Tag | Content |
---|
EnhancerAtlas ID | HS074-00268 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:28497590-28498960 |
Target genes | Number: 20 | Name | Ensembl ID |
|
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 | TGGGAGGCCG AGGCAGGCAG ATCACCTGAG GTCAGGAGTT CAAGACTGGC CTGGCCAACA 60 TGACGAAACC CCATATCTAC TAAAAATACA AAAATTAGCT GGGTGTGGTG GCGCACATCT 120 GTAATCCCAG CTACATGGGA GGCTGAGGCA GAAGAACCAC TTGAACCCGG GAGGGGGAAG 180 TTTCAGTGAA CTGAGATTGT GCCACTGCAC TCCAGCCTGG GTGACAGACC GAGACTCCAT 240 CTCAAAAAAA AAAAAAAACT TGACCTCACA GGATAGCCCT GATGTTGAAG ACAGACAACC 300 TCTACAGTGC TAGGCATATA GAAGGTACTC AATACATGAG TTACTTCCTG TTCTGACATG 360 CCCTGTTGCT TGATATTTGT GCCCTGACCT GGCCGTGCCG ACCACACCCT CTAATGTTAC 420 CTCTCACAGA GTGGTTTCAA TACCATTTCT CCAAGATGCA GAAGGATTTG AGCGACGAAT 480 TAAGGGAGGA GAAATCCTGA CCTCTGGGGA ATTCTGTGCC AGGCTCCCTA CAATTCCCAG 540 CGCAAGGGAC CATGCACATT TATTGGCTGA TGAATGAAGC ACCATGTCTG GGAGAGGTTA 600 CGGACAGGGT CTAGGGCACG AGGGATGAGG ATGATCTGGG TACCAGTCAG AGTTACCCAG 660 TGTTCCTTCT CATTGGGGAC CTCATCCTGG CCCCAGATAT GTATATTACA TTGAGGAGAC 720 TCAGCCTCTG CTCAGTTGGC CTAGGAAACC CCAAGTCTGG CCTGGGTCTC TCCTCCTGGC 780 TCCCAGATAC CCAGGTGGTA TCTGTTTGTG AGTTACCCTA TCCAATTTTG CTTCCAGGAC 840 AGGGCCAGGA AGAGGGAGGG AGGAACCATC TCCTCTGGGC TGCCCCAGCA CTGGGCACAT 900 CATGCCTCTG TTATGCCTCT GGTTTTTGTG TGTGTGTTGC GGGGGTGGGG GGTTGAGACT 960 GAATCTCAGT CTATCACCTA GGCTGGAGTG CAATGATGCA ATCTCAGCTT ACTGCAACCT 1020 CCGCCTCCCA GGTTCAAGCG ATCCTCATGT GTCAGCCTTC CAAGTAGCTG GGATTACAAG 1080 CGCATGCCAC CATGCCTGGC TAATTTTTAT ATTTTTAGTA GAGACAGGTT TTCACCATGC 1140 TGGCCAGGCT GGTCTCAAAC TCCTGATCTC AGGTGATCCA CCCACCTCAA CATCCCAAAG 1200 TGCTGGGATT ACAGGCATGA GCCACCGCAC ACAGCCATGC CTCTGTTATA CCAGGAATCA 1260 CGCTGACATC TTCCCAGCCT GGGAGTTCCT GAGTCCTGCT GGTGTCCTCG TGGCCAGTCC 1320 AGGACCCCGT CCAGGGAAAA AAGCAGGGCT GGGCACAGGC CCTGGCGTCA 1370
|