| Tag | Content |
|---|
EnhancerAtlas ID | HS050-08910 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr10:79802920-79804390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX3 | MA0684.1 | chr10:79803889-79803899 | TTTGCGGTTT | - | 6.02 | | ZIC1 | MA0696.1 | chr10:79803344-79803358 | GACCACCTGCTGTG | + | 6.81 | | ZIC3 | MA0697.1 | chr10:79803344-79803359 | GACCACCTGCTGTGT | + | 6.41 | | ZIC4 | MA0751.1 | chr10:79803344-79803359 | GACCACCTGCTGTGT | + | 6.38 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I078041 | chr10 | 79801521 | 79804070 |
|
Enhancer Sequence | CCGGGTAATT TTTTGTATTT TTAGTAGAGA TGGGGTTTCA CCATGTTAGC CAGGATGGTC 60
TCGATCTCCT GACCTTGTGA TCCGCCTGCC TTGGCCTCCC AAAGTGCTGG GATTACAGGT 120
GTGAGCCACC GTGCCCGGCC TAATCTGCAT GTTAACTCCA AGAAGCATGT CTTCCTGGAC 180
CCACGCTGGA AAGGGTGTAG AGCAGTTAAG CATCTTACCA GTGTCTCACC CATGAAGTGG 240
TGGGGATGGG ATTGGAATGC AGTCATCTGA CTCCAAAACA CTGCATTTTT TCAGGCACTC 300
CAGTATTAAG CTACTTTGCA CTGTGCATAT AATGGTATAT AAAACTCATG ACTGCCAGCA 360
GGGTGCCAGT TGCCATGGGT TTATTGAACA AGTGTTAGAT GGCTAGCCAA ATTCCCAATT 420
TACTGACCAC CTGCTGTGTC CCTGTTCTGC AAGTTGGGGA TAAAGAAGCT GTTCTGTCTT 480
GAAAGCTCTG AGGTAGTTAA TGACGATCCC ATGATCTGGC TTCTGTTCCT TTCTGTGAAG 540
TAGCAGATAG TGTATGACTG TGACGTGATA GAAATTGAGA GCCAAGAAGA TCAGTGCAGG 600
GAGGCTGGGT CTTGGAAGGC TTCCAGGAGA CATACAGCAG TCCCCACCTA TCTAGTTTCA 660
GTTGCTGTCG GTCAACTGCA GTCTGGAAAA TTATCATGGC TAAATGGTCT GGGATCACCC 720
AAAAGTGATG ATCCTCTTGA AGTGTCATCA GAAGGTCAAT AGTAGCCTAA CACGTCACCA 780
TGCCTACGTC ATTTACCTCC CTCTCCCTTC CACATAGGCA TTTTATCTCC CATCAAGAAT 840
GTGAATACAT GTACGTATTC AGAGGAAAAG AGTTCATGCA GCCTACTACA GTATAATTAT 900
TAATATCTTA CTCCCTAAAT TATGAACTTT AATTATGTAT ATATAGCAAC AAACTTGGTG 960
TAGATAGGGT TTGCGGTTTC AGGCATCCAC TGGGGGTCTA AGAACGTTTG CCCCATGGAT 1020
AAGGGAGGAT TACTGTAACA CCAGCAGTGG CAAGAGACAT GATCTGATTT GGATGCACAG 1080
GAGAAAGTTC TCATTTGAGG CCATGAAAAA TAGGAAAGAA AGCAGGGAGA TGGGAGCAGG 1140
CAGTGTGGGA CAAGGTGAGA CCAGTCATTC TGCAAGGGGA AGAGAGGATG ACACTGGGGA 1200
GGTGGGAGCA GAGTGGGTAG GTAGGCATTC TCTTGAATCA ACAAGATGGA AGGCCCTACA 1260
TGACTGATGC CTTTGAGCAG AGTTTTGCAC AATGCATTTC TGGTGGGAGA TACTCCATTT 1320
CAAAAATAGT CTTCAGGTTG GCTGCTAGAG CACAGAAGTA TGACACCTGA CTCATTTGTG 1380
CTGGCAGAGA GGCTCTCCTG GGTTTTAGAG CTTTGTGAAC ACACCTCCAT ACATTAATCC 1440
AACTGTCCTT CCCCATCCAC TCACCCTTGA 1470
|
