| Tag | Content |
|---|
EnhancerAtlas ID | HS184-20764 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:118975940-118977340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr3:118977169-118977180 | TTTGTTTACAT | - | 6.14 | | NFYA | MA0060.3 | chr3:118977109-118977120 | TCTGATTGGCT | - | 6.32 | | Stat6 | MA0520.1 | chr3:118976005-118976020 | ATTTCTCTAGAAAAG | - | 6.49 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I119257 | chr3 | 118975222 | 118978125 |
|
Enhancer Sequence | AGAAGTGCAA TCAGAGTTAA GTCAGTCAAT GTACAATTCT AAATTATTTT AGACAAGGTT 60
GACTCATTTC TCTAGAAAAG CACAGGTTTC AAAATGGAGA AGCCCCAGGA ACCTTGGATT 120
CAGATGAACC CATTATTGCC GGTCTTCTTG TAACCTTATG TACCAGAGGC CTTTTATGGA 180
ACCCAGCCCA GTTTCTGTTG AATCCAATCT GACACAAAAC CCAGTCCAAC TTGTGAACCC 240
AGTCTGGATT TAAGATGCTC AGATAAACTC AGGGATCACA ACACAAGTTA TGGAGCTCAT 300
ATTCAATTGG GACTTGCTGA TGACAACCTC CAAATGTGCA GTGAGAAACA GTGAGCATAA 360
GGGGTTTAGG AAGATACCTA CAGCTGTTTG CTCATTGCTC CTAAAGGTCG TCATCAGGAG 420
GGCACCTTTG GATCTCACTT ACAATGTAGC AGGACAAGCC GCAGACAAAA CCTCTCAGAC 480
ACTGAGTTAA AGAAGGAGGG GCTTTATTTG GCCAGGAGTG TCAGCAAGAC TCAGGTCTCA 540
AAAACCGAGC TCTCCAAGTG AGCAATTCCT GTCCCTTTTA AGGGCTCACA ACTCTAAGGG 600
GGTCTGCGTG AGAGGGTCAT GATCGATTGA GCAAGCAGGC AGTACATGAC TGGGGGCTGC 660
ATGTACCGGT AATCAGCATG GAACAGAACA GGGCAGGGAT TTTCACAGTG CTTTTCCAAA 720
CAATGTCTGG AATCTATATA TAGCATAACC GGTTAGGTCG AGGTTGATCT TTACCTACCA 780
GGCCCAGGGC GCGGCATTGG GCTGTCTGCC TGTGGATTTC ATTTCTGCCT TTTAGTTTTC 840
ATTTCTTCTT CCTTTAGAGG CAGAAATTGG GCATAAGACA ATATGAGGGG TGGTCTCCTC 900
CCTTAACAAC ACCAGATCTG TTCAAATAAA AACTTTCAAC AAAGTAAATT TAACAGTTTG 960
TTTCAGAAAA GAACAATTTA TGCATCAGGC AGCTCTCAGG ACCAGAAAAG GTTCAGAGAG 1020
CTCCACTCTG AAGGGGGGCA GTGAGTATTT ATAGACAGAA CAGGGAAGTA AAGTTCAGAA 1080
ATAGCTTGAT TGGTTATAGC TAGACACTTG CCTTATTTGG ACATGGTCTG CACAGTTGGC 1140
AGCCTGTGAT TGTCTGAAGC TCAGCTGCTT CTGATTGGCT GAGAAACAGC TATCTTATAT 1200
GAAAAATGTG CTTCTAAGTT AGGTTTCAGT TTGTTTACAT ACTAAATTAG GTTGCAGTTT 1260
GTTATGCAAG GACTCAAAAT ATGTTTTGGT TGTTGTTCTT TTCTTTTTTA AAACGAGCTT 1320
TCTCTTTTCA TTTTCCAAAA AGATTCAAAA TATAAAGACA GCCTCAAGGC CAAATTTAAT 1380
TTAACAGACA ACAGATATTG 1400
|
