Tag | Content |
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EnhancerAtlas ID | HS050-00657 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:13946190-13947040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:13946210-13946222 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr1:13946210-13946222 | ACTAAAAATAGA | + | 6.32 | ZNF263 | MA0528.1 | chr1:13946641-13946662 | TTTTTCTTTCCTACCTCCTTC | - | 6.03 |
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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 |
GH01I013618 | chr1 | 13945214 | 13947400 |
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Enhancer Sequence | AGCTGCATGT TAACACATGC ACTAAAAATA GAGTCATCCC CTTGTGTGCG CTGGAGGACT 60 TGTTCCCTGA AACATTGCCT TTTTCTTTGC TCTTCCTGAA GCTTAAAATC GGGTTAGAAC 120 ATATAATAGA TCCTGGATTT TTCAACTCAG TAAATATAAA TGATGTAAGT GTGGTTATTG 180 GTCAACAATG CAGAATGAGT CTAAAATCAC ACTCACTGGT GTGAATGGGA GTTTTTTTGG 240 CTCAGGGGCC CAGCATGCAG GTACGTACCT GGTACAGGCA AAGCCAGCCT GAAAGCACTA 300 AACACTATTC CTCAGCACTG TTTCTTACTC TGAGATTATT TTATCAGATG CTGACTCAAA 360 GCACAGCGTG TTCTATTTCT ACATCCAAGG GCTCCGGGCC ATAGTACAGA CAGTCCTATG 420 CGTGGTTCTG AGACCTTGCT CCTCCTCCCA TTTTTTCTTT CCTACCTCCT TCTCTACTGC 480 TGCCTCTGCC TTTCCACTGA TGCAAATTTT TGAGAAAACA ATCACGTGCT GGTCACATAC 540 CAGGGCGATC AGCAAATGTT TCTGAAGTGA CGGCTTCCCT CTGGATGCTG CTGAAGTAGT 600 CAAAGAGGTC GTCTGAAATA TTTGTTTGAA TAAATGAGCT TACGGTCCTC CGCATGTAAC 660 CTCAGGAAGG TGTGCAGGTG TCCTGACCGA AGCAGGAGGT GGACCCCTTC CTGTTGCTCC 720 TGTTCCCACC CTTCCACAGA GCATCTGTAG GTGAGGCTGG ATCTGTGGAT GGCCCAGGGC 780 TCACTGGAAA GGGAGTAGGA TTCTTGTCCA GCAAGATCCA GAAACAAAAG ACACTCCCTT 840 GGGTATAACT 850
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