Tag | Content |
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EnhancerAtlas ID | HS048-19728 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:10550080-10551290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr2:10550854-10550869 | GACTTCCTGAGAAAT | + | 7.77 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_31666 | chr2:10550764-10551529 | Gastric | SE_47142 | chr2:10539677-10552485 | Panc1 | SE_51031 | chr2:10544683-10550562 | Sigmoid_Colon |
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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 |
GH02I010403 | chr2 | 10544013 | 10552288 |
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Enhancer Sequence | TAATTTTTTA TATTTTTAGT AGGGACGGTT TCACCATGTT GCTCAGGCTG GTCTTGAACT 60 CCTGAGCTCA GACAATCCAC TGCCTTGGCC TCCTGAAGTG CTGGGATGAC AGGTGTGAGC 120 CACGGCGCCC CGGCCAGCCT GGGTCTCTCA TAAGCATTTG GTGTTTCCCA CCTCTCTGGT 180 CGCCTTCCCT CAAAGCATCT CAGAGTCTGG TTGGCCTGGC AAGCTTCGGG GATCTGACTG 240 ATGAAAGCAT TTTGGAGCAA TGGGATGAGA TGCCAACCAA TGCCGTCAGC CGGCACTGAG 300 GTGGGATTAA CAGGACAATC AAGCCCTCGG TTCCCAGGAG CCTCACTGAG CAGCTGCTAG 360 AACTGTGCCA CTAAACAGGC TTTAATTTAC AGGCAATACC GACTCTGGGT TAACTATTTC 420 TCACAGGGCT CCCCAGCTGC ATGTTTACAT TTCTTTCCTT GTTCCTCTTT TTCTTCTTCT 480 TCTTTTTTTT TTTTTTTTTT TTTTTTTACA ATTCAGCAGA TTAAGAACAA TAGCAGGGTA 540 ACTGAGAACC ACAGAGGTGG CTGTAAGTGA CTCATTAACT CCCTCTCCCA TGTTTCCATC 600 ACCGTGAATT ACAACGTCAT CTCTGATGCC CTCAGACAGC TGTTACTAGT TTGATCCGAG 660 CCTTGCTTGA ATATGAATCT TTTTAAGCCG AGCAGGAGAT GGTTCTGCTC TCAAATAGAC 720 TGCCCTCCCC TGGGCCTCCC ATTTCTTACC CCACCATCCT CCTTGGAGAT GAAAGACTTC 780 CTGAGAAATG AAGGCTGGGT TTGCCTAATT ACTGGAGCAA GGTGGCTGTT CTGCTGGGAA 840 ACGTGAGTGG TGGCTTTCTG TCTCTGCAGA AAGGCTTGCT TTTGCTCGGT CGTCTTACTA 900 GACAGCCAAG CACCAATAAG GTTGGCTCCT TTGCTTAATG AATGACAGAG GGGTCACAGC 960 AGCATGCAGC ATTCCCCCCG CCCCCCGTTT CTTGTGAGGC AGCCTGCGTC GGGCCCGACA 1020 GCCTCCAGGA GAGAGCTAAA ATGAGGTCCT TCAGATTACA TATTTCATCT GGGCCCTTGT 1080 TAATAAGCAA ATGCTGGCTG TCCCAGTGAG TGACTGGGAG TGTGTGTGTG GCCGTCACCT 1140 TCATTTGGCA TTCATGGGCT CCATTTACCA GTTTCATAAA AGTTCCAGTG GGGAGGCCAT 1200 CTTGCAAAGC 1210
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