Tag | Content |
---|
EnhancerAtlas ID | HS145-11687 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr19:33764270-33765780 |
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 | TGGGCCAGGA ACACGATCTG ATTGACTTTT GCAAGGATCC CTGGCTGCTG TTGAGAGGTG 60 GAGGGCAGGA CCTGCAGGGC GGGAGGCCGG TGCTCCTGGG AGGCTGCCGT GTGGATAAGA 120 GTCGGGGGCC AAGTCTCCCG CTGGAGCAGC ATGGAAGGCT GGGCCGGACG TGGGCGGTGG 180 GCAGGCCCCA GGACTGCTGC TCTTGGCCTG GCTCTGGCGT TGGCTTAGCG TGCAGCCGCG 240 GGGGAGCCGT GTGTGGGCAC GTCCCTGTGC TGCCGCCCCC GCTGCCCCAG AGACACAGCC 300 ATAGGCAGGC TGGCTCCCCT GGGCCTGGCT CACACGTGGT GGAGGTGATC AGGGATGACG 360 AGGCGGGTCG CAGGGTGGCA GGGACCTACA GGGCCCCAAG GCCAGCCCGG GGGACAGAGG 420 ACTCCCTTGC CAGGTCCTTG TTCATTCATC CCCCCCCTTT GTATGGTGAG ACCACTGGGA 480 GCCAGACACA GCCCTGCCCC AGGGGCCATG GGGAAACGAG TGTCTGTCTC TGGTCCGGGG 540 CCAACCTCAA GGTGGGTGTC CTCTCCTGCA GCAGGGCCAC GGGCACCTTC CGGCTCCAGC 600 CCCAGCCCAG CCAGGCTCTG AGGGAGCCTG AGGCTGCCTC TCCTCCTCCA GGTTCCTGTT 660 TCCCGGGTGG CCCCAAAGAC AGAAGATGGT GTGAGGTTCA AGGGCTCAGT CCCAGGCTCG 720 GATTTCCTGG GCGTGTCAGA TTTCCTGGGC GCTGTGTGGC TGGTGTCTGC CAGGGAGGCC 780 ACTGAATAAC GTGAAGACCA CTGGGAAAGC ATAGCAGAGT GTGCAGTGGC TGAGTCTGTG 840 TGTGTGTGTG TGTGTGTGTG CGTGCGTGTG TCTGTGTGGG TGTGGGGTGT GACTCACACA 900 GGCCTGGGCT TCATGATGTC TCTTGGGAGC AGGAAGGTCT GTGTGAGTCT GTGTCTGTCT 960 GTGTGTGCAT GTGTGTGTGT ACCCGTGTGA CTACAAGCAT GTGTATGAGT GCACACAGTT 1020 GGTGCAGGTG TACCTATGTG TCTGTGCACA TGTGTGTGCA TGTCTGTGAG CGTGTGTGCA 1080 TGTGGTTATG AGTGTGTCTG TGGGTACGCA TGTGACTGTA GTGTGTGTGA CTGTGTGTGT 1140 GCACGTGTGT GTGTGTGGAC ACAGCCCTCT CTGGCCTGCA CTCCTGGAGC CTGTTTTCCT 1200 GCTCCACCTC CCTCCTCGGC AAGTGTTGAC TCAGGGAGGG ATAGGCAGCC TTGGTTCAGG 1260 ATTTCCTGGT CAGGCAGAAG TGGTGCCTTG AAAAGGGAAC AATCTCGTGC TAAAGTGGAC 1320 GCTGAGGGTC CACACAGTGC AGTGCTCTAG GGTGCCCAAG GCCGAGAGAC CTTGTGCCTT 1380 CCTTGCCTGG GTTTACAGTG GGGGTCCCAG AAAGCTTTGC CCCTAGGGTG GCCCATAGGA 1440 TGTGCCCTCA GGCTTTTTCT AAATGCTTCC TGATCTGGGC TGCCCGGGGT GGGGGCTCTG 1500 GAGCTGGACA 1510
|