| Tag | Content |
|---|
EnhancerAtlas ID | HS095-04694 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr10:128038890-128039990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr10:128039614-128039625 | GCAGGGTGTGG | - | 6.62 | | Myog | MA0500.1 | chr10:128039817-128039828 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr10:128039817-128039828 | CTGCAGCTGTC | - | 6.14 | | ZNF263 | MA0528.1 | chr10:128039002-128039023 | AAGGGAGGAAGAGGGGAGAGG | + | 6.52 | | ZNF263 | MA0528.1 | chr10:128039005-128039026 | GGAGGAAGAGGGGAGAGGAAT | + | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I126349 | chr10 | 128037745 | 128042107 |
|
Enhancer Sequence | CAGCATAAAT CAGAGCCACA TGGAGAGAAA CTCTCCTCTT GAAAATACAC ACCCACACAC 60
AGAGTCGGCC AAGCCCGAGT GAAGCAAGTT CTCTACAAGG CTGACTTTGA GAAAGGGAGG 120
AAGAGGGGAG AGGAATTCAG CCCCGGGACA GAGACAGCTG CCTGGGCATG GCCACCACAA 180
CTAGACTCAC CTGGCCCTGT CAACTCCATC ATTCTAGGAA GTTCCTGCTC CAGAGCCTGA 240
CTCTGTCCAT CTCTTGGAGC ATTTTCCGCA GTGACCTGCA TGTGTGAGCA GCTGTGTCTG 300
TTGTCAGTGG CAGTCTTGTG TCGGATGTCT CCCAGTTGCC AGGCACTTGA CAGATTACAA 360
AGTGCTTCCC ACATGTGTCA CCTCACATCG GTGCACAGGA ATGCTGCAGG AAGTTTGATT 420
CATCCCATTC TACTGAGCAG GGGATAGGGT GAGTGGGAAG TGAGCCTTGG AGGCCGGGCA 480
CCTGGCCAGA ATTCACGCCT CTGGCAGTGG GCAGAGCTCA GGCTCACATC CAGGGCTCTG 540
CCTTGCCATG GGTACCTCAG ATCCAGAGTA TCCTGTGACC TGAACTGCTG CCGACCCCCG 600
GAGCCCTGCC CCTTCCCCTG TCCAGGCTCT CCTGCATGGC ACCTTTGCTC ATGCTGGTCT 660
TCCATCAGTC TGGGCCATGT TCCCCCACCA CAGTGTACCC ATATCGGTCA CATAGTGAAA 720
TGAAGCAGGG TGTGGAAAGC AGGCCATGGC CAGGATTTCA AGCGAAGCTA GGCTGTGGCA 780
GAGGTGTCCA CGGGCAGTGC CCTCAGCCCG GAGGCCCAGA CCCCACCTGT TCAGCCCAAA 840
GCTGGCACCA GACAACATGT GCCCTGCTCC CCCACCCCAC CCTGCCCTTC CCTTCTGTCC 900
CAACTTCCCC CTTTAGTCTC GGCTTTCCTG CAGCTGTCCG GACCTCACCA GATGTGTCCT 960
GGTTGTGACT GGCTTCTGGG AGCTCTGTCC TCTGCCAGCC CTATCCAAAT CAAGAGGGTT 1020
CCCACTGGAT AGGCCAGTTC TTGGCCTCAC TGGTGGTCAC CATCCTGCAT GCTTGCACTA 1080
CAATGGATCC CTGTCTGAAG 1100
|
