| Tag | Content |
|---|
EnhancerAtlas ID | HS148-00900 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:110777560-110778950 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| 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 | GGCCCCTGTT TCAGAGACAG AGTGAAGAGC CTGGCCTGGT GTCATGTGTC TACCTGTGAT 60
ATGACATATA GTAGCGGCAC AGTGTCAGCT CCCTCCCTGC CCTGTTCCTG TCACTCTCAG 120
ACTTTTCTCC ACAGACTTCT GAGATCTCCG TGTCCAGCTG CACCAAGAAA GGACAAGAAC 180
ACACCCGGGA GCTGTCTTGG GCAGTGTAGA ACAGCAGGGT GAGGACGGAA TGGCCGAGGA 240
GAGGGAAGAA GCCAGGGGAA GCCTGTTCCT GAAGTGTAAG GAAAGATCGG GCTTGGAGCC 300
TGGGCCAGCC GAGGCAAGGG GGTGGCAGGC AGCCAGTGTC AATTAAAGAT AAAATTTCTC 360
CTCCGGTAGT GGAGGGCAAA CAGTGGCTGT GGCCCCCCTA GACAGGAGAA AGCCATTTGC 420
AGCCAGGCTG GCCTTGGAAA AGCTTGGCCA GGCGATAATG GGACGGGATG CGCTGCTGAC 480
TCCATAATGA TATTACGCAT CAGGGCCCAC GGCCAAAGTG GCTGTTTTTT CTGTAGATCG 540
ATGTGGAACC ATTTCATGGT CAGGGGCTGA GAACCCAGCC AGCAGCAGGG GTACTAGATG 600
CCAGAGTGGT CCTGAGGGGA CTGAAGGGGT GGCAACTGGG GTCCCCAGTG ACCGTTTCAG 660
GCTGCTGGAA GAGGAGGGGG CAGTGTGCAG GAGGGTGGAG GGGTGGACGA GAGAAGCAGC 720
AGACTGCCCC TCCTCCCCAC CTCACAGAAA CAGCAGGCCG TGCTGTCAAG GAAGAAAGGG 780
CTCTGGCTTC CTCCTGTTCC CCAAAGCTGG AGTCGAGCCC AAGGTAGGGA GCTGGTTAAA 840
AGAACAGGAC ATTGTTTAAA AGAATAAGAC AGACTTTTGA AGTCAGGCAG ACTTGGGTTT 900
GAGTCCTGAC TCCATCACTT CCTTGTTGTG TGACCCTGGG CAAGTTACTC AGCCTCTGTG 960
AACGTCTATT TCCTCATCTT TTAAATGTAG TATCTGCCTG AGGCCGTGTC TCTCTCATTG 1020
AGCCATGAGG AGAAATGAGT CGGCGCCTGT AAAGCCTCGC GCACAGTGCC TAGCACATAA 1080
CCATTGCTAG AGGGAGAGGG GAGTATTTTG GGGCAACTCA CTCCAGTAAC AGATGACCAG 1140
TTTGGTTTGA TGACCTCACT TTTCAGTGAA TCAGCCTCAT TTCACTGAAG TCCTTAGTCC 1200
TTATCTCCTT GTGAAGGAAT AAGAGGGGAT GATTATACCT AACAGCGAAC ATTTATTGAG 1260
TGCTGGGCAG TACATTTCAT GCTTATAAAG ATGCATTCCA AGATTGATGT TATCCTTACC 1320
TTTGTTTTAC GAGGAGAAAA CCAACACAAC AATGTCAGGT CATTTCTCCA AAGTCACACA 1380
GCCATTAAGT 1390
|
