Tag | Content |
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EnhancerAtlas ID | HS082-22942 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr3:16281100-16282590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr3:16281877-16281888 | GATGAGTCACT | - | 6.02 | JUND | MA0491.1 | chr3:16281877-16281888 | GATGAGTCACT | - | 6.32 | STAT3 | MA0144.2 | chr3:16281973-16281984 | TTTCTGGGAAG | + | 6.02 |
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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: 1 | ID | Chromosome | Start | End |
GH03I016238 | chr3 | 16280447 | 16282664 |
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Enhancer Sequence | GCCACTGCTA TCATAATCGG TCAAACACTC TGGGAAGCAA TGGTGTTCTG ATTTCTTTTA 60 CTGCACAGCT TCCAATAAAA TTTGTGGCCC AGGTGTGACA ACCAATAGAA CTCTTTCACT 120 TTATTCTTGT CTCTGAGATT CTGGTTTCTA CTTGCTTTCT AAAAGAAACA TAAAAGGCAA 180 GTAAGCATGG CGTGTAAAAG TGAAGGGGGT GGGCTTCCCA TGGGATATAT GATGATTTTC 240 TTCCTTTGTT GTAAACATAT GATATAGGAA GTTGCGTGAG AATCTTGCTT AAAACAATAG 300 TGACAACCTT TTAACCCCAT CTGCTTCCCA TTAATGGGAA AAGCCGTTAC ATGGTAGTGT 360 CAAGGGGCCT CTGGATTTTC TCAAGGCTTT ACCATAAGAC AGATGCTTAA GACAAAATCC 420 TCCAACCCTT TGGTTCTAAT CCTCCCCTTC TTAGTCCATT CAGAAAGCAC AGAAGGTAAT 480 GGCATCTGGC CGATACTCAT GAGGGCTGGG TTGGTAAAGT GAAAACCTTT CTGTGCTGTG 540 ACAAATTTCA CTGGCTGTGC TTTAGGTAGT TTGCAAAGCA CAAAGTTAAG TTTCTGGATG 600 ATATGTTCAT GATTAACAAA CCAGATTATA ATGCCCTTTC CAGAGTGAAT TCTAGTTCTT 660 AGGATTACTT TGCAGATTTA AAAACAATAA ATATTTATTA AATATCTGTT ATTTACCAAG 720 GTCACACCTC TAGGGCCTTG TCCCGTGTGT TTTCTGAACC ACTGGCGTGG ATGACTTGAT 780 GAGTCACTCA TGAATCAGAA AATTGCAAAA TATCATCTTC ACTGAATTTT ATGTCAGCAC 840 AGACTCAGTC AGAGTTGAAT ATGGACTCCC TGGTTTCTGG GAAGGCAGAG ATATTTCAAA 900 AACATTTCCA GGAAGGCAAT CAAGTGCTCC TTTTGATGCA TTTGCCAAGT GGGACACAAA 960 ATAGACCTAT ATTTGTAAAT AACAATCTTT TTCAAACACT GCCATGGGGA TATGCCCAGC 1020 TTATAGTGAT CCTTAAAATA TGTATTGTGA AGTAATAATC CACCTATGTT TCAGTAATTT 1080 CCAAGTGTTT CTCCAGCCTT GACTCCAACC ATGAACCTCA GATTCACACA CTCAAGCACC 1140 TTCAATCTAC ACTAGAGCCC GAGTAATCAA CCTAAAGCAC TCTCCTTCCA TAATCTCTTC 1200 TATGACTCCG CATCACCTTC AGAGTAATGA CCCGCCTCCC CAGCACAGCC TGACTACAAG 1260 TTCCTCCCTG ACCCTGCCTC CACCCTCTGG ACTCACCTGC TACTATTTGC CCCATCTCTG 1320 AACACCAAAG TTTTTGTAGT TCCCAATACA ACACCCTTTT CCTTGTCTCT GCTCTAACCA 1380 TGCTCTGTTC CCTCTGCACA GAATGCCCTT CCCTCCGTTT GCCAGCTTCT TCTTACCTAT 1440 CATGCATGAC TCATATACAT CATGTCTCTG GAGGGTCTTC CTCGAACCCC 1490
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