| Tag | Content |
|---|
EnhancerAtlas ID | HS113-09774 | Organism | Homo sapiens | Tissue/cell | Keratinocyte | Coordinate | chr12:132643130-132644230 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr12:132644135-132644152 | ATGTGGGCGGGGCTGGG | - | 6.63 | | SP4 | MA0685.1 | chr12:132644134-132644151 | GATGTGGGCGGGGCTGG | - | 6.17 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCACCTTCCT CAGCGCCCTC CCTGCACGTG TGACGCGGTG GCCCCCAAAA TGCCTCTGAC 60
CCTGCCTGGT CTTCCTAGAT GTTCTGCACC AGCTTTGCTG GTGTTTTCAG GGTGCCTACG 120
GGGACCCCTC ATCCCGCAGC CTTCACAGGG GGTGGGGTTC ACTCCTCGGA TCTCACGGGG 180
GCTAACGTGT CCCCCGGAAA GAGATGTCCC CGTCCTGGCC CCCAGCATCG GCGAGTGGAC 240
CTTATTTGGA AATAGGGTCT TTGCAGATTA AGGAGCCAGC TGAGATCATC CTGCATTCAG 300
GGTGGGCCAT CAGTCCGGTG GCCGGTGTCC TAGTCAGAGG CGTGAAGAGG AGGGCGGAGG 360
CCGGAACTAT CCATCGGCTC CGAGGGTGGA GCAGGGGCCT CTGGGAGCTG GAAAAGGCAG 420
GAATGGGTCC TCCCTGAGTC TCTGAGGGCC CCGCCTGCCC ACACCTGCCC ATATTTGCCC 480
CAACCTGCCC ACACCTGCCT CAGGACAGCA TCTCGGTCTC CTGGCTGCCA GACTGTGATG 540
AAGATGCATG GTTCTAGGCC ACTGGCTTGT GGTGACTTGT TGCATCAGCT GTGGGGAGCT 600
CACACGGTAG CGCCTGTCTT GGGGGGTGCT GGGCGGGTGA CCTTCAGGAG ACCCCTGGGG 660
CCCCGCTGCC CTCCCAATGC CTCCAGTCCC AGTGTCTCTG TGGTGGCATC CTGTGCTGAG 720
GATGGTGCCT CGCGGAGCCT CCACTGCCCC TGTGTGCTCC GCACCACGTC TGTCTCGATG 780
GCGCCCCTCG AAGACCTCGG GAAGCTCCCC GTTCGCTGTG GCCCCCCGGG GTCTGTCCCC 840
TGCAGCACTG TTCTCTGGGG GCTCGTGGTC CGAGTTCTGA TACTGCAGGT GGCAGGTCCC 900
CTGAAGGCAT AGTCAGAGGC TTTGCTCTGG GCTGGCATGG AGGTATGGGC GTGGCGGGGT 960
GTGGCTGGGC GTGGAGGGGC ATGGAGGTGT GGGCAGGGCA TGGAGATGTG GGCGGGGCTG 1020
GGCGTGGAAG GGCGGGGTGT GGAGGTGTGG GCGGGTTGGG CACCTCTGGG GGTTCTGGGA 1080
AGACTCGTTG CTGACTTCTT 1100
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