Tag | Content |
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EnhancerAtlas ID | HS184-11574 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr15:76825310-76826240 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr15:76825594-76825605 | ATATTTACATA | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGACACAGG GTTAAATAAT TACCTTTTAG AAACTACAGT TTTGTAGGCA AAACAATAAG 60 TAATTATATT ATGCAGCAGA AATGATCAAT TATTATGCAG CAATGATGTA GCTGGGCAAG 120 GATGTTAAAC AGTAAACTGG GAAAAGACTT CCTAAAGGTA GAGATTACTG AGATTAGTTT 180 TGAAGAGTAA GTAGGGGCTG GCTTTGCGGA GTGGGTATTT CAGAAGAGGA AATGGCAGGT 240 AGGCAGTAAA GAAGGAAGTG CACTGTTAAA AATCAAATAC GTCAATATTT ACATACACTT 300 CATGTGCCAC ATAACGATGT TTCAGTCAAC AATTGGCAGC ATATACAACT GTGGTCCCAT 360 AAAATTATAA TAGTCTATTT TTACTGTATC TTTTCTATGT TTAGATATGT TTAAATACAT 420 GAATACTTAC CATTGTGTTA CAAATGCCTG TAGTATTCAG CATAGTATTC AGTACAGTAA 480 CATGCTGTAC AGATTTGTAC CCTAGGAGCA ATAGAGTATA CCATATAGCC TATGTGTGAA 540 GCAGGCTATA CCATCAAGGT CTGTGTAAGT ATACTCTATG ATGTTTGCAC AACGATGACG 600 CTGCCTAAGG ACACATTTCT CAGAATGTCT CCCTATTGTT GAGCAATGCA TGAGTGTACA 660 TATGTATGAT CTATGGACAT ATCTTAAGCA ATGTTAAAAT TATTACACAT TTCCTTCACT 720 CTTGCTCAGT AAATAATTGA GTAAATGCCT GAAATTGAAA CAGTCTTTAA CTGGCTGTAA 780 TAGTTGACAT GACCACTGTG CAAGTAAAGG GCTACTCCTC CTCTGTCTAT CTATCAGCAC 840 ACTTTTCTGA TCTAACTTGG TCAGAAGATG CTAGGAAAGA ATATCACCAC AGAAAACACA 900 TTCTACAATG TGAGTTTCCA CATTTCACTT 930
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