| Tag | Content |
|---|
EnhancerAtlas ID | HS110-02377 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr19:34310140-34312350 |
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 | TGTATTTTTA GTAGAGGCGG GGTTTTGCTT TGTTGGCCAG GCTGGTCTTG AACTCCTGGC 60
CTCAAGTGAT CCTCCCACCT TGGCCTCCCA AAATGCTGGG ATTACAGGTG TGAGCCATTG 120
CGCCCAGCCA GGAATTGTTT ACTTTCAATT GTGTACTTGA AGCTCTGTAA ATTTAACAGG 180
AAGAGAGACC ACATTGCAGT TTTCCACTTC GTCATGACAC TGAACATGGA TTACCCCAAA 240
TGCATTGATT TGCATGTAGA GAGAACCACC TCTCAGGCCT CAAGACTAGC GTCTCCATAG 300
CAAAGGAAGC TTCTGTGAAA TTCTAATGAG AGACCCAGAG AAAGAGGCAG GCACACTCCC 360
GGGGACACAC AAAGGAGAGG GGTTAGGGGT CAGCTGCATT TGGGGTTTTG TCTTTATTTC 420
CATTACACAG AACAGCCAGT CCCGACAGCG CCCAGGCCCC ACAGGACAAT GCTGTTCCTG 480
GACCCGGAGC CATGGCCGTG GAATAAGAGC TAGGTCTTCA GGGCCTCCTC CTAGGATCCT 540
TCTTAACACA GAAATCACAA ACCAGGCCAA AGTCTTAAAA AGCAGAGCCT GGGAGGGGCA 600
GGGACGCCCA AGCCACGCTG GGGCCCGGGA GGCCTCCCGT CCTGCCCGCG GGAGAACCCA 660
GGCCGCGCAT CCCTGGCTGG ACGGCGTCAC CAGCCGTAGC TGGGCCAGGC CTGCTGCTCA 720
AAGCCCGTGT CTAGGATGTC ACCAGAGCTC CCTTTTCTGT GTCCTGGACC CGGTTCAGGG 780
CCCCCGAGGA AGCTGCGGTT TGGGGCGAGC CGATTGCACC AGCAGGGCCG GGCTGCTGCT 840
CCCGGGGCTG ACGCGGGCCA CGCCCTCCTG GACGCGGACA CACCCCCATT TCCCCGGGCC 900
CACAGAGCCA CGCCTGGCCC TGCAGCCAAA CAGCGGGAAG GCAGATTGGT ACGAGTAGGT 960
ACAAGGCCCT GGAATTCTCG CCCGGTTGCC ACACACTGCA CGGAGCATAA TTGGGGGAGG 1020
TTGTGCAACT GCCCGGGAAG CCGGGGCTCG CAACGAGGGC TCTCTCCAAG TCCCCATCAC 1080
AGGCCTCCGG GGAGCCTCGG GACAGAGCCT GACGCCACCT TCGGGTGACA TCGATGGCCT 1140
CGCTCTGGCA GAGGAGTAGT GTGGCTCTGC CGAGAACTGG GGAGCCCGGG TCCCCGCAGG 1200
GCCAAGGGGA GGGAGGGCTG GCGGAAGGGG CCGCGCCCAC AGCCCCAGGT GGCAGCAGCG 1260
GCGGTGGCGG TCCCGACTGG CAGAGCCTAA CGAGAACAGG GCCTATCCCC AGGGGCCCCG 1320
GGCTGGACGC AGACCAGATC TCGCGGGGGT GGGCTGGGAG GCGCCCGCCA GAGGCCGGAG 1380
GCTGACAGTG CCTTTCCTAT CCTATGGGTC TATTGTGGGC CCGCGGAGCC CCCATGGGTG 1440
GGTCCATCCC CGGGCCCAGT GAGTCACTTC CCCAGGCCCC GGAGGCCTTC GTGGAAGGTG 1500
CCTCCCTTTC CGGCAAAGCA TCCTTTGTTC TCCTGCTGGC TTTGCTTCCC AATCCTCTCT 1560
GAGTTGCAAC CTTGAGGGTT TTAGGGGCAC CAAGCTCCCA GGAGCACAGA GGTGGGCTTG 1620
GGTGCCACCT GGAGAGCGGG CTGCAGAAGG CTGCAGCTGC TTTTTTGCTT CCTCAGTTCC 1680
CTGCCCTCTC AAGGCCCAGG CTCTCCCACC TCCCCAGACG TCTGGGGAAA CCCACACTGC 1740
CCTGCATAGG TTGTGGTGTG CAGCCTCCGG ACTGCAGATC CTGAACGCGC ATCAGGAGGG 1800
AGGGAGGGAG GTTTCGATGC TCTCGCCCTG GCCAGCACCG CTCTGAGTTG CTGAACTGGC 1860
CTCAAGGCTT CTCTTGCATC AGGGAGAGGC TTCCGGCACC ACCACTGGCA CTCCTCCTTC 1920
TCCCTCCCTT TAGCCTCCCC CAGTTCCCAT GCCCAGGTGG AGGAACCCGT GTAGAAGCCC 1980
AGCCCAGGGA GGGAATTCAT CAAAGCACCT TCCCACACAG CCTCTAGTTT GCCTCCTCTC 2040
CACTCCCACC TTCCAGCCCC AGCCTGGCTA GCCACGTGGG GGGCTCCTGT GCCAAGGAGT 2100
GCCCAGCTGC CGGGTGAGTG AGCAGCCCTG CACAGAAGGC AGCTGACTAC CATACACACT 2160
ACATGTGTGG AGAGCACCAG CCTTGCAGCC TGGCGAGGCT CTTGCTTTGA 2210
|
