Tag | Content |
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EnhancerAtlas ID | HS113-13561 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr16:4793160-4794260 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr16:4793451-4793469 | CCAGCCTGCCTTCCTTCT | - | 6.27 | HES2 | MA0616.2 | chr16:4794072-4794082 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr16:4794072-4794082 | GGCACGTGCC | - | 6.02 | Nr5a2 | MA0505.1 | chr16:4793162-4793177 | TCTGACCTTGAACAC | - | 6.39 | ZEB1 | MA0103.3 | chr16:4793708-4793719 | GGGCAGGTGCG | - | 6.02 | ZNF263 | MA0528.1 | chr16:4793457-4793478 | TGCCTTCCTTCTCCCTCCTCC | - | 6.37 | ZNF263 | MA0528.1 | chr16:4793460-4793481 | CTTCCTTCTCCCTCCTCCTCC | - | 8.51 | ZNF263 | MA0528.1 | chr16:4793463-4793484 | CCTTCTCCCTCCTCCTCCTTC | - | 8.95 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH16I004743 | chr16 | 4793202 | 4793801 |
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Enhancer Sequence | GGTCTGACCT TGAACACTGG AGCCCACGTG AATCCCCACA AGCAGCACCT TCCTGGGCCC 60 CTCAGACACA GAGGGCTGCA GGCTGGTCAC AGACAGTCCT GCAGCCCACA CAAGTCTTCC 120 CTGCTGGCCC CGCCCTAAAC ACTCATGCTG CCAGTCCCCA AAAGACTTCA TTCATTCAAC 180 ATATATGTGA CCGCCTGCTA CGTGCCAGGC GTGGGCCAGG TCCTAGGGAC AAAGGAGAGG 240 CCTCCGCACC CCACCCCATG ACCCATACCT CCTCTTCCCC ACCTCCCTGG GCCAGCCTGC 300 CTTCCTTCTC CCTCCTCCTC CTTCCTGGGG GAAGGAAGCC CCACCTTCTG TGCGCAGTCA 360 GCTCCTAAGC ACGCTCCCGC TTCCCCTGGC CTCCCCATTT AAAAAGGGAG GCAAAGGATG 420 TCACCACTGT CACTACACTC ATGGCTTTGC TCTGGGAAGT CCTGCAAATA AAATGAAAGT 480 TCTCCAACCC CTCCCTATCC ACTCGGGCCA CAAAGGCGAG GGGAGGCAGG TCTGAGGCAG 540 AGGAGCCAGG GCAGGTGCGG CGCTTCCGCC TCTGGTCCCA AAGCAAAGAC TCCCCTGTGA 600 CTGACAGCCC GTGTTATGTT AAATACATTT TGTTGGTTTG TAATTCAAAT CCCATAAAGC 660 AGGAGGTAGA GAGCCAACCA TTCTGGAGGA CATGTGTGTG CATGTGTATG TGTGTGTGTA 720 ACTGGCACTC CCTTTGTGGA GGGGAGTAGG GCAGAATGTA TTCTTTTTTT TTTTTTTTTT 780 TTTTTTTGAG ACAGAGTTTC ACTCTTGTTG CCCAAACTGG AGTGCAATGG CACGATCTCG 840 GTTCACTGCA ACCTCCACCT CCCGGGTTCA AGCGATTCTC CTGCCTCAGC CTCCTGAGTT 900 GCTGGGATTA CAGGCACGTG CCACCACGCC TGGCTAATTT TTTTTGTATT TTTAGTAGAA 960 ACGGGATTTC ACCATGTTAG CCAGGCTGGT CTCGAACTCC TGACCTCAGG ATCCGCCTGC 1020 CTCAGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC CGCGCTTGGC CGAATGTATT 1080 CTCTGTTTTA AAGGCACATA 1100
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