| Tag | Content |
|---|
EnhancerAtlas ID | HS172-00758 |
Organism | Homo sapiens |
Tissue/cell | SGBS_adipocyte |
Coordinate | chr1:153478940-153480080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:153479529-153479550 | TGAAGAGGGGAAGGGGGAAGA | + | 6.03 | | ZNF263 | MA0528.1 | chr1:153479781-153479802 | CCCTCCTCCCACCCATCTTCC | - | 6.16 | | ZNF263 | MA0528.1 | chr1:153479784-153479805 | TCCTCCCACCCATCTTCCTCC | - | 6.53 | | ZNF263 | MA0528.1 | chr1:153479769-153479790 | CCCCCCATGTCTCCCTCCTCC | - | 6.86 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_02992 | chr1:153478832-153481149 | Bladder | | SE_28418 | chr1:153478695-153480927 | Fetal_Intestine | | SE_36529 | chr1:153479156-153480743 | HMEC | | SE_52579 | chr1:153478743-153481142 | Small_Intestine |
|
| | 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 |
| GH01I153506 | chr1 | 153478735 | 153481271 |
|
Enhancer Sequence | TACATCACCC CTGTACGCAC AGCCACATGG CACCCAGGTC CACATGGGCA GTGAGCCACC 60
ACCTCTCATC TGCTTCCTCT GTCACAGGAC TACAAGGGGC TGAGCAAGGT AGGCATGGTC 120
AGGGTGCCAG GCATCAAGGG ACAGGGCTAT CGGATCAGCC GGGCCTGTGC TGTGACAGGT 180
AGGAGTGAGG CAGTATGATT GGGAGCACCA CCAGCACCAC TAAAAATGGG GAGAGAAAGT 240
TCCGCTAGGA ATGGGGTTAT CAGAAATGGG AAGAGACGGT GGTCAGACCT GTGTGGGTGA 300
AAATGAATGC AGGAATGACA CCAAAGACCG GCTAGCTTCC ACAGCCCTTT GCAGGATGCT 360
CTGAACTTGC TGAGCCCTTT CACACCCGCC ACCTGGTCCC TGTTGACCCA CCAGCTGTAT 420
GCAGCTGACT ATCTTCACCA GCTCCTTGAA CAAGAATTTC CATTTCCAAG GCCAGGGTGG 480
GGGAGGCTGC AACATTTTTT GCCAGAGAAT CCAAAGAGCA CATGAGTCAG CTGCCTGGGT 540
CAAGGCCCAG ATCCCTGTGG CGGGTCAGCC AGAGAGCAGG AGCTGGCCCT GAAGAGGGGA 600
AGGGGGAAGA AAGAAACCCA GAGGGCTCAG AGAGCACAGG ACCCTGCCCA CGTGGGCCAC 660
TCTGCAGAGG CCAGGCCCAA GGCTGAGTTG GGCCTCCCAC ACAGACATGG AATGAGAAGG 720
CTGTCAGTGC AGGACAGGGT GAGGACACAC TCAGCGGGCA CGGCTTTCTC CCCTAACAGC 780
CACTCCACCC AGGGGCCAGA AACTGACTTC ACCTCTGCAC TGAATTCCTC CCCCCATGTC 840
TCCCTCCTCC CACCCATCTT CCTCCTGGTG CTTCCAGCAG AGCCAAGAAG GCTTCGCCCC 900
ACCTACTCCC CTCCTGCTGA CACGGACCCC CCACACACAC ACCCAAGGAA CAGGAATACC 960
AAAAATGATA CTACCAGAGT GAAGCGTGTC CTGCAGACAT TATCTCTTTA ATCCTAACTA 1020
TAATAGTCCC TATTTCAGAG ATGAGGCAAA TGTGAGAGAA CAAGTAACTT TCCCAAGAAC 1080
ACACAACCAA GAAAAAAGAA AGCCAAGATT CAAGTGCAAG TCTGCCTGGG GGTCTGGAGC 1140
|
