| Tag | Content |
|---|
EnhancerAtlas ID | HS196-01464 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr1:110777970-110779240 |
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 | AGCCATTTGC AGCCAGGCTG GCCTTGGAAA AGCTTGGCCA GGCGATAATG GGACGGGATG 60
CGCTGCTGAC TCCATAATGA TATTACGCAT CAGGGCCCAC GGCCAAAGTG GCTGTTTTTT 120
CTGTAGATCG ATGTGGAACC ATTTCATGGT CAGGGGCTGA GAACCCAGCC AGCAGCAGGG 180
GTACTAGATG CCAGAGTGGT CCTGAGGGGA CTGAAGGGGT GGCAACTGGG GTCCCCAGTG 240
ACCGTTTCAG GCTGCTGGAA GAGGAGGGGG CAGTGTGCAG GAGGGTGGAG GGGTGGACGA 300
GAGAAGCAGC AGACTGCCCC TCCTCCCCAC CTCACAGAAA CAGCAGGCCG TGCTGTCAAG 360
GAAGAAAGGG CTCTGGCTTC CTCCTGTTCC CCAAAGCTGG AGTCGAGCCC AAGGTAGGGA 420
GCTGGTTAAA AGAACAGGAC ATTGTTTAAA AGAATAAGAC AGACTTTTGA AGTCAGGCAG 480
ACTTGGGTTT GAGTCCTGAC TCCATCACTT CCTTGTTGTG TGACCCTGGG CAAGTTACTC 540
AGCCTCTGTG AACGTCTATT TCCTCATCTT TTAAATGTAG TATCTGCCTG AGGCCGTGTC 600
TCTCTCATTG AGCCATGAGG AGAAATGAGT CGGCGCCTGT AAAGCCTCGC GCACAGTGCC 660
TAGCACATAA CCATTGCTAG AGGGAGAGGG GAGTATTTTG GGGCAACTCA CTCCAGTAAC 720
AGATGACCAG TTTGGTTTGA TGACCTCACT TTTCAGTGAA TCAGCCTCAT TTCACTGAAG 780
TCCTTAGTCC TTATCTCCTT GTGAAGGAAT AAGAGGGGAT GATTATACCT AACAGCGAAC 840
ATTTATTGAG TGCTGGGCAG TACATTTCAT GCTTATAAAG ATGCATTCCA AGATTGATGT 900
TATCCTTACC TTTGTTTTAC GAGGAGAAAA CCAACACAAC AATGTCAGGT CATTTCTCCA 960
AAGTCACACA GCCATTAAGT AGCAAAGCTG GGATTCAAAC TCAGTCTGGC TCTGTGGGTC 1020
CAATGCTTAG CCACTCTCTG AACTGAGTGG GGCTTGTGAG TCATAACCTC CAGTGTAGGA 1080
GTTTGTGCTT TTAGTGTTAT TTCCTTAACT GCAATTGATT CTCATAGCAA AGGTATTGTT 1140
TTCCCCTTTT ACAGATAAGA AACCAAGGCT TGGAGAAGTG AATCATTAAA CTCACTCTCC 1200
CTTTTACGTG TATGTACCCC ACCCCACACA CACATAAAGC GAGGAGGAAT GTCCTCTTGG 1260
GATTCATTCA 1270
|
