| Tag | Content |
|---|
EnhancerAtlas ID | HS183-09945 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr7:72857150-72858310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr7:72857681-72857691 | GGGGCGGGGC | - | 6.02 | | SCRT1 | MA0743.1 | chr7:72858225-72858240 | TCCCACCTGTTGCCT | - | 6.29 | | SP1 | MA0079.4 | chr7:72857679-72857694 | AAGGGGCGGGGCCTC | - | 6.18 | | SP4 | MA0685.1 | chr7:72857677-72857694 | AAAAGGGGCGGGGCCTC | - | 6.79 | | ZNF263 | MA0528.1 | chr7:72858198-72858219 | TAAGAAGGAGGAGGGGGGAGG | + | 6.53 |
|
| | 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 |
| GH07I073441 | chr7 | 72856010 | 72859944 |
|
Enhancer Sequence | TGAAGCACCT GGCAGGAAAG AAAGAACAAT GTTATTACAG ATTCAAGACA GGAGGAAGAA 60
TGGACAGGGC AGAAAATAAG TGTATCTGCT CAAAAAAGGA AGAGAGTTCA ACTATTTCCT 120
TGGCGCAGAG GTGCTGAAAC CTTCTGATAT TCAAGTCAGG GAGCACCCTC GGCCCAGGTG 180
GCAGGCATCT TCCCAGTAGT CCACTCACTC GCCTCCCCCG GGGCCACGGC AATCAAAGCA 240
GCAAAGAGCA GGCAGCGGGG GCCGCCTTTA CCAGCAGTCC TGCTGGAGGT CGGCTGAAGG 300
GGGCTACTGT CAACAGGACA CTAGCTCTCA GAGAACAGGT GGACCTGGGG TTACAGTGAC 360
ACCATGGAAG GGCATCAACA AGCCACTGCA GAAAGCAAAA CATGCTATCT GGGCCAACAG 420
CAGCCAATTC TGTGGGGGTG GGGTGCCTCT GGTAAGAAAA GCAAGAGGTC CAATTCCCTT 480
CCTGGGCTCT TCCACCGTAG ACATGTGAGG GTTAAGTGGC TAAAGAGAAA AGGGGCGGGG 540
CCTCCATTCC AGGTAGCCAT AACAAAAGCT GTGATTCACA GCAGAGGCCA CAGAGCCCAA 600
GGCTGTGGCA AACCGAGCAT CTTCTAATGC CTTATGATCT CCCAAATGGC CTGCCTTAAG 660
CCCCTAACTC CAATTTGATC TGTCAAAACA AGCACCTTTT CAAGAGTTTC TTTTTTGTTC 720
TTTAAAGCTC AAGTGAGATC TAAAAACTAC TAAAATTACA TTGGTTAAGG AGCAGAGGGG 780
AGGGTAATGT CCCTCCCATA ACAACTGTCG ACTCAACAGT AAGTGAGGCT CCAGCATTGC 840
TGACATTCCC ACAATGAAGA CCCAGCCCCT CTGAGCCCAC TGGAGACACA TGGATACTAT 900
TTTTAAATCC TTAATAAGTT GCAGGCTGCC CGCTAACTAG TTTGCAGGCT ACAGCAGGGG 960
AATGCCGGAC ATAGCTGTTC CTGGAGGCCT TGCTGCTTCT GTCTGCGTAC AGGCTCACCC 1020
ATCTGCCTCC CCAGCCTCCC AAGTTTGGTA AGAAGGAGGA GGGGGGAGGC TCCCCTCCCA 1080
CCTGTTGCCT GATGAATTCC TAATTGCTGG GGTAGGGAAT AAGAAACAGA AAGGTTAGAG 1140
AAGGGATGAT AAATAATTCT 1160
|
