| Tag | Content |
|---|
EnhancerAtlas ID | HS113-23627 | Organism | Homo sapiens | Tissue/cell | Keratinocyte | Coordinate | chr22:28408000-28410230 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr22:28408984-28408995 | CCACACCCTGT | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 28408050 | 28408090 | | chr22 | 28408794 | 28409005 | | chr22 | 28409651 | 28410158 |
| Enhancer Sequence | AAAGAATGGA GAGTCCAAAT AACCTTCAGA GGAGCGGGGA TCCCTGGGAA ATGCAGGCCT 60
CAGGGCGAGC AGGAGGGAAG GCTGGTAGTA AGTCACTGAA ATGGTTTGCA TGACAGTCAG 120
TAGCAGTAAA GAAAACTTGG AAAAGCAAAG GAGCTAGGTT TATATTTCTT CCTCCAAGGT 180
ATGGCACATA AATCAGGGTA AGTGATGATG GTATCTCAGA AGCTTTAAGC TGGAGAATTC 240
TCTGCAGTTT TGGTCATCTC ATTAAAAGGA GGACGCAGGA GAGGGTCATA ATCCTAAGAA 300
GGGAAGGACA ACCGAGCACG TGCAAGGACT GCAAGAATGT GCATGCAAGG ATGTGATCGG 360
ATCCGGGAGG CCCAGGAGCA CAGGGAAGGC TTGGAGGGAC AGTGGCAGTG ACCCGGCACT 420
CGGAAGAGGT ATCTGGGCAC AAGAAGCCAC TGCTCGCCAG GCACACATTC ACTGCTGCTG 480
CTGCCTCAGG GGCTTTATGC ACCTGTATGT TTTTTTTGAG ATATGGTTCA GTTCTGTCAC 540
CTAGGCTGGA GTGCAGTGGT ACGATCATGG CTCATTGCAA CCTCGATCTC CCAGGCTTAA 600
GCGATCCTCC TACCTCAGCC TCCCGAGTAG CTGGGACTAC AGTTGTGCAC CATCATGCCT 660
GGCTAATTTT TGTATTTTTT GTAGAGACGA GGTCTCACTA TGTTGCCCAG GCTAGTCTCG 720
AACTCCTGGG CTCAAGTGAT CTGCCCGGCT CGGCCTCCCA AAGTGCTGGG ATTACAGTCA 780
AGAGCCACTG TGCTTGGCCA GGTGCTTTAC ACATTTGTCT AACCTGCTCT AACCTGTTGC 840
ATTGGGTGTT ATCATCCTCA TTTTCTAATG AGGAAACAGA TACTCCAGGA GGGGAAGCAG 900
CTTTGCCATT GTCACCCAGC CAGAAAAGGG CAGTGCCAGA TGCAAATCCA GCTCTGCTGG 960
TTCCCAAAGG CTCTGTGCTT TCCACCACAC CCTGTCCCCA AGCCAGAGAA CATCCAGAGG 1020
GCACTGGCAG GTAGCGCAGC CTCCTGACAA ATATTAGGCA AGACACATCC TTGGAAGGCC 1080
AGGCAGGGAA GGTATAGGCA TTTTCTGGGG ACAAAGAAAT CATTGTGCAG ATGTGGTTTC 1140
CCGGGGATAC ATTTCTCCTC CGTCATTTGG CTGGAGCAGA AGAGAGAGCT GCTGAAGGCC 1200
ACTCCAACAG CTGTGAGACA AATCTCCCAC CTGGCTGCAG ACTGCTGGGA AGAAGGGGCC 1260
ATGCAGCCTG GCTAACAGCA GCCTGCTCGC CTGCTGCAGG CTCCCTGGGC TTTCCTAACA 1320
GTCTACGCAA AGGCATCTGA TGGGCTCACC GTTGGGATTT GCGAAGATCC TGAGCCCTCC 1380
AGCACTCTCT GCTCAGTCAG AGGGCTGTGT TTGAATTAAA AAGTGATGTG CAAAGACCAG 1440
GGCAGGTGAA TACACACCAC AGAAAACCTG TCTGTGGCAG ATTATGCAAG GGTGTCTTTA 1500
ACGTTAGACT CTATGGTGGA GTCAGTGATT CCCAACAATA TCTGAGGCTG AGGGCAAGAG 1560
GGAGGTGGGA ATTGATTCTC TGAGACTCCA TCTCACCAGA AAGCATAGCC CTGGCTCGAA 1620
GTTGCTCAGA CAAGATTCTA GGATGAGAGG TGGGGAGGTG GGGAAGCATT CATTCCCAGT 1680
AGGGTGTGGG CGCAAGGTGC AAAGAAGCCC TCTGGGAAGG GCACAGCCAC GGCCACATCC 1740
CCGAGGCGTC TGCTAGGTGG GAAAGGGCAC ATCCACGGCC ACATCCCCGA GGCATCTGCT 1800
AGGTGGGAAA GGGCAGCCTC GTCCTCACAC TGATGCACGG CCCCTACTGA CAACTGCTTA 1860
GAGGTGCACC TGCGCCTCCC TGAGCCGCAC CATCACTCTG TTGGGCAGGC TGGGAAGGGA 1920
GCATCATTTC ATTTTGTACA TGAGGTCACT GAGGCTGAAT GTACCCGGCT TGTAGGGAGC 1980
AGAGCTAGGG CTTGAACCCA GATTTGCAAC TTAAAGCTCA AGGCCTCATC CACTACCAAC 2040
CAACCAACCA AGTCTGTGCT CCACCTTATT TTTCAAATGC TCACTGAGAA GCTGGACAGA 2100
GCGGACTTGT GTTCTGGAAA GCCTCCGGTT GTCTCGGGAG CCCATTTTGG TGTCTAAGAG 2160
GGATACATGT GGGCGCTGAC TGGTAAGCGA TGTGTTCTGA TGCGGAGGAG CCTTGTGCCC 2220
CCAGGAGGTG 2230
|
| |
|
|
|
