Tag | Content |
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EnhancerAtlas ID | HS040-00753 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:19700820-19701340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA(var.2) | MA0730.1 | chr1:19701281-19701298 | TGACCCTTGCCTGAACC | - | 6.22 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_05833 | chr1:19698064-19702209 | Brain_Hippocampus_Middle | SE_28013 | chr1:19699343-19705753 | Fetal_Intestine | SE_28668 | chr1:19695814-19705798 | Fetal_Intestine_Large | SE_45720 | chr1:19700640-19703276 | Osteoblasts | SE_51211 | chr1:19700896-19702318 | Skeletal_Muscle | SE_52345 | chr1:19700196-19701659 | Small_Intestine | SE_65446 | chr1:19700991-19701750 | Pancreatic_islets |
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| 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 |
GH01I019368 | chr1 | 19694981 | 19705508 |
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Enhancer Sequence | TCTGAGCTCC AACGTGGCAG GAGCCTGGCA GCTCTCAGTC ATTCGATGGG GTTGGTGGTC 60 ATGAGGCTGG AGCTCAAGCC AAACATAGTC CTGATTGCGA TTCATCAGGA TCCAACAATT 120 CAGAAGCACC TGGAATCGTG AATTAAAGAC CCTGTCAACA CAGTCTGCTC TTCCAACCCC 180 CAACCACCAG GGGCGCAGGC CAAGCTCTAG CTTGAAGTGT GTGGTCTGAA AGTGGCAGCT 240 GCACCTGTGC AGCCCTCCTG GGCACAAGGG CGAGCCCAGC CTGCTCTCAA GGGGTGGCTT 300 CTCCGGCCAC TCCCCTTTTC TCCTGGCAGG GTGGGTCTGG CTGAGGCTCT GGCCATCTCT 360 CACAGGCCGG GGACACCAGC CACTTTCCTG GCCCCTCAGG CAGCAGCTCA GGGTGACCAA 420 GCCAGCAGAC GGGAGCATTG GGTGGAGGTC TCCTCTCAGA ATGACCCTTG CCTGAACCCA 480 TCTGCCAACC TGAACAGAAG ATAGGTGGGA GAGCTGTGGC 520
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