| Tag | Content |
|---|
EnhancerAtlas ID | HS002-04923 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr19:34310270-34312370 |
Target genes | |
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 | GGAATTGTTT ACTTTCAATT GTGTACTTGA AGCTCTGTAA ATTTAACAGG AAGAGAGACC 60
ACATTGCAGT TTTCCACTTC GTCATGACAC TGAACATGGA TTACCCCAAA TGCATTGATT 120
TGCATGTAGA GAGAACCACC TCTCAGGCCT CAAGACTAGC GTCTCCATAG CAAAGGAAGC 180
TTCTGTGAAA TTCTAATGAG AGACCCAGAG AAAGAGGCAG GCACACTCCC GGGGACACAC 240
AAAGGAGAGG GGTTAGGGGT CAGCTGCATT TGGGGTTTTG TCTTTATTTC CATTACACAG 300
AACAGCCAGT CCCGACAGCG CCCAGGCCCC ACAGGACAAT GCTGTTCCTG GACCCGGAGC 360
CATGGCCGTG GAATAAGAGC TAGGTCTTCA GGGCCTCCTC CTAGGATCCT TCTTAACACA 420
GAAATCACAA ACCAGGCCAA AGTCTTAAAA AGCAGAGCCT GGGAGGGGCA GGGACGCCCA 480
AGCCACGCTG GGGCCCGGGA GGCCTCCCGT CCTGCCCGCG GGAGAACCCA GGCCGCGCAT 540
CCCTGGCTGG ACGGCGTCAC CAGCCGTAGC TGGGCCAGGC CTGCTGCTCA AAGCCCGTGT 600
CTAGGATGTC ACCAGAGCTC CCTTTTCTGT GTCCTGGACC CGGTTCAGGG CCCCCGAGGA 660
AGCTGCGGTT TGGGGCGAGC CGATTGCACC AGCAGGGCCG GGCTGCTGCT CCCGGGGCTG 720
ACGCGGGCCA CGCCCTCCTG GACGCGGACA CACCCCCATT TCCCCGGGCC CACAGAGCCA 780
CGCCTGGCCC TGCAGCCAAA CAGCGGGAAG GCAGATTGGT ACGAGTAGGT ACAAGGCCCT 840
GGAATTCTCG CCCGGTTGCC ACACACTGCA CGGAGCATAA TTGGGGGAGG TTGTGCAACT 900
GCCCGGGAAG CCGGGGCTCG CAACGAGGGC TCTCTCCAAG TCCCCATCAC AGGCCTCCGG 960
GGAGCCTCGG GACAGAGCCT GACGCCACCT TCGGGTGACA TCGATGGCCT CGCTCTGGCA 1020
GAGGAGTAGT GTGGCTCTGC CGAGAACTGG GGAGCCCGGG TCCCCGCAGG GCCAAGGGGA 1080
GGGAGGGCTG GCGGAAGGGG CCGCGCCCAC AGCCCCAGGT GGCAGCAGCG GCGGTGGCGG 1140
TCCCGACTGG CAGAGCCTAA CGAGAACAGG GCCTATCCCC AGGGGCCCCG GGCTGGACGC 1200
AGACCAGATC TCGCGGGGGT GGGCTGGGAG GCGCCCGCCA GAGGCCGGAG GCTGACAGTG 1260
CCTTTCCTAT CCTATGGGTC TATTGTGGGC CCGCGGAGCC CCCATGGGTG GGTCCATCCC 1320
CGGGCCCAGT GAGTCACTTC CCCAGGCCCC GGAGGCCTTC GTGGAAGGTG CCTCCCTTTC 1380
CGGCAAAGCA TCCTTTGTTC TCCTGCTGGC TTTGCTTCCC AATCCTCTCT GAGTTGCAAC 1440
CTTGAGGGTT TTAGGGGCAC CAAGCTCCCA GGAGCACAGA GGTGGGCTTG GGTGCCACCT 1500
GGAGAGCGGG CTGCAGAAGG CTGCAGCTGC TTTTTTGCTT CCTCAGTTCC CTGCCCTCTC 1560
AAGGCCCAGG CTCTCCCACC TCCCCAGACG TCTGGGGAAA CCCACACTGC CCTGCATAGG 1620
TTGTGGTGTG CAGCCTCCGG ACTGCAGATC CTGAACGCGC ATCAGGAGGG AGGGAGGGAG 1680
GTTTCGATGC TCTCGCCCTG GCCAGCACCG CTCTGAGTTG CTGAACTGGC CTCAAGGCTT 1740
CTCTTGCATC AGGGAGAGGC TTCCGGCACC ACCACTGGCA CTCCTCCTTC TCCCTCCCTT 1800
TAGCCTCCCC CAGTTCCCAT GCCCAGGTGG AGGAACCCGT GTAGAAGCCC AGCCCAGGGA 1860
GGGAATTCAT CAAAGCACCT TCCCACACAG CCTCTAGTTT GCCTCCTCTC CACTCCCACC 1920
TTCCAGCCCC AGCCTGGCTA GCCACGTGGG GGGCTCCTGT GCCAAGGAGT GCCCAGCTGC 1980
CGGGTGAGTG AGCAGCCCTG CACAGAAGGC AGCTGACTAC CATACACACT ACATGTGTGG 2040
AGAGCACCAG CCTTGCAGCC TGGCGAGGCT CTTGCTTTGA AGAAATAGAA GACTAATTAT 2100
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