Tag | Content |
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EnhancerAtlas ID | HS113-07005 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr11:77842520-77844010 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr11:77842978-77842993 | TGGCCTCTGCCCTCT | - | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 77843035 | 77843321 | chr11 | 77843617 | 77843712 |
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Enhancer Sequence | CACCTGTAGT CCCAGCTACT CAGGAGGCTG AGGCCAGAGG ACGGCTTGAG CCCAGGAATT 60 TGAGGCTGCA GTGAGCTATG ACTGTGCCAC TGTAATCTAG CCTGAGCAAC AGAGTTAGAC 120 TCTGTCTCTA AAATTTTTGA CCACCATCTC CAGCTAATTC TTTGTATTTT TTGTAGAGAC 180 GGGGTTTCAT TATGTTGCCC AGGCTGGTCC CAAACTCCCA AGCTCAAGCA ATCTGCCTGC 240 CTTGGCCTTC CAAAGTGCTG GGATTACAGG TGTGAGCCAC TGCACCCAGC CCTGTCTCTA 300 AAAATTAAAA CAAACAAAAA CCTACCATCT CTTACTTGTC CTATGATAGC TTCTTAAATT 360 GAACTCCCCA TCTTCACTCA GGCCCTTCAT TAATCTAGCT TTCACATTGC AGCCAAAGTA 420 GTATTTCTAA ATCACGAATG TTATATTTCC CTTTTAACTG GCCTCTGCCC TCTGGATAAA 480 ATCTAAAGTA CTCAACATAG TCTAAAAGAT ATTTTTGGAT CTCGCTTACT CACCTTTTCA 540 GCCCATTTCT CACCATCCTC CCACCTGTCT TTGTCTTACT CTACATTCAC CTTTTCCCTC 600 TGCCTGCAAC ACTCTGTGTG AGGTAGGTTC TTTAACTCTT ACCATTTCAC CAGTGGCGTA 660 GAGAAGCAGC TTGCCCTGTC ATGTAGCCAG TATGCAGCAG AGCCAGATTC TAACCAGGGC 720 AGTCTGACTC CCTAGCTACG GCTCTTAAAC CACCAAATAC TTCCAAAGTT AGTTGTTATT 780 TTCTCTGCAA ATCCTTCCTG ACCTCAAGGC AAAATAAATC TTTAATTTGT CCATTTCTAT 840 CTCTAATGCC ACCACTCCAA TTCAAGTCAG CATCTTCTCT CATGTAGACT TTCTCAAAGG 900 GCACCTAGCC TTCCTGACTC TCCTTCTGCC TCCTCCAATC ATTTATATGG GAGCCAAAAA 960 ATATTTTATA AATGCAGATC ATTTCCACTG AGCTTATAAA ATCAAAATCT AAATTTTTCA 1020 TCCTGGCTTT ATAAGCTCCG GCATGATTTG GTGCCTATCT TTCCAATTTC ACTGTGCATG 1080 TTTCTGTCTC TGTTGCTTAT TCCATGCCAG CTACACTGGC CTTATCATAG CTGCCCAAAT 1140 AGGTCAATAC TTTCACACCA CAGGGCCTAT ATTTATACAG TGTGCTCTTT CAGATAAGTT 1200 CTACACACTT GCACACACCA CATACTCTGC ATGGATGGCC CTCTCATTCA CACTTTAGGC 1260 CTCCAATGAT GTCAGTTCCT CAGAGACATT CTCTGACACC TAACTGAAAG TACATCTTCC 1320 TTCTTGGTCG CCTGATAGGA TCCTGTTCTT CTTCTTCCAT TTTTTTTTTT TTTTTTTTTT 1380 TAGATGGAGT CTCACTCTGT CGACCAGGTT GGAGTGCAGT GGCGCTATCT CGGCTCACTG 1440 CAAGCTCCGC CTTCCGGGTT CATGCCATTC TCCTGCCTCA GCCTCCCCAG 1490
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