| Tag | Content |
|---|
EnhancerAtlas ID | HS040-11165 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr14:104560420-104561600 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr14:104561156-104561175 | TGGCCAGCAGAGGGCGCCC | + | 8.45 | | REST | MA0138.2 | chr14:104560980-104561001 | AGCACCACCCAGGACAGGACC | + | 6.06 | | ZNF263 | MA0528.1 | chr14:104560804-104560825 | TTTTCTTCTCCCTTCTCCCCC | - | 6.76 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24313 | chr14:104560233-104560819 | Colon_Crypt_2 | | SE_24938 | chr14:104558133-104561752 | Colon_Crypt_3 |
|
| | 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 |
| GH14I104094 | chr14 | 104560234 | 104560819 | | GH14I104095 | chr14 | 104561081 | 104561230 |
|
Enhancer Sequence | CAGGAAAGGG CAGGGTCCAC GTGTCAGAGC TGCGGGCAAG GCTCTGAGTT CCTCTCCCCC 60
ATGCAAGCTG GGGGTGGGCG TATAGGGCCA AGTCGACTTC CCAGATGAGG ACACAACGGG 120
AACAGTTGTC TTAGCCTGTC CCAGTTAGTA TCTGGGGCGC GGTGTGTGGT GTGTGATGCT 180
ACCTCGAGGG CCAGCAAGCT CCTTGTGCGT GGCTGGTGAC CTGCTCACTG CCCTCTGTCC 240
GTCCCCGCCC AGTTGGAGTC TTAGTGGATT TAGTGGAGTC TTGGTTGGAG TCTTAGTGGA 300
CCACAGCACC TCTCAAAGAC TCTTGTGGTT TACAGCGACC TGTGTGCTCC CCCTGCAGGC 360
AGAACCACCC CCCGCCCCAT CAGCTTTTCT TCTCCCTTCT CCCCCATCAC AACACGCTCC 420
CATGTTACCG GAGCTGCCTC CCCTAGTAGG GGGCCTCCTG CCCGCTCCAG TCCCAATTCT 480
CACCTGCTTC CCTTACGAAC CCCCTGCTCC CCTGAGTGGG AACATCTAGG CTTCCCCTTC 540
CCAGCAGCAG GGTGGCAGGC AGCACCACCC AGGACAGGAC CCTCCATTTG TAGCCGGCAG 600
CCCTCACCGG GCAAGGCGTG ACTGCTTTTT GAGGCCCACG AAGCTGCCCT GCGGTCCTTG 660
CTGCAGGGAG CAGCCCTGGG CAGCCTCACA AAGGCCTTCT CGGCTCAGGT GGCCCAGCCT 720
GCCGTCTTGC CGCGAGTGGC CAGCAGAGGG CGCCCTTCCC CTCCTTGGCC TCCGCTCCTC 780
TGCAGTTCCC AGGCCTACGG GGCTTGGTCT TTTAATGGCC CCCCGGGCAG GCCCAGGCTT 840
CGTATGGAGC CCTGGGCTCT CGGAACGGTG CCCTGGCAGC CGCAGCCTGG GCCAGCCACC 900
CTCCAGGGGG TGGTGGCCGG AGGACGTCCC TGCATGGCCA GCTTCACTGC TGCCCTTCGG 960
TGTCCTGCCC GGCCGCCCAG GTCCAGATCC AGGCAACCTC CAGGATCACC TGCTGGTTCC 1020
CGGCCATGGC TGTGCCTTGA CCCTGCAGGC GTCCTTGTGC CCACCGTTGT GTTCTTGCCT 1080
GACCCGCGGT CTGGGCTTCG AGGCTCGTGC ACCACCACAG CCCCCTGCTG CCATGGAGAG 1140
GCGCTCTCCC GCCCTTGGGG AGTGTGCAGA GGCCCCTTGG 1180
|
