| Tag | Content |
|---|
EnhancerAtlas ID | HS050-65378 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr8:27532550-27534080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr8:27533090-27533105 | GAGGTCAGGAGTTCA | + | 6.22 | | Sox3 | MA0514.1 | chr8:27532942-27532952 | CCTTTGTTTT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH08I027675 | chr8 | 27532518 | 27533117 | | GH08I027677 | chr8 | 27533578 | 27533648 | | GH08I027676 | chr8 | 27533701 | 27533850 |
|
Enhancer Sequence | CCTCCTTCTA AGAAGAGCAG GGGCTTGCTG GAAGCCACAG ACCTGGCTCA TGTCCTCTGA 60
GTGCCTCTAA AAACCCCAGG CCAGCCCACT CCTTTCACCC TGGCGACCTC ACCACCTCTC 120
CAACCCAGGC AGGACAGGGG GCTGGGCAAG CCTTCTGCCG TCCCTCCAAC TCGTCTCTAG 180
CCAGGGCTGA GCTGACAACT TCTGTTGCGC CAGCCCTGGA TACACCTGTC AAAACAGAGC 240
CGCGGGAGAG GAGAGCAGAG AGCTGAAAAA CATGGTCTGA CCACAGTGAA CTTTCCAGTG 300
GGGCTGGGCT AGGCTGGGCT GGCAAGCCTT GACCTGTGGG TGGTGTGCTG AGCAGCCTGG 360
CTGGGGATTG TTTGACCTGC AGGAGCACAG GCCCTTTGTT TTGCTTGCCT TCTTCTGTCT 420
TGCCCTTTTG TTTTCTTTTG AACACTTCCA AGTGCAAGAC TCTGTGCTTG GTGTGGCAGG 480
CGGTATACAC AGGCTGGTGT AGTGCCAGGA CTTTGGGAGG CCAAGGCAGG TGGATCACTT 540
GAGGTCAGGA GTTCAAGACC AGCCTGGCCA ATATGGTGAA ACCCCGTCTC TACTGAAAAT 600
ACAAAAATTA ACTGGGCAGG GTGGTGTGCA CCTGTAATCC CAGCTACTTG GGAAGCTGAG 660
GCAGGAGTGT TGCTTGAACC TGGGAAGTGG AGGTTGCAGT GAGCTGAGAT TGTACCACTG 720
CACTCCTCCC TGGGTGACAC AGTGAGACTC CATCTCTAAA TAAATGAATA AATAAATAAA 780
TGCAGATTGT GGGCCTCCCC CCCAGAAACT CTGATTCAGA ATCAGGGACG CGGTGGGATG 840
GGAGGAATGG GGCGGGACGG GGTGTGGGGA GGTGGGGGAG GAACGTGTAC TTCCCCCAGT 900
TTCCCAGGGA TTCTGACGCC CCAGATAAAA CTTGAGAGCC ACAGGTGTAG GAGATATAGA 960
AAAATATTGT TTTTTGATTT ATGTATATAA TTTCAATTAA TCTTCACAAG CAAAGTGTGT 1020
TTGCATTTTA TAGATCAGAA AACAAGGCTC AGAAAAGCTA ACTCGCTCAA GGCCACATAG 1080
ATGTTAAGTG GTTTCAAACC CAGGATTTTT AGAAGCTGCT ATACTGAGCT GCTTCTTACA 1140
GAAAGGTGGC ATTGGAAATT AGATAAGACC TGTGTTTGCA TCTGAGATTG CTGAGTTCCA 1200
CAGAATCAAC TTGCTCAAGT TCCCAGAGCC AGCTAGTGAC AAAGCTGTGA CAAGGCTTCA 1260
CACTGAGGGC TGCTGGGTTT CCCGGTTCCA GCTGCCTCGT TACTAACACC ACCAGTGAGA 1320
GCAGTGCAGG AGATGGCAGC AGGAGTGTGC TTCTGGCTGG GAGAGTTGGC AACTTCTCAA 1380
AGGAAGCCAG GTGCTGACCT CAGCCAGGCC CCCGACTTCC CTGAGGCCTT TTCCCTAAGC 1440
CCAAAGTCTC CAACATAGGT GTCCAACGAA ATCCCCTGAA GTGAGGAACA AACTATTAAA 1500
TATTAGAACA TCTCAATGTG TTTCATCTAT 1530
|
