| Tag | Content |
|---|
EnhancerAtlas ID | HS184-14401 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr17:79466250-79467630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr17:79467322-79467337 | AGGTCAGCCTGTCCT | + | 7.24 | | INSM1 | MA0155.1 | chr17:79467114-79467126 | TGCCAGGGGGCA | + | 6.62 | | ZIC3 | MA0697.1 | chr17:79466793-79466808 | GAGCAGCAGGGGGCC | - | 6 | | ZIC4 | MA0751.1 | chr17:79466793-79466808 | GAGCAGCAGGGGGCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr17 | 79467092 | 79467468 | | chr17 | 79466809 | 79466898 | | chr17 | 79466947 | 79467007 |
| Enhancer Sequence | CCGCCTCGCC CGGGACAGCG CCCCGGCCCT GCTCCCCGCT CTACGGCCCC GCGCCCCGGC 60
CATCTGCGGC TCCTCTTGCT TCGCGCCCGC GCCGCGCTCT GCCCACGCCC AGCCCCGCAG 120
CTTCTCTGTG ACCCCCGCCT GCCGCACCCC GGCTAGGGGC TTATTAGCGC CACGGAGCTG 180
AGCTGGACGT GTCCAGGATC TGGGGAGGGA GCAGCCCAGA GAGGGCAGGG CCTGGCCAGG 240
CCTCCCCAGG CAGCCCTGCG GTCCTGCAGC CACGAGGGGA GGGGACGCCA CAAATCCGGG 300
TGCCGACCCG GGCCAGGAGA GTCGGGAAAT GGGCCTTGGC TGGGACCCAG GCCGACTCTG 360
ATCCCGCGGG CCTCGTAGCC CCTCCAGCCC TCGGCCATGC AAAGTGGGGG TCCCACGGGA 420
TGAGCCCCAG TGTGGGAGCC CAGCTCGGAC AGACATCACC CCTCAGTCCC CCGACCCTCC 480
GCCCCAGGAG AGAAGCTGGA CGCTTGCCTG GGCGACCAGG TCCAGGCCAC CCTAGGCAGT 540
GAGGAGCAGC AGGGGGCCAT GGCGAGAGGA CAGGGAGGGC CTCTGTTGGG CCTCGGAGGT 600
GGAGACCCCA CTGCTGAGCC ACAGCTGGGG CATGCATTGG CTTTCTTCTG AGCATCTGTC 660
TGGGGAACCG CCGTGGGAGG AGCAGAGCCC CTCGGGCACT GGTAGGGAAG CCAGGCTGCC 720
AACAGCCCTG CCACCCTGGC TGCAGGTTCT GGAGCCGGGG ACCCTCTAGG CTGAAGTTCT 780
CCAAGTGGGT TGAGCCCAGG TATCCGTTTA TCCTAGGTAG GCCTCCATGC CTGAAGGTCC 840
CGGGCTCCTC TGGACCACCC GTCCTGCCAG GGGGCAGACA GGCCTCCTGT CCCTTCCTGT 900
TCTGTTCTGC TCCCTAAACT CCAAGCTAAG TGTGTCCCTG GGCAGCTGGG TCTTAAGAGC 960
CTGAAAGGCT GCATGGAGTC TGTTTGTTCG TTCAGAGGAA TCTCAGCTAT TTCCTGGGAG 1020
GCTCCATCTG AGCCTGGTAG GTCCCGGATG AGGGGTGGGT GGCCCGGTGA GCAGGTCAGC 1080
CTGTCCTCAG GGGCTTGCAG CACACCCGCC AGGGTGGCAA TTATCCAAAA TATAGAAAAC 1140
AAGTGCCACT GAGGATGTGA AGCAACTGGA ACTCTTGTCC ACTGCCGATG GGAATGCAAG 1200
ATGAGGCAGC TGCTGTGGAG AACTGTTGGT TCCTCAGAAA GGTGCACAGA ATGACCCTAT 1260
GACCAGCAGT CCACGCCGGC CACAGACCCC AGAGAACTGC AGGCAGGCCC TGGAACACAT 1320
ACTTCACAAG CAGAATGTAG TATAGACATA TACTGCAGTA TTTCTCAGCT TTAAAAAGGA 1380
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