| ID: 127886615 | NANOG hESC enhancer GRCh37_chr17:35814497-35815074 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37454395..37454972) | | |
| ID: 127886614 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:35768105-35768789 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37408018..37408702) | | |
| ID: 127886613 | H3K4me1 hESC enhancer GRCh37_chr17:35712269-35712768 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37355326..37355825) | | |
| ID: 127886612 | NANOG hESC enhancer GRCh37_chr17:35499293-35499794 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37142369..37142870) | | |
| ID: 127886611 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:35464619-35465223 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37107684..37108288) | | |
| ID: 127886610 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:35464014-35464618 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37107079..37107683) | | |
| ID: 127886609 | H3K27ac hESC enhancer GRCh37_chr17:35460987-35461591 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37104052..37104656) | | |
| ID: 127886608 | NANOG hESC enhancer GRCh37_chr17:35446662-35447163 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37089727..37090228) | | |
| ID: 127886607 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:35422902-35423456 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37065602..37066156) | | |
| ID: 127886606 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:35421791-35422346 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37064491..37065046) | | |
| ID: 126862545 | BRD4-independent group 4 enhancer GRCh37_chr17:35453499-35454698 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37096564..37097763) | | |
| ID: 106635523 | small nucleolar RNA, H/ACA box 90 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37244801..37244975) | | |
| ID: 100420063 | high mobility group box 1 pseudogene 24 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37143461..37144379, complement) | | |
| ID: 100419621 | ribosomal protein L24 pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37454156..37454973) | | |
| ID: 100271604 | ribosomal protein L18a pseudogene 12 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37162580..37163196) | RPL18A_7_1543 | |
| ID: 100271251 | ribosomal protein S2 pseudogene 49 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37140569..37141413, complement) | RPS2_24_1542 | |
| ID: 284099 | chromosome 17 open reading frame 78 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37375985..37392708) | | |
| ID: 6871 | transcriptional adaptor 2A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37406886..37479725) | ADA2, ADA2A, KL04P, TADA2L, hADA2 | 602276 |
| ID: 31 | acetyl-CoA carboxylase alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37084992..37406836, complement) | ACACD, ACACalpha, ACC, ACC1, ACCA, ACCalpha, Acac1, hACC1, ACACA | 200350 |