| ID: 127882533 | H3K4me1 hESC enhancer GRCh37_chr7:73995345-73995846 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74581016..74581517) | | |
| ID: 127409573 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74075507-74076155 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74661176..74661818) | | |
| ID: 127409572 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74031728-74032292 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74617409..74617973) | | |
| ID: 127409571 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74031162-74031727 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74616843..74617408) | | |
| ID: 127409570 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74002117-74002703 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74587788..74588374) | | |
| ID: 127409569 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74001529-74002116 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74587200..74587787) | | |
| ID: 127379775 | H3K4me1 hESC enhancer GRCh37_chr7:74203411-74204070 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74789067..74789726) | | |
| ID: 127379774 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74201830-74202532 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74787486..74788188) | | |
| ID: 127379773 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74186639-74187184 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74772292..74772837) | | |
| ID: 127379772 | H3K4me1 hESC enhancer GRCh37_chr7:74181785-74182286 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74767440..74767941) | | |
| ID: 123956164 | Sharpr-MPRA regulatory region 2459 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74581480..74581774) | | |
| ID: 113218504 | microRNA 10525 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74595968..74596026) | | |
| ID: 106029312 | Williams-Beuren syndrome medial block B recombination region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74733937..74869227) | | |
| ID: 101926943 | GTF2I antisense RNA 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74688937..74728918, complement) | | |
| ID: 100873752 | PHB1 pseudogene 15 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74741457..74742121, complement) | PHBP15 | |
| ID: 653361 | neutrophil cytosolic factor 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74774011..74789315) | CGD1A, NOXO2, SH3PXD1A, p47phox, NCF1 | 608512 |
| ID: 84163 | GTF2I repeat domain containing 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74796151..74851605, complement) | FP630 alpha, GTF2IRD2A, GTF2IRD2 | 608899 |
| ID: 9569 | GTF2I repeat domain containing 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74453906..74602605) | BEN, CREAM1, GTF3, MUSTRD1, RBAP2, WBS, WBSCR11, WBSCR12, hMusTRD1alpha1 | 604318 |
| ID: 2969 | general transcription factor IIi [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74657718..74760692) | BAP135, BTKAP1, DIWS, GTFII-I, IB291, SPIN, TFII-I, WBS, WBSCR6 | 601679 |