Tag | Content |
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EnhancerAtlas ID | HS105-30140 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr16:21180520-21181480 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr16:21181198-21181209 | GGTGACTCATG | + | 6.62 | FOSL2 | MA0478.1 | chr16:21181197-21181208 | GGGTGACTCAT | + | 6.14 | JUNB | MA0490.1 | chr16:21181197-21181208 | GGGTGACTCAT | + | 6.32 | JUND | MA0491.1 | chr16:21181198-21181209 | GGTGACTCATG | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGACTTAGTT CATTGCTTCT CAAACTTTAA TGTGTATGCA CGACACCTGG GGAATCTTGT 60 TTAAAAGGCA GTCTGATTCA TCAGGGCCTG AGATTCTGCA TTTCCTTTTT TTTTCCCCTT 120 TTTCTGGAGA CAAGATCTCC CTCTGTTGCC CAGGCTGGAA TGCAGTGGTG CAATCCATAG 180 TTCACTGCAA CCTCAAACTC CTGGGCTCCA GTGATCCTCC CACCTCAGCC TCCCAAGTAG 240 CTAGGACTGT GGGTATGTGC TGCTATGCCA AGCTAGTTTT TAAATTTTTT GTAGAGATGG 300 AATCTTGCTG TGTTGTCCAG GCTGGTCTCA AACTCCTGGC CTCAAGCAAT CTTCCTGCCT 360 CGACTTCCCA TAATGCTGGG ATTACAGATG TGAGCCACCA CGCCCAGCCA GATTCTGTAT 420 TTCTAACAAA CTCCTAGATG ATCCAAGTAG CTAAGCCTAT TTGTGTCTGA GTGGCTTCAA 480 CTATGAGAAC CTCAGCTGTA AAGTAGGAGG CAGATGGTAT GTACCTTACA TCAATGCACC 540 TTTATGCCGA AGAGGTCTTC TCAAGAGTGT GTTTGGCAGG AGAGCCATGA CTGGGTCTTT 600 CCTCCTTTCA CAAGGCTTGA CCTTGGGTGG GGACCTCAGA CTTGCCACCT CTCCACAGCT 660 GCCTAAGATA GCTGCCTGGG TGACTCATGT CTTGGGAGAA GTCTTGTTGT AGTGACTTTT 720 TTTTTTTTTT TGAGACGGAG TTTCGCTCTT GTTATTCTTA TTATCATTTT TGAGATGGAG 780 TCTTGCTCTG TCTCCCAGGC TGGCGTGCAA TGGTGTGACC TTGGCTCACT GCAACCTCTG 840 CCTCCCAGGC TGGAGTGCAA TGGTGCAACC TTGGCTCACT GCAACCTCTG TCTCCCAGGT 900 TCAAGCAATT CTCCTGCCTC AGCCTCCCCA GTAGCTAGGA TTACAGGCAC ACACCACCGT 960
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