ID: 132088597 | Neanderthal introgressed variant-containing enhancer experimental_1250 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169531606..169531775) | | |
ID: 129931898 | ATAC-STARR-seq lymphoblastoid active region 2078 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169696872..169696921) | | |
ID: 129931897 | ATAC-STARR-seq lymphoblastoid active region 2077 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169680485..169680734) | | |
ID: 129931896 | ATAC-STARR-seq lymphoblastoid active region 2076 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169658989..169659078) | | |
ID: 129931895 | ATAC-STARR-seq lymphoblastoid active region 2075 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169604869..169604978) | | |
ID: 129931894 | ATAC-STARR-seq lymphoblastoid silent region 1546 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169485589..169485768) | | |
ID: 129931893 | ATAC-STARR-seq lymphoblastoid active region 2072 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169485349..169485408) | | |
ID: 129388627 | MPRA-validated peak449 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169539087..169539287) | | |
ID: 129388626 | MPRA-validated peak448 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169526607..169526807) | | |
ID: 129388625 | MPRA-validated peak447 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169510738..169510938) | | |
ID: 127270801 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:169636965-169637470 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169667727..169668232) | | |
ID: 127270800 | H3K4me1 hESC enhancer GRCh37_chr1:169555695-169556194 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169586457..169586956) | | |
ID: 127270799 | H3K4me1 hESC enhancer GRCh37_chr1:169555193-169555694 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169585955..169586456) | | |
ID: 120893165 | Sharpr-MPRA regulatory region 5964 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169485951..169487001) | | |
ID: 112577512 | Sharpr-MPRA regulatory region 2803 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169576331..169576625) | | |
ID: 107985745 | uncharacterized LOC107985745 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169662332..169683932) | | |
ID: 10560 | solute carrier family 19 member 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169463909..169485970, complement) | TC1, THMD1, THT1, THTR1, TRMA | 603941 |
ID: 6403 | selectin P [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169588849..169630124, complement) | CD62, CD62P, GMP140, GRMP, LECAM3, PADGEM, PSEL | 173610 |
ID: 6402 | selectin L [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169690667..169711620, complement) | CD62L, LAM1, LECAM1, LEU8, LNHR, LSEL, LYAM1, PLNHR, TQ1 | 153240 |
ID: 2153 | coagulation factor V [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169511951..169586481, complement) | FVL, PCCF, RPRGL1, THPH2 | 612309 |