| Tag | Content |
|---|
EnhancerAtlas ID | HS091-15457 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr15:79029550-79030980 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr15:79030648-79030667 | TCCTGCCCCCTAGTGGCCA | - | 7.89 | | Klf1 | MA0493.1 | chr15:79030732-79030743 | AGGGTGTGGCC | - | 6.32 | | ZNF263 | MA0528.1 | chr15:79030159-79030180 | AGAGGAAGGAGGAGGGGATGG | + | 6.02 |
|
| | 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 |
| GH15I078737 | chr15 | 79030177 | 79031145 |
|
Enhancer Sequence | TGAAAAGTAT TTTAAAAAGT TATGAAAAGG AAGTTACGGG ATTTTTTTTT AAGTCATGGG 60
ATAAAAATAA AAGCAGGTCT CTGTCGGCAC AAGCCTGGAG AAGTGGGACT GGAGACTTCG 120
CCCCCGCCAT GGACCAACCA CCCCTTCCCA GTCACCCCTT TACCATTAGG GTGGCAAGAC 180
AAGATCCCTG CCTAATGGGG GGAGATAAAC AGACCCTTTG GCACCTGACC AGGGCTGAGT 240
CCTTAAATTT CTGGATGATG ATGATTGTTA TTTAAGAGCC AGAGGCTGGC GGAGTTGGTT 300
TGTTTGGAGG AGGCCTGATG GCCTCCCCTA CTCTCACCAA AGCAACTTTT CCCTCAGGGG 360
GCTCCCATCT TATTCAGAGA GGCAGCTGAG GCGGGACAGT GGGGCTAACT GTAGAGCAGG 420
TGAGGGCTCG GGCTGCTGGG GTGGCCCCCC TTCCCCAGTG TACACATAGT ATCTGTGTAA 480
CATTTTGTAT ATTCCGGGGG GTAGGGCCAC CCCTTGTATC ATACCTACCA GAGGCTGGAG 540
CTGGCATATG AGGAGGAGGT TCTAATCATT ATTTACGGCT GGGAAACTTA TTTATTGATA 600
GCATAGGACA GAGGAAGGAG GAGGGGATGG GGTCCTGGCT GCCTTGGTGA TGTGACTCCT 660
GTTTATTTTG CTTTCCATTT TGGAATAAAT GGATTTAGCC ATACTGCTCA GCCTGGTGGG 720
TTCCCATTTC CCTCACTGGG TCCTGGAGTT TGCGCCACTG AATGAAGAGC CCCAGAGTGA 780
GCATGTCCAG CTGGGCTGTT GGGGACCTTC CAGGCCTGTT ACCTGTATGC TGCCTGGTGA 840
CACCTGGTAG ATTGCATGGG GATTGCTATG GCGCCTATGG GGCACAGTCC GGCCCTGACA 900
GCCAACAGGC TCAGAAGCCT GATCTAGCGG TGGCCGGGAA GGCAGATACG AGCACCCAAG 960
GCCACTGACT TCCATTCACC CCAGTCGTCT TCGGTTCCGT CCCCTTGCCT CCCTCTCCTG 1020
TCTGCACAGG GTGGCCTGTT CTGTCTGGCC CTCTAGAGTG TCAGCTGCCC CGCAGGCTCC 1080
TCCAGGCTGA GTTCATGGTC CTGCCCCCTA GTGGCCAGAG CCAGCTTCAC AGGATAAGAG 1140
CCAGCTAAGC TCCAGGGGCT TTCCAGGAAG TGTCCCTTGG AAAGGGTGTG GCCTTTTCAC 1200
CGCTCCCAAC AGCACCCTAG AAATGGCTTG GCTTTTTCCC TCCCCTCAGC TCCACAGAGA 1260
ACACAGCCAG CAGAGGACAC ATTCCCCATC ATCCAGAAAT GGGTTTGATT CTCAGCCAAG 1320
GGACACCAGG GCTGGTAGAG ACTGTCAGGC CACACAGCTG CCTGCACAGC ACCCCCATGC 1380
TTGGTGGGGG GTGGGAGGGA TGGCGGGGGG TGGGACGGTG GGGGGGTGGG 1430
|
