| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23315 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:12312380-12313850 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:12313647-12313665 | GGAAGGAAGGGAGGGAGG | + | 8.13 | | Nr2f6(var.2) | MA0728.1 | chr19:12313672-12313687 | TGACCTCTTAAACTC | - | 6.27 | | RUNX1 | MA0002.2 | chr19:12313767-12313778 | CTCTGTGGTTT | + | 6.14 | | ZNF263 | MA0528.1 | chr19:12313249-12313270 | AGAGGAGAGAGAAAGGGAGGA | + | 6.84 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 12313455 | 12313555 | | chr19 | 12313174 | 12313445 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I012202 | chr19 | 12313221 | 12313370 |
|
Enhancer Sequence | TCCTTCATCT CTTTATTATT ATTTTTTGAG ATGGAGTCTC GCTCTGTTGC CCAGGCTGGA 60
GTGCAGTGGT ACGACCTCCG CTCACTGCAA CCTCTGCCTC CCGGGTTCAA GCGATTCTCC 120
TGCCTCAGCT TCCTGAGTAG CTGGGACTAC AGGCATGTGC CACCACGTCC AGCTAATTTT 180
TTGTATTTTT AGTAGAGACG AGGTTTCGCT ATGTTAGCCA AGATGGTCTC AATTTCCTGA 240
CCTCGTGATC TGTCTGCCTT GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACCGC 300
ACCTGGCCTT TATTTTTTTA ATTATTATTG TTATTATTAT TTTTTGAGAC AGAGTCTTGC 360
TCTGTCACCC AGGCTGGAGT GCAGTGGTGT GATCTCAGCT CACTGCAACC TCTGCCTCCC 420
AGGTTCAAGC AATTCTCCTG CCTCAGCCTC CTGAGTAGCT GGGATTACAG GTGTGCATCA 480
CCACGCCCGA GTTATTTTTG TAGATCTTCT CTTGCTCTGA CTTGCTAACC CACTGTCCTG 540
CCTGATGGCC AACATGTCCA GTGAGCTACT GCTGGCTAGA AAGCTGGTGC TTCGAGTGTG 600
CTGCTCTGTG TTGCATGTTG AGCCCTACCA AGTATGGGTT CTATATTCAA CTGACTGAGT 660
CTGCCTTTTT AAAAATAATT CTTTGGCATT TAAGAGTAGG ACTATGCTAT TGGACCCCTC 720
CTTCAATTGA TGCTGGATCT ATCTGTGTGT TTAGAGTGAA GCTGTGCCTG ATGCTGGGTT 780
GGCCCGGTGT GCAGGGTGCC AGGGTGCAGC GGGAGGGTGG ACTATATACA CCCTGTACAA 840
GAGGTGCTCC TGAAACAGTA GTCATTTAAA GAGGAGAGAG AAAGGGAGGA AAGGCAGCCA 900
TCAGGTGGCG CACTGAGTCC ACACCCCAAA AGGCAAAGGG CTCACCAGGA CCTTAAGGAC 960
CTCTGCTGCT GCTGCTGCTG CTTCAGGTAC CTTTATCACA ACAAATATCC TGACCCTGGG 1020
GCATAGACGG GACAATATCC ATGATTCCCC AGTGGCATAA CAAAGGGGTT AGTTTAAACC 1080
TGACATAGGC TAGAGATCCT TAAACCCTAT GAAGGAACTA TTGCCATGGA GGAGGCCCCT 1140
AACTCTGATG ACACTGAACT GAGCCTCTCT GGAGGAAAAA AAATTGTAAC TGTCCCATTA 1200
GAGAAAGTAC CCCTTTTCCT TGAAGTATAT CCACTGACCA AAAAGAAAGA AAGAAAAATA 1260
AAAACATGGA AGGAAGGGAG GGAGGGATCT CTTGACCTCT TAAACTCTTA GCCTGGGGAA 1320
CCTAGTGTGA CCCCATGTCT CTCTTTTTTT TTTTTTTAAA CAATGCTAGT AATAAGAGGG 1380
TTTAAACCTC TGTGGTTTAC TGATTTACTC TATTAAAGTA ACTTATCATA CATATTTTTT 1440
ATGTTTGTGG TGGGATGCTA AATATTAGGA 1470
|
