Tag | Content |
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EnhancerAtlas ID | HS184-08389 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:104575790-104577420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr12:104577326-104577338 | GAATGTTTGTTT | + | 7.22 |
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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: 2 | ID | Chromosome | Start | End |
GH12I104180 | chr12 | 104574321 | 104576769 | GH12I104183 | chr12 | 104576821 | 104576970 |
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Enhancer Sequence | AGTAGAGACG GGGTTTTACC ATATTGGCCA GGCTGGTCTT GAACTCCCGA CCTCAGGCAA 60 TCGCCTGCCT TGGCCTCCCA AAGTGCTGGG ATTATAGGCG TGAGCCACTG AGCCAGGCCG 120 ATCACTGTTG TCTATAATTG TTTTACTTAT CCACCCTTCT CTGTAGATTA GTGGCTTGTT 180 GAGGACAGGA TATGTAGGGT CCTCCAGCGT CTCCCTACCC GCTTTCTTTC TCAGCCTGCC 240 TGAGAGTGCC TTTGGCCTCT CTGCGACCCA GCCAGCTGCA TGTTTTCCCT GCAGGCTTGA 300 ACCCAAGCCA AGGCCTTGAA CATTCCCAGG CACTGATGAA GTTGCCTAGT TTGGTTTAGG 360 TTGTTGCTCA AGACACTGAC CTGAGCCAAA TTCTTTAAAC CCTCATGTAA ACTCCACATT 420 CTGACCCCGT CATGGTGGAC ACACCTAGGT AGAACATTGC TTTCTCTCTT GACCACTGGG 480 GGATACATGG CAGCCCACTC TGTAAGTCTG TCCCACTAAT AAACACTTTG GACTGATCAT 540 CCTTGTGTTT AGTGCTTCTT TCTCTAGAAT CCCATCCAGC CCCATCTCAA GACCATTTGG 600 GGCTCTCTCT TGTGGGAACT TCCCTGCCAC TGCTTTGGGG GCAACTCCAG CCACAAGTTT 660 GGTTGGAAGG AACAATGTCT TTTATTTCTG ATTCCTAGTT ATCTATCACA GTTCCCTGCA 720 GACATAAGCC ATTCAATGAG TAAATGATTC TAGTGAATTG CTTTCTAGCG AAATGTATGC 780 AGGTAGATGC CATGCAGGTC AAAGGTGGCA TCAACACCAG CTGGCTGCTC ATGGCATGTC 840 CTCCTCAGGC CCAGCTGCAC TCTCCACTGC AAATTCCATG AGATATATCT ATATCTTTAC 900 AATAATTTTC CCACCCGTCC CCCCATTAAG CCACTTCAAA TAGGTTCCTG TTGTTTGCAA 960 CTGGAAATGT CCTAAGCAAA ACATTACCTC ATAGCCTTAT TGAATTGGAT CATTGTATTG 1020 ATTTGTGCAT CTCGCTGTAA ATTTTATCTT AAAAAAAACA CAGGAGAAAA ATTACCCCAT 1080 GGGGTTGCCA GGAGGCAGAC ATGAGATAAT GCTTGCACAA TGCTGTGTCA GTCAGGAATA 1140 TTTTGGAAAC AAGTGACCTA AACACAAAAC ACAAACCAGG TTAAGTAAAA AATGGAATGC 1200 ACAGGCTCAC AGAACTGGAA AACCTAGAGG TAGGTCTGTG TGTTTGTTCT CTATTGCTGC 1260 ATACCAAATT GCCGTAGCAC CAATTTAGCA GCTCACACCA CCACCCACGT ATTGTCTCAC 1320 AGTTCAAGAC TGAAATCTTG GGGTCAGCTG GGCTGAGTTC TCATCTGGAG GCTCTGTGGA 1380 TAATCTGCTT TCAACCCCAT TCTTCTTGTT GGCAGCATTC AGTTGCTCGC AGTTGTAGGA 1440 CTGAAGTCCC ATTTCCTCCC CAGCTGTGCT GCTCTCAGTT CCTAGAGGTT ACCCATGGTT 1500 CCTTCCCATG TCCCTGCCAC AGGCAGATCA CAGCATGAAT GTTTGTTTTC TTCCAGATTA 1560 ATTAGAGCGT CTCTCTCTGA CTTCCTCTTC TCACCTCAGA TGATGAGGCA CCCAGATCAT 1620 CTCCCAATCC 1630
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