| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00835 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:28497370-28498630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:28497991-28498002 | CCACACCCTCT | + | 6.02 | | NKX2-3 | MA0672.1 | chr1:28497745-28497755 | ACCACTTGAA | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:28497617-28497632 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09203 | chr1:28497615-28504223 | CD14 | | SE_60762 | chr1:28495302-28510214 | DHL6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAAGGTGGTG GGCGCCTGTA GTCCCAGCTA TTCGGGAGGC TGAGGCAGGA GAATGGCGTG 60
AACCCGGGGT GCAGAGTCTG CAGTGAGCCA AGATTGTGCC ACTGCACTCC AGCCTGGGCA 120
ACAGCGAGAC TCCATCTCAA AAAATAAATA AAAATAATAA ATAAATAATT AATACAAATT 180
AGGCTGGGTG GGGTGGCTCA CACCTGTAAT CCCAGCACTC TGGGAGGCCG AGGCAGGCAG 240
ATCACCTGAG GTCAGGAGTT CAAGACTGGC CTGGCCAACA TGACGAAACC CCATATCTAC 300
TAAAAATACA AAAATTAGCT GGGTGTGGTG GCGCACATCT GTAATCCCAG CTACATGGGA 360
GGCTGAGGCA GAAGAACCAC TTGAACCCGG GAGGGGGAAG TTTCAGTGAA CTGAGATTGT 420
GCCACTGCAC TCCAGCCTGG GTGACAGACC GAGACTCCAT CTCAAAAAAA AAAAAAAACT 480
TGACCTCACA GGATAGCCCT GATGTTGAAG ACAGACAACC TCTACAGTGC TAGGCATATA 540
GAAGGTACTC AATACATGAG TTACTTCCTG TTCTGACATG CCCTGTTGCT TGATATTTGT 600
GCCCTGACCT GGCCGTGCCG ACCACACCCT CTAATGTTAC CTCTCACAGA GTGGTTTCAA 660
TACCATTTCT CCAAGATGCA GAAGGATTTG AGCGACGAAT TAAGGGAGGA GAAATCCTGA 720
CCTCTGGGGA ATTCTGTGCC AGGCTCCCTA CAATTCCCAG CGCAAGGGAC CATGCACATT 780
TATTGGCTGA TGAATGAAGC ACCATGTCTG GGAGAGGTTA CGGACAGGGT CTAGGGCACG 840
AGGGATGAGG ATGATCTGGG TACCAGTCAG AGTTACCCAG TGTTCCTTCT CATTGGGGAC 900
CTCATCCTGG CCCCAGATAT GTATATTACA TTGAGGAGAC TCAGCCTCTG CTCAGTTGGC 960
CTAGGAAACC CCAAGTCTGG CCTGGGTCTC TCCTCCTGGC TCCCAGATAC CCAGGTGGTA 1020
TCTGTTTGTG AGTTACCCTA TCCAATTTTG CTTCCAGGAC AGGGCCAGGA AGAGGGAGGG 1080
AGGAACCATC TCCTCTGGGC TGCCCCAGCA CTGGGCACAT CATGCCTCTG TTATGCCTCT 1140
GGTTTTTGTG TGTGTGTTGC GGGGGTGGGG GGTTGAGACT GAATCTCAGT CTATCACCTA 1200
GGCTGGAGTG CAATGATGCA ATCTCAGCTT ACTGCAACCT CCGCCTCCCA GGTTCAAGCG 1260
|
