| Tag | Content |
|---|
EnhancerAtlas ID | HS040-28670 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr5:137998220-137999670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr5:137998812-137998830 | CCTGCCTTGCTTCCACCC | - | 6.03 | | REST | MA0138.2 | chr5:137998468-137998489 | TCCAGCACCCAGGACAGCGCC | + | 9.37 | | SOX10 | MA0442.2 | chr5:137998365-137998376 | AAAACAAAGAA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 137998609 | 137999000 | | chr5 | 137998421 | 137999116 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I138662 | chr5 | 137998488 | 137999089 |
|
Enhancer Sequence | CCAGGCATGG TGACGCATGC TTATGGTCCC AGCCACTTGG GAGGCTGAGG TGGGGGGAAT 60
CGCTGGAGCC TGGGTGGTTG AGGCGGTAGT GAGCCGTGAT CATGCCACTG CACTCCAGCC 120
TGGTGACAGA GGGAAACCCT GTCTCAAAAC AAAGAAAAAG AAAAAAGAAA CGTGTGGAGT 180
GGGTACTAAG TCTGCCTGTC ACACACTGGG ATGTTATGCA CAGTAATGGC AGGGCCCACT 240
GCCACTCCTC CAGCACCCAG GACAGCGCCT GGCACATAGT AGATGCTCAG TAGATACTGA 300
TTACTGAGTG AATGTGCTAG ATCTCATGAT AAATGCGGTG AGACTCTTCC CTAGCCTTTC 360
ATCCAGCACG GGTTCCATGC AGGTACCTTG AGAAACACAT CAATACCCTA CCTCCTCATC 420
CTTCCCATGG AATGATGCTA TGGGACTCTT AGTAAATGCC CCACAAAGTG AGAGATGGGC 480
TCCTTGAGAC ATGTAGGGGT GGCAGTGCCC TGATTGGGCA CCCCACAAAA GGGAGGCACC 540
ATCTGATGCC TCAAACCACA ACTTCCTCTT CCACCCACGT CAGAAATATT TGCCTGCCTT 600
GCTTCCACCC TCTTCTCAGG CAAATACCAC TCACCCCTCC TATCTCCAGC TGCCATCTCC 660
ATCCTCATGA TGTGTCTCTC TTACTGTACC AGGCACCTCT TGTGCACCAC AACCAGCTCC 720
ACGCTGGCTT CAACCTGTTC ATGCGTGATC TGGCAGTGCC ACACCCGCAG GCCCCTGAAT 780
TTACGCCCCT GCTCTTTGCC CCAGGGCTTC TCTGTTGGCA GGAAACTGCC TGGCTTTCCT 840
GCTTGGGCAG CCCAGTGGTG CAGGGCAGTT AATTCCTTGG GGGAAACTCT TGGCAAGGGG 900
GGGCAGGAAC CACTGGATAA ATGCTTCTCT CTTTCTTGCC CTGGGTGGAC AGTTGCGAAT 960
TCTTCATGAA GCTTTTCAGA ATGCTCCCTG GTTGCTTGAA GCTGTGACCA ACTCAAAAAC 1020
TCTTCTCCTT TGGGCTCTCT TCTGTCGTCA CCTGCTCCCT GGATCACAGC CTTTGATCAG 1080
GGTCAACTTT CAGGGGAGGT TGGCTTAAAT CTCCCTGACT TCCCTCTGCC CTCTCTGCCT 1140
CATCCACCCC GGTTTCCTTT TAGTTCTTCA GCTCTTTCCC ACACCAGGCC TTGCCAACAA 1200
GCTTTCCATA TTCCCTGGAG TGCCTTTCTC TCTGCTTGGG AAATCTCTCA GCTGAGACTT 1260
GCATGACCGG AAGGAAGCAG TCACAAGAAC ATCGGGGAGA AAAAGAGTTC CAGGCAGAGG 1320
GAACAGCCAA GGCAAGAGCA CTGAGGTAGG AGTGAAGTTG GCATGCTCAG GGCAGAGCAG 1380
GAGGGCCTTT GTGGCTTCAG CAGAGTGAGA GAAAGAGGGG CATAGAGTGC AGTTGGAGAG 1440
ACCATGTGCA 1450
|
