| ID: 129933383 | ATAC-STARR-seq lymphoblastoid active region 15507 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27430518..27430817) | | |
| ID: 129933382 | ATAC-STARR-seq lymphoblastoid silent region 11302 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27428999..27429148) | | |
| ID: 129933381 | ATAC-STARR-seq lymphoblastoid silent region 11301 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27409572..27409761) | | |
| ID: 129933380 | ATAC-STARR-seq lymphoblastoid silent region 11300 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27409292..27409481) | | |
| ID: 129933379 | ATAC-STARR-seq lymphoblastoid silent region 11299 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27409172..27409221) | | |
| ID: 129933378 | ATAC-STARR-seq lymphoblastoid silent region 11298 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27409072..27409151) | | |
| ID: 127272959 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:27665383-27665925 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27442516..27443058) | | |
| ID: 127272958 | H3K4me1 hESC enhancer GRCh37_chr2:27618171-27618672 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27395304..27395805) | | |
| ID: 126806174 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr2:27681686-27682885 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27458819..27460018) | | |
| ID: 126806173 | BRD4-independent group 4 enhancer GRCh37_chr2:27676057-27677256 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27453190..27454389) | | |
| ID: 106481491 | RNA, U6 small nuclear 986, pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27475494..27475595, complement) | | |
| ID: 200634 | keratinocyte associated protein 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27442381..27446481) | KCP3 | 619261 |
| ID: 64838 | fibronectin type III domain containing 4 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27491883..27495200, complement) | FRCP1 | 611905 |
| ID: 29959 | nuclear receptor binding protein 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27427790..27442259) | BCON3, MADM, MUDPNP, NRBP | 606010 |
| ID: 26160 | intraflagellar transport 172 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27444377..27489743, complement) | BBS20, NPHP17, RP71, SLB, SRTD10, osm-1, wim | 607386 |
| ID: 5496 | protein phosphatase, Mg2+/Mn2+ dependent 1G [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27381199..27409591, complement) | PP2CG, PP2CGAMMA, PPP2CG | 605119 |
| ID: 2498 | ferritin heavy chain 1 pseudogene 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27392623..27393576, complement) | FTHL3, FTHL3P | |