| Tag | Content |
|---|
EnhancerAtlas ID | HS052-27044 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr3:128764360-128765680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr3:128765654-128765675 | GGAGGCGGCGGGGGAGGATGA | + | 6.18 | | ZNF263 | MA0528.1 | chr3:128765651-128765672 | GGGGGAGGCGGCGGGGGAGGA | + | 6.8 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_53691 | chr3:128765377-128766212 | Spleen |
|
| | 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 |
| GH03I129045 | chr3 | 128764383 | 128766418 |
|
Enhancer Sequence | AGGAATAAAT TATACTAATT CTCCACAATC TCTTGCAAGA GATAGAAGCA GAGGGAATGC 60
TTTCTAACTC ATTCTATGGG GCCAGCATGA CCCAATACCA AAACCCAACA AGACATTACA 120
AGAAAAAAAA ACTACAATTT GCTCCGGCGG AAGTGAGGAG CAGGCCTGGG CCCTAAGGGC 180
CGGGCCTCGA CCCCCCGCAG GTCCCCGCGG TCCCGGTCCC CCGCCCGGGA CATCTGATGG 240
ACCGAGCCGC GCCCCCGCGG AGCACCACTT CGGAGGCCTG AGAGCGGCGA CCGGGCAGGG 300
CGTGGCCTAC ATCCCGGAGC CTCGCGCCTT CTCCTGCGCC GACTTCTGCA GGGCCTCCGG 360
CTGCTCGAGC CGCCCTGCGC TGCTCCCGCG CCTGCACCCG AGGCTGGGGC AGCGGCGGCG 420
CTGGGTGACG CCGGAGGGGG CGCCCGACTT GAACCAACTG CGGCGGACCC GGGAGCCGGG 480
GTCCAGGAAT ACAGCCCGAA CCCCAAGAAT ACAACCCGAA CCCCAAGAGT ACGTGCCCCT 540
CAGAGACTGC AGCGGCTGCT GAGAGGAGCA CATCCAGGGC GGCTACTGCC CCAAGGGGTC 600
GCCACCTCTG GGACTGGCAT CCGTTCAGGG GCCCTCGGCA AGGGACATGT CCGCCCGGCC 660
GTGCGCCTCC CGGCCCAGGG CGCGCTGGAC GTGGACGCCC CTCGCCTGGT CTGCGCTGGC 720
CCTGCGGGCA GCTGGACCTG GTTCCGCGCC CACGCCTTCC GCTCCTCCAG CTGGTCCCGC 780
AGCTGGTCCC GCAGCGCCGG CGGACAAGAG AAGTGGCTCC TCGTCCCCAG GTGCGCGAGG 840
AGGCCCTGGG GACTCCCGCG GCTGCCTGCC CGACGGCCGG ACCTCCCGGG CACTCCCGAC 900
GCGCCTGCAC CCGCGACTCC AGCTCGCGGC CTGCCCTGGA GCTCACGCGC AAGGTGGGCG 960
AGATGGTGCT GATGCCAGTG TGGGGCACCA CCGGGTTCAC AACCTGCTAA GGCCGAGGTA 1020
CGTCCCGGCC ACCCAGGCCT GGAGCTAGAG TGTGCGCCCG CCTTCGACCA TGGGCCCTTC 1080
CGCAGGAAGA GGGCAGCGCC CCTCCAGACT GTCCCTCCAC TAGGAGGCGT CGCCGGGGCC 1140
CCGGCCTTTG TTTCACCCTC GCGCGCTCCT TCTCCGGCAT ACTCGCTCTG GGTCCGCCGC 1200
TGCCGCTCAT CATGAGGTCC TGCTCGGGCA TCAGCTTGGA AGAGCTTTAC CACTTCCCCA 1260
GGGTTCTCAC TGAGAGGCAG CTCCTAGTCC TGGGGGAGGC GGCGGGGGAG GATGAGGCCT 1320
|
