| Tag | Content |
|---|
EnhancerAtlas ID | HS053-01495 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:55486770-55488310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:55487917-55487936 | TGGCGCCCTCTGCTGGTCT | - | 7.51 | | EWSR1-FLI1 | MA0149.1 | chr1:55488016-55488034 | TATTCCTTCCTTCCTCCC | - | 7.54 | | EWSR1-FLI1 | MA0149.1 | chr1:55488020-55488038 | CCTTCCTTCCTCCCTTCC | - | 9.6 | | ZNF263 | MA0528.1 | chr1:55487392-55487413 | GGAAGAGAGGGGAGGAGAGGA | + | 6.02 | | ZNF263 | MA0528.1 | chr1:55488012-55488033 | TCCCTATTCCTTCCTTCCTCC | - | 6.04 | | ZNF263 | MA0528.1 | chr1:55488004-55488025 | TCCCTCTCTCCCTATTCCTTC | - | 6.08 |
|
| | 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 |
| GH01I055021 | chr1 | 55487341 | 55488393 |
|
Enhancer Sequence | TCTTGTTCAC TGCTGTACCC CAATGTCTGT AACATGGAAG GTGATCAAGG GAGGTTTTGT 60
TCTGTTTGCA TTTTTTTTCT TTTTGAGATG GAGTCTCCCT CTTGTCACCC AGGATGAAGT 120
GCAATGGCGC GATCTCAGCT CACCACAACC TCCGCCTCCC AGGTTCAAGC GATTCTCTGC 180
CTCAGCCTAC CGAGTAGCTG GGATTACAGG CATGCGCCAC CACGCCCGGC TAATTTTGTG 240
TTTTTAGTAG AGACAGGGTT TCTCCATGTT GGTCAGGCTG GTCTTGAACT CCTGACTTCA 300
GGTGATCCAC CCGCCTCAGC CTCCCAACGT GTTAGGATTA CAGGTGTGAG CCACCGTGCC 360
CGGCCTGCAT TTTGTTTTTT TAGGGTGGAA GAGATCTGAG CGTGCTGAGA GGCTGGCAGG 420
AAAAAGGGTG AGTAAGCCTT GATGTGTACA AAAGAGAGAC AGAGAGAGCC AGGCAGACAT 480
GTCAGAGAAC AGCAACAGCT CTTCCCTTTA AGCCGGCAGG GAGTGGGGAC ATACAGGGTG 540
GAGAGGGGCT GCCTGTGGCA GGTGCCAGGA AGACCCCAGT GGCCTCCTTT TCTCCATGAA 600
GTGGCAGACA AGGGGCTTCC TGGGAAGAGA GGGGAGGAGA GGAGAGGGTG GAGACTGGTG 660
ATGTGCATTG GGCCCAGAGC CATTCTTGAG CAGGTGGAGA GGAAAGCATT TTTGAGGCCG 720
GCGTGCTGGT CATGACCCTC TTTTGTTCAG AATCTCCCAG AGTCCCCTAA CCTCAGGAGA 780
GGGCCATGCC TTGGCCTCGA GAGGCGTTAA AAACCAGCCT CCCATCTCAG TGTCTCCAGC 840
TGGGCCATGC ACTGCTTCCT ACCACCATTA TAACTGGACC ACAGATCCCG AGCTGCCACC 900
TCCAGGAAGC CGGCCCGGAT TCAGTGCCCA TCTGACTGAG TTCCCGCAGC ACCTAGCCTG 960
TCCCTTCTGT GAGACTTGGC TCCTCTTGCC TCCTATCACA GTCGCCTGTG CTCTCATCTG 1020
CCTCCCTGTG GACTCTGAGG ATGAGGCGAG GGCTGATTCA GCTCAGGGGT GAGAGCAGGT 1080
GCCAGCAGCT TATGGGCTGG GCCGGGCCTG GGCAGTGGGC AGGCCGTGGG CTCAGATGAC 1140
AGGTACCTGG CGCCCTCTGC TGGTCTAGCT GGGCAAGGCT GCTGCTCCAG AGTGGCCGGA 1200
AGCTTCCTGG GAGAGGCCTG GTTCTCTGGG CCTGTCCCTC TCTCCCTATT CCTTCCTTCC 1260
TCCCTTCCTG AAACTGCGTC CTCCAAATCC TGCTCCAGCA CCAGCAACCC CCTGCTTTTC 1320
AACAGCCTCT GGCAGCGTTT CGGTCCCTTT CTGGCCTTGA CTGGAAGGCC CCTGTCCCCC 1380
AAGGACACTG CTGCCGTCCC TGCAGTCCTT TCCCCCCGCC TGAGAGGGGT AGGGTCTCCT 1440
TGCTCTCAGT GCCCCACTCT CTGGATCATT GTCCTTCTCT CCTCCATAAA CGCAGTCATG 1500
CGCCACACAG CAATGTTTCA GGCAACGACA GACCACATAC 1540
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