| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00670 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:24518770-24519940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr1:24519696-24519707 | TCTGATTGGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:24518790-24518805 | AAGGTCAGAAGTTCA | + | 6.22 | | RARA | MA0729.1 | chr1:24518790-24518808 | AAGGTCAGAAGTTCAAGA | + | 6.64 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_43744 | chr1:24512289-24520429 | MM1S | | SE_60528 | chr1:24506792-24533781 | DHL6 | | SE_67315 | chr1:24512289-24520429 | MM1S |
|
| | 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 |
| GH01I024188 | chr1 | 24515091 | 24519970 |
|
Enhancer Sequence | CTGAGGTGGG TGGATCTCCT AAGGTCAGAA GTTCAAGACC AGACTGGCCA ACGTGGTGAA 60
ACCCCATCTT TACTAAAAAT ACAAAAATTA GCTGGGCGTG GTGGCATGTG CCTGTAATCC 120
CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CGCTTGAACC TGGGAGGTGG AGGTTGCAGT 180
GAGCCAAGAT CATGCCACTG GACTGCAGCC TGGGCAATGA CAGCAAAACT CTGTCTCAAA 240
ATAATAAAAT AAAATAAAAT AATAATAATA ATGTGCAACA GGGGAAACAA AACCACATTA 300
CTCTGTGTGT GTGTGTGTGT GTGTGAGAGA GAGAGAGAGA GAAAGAGGGA GAGAGAGAGA 360
GAGAGGGAGT TCACAGCCTC TCCCTCTCCT GTCTACTAAG ATAATTATGC GCAGGCTGGC 420
AAAGTGTCCC ATAGGACTGG GAAAAGGCAG GAGAGGAGGC AAAATGTAAA AGCCAATTGG 480
GGCTGGGTTT TAAAAGTCAG TTTTGGGGGA CATGTGGAGA GAAAAGGAGC AAGTGCAGGG 540
ACCAGCTGCT CTAAGAGCTG AATGTGAGTG TGAATATGAG ATGTATGGAA AGAGAGGTGG 600
AGAAAATGGA TTTCCAAATT TTTGGCTCTG TGTCAGGACT GAAATTTCTT TTGGCATTTT 660
CCCCCCCCAA GAAACTAAAG ATTTTAAACC ATTGTTGTTT TGACTATTAT TCTTCTTGCT 720
GTTGTTTTAA TGTAATGCTG GAGGCAGGCA GGGCCCAGTA CAAGAACAAG GAGATCATTT 780
GTATGTGGGA GTGGAATTTA AGACTTTACC AGCTGCAAGA ACACAAACTC TAAACTGACA 840
TAAGTGCAAA AGGAATTCTG CAAGTTCCCC AGATTGAGAA GTTCAAGGAT GGATGTGGCT 900
CTGGGACGGC TCTAGTGGAA ACAGATTCTG ATTGGCCTGG CTTGGGTCAC ATGCCATTTC 960
CTGAGCCAAT CGATGTGGTC AGAAGAATGG GCTACTGTCA TTGGCCTCTC TGGGTAGAAT 1020
GCCCATCCCG GGGGAGAGGG GTAAGGGAGT ATTCTGATTG ACAGCTCCTC CAACTATAGG 1080
AACTGGAGGA AGATTGGTTC CTCAGAGGAA TGGAGGCTGC AGAGGCAAAC GGCATACACC 1140
CACTGCTGGG TTGCAGAGGA GGAGTCCTTA 1170
|
