Tag | Content |
---|
EnhancerAtlas ID | HS184-15436 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:33764800-33766150 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:33765463-33765484 | TTTTCCTGCTCCACCTCCCTC | - | 6.06 |
|
| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09601 | chr19:33763698-33766425 | CD14 | SE_23205 | chr19:33764413-33767578 | Colon_Crypt_1 | SE_23808 | chr19:33764326-33767580 | Colon_Crypt_2 | SE_24807 | chr19:33763936-33767669 | Colon_Crypt_3 | SE_27406 | chr19:33764404-33766196 | Esophagus | SE_27669 | chr19:33764408-33767743 | Fetal_Intestine | SE_28569 | chr19:33764450-33767650 | Fetal_Intestine_Large | SE_31890 | chr19:33764433-33767612 | Gastric | SE_35421 | chr19:33764588-33771627 | HepG2 | SE_43051 | chr19:33764035-33767549 | Lung | SE_50571 | chr19:33764237-33766629 | Sigmoid_Colon |
|
| 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 |
GH19I033273 | chr19 | 33764308 | 33767610 |
|
Enhancer Sequence | TGGTCCGGGG CCAACCTCAA GGTGGGTGTC CTCTCCTGCA GCAGGGCCAC GGGCACCTTC 60 CGGCTCCAGC CCCAGCCCAG CCAGGCTCTG AGGGAGCCTG AGGCTGCCTC TCCTCCTCCA 120 GGTTCCTGTT TCCCGGGTGG CCCCAAAGAC AGAAGATGGT GTGAGGTTCA AGGGCTCAGT 180 CCCAGGCTCG GATTTCCTGG GCGTGTCAGA TTTCCTGGGC GCTGTGTGGC TGGTGTCTGC 240 CAGGGAGGCC ACTGAATAAC GTGAAGACCA CTGGGAAAGC ATAGCAGAGT GTGCAGTGGC 300 TGAGTCTGTG TGTGTGTGTG TGTGTGTGTG CGTGCGTGTG TCTGTGTGGG TGTGGGGTGT 360 GACTCACACA GGCCTGGGCT TCATGATGTC TCTTGGGAGC AGGAAGGTCT GTGTGAGTCT 420 GTGTCTGTCT GTGTGTGCAT GTGTGTGTGT ACCCGTGTGA CTACAAGCAT GTGTATGAGT 480 GCACACAGTT GGTGCAGGTG TACCTATGTG TCTGTGCACA TGTGTGTGCA TGTCTGTGAG 540 CGTGTGTGCA TGTGGTTATG AGTGTGTCTG TGGGTACGCA TGTGACTGTA GTGTGTGTGA 600 CTGTGTGTGT GCACGTGTGT GTGTGTGGAC ACAGCCCTCT CTGGCCTGCA CTCCTGGAGC 660 CTGTTTTCCT GCTCCACCTC CCTCCTCGGC AAGTGTTGAC TCAGGGAGGG ATAGGCAGCC 720 TTGGTTCAGG ATTTCCTGGT CAGGCAGAAG TGGTGCCTTG AAAAGGGAAC AATCTCGTGC 780 TAAAGTGGAC GCTGAGGGTC CACACAGTGC AGTGCTCTAG GGTGCCCAAG GCCGAGAGAC 840 CTTGTGCCTT CCTTGCCTGG GTTTACAGTG GGGGTCCCAG AAAGCTTTGC CCCTAGGGTG 900 GCCCATAGGA TGTGCCCTCA GGCTTTTTCT AAATGCTTCC TGATCTGGGC TGCCCGGGGT 960 GGGGGCTCTG GAGCTGGACA CTCCTCTGAC TGCTGTGGAG GCAGGGACAG CACCCCCACA 1020 AGAGGTACCC CAAGAGAAAT GGGGGCCCCC AATGTCCCCA GGCACTAGCT GTCCCAGGTT 1080 CCCTTCCACA GTGGGCAGCT TTACCCCTGC ACCGCCCCAT CCCCCAAAGC CTTAACAAAT 1140 AAAAATGAAG CTCTTTGAGG CTAAGAGTCT ATTCAAGCTC CAAGAGCTCT CTGCCATGTT 1200 GGGAGGAGCC TTCTAGAAGC GCTGCTTCTC TCAGGGGCTG GGAGGGCTGG CCTCACTGGG 1260 TACGCCTGAG AGATGCAGCA TCTTAGTCGG CACCCATCTG CCGCGTCCAC ATCTGGGCTG 1320 TACCAAGGTC CCCCAGAGGC GCCACTGTCC 1350
|