| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04402 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:159157780-159158890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:159157955-159157966 | CCGCAGCTGTC | - | 6.32 | | ZNF263 | MA0528.1 | chr1:159158045-159158066 | TCTCTCCCTTCCCTCTCCACC | - | 6.02 | | ZNF263 | MA0528.1 | chr1:159158048-159158069 | CTCCCTTCCCTCTCCACCCCC | - | 6.12 | | ZNF263 | MA0528.1 | chr1:159158280-159158301 | CTCTCCTCCCCCACCTGCCTC | - | 6.13 | | ZNF263 | MA0528.1 | chr1:159158097-159158118 | CTCCCCTCTCCCCTCTCCTCT | - | 6.98 | | ZNF263 | MA0528.1 | chr1:159158268-159158289 | CCCCTTTCTCCCCTCTCCTCC | - | 7.09 | | ZNF263 | MA0528.1 | chr1:159158271-159158292 | CTTTCTCCCCTCTCCTCCCCC | - | 7.29 | | ZNF263 | MA0528.1 | chr1:159158083-159158104 | CCCTCCTCTTCTCCCTCCCCT | - | 7.87 |
|
| | 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 |
| GH01I159187 | chr1 | 159156991 | 159158926 |
|
Enhancer Sequence | CCTACTTCTC TCTATTTGTG ACTGTTTTTC TCTGTTTTCT CCGCTTTACT CCTTCTCAGC 60
ATTTGGGCAT TAGCGCTTCT CCCATTTAAG AACAGAGTAA TTCCTAAAAT CTCCTGGAAG 120
CTGTCTGTGA GGAGCAGAGA AGAGGGGAGG TGCCTCCATG GAGGCCAGGG AACCTCCGCA 180
GCTGTCTCAG AGTCCCATTC CCATGCTAGG ACTCTCTAAC GCTGCCTGCT TCCTGCCTGA 240
CTCCCTCCCC TCTCCGGCCT CCCATTCTCT CCCTTCCCTC TCCACCCCCT CTTTATCCTG 300
TACCCCTCCT CTTCTCCCTC CCCTCTCCCC TCTCCTCTCG CCCCTCGCCT CTCTTTCCCT 360
TTGCTTCTGA TTAGGCAATT CTCTCCCTAG TCCTGTCCTT TTCTTCCTCA GGGACCCTAA 420
GCCCACGTCC CACTTTTCTT TGTAATCTCG ACCTCCCGGC CCCCGCGCGC CCTCTCTCGG 480
TCCTAGCGCC CCTTTCTCCC CTCTCCTCCC CCACCTGCCT CTCCCCAGCT GGCTCTGAGT 540
CGCGCTGGGA CGACTGGCGA AGTTCACCCG GGACTCCAAA GCCCGGACAC GTAGCAGCTC 600
TGGGCTCTGC TCAGCAGCGG ATGAGCTCAC TGAATTTTGC GCACTTGATT GGCTACTTCG 660
GGGCGCTGCG GCGGGAGACC CTGAAAAGAT TCGCAAGGCC GGTTTCTTTG TCCCTCCGCC 720
TCTTCAGGTT GGGCTAGGGA CTTAGGCCAT TGGGTATTTC TTGGAAATGG AATTCCAGTA 780
ACCAAGAAAG GAATAGGCAG ACAGGTAGGG GTAAGGTAGG TGCCAAAGGG AGCATGGAAT 840
TGATTTAAAA TTGTCTGCAG GGGGATGTAG GAAGTAAGTT TCTTGGTTTC CTTAGTTTTC 900
CTTGCAATAC CTCAAGAAAG GCGTTAGGAG CCACCTTATA GGAAGAGAGG TGAGGAGGTG 960
ACGCAGGCCC TGGAAAAGGG GTTTGTTGTC CCAGAGGAAG GAGCAGACTC AGTCATTTAG 1020
AGGGGCTAAG GGTAGAGTAG GGAAAAAAGA TAATTTGAGT AGCCCATAGA AGGTAGCAAT 1080
CTGGGAAGAC ATGGTACAAC TTTCAGCCCT 1110
|
