Tag | Content |
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EnhancerAtlas ID | HS108-03697 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:197644270-197645660 | Target genes | | | 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 |
GH01I197675 | chr1 | 197644531 | 197645330 |
| Enhancer Sequence | ATTAAAAAGA AAAAAGAGCA AATATCTTAA TGCAGCAGTC ATCCTCACTG AACAATATTT 60 TTGCTACCAC TTCTTTGCCA CTAAAACTAA GGTCTACAGA AGTCATCAAT ATCTGAATAT 120 TTAAACCGTA TACATAAATA TAGCATTGAG TGTTTTAAAG TAGAATTTCT TGCATTCTTT 180 TAAAAAGGTA GACTACAATA AAGTGTCAAC TAAAAATAAA ACATTATAAA ATTCCAATAC 240 CAATACCTAA GAAAGCTTCA GTGCCTTAAT GCACATAAGC AGAAAGAAAA GGATCTTGTA 300 AAAAAAAAAA TCATCTACTC TTAGGGCAGG GTACCCTGGA TTGCTTATAA TCATAATCAT 360 GTACCTTTAA AAATATGAGC ACAGACTCTA TATTAAGCGA AAGCTAACTG TTTCACCACT 420 GACAATATTT TGTTAAATGT AGTTAAAAGA GTCACTAAAC TTGCAGTAAG TTAAATTCTG 480 TAAACTGAAA AACAGTTCAT TGCAAATGAG ACCAGTTCAT TTTCATTTGA CCATTGCTTA 540 ATCCTTATCT TGTACTTCAT AAAGTGAAAC CATTCACCAT TTTTACTATA CATGTGAACA 600 CTATTCAGAC CTCCTCCTAT AAAATTGTCC ACATAATTTC TGTAACAATA AAGAACATAT 660 ATTCAAAATT CAATATCTCC CTCTAAATAC ACAAATTAGT AATATATTTC ACATCAATTT 720 TAAGACTCAA GACGAACGCT TCCCAGTTAG TTGCTCAATC TTTCACACCC TCCCCCTCCC 780 TTCTTCCACA AGCAACACAC GTGCATACAC TTCTGTGAAA CAGCCTCAGC TCGCTTCCCA 840 ACTGGCAGAA GCATCCCTCA GGGGACAAGT CTTTAAACCT CCGCACTCTT TAAAATTCAA 900 CCAGCCAGCA GGTCTATAGA CTAGTGTATA AACAGTATAG ACAAAAAAAA AAAAAAATCC 960 TCTCTCAGCT TATGTCAGTG ACAAAGCAGC TCAGCAGTTG ACTGTTTCTC CCCTGACAGT 1020 ATAAACTGGG TTTACACAGA TCAATAGCTG GAAGTCCTAC CTAGCTCCCA GGGCTTGGTT 1080 TTCTTCCTTA ATTACAGGTG CTATTGAAAC TGAAGTGTAA AAAGAAAAGA GAGAGACTTG 1140 GAAGGAGGCA TAAAATGCAT GCAAATAGCT TTTATGGATC CTCTTAGCAA TAGTATTAAT 1200 TGAAAATTAT ACTTCCACAT TTATTACAAA AGTGTGTGTG AAGGCTGGTA TTTTCACTAC 1260 ACAGTGTTTT TAATATGACA CATATACAAA CACACACACA CACACGCACA CACGAAATCC 1320 TAGGTTAGCA TCCACAGATT ATGTGAAAGG TTTAAGACAA TACTCTCCAG AAGTTATCAA 1380 TTTTTCCTTT 1390
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