Tag | Content |
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EnhancerAtlas ID | HS184-31663 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:130809340-130810090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr9:130809702-130809719 | TAGGTCACCACGACCTG | + | 7.04 | ESR2 | MA0258.2 | chr9:130809703-130809718 | AGGTCACCACGACCT | + | 6.56 | Nr2f6(var.2) | MA0728.1 | chr9:130809890-130809905 | TGAACTCCTGACCTC | - | 6.22 | Sox3 | MA0514.1 | chr9:130809441-130809451 | AAAACAAAGG | - | 6.02 |
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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: 1 | ID | Chromosome | Start | End |
GH09I128045 | chr9 | 130808214 | 130810930 |
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Enhancer Sequence | GATGGTTATT AAGGTGCACA CCGGCTCAGT GGATTCACAT CCAAAAAGCT GAGCATTGAA 60 CAAAAACAGA TTTTAGCTTA TATAGGCTAG CATACAAAAG CAAAACAAAG GCAGTGAATT 120 TTACAGTGAC AAGTCACATA ATCCATAGTA TAGCTGCTGA CCTGGCACTA ACCTATGGCC 180 TTGCATAGCT AGTGGCCTAG CAGTGGCATC GAAAGAAAAG CAGGAACTTT GCAAATCTTA 240 CTAAATACAA CCATTGGCAA ACATGGCCAT AACTAATAGT TCAGTACATG AGAGACAGTA 300 AAGGAATTTG TTTTTCTTCT TTTAACTTTG CTCGGGGGTG TCTGGAGCTG ATTTCTGCAG 360 GCTAGGTCAC CACGACCTGT CTATAGCCTT GCTTGCAGCA GTGAAAAACG TGTTTTTCGC 420 TTAACCCTTA CTTTCCTTGG AGTGAATAAA CGCAGTATTT ATTTTTCTTT AAATTTCTGC 480 CTCAACACAC TTGGCTAATT TTTGTATTTT TAGTAGAGAC AGGGTCTCAC CATGTTGGCC 540 AGGCTGATCT TGAACTCCTG ACCTCAGGTG ATCCACCCGC CTCAGCTTCA CAAAGTTCTG 600 GGATTACAGG CATGAGCCAC CGCACCAAGC CAATTCTCAT GGTCTTAATT ATGGTGATGT 660 TTTCACAGAT AGAAGAGATT CCATGTGTGG GGCCTGGGAA TCTGCATTTT AAAGAGTTTC 720 CAGGAATTAG GCTGGGTGAG GTGGCTCATG 750
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