| Tag | Content |
|---|
EnhancerAtlas ID | HS050-42966 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr20:62008510-62009800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr20:62008898-62008914 | TGTTTCCATAGCAACC | - | 6.31 | | RFX1 | MA0509.2 | chr20:62008898-62008914 | TGTTTCCATAGCAACC | + | 6.32 | | RFX2 | MA0600.2 | chr20:62008898-62008914 | TGTTTCCATAGCAACC | + | 6.71 | | RFX2 | MA0600.2 | chr20:62008898-62008914 | TGTTTCCATAGCAACC | - | 6.83 | | RFX5 | MA0510.2 | chr20:62008898-62008914 | TGTTTCCATAGCAACC | + | 6.86 | | RFX5 | MA0510.2 | chr20:62008898-62008914 | TGTTTCCATAGCAACC | - | 6.8 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 62008800 | 62009200 | | chr20 | 62009200 | 62009781 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH20I063377 | chr20 | 62008841 | 62008990 | | GH20I063378 | chr20 | 62009061 | 62009230 |
|
Enhancer Sequence | AGCTCAGTTC TTTGGCCCTT GGTCTGGGGT GACAGCCGGG GGCACCCAGG CCCCTCCAGC 60
TCGGAGCTGC ACCAGGGACG GGTGCGTCCG GAGGGAGCAT CAGCAGCCAG TCACGGTAGT 120
GGCTTCGCCT CTGCACATCC AGATCAGGGA GAAGAGGGAA AGGCTTCCAT CCCACGGTTG 180
GCTTTGCCGA GACGTTTCTA AATAAACGAG CTTTGCGGGG CGGCAGGTTG ATGCATCTGG 240
AGTGTGGGGT CTCCTCCAGC TTCCGGAGCA CACGCCTCCC ACCGCACCGC CACCTCCCCG 300
GCTCTGAGAG GAAAACTCAT TCATCTTTCA ACACTTCATC CCCGGCGAGA CCCTCCGGGC 360
CCATCCCCCA CCCCGAATAG CCTGTGTGTG TTTCCATAGC AACCTGCACG TGCCTCTGTG 420
GGTCACATTT CATGAGGCCG TGAGCTCTTT GAAGGCACGG CCTTGACTTG AATCATTCAC 480
AGGGTGCAGA GTGGACGGGT GAACCATGAC CCTAAGCCAG CCTGGGGGGC AGGTGAGCCA 540
GCTCCCTCCC ATGCCATTCT CTGGACCATA GCTCATGCAC CCCGATTGCG TCTTACCGTC 600
ATTTGACAGA CAGAGGCCAA GGCCCACAGA AAGGGGGCCC TCCCCTTCAG CAGCAGGGAG 660
ACGGCGGTCA TGCTGGCCCG AGACAGGACG CCCCTCCTGG GGAGACGGAG CTCTGCAGAC 720
GGGAAAAGCC AGCTGCCCCC CTGCACACCG GGGTGCGGGG CAGCCCTGCT TCCTTGGAAC 780
AAAGGCTGCA CTTGCAGAAG TAGCTCAGAC TTTCACCTGC TTCAAACCCT GGGCCGTCTT 840
CTGGTCTCAA GGCCAGGAGG CAGGGCCCAC CGTCTGCTCC CTCCTGCTGG ATGGAGCCTG 900
GGGAAGCTGA GGATAATGGG GGCGTGGGGA GGGCTTCTGA GCCCCCGTGC TGAGCAGCAA 960
CACCAACCCT CCCAGTGCTG GTGAGAATTC CGGAGCAGCT GGTTTACTCC GTCTGGCAGG 1020
CGTTTCCCTC CCAACAGCAA AGCATCCCGG GCTTCTAGCA TCTACCTTGT AAATATCAAG 1080
GGCATTGCAG GGAAGCTGAG CTGGCACTGG TGAGCTGACG TCAGCAAAGG GTCAGCCCCG 1140
GGGCCGGGGG TGTGATGGCA CAGCTGTGGC CCAGCCCTGG GGGCTTCATC GCTGCTGAGT 1200
ACCTCGCAGT GCGGGAATCG AAAAAGCCTC CTCCCTCGGC ATCGAGCTGT TCTTGCCCCA 1260
GAGACATCTG AACAACGAGT ATTGTTTCAG 1290
|
