| Tag | Content |
|---|
EnhancerAtlas ID | HS092-25887 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:241855400-241856830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:241855631-241855652 | ACCTCCACCTTCCCTTCCTTC | - | 6.01 | | ZNF263 | MA0528.1 | chr2:241855672-241855693 | CTCTCCCCTGCTTGCTCCTTC | - | 6.02 | | ZNF263 | MA0528.1 | chr2:241855692-241855713 | CCCTCAGCCCTTCTCTCCTCC | - | 6.1 | | ZNF263 | MA0528.1 | chr2:241855634-241855655 | TCCACCTTCCCTTCCTTCCCC | - | 6.46 | | ZNF263 | MA0528.1 | chr2:241855643-241855664 | CCTTCCTTCCCCTCCTCTCCC | - | 6.88 | | ZNF263 | MA0528.1 | chr2:241855640-241855661 | TTCCCTTCCTTCCCCTCCTCT | - | 7.47 | | ZNF740 | MA0753.2 | chr2:241855863-241855876 | CCGCCCCCCCCAT | + | 6.67 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 241856097 | 241856248 | | chr2 | 241856600 | 241856800 | | chr2 | 241856139 | 241856600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I240912 | chr2 | 241852134 | 241857947 |
|
Enhancer Sequence | ACCCCGCAGA GGCCCCGGGC GGGAAACGGG CAGGCCCAGA AGGACCCACA GGTCGCGGAG 60
GGGACGCCCT GCCTGTACCC GCCGGCGCAG GTGGCAGCGC AGAGTCCCTG GGAGGGGCCT 120
GGGGAGTGGG CGGTGCCGAC CCTCAGGACC ACCCTGGAGC CGTGGGGAAG GAAGCAGCAT 180
CGGCGGGGTC CTAAGCGCTT AGGCTGGCGG CACAGGCCTC CGGACACGCC GACCTCCACC 240
TTCCCTTCCT TCCCCTCCTC TCCCATCCCT GCCTCTCCCC TGCTTGCTCC TTCCCTCAGC 300
CCTTCTCTCC TCCGGGTGGT TCCATGGGGG CGGCGCTGCC CTCACACTCC AAAGTCGCGC 360
CCACTCTACG CCCCCTGCGC CCCCCTCTGC GTCCCCCTGC GCCCCCCTGC TCGCCCCCTC 420
CTTCCCCGGT GCCCCCCGCC CACCTGCACG ACCCCTGCGT CCCCCGCCCC CCCCATGCGC 480
TCCCCCCGTG CCCCCGCGCC CCCGCGCCCC CTGCGCTCCC CGCTCCCCCC GTGTCCCCCT 540
GAACGCCCCC TGCGCTCCCC CCGCGCTCCC CGCGCCCCCC TCCGGCTCCA GCTGGGCCGC 600
GGCCTATTGC AGGCACCCGT CCACAGATGG AACCCATTAC GCCCCAGCGC CTCTCGGGAC 660
GTCCCGCTAA TAAGTGACCC TCTGTAAATG TTAGGAATGA GTCAAGTTTA CTCCGCGCTG 720
CAGCCTTCCC GTTAGCGGGT GGCGCCGCCG ATGCCCGGGG GAGCGCAGGG CGGGAGCTGC 780
TGAGCAGGCG GAGGGAGGGC GGGGCAGAGC CCTTCCCAGT CTGGGGGATT GAGCGGAGCA 840
TGACGGTCTC TGATCAAGGA GCCTGGGGTG CCTCTTGCCA CCCTGCTGGG CCTCCGTTCT 900
CCGCTGTGCA AAATAAGGGG TTTAGAACAG AATGGCTGAG CCCCTTCCAG CAGCTCTCCT 960
CCTGGTTGGT GGTCTTGGCA CCTGGGTCCC AGCTGGGCCC AGGAGGAGGA GCAGGGACTT 1020
CCCTCCCCCT CCCCCACTGG GCTGCTGCTC CCAAGGGGGG CCCATTACTC CCTCCAGAAG 1080
AAGAGGCAAT GGGGGAACCT GCAGTGAAGG CGCCTCCCAA GACCTCCCAG GGGACTGAGA 1140
GACAGACCCT GGTGCACGGG CTGTCGGGAG GACGGGCGGG CTGGCCCCAG ACCTCAGCTG 1200
ATAGTGGGGA GGCGTTTGCT GAGTGGCTGC CCTTTGCAGG GCAGCAGAGT CGGAATAGGG 1260
CCTCTCCAGG CGCCATGCTG AGCCTGGGTC TGCGGTGACT CTCCAACCCC GGCGAGGGGG 1320
GCCGCGATCT TTGGGGTGCA GATGGAGGAG GAGGCCTGTG TCCAGGGAGC ATCCGGGATA 1380
GCCAGACAGC ATGCACCAGG TGCAGGAGGC CTGGCTGGGG TTGGGAGGAG 1430
|
