Tag | Content |
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EnhancerAtlas ID | HS184-09326 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr13:96756590-96757640 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr13:96757329-96757350 | AAAAAGAAAAAGAAAGAAGAA | - | 6.87 | ZNF263 | MA0528.1 | chr13:96757534-96757555 | GAGGGAGGGAGAGAAGGGAAG | + | 7.2 | ZNF263 | MA0528.1 | chr13:96757530-96757551 | GGAGGAGGGAGGGAGAGAAGG | + | 8.48 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 96756681 | 96757146 | chr13 | 96756741 | 96757283 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I096104 | chr13 | 96756881 | 96757030 |
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Enhancer Sequence | GGATATGACA GATTTCCATG GCTTGAGACC TGGAATACAT GGAACTTCTG GGCTGGAGTA 60 GGTCTTGGAG GAAGGTCAAT AAGCTGATAG AAAACCCTAA GATTCACACT GTGATTTTCA 120 CGCTTTGACA TTTGTGGACT TGCTGACCCT GAAGGAACTG CCTCTCCTAG GGTTAGCTAA 180 TTCCTAGAGT TAGTAAATGA CTCACCTTCC AGCACACTTT TTGTATGCAA ACCAACCTAT 240 CTAGAGCCCA CACCCCTAAC TACTTGCTTT AGTGGGCTCT TGCAATATAG TCCACTATCC 300 CACTGCTTTA ATCACTCCAG GGCCAGACAC CAGACAACTG CCCCAGGGCC TGCTGAAATG 360 ATTCAAACTG GCCAGTCCTA AACCTGCTTA CCCTGTCTCA CTGGTTTCTT TCCATGGATA 420 CCACAATAAA GGCTCTTGGC CGTGTTTTCC CCTCTCCCTT GGCTTCCTGA CTGACCCCTG 480 TGCTTCCCTT TGTGGCCCGG TGTGGTGTGG CCTGCTTCTT ATTTCCAGGG ATCTCCCAGG 540 GAGCATAAAA TCCTTCTTTT TCATGATGGT TGTTTATGTG TCTGCTTGTC TTACTGTACT 600 TGCCTAAAAC AAAGCCTGGG TATCCTTAAA ACAGTTATCA AGATTGGAAA GGACACAATA 660 ATGTACAGGG CAAATAATGT AATTATTTGC ACAGGACAAA TAATGTAATT AACCAAAGGC 720 ATAAAGATGG AAAAAAAAAA AAAAGAAAAA GAAAGAAGAA AAGTGCAGAA GCCAGTGATC 780 AGAGTACAGG TGCAAAGTCA GATTGAGACT AGACATAGGA TCAGACTAAT TTGTGCTGTC 840 ACACCCATGA TGTGACATGG ATGTGGATTG ATTTGAGAGA TTGGAGTCGG ATCAAGTCTC 900 CAAGTCACAT GGTTCTAAGC TGTGGAAAGA CATGGAAGTA GGAGGAGGGA GGGAGAGAAG 960 GGAAGGGTTT ACAGCTGTGA AACCCAGCAA AACCTGACAC AGACAATTCC TTATAATTTA 1020 AGTAATATTA TAGGCCAGGC ACAATGGCTC 1050
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