| ID: 127895972 | H3K27ac hESC enhancer GRCh37_chr22:35695462-35695984 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35299469..35299991) | | |
| ID: 127895971 | H3K27ac hESC enhancer GRCh37_chr22:35652780-35653280 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35256787..35257287) | | |
| ID: 127895970 | H3K4me1 hESC enhancer GRCh37_chr22:35573611-35574112 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35177618..35178119) | | |
| ID: 127895969 | H3K27ac hESC enhancer GRCh37_chr22:35554225-35555056 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35158232..35159063) | | |
| ID: 127895968 | NANOG-H3K4me1 hESC enhancer GRCh37_chr22:35531129-35531665 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35135136..35135672) | | |
| ID: 127895967 | H3K4me1 hESC enhancer GRCh37_chr22:35419897-35420488 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35023906..35024496) | | |
| ID: 126863132 | MED14-independent group 3 enhancer GRCh37_chr22:35567219-35568418 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35171226..35172425) | | |
| ID: 126863131 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr22:35472054-35473253 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35076061..35077260) | | |
| ID: 125446225 | Sharpr-MPRA regulatory region 1139 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35154634..35155170) | | |
| ID: 124905110 | uncharacterized LOC124905110 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35072782..35075971, complement) | | |
| ID: 106479088 | RNA, U7 small nuclear 167 pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35249772..35249833) | | |
| ID: 105373017 | uncharacterized LOC105373017 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35232643..35261525, complement) | | |
| ID: 104310353 | long intergenic non-protein coding RNA 1399 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35119824..35231056, complement) | | |
| ID: 114657 | COX7B pseudogene 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35194401..35195027, complement) | bK714B7.1 | |
| ID: 91464 | intestine specific homeobox [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35066158..35087387) | Pix-1, RAXLX | 612019 |
| ID: 10043 | target of myb1 membrane trafficking protein [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35299275..35347973) | IMD85 | 604700 |
| ID: 10042 | HMG-box containing 4 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35241536..35295807) | HMG2L1, HMGBCG, P53N, THC211630 | 604702 |