| Tag | Content |
|---|
EnhancerAtlas ID | HS091-45063 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:139705180-139706890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr7:139706078-139706089 | CCACACCCTGC | + | 6.62 | | Myod1 | MA0499.1 | chr7:139706225-139706238 | TCCAGCTGTTCCT | + | 6.09 |
|
| | 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 |
| GH07I140005 | chr7 | 139705761 | 139705870 |
|
Enhancer Sequence | ATCACACCAC TGCACTCCAG CTTGGGCGAC AGAAAAAGAC TCTGTCTCAA AAAAAAAATA 60
AATAAATAAA AGATAAAGTT ATGAAGACTC TCAAGACAGC GCCACAGAGG ATTAACCCCC 120
GCACAGAGCC CTTTTCATTG GTCACTTGCT CAGCCAGCTG CCCCAGTGGC CTGTGATGGG 180
AGTGGGAAGT GTGGGGTTGG GTGATAACCT TCTAAAGTTA GAACCGTTCC CAGAAATGCA 240
GACGGGAGAG CTTTGGGAAA ACCATCCAAA CCTTGTTATT TTTTATGACA AAGTAGGAAT 300
GCCACCCTGG CCCTCTAAAT TCATAAACAG TCACAGACAT GGGATTAAAC TACATATAAT 360
TTCTGCAACG TGGCTTATAG GCATCATTAA ACAGCTGCAA TATGTTGAAT GGCTATGTCA 420
TCATAGATTA GCTACGATAC TGGCTATGGA CTTCAAGACT CCATGTGTCC TGGCCCCTGC 480
CCTTCCACCC CTCTGACCCG AGATGCAGTT CTAACAGGTT CCCGGGTGAT GCTGCTGCTG 540
CTGACCCTTG CCCATCCCGG AGCTCACTTT GAGAGCTGGC TGAGATCCCA GGCAGGGTGG 600
CCAGTGGCTG CTCCAGGGCT GTGAAGGGCT CCCCCTGCAG ACGGAGGAAC TAGGCCTCCC 660
AGCGCCTGTA ACTGGAACGT TGGCGGCTTG AGAATGGACT TGCCCTGAAG GCCGGCCTCC 720
TGCTGCTCTG GGAAAAAGAG GGAACAGAAG AAAGCAATCC GCCACCTTGG GGACTCCTCC 780
TGGATTAGCA TTATCTAGGT GAAGAAAGTG AGACCATCAC CTACCAACCA GATAACTCAT 840
TCCACCTCTG TGGGCAAACT GGCAGAGCAG CAAATAAGCT TCCTTAATCC CAGTGCGCCC 900
ACACCCTGCT CAAGAGCTCA TGGGCACGTG TTCATCTTCA GGCCAAAGAT GGGGAGCCAG 960
GGAGTGACAG ACTGTCACTC CAGGAGAGTC ACCCGGGGGT GTTAGGATCC CCACATTTGC 1020
ACCCCCTGAA ATCTAATCAG CATTTTCCAG CTGTTCCTAA TCTGACCTGT GCAAATGGAA 1080
TCTCATTGGA ACTTGCATTT TTCATTATAG TAACTCATAT GGCCTCTGTG TTTCGCCTGT 1140
TCATAGCCTT TGACCATTTT TCTAGCTAGT TGTCTTTTCC TACTGACTGA TAGTAGCTCT 1200
TTGGTTTTTG TTACTGTTAG TCCTTTATAG ATGTGGCAAA CTTTTTTATT TGCTATTTCA 1260
CTATTTGCCT TTTGACTTCA TAATGTGCCA TGACTACCCA TGTGACAGGC TCTTTGAGCC 1320
TCAGTTTTCT CATCTAAGAG ATGGGGAAAC AGTCACCACA CTGGCTTAGT GGAGCATCAA 1380
ATGCGGTAAC GTCTATGCTG CACTTGGTCG GCCACATCGT CAGCTCCCAA TAAATGCTGG 1440
CGGCTGTGGT TGCCGCTGCA GTTTTATAAC CAAACTTCTC TGTATTACGA AGACCCCTGA 1500
GCCCCAGGCT AGCACCGTGA AATATAAGCA CAATAGAACC ACTGAGCGCC AATCAGATGC 1560
AATTTGGGTC ATACCGACTT TCCATTTTGT GGGGTTTCTG TTTAAATGTT TGCCAAAGTT 1620
GGAAACGAGA TTGAAATTTA AGGAAAAGAC AAAATGCTGT GAGATTTGGG CTAACACGAA 1680
CTTCTCCCTT TGTCACGACC CCTCCATCAG 1710
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