Tag | Content |
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EnhancerAtlas ID | HS184-29914 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr8:101675220-101676370 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr8:101675973-101675984 | TAAGTAAACAT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 101675322 | 101675409 | chr8 | 101675559 | 101676218 |
| | Number: 1 | ID | Chromosome | Start | End |
GH08I100663 | chr8 | 101675620 | 101676434 |
| Enhancer Sequence | TTATCCTAAG CAAATTAATG CAGGAACAGA AAACAAACTA CCACATGTTC TCACTTGTAG 60 ATGGGAGGTA AACATCAGGT CCACACAGAC ACAAAGCTGG GAACAACAAA CACTGGAGGC 120 TCCAAAAGGA GCGGGGGTTG GAAACCTACC TTTCGCGCAG CGCGTTTGCT ACTTGAACGA 180 CGGGACCATC AGAAGCCCAG ACCTCAGCAC CATGCAATAT ACTCCGTCTA ACAGAGCTGC 240 GCAGATACCC CCCCCAATCC AAAATTAAAA TGAAAAGATA AATAAATGAA AATTAGGAAT 300 GTTTGATTCC CACTGAGCAG TATCTTTGTA TTTGAGAGTT AAAAGACAGA AATAGCTCTT 360 TTCTCGACAG TACAACTGGA AATAACCCAA CCAAGCCTTT TTTGAATGCA CAGGGCTTTT 420 GAGGAATGCT TTTTCAGAGT TGTTTTGTTT CTGCTTTTGG TGCTTTTTGG CTCCTCTTCC 480 TCAGTTGCGA GGATACCATG TGAATTAAGA CGGCGATGTC CCCCAGCTCT GAAGCAGTCA 540 CAGTGGAGCC CTCTGGAAAC CCTATCGGAG TAAAAGGTCC TATAAAGAAG ATTTTGTTTC 600 TTCAACAGAA ATGAGAACCG TAGCTCCATG GCCGGAGAAT AAAGGAAAGG CGTTTTCAGC 660 CATGCCAGTG TGCACTGTAA ATAAGAATGT GGCTGGGTAC GTCCTGCCTG CTGAGCTTGT 720 CTTACTATTC AACTATCGGA CTTTGATTTT GGTTAAGTAA ACATGAACTT GGGGACAACC 780 AGCTTTTCTG CATCTCTAGT CAGGGAGTTG TAGGCGCAAG GTTGAGCTGG TGGCTCTGGC 840 AGTGAGCTGG CCAAGCGAGG TGGCCTGGTT TTCAGCCAAG AAAGGAGAGA ATGAATATAT 900 AGTGGATACC TATGGCGGAT CTGGCACTGT GGATGGGCTG TGGGTCCCAC AGTAGATGTC 960 TCTGTGCTCA CACAGTCTTA CAGGGAAGCC AGACATTCAG GAAGAAAGAA CACAAGTGGA 1020 TTCGATTCCA AGCGTGATCC ACTCTAGGAA GGGCAAGCAC AGAGAAAAAG GTTGCCTCTT 1080 GAAAGGGAGA CAATGGAGTG AGGCCTGAGT CTGCTGTTTC CACATAAATC TTATGGAACT 1140 AGTTGATTCT 1150
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