Tag | Content |
---|
EnhancerAtlas ID | HS110-03318 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr22:42695880-42698180 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:42697687-42697705 | GGAAGGTGGGAAGCAATG | + | 6.3 | EWSR1-FLI1 | MA0149.1 | chr22:42696059-42696077 | CGTTCCTTCGTTCCTTCG | - | 6.54 | EWSR1-FLI1 | MA0149.1 | chr22:42696055-42696073 | CTTTCGTTCCTTCGTTCC | - | 6.95 | MYC | MA0147.3 | chr22:42697442-42697454 | AGGCACGTGGCC | - | 6.07 | SPI1 | MA0080.4 | chr22:42697165-42697179 | GAAATGCGGAAGTT | + | 6.68 | SPIB | MA0081.2 | chr22:42697167-42697179 | AATGCGGAAGTT | + | 6.27 | ZNF263 | MA0528.1 | chr22:42695935-42695956 | GAGGAAGAAAGGAGAGGAGGG | + | 6.03 | ZNF263 | MA0528.1 | chr22:42695944-42695965 | AGGAGAGGAGGGGAAGGAAGG | + | 6.1 | ZNF263 | MA0528.1 | chr22:42695953-42695974 | GGGGAAGGAAGGGCGGGGAGG | + | 6.26 | ZNF263 | MA0528.1 | chr22:42695956-42695977 | GAAGGAAGGGCGGGGAGGGGG | + | 6.33 | ZNF263 | MA0528.1 | chr22:42695938-42695959 | GAAGAAAGGAGAGGAGGGGAA | + | 6.36 | ZNF263 | MA0528.1 | chr22:42695947-42695968 | AGAGGAGGGGAAGGAAGGGCG | + | 6.4 | ZNF263 | MA0528.1 | chr22:42697672-42697693 | GGAGCAGCAAGGGAGGGAAGG | + | 6.82 | ZNF263 | MA0528.1 | chr22:42695966-42695987 | CGGGGAGGGGGAGGGGGAGGG | + | 7.01 | ZNF263 | MA0528.1 | chr22:42695914-42695935 | GGAGGAGGGGGAAAGGGAGCA | + | 7.5 | ZNF263 | MA0528.1 | chr22:42695908-42695929 | GGTGGAGGAGGAGGGGGAAAG | + | 8.08 | ZNF263 | MA0528.1 | chr22:42695911-42695932 | GGAGGAGGAGGGGGAAAGGGA | + | 9.32 |
|
| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_23330 | chr22:42695863-42698813 | Colon_Crypt_1 | SE_23842 | chr22:42695766-42696384 | Colon_Crypt_2 | SE_23842 | chr22:42696407-42698797 | Colon_Crypt_2 | SE_25072 | chr22:42695921-42698957 | Colon_Crypt_3 | SE_50938 | chr22:42695852-42698100 | Sigmoid_Colon | SE_56829 | chr22:42695891-42696837 | VACO_400 | SE_56829 | chr22:42697117-42697976 | VACO_400 | SE_65474 | chr22:42695910-42696986 | 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 |
GH22I042298 | chr22 | 42694880 | 42697851 |
|
