| Tag | Content |
|---|
EnhancerAtlas ID | HS091-15453 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr15:78909480-78910950 |
Target genes | |
SNPs | | Number: 4 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr15:78910916-78910935 | TCACCACCAGGGGGCAGCA | + | 8.06 | | EWSR1-FLI1 | MA0149.1 | chr15:78909480-78909498 | GGAAGGAAGCAGGGAGGG | + | 6.98 | | ZNF263 | MA0528.1 | chr15:78909481-78909502 | GAAGGAAGCAGGGAGGGAGAA | + | 6.27 |
|
| | 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 |
| GH15I078618 | chr15 | 78910841 | 78911170 |
|
Enhancer Sequence | GGAAGGAAGC AGGGAGGGAG AAGGAGACGG TAAAAGAATC AGCCTGGTTT TACTTCCCGT 60
GGCACCACCC ATCTTGGTGA CTCCCCACCC CTGCTGCATG TGACCGAACC ACATCCATGC 120
CATGATCACA TAGTCCAACT TCTCCTGTGG GTGTAGTGCA GGAGAGAGCA CACGGCTGGC 180
TCTGCGGGCC ACCTCCTGGC ACTAGGGAAG CCACTGCCCC CATAACCATG AGCAAGCCCA 240
GCCCCTCATC AACCAAACAG GGCCTACTCG TGCTTTCTCT GGTCACTTCT AGTGCCAGGT 300
GGAGACTCCT GGACTTCATG CATCATGTCC AGGTCCATGT GCCTGTTTAC AGCCCCTGAA 360
TGGCTCTCCA GGGGTGTTTT CCAACATAGA CACTCTTTCA CCCCAAGGTT AAGCAAGACT 420
GGACTCTGAA AGATTCCGGG GGAAGAATCC ATGACCCCTG CAGGGCCCAG GAAGTGTCTG 480
GGTCCAGAGG CTGGGAGGTC TGAGTCCTGA GCACCAGAGG AGAGAGGGGT GAGGCTGCGG 540
CCACAGAGGG AACGTGTGCA TCAAGTACTG GGTGGGGCAC TGTGCCCATC TGGCTTTCCA 600
ACCTCCTGGG GATGAAGGCT GTGTGTGCTG AGTGCTCAGC TGGCCAGGCT GGCAGAAGGG 660
TCACCCGCAG GCCAATGGGC CATTATGTCT CCTGGCAAGT CTGGACAAAG CCTCCCTGGG 720
GAGGACATGT GGAAGGCAAT TTCTTGGCCT CGATCTGAAC AGGAAAATCT ACTCCCACGC 780
TACCAACAAC AGCAGCATCT TATTCTGACT TAAGAATGAG TATAGGGGCT GTGCACAGTG 840
GCTTCTGCCT GTAACCCCAG CACTTTGGGA GGCTGAGGTG TGTGGTTTGC TTGAGATCAG 900
GCGTTCGAGA CCAGCCTGGG CAACATGGCG AAACCCTGTC TCTATAACAA ATCCAAAAAT 960
TAGCCAGACG TGGTGGTGCA CAGCTGTGGT CCCAGCTACT TGGGAGGCTG AGGCAGGAGA 1020
ACTGCTTGAA CCCTGCTGGT GGAGATTGCA GTGAGCCGAG ATCACGCCAC AGCACTCCGG 1080
CCTGGGTGAC AGAGCGAGAT CCCGTCTGGA AAAAAAACTG AGTTTTTAGC AAGAGGGAGA 1140
GAAGGAGGTG TCTCAGGCAC CACCCCAGGG TTTGGGGGCA GGGCTTCAAT CTCAGGTTCG 1200
TACTCTTCTG TTGTGTGAAC ATGGAGAATG TCTTTCTCCA GGCTGCAACC TGTCCATCTG 1260
GGACTTGAGG GGTTGGGCCC TACAGTCCTT CCAGGGGGAC TGTAGGGCAG TGCATGTGAC 1320
CTCAAGCCTT AGAAGAGATA TATCTGCCAG TCAGTGGACC CCAATCTGGG TTCCACAGAA 1380
GTAAATGAAG CCTGGTCTTT AGGCCTTTCT TGGTTCACCT AAAGCAAATA AAACAGTCAC 1440
CACCAGGGGG CAGCAGTGCC TAGGGTCTGG 1470
|
