Tag | Content |
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EnhancerAtlas ID | HS191-21492 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr2:149476930-149478250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr2:149477669-149477680 | AGAGATAAGAA | - | 6.32 | Gata1 | MA0035.3 | chr2:149477669-149477680 | AGAGATAAGAA | - | 6.32 | Gata4 | MA0482.1 | chr2:149477668-149477679 | GAGAGATAAGA | - | 6.32 | TCF7L2 | MA0523.1 | chr2:149476949-149476963 | TACCTTTGATCTTT | - | 6.46 |
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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 |
GH02I148720 | chr2 | 149477581 | 149479021 |
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Enhancer Sequence | TCATCTTTGT GGGCTTATCT ACCTTTGATC TTTGAGGTTG CTGACCTTTG GGTGGTATTT 60 TGTGGTTTTT CTTTGTTGTC GTTTTCTGTT TGTTTTTCTT TTCATAGTCT GGTCACTCTT 120 CTGTAGGGCT GCTGCAGTTT GCTGGAGGTC CGCTCCAAAC CCCAGTTGCT CTGGTTCTTC 180 CTGTACCTGG AGGTATCACC AGTGACGCCT GCAAAACAGC AAAGATGGCA GCCTGCCCCT 240 TCCTCTGGAA GCACCATCCC AGGAGGGTGC TGACCTATTG CCACCTGAAC ACGCCTGTAG 300 GGGGTGGTTG GAGACCCCAG TTGGGAGGTT TCACCCAGTT AGGAGGAATG GGATCAGGGG 360 CCCGCTTAAA GCAACAGTTT GGCCTCTTTT TGTTAGAGCA GCTGTGCTGT GTTGGTGATC 420 CCTTTAGCCA CCATTTGATC TGGGCTCTCC AAGCCCCACT GGCTGAACTG GCTGAGGAGC 480 CCAAACAGCC AAGGTGGCAA CCTGCCCCAC TCTTCAGGCA CTCCATCCCA GGGAGAAATT 540 GGAGCTCTTT CGGCCCATAG AACATGGGTG GTGACTAGAG GCTCTGGCTG GGAGGACCCG 600 CCCCACAAGG AGGAGTGGAT TGGGGGTCCT GATTACAGAA TCAGTCTGGC CATGCCTTGA 660 CAAAACAGCT GTGTCATGGT AGGGAACTGC CTCTGCCCAG GTAGCAGCCC TCCCCTCTCC 720 TGGACACTTT GTCCCAGGGA GAGATAAGAA AGGTAAGAGC TCTGTCAGGC CATGGCTGGA 780 GGGCCTGGCT GGGAGGTCCC ACTCAGTGAA GAGGAATGGA TTGGAGCTTC ACTTAAAGAA 840 GTAATCTGGT CAATATCTGG CAAAGCTGCT GAGTTGTGCC ACTGGGGGGA CCCTTTCTCG 900 TCTGGACCAT TTGGACTCTC CAGGGTCTGC AGGCTGGAAC AGCTGTGTTG ACCAAACAGC 960 AGAGATGGTG CTGGCCTCTC CCCACAGCCT ATTGCTGGTG GCTGCTTGGA ATTCCAAGCC 1020 AGTGGGTCTT ATCTTGTGAG GTGTCATGGA AGTGGGCCTG CAGAACAAGG CTGCTCAACT 1080 TTCTGGATTC CAACCCCTCT CGGGGGGTAT ATGTGGACCT CCCGCCTTGT CTGAGTTGCA 1140 GACACGTTTG TTGGAGATCC CGGTACTGGA GTATGTAAAG CTCTTGGGTC TCTGTGCATG 1200 CCTGAGCAGC TGCTCTGCTG AGACTCCACG CAGCTCCGTG TGTTGGCCCC AAGGCCCTGG 1260 TGGCGTGGAC TCATAAGGGG ATCTCCTGAT CCCCGGGTTG CAAAGATCCA TGGGAGAAGC 1320
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