Enhancer Sequence | GAAAGGGGTA GAAGGGAAGC TTGGAGCGGG TGGAGGAGGA GGGGGAAAGG GAGCAGAGGA 60 AGAAAGGAGA GGAGGGGAAG GAAGGGCGGG GAGGGGGAGG GGGAGGGGCG CGCTGAAATC 120 ACCCGCAACA TCAAAGCCTT CCCCAGCCGC AAAGCAGTCA CGTGCAGCCT GGTTCCTTTC 180 GTTCCTTCGT TCCTTCGCTG GTAGAAGCCG CTGGGCCTGG GGCTGCTGAA GGAATTTTAA 240 AACGAGGCAG ATTGTCTGGA ATATCAGGGG GTTAGGGGAA TGCGGTTTTA TCTCAAGGCA 300 GGGTAAGGGG AGGCAGGTTT TGAAACCTGT TCCCCCAAGG AGAGCGGCAG GGCTTTGGGG 360 CCTCTGCTAG GAGGCTGGGC AGGTGGCCAA GAGTGAAGAC CACCCAGCTA CTCCTGCCGG 420 TGAGAGCTCG TGGCTGGGCC AGCCCAGATA TCAACAGAAG CCAGAAATCT AGATTTGTAT 480 GTGAAAACTT CCCTGTTTTA ATTTTGGCTC AAACTAAAAA AAAAAAGAAA AAAAGCGCCA 540 CATGGGCCAA ATAGAGCATG TCCTGACTGG GGCCCAGAAC CTCGGTCACC TCCCACTTCT 600 GATGGTGGGC AGCAACGCTT TTGTTTCCCA GGGGGCACTG AGGCCCAGGA AGGGAAAGGC 660 ACTTGTTCAG GGACACACAC AGTGAGTGCT CAAGGGGTGC GGGCTAAGAC TTGGGGTCTC 720 AGGACTCCCA TGCCTGAAGC CTCCTGCGGT CAGCAGCCCA AGGGGCAGGG CTGTGGCTGC 780 TGGGAAAGGG AAGTATAGGG AGGTTAGTGG CAGGGGAGGG TCTCAGAAAA CCCCTCGTCC 840 AGCCCAGGGC CAACACACTC AGCCCCACTC ATCACCCTGA TGACTAACCC AGGCCTGCCT 900 CTCTGCCTTT GCCTCTGCTC AGCCCATCCT CCCTATCCAC TCCTGACATT CCCTCCTCCC 960 CCTGCCAAGA CCTGGGCAGC TTCCCCTCCC CCGAGCCCCA CCTGCAGAAT GCACCATGCA 1020 TTCAACCATT CATTCTTCTG TTGCTCCCCA AGGCCCTGAG TCAGCCTTAA CCCCACCTTC 1080 AGAGGCCAGG ACAGGGGAGG GTGTTTAGGA TAGAGAGGTG TGGCCTCCAA GGAGGAAGCA 1140 GCTACCTCTG TAGGGTGGCG GTAGGGGAGT CTCCCCAAAG GAAGGTCCTA GGGCAGAGCA 1200 TGGCATCTGC ACTTACCAGG GTGGAGGTGT AAATGGCTGC TGGAAGCCAG AGGCAAGGCT 1260 GGGAGGAGGT GGATGTGGGG GTTCAGAAAT GCGGAAGTTT ATCTTGCGGG CACTAGGGAG 1320 CCGTTGGAGG TGTGTAAGCA GGAGAGAGGT CGGCTCAGAT CTTCACTATG GGGCTGTCAG 1380 GACAAGGCGA GGATGGAGTC ATTCATAGGT TCAACAAGTG TTTGCTGAGC ACTTACTCTG 1440 TGCCACGCCC CAGGGAGACA GAGGAGAGCC AGACAGACAA GGCGTGCACC TTGGGGAGAC 1500 AGACGTGACC ACACAACCAC CACCACAGGG TGAGGGGGCT ATGGTGGGGG CTGGACTGGG 1560 TAAGGCACGT GGCCTGGTCC CTCCAAAGAG GAATCCACCT GCAAGGTGAG GACAGGAGGG 1620 GACACTGTTC CCAGCCAAGG AGGTGGCATG CACACAGGCC CAGAGGTGGA GAAAGCAGGG 1680 CTTCCTAAGT CAAAGTGATT CGACAGGCGG AGGTGTCTGC AAGAGCCATG CCAAAGGTGA 1740 CAGAGCTCCC TGGCGTAGCT CCAGGGCAAT GGAAACCTTT GGGAGGGGTC TGGGAGCAGC 1800 AAGGGAGGGA AGGTGGGAAG CAATGTTTGC AGGCTGGGGA GACCTGGCTG CGTCCCTTGG 1860 CTCCCTGAAG TCTGTCGTGG GGAACAGGGG ACTCCCTTTC TCACTGCCAG CGGGCAAAAC 1920 CCGAGCAGAT GGGCAGCCAT TCCCCTGGTA GATTTCAGTT CTCCGAGGAG GAGCACTCCA 1980 GTGCACAGCC GCTTGGCTGG ACGGCCACGG GGGCTGGTGT GAGCAAGACT CAGGGCCGGC 2040 AGGCCTGGAT TCCGGGCCCA GGGCTCGCAA GTACAGCTGG ACGACCTCAG GCAGGTCCCT 2100 CAACCTAAGC CCCCAGAGGA AAGGCCTCTT GGAGGAGCTG GGAGAGAACC CCCTGATGGG 2160 TCTGCATGGC ACAGACCCAC CTCTTAGCCC AGAGCAAGAG CCGGCAAAGG AGGGACAGCT 2220 AATGGGACAG GAGGCAAAGG GGCCAGTCTG GGAGAGCTGA GGGGCCCCTC ACTGGGCAGG 2280 TGCCTTGATG CTGCCTTAAG 2300
|