| Tag | Content |
|---|
EnhancerAtlas ID | HS040-12820 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr16:3005190-3006360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr16:3006123-3006144 | TGAGCAGGAGGAACAGGAAGA | + | 6.5 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 3005233 | 3005437 | | chr16 | 3005477 | 3006081 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH16I002953 | chr16 | 3003742 | 3006941 |
| Enhancer Sequence | GCCTCTACTG TCTCCCTCGG TGTCTCCCGG AAAGATCCCA AGCCCCAGGC CGGGGAGGGG 60
CCGCTTCTGC CCAGTCCCTC CCTCCTCCAC GCCTGACACC TGTGGGGCCA GTGCAGGAGC 120
CCCACCTGTG TCTACACCGC CCTCCCCTCC TGGATTCCCT GTCACTCCGG CAACAGGAAC 180
AGTTGTTCTG AGCACTTGTC ATGTTCGAGG CAAATACTCC TCCTTTCTGT GAAGCAATGT 240
GGGGTGGGGG TCCTCCTTCT ATCCAAAGCT GAGGGCCCTT CTAGTGCCCG TCAAGCCCTC 300
GAGGTGGGGA TGGCGGGGTA GGCAGCTAGG AGGGACTAGG CCCCCCTGAG GGGGGCTTCC 360
AGTCACCCCT CATTCAGACT GAGTGGAGAC CAGCTGCGGC CTTCCTGGGG ACAGGACACC 420
CCCAGCCCTG CCAGCGAGTG AGCCCTCACC GGGCCTGCAG GCCTGAGGCA GGGGGAGCCG 480
GGGAGCGGGG TGAGCCGCTG AAAGTCCGGG GGGTGGGCAC TGCTTTTTAG ACAGCAGCAG 540
GTCAAAGTCA GGAGGGTGAG GGTGGCCAGG ACTCTGAGGG CAATGAGGGT CCCCGGGACA 600
TGCGAAGCCC CGCATCTGCC ATGGTGCTGG GGGAGGGGCC CGTGGAGGAG GGGGTGGGCG 660
GGGTCGAGCA GGTGGCTCAC CTCCTTGTTC CGCCTTCCAG GAACCAGGTC ATGGTCGTCC 720
TCACTTGCTG GGAAGGGCGG GACTGGCTCT GCTCGCCCCC ACACCAGCCC CCAGACCAGC 780
TAAGGCTCTT GGTCTCTCAC CTTCCAGGGG TCCCGTGCCC CCCCACCCTA CTCAGGCCAT 840
GCACCACTGA CCGGGCCTGG CCCTACCTGT GGACAGCCTC CCTCCCCAGG GTGCAGGAAG 900
GGGCCTCTCT CCATGGAAAG TGAAGCCTCA ACCTGAGCAG GAGGAACAGG AAGAAAGGGC 960
TTGGCTCACC CGCCCCCAGC CCCTGGAGCT GCCCGTGTGG GCCCCTTCCT GCCCCTGTGC 1020
AACAACACAG TGAGCTGTTC GGACAGACAG GCAGACAGAC AGACAGACAG ACTCCTGCAT 1080
TCAGAAAGAG CCCCAGCCCA GCCAGGGCAG GGCAGCTTCC AGCAACTCTT GCAGACATTT 1140
TGGAGGCCAA GGCCGCTAGC GCCCCAGCAG 1170
|
| |
|
|
|
