| Tag | Content |
|---|
EnhancerAtlas ID | HS050-03661 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:110777150-110779490 |
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 | GCCTGGATAG GACGGGGAGA TGGTGAGTGA TGGTCAGACG TGGCCCTTGG CTCTCACTGT 60
TGTTATCCCT CTCACGTTCA CATAGGGGCA CACGCAGGGC CAGCTTCATG GGTGTGCAAC 120
CTGTGCAGCC ACTCAGAAGG GCCCCATGCT GGGTTTAATG CTTGGCTGTC ACCATCATGA 180
AATTAATAAT GGTTGAACAG GGGCCCTGCG TTTCCATCTT GCACCAGGCT CTGGCGGGTC 240
TGGTTGCCTG CTTGCCTCTC CTTATTCTTG TCTTACTCCT CACTCTTACT CTGGGCATCT 300
GTGTAGGACC ATAGGGGCCT CAATTCAAAG TCTTGCTTTG CTGCTTGCTA GCTGGGTGAC 360
TTGGGGGTGA CTCACCGAAA TGGTTTCCCT GTTTGTTAGG GAATAATGAT GGCCCCTGTT 420
TCAGAGACAG AGTGAAGAGC CTGGCCTGGT GTCATGTGTC TACCTGTGAT ATGACATATA 480
GTAGCGGCAC AGTGTCAGCT CCCTCCCTGC CCTGTTCCTG TCACTCTCAG ACTTTTCTCC 540
ACAGACTTCT GAGATCTCCG TGTCCAGCTG CACCAAGAAA GGACAAGAAC ACACCCGGGA 600
GCTGTCTTGG GCAGTGTAGA ACAGCAGGGT GAGGACGGAA TGGCCGAGGA GAGGGAAGAA 660
GCCAGGGGAA GCCTGTTCCT GAAGTGTAAG GAAAGATCGG GCTTGGAGCC TGGGCCAGCC 720
GAGGCAAGGG GGTGGCAGGC AGCCAGTGTC AATTAAAGAT AAAATTTCTC CTCCGGTAGT 780
GGAGGGCAAA CAGTGGCTGT GGCCCCCCTA GACAGGAGAA AGCCATTTGC AGCCAGGCTG 840
GCCTTGGAAA AGCTTGGCCA GGCGATAATG GGACGGGATG CGCTGCTGAC TCCATAATGA 900
TATTACGCAT CAGGGCCCAC GGCCAAAGTG GCTGTTTTTT CTGTAGATCG ATGTGGAACC 960
ATTTCATGGT CAGGGGCTGA GAACCCAGCC AGCAGCAGGG GTACTAGATG CCAGAGTGGT 1020
CCTGAGGGGA CTGAAGGGGT GGCAACTGGG GTCCCCAGTG ACCGTTTCAG GCTGCTGGAA 1080
GAGGAGGGGG CAGTGTGCAG GAGGGTGGAG GGGTGGACGA GAGAAGCAGC AGACTGCCCC 1140
TCCTCCCCAC CTCACAGAAA CAGCAGGCCG TGCTGTCAAG GAAGAAAGGG CTCTGGCTTC 1200
CTCCTGTTCC CCAAAGCTGG AGTCGAGCCC AAGGTAGGGA GCTGGTTAAA AGAACAGGAC 1260
ATTGTTTAAA AGAATAAGAC AGACTTTTGA AGTCAGGCAG ACTTGGGTTT GAGTCCTGAC 1320
TCCATCACTT CCTTGTTGTG TGACCCTGGG CAAGTTACTC AGCCTCTGTG AACGTCTATT 1380
TCCTCATCTT TTAAATGTAG TATCTGCCTG AGGCCGTGTC TCTCTCATTG AGCCATGAGG 1440
AGAAATGAGT CGGCGCCTGT AAAGCCTCGC GCACAGTGCC TAGCACATAA CCATTGCTAG 1500
AGGGAGAGGG GAGTATTTTG GGGCAACTCA CTCCAGTAAC AGATGACCAG TTTGGTTTGA 1560
TGACCTCACT TTTCAGTGAA TCAGCCTCAT TTCACTGAAG TCCTTAGTCC TTATCTCCTT 1620
GTGAAGGAAT AAGAGGGGAT GATTATACCT AACAGCGAAC ATTTATTGAG TGCTGGGCAG 1680
TACATTTCAT GCTTATAAAG ATGCATTCCA AGATTGATGT TATCCTTACC TTTGTTTTAC 1740
GAGGAGAAAA CCAACACAAC AATGTCAGGT CATTTCTCCA AAGTCACACA GCCATTAAGT 1800
AGCAAAGCTG GGATTCAAAC TCAGTCTGGC TCTGTGGGTC CAATGCTTAG CCACTCTCTG 1860
AACTGAGTGG GGCTTGTGAG TCATAACCTC CAGTGTAGGA GTTTGTGCTT TTAGTGTTAT 1920
TTCCTTAACT GCAATTGATT CTCATAGCAA AGGTATTGTT TTCCCCTTTT ACAGATAAGA 1980
AACCAAGGCT TGGAGAAGTG AATCATTAAA CTCACTCTCC CTTTTACGTG TATGTACCCC 2040
ACCCCACACA CACATAAAGC GAGGAGGAAT GTCCTCTTGG GATTCATTCA TTAATTAGCA 2100
GCAGGCAACA CCCAGCTCAG TGACTGCTTG GTTCCTTCCC TCTGCGACCC CACTGGAGTT 2160
TTATTCTCTG ACGCACAGAA GTGGGTAAGT GGGGGTAGGA CTGCTCTGGA ACCCAAGTTA 2220
CATGAGGAGT GGCTCAAGCT GGAGAAGTCT TGGAAACCTG ATCCCAACTA CCAGGTGTTT 2280
AAAGGGTACC TGTGGGGAAG TGGGTTTAGA TTCTTCTCTG ATTGCAGAGA GCAGATCCGG 2340
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