Tag | Content |
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EnhancerAtlas ID | HS108-36017 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr6:158675950-158677430 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH06I158256 | chr6 | 158677046 | 158677848 |
| Enhancer Sequence | AAAATTAACT GGGCATGGTG TCAGGTGCCT GTAGTCCCAG CTACTCAGGA GGCTGAGTCA 60 GGAGAATCAC TTGAACCCAG GAGGTGGAGG TTGCAGTGAG CTGAGATTGC GCCACTGCAC 120 TCCAGCCTGG GTGACAGAGT GAGACTCTGT CTCAAAAACA AAACAAAACA AAAGCAACAG 180 AAAAACTCTG TGTCCCTTGT CTTACTCCCT CACCCCCACC CTGTGGCCTC CCTCTGCATG 240 GATCCTGTCA TGTTTATGAA TCCCCCTGCA GGTGTTGCTG GAGGGGGCTT TCTCTTGGCA 300 GTTGTAGACA CTGTTGGGGA CCAGAGCATG TACCCTAAAT TGATAACCGG CAGACCCTGT 360 CGAGTGCATA TCTAATGTTC TTTCTTCCCT TCTTTCTAAG TAGAATTGGA ATTTTGTTTA 420 GAGAGCCTCT TGTCTCCTGT GTGACTCTGG GGAAGGTGAT CTTATCCCTA GCACTGGGGT 480 AAATCCTGAC TGGTTTCAGC TAGTCACATG GGTCCCATTC TCCGTAGGTG ATGACTGTAG 540 GGGTGAGCCA GAGACCTAGT TCTGGTCAGT GAGATTAGTG GGAGGTCTGT CCAGAGGTTC 600 TGGAAAACTC AGCCTTACAG CAACAACTCT AAGAATGGTG GCCTTTTCTT CCTCTGAAAG 660 TTGTCATGTC TGGGTGTGGT GCCTGGAACT GTTACAATTG TTTTGCTACT GGTCTGAGCA 720 TGAAGCCAAC ATCAGGTTAA GGACTGAGCC AAGCCAACAG CAGAGAGAAC TCTGCAGAGC 780 CCCAGTGCAC CATGCTTGGC ACCCACTAAC CTTGGACTTG TTCTGTGAAA TAAATTTTCT 840 TATTGTTTAC ACCAATTTAA GTTAGGGTTA TCTGTTATTT GCAACCGAAG ATGTGCTAAC 900 TGATGCAATA GCTGTCATTC TTTCCCTCAT TGCATGAAGA AGTACAGGGT ATAAAGGCAG 960 AATTGATCTA GTCAGAAGGT CAGAGGTGGC TTCCCTGGGG AAATGCAGAG GCCTTGGTGG 1020 GAGAGATCCC TTTTCTTGCT GGGCCTCGTG TGCCACATTT AAGGATTTTG GTCTTTATCG 1080 CAAGAGCAGA GCCTGTTATA GGTTTAAGTA CTGGGCTATG GCATGAATGC AGTGAACTCT 1140 TACTATTTAA AGTAACTCTC TAGTTACTTA AGCTACTCCT CCTGAAGAAC ACCTTGGCTT 1200 AACATTCCAG AGTTGAGTTT GATTTGCTGA GCAGGCAAGG AGCAGTCAGT GGTTAAGGCT 1260 TTGGTGATTA GTAGGTGTGT CCAGAAAGCA CAGAAGAGCA TCTTTGCTTG GAATCTGATG 1320 AAGTGAACAG CCCAGATTGT TTTCTTTTTT CTTTGCCAGT GCGTGCATGT GTGTATGTGT 1380 TTCTGTATGT ATGTATATAT ATAACTTCTG TGTGTGTGTG TATACGTGGT ATGTATACTA 1440 ACATGTACAC ACATATACCA CACTCACACA GGCAGCTTTC 1480
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