| Tag | Content |
|---|
EnhancerAtlas ID | HS184-28014 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr7:50535320-50536710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REL | MA0101.1 | chr7:50536168-50536178 | GGGGATTTCC | + | 6.02 |
| | | 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 |
| GH07I050467 | chr7 | 50535499 | 50536470 |
| Enhancer Sequence | TCATTCTGGA AGAGACAATG GCTAATGCCC ATCGAGTTGC TCCTCTGTGC TTGAGGTGCC 60
AGCGCTCACC ACTGCGGCAT CCTCAGGACA GCCCACAACA CAGAAGATAT CATGATTATC 120
CCCATTTTGG AGATAAGAAA ACAGGCTGGG AGAGGGTGAG CGACATGCCC AAGGTGCACC 180
CGGAGGCCTT GGCTGAGCTA GGATTCTAAG GCAGCCTGAT GGAGCTGCAG CTCTGTGGCT 240
GCCACAGCTG TTGCTCCTCC TCCGCGTTTG CCACCTAGAG CTGGGCATCC TGTCCGCTCT 300
GTCACATTCA GAAACGGCCT TCCTCTCATT GAATATCACA CTGACCTTAT TTCACTTCCA 360
AATAGTTATA GAACTCAGAA GCTATTCAGA CAGCATGTGA TCCTAGGAGA AGGAGCCCTC 420
CGTGGCGTAG GCCCGTGCCT TGCTCATTCT AAGCCCGCGG ATACAGCAGG GCCCCCATGT 480
TGCAGGTGCT GGGGAGGACC TGCGGAAACG CGGCGCCTCG CGGGCAGGGG GTGGCTGGGA 540
CAAAAACACG TGTCATACGA GTGGTTCCTC GTCATGCCAC CAGAGAGCGC CAAAGACCTC 600
GGCCTCATGG GCGATCCCGA AAGCCGGTTC CCGCCCAAGG AGACAGGCTT TGAGCATCGC 660
TGGACTCTGC TCCTAAGGCA GGATTGGGTC CCCTTTAAGA AAGAAGTGGA GTGTGTTTTA 720
AACAGGAGCC AGCATGATCA TAACTAGTTG TCCTTGAGCT TAAAGACGTC ATCATTGTGG 780
GGAGATAAAT CCCTTATTTT TTGGCTTTCT TTCCCCAAAA AAGCTGAATT CGTCTCAAAT 840
GGGTAGAGGG GGATTTCCTA CCCAGGAATT CATATACATA CTCCTTTCCC AGTTCTCGCC 900
CCCAAACAGG TCCTCATAGT GCTCGGCAGC TCCTGGAACT GTCCTCACCG AAGCTTTGGG 960
AGTAGGCAGT TCATGGCACA TCCTAGGCAT TCTATGAAGC TTGCAGATGG ATGTGTTTAT 1020
ATATGCTGTG CCACAGAGGA GGTGGCTGGG GACACCTGCC CCTGCACACC TGGTTGTGAA 1080
GTGGCAACAG GACTTAAAAT GGAGGGCTGT TACCATCACT AAGGCTGAAT ATCATAAGTG 1140
TGCTTGTTCC CATGAAGCCT GGGGACCTCT GTCCATCAAG ATGAGGCCAC AGCTTAGGAA 1200
GGACACCAGG ATCAGAGAGA GCCAGCAGAA CAGCAGCAGG CCTTCTGCAG CTGGCTAAAC 1260
GGGTGGCTCT AGGCAGATCC AGGCTCATAT TCAGGACTCA GTTTCCTCAT TTTTTTTTTT 1320
TTTTTTTTTT TTGGTGAGAC GGAGTCTTGC TTTGTCACTC AGGCTTTAGT GCAGTGGCAC 1380
AATCTCTGCT 1390
|
| |
|
|
|
