| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23077 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:7188580-7190480 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr19:7188659-7188669 | ACCACTTGAG | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr19:7188666-7188681 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr19:7189893-7189908 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41206 | chr19:7188996-7189880 | Left_Ventricle |
|
| | 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 |
| GH19I007188 | chr19 | 7188237 | 7189850 |
|
Enhancer Sequence | ATATTAGGAA GTTCTAATAG GGCTAAGCAC AGTGGCTGAT GCTTGTAATC CCAGCACTTT 60
GAGAGGCTGA GGTGGGTGGA CCACTTGAGG TCAGGAGTTC AAGACGACCA GCCTGACCAA 120
CATGGTGAAA CCCGTCTCTA CTAAAAATAC AAAAATTAGT CGGGTGTGGT GGTGCTTGCC 180
TATAATCCCA GCTACTCGGG AGGCTGAGGC AGTAGAATCG CTTGAACGCA AGAGGAGTTT 240
GCAGTGAGTC AAGATTGTGC CACTGAACTC CAGCCTAGGT GACAGAGCGA GACTCTATCT 300
CAAAAAAAAA AAAAAAAAAA AAAAGGGAGG GGGGATTGTT AATAAGAGTC CCTTCCTTCC 360
TTCTTAAGGC TGTTGCAAGA AATAAACAGG ATGACGTCAG TAACACATCA GATTCTTTGA 420
TAGAGACATT TTTAGGCTTG ATAGAAATTA ACTACAGAGG GTATCTATAA TTATCATAAT 480
TATCAACATC ATTAACACTG ATCTGTCTGT GGGAACCTGA GGGCTGAAAT TCAATTGAAG 540
GAAGCAATAT ACAAGGCAGA CAACAATGAT CCAGGACCCA CGGAGTTCCA GCACTCTGGC 600
AAGGAAACAC ACACACAAGA GGAAGGGGCT TGTTTCCTGG GCTGGAGCCA CTTCAGAGGG 660
TCAGCCCTTT CATTCAAAAG AGGCGTCATC AATGGCCTAA CACAAACCTC TCAAACACAT 720
AAGTCCTTCC GGCCTAGACA ATGGGAAGAA AAATTATCCA ACCATTGCAA ACAAGGCCAG 780
AGGCTGCGAG ACTTTGCAAT CCTGTGTTGG AGCCCTAGCT GACAGGCCTA TCTGAGCTAT 840
TTCATTTGTC AGCACAGGAG TTGGTCAACT TTTTCTGTAA AGGGCCACAA GCAAATACTT 900
GAGGCTTTGC AGGACATATG GTGTTGGTTG AAACTACTCA ACTCTGCCAC GATGGCATGA 960
TAGCAGCCAC AGACATATGT ACATGAAGAG GCATGGCTAG GTCCAATAAA ACTTTATTTA 1020
TAAAAGCAAG TGATGGGCCA GATAGTTTAT CAACCTGCAC TAGTTAAATG TACCTGTAAT 1080
TGATTTTACT ATTACTTTTT TTTTTTTTTT TTGAAACCGA GTCTTGCTCT GTTGTCCAGG 1140
CTGAAGTACA GCGGTGCCAT CTCCGCTCAC TGTAAACTCT GTGTCCCAGG TTCAAGCAAT 1200
TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG ATTACAGGCA CCCACAACCA TGCCTGGATA 1260
ATTTTTGTAT TTTTAGTAGA GACTGGGTTT CAGCATGTTG GCCAGTCTGG TCTTGAACTC 1320
CTGACCTCAA GTGATCTGCC CACCTTGGCC TCCCAAAGTG CTGGGATTAT AGGCATGACC 1380
CACTACGCCT GGCCGATTTT ACTATTTCTA TTAGGAACTA GACTCAAGGA AATTAGAGTT 1440
AACTTACAGA CAGATATGCT ACAAATTATT TTCATCTCAG AGAAAAGATA CTCTCAGCTG 1500
GGCATGGAGG CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGCGG GAGGATTGCT 1560
TGAGCCCAGG CATTCGAGAC CAGCCTGGGT AACAGAGTGA GATCCTATCT CTCCTTGCCG 1620
AAAAAAAAAA GAAAAAAATC ATCCCCAAAG ATTACAGTTT TATTGTCCTA TGGGACATTA 1680
AGCAGCCTCA CAGCTAACAC TGCCTTCTTA TTTCAGTGAC TATACATGTT TTGGCTTTAT 1740
AATCCTGCTG TTCCCTCACT AATGGGTTAA ATAAACATGC TGACCTGTGT TCTTTGGTGG 1800
TTTTTTTTTT TTTTTTTTTT TGAGACAGAG TCTCACTCTG TTGTCCAGGC TGAAGTGCAA 1860
TGGTGAGAAC TCAGCTCACT GCAACCTCCG CCTCCCGGGT 1900
|
