Tag | Content |
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EnhancerAtlas ID | HS091-48317 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr9:115123580-115124950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr9:115123966-115123985 | CAGTGCCACCTGGTGGTGA | - | 7.95 | Lhx3 | MA0135.1 | chr9:115124772-115124785 | AAATTAATTATTT | + | 6.78 | Nr2f6(var.2) | MA0728.1 | chr9:115123597-115123612 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH09I112361 | chr9 | 115123881 | 115124030 | GH09I112362 | chr9 | 115124081 | 115124280 |
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Enhancer Sequence | GTTGGTCAGG CTGGTCTTGA ACTCCTGACC TCAGGTGATC TGCCCATCTC GGCCTCCCAA 60 AGTGCTGGGA TTACAGGTGT AAGCCATGGC ACCCAGCCTA AACTTCATAG ACTTTAGAAG 120 CCACAAAACA AGGGAAGATA ACTTTGTCCA TTTTATGGTA ATTTTGAAAA CGTTAATAAT 180 ATAAAATGGA TTGGAGTATC ATATCCTGTT TTAATGATTC AAAGCATTAT TTTCATTAAG 240 ACATTTAAAT TTCTACCTTA TTTTCCTTTT TTGAGAGCTA TAGAAAACTT TGTTATTTTT 300 GCCTTAACCC AAGTCAATTA TTATATCACA ATATTGTTAA TAAATTAACA TTTTGTGGCA 360 TTATACAATT TTGAATTTTA AAATAACAGT GCCACCTGGT GGTGACTCTA AACATGTTTT 420 TATTTCTCTT CGGTATACAT ACCAAAAAGT GGAATTGCTC TTTTGACTGT GGACATTCGG 480 GAACTAGCAA GTGTGTTTAA CCTGAGAGAC TGCCAAACTG TTTTTCAAAG CTACTGAACC 540 ATTTTATACT TCCACCAGTA ACGTATGAGG GTTCTAATTT CTCCACATCC CATCCGACAC 600 TTGTTACTTT CCTTTTTTTT ATTATAGTCA ACCTAGTGGG TGTACAGTGG AATCTCATTG 660 TGGTTTTGAT TTGCATTTCC CTAAGTAATG CTATTGAGCA TCTTTTCATG TGCTTGTTGC 720 CATTAGTATA TCTTCTTTAG AAAATTATCT ATTTGGGGAC AGGCATTGTG GCTCACACCT 780 GTAATCCCAG CACTTTGGGA GGCTGAGGCA GGAGGATTGC TTGAGTTCAG GAGTTTGAGA 840 CCAGCCTAAG CAACATGGCA TGACCCTGTC TCTACAAAAA GTATGAGTCT GTAGTCTCAG 900 CTACTCAGGA GGCTGAGAGG GGAGGATAAC TGAGAGGGAG AGGTTGAGGC TGCAGTGAGC 960 CATGGTTGCA CCTGAGCAAC AAAGTAAGAC CCTGTCTAGC AAAAGGAAAA GAAAAAATAT 1020 CTATTCAAAT CGTTGCCCAT TTTTTAGTTG GGTTGTTCAT TTTTCTGTAG CTGTTGTAAG 1080 AATTCTGTGT ATATATTGGA CACTGGAGCC TTATCAGGTA TATGATTTAT AAGTATTTTT 1140 TCTCATTCTC TAGGTTGTCT TTTCACTTTC TTGATAGTGT CCTGGGATGC ACAAATTAAT 1200 TATTTTAATT CTTATGAAGT TCAATGTATC TTCTTTTTTT TCCCTTCTGT GGCTTGTGCT 1260 TTTGGTGTCA TATTTAAGAA TCCATTGTCA AATCCAAGGT CATGAAGATT TACCCTTATG 1320 TTTTCTTTCA AGAGCTTTAT AATTTTAGCT CCTACATTTA AGGTCTTTGA 1370
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