Tag | Content |
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EnhancerAtlas ID | HS043-29192 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr3:72663430-72664620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr3:72663446-72663458 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr3:72663450-72663462 | AAACAAACAAAC | - | 6.32 |
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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 |
GH03I072614 | chr3 | 72663945 | 72665029 |
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Enhancer Sequence | GGACAGAAAC AAAATGAAAC AAACAAACAA ACAAAACAAC AACAACAACA ACAAAATGGA 60 TGGAAAGCAT GTGGCAGCTA CAAAAATGCC CCTCTCAGAT CTCCTGTCAT GGGGAGGGTA 120 GTTGACTAAT GGCCCCAGCT GCTGCTCTCC AAATCTGAAT CCATCACCAC ACTGTGACCA 180 AGACCATTTT TTCCATGGCT GCTCCCTGAC AGTGAAAGAG CCCAGCAGGG ACTCCAGGGC 240 AGATCCGTTT CCGCAGGAGA CAGGCCCATA GCCACACCAA ACTGCAAGGG AGGCTGGAGA 300 ATATAGCCTT TATCTTAGGC AGTCACGTGC CCAGCTAAAA ACTATGAGCT TTTATAAGAA 360 GGTGCAAAAG GATATCGTGG ACAACTAGAA ATCTCTGCCA CTGAGATTTT AATTTTCTGG 420 ACATAACCAC AGATGGTTCC TCCCTCTGGT TCCCTTTCTG CCTTCTAATT ACTCCTGTGC 480 AGTCCTTCTT TACAATGCAA TGTGCTTACC TCCCATCCCC CACACCACCA TCAAAGTTCA 540 CACTTGGTTA TCTTTCTCCT ACTGTTGTAA AAATAACCTC TTGCTTCTTC CCTCTCTGTG 600 GCAAATTCAT CCTGGCTAAG CCAACCACAT GAGGCTTCTT AAATGCCGCT TTGTACACAC 660 TTCCTCTTGT TTCTTACCAT TGAAGCCCCT TGTCTATGGG GGGAAAGAAC AACCTCTTTG 720 GTCTTTTTCT CTGGACTCTC CCTAATCTGG CCTCTTCCTG ACTACTTGAA GCTCATTCTC 780 ACCATGACCT GGCAAACTGG GGCTGCTTCT CTTCACCAAT ATACAGCTCC TCACCAGTTT 840 TTTGTTTTTG TTTTTGTTTT TCATGTTTAT TGCCTGTTGT TTACCCCAGG TCCTCTGTCT 900 TTTTTGACCT TCTCCTGGAC CGTTGGTCTT TTGCAGATAA AGAACAGATT TTCAGACTAC 960 CTCAAGCCAT TACTCCAGTG AATTGCAAGG ACACATATAA CATATTGATA ACAGGGATCT 1020 CAAGAGAAAC CAAGAAAGGT GAACTGCTGA GCTTCCTGGA GTCTGGAATA GACTTTAGAA 1080 TTTGACAAAG CAAGTTGGTT TGTTGGTTAA ATTGTGGACT TTGGAGTCCA ACCGGCTGGG 1140 TTTTTGAGGC TTGGTTCTTC CAGTTACTAG CTATGCGATC TTGAGCAAAT 1190
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