| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05765 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:65692130-65693430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:65692214-65692235 | GGAGGCAGAAGGGGAAGGAGA | + | 6.34 | | ZNF263 | MA0528.1 | chr11:65692215-65692236 | GAGGCAGAAGGGGAAGGAGAG | + | 6 | | ZNF263 | MA0528.1 | chr11:65692211-65692232 | GAAGGAGGCAGAAGGGGAAGG | + | 7.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAAAGGGAGA AGGAAGAAGC ATGGGGCACC TACCACACCC CTGCCCTGGG TGCTGCTGGA 60
CCTGGGGCCC CAGAGGCTGG GGAAGGAGGC AGAAGGGGAA GGAGAGTTGA ATGACTGAGT 120
GAACCTGCTC GTCCTCTCCC AGCCTCATCC CTGGCCTGGT CAGGGAGCTG ACGTGCTATG 180
GGATCTCTTG ATTTCCCCTT TCCCTCTCTG GGCTTTGCCC TCCACAGCCA TGAAATAGGT 240
CTGCGGATGC CTCCCCCGTG GTTGATGGGA GGCAGGAGGC GTTGCAGCAG CACGTTGCTC 300
TGTGCTTGTC AGGTGTGAGG CCACCATCAG TTTCCCTGCA CCCCCGAGCC CTCCTCTAGG 360
AGAGATGTCC TCATACCCCC ACCTTATGGA TGAGGAGACT GAGGCTCTAG AAGTGACATA 420
GTGGCCCAGA GGTAGGCAGG GGTTTGGTCT AGGCATGTAT GTCGTCCAGG ACTTGGAGAG 480
GTGGAGTTAA CAGCTTAACC CCCAATACAC ACCCGAGGGC CATCCCTTTC TCTGGAGCAG 540
GGACACTTGG CTCCAGGACA TAGACACGAC CAAATTCCCA CTCAATTAGG CTATGGGCCC 600
TGAGGCAGGG GACTGGCACC CGTGCTCTGG ACAATCTACC AGGGGCCTGG TCCCTCCCCT 660
CTTTGGTGCA GGGCCTTTGA TGAGAGTGGG TCTGGACTTT CTCGGGGGGC TCCTTGTATC 720
CGGAGAGTGA CAGGGCTATG TGACTGCCAC CTCCCATCAT CAGAGTGAAC TATTTCTATT 780
CTGAAATCCC ATTTTTCCTA TTGTGTGTTC AAATGTCGTT TTAAAAAATG GAATAAGGAC 840
TAAGATTTTT GCCAGTAATC AGAGAGCTGC AAAGAAAAAC AGGATCCCAC ACAATGCCCA 900
TCAGATAAAA CTGAAAACCG GATAAAACCT GTTGCTAGTG AGGATGCCAG TGAATGGAAT 960
TCTGGCATTT GGTAGGCATG TAAGTTAGTG GGGATGTTTG AAAGGGCATT TTGGCAGTTG 1020
TGTGTCCCCT GGCAGGTCCA CTCCTGGGTT AAACCTCTCA CAAGCAGAGA GATGTGTCCT 1080
AGGCATGGTT TGAGGTGGCA GAAAAATCAG TGTCCATCAA TGGAGAACTG CCTGGGCAGA 1140
AGGCAACAGG GATAGAGCTT AAATGCAGAG TGCTGAGTGA CAAATAGTCA AATAGAGAAC 1200
AAGAAACAAA AAACGCAGAC ATACATGAGA ATCCTTTATA CGGCATTTCT GCCACTTACT 1260
CTGTTACCTT GGACAAGTGA CTTTAAGCTG TCTCTACCTC 1300
|
