| Tag | Content |
|---|
EnhancerAtlas ID | HS091-28044 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:169705510-169707340 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:169705851-169705872 | TCTTTCTTTCTCTTTCTTCTT | + | 6.72 | | Nr2f6(var.2) | MA0728.1 | chr2:169707206-169707221 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr2:169706084-169706099 | TGAACTCCTGACCTC | - | 6.22 | | Nr5a2 | MA0505.1 | chr2:169707214-169707229 | GAGTTCAAGGCCAGC | + | 8.25 | | Nr5a2 | MA0505.1 | chr2:169706076-169706091 | GCTGGCCTTGAACTC | - | 8.25 | | RARA | MA0729.1 | chr2:169707206-169707224 | GAGGTCAGGAGTTCAAGG | + | 6.73 | | RARA | MA0729.1 | chr2:169706081-169706099 | CCTTGAACTCCTGACCTC | - | 6.73 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 169706198 | 169706551 | | chr2 | 169706063 | 169706107 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I168849 | chr2 | 169706201 | 169706350 |
|
Enhancer Sequence | TATACCATAG ATGAATTAAC AACACAGGGA TATAGAGGAA TACCATACTG AATCAGGCCA 60
ATGGGCTCCT GTAGGAATTT CAAGAGGTGA GCAAGGAGAA CCCAGTGATC TTTGTGACTC 120
TCCATTCTCA CCTCTCTTGC ACTGCCAAGG GCCTTGAGAC ATACCCATCT TTCTTCTTCC 180
CTATGGTCGT GTTACCCACC AACTTCTCCA AAGCCTTGTT CATGAAAGAT GATTGCTGGT 240
GCTCTTTGTG GGATGCAGGA GTTGGGATGG TGGGTATGAG AGCAACTGAG CTGGACTTCC 300
CTGGATAAAA GGATGAATGC CCAGGCCTTG TATTTTTTCT TTCTTTCTTT CTCTTTCTTC 360
TTTTCTTTTT TTTGAGATGG AATCTCACTC TTTTGCACAG GCTGGAGTGC AGTGGCATGA 420
TCTCAGCTCA CTGCAACCAC CACCTCCCAG GTCCAAGCGA TTCTCCTGCC TCAGCCTCCT 480
GAGTAGCTGG GACGACAGGC GCCCGCCACC AGGCCTGGCT AATTTTTGTA TTTTTAGTAG 540
AGACGGGGTT TTGCCACGTT GGGCAGGCTG GCCTTGAACT CCTGACCTCA GGTAGTTCAC 600
CCGTCTCGGC CTCCCAAAAT GCTGGGATTA TAGGCATGAG CCACCGCACC TAGCCAGGCC 660
TTGTTTTTAC AAAAAAAAAA AAAAAAAAAG ATGGGAAGAA TTTTGTCTTG GACACCTGCC 720
ATCTCCATCA AAGCCCAAAG TCCCCTGGGC ACATACCCAG CAGCCTTACA CTGCCCCCAC 780
ATGGCCTTGG AGTCTCCCTG AATACTCTGC CTGAGCCAGC CTTCTCTAAG AATGCTTAGT 840
TGCTAAAGCT TTCTGCCCCC TGTAAAACCA CCAGTCAGCA ACTCAGTTGG CATGGGTCCA 900
ATAAGTAACA TTTTCTCATT TTTTTTTTTT TTTTGAGACA GTTTCACTTT TGTCACCCAG 960
GCTGGAGTGC AGTAGCATGA TCTCGGCTCA CTGCAAACTT CACCTCCTGG GTTCAGGCAA 1020
TTCTGCCTCA ACCTCCTGAG TAGCTGGGAT TACAGGCGTG TGCCACCATG CCTGGCTAAT 1080
TTTTGTATTT TTAGTAGAGA TAAGGTTTCA CCATGTTGGC TGGGCTGGTC TCAAACTCCT 1140
GACCTCAGGT GATCCTCCCA CCCTGGCCTC CCAACGTGCT GGGATTATAG GCATGAGCCA 1200
CTGTGCCCGG CCTCTAAAAT GTTAATAGCT AACAAAGCAA ATGTGATTCC CCTCACTTTC 1260
TTATTTACCC TTCCTACCTA AAAGTCATAA GTCTAATAAT GAAACTTCTG TCATCTCACA 1320
CAAAATAAAG AGGCTATGTG TCTACCTGCA AACAGCGGAC TCTGACTCCC AGGCCTAATT 1380
TTAGGCAGAA TTATAAATTG GTCAGACTTT GGGATTCTTC TCTTGTCAAA TAACCTCCTT 1440
AAACAGAGAA TTTGTGGCCT GTCATTCTCT TCCCTGCAGA CTAGCAGAAC GCCTTGAATG 1500
TACTATAAAC AATTCTAAAA CTATTGGGTG TCTCAATGCA TTTCCAAGAC ATGGATATGG 1560
GCTTTCCTGG GCTTCACCCT CTGGAATTCT TCCCAATTTT TTTTTTTTTT TTTTTGTAAA 1620
AACAAGGCCT GGCTAGGCGC GGTGGCTCAT GCCTGTAATC CTAGCACTTT GGGAGGCCAA 1680
GACAGGTGGA CCATCTGAGG TCAGGAGTTC AAGGCCAGCC TGCCCAACAT GGTGAAACCC 1740
CATCTCTACT GAAATTCTCT GGAATTCTCT GGAATCCATG ATTGTGTCTC AAATGCTTCC 1800
TTTTCTTCTT TTCTCCCCCT TCCTCATAAA 1830
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