| Tag | Content |
|---|
EnhancerAtlas ID | HS183-03032 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr3:13692330-13694540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr3:13693529-13693547 | CACTGAGCTTTTGGCCTC | - | 6.04 | | TFAP2C | MA0524.2 | chr3:13694478-13694490 | TGCCCCGGGGCA | + | 6.74 | | TFAP2C | MA0524.2 | chr3:13694478-13694490 | TGCCCCGGGGCA | - | 6.74 |
|
| | 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 |
| GH03I013650 | chr3 | 13691756 | 13692500 |
|
Enhancer Sequence | GAGGTGGGGG TGCGTGAACG TGGATGGGCA GAAATAACAT CTTTTGTACT CTAATTGGAA 60
CATAGCATGT CCTTTAATTA TGAACGCAAT GAGCTATAGT AGCACTACTG ATTTCAGAGA 120
TGGCGCAATC TCGCTTTCCT TCCTTAGTAC TTTGAAATTG CAGTGGGTAT TAGACCCGCT 180
GCTAGACCGT GTCATTCACT GGGTTAAGAA GGAAGCCCAG GTAGCGCCAC GTCACAGACC 240
CCTTTTAGTA TTCTGATAAC TATAATTTAA ATCTAATCGG CATTTAAGAG CCTACAGGCT 300
TGCCCAGACT GCCAAAGGCG TCTCTGGCAC ACACACACGC ACACACACTA ACATGCACAC 360
AAGCAGACAC ACATGCACGC AGACACGCAC ATGAACACAT GCACACGCAC ACTTGCATGT 420
ACACACGTGT GTACACATAC ACACATGCAT GGTTGAGAAC CTCTCTGGAG AGGAAAGGCA 480
ACACCAGTGT GTCCGCTATG TAGTGGTTTA TCAGACAGTT TATTGTGGAC ATGGACATGA 540
ATAAGAAAGG GGCACTGCTA ATTAGGCCAA GGCAGTGGAT ATGAGGTGGG ACTGTCCCTA 600
GCACACTGGG ACCAGGGCTA CCCTGAGGCC TGCAGGACAC CGGGAGCTGT GTGTGAGTTT 660
GCATCTCTGT AGGCGCGTGG CTGTGAGTGT GGGGGAACCT GGTGAAACGC ATCTGAGGAG 720
GGGAGGGGGT GTCTGCCACT GTTCTGGGTG TGTGTGTATG TGTGTGTGTG TGTGTGTGTA 780
TAGGGCATTC TGATCTCTAG TACCTGGGTT CTAGCAGATG CCTGACCTAC AGCCCTGTGT 840
TCAGCCTGGT CATTCCAGCT CTCAGAGAGA CCTTGCCCAG CCATTTCCTG GGGTAGCAAA 900
TGGTCTGGAA CCAGTCTGTC TTGCCTCCCC TGAGGGAGAC AGGCGGGCTA CTTGTGTAGC 960
CTTCTTACCT CACTAAACTC TTCCTTCCTT CCATGATGAT CCCCGTTTTA CAGACACAGA 1020
AACTGAGGCC CAGAAGAGCT GAATATTTGG CCCAGGCCAC ACAGGGAGTC CAGCCACGGG 1080
TGATGAGGGG CTGAGGATCG GGGAGGGACA GGAAACCTGG CCTTTCTGAG CCTTGCTGTC 1140
CTTATCTGCT GCGTCAGGAG GTGAGAGGAA GATGTTTGGG GCTGAGCTAG CAGAGAGGAC 1200
ACTGAGCTTT TGGCCTCTCC CCTGTGTAAA CCCCACCATG ACTCCCCATT GCCACGGCAT 1260
CAAGTCCCAG TTCCATGGCC TGACATTCCG GTCCCTGCCC CCTTCAGATT CATTGCCCAT 1320
CACTCCCCGT CCACTCCCTG CACTCCAGCC ACCCTGGCCA CCAGCCCTTC CTAGCACCCT 1380
CCAAGACCCT TCTCATCTCC ACGCCTCTGC CCATTCTGTA CCTGGCAAAC TCCTACGCAT 1440
CCTGCAATGC TCAGCTCTGA GCACCCCACA CAGAGTTGGC ATCTGCCTGC TGTGTGCCCC 1500
CACCGCCCTC ACACATCCCT GCAGGTAGTC CTTCTCAGGA CTGATGCAGC AAAATAAGAT 1560
CCGAGTCCCC AGCACCTAGC ACCGTGCATA AAGCAGGCAC TAACAAATGC GTGTCGAATG 1620
AATAAGCAAA TGTGTGCGTG CACACTCCAC CCGCCCCCCT CCTCATGAAC TGCTTGAGAG 1680
AAGGGCTGGG TCCTTTCCAG CTACTCAGGT GGCAATCGGA GTTTGTCCAA TGTCCAGGCT 1740
GGAGCCAGAG TTGAAGGGAG GAGCAGGCTG GGGGTGGTGG TGGCTGCATT TGGTGTTAGG 1800
AGGCCCAGGC TGGGCCTGTG AGCTGGACAC CCCACCCCAA CACCTGAGGT ATCTGCTCCA 1860
GGTCCCTCTC TGCATGCTCC TGGATGGGGC TTGGCTGTGG CTTCCACTCA GGCCCCTGGA 1920
TATCCCCACT GCAGCTTGGC CCTCTGTGAC TCACTCTTTC TTGGCCCTAA AGGTCAGTGC 1980
AGGGCCAGGC CTCGTCCTCT TCTCTGTCCA TTTATCAGGT CGGAAGCTCA AGGCTGACCT 2040
GGCTGGGGCC AAGGTTTATG TGCTTGTTCA CCCCACCCAG CACCTCTGAC CTTGTGAAAC 2100
ATGCCAGGAA GGGTGGGGAC AGGAAGGTGA CACTAGGGCC TCTGTGTCTG CCCCGGGGCA 2160
CTGTCAGCTG GGTCAGGATT TATGCCCTGA TGTTCCCACC CCCAGACCTG 2210
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