| Tag | Content |
|---|
EnhancerAtlas ID | HS113-00051 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:1873860-1875360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:1874294-1874305 | AGAGGGTGTGG | - | 6.02 | | MYC | MA0147.3 | chr1:1874008-1874020 | GGGCACGTGGGG | - | 6.07 | | NR2C2 | MA0504.1 | chr1:1874393-1874408 | TGACCTCTGACCACT | - | 6.05 |
|
| | 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 |
| GH01I001942 | chr1 | 1873910 | 1876089 |
|
Enhancer Sequence | CGGGAACCAG ATGCTTTCCG GGAAGAGCAC CTGCCAGGCA GCCCCTGGGT GCGGGGCCCT 60
GGAGGGGACA TGAGGGGTGG AACCCCTCCC TCCAGGGCTC TGCCCGCCTC CTGCCCAGGG 120
CATCCCCACA TCCTGCAGCT CAAGCACAGG GCACGTGGGG GGCCTGGGAC GGCCACAGGC 180
CTCGGTTATG ACAGCAGCCT CCAACCCAAG ACGAGCCTGA GAGAGCCAAG GTACCCGCCA 240
GTCACCTGGG AGGCCATGCG TCTGTCCGGT CCCTACCTCC GGCTCCCTTA AGCCAACGGC 300
CTCCTCAGGA CCACCTGGAG CCTCCCTGTT CCCACAGTGA AGCCTCCCTC CCCTCCCCCG 360
TCTTGGAGCC TCTGCTAAAC AGTGTTGTGG CCGCCCCGCC ACAGCTGCCC CGGGCAATCC 420
ACGAGGGGGG ACCCAGAGGG TGTGGCAGTG AGAAATCTCC TCCCTCCTGT GCTTCCATGC 480
GACAGTCACC CATGCTGTGG CAGCCTCATC TCCGTCCATC ACAGACCTGC CTCTGACCTC 540
TGACCACTAC CCAGAGGCCA CCCACAGTGC GTCTGGGCAC GCCAGCCTCT GCACCCCTAC 600
TGCTGGGCCC CATGGGAGGC GGGCGCCCGG GTGCTCAGAG ACCGCGCCCT CCCCGTCAGG 660
CAGACGCTGC TCTGCCTTCC GGTTCCCTTA TGGGGCCAGA GTCTATACAA ATGAGCACAC 720
AGCTACACTG AGGTACACAC AACCACAGCC GGAGACCATC CACAGAGCTG GGCCCCACTC 780
AGCCCTCAAT GCCCGACAGA CACGCCTGGG CCCTTTCTGT CAAGTTTCCA AGGCCACTGA 840
GAGGCTGTAG TAGGACGATG CCGGAGGCGA GCAGACTCCA CCGCAGACAC GCCAACACAC 900
GCAGCTGGCT CCCGGGTCAC CGCAGGCTGC ACATTCCCGG CCCATGCCGG GCCCACAGGA 960
GTCCGACAGC AGGAGGACAG GCGCCGCGGG AGCTGTTCCT ACCCAGGTCA CCGGGGAGAG 1020
GTGGCTGTGC CTGGGGCCGG TGCCCGGGGC CTCTGTGTCC GCACACCCTG CTCCTTGGTG 1080
CTGGTGGCAC AGGGGCTCCG TCATGGAAAC CCCGCAGGCC CAGCCTCGCC GTCCCTCTGC 1140
GCTTTCCCAC CGGCGTGGCT GTTCAGGGCA GGCTGCTTGC TCTGATGTCT GGAGCCCTTG 1200
CCAAACCCTG CAAGTGGAGG CTTCCTCCTC CAGGCTCACC CTGCCTGTGT CCACGAGGGG 1260
CTGAGGACTC TGGCCGGGCC CAGGCGGGCA GTGCGTTTCC TGTGGCTGCT GAAAGGATTT 1320
GCCCCAAGCT TAGGGGCCCC ACAACACAGA GGCACATTCA TTCTCTCCAC GTCCTGGAGG 1380
TCAGAAGCCA AGACGGAGCT AAGGCCAAGG TGCGGGCAGG GCCGTGCCCT TGTGGCTCTA 1440
CGGGACAGGT TTCTCCTCTC CTTTCACAGC CTCTAGAAGC TGCAGTGTCC CCGGGCTCGG 1500
|
