| Tag | Content |
|---|
EnhancerAtlas ID | HS089-09235 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr3:121748870-121750250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr3:121749938-121749959 | CCCCTTTCTTCCTTCTCCACC | - | 6.18 | | ZNF263 | MA0528.1 | chr3:121749185-121749206 | AGGGGAGGGAGAGAGAGAAAA | + | 6.34 | | ZNF263 | MA0528.1 | chr3:121749935-121749956 | TTTCCCCTTTCTTCCTTCTCC | - | 6.66 | | ZNF263 | MA0528.1 | chr3:121749174-121749195 | GAAGCAGGGGGAGGGGAGGGA | + | 7.39 | | ZNF263 | MA0528.1 | chr3:121749180-121749201 | GGGGGAGGGGAGGGAGAGAGA | + | 7.57 |
|
| | 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 |
| GH03I122030 | chr3 | 121749020 | 121749860 |
|
Enhancer Sequence | CTAAAGTATC TTTAAGGGTG ACCTCTCTCA GAGAAAAGTC TTGCTAGGAT CCACCCATTC 60
TAAGTAGAAG TGTAGACTCC ATGGTCTGCC AAAAGCCACT TATAAAACCA AGGAACTTTA 120
ATTGCACTTG CCATGCACAG CCTAAGAATC TAATTCTTTC AACATTTTAT TATAAGGGGA 180
GAAACCAAGG ACAAATGGGG GCTGCATTCC TAGGACTAGA GCCGCAGAGA AGAGGTTCAA 240
GTCCTCAAGT CATAGCAACA AAGGTAGAGT GTCTGAAGTT TGCCACCACC TCCTTTGACA 300
ACATGAAGCA GGGGGAGGGG AGGGAGAGAG AGAAAATTAT TAATCAGTAT GGAAACAGAC 360
ACAATACCAC TCAGCCACAT GCTTCTCCCC TTCCCTGTCA TTGCCACTTG CCACTGTCCC 420
CACATTCCCC CATCTCTTTG CCACCTCTTC TTGACCAAAA TGCAAGAGGC TGTGATTGGT 480
GGATGTGAAT TCCTTCTGCT GAATCATGCC ACCACTCTGC AGCCAACTAT GGATGGTTTT 540
AATGGTTTCC CTTTCATTAT CTCTGTGAGC TCAGTCCCAG AACAAAGAGG CAAGGGTTTT 600
TCTCTCTCTC TCTCTCTCTC TCTCTCTCTA AGTGTTTCTT ACTCTTCTGG CAAGGCTCAG 660
TTTGATGTTC AGAGTCAGAA CTACTCTGAA ATTATGAGGT CAGTCCACAT ACATCTCGGT 720
TAAGCTCAAT GAGGATCAAA ATATCCTATT CTTTCCAGCT CACTCCAGAA AGTCTGTTTC 780
AATTAGTATT TGGGGAGGCC CAGGAAGCAG TAGCTTATTA AAGTTCCCAG GTGGTTCTAA 840
TCTGCAGCCA GAGCTGAGAA GCTAGTTAAA GCATGAGTTG AATGAGAGAA TGTCTTGCAT 900
CTTGGTGACA AAATAGGGCA TTCCCCAGGG CAGCCCCTAA ATGGAACACT TTCTAACATG 960
TTTTCTATCT CAGCTTCTCT TTGCTAACTT TCTCTTTTTC GTCGCCTAGA GTGACAGACT 1020
AGGAGAGTAT CTACTCCAAA GCTCATGGCC CTGAGATGTG TAACATTTCC CCTTTCTTCC 1080
TTCTCCACCA GAACAGCATA ACATGTGATA TTACATTCAG ATGGGAATGA ATCTCCGGAC 1140
ATTGCCACAA GTAGCTGCAT AACTCTAAAT AAGTAACAGT CTCTCTAAAT ATTAGTTTCT 1200
TTATTTGTAG CACCAGGGAG TTAACTAGAT CAGTAGTTTT CACACTGTGT TCTGAGAATT 1260
TCTGACATCC TGTGGAGTAC CTAAGGGGTT GTCTCTGCCA GGGAGGTCAG TTTGAAAAAT 1320
CACTGGACCA AATGATCCAG AAGTTCTTTT CAGAACCAAC ATTCTACAAC TCAGACTTTG 1380
|
