Tag | Content |
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EnhancerAtlas ID | HS048-01134 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:43467580-43469140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata1 | MA0035.3 | chr1:43468607-43468618 | TCCTTATCTGT | + | 6.14 | IRF1 | MA0050.2 | chr1:43467896-43467917 | TAAGAGAAACTGAAACCCCAT | - | 6.34 | IRF9 | MA0653.1 | chr1:43467898-43467913 | AGAGAAACTGAAACC | + | 6.1 |
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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 |
GH01I043002 | chr1 | 43467753 | 43469213 |
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Enhancer Sequence | TATCACCTGG GGGTTAGGAT TTCAACATAT GAATTTTGGG AAGACACAAA CATTCAGACC 60 ATAGCAGAGG ACAAGGTTTA ATGTCCAAAT GTACCCACTT GGGCTATGGG GATTTTGGAC 120 AGAACCATCT TCCTAGAAAG GAATGTGATG GGGCAGGCCC TATGATGGAC ACTTCCCATA 180 TAGAAGATCA CCTGTCTTGC AGATGGTCCC CTCTCTTGCA GGTGGACACC TGTCTTGCAG 240 ACCTCCAATC CTAAACCCTC ATTCCTCCCA AGCCGTGAGG TTCACTGTTA CCTGACACTG 300 CTCTTCATCC AGCCTCTAAG AGAAACTGAA ACCCCATTTA TAGCACTGCA CGTTTTTACT 360 CTTGAGCATT GATTATCTTC TTCCTTCCTC CTAAGCTTCC CACTCCTTCT TCCTCTGCTC 420 ATTCACAGTC AGAACTGAAA GGACATGGAA AAATCACACA GTCCAATCTG GGCACGTGGC 480 AGGTGAGAAA AGTATGACCC AGAGAGGTGA AGTGACTTGC CCAAGTTAAT GCGTAGGCTA 540 AATGTAAATA TAGGCCTCCT GATTTTTACT ATTAGTGTTT TCTCCCCACT AGCCAGTAGT 600 TGGCCCCAGT AGGCATGCCT CCCCCCAACT TCCACTGGGG TCTAATGGGG CAGAAAAACT 660 GGTGCTGCAG CCCAATGGAG GCAGACAGGG CCAAGGAGCA GGTGACAGCT ATGACCCAGA 720 CTAGGTGGCG GGTAGCAGGA ATCCCATCCC ACCAAGATCA GGCTTCGGGG TTTGGTGGGT 780 GAATGCATGA AGGCCTAGGT CCAGATTTGG CTAGAAGATG AGAGGTGCAG AGGCAGGGGA 840 CTGGCTGATT TGGAGCCAGA ATCGATAGAC CTGTATTACT TTCCTGTGGC TGCTGTAATA 900 AATGATGATG AATTGGGTGA GTTCAAACAA CAGAAGTGTA TTCTCTCACA GTTCAGGAAG 960 CTAAAAGTCT GAAAGCAGGG TGTCAGCAAG GCTCCACTCC CTCCCCAGAC TCTTGGGGAG 1020 AATCCATTCC TTATCTGTTC CAGCTTCTGG TGGCTGCAGG TGTTCCTTGG CATGTGACTT 1080 TATCACTCTC ATCTTAGACT CTGTCTTCAC ATGGCCTTCT CCTCTATTTG GGTATGTCTT 1140 CTCCTCTCTC TGTCTGTCCC TCTCCTCTCT CATAAGAACA CCTGTAATGT CATTTAGGAC 1200 CTACTTGGAC AATTCAGGTT AAGCACCTCC TCTTAAGAAC CTCAACTTAA TCACATCTTT 1260 TGCTATATAA GATAATGCTC ACAGGTGTCA GGGATTCCTG TGGGTATCTT TTTTTTTTTC 1320 TTTTATTTAT TTTTGAGACA GGGCCTCACT CTGTCACACG GGCTGGAGTC CAGTGGCACG 1380 ATCGTAGCTT ACTGCAGCCT CGAACTTCTG GGTTCAAGTG ATCCTCCTGC CTCAACTTCC 1440 TGAGTAGCTA GGACAACAGG CACCATCAGC ACACCCAGCT AATAACTAAA TTTTTTGTAG 1500 AGACAGCATC TCACTATGTT GCCCACTATG TTGTTCAGGC TGGTCTTGAC CTCATAGGCT 1560
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