| Tag | Content |
|---|
EnhancerAtlas ID | HS040-13531 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr16:56722980-56724140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr16:56723761-56723782 | GGAGGAGGATGGAGAGTGGGT | + | 6.25 |
|
| | 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 |
| GH16I056690 | chr16 | 56723101 | 56723250 | | GH16I056689 | chr16 | 56723321 | 56723470 |
|
Enhancer Sequence | AATGGACTCC AGCTAAATTA GGCAAAACAA ATTCATTGGA AAGATACTGG AGACCCATGG 60
AGTCAACTAG AAGGATGGAA AACTAGGCTC AGAAAATGGG TGGTTGCTGT GAGTGGTCAG 120
GTAGCAGGTC ATGTCACAGG ATCAGCCCGG CTGGGCTGCA GCAGTTTACA CAGCTGTCAC 180
CACTGCTTCT GCTGTTCCCA AATGCCCCCA CCACTGCCAT TGGCCACTGG TACTATGAAT 240
GAGTTCTAAA CTATTCACTG AATTCTTTGC TTCCAGCTTA GGATTCAAAG TCTCAGGAAG 300
TCCACTGGCT GGCAGTGGGG AGGAGAATCT GGCCACCTTC GGGTTCCCTA GTGGGACGTG 360
GGACTCTGCA CACCCTGAGA CTCACTGTGG AGTTTCTTCC TATACCAGGA AGAGTCCTGG 420
CAGGAGATCA GTGAGTCATT GGGGAGAGTT TAATAAAGGG GTGTTTACAA AGGAGCAGGA 480
AGGATTAAAA GAAATGAACA AAAGATGCAA AGACTCCCAG GCCTGCAACA CTGGGGAGCA 540
ATTGCCAGGC CCGGGCATGG CTATCCCTGG AACCCAGAGA AAGTAGCTGC AGGAGAGGGT 600
GTCCCAACGG GAGCTGTGAC TCTCAGGTTG CCACACAACT CGGTGAAGAG GGAGTCCATT 660
CTGTGACCTC CTCTCCATTC TGTGACCTCC TCTTCTCGTC TCCCATCTCC TGCCAATGCG 720
CTCATTGGCT GAACCCAAAC AGATGCTGGC CCTACCACTC CCTCCCTCTC TCTGGGTGGC 780
GGGAGGAGGA TGGAGAGTGG GTCTAGAAAA TACCCAGCAC ACCTGCAAAT AGGCTGTGTC 840
CCGTCACTAA AGGCCATGTG CGTCTCTTCC TTACACCCTG GGAGAATGGA ACTAATCTAA 900
AGACAAATTC AGCTTACGGG GTTGGAGGGG GTCGGGGTGA TGGTGGAAGC CTTGTATGGT 960
GGAAGCAGGA GTCAGGGTGG GGTGGAGGTA GTGCAGGCAT GTGAGGGCTC TCAGAATGTC 1020
TGTCTGCAGA TGTGGCTGAG CAAGTCTGCT CAGACTCCCG TGAGGAGTGG AGGTCGGGGA 1080
AGAACCTGAA TCACACACCT GTGTGTCCCC ATGGGACACT TACCTGGCTT CATTTGTGGC 1140
ATCACAATAC CTACTAAGCC 1160
|
