| Tag | Content |
|---|
EnhancerAtlas ID | HS108-03883 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:204775830-204776960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:204776244-204776263 | TGCTGCCCCCTAATGGCAG | - | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 204775985 | 204776903 | | chr1 | 204775838 | 204776474 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I204806 | chr1 | 204775721 | 204776774 |
| Enhancer Sequence | GCAAAAACAG GCAAATAGGA TTCCATTAAA CTAACAAGCT TCTGCACAAC AAAGGAAATG 60
ATCAGCAGAG TGAAGTGACG ACCTACAGAA TGGGAGAAAA CATTCATATA CTTCGCATCT 120
GACAAGGGGT TAATATCCAG GACACACACG GAACTCAAAG AATTGTAAGT CTTAAACGAT 180
GGCTTTAAAC AAATTTTGTG AAAATTTAAC CATCAGGTCT GGTATAAGCC AGCTCCAGGA 240
CACCACTGGA AGGGTTCCTG TTTTGGAAGC TGGACTCTGT CCTCCTCTTG GAGCCCTCGG 300
AGAGAGCAAG CGAGGCTGCT CTGTTCTGGA GGCTCCGTGC CCCTGAGGCC TTTGACCCCG 360
TTACCCGCGT TCCTCCCCTT GAAGCCCGGT CCCGCTCTCC CAACACCAGT GTTCTGCTGC 420
CCCCTAATGG CAGCTTCTGC CATCTGCGGC TGTCCGGGAG CTAGATCCAC CGCAAAGTCC 480
ACCAGCTCCG CTCCAGGATC AGAGACCCCT GAGCAGGTTA AACAATCTTC CCCCTCCACT 540
CCAGACTTTT GGAACCCAAG GACGGCCGGG TCAGAGTACC CAGGACCTCA AGCCCCGCTG 600
CCCCTTGTCC ATCCCAGAAT CGTGGTTTCC CACTGCCCTC TGCAGTGCCG CGGCGAAGTG 660
ATGAGCCCGG CACTGTGGCG CCACCTAGTG CCTCTGCTGG GTCAGTGGCA CCTGCACCTG 720
CACTGCCAGC CCCCTGCTGG GAGAATTCCG ACTCAAGAAC TGTAGTTTGT TGTGTGTTGT 780
TTTTGCTTTG GGGCTCACTG GGAAACTCTC ACCAGTCACC TGCATTACAG CCTGGGGCTT 840
CCTGTCACTG TAGAGCAGGT AAGAAGAGGA GGGAAAGAAA AGACCTCAGC AGCACAGCAC 900
CAGACCTTCC TCCACTTGGT GGGGCCTTCT GACCACGAAT GGTGAATAGT CCAACTAACA 960
ACTAAAAGCT CCAGCTGGGA GGACCCTGGA GCTCCCCTGA GCCTGTGGCC TTCAAACGGT 1020
ACTGACCAAG CCCATCAGTA AGCAGTGCAT TTTACAACGC AACAGTCCAG GACACCCCTG 1080
CGTTGAAAGA ACTCAGGAAG CAATACTTAC CCTTAGTATG CATAGCGTAT 1130
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