Tag | Content |
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EnhancerAtlas ID | HS098-16680 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr13:113176820-113177560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr13:113177138-113177149 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr13:113177138-113177149 | CTGAGTCACCC | - | 6.02 | NFE2L1 | MA0089.2 | chr13:113177134-113177149 | AGTGCTGAGTCACCC | - | 6.67 | Nfe2l2 | MA0150.2 | chr13:113177136-113177151 | TGCTGAGTCACCCGT | - | 6.08 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CAGCTGTAAA GAACAACAGG GAAGAGCACA CATGCATATG TAATTTGTAT TTCCACAGAG 60 GAGAAATGAA GGCACATACA TCCAGACTCA GGGCCAACCA CTGCCTGTGG CATCAGTAAC 120 AGACTGACCG CAGGCACAGA CAGCTGGACA TTCCACAAAG GAGACCAGAG CCCTAAGACC 180 ACACACATGA AAACAATTCT GCCAGCTGGG TTCACAGCAG ACACCTACAT GTGTGTCTTC 240 ATGATTTCCA AATCCCTTAA TACACTGTAA CTAACCGTAA ATCTCACCAA AACACACTGG 300 TAATAGGGCA AGTCAGTGCT GAGTCACCCG TCCATACCCA TAAGATGTTT CCATAAATTA 360 GTCTTAAGAC CAAAACAGCA CATGCAAATA AGCTTTGTGA ATTGTACAAC TCGCAAAAGT 420 TGAGTAGTAG TATCATGCAC CATAGAGTGA ACTCTACGGA GATTGGTGGA GATGTCTAGG 480 GGACAAAACC AGATTGTCAC CAATAAAGAC GCCTGACTCT AAGCAGTAAC ATAGCGGAAG 540 AAAGCATTTC CATAGCTTTC TATTGAGAAG AAATTGCAGG TGGAGACTAT ACACATAACA 600 GAGCTTCTTA CAGTGCTGAT TTACATCTGC AAAGCACAAA ACCATTTTTA AAACTTATAT 660 GAATACTTCA TTTCATTAAA CCCACAATAA TACTTAAGCT AGACAATAAC CCCAGTGGGA 720 GGAACAACCT CAGACTGAGA 740
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