| Tag | Content |
|---|
EnhancerAtlas ID | HS040-34085 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr8:144959470-144960630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr8:144960595-144960615 | TGTGGGTGGATGGGTGGTGG | - | 6.45 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH08I143885 | chr8 | 144959402 | 144959607 | | GH08I143886 | chr8 | 144960453 | 144960673 |
|
Enhancer Sequence | CCTTTACTGA CGTCCCTGCC CCCAGCCTTC CCTCCCAGCC ACAGCTTGGC CCGTCCCATC 60
CAGCTGTCAG TGTGGCCAGT GCAGCCAGTC GAGCCACAGC CTCAGTGTTT TCCTCTTGAC 120
CCTGCCTCCT GCCGCCACTT GTTTCCAGGG AAACCAGGAC CCGGCCCCAG CCATGTAAGT 180
AGGAGAGACT GGGAAGGGGC TTCTCACCCT CCCCCTAGTT TCTTGCACCT CGGGGGAGGT 240
GAATAGGCCA GGGTTGGAGG AACTCACTGC TCCCAAGGCC CGTCTGGCCC ACTGGACTGA 300
GCCCCCACGC TGGGCAGGCA GCCAGAGGGA GGGATTGCTG GCGGTGGATG CCAGGCCTGC 360
CCTGGGAGGA TCTGGGGGCG GGCAACATGG GGGTGCTGAT CACACTCCTG TGGGCCAGGG 420
ACTGAGGAGC TACAGGTGGG CTCTCCCGCC TCCTCCTCTG CAGCCATGCA GACCTCAAGG 480
ATCCCTGTCT CCTCACCTAC ACCCTCGATA GCCTCTCCAT TCCCCAGCTG CCCCACCCCT 540
GGGGACCCGA CAGCCCCCAC CCAAGACTTC CCACCACCCC AGACTGGCCG GTCTCGCTGC 600
CAGGAACCTC CACCCTGTGG CCACGCCTTT CCCACCCAGG CCTGGAATGA ACCTGCCCCT 660
CCCCAGCCTG GAGCCCCCCT CTCCCAGGCC TGACAATGGG GAGAGGTGAC TCCCCAGCGC 720
AGGAGTGGGC GCCCCTGGTC CCTGCAGGTG CAGGGTGGTC AGCTGTGTCC GCAGGTGCCA 780
GTGCAGACCC TCCCCCCACC CGCTGAGTCC TTCATCCAAC ACTGGCCTCT ACCGAGGAGT 840
GGATGCTGTG TTGGGCACAC AGGCCAAAGC CCACCTGTGC CCACCACTGT GCTGGGCCCC 900
AGGCCCAGCA GGAGCCACCG CTGCTTGGGT AAGAGAGGGG ACAGAGAGCA GGGGCCCAGC 960
CTCCGGGCAG TCTGGACAGA CACTGGGAGT CCCTGTGGGG CCCAGGCCCA CCCCTGCCCG 1020
GGCATGTCTT TCTCACAGAG TTTGTGCTGC TGTTGCCTGG GGAACTTTCC ATCAGAAGAT 1080
GCTGGGTGGG GTGGGTAGGC AGGCCGGGCG GGCCCGCAGA CGCGCTGTGG GTGGATGGGT 1140
GGTGGACGCC TCTCCCGGGA 1160
|
