Tag | Content |
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EnhancerAtlas ID | HS050-06379 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:232454570-232455700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PBX1 | MA0070.1 | chr1:232455410-232455422 | CCATCAATCATT | + | 6.07 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27584 | chr1:232454562-232456994 | Esophagus |
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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 |
GH01I232319 | chr1 | 232454898 | 232455086 |
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Enhancer Sequence | TGACTCTATT AGGGAAATGG TGTGCTAATC CAGGTTTTGT TATCATTTCA GCCTGATGGC 60 AGATTGTCCA TGAAATCTTT CTAGATTCAT GGAGGGAGAA GCTTTGAGGA AATGAATTCA 120 GGAATCTAAC GCAAAGAAAA GAAAGCGGCA TAAACTTTCC CCCACCCCAG ACCTGACATG 180 AAACCCTAGG CGATCCCTCC TTCTCAAATG TTCATACCAT GTGCCCTGAG TTATTTACCT 240 AACAATGGTC ATTCTTCTAA TAACAGATCC TGGGATTCCT GAAACCATGC TTTCTCTCAG 300 TGCTGTTGTC TCTGGGCACA TACGCTGTTG AGATGGCGAC ATCACACACC CTTGAAATAG 360 CAGTTGCACA AAGCAAACGT TTGCCCCAAG CATGTCAGAC TTTTGACAGG CTGCAACATG 420 ATAAGTTACC AGACGTGTTC CCACAGGAGC CTGCGTGAAT TGATTGCAAC CAGACTCACC 480 CGATGACAAG TGACAGACAG CGGATAATGC AGGGAGGTCA GGTGGGCTGC CAGGCCCAGG 540 GCCAATTGCT CCCTGGAGCC CATCAACAAG GGACAGGACT CGGCAGGACC AGGCCGGCAG 600 CCATCCTGGT TGGCTTCCAG CGGGTACAAG GAGAAATTGC AGCTGGCAGA AGCGCAGACT 660 CCTGGTGCCA CTCCAACACA GTGAGGGTAG AGGAAGGTGA GAGGAGGGTG TTACTCTTTA 720 AAAGAACTCA GATTGCATAT GAAATGCATC TCTTTCTTCT TGCTTTTGAT CCCAAAATGA 780 AAAGAGCTTA ATCTCCTATC TGAAAAGAAG CTTTTCCTAT GCTCTGCTGA CACGAACAAA 840 CCATCAATCA TTGCCTGGAT TTCCTGAACC TCTCAGTACA GAGGCTTCCA GGCCAAGAAG 900 GGTTGAGAAA GGCCTCCTTC CAGCTGAGGA CAGTGAAGTG TGGTAGGAAG CAGGAGTCTC 960 CCAGAAAGGG CATACCCTGT CTGATCCCTC CCTCTGACAA CCTGCTCCAC AAAATGATGT 1020 GGGGAGAGAG GGGTCATGGC TCAGACTCTG GGAAAACAGT GGCTTAGAAA TTGATAAGTA 1080 TTCAGACTGG ACTTGGTTCC GAAACTGATT AAGCCAAACA TCCTTTTCCC 1130
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