| Tag | Content |
|---|
EnhancerAtlas ID | HS183-03606 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr3:186508190-186509510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr3:186508636-186508647 | AAGAGGATTAG | + | 6.62 | | Crx | MA0467.1 | chr3:186508706-186508717 | AAGAGGATTAG | + | 6.62 | | EN2 | MA0642.1 | chr3:186509163-186509173 | GCTAATTGGG | - | 6.02 | | SPIB | MA0081.2 | chr3:186508547-186508559 | AAAGGGGAAGTG | + | 6.07 |
|
| | 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 |
| GH03I186789 | chr3 | 186507781 | 186509050 |
|
Enhancer Sequence | ATTACCTAGG TAATTGAATG TTCGGTATTA AAGATGTTTC TAGGTGAGAC TAGACATACA 60
CTCTGCCAAC TGGCCCCCGT GCCCCCAGTC ATTTCTGTTC CACACCTAAG TTCCATACTT 120
TCCTGGGAAG GCTTTGGGAG AACGGAAAGG GCCAGAGTAA CTCCAGTCAC CACTAAGCAA 180
CCAAGGTGCT AACAACTGTG CTTTTAAAGC CCTTTAATGG CTTTGTGAAC TTCCAAGTTT 240
GGGCACACAT GGATTATAGC TTGTTCTGGT CAGTGGATGA AGATTAAGTT TTCCCCTAGC 300
GGCTATAACG ATTCCTCAGA ACAGTGGCCA AGATCAATCA AAAAGACTGA TTTCTTTAAA 360
GGGGAAGTGC CCTTTCTCTC AATGTCTCCA TGTAAAGATG CCACTAATGA GATTGGTTTA 420
AAAAGTCCAC AATATCCAGA AAATTAAAGA GGATTAGTGG TACCAGTCTT GTCATATGGA 480
AGGCCTACCG TGAAGGTGAA AAACGTCATA GAAACAAAGA GGATTAGTGG TACCAGTCTT 540
GTCATATGGA AGGCCTACCG TGCAGGTGAA AAATGTCACA GAAACAAAAG TTGTTAAGTA 600
GTAGTGATTC TGAAGTGAGT TTTTACATGG GAGTATCCAA AGACAAGTGG GGTACTCCAT 660
TCTCTTTAAT AAATGATTAC TGTAAGTTGG ATATGCCTTT TGTTTATATA CAACTGGCAA 720
AATAGTTTTC ATGTATAAGA ACATCTGCTA AAATTGATTT AACTGCCAAA GGCATCTCTT 780
ATAAAATCTA AAAACTGAAG GCTGGGTGCG GTGGCTCCCA CCTATAATCC CAGCACTTTG 840
GAAGGCTAAG CGGGGGGCGG ATCACCTGAG GTCAGGAGTT CCATACCAGC CTGGTCAACC 900
AACATCGTGA AACCCCGTCT CTACTAAAAA TATACAAATT AGCTGGGCAT GGTGGCAGGT 960
GCCTGTAATC CCAGCTAATT GGGAGGGTGA GGCGGGAGGT GGAGGTTGCA GTGAGTCGGT 1020
ATTGCGTCAC TGCACTCCAG CCTGGGCGAC ACAGCAAGAC TCTGTCTCAA AAAAAAAAAA 1080
ACAAAAAAAC TAACAACTGA AAGTGTCCTT TTCTTTCCTG AAATGTCTGT TACATGCCTG 1140
ACAAACTGAA AAGTCAGTGC TATCTCCTCA CCTCAAACAC TCTGATACTC CCAGGTTATT 1200
CCCTTATACT TCCTAGTGCA GTACTTGGCA CTTGCTAAAC ACCCAGTATT TGTTGGATGA 1260
AAATTTCCTA AAAGCCACAA AAAAGCCAAC TAAAAAGAAA TTCAGAATAT CCAGTACTCT 1320
|
