| Tag | Content |
|---|
EnhancerAtlas ID | HS184-02418 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:210539870-210541340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:210540284-210540302 | CTCTCTTTACTTCCTTCC | - | 6.04 | | MEF2A | MA0052.3 | chr1:210539964-210539976 | TCTAAAAATAAA | + | 6.07 | | RREB1 | MA0073.1 | chr1:210541247-210541267 | CCCTCCCCCACCCCCCACCC | + | 6.27 | | ZNF263 | MA0528.1 | chr1:210541248-210541269 | CCTCCCCCACCCCCCACCCCC | - | 6 |
|
| | 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 |
| GH01I210366 | chr1 | 210540261 | 210540410 |
|
Enhancer Sequence | AATTGCTTGA ACCCGGGAGG TGGAGGTTGT AGTGAGCAGA GATCGTGCCA CTGCACTCTG 60
CACTCCAGCC TGGGTGTCAG AGTGAGACCT TGTCTCTAAA AATAAAATCA AAAACAAGAA 120
ACAATTTAAA AAGTCTCCAT GCATTGCCAA ATGCCCCCAG GAGGCAAAAA TCATCCCCTT 180
TTAAGAGCAG CTGGTCTATA GCAATATTTA AGGGCTCTTA AATGACCACT CCCTTGGTCA 240
TGCCGATTTG CCATTCTTAC CTTTACTCAT CCTGTTCCTC TTCTGGATTG GGGCTCACGC 300
CTTCCCTGTC CGGCCCTTAC TCAGACTTCA GATCATAGCT GGCTCCCTGT CACGAAGCAT 360
TGCCTGAAGC TCAAGCTGAG CTTGGTGCTC ATAGTTCCTG ACACTTCCCT GCCTCTCTCT 420
TTACTTCCTT CCACAAATAC AGCTTTCAAT GAGAGTGTCT CTGTGCTCAA GTCCATATGG 480
AGCGCTGGGG ACAGTGGTGA GCCAGACAGA CAACATTCCT ATGCTAGTTT CTCCTACTAG 540
GGACAGGCTG ACCGCAAACA AATGAACAAT GGCCACAGAT TGAGCTAAAT GACATGAAGG 600
CAGTAAACAG GGTGATAGGA TAGCACTCTT TTGGGTGAAA TCGTGTACCC TATTATGACA 660
AATTTATTTG TAGAATTTTA TTTGATGTTG TCCTTTCTGA CTTAGATTGT GGGTCCCACA 720
AAAGCAGGGC TGGGATTTAA TCATTTCTGT ATCTTCAATG CCTGGAGCAG AGTCAGTGAG 780
TATTTTATTG AATTTAACTG CAGGAAAGAG TGAAGGGCCA GGTTGCAGCA TGGAGGTGAG 840
AAATACATTG GTCCTACGTG CCTCTAGATA GCCATGTAGG TAAGTGGGCT AAGTGGGACA 900
GTGTGTAGAG TCAGAGTAGG GAGACACCAT TCTGGGCACA AAAAATCACA AACTGCTTCT 960
GGGAGAAGGG GGCTGACCTT CACCTGAGCT CCAGAGAATG AGTAGGATTT GGCAAGATCA 1020
TCAGTAGAGG AGATGCTGTT CCAGTGGTGT TGCTATGGTT AGAAAAGGGA AGAATGTATT 1080
AGGGAAATGG TGAGTCAAAG TGAAGCTTCA CTTAGGGCAG TGAAAGGGAG CTGGACCTGA 1140
CTGTAGTCCT CCAGTTTTTG ATGATGTTCA GGTTTGGAGG ATTACAGCCC CAATCAAGAA 1200
TGCTTTTGAT CTTTGTCATT TCTTTGAGGG TAATGCTGAT TGCACTTGCC AAGACAACAG 1260
AAGTGGTGTG GGTGCTTGCG TAGGTGCGGC TGTCAAGGGC TGTTCAGACT CCATATGCTT 1320
TGGTTTTTGC ATCCTTTTTT TGTAATGTTT GCTCTTCCAG GCTGTCAGGG TAAAAGCCCC 1380
TCCCCCACCC CCCACCCCCT GCAGGCTCCA GTGTGCTGTG CTAGAATGGG GTGAACCCAG 1440
CCTTGCTGGG TTCTGGGGTG ATCTGTCGTT 1470
|
