| ID: 128772435 | melanoma risk locus-associated MPRA allelic enhancer 22:38608227 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38212148..38212292) | | |
| ID: 127896198 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:38685261-38685970 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38289255..38289964) | | |
| ID: 127896197 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:38679509-38680035 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38283503..38284029) | | |
| ID: 127896196 | NANOG-H3K27ac hESC enhancer GRCh37_chr22:38667767-38668476 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38271761..38272470) | | |
| ID: 127896195 | H3K4me1 hESC enhancer GRCh37_chr22:38659892-38660392 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38263886..38264386) | | |
| ID: 127896194 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:38624990-38625720 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38228984..38229714) | | |
| ID: 127896193 | H3K4me1 hESC enhancer GRCh37_chr22:38620666-38621166 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38224659..38225159) | | |
| ID: 127896192 | H3K4me1 hESC enhancer GRCh37_chr22:38618750-38619250 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38222743..38223243) | | |
| ID: 127896191 | H3K4me1 hESC enhancer GRCh37_chr22:38609813-38610394 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38213806..38214387) | | |
| ID: 126863147 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr22:38614213-38615412 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38218206..38219529) | | |
| ID: 106635525 | small nucleolar RNA, H/ACA box 92 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38224479..38224720, complement) | | |
| ID: 106481115 | RNA, 7SL, cytoplasmic 704, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38231721..38232000) | | |
| ID: 25829 | transmembrane protein 184B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38216395..38273010, complement) | C22orf5, FM08, HS5O6A, HSPC256, SLC51C2 | |
| ID: 23764 | MAF bZIP transcription factor F [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38201994..38216511) | U-MAF, hMafF | 604877 |