| Tag | Content |
|---|
EnhancerAtlas ID | HS047-01830 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:110777520-110779400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr1:110779120-110779131 | ACAGATAAGAA | - | 6.14 | | Gata1 | MA0035.3 | chr1:110779120-110779131 | ACAGATAAGAA | - | 6.62 | | JUND(var.2) | MA0492.1 | chr1:110778708-110778723 | GATGACCTCACTTTT | - | 6.05 | | Sox3 | MA0514.1 | chr1:110778878-110778888 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65653 | chr1:110775910-110779459 | Pancreatic_islets |
|
| | 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 |
| GH01I110234 | chr1 | 110777486 | 110779509 |
|
Enhancer Sequence | CTCACCGAAA TGGTTTCCCT GTTTGTTAGG GAATAATGAT GGCCCCTGTT TCAGAGACAG 60
AGTGAAGAGC CTGGCCTGGT GTCATGTGTC TACCTGTGAT ATGACATATA GTAGCGGCAC 120
AGTGTCAGCT CCCTCCCTGC CCTGTTCCTG TCACTCTCAG ACTTTTCTCC ACAGACTTCT 180
GAGATCTCCG TGTCCAGCTG CACCAAGAAA GGACAAGAAC ACACCCGGGA GCTGTCTTGG 240
GCAGTGTAGA ACAGCAGGGT GAGGACGGAA TGGCCGAGGA GAGGGAAGAA GCCAGGGGAA 300
GCCTGTTCCT GAAGTGTAAG GAAAGATCGG GCTTGGAGCC TGGGCCAGCC GAGGCAAGGG 360
GGTGGCAGGC AGCCAGTGTC AATTAAAGAT AAAATTTCTC CTCCGGTAGT GGAGGGCAAA 420
CAGTGGCTGT GGCCCCCCTA GACAGGAGAA AGCCATTTGC AGCCAGGCTG GCCTTGGAAA 480
AGCTTGGCCA GGCGATAATG GGACGGGATG CGCTGCTGAC TCCATAATGA TATTACGCAT 540
CAGGGCCCAC GGCCAAAGTG GCTGTTTTTT CTGTAGATCG ATGTGGAACC ATTTCATGGT 600
CAGGGGCTGA GAACCCAGCC AGCAGCAGGG GTACTAGATG CCAGAGTGGT CCTGAGGGGA 660
CTGAAGGGGT GGCAACTGGG GTCCCCAGTG ACCGTTTCAG GCTGCTGGAA GAGGAGGGGG 720
CAGTGTGCAG GAGGGTGGAG GGGTGGACGA GAGAAGCAGC AGACTGCCCC TCCTCCCCAC 780
CTCACAGAAA CAGCAGGCCG TGCTGTCAAG GAAGAAAGGG CTCTGGCTTC CTCCTGTTCC 840
CCAAAGCTGG AGTCGAGCCC AAGGTAGGGA GCTGGTTAAA AGAACAGGAC ATTGTTTAAA 900
AGAATAAGAC AGACTTTTGA AGTCAGGCAG ACTTGGGTTT GAGTCCTGAC TCCATCACTT 960
CCTTGTTGTG TGACCCTGGG CAAGTTACTC AGCCTCTGTG AACGTCTATT TCCTCATCTT 1020
TTAAATGTAG TATCTGCCTG AGGCCGTGTC TCTCTCATTG AGCCATGAGG AGAAATGAGT 1080
CGGCGCCTGT AAAGCCTCGC GCACAGTGCC TAGCACATAA CCATTGCTAG AGGGAGAGGG 1140
GAGTATTTTG GGGCAACTCA CTCCAGTAAC AGATGACCAG TTTGGTTTGA TGACCTCACT 1200
TTTCAGTGAA TCAGCCTCAT TTCACTGAAG TCCTTAGTCC TTATCTCCTT GTGAAGGAAT 1260
AAGAGGGGAT GATTATACCT AACAGCGAAC ATTTATTGAG TGCTGGGCAG TACATTTCAT 1320
GCTTATAAAG ATGCATTCCA AGATTGATGT TATCCTTACC TTTGTTTTAC GAGGAGAAAA 1380
CCAACACAAC AATGTCAGGT CATTTCTCCA AAGTCACACA GCCATTAAGT AGCAAAGCTG 1440
GGATTCAAAC TCAGTCTGGC TCTGTGGGTC CAATGCTTAG CCACTCTCTG AACTGAGTGG 1500
GGCTTGTGAG TCATAACCTC CAGTGTAGGA GTTTGTGCTT TTAGTGTTAT TTCCTTAACT 1560
GCAATTGATT CTCATAGCAA AGGTATTGTT TTCCCCTTTT ACAGATAAGA AACCAAGGCT 1620
TGGAGAAGTG AATCATTAAA CTCACTCTCC CTTTTACGTG TATGTACCCC ACCCCACACA 1680
CACATAAAGC GAGGAGGAAT GTCCTCTTGG GATTCATTCA TTAATTAGCA GCAGGCAACA 1740
CCCAGCTCAG TGACTGCTTG GTTCCTTCCC TCTGCGACCC CACTGGAGTT TTATTCTCTG 1800
ACGCACAGAA GTGGGTAAGT GGGGGTAGGA CTGCTCTGGA ACCCAAGTTA CATGAGGAGT 1860
GGCTCAAGCT GGAGAAGTCT 1880
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