Tag | Content |
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EnhancerAtlas ID | HS048-35179 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr8:9434900-9435940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr8:9435348-9435363 | AAAGTCCAGAGTTCA | + | 6.04 | Sox3 | MA0514.1 | chr8:9435477-9435487 | AAAACAAAGG | - | 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 |
GH08I009577 | chr8 | 9434959 | 9435830 |
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Enhancer Sequence | AGCCTGGGTA ATTTATAAAG AAAAGAGATT TAACTGACTC ACAGTTTTGT AGACTGTACA 60 GGAAGCATGG CTGGGGAGGC CCCAGGAAAT TCACAGTCGT GACGGGAGGT GAAGGGGAAG 120 CAGGCATGTC TTATATGGTC AGGGAAGGAG GCAGAGGAGA GCAGGAGGAG GTGCTACACA 180 CTTTTAAACA ACCAGATCTT GTGAGAACTC ACTATTACGA GAACAGCAAG AGGGAAATCT 240 GCCTCCATGA TCCACTCACC TACCACCAGG CCCCTCTTCT AACACTGGGG ATCATAATTT 300 GACATGAGAT TTGGGTGGGG CCACAAATCC AAACCAAATT TTTTGGTCCC TGGCTCCTCC 360 CAAATCTCAT ATCCTTCTCA TATTTCAAAA TACAATCATG CCTTCCCGAT AGTCCCCAAT 420 AGTCTCAACT CATTCCAGCA TTAACTCAAA AGTCCAGAGT TCAAAGCAAA GCAAGTCCCT 480 TCTGCCTGTA AAATCAAAGC CAGTTAGTTA GTTACAAGAT ACAGTGGGCG TACAGGCATT 540 GGCTAAATAC TCACATTCCA AAAGGGAGAA ATCAACCAAA ACAAAGGGCC TGCAGGCTCC 600 ATGGACTTCG AAACCCAGCA GGGCAGTTGT TCAATCTTAA AGTTCCAAAA TAATCTCCCT 660 TGACTCCACG GCTCACATCC AGGCCACACC AACACAAGGG GTGGGCTCCC AAGGCCTTGG 720 GCGGCTCCAC CCCTGTGGCT TTGCAGGAGT CAGCTCCCAT GGCTGCTCTC AAGGGCTGGT 780 GCTGATTAGG GAAATGGAAG TTTGCACTCA GGCTTTATTC AGATCCGTAG AGAAGGAGAA 840 TAATTCAACC TTCCTGGGTC AGGACAGCAC TTATGGCCCA GTGGAAGAGT AGGGCATTGA 900 TGGTAGAGGG AAGGAAGTCG AAGTTAGAGA ATTAAAGAAA ACCTAACATC CGTAAAGTTC 960 TGCAGGTATT TAAAAAACAA AACCAGGAAC CCTGGTAAGA TGCTGACAGT TTACTTGAGC 1020 ATGTACCCTA TGCTTTTACT 1040
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