Tag | Content |
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EnhancerAtlas ID | HS047-04711 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:101355330-101356190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr10:101356062-101356080 | GCCTGCTTCCTTCCTTAC | - | 6.22 | Nfe2l2 | MA0150.2 | chr10:101355803-101355818 | TGCTGTGTCATGCTC | - | 6.4 |
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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 |
GH10I099595 | chr10 | 101355368 | 101356290 |
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Enhancer Sequence | CTTTCCATTC TGAGACCCCA TGTTTGTTAG CTTGTTTGAG TGAATGAGTG AGCTCTGAGC 60 CTTCCCTCAA CACACACACA CCTCTACAGT CCTGTACTCA TGTCCCCTTC CTTGCTATTT 120 CCTCTGTGTG GCCTCTGCCA AGCACAACCC CGAACGCTTA TGTGGGAAGG AACCCAGAAG 180 GGGGTCTTTA CCCAGTACTC AGTCTTTGCA GAGCTGGGAG CAGCCTGCTG CCCCCACAGG 240 GTAAGATGAT TTCTTTCACG CTGCATTAGC CTATGAGACA GGCGTTCTGG CATGCTGTTC 300 CAGGAATCCT CATGAAAGGC CTGAAGGGGT AGGGGGAAGC AGGTATTCAT TGCAAAGCAT 360 GAGGTTGAGC TGCTCTTTCC ACCTGGAGGG TGATCTGAGC TCAGCCCACT GCACTGCAAC 420 TGGACACCAG GCAGCAACTG GCAGGGAGGT CCTGGAAGAG CTGGTGACAC TGATGCTGTG 480 TCATGCTCCT CAGAGGACAC GACCCTGCCC TGCCCAGGGA TTATAAATGG CTCTCCCGGG 540 TATTGTTGGG TTTCTTTCCT TTCTACAATG AACTAACAGT CTCTGGACCA CAGAACTATG 600 GAGTATTTGA GTCATGGGAG GAGAGGAATA GTGTTGGGCA AAGAGACTGG TGGGAAAGAG 660 GGGGACCCGG GCATGTACCC GGGCTGATGG GTGTGCACTG TGGGACCTGG ACCTGCCACA 720 TGACTCCTCT AGGCCTGCTT CCTTCCTTAC CAGATGGCCA TGAGCTTCAC AATTTTAATG 780 ACACCTACCT TGCAGCATTG TTTTAAGGCT TAAATTGGTT TACTTGCTCA ACAAATTACT 840 TATTAAGTAC CTATTGTGTT 860
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