| Tag | Content |
|---|
EnhancerAtlas ID | HS098-27726 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:34310350-34312190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr19:34310995-34311010 | GGCCACGCCCTCCTG | + | 6.46 | | POU2F2 | MA0507.1 | chr19:34310384-34310397 | TTGATTTGCATGT | + | 6.12 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_26999 | chr19:34310151-34312404 | Esophagus | | SE_32421 | chr19:34310338-34312371 | Gastric | | SE_54276 | chr19:34310171-34312632 | Spleen |
|
| | 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 |
| GH19I033819 | chr19 | 34310149 | 34312946 |
|
Enhancer Sequence | GTCATGACAC TGAACATGGA TTACCCCAAA TGCATTGATT TGCATGTAGA GAGAACCACC 60
TCTCAGGCCT CAAGACTAGC GTCTCCATAG CAAAGGAAGC TTCTGTGAAA TTCTAATGAG 120
AGACCCAGAG AAAGAGGCAG GCACACTCCC GGGGACACAC AAAGGAGAGG GGTTAGGGGT 180
CAGCTGCATT TGGGGTTTTG TCTTTATTTC CATTACACAG AACAGCCAGT CCCGACAGCG 240
CCCAGGCCCC ACAGGACAAT GCTGTTCCTG GACCCGGAGC CATGGCCGTG GAATAAGAGC 300
TAGGTCTTCA GGGCCTCCTC CTAGGATCCT TCTTAACACA GAAATCACAA ACCAGGCCAA 360
AGTCTTAAAA AGCAGAGCCT GGGAGGGGCA GGGACGCCCA AGCCACGCTG GGGCCCGGGA 420
GGCCTCCCGT CCTGCCCGCG GGAGAACCCA GGCCGCGCAT CCCTGGCTGG ACGGCGTCAC 480
CAGCCGTAGC TGGGCCAGGC CTGCTGCTCA AAGCCCGTGT CTAGGATGTC ACCAGAGCTC 540
CCTTTTCTGT GTCCTGGACC CGGTTCAGGG CCCCCGAGGA AGCTGCGGTT TGGGGCGAGC 600
CGATTGCACC AGCAGGGCCG GGCTGCTGCT CCCGGGGCTG ACGCGGGCCA CGCCCTCCTG 660
GACGCGGACA CACCCCCATT TCCCCGGGCC CACAGAGCCA CGCCTGGCCC TGCAGCCAAA 720
CAGCGGGAAG GCAGATTGGT ACGAGTAGGT ACAAGGCCCT GGAATTCTCG CCCGGTTGCC 780
ACACACTGCA CGGAGCATAA TTGGGGGAGG TTGTGCAACT GCCCGGGAAG CCGGGGCTCG 840
CAACGAGGGC TCTCTCCAAG TCCCCATCAC AGGCCTCCGG GGAGCCTCGG GACAGAGCCT 900
GACGCCACCT TCGGGTGACA TCGATGGCCT CGCTCTGGCA GAGGAGTAGT GTGGCTCTGC 960
CGAGAACTGG GGAGCCCGGG TCCCCGCAGG GCCAAGGGGA GGGAGGGCTG GCGGAAGGGG 1020
CCGCGCCCAC AGCCCCAGGT GGCAGCAGCG GCGGTGGCGG TCCCGACTGG CAGAGCCTAA 1080
CGAGAACAGG GCCTATCCCC AGGGGCCCCG GGCTGGACGC AGACCAGATC TCGCGGGGGT 1140
GGGCTGGGAG GCGCCCGCCA GAGGCCGGAG GCTGACAGTG CCTTTCCTAT CCTATGGGTC 1200
TATTGTGGGC CCGCGGAGCC CCCATGGGTG GGTCCATCCC CGGGCCCAGT GAGTCACTTC 1260
CCCAGGCCCC GGAGGCCTTC GTGGAAGGTG CCTCCCTTTC CGGCAAAGCA TCCTTTGTTC 1320
TCCTGCTGGC TTTGCTTCCC AATCCTCTCT GAGTTGCAAC CTTGAGGGTT TTAGGGGCAC 1380
CAAGCTCCCA GGAGCACAGA GGTGGGCTTG GGTGCCACCT GGAGAGCGGG CTGCAGAAGG 1440
CTGCAGCTGC TTTTTTGCTT CCTCAGTTCC CTGCCCTCTC AAGGCCCAGG CTCTCCCACC 1500
TCCCCAGACG TCTGGGGAAA CCCACACTGC CCTGCATAGG TTGTGGTGTG CAGCCTCCGG 1560
ACTGCAGATC CTGAACGCGC ATCAGGAGGG AGGGAGGGAG GTTTCGATGC TCTCGCCCTG 1620
GCCAGCACCG CTCTGAGTTG CTGAACTGGC CTCAAGGCTT CTCTTGCATC AGGGAGAGGC 1680
TTCCGGCACC ACCACTGGCA CTCCTCCTTC TCCCTCCCTT TAGCCTCCCC CAGTTCCCAT 1740
GCCCAGGTGG AGGAACCCGT GTAGAAGCCC AGCCCAGGGA GGGAATTCAT CAAAGCACCT 1800
TCCCACACAG CCTCTAGTTT GCCTCCTCTC CACTCCCACC 1840
|
