| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00040 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:1873370-1875800 |
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 | GCAATGAGAA CAGAGGAGTG GCCAGTGGCG AGGAGCGCCT CGGAGCCCAC AACCTCCCAC 60
GTCCTCCTGT CCCGGCCTTG GCGTCCTGGC ACCTACCGCG GCAGGAACTT GAGCTGCACG 120
GAGTAGGACG ACTGTGCCTG GATATAGCCT GTCTTGGGCA GGAGCTCCAG GTGGGCCCTC 180
AGCTCCTTGC ACACCTCGAA CTTCAGGCGC AGGGCAGCTT TCGACCTGTG GGCGTGTCGC 240
AGGGCACTGG GTCAGGTGCC ACAGTCGTGA TTCTGTGTGC GCTCAATGCC TGGAGTTATT 300
AAAACATTTC TGGCACCCAA GCCCCCGAGA GGTGCTCAGA GCCCACCCAC TCCAAGCCAT 360
GCACGTGCAC CTCGACAATC GGAGTCCTCA AAGCCCTGCT TTGTAAGGGC TGTTTTTTCT 420
GAAATGAAAT CTGATGAAGA ATTCTTAAAA ATAACCACAT CGAAACGGAA GCACGGTCCT 480
AATGGGCTCT CGGGAACCAG ATGCTTTCCG GGAAGAGCAC CTGCCAGGCA GCCCCTGGGT 540
GCGGGGCCCT GGAGGGGACA TGAGGGGTGG AACCCCTCCC TCCAGGGCTC TGCCCGCCTC 600
CTGCCCAGGG CATCCCCACA TCCTGCAGCT CAAGCACAGG GCACGTGGGG GGCCTGGGAC 660
GGCCACAGGC CTCGGTTATG ACAGCAGCCT CCAACCCAAG ACGAGCCTGA GAGAGCCAAG 720
GTACCCGCCA GTCACCTGGG AGGCCATGCG TCTGTCCGGT CCCTACCTCC GGCTCCCTTA 780
AGCCAACGGC CTCCTCAGGA CCACCTGGAG CCTCCCTGTT CCCACAGTGA AGCCTCCCTC 840
CCCTCCCCCG TCTTGGAGCC TCTGCTAAAC AGTGTTGTGG CCGCCCCGCC ACAGCTGCCC 900
CGGGCAATCC ACGAGGGGGG ACCCAGAGGG TGTGGCAGTG AGAAATCTCC TCCCTCCTGT 960
GCTTCCATGC GACAGTCACC CATGCTGTGG CAGCCTCATC TCCGTCCATC ACAGACCTGC 1020
CTCTGACCTC TGACCACTAC CCAGAGGCCA CCCACAGTGC GTCTGGGCAC GCCAGCCTCT 1080
GCACCCCTAC TGCTGGGCCC CATGGGAGGC GGGCGCCCGG GTGCTCAGAG ACCGCGCCCT 1140
CCCCGTCAGG CAGACGCTGC TCTGCCTTCC GGTTCCCTTA TGGGGCCAGA GTCTATACAA 1200
ATGAGCACAC AGCTACACTG AGGTACACAC AACCACAGCC GGAGACCATC CACAGAGCTG 1260
GGCCCCACTC AGCCCTCAAT GCCCGACAGA CACGCCTGGG CCCTTTCTGT CAAGTTTCCA 1320
AGGCCACTGA GAGGCTGTAG TAGGACGATG CCGGAGGCGA GCAGACTCCA CCGCAGACAC 1380
GCCAACACAC GCAGCTGGCT CCCGGGTCAC CGCAGGCTGC ACATTCCCGG CCCATGCCGG 1440
GCCCACAGGA GTCCGACAGC AGGAGGACAG GCGCCGCGGG AGCTGTTCCT ACCCAGGTCA 1500
CCGGGGAGAG GTGGCTGTGC CTGGGGCCGG TGCCCGGGGC CTCTGTGTCC GCACACCCTG 1560
CTCCTTGGTG CTGGTGGCAC AGGGGCTCCG TCATGGAAAC CCCGCAGGCC CAGCCTCGCC 1620
GTCCCTCTGC GCTTTCCCAC CGGCGTGGCT GTTCAGGGCA GGCTGCTTGC TCTGATGTCT 1680
GGAGCCCTTG CCAAACCCTG CAAGTGGAGG CTTCCTCCTC CAGGCTCACC CTGCCTGTGT 1740
CCACGAGGGG CTGAGGACTC TGGCCGGGCC CAGGCGGGCA GTGCGTTTCC TGTGGCTGCT 1800
GAAAGGATTT GCCCCAAGCT TAGGGGCCCC ACAACACAGA GGCACATTCA TTCTCTCCAC 1860
GTCCTGGAGG TCAGAAGCCA AGACGGAGCT AAGGCCAAGG TGCGGGCAGG GCCGTGCCCT 1920
TGTGGCTCTA CGGGACAGGT TTCTCCTCTC CTTTCACAGC CTCTAGAAGC TGCAGTGTCC 1980
CCGGGCTCGG GGCCCTTCCT CCATCTTGGA AGCCGACAGT GCAGTGTCTT CAAATCGGCC 2040
TGACTCTGAC CCTCCTGCCT CCCTGTGACG CCTCCCGTGA TGACACTGGC GCCTCCCAGA 2100
TGATCCTGGA TCACCCCCCA CCAAGGTCCC TCTCCCCAAC CATGTCTGCT AAGCCCCCTG 2160
CTTGCCACAC AGGATGCCGT TCAGGGCCTG GACAGCAGCC GTGGCAGCCC CAGGTGCCAT 2220
GTCCCCGCTG GCCACTGGGG GGCTCACCGC GTGTGCACAG GCAGGCAGCG GCTCACCCCG 2280
TGTGCGTGGG TCACCCCGTG TGCGTGGACA GGAGGGGGCT CACCGCGTGT GCACAGGCAG 2340
GCAGCGGCTC ACCCCGTGTG CGTGGGTCAC CCCGTGTGCA TGGACAGGAG GGGGCTCACC 2400
GCGTGTGCAC GAGCACAGAG TCCTGGTAGA 2430
|
