| Tag | Content |
|---|
EnhancerAtlas ID | HS138-02061 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:110777880-110779530 |
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 | GGTGGCAGGC AGCCAGTGTC AATTAAAGAT AAAATTTCTC CTCCGGTAGT GGAGGGCAAA 60
CAGTGGCTGT GGCCCCCCTA GACAGGAGAA AGCCATTTGC AGCCAGGCTG GCCTTGGAAA 120
AGCTTGGCCA GGCGATAATG GGACGGGATG CGCTGCTGAC TCCATAATGA TATTACGCAT 180
CAGGGCCCAC GGCCAAAGTG GCTGTTTTTT CTGTAGATCG ATGTGGAACC ATTTCATGGT 240
CAGGGGCTGA GAACCCAGCC AGCAGCAGGG GTACTAGATG CCAGAGTGGT CCTGAGGGGA 300
CTGAAGGGGT GGCAACTGGG GTCCCCAGTG ACCGTTTCAG GCTGCTGGAA GAGGAGGGGG 360
CAGTGTGCAG GAGGGTGGAG GGGTGGACGA GAGAAGCAGC AGACTGCCCC TCCTCCCCAC 420
CTCACAGAAA CAGCAGGCCG TGCTGTCAAG GAAGAAAGGG CTCTGGCTTC CTCCTGTTCC 480
CCAAAGCTGG AGTCGAGCCC AAGGTAGGGA GCTGGTTAAA AGAACAGGAC ATTGTTTAAA 540
AGAATAAGAC AGACTTTTGA AGTCAGGCAG ACTTGGGTTT GAGTCCTGAC TCCATCACTT 600
CCTTGTTGTG TGACCCTGGG CAAGTTACTC AGCCTCTGTG AACGTCTATT TCCTCATCTT 660
TTAAATGTAG TATCTGCCTG AGGCCGTGTC TCTCTCATTG AGCCATGAGG AGAAATGAGT 720
CGGCGCCTGT AAAGCCTCGC GCACAGTGCC TAGCACATAA CCATTGCTAG AGGGAGAGGG 780
GAGTATTTTG GGGCAACTCA CTCCAGTAAC AGATGACCAG TTTGGTTTGA TGACCTCACT 840
TTTCAGTGAA TCAGCCTCAT TTCACTGAAG TCCTTAGTCC TTATCTCCTT GTGAAGGAAT 900
AAGAGGGGAT GATTATACCT AACAGCGAAC ATTTATTGAG TGCTGGGCAG TACATTTCAT 960
GCTTATAAAG ATGCATTCCA AGATTGATGT TATCCTTACC TTTGTTTTAC GAGGAGAAAA 1020
CCAACACAAC AATGTCAGGT CATTTCTCCA AAGTCACACA GCCATTAAGT AGCAAAGCTG 1080
GGATTCAAAC TCAGTCTGGC TCTGTGGGTC CAATGCTTAG CCACTCTCTG AACTGAGTGG 1140
GGCTTGTGAG TCATAACCTC CAGTGTAGGA GTTTGTGCTT TTAGTGTTAT TTCCTTAACT 1200
GCAATTGATT CTCATAGCAA AGGTATTGTT TTCCCCTTTT ACAGATAAGA AACCAAGGCT 1260
TGGAGAAGTG AATCATTAAA CTCACTCTCC CTTTTACGTG TATGTACCCC ACCCCACACA 1320
CACATAAAGC GAGGAGGAAT GTCCTCTTGG GATTCATTCA TTAATTAGCA GCAGGCAACA 1380
CCCAGCTCAG TGACTGCTTG GTTCCTTCCC TCTGCGACCC CACTGGAGTT TTATTCTCTG 1440
ACGCACAGAA GTGGGTAAGT GGGGGTAGGA CTGCTCTGGA ACCCAAGTTA CATGAGGAGT 1500
GGCTCAAGCT GGAGAAGTCT TGGAAACCTG ATCCCAACTA CCAGGTGTTT AAAGGGTACC 1560
TGTGGGGAAG TGGGTTTAGA TTCTTCTCTG ATTGCAGAGA GCAGATCCGG AAATAATAGG 1620
TGGAAATGTT AGGAGGGCAG ATTGGGTTTA 1650
|
