| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04219 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:154779360-154780600 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:154779494-154779515 | TCCTCCTCTTTCTCTTCTTCC | - | 6.37 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGCCATTCC CCACCAGGGT GCCCAAGGAC TCCCACCAAA TTAGAATGTG GTCCCAGCCC 60
CGGGAACTAA ATTTATCCTG AAAGGACATT TGGATCAGAA TGTTCTCTGC TACAAGAGAT 120
CCTGTCCCTC ATTGTCCTCC TCTTTCTCTT CTTCCAGAGC CAGGCAGTAT TGGCTGTAAA 180
ACTCAGCCCT GTCAATTCAG CTTGAAAACC ACACATACAC ATGCAGTCAA CCCGCAGCAA 240
CAGACACCAC ATGTTTAGAT TTGAAAGATG GGAAAGACTG AGGCAAGCAG GAAAGGAGAG 300
GCCGAGGACA TACAGAGAAG GTGAAACAAG GTGGTTTTGG TGAAGCTGAG CGCAGGGTCA 360
AAGAGGAACT GAGAAGAGGA AAAAATGTCC CCTGGTGGCT GTGGACAACT CGAGCCCGTA 420
ACCCAACAGC AGCTGGGGCA AGTCATTCCC TCTACAGCGC CAGCTGCTCC TTCCCAAGCC 480
ACGCAGCTCC TCCTACCTGC CCCCGCACTT CAACCTTTTG AGCCCACTTA ACACTCAGAA 540
GCCCCCCGCA CAAAGTCGGC TTTGGGTGAT GTCACTGCTG CTGCGGGTGA CAGCCAGGCC 600
CTGGGGATAG AAGCCTGCTC TGGGATGGTG GCGGTTTCCA GCCACCCCAC CAAACCTGCA 660
AGGTTGAATT CTGCAGGCAA AGGAAGGATG TAAACTCCCT GCCTGGGGGA GAAGCTAAGT 720
CCCCGAGGCT GCTGGAGAAG AGTGTATTTT TAGGCATAGG CTTGATTTGT GAACAATAAG 780
GGAAGAGCAA AATTGTAAAA TCCTAAGGTT CTTGTGAAGT CTGATCAGTG TCGCTCCTGC 840
TAAACATCCA AAAAGATCCG ACAGAGCAAG ACAAACTCGG GCTGCCCTCA AGCCCTGGCT 900
CCTGGTTGGG TGGTGTTCAG TCAGTGAGAT CAGAACCTCA GCGTTTTGGG GTGGGAGGGG 960
TGTTTTTCCA TTCCTCTGAC TCTTAAACAA GAGTGTACCA GGTGGCTCTC ATCTTTAATC 1020
CTAACAATCT CCCAAGGAGG GAGATTCATC CACCATTCCT CTAGCCCAAC CCTGTACTCT 1080
AAGGTCAGAG CAGGTCCCAG TGATTGAGGG GGGTTCAACC TGTACCATAA TCTACACCCG 1140
TCTCCCATCC CCATTCTTAC CTCTCAGTCT TTGATACAGA CTATTGACAT TCTCTCCATC 1200
TTACATAAAA TGCTTTGCAG GTGCAACCTG AAGACAAATT 1240
|
| |
|
|
|
