Tag | Content |
---|
EnhancerAtlas ID | HS112-07457 | Organism | Homo sapiens | Tissue/cell | KELLY | Coordinate | chr2:18285790-18286680 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr2:18286638-18286649 | AGTGACTCATC | + | 6.02 | JUND | MA0491.1 | chr2:18286638-18286649 | AGTGACTCATC | + | 6.32 | MEF2A | MA0052.3 | chr2:18286156-18286168 | TTTATTTTTAGC | - | 6.04 | MEF2C | MA0497.1 | chr2:18286155-18286170 | TTTTATTTTTAGCAG | - | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACAGGCCTT TCTCACAGCT ATTGTCAGAG GTGGTAACTG TCTCAGTGGC TAATTCCACC 60 TTTCACATGG GACCCCACCT CCTATATCTA GAGTGTTGCC TGGTCCCTGA TGTGGTGGAA 120 AAATGTCAAC TTTACAATGA CCCTAAGGTT CACTGTTGCA CAGGTATTTT GACCACGTGG 180 TCTTCCTGAA ACAGGGACAT TTTGTCAGTT CAGACTAACC ACAGACCAGG TTGTTGATTT 240 TACCTGAAAG TATTTTCTGT CACCTTTGAA ACACTAGGTG GCTAATATGG TAAACACATT 300 ACAGTGAGTG ACCTACTTAG ATCTGTTTAA ATCGGCCTTT GCGTGAGTTT TGGTTACAAT 360 GATTCTTTTA TTTTTAGCAG GAATGAGAGA TGAATGCCTT CTTGCAGATC AGGGTCACAT 420 TTTCTTGCCT TCGTCAAGTA GGGCAGAACA ATTAGTCCAG TTATCCAGGC AAGAGACTCT 480 AGGCTTCTGA GATTCAGATT CTCAGCACAG AGGCAGCCTG GGCCCCTGTG CATAGCCTGA 540 GCCCCTGAGA GGGCCTTGAT AAGCTCTTGA TTAAGTCTGC TCCCATTAGG TGCTGACAAT 600 TCACGCTAAA CAGGAGTGTG GGTGCTGGAA AATGAAGCAA GTGCAGAGTC AGTAGTAGTC 660 TGGATTCTAT TTCTGTTTTT CTCTCCAGAT AACCTTGGGG AAAATATTCA CCTCTTTGAG 720 CCCCAATTCT GCCATTTGTG TTTTGTTAAA AAAAAAAAGG AGGGAAAAAA TCATCTACTA 780 AATCACACTG CTTTATAGGT GCAACCGTTT CCTAGGAAAT ACTTTAAACT AGTTCATACT 840 AAAGTGTTAG TGACTCATCA ATTCACTGGC CTTCTGTTTT TAAAGGAATC 890
|
| |
|
|
|