| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23799 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:33588810-33589950 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:33589169-33589184 | CAGGTCAGAAGGTCA | + | 6.56 | | RARA | MA0729.1 | chr19:33589169-33589187 | CAGGTCAGAAGGTCAAGC | + | 7.09 | | SOX10 | MA0442.2 | chr19:33588928-33588939 | AAAACAAAGAA | + | 6.62 | | SPI1 | MA0080.4 | chr19:33589799-33589813 | TACTTCCTTTTTTT | - | 6.3 | | SPIC | MA0687.1 | chr19:33589799-33589813 | TACTTCCTTTTTTT | - | 6.79 |
|
| | 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 |
| GH19I033097 | chr19 | 33588371 | 33589650 |
|
Enhancer Sequence | AATTCGACAG CCACAAACCT AATGGCAGGA CCAAGTGTCA GGGTATCAGG AAGGAGGGGC 60
TGCAAGAGCG ATACAGGAGC ACCAGCCTCT GTTGTTGGTC AAAGTCACGG TAAGAAACAA 120
AACAAAGAAG CGAGGCCCAG CATGGGAAGT GAAACAAATG CAGGATTCAG ACCTGGCCAA 180
GGCCAAAGCC AGCTGTCAAG GTGGGGCCCA GGTGGGAGGG AGGGAGAGGT CTGTAATCAG 240
GGAAAGAGGA ATGCCTGGAC CAGTGACCAC ATGGCTGGTC AGAGCTGGCA GTGGGTCAAA 300
GGGAAGCACC CAGAGCTCGA GGAACTGGGC AGGTGGCCAA AGGAGGCCAA CACATGCAGC 360
AGGTCAGAAG GTCAAGCCAG GGGACCAGGA GGCAGGTACA CCAACAGCCT GCAGCAAGAT 420
GGAGCTGGGC GCCCAGTCCG TCTTCTCCCT TGAGTCCCTG GCTCTGAGGA GGCTCTTGTT 480
GGGATAAGAG GCTGACATCT CTCAACACAA CTTTAACTTC ATGCTGTGTT GAAATTTCAA 540
GGTGAATCAG ATCCTGTGGT TTGAAGTCAC ATTTCAGTTG TTTCCAGAAA AGGTGCAGGG 600
CCAGACAGTG TAGAGTCGGT ATTAGCAGCA TGTGATTTGG AGTCAGTCAG ACCTGGGTTT 660
GGATGCCAGC TCTCCATTGC CCAGCTTTGT GACCTTAGGC AAGGCTCATA ACCTCTCTGG 720
GCATTGGAGT CCACATTTGT AAAGTGAGGA TAAAATCCAC TCCAGAGGTG GTTGTGAGGA 780
TTAAGTGGCA TAACTCAGTG TCTGGCAAAG CACCTGTCCC AAAGACTGAA GAAGTGGCAC 840
CTACTATTCT TTGGTTATCA TACAGTCATG TGTCACTTGA CTGGGATGGT ATGACAGGGA 900
ACCCAGGGTT TTACACAGGA CACTGGAAGG GCATGTGTAC CCAGTGTTAG GAGACTTAAC 960
CTCCGGGTGG TCAGTGGGCT GCTAGTACTT ACTTCCTTTT TTTTTTCCTT CCAATGTTTT 1020
TCTTTTTTTT TCCCCTGAGT CATTTAGCTT CTGAGCCTTC TTCCTTTTGC CTCCCTATAG 1080
TTTCTGATTT CTGTCCCCAA ACTATGGATT ATTTTTATAT AACTTAAATG AAGATATATT 1140
|
