| Tag | Content |
|---|
EnhancerAtlas ID | HS118-09096 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr19:7961790-7963130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr19:7962051-7962072 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | | IRF1 | MA0050.2 | chr19:7962045-7962066 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | | Nr2f6(var.2) | MA0728.1 | chr19:7962277-7962292 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH19I007896 | chr19 | 7961822 | 7962913 |
|
Enhancer Sequence | CAATGCTCAG TTTTATCCCT AGAATCTGGA AAGGACTGCA GTTGCTATAT GAGTTTGTTA 60
CTTCTGTTGT AACAAAGTAG CAGGGATTGA GTGGCTTAAA TAACCAGAAA TGTTTCCTCT 120
TCTGGGTCTG GTTCTGGAGG CCAGAAGTCT GAGATCAAGG CGTCAGTTGT CAGTGAGGGA 180
GAATCTTCCA AGCTTCCCTC CTAGATTTTT GCAGCTCCAA GAGTTCCTTG GCTTGTAGAT 240
GACATTCTCC CAGTATTTTT CTTTTTCTTT TTCTTTTTTT TTTAGACAGA GTCTCCCTCT 300
GTCGCCCAGG CTGGCATGCA GTGGTGCGAT CTCGGCTCAC TGCAACCTCC GCCTCCCGGG 360
TTCCAACAAT TCTCCTGGCT TAGCCTCCCA AGTAGCTGGG ATTACAGGCG TGTGCCACCA 420
CGCCCGGCTA ATATTTTTTT GTATTTTTAG TAGAGACGTG GTTTCAGTAT GTTGGCCAGG 480
CTGGTCTTGA ACTCCTGACC TCGTGATCAG GATCAGCCTG CCTCTGTCTC CCAAAGTGCT 540
GGGATTACAG GCATGAGCCA CTGCGCCTGG TCGAGACAGT TTTTTTTTTT TTTTTTTAAG 600
CAAGCTCTGT CACCTAGGCT GGAGTGCAGT GGCGCAATAA TAGCTCACTG TAACCTTGTA 660
CTCCTGGCCT CAAGCAATCC TCCTCTACCA CCCCCGCTTG GCCCCCCCTC CCACTGCCTC 720
CCAAATCACT GGGATTACAA GCCTGAGCCA CCGCACCCAG CCTCTCCCTG TATCCTCACG 780
TCATCTTCTG TCTTTGTGTC TGTCTCTGTG TCTATGTTTC CCCTTTCTCT AAGGCGCAGT 840
CATACTGGGC CCACCCTACT GGCTTTGTCT TGACTACCTC TGCAAAGACC CTATTACCAA 900
ACAGGAGCCG CCTGACCCAG CTCAAATAAT ACCACATTCT AAGGATTCGG AGTTGGGACT 960
TCAACATCTT TTGTGGGGAC ACGATTCAAC CCAGCTCCTT TTCTCAGACA AAGACCAGTG 1020
CTTTGTCAGT TGTGGTGGCT CATTCCTGTA ATCCCAGCAC TTTGGGAAGC TGAGGCAGGG 1080
GATCACTTGA GGCCAGGAGT TCGAGAGCAG CCTGGCCAAC ATGGTGAAAC CCCATCTCTA 1140
CTAAAAATAC AAAAATTAGC TAGGCGTGGT AGTGCGTGCT TGTAGCCCCG GCTACTCAGC 1200
AGGCTGAGGC AGGAGAATTG CTTGAACCAG GAGGGGAAGG TTGCAATGAG CCAAGATTGC 1260
ACCACTGCAC ACAGCCTGAC AGAGCGAGAC TCTTGTCTCA AAAAAAAAAA CCAAAAAAAA 1320
AAAAAACAGT GCTTAGAGGT 1340
|
