Tag | Content |
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EnhancerAtlas ID | HS129-38669 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chrX:54500510-54501470 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chrX:54500974-54500992 | CGTTCCTCACTTCCTTCC | - | 6.74 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH0XI054474 | chrX | 54500642 | 54501556 |
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Enhancer Sequence | TATCTTCAGG CTGTCCTGGA ACCAATTCCC CATGGAGACC AAGGGACAAC TGTCATTTAC 60 TATGTCATAC TCATCTAACA AACACATCCA CGGTGTCCCT GGGTCTTAGC CATAGGCCCA 120 GGAATACACA CACTGTGGGA CACTTGCCTC CTCCTAAATA GTCACATACA AACTCTGCTG 180 TGAAAACATA CACACACAAA GACCTCTGCA GCCTCCCTTC CAGGGTCACA CAGGCAGAAA 240 GAGTCACAGG GGATTTTAGG TCTCCCAGTC CCGGAGGGAA GAAATAGCCC AACCCACAGG 300 GTTCCAGCAG CTTCCCTAGG CCCCTGACCT CACCCCTGGC TACATCCCAG CCAGGTCCAC 360 CCCAGGGGAC TCAGATCAGG GTCCTTTCCC AGCACTGAGG GAACAGGGTG CCCCAGGCCC 420 CAGGCCGAGC GCCCCTCCCC AACTCTGTAC CTTGCTTTGG GTGTCGTTCC TCACTTCCTT 480 CCCCACCTAA GCTGGCAGGG CCTGGCCAGG ATGGAGGAGG CGCTCCTCTC CACTCAGCTG 540 TGCCGCTTAC CCTGCCCTGC TCAGCACATC CTGGCCTGGT CTTGCCCTGC CCTCCCCCTG 600 GGCGTGGGGG TGAGGAAGAT GAATCACCTG GAGGGTGGCA CAGGCGGAGA TGTGGTTGGA 660 GAGACACATG GCCAGAGCAA GGGAGAGAGA CAGAGAGGAG CTGACAGGGC CAGAGAGGCA 720 GTGAGTAAAG CCAGGCACCC TGCCATGCAG AGACCCCTCC TCAGATATAC ACACATAGGT 780 GCCAGGGTCC CTGGTGCCCC TTGTCTGCCT CCTTGGGCCT GGAGGAGCCC ACCTATCTCC 840 ACACCTCAAA GCAGGCAGGC CTCTCTGGGC AAGCCCTCCC TACCCTATCT GTAGCAAAGC 900 AGCAGGGTCC CTGGATAATG CTGCTCTCCT TCTCCTCCAG TGCTGGTCCT CGGGATGGAG 960
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