Tag | Content |
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EnhancerAtlas ID | HS180-50785 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chrX:20430630-20432310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chrX:20431040-20431060 | AGGTTGGGGGTTGGTGGGGG | - | 6.32 | RREB1 | MA0073.1 | chrX:20431041-20431061 | GGTTGGGGGTTGGTGGGGGG | - | 8.14 |
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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 |
GH0XI020412 | chrX | 20430635 | 20433205 |
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Enhancer Sequence | CTGCATCTAT TGACCCATTC TCTAAGCTCC CTCCCCTTAC CCCAACCCCC AACAGGCCCT 60 GGTGTGTATT GTTCCCCTCA CTGTGTTCAT GTGTCCTCAA TGTTTAACTC CCACTTATGA 120 GTGAGAACAT GTGGTATTTG ATTCTCTGTT CTTGTGTTAG TTTGCTGAGG ATGATGGCCT 180 CCAGCTTCAT CCATGTCCCT GCAAAGGACA TGATCTCATT CCTTTTTGTG GCTGCATAGT 240 ATTCCATGGT GTATATGTGC CACATTTTCC TTACCCAGTC TATCATTGAT GGGGATTTGG 300 GTTGGTTCCA TGTAAATAGT GCTGTCTCCT GTGGGCTTCC CCTGAGGCTG GGCCCCTGTA 360 CTCCCGATGC CACTCAGATT TGTGCCTACA GGGCCAAGAT CAGCTCGGCG AGGTTGGGGG 420 TTGGTGGGGG GGGACTGGCA CTTGTGTCAG AGAAATGCCA GAAAAGCTCT GCCCAAGAGC 480 CGGAAGTTGC GTCTGTGTGT ATGTACTTCT TTGCTTTTGT TGTGTTCTCA GCCCTCGCAG 540 GGACTCTAAC CACTTCCCCC TGAACTTCAG GCCGTACGGG AACCTCACCT CTCTTGCGGT 600 AGTGGTCCTT CTAAATTCGG GCCACTCGAC TCATTCCTTC CTGTCTCATT TTGTTCTTCC 660 TGCCTCTTCT GTGCATGGGG GCTACATTAC TGATGCTGCG GTTGCCCAGT TGGAGAGGAG 720 AGCAGTAGTA TAAGAAAAGC ACCCTGGACC TGTGCCCCTC AAAGCGAGGT CCCTGGGCCA 780 GCAGCATCGG CTTTACCTGA GAACTGCTTA GAAATGCAGA CTCTCTGGTG CCACCCCAGA 840 CCTCCTGGAT CTGCCTCTGT ATTTTAACTG GACCCCCAGA GGTGTCGTCA AGCCTGAGAA 900 ACACCAGCAT CTGGTTACAG CTCGCCAGCC CTTTAGCTCT GTAACCTGGC AAGTCTCTTC 960 GCTTCTCTGT CGGACACACT GATTTCCCCT GTGTCAAATT AGATGCATTT AATTATGTGG 1020 TAATTCAGAT TACTTTGTTG CTTCATCAGA GAAGTACAAA GGTGTGGGAA GTGGCAGAAA 1080 ATCATATTGT GCACAAAATC AAGAACTTTT AGAGCTGGAA AGAACTTGAT TGACCACCTC 1140 CTCCAGTTCC CTCTTGTTTT ATAGCCACTT AAGGTCAAGC CTTGCTAAGG AGAATGTCAG 1200 TCTCCTCCAT CCTTCCAGGA GAAACACAGC CCCTGCAGTC AGAAGAGACA GGAAGGCCAC 1260 ATGAGACAGG AGGGAATGAG CCGACTGGCC TGAATTTAGG AGGACCACTA CCATAAGAGA 1320 GGTGATGTTC CCATATGGCT TGAAGTTTAG GGGGAAGTGG ATCCCTGATA TGAAAATTGT 1380 GGTCCCTGAA CCAGTAGCAT TACAGTCACC TGGTAAGAGA GGCAGTGGGT GGTGTGCGAG 1440 AAATGCGGAT TCTCAGGCCA AGGCTCATAC CTACTTGATA AATAGAGTCA AAATCTCTAT 1500 ATACCAAGAA CCCCGGATGA TCTGTAAGCA CAGCCAAGTT TGGGGAGCGC TGGGCTAAAT 1560 GACGCAGTCA CTGGGAATGC TTGAAGACAA ATGAAGCCCA GAATAGAAGC GTCATTTCCC 1620 AAGTAGTAAG AGTGCTGGCC CTGGAAGCAA AGAAATGTAG ATTTGAATTT CAACTTGCCA 1680
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