Tag | Content |
---|
EnhancerAtlas ID | HS176-39652 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr8:41604850-41605790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr8:41605602-41605614 | GGTGACGTCAGC | + | 6.14 | CREB1 | MA0018.3 | chr8:41605602-41605614 | GGTGACGTCAGC | - | 6.14 | IRF1 | MA0050.2 | chr8:41605411-41605432 | GAAGGGAAAATGAAACCAGTC | - | 6.71 | IRF2 | MA0051.1 | chr8:41605415-41605433 | GGAAAATGAAACCAGTCT | + | 6.17 |
|
| 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 |
GH08I041747 | chr8 | 41605273 | 41605943 |
|
Enhancer Sequence | AGGCCCAGAC CGAGTGTCAT TTTGCCTGTG ACTTTACCTG TCCCCTCTCT TTGCCACACT 60 GTACCTTATT TCTAGCCCCC TAAAAGTGGA TTGCTTTCTT GGCCATGTTC CACGGACCTT 120 GATAACTCTC TCAAGACCCT CATCACACAG AATTGCATTT ATCTGCGCTT GTGCCTGTCT 180 ATCCCAAAGG CCTGAATTCT TTGAGATCCT GTGTTTTGCT CACCTTGGTA ATCAGGTCCT 240 AGCATGGAGC CTGGTGCATA AGGTTTGCAG AATTCAATGC ACCTTCATGG AACCTGCCAC 300 ACACAGGCCT ATCTTTTTTC TTTGTCTCTA AGCACTATGA AGATCATGTC TAGTCTTCAT 360 ATTCTAAATT CCTAGAGCAA TGAAACCATA ATGTGGAGTT TAGAGAGTGT GTGTTCCTTG 420 CACTACATTC CGGATCGTTC CTGAAGGTGC TAGTCACCCT TTTCCCAGTC CCTAGGATTC 480 CATGGAATGT CCCTGCTGTG ACTACAAATG AAGATTTTTA TGTAACTGAA CTGGTCAATT 540 AGCTCTTCCT TGGCTGCAGA GGAAGGGAAA ATGAAACCAG TCTGGGGCAG ATCACCCAGA 600 GCAATAACAG GCTTGCTGCG CAGTGTCAAA TCCATCCTCT GAGTCAGTAC AGAGGCTTGG 660 GCTGGGTGTC TCAGTCCTGG GCTCTGAGAC TCTTCACCTC TCTGAGTCTC CCCAGCCTCC 720 CTGGTCAAGC ACCTGCTCTA ACCAACTCTC AGGGTGACGT CAGCATTAAC GGTGTCGCAG 780 GTACCAGGTG CCAGGCATAG GGGCACCTAG CTGCATATCT GGTTTAACTA TTTAACACAG 840 AACACTCTTC TCCCAGGTGA GGGCTCCAAT GAAACGTTCT TTCTTCCTCA TCCCTATTCC 900 AGAGCTGCAC CAAGGCAGCA AGTCTAAAGA AGTTTAATAC 940
|