Tag | Content |
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EnhancerAtlas ID | HS113-30980 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr6:3013350-3014470 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr6:3013914-3013929 | GTGCTGACTCATCAG | - | 6.22 | MAFF | MA0495.3 | chr6:3013914-3013929 | GTGCTGACTCATCAG | + | 6.3 | NFE2L1 | MA0089.2 | chr6:3013913-3013928 | AGTGCTGACTCATCA | - | 6 | NFYA | MA0060.3 | chr6:3014231-3014242 | TCTGATTGGTT | - | 6.62 | NFYB | MA0502.1 | chr6:3014232-3014247 | CTGATTGGTTCAGAT | - | 6.81 | Zfx | MA0146.2 | chr6:3013432-3013446 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_10010 | chr6:3012114-3014720 | CD14 |
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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 |
GH06I003013 | chr6 | 3013881 | 3014030 |
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Enhancer Sequence | GGCTAGTTTT TTGTATTTTT AGTAGAGACC GGGTTTCACC GTGTTAGCCA GGATGGTCTC 60 GATCTCCTGA CCTCGTGATC CACCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT 120 GAGCCACCGC GCCCGGCCGA TGTAACACTA CTTTAAACAC TTTACCTAAT TGGGTAAAGA 180 TATCCACGTA GCCAATATCA CTCACTCCAA ATCCCGACTG CCATGTAAAT AGGAATGAAG 240 GATATTTCCA TTATTCCAGT GGTCCAAGAA TCATCTGAAA CCTGCCAGTC TTGTTGCTTC 300 CCTTCTCTTC CCGTTCCTGC CCTGAGACAT TCTGGGGCTG CTTGAGAACC ACATTTATCT 360 GCACAAATGT TTATCAGGGT AAATCAGGCC AAATGCATCT CCTTAAATAT CCTGCCTTAA 420 ATATCCTGAT CATTAAGAGG AAAATCTCTG GTTTCTACCC TCTCAGTGGT TGCTTCACCC 480 CCAGCCCAGC CACCTTCCTG TATTTGTTCA CAAGGAGGTG ATGCCACTGC AGAGTGAACT 540 GGCCCAGCAA AATGCCCTCC AGGAGTGCTG ACTCATCAGG CCACTTCCCG CCACTGCAAG 600 GAAGATGTGC AGGCATGGCT GTGGCTGTGT AAACCTGGCA GCAGAGTACG CACATGAGCT 660 TTGAGGGAAT TGTTGGGTGA CAGAAATTCC TGTCCAACTA GAAGGAAAGG GGAATCTATT 720 ATAAGGGCTC TGGTCACTTG GGCCTCCTGG ATCCCAAGGA CAGAGCTGTA GCTGCTCTCG 780 TCCACAGATT CCCATCTGCT CCTTTCTGCC TCTTGGCTCT GTTCTCTCTC ACTGCTTGCC 840 AGGGACTGGA TCCCCTAGAT CCAGAATTTC CAACCAAGGG ATCTGATTGG TTCAGATCAT 900 TTCTGTTTTC CAACCCTGCT TGAGGATGCG GAGTGGGCAG GAGAACGAGA GCACTGTTCG 960 CATGAGTCCG CCATGTGAGG GCAAGGCAGG GGGTGAGCGG CATGTGACCA CTTTCCAGAC 1020 AAAACCACCT TTCCAGAATG ATGAGGTTCC CAAGCCTTCA TAAAAGCAAC CTGCATGTGC 1080 GGGAAGAGGG CTGCCTCATC CCTGCCCAGG CTTGCCTCTG 1120
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