| Tag | Content |
|---|
EnhancerAtlas ID | HS050-56417 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr5:167604360-167606670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr5:167605076-167605087 | CTAATCCTCTC | - | 6.02 | | Myod1 | MA0499.1 | chr5:167605459-167605472 | GGAGACAGCTGCA | - | 6.24 | | Myog | MA0500.1 | chr5:167605462-167605473 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr5:167605462-167605473 | GACAGCTGCAG | + | 6.14 | | ZNF263 | MA0528.1 | chr5:167605640-167605661 | AGAGGAAAAGAAGGAAGGGGA | + | 6.05 | | ZNF263 | MA0528.1 | chr5:167605637-167605658 | GGGAGAGGAAAAGAAGGAAGG | + | 6.14 |
|
| | 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 |
| GH05I168177 | chr5 | 167604964 | 167606356 |
|
Enhancer Sequence | GTGTGATTAT TTTTATTTTA CAGATGAAGG AACCAAGACT CAGAGAGGTA AAGTAACTAG 60
CCCAAGGCCA CACAGCCAAT ATTTTGCTGA CCTGGGGTTG AACACAGATC AGCTGCCTCT 120
AGATCCCGTG ATCATAATTG GCAGTATGAT ACTAATTCCT ATTATCTACA CCATAGAGTA 180
GATGCGAAGA TTAAATGACA GCCAGGCACA ATGGCTCATG CCTGTAATCC CAGCACTTTG 240
GGAGGCTGAG GCAGGAGGAT TGCTTGAGCC CAGGAACTTG AGACCAGTCT GGTCAATATA 300
GCAAGACCTT GTCTCTACAA AAAATTAAAA AATTAGCTGG GCACAGTGGT GGGTGCCTAT 360
AGTCCCAGCT ACTCAGCAGG CTGAAGCAGG AGGATCTCTT GAACCTAGGA ATTTGAGGCT 420
GCAGTGAGCC AAGATTGCAC CACTGCACTG CAGCCTGGGT AACAGCACAA GACCTCATCT 480
CTCAAAATAA ATAAGTATAA AACAAAATAA ACGAGAAAAT CTCCAGCGAG TGCTAAGCAC 540
AGTGCTTGGA ACATGGCAGC AGCCACGTTT AGGAATGACA CCGTTTAGAA ATTAGTACTT 600
CCAACTCCTC TAATTCCACA GGAAGCTCGT AGAATAGCCA AGTCCGGGCC CTTCTCCCAG 660
CTGGCAGTCT GGGGCATTTC TTTATGCAGC AGAAGGAGAA GCATCATGCG CCCCTACTAA 720
TCCTCTCCAC TCTGGGGCCA AGCCTCCCAT CTTCCCCCCA GGGACAAGGT CTCCCCTCAG 780
GCGGAAAGTA ACTGTTCACC TTGTTGCTCT GAGGTGTCGG TGGTGACAGC CCCTTTTCTT 840
TCTGAGGGCC CCAGCAGGTC ACTGTCTGGC ACCAGGCTGC CACCCCCTGC CGGGCCTCGG 900
CTGCACTGGC CGTCGGCTCA GTTCTGTGTG ACCTGTCAGT GGGCTCTTTG AAATGGAGGT 960
TGATGAGGAA CAGAGCAGGG TAGACCAGGC AGCGAGAGGC CAGGAACAGC AGGCAGAGGG 1020
CAAGCATTTG GGGAAATCAG AGGCCAAGAG CAGAGGCCCC TGCTCTCTGT TGCCAGTGGT 1080
TTTTGTAACA GCAAAGTGGG GAGACAGCTG CAGCCAGGAT AGAAATCCCC CAGGTATAAA 1140
AAACGTGGCT CTAGGCTAAC AAGGGTGAGA CTGTGCCAGA GAGGCCTGTC AGAGGCTGTC 1200
CAAGGTGGGA AATTTCTGAT CAAATGAGAT GATTCCCAGA GGCCCTTTCT GGGTTGAGAG 1260
TCAGCAGGGG CGGGACAGGG AGAGGAAAAG AAGGAAGGGG AAAGAGACAG AAAAAACAAC 1320
TAAGAAATGA ACATGTCTTC TGAAGCTTCA GTATTTCCCT TCATAAGTCC TGTGACATTC 1380
AGAGGGTACC TATATATGGC TGTGACTGCT TCCAGCCCCC TGTGAAAAAC CGAGAACAGA 1440
AGTCAAGAGG CTTTGGAGGA GGCTGGGCAT GGTGGCTCAC GCCTGTAATC CCAGCACTTT 1500
AATTCCAGCA CTGTAATTCC AGAAGTCAAG AGGCTTCGGG AGGCCGAGGC GGATGGATCA 1560
CTTGAGATCA GGAGTTCAAG ACCAGGCTAG CCAACATGGT GAAACCCCAT CTCTACTAAA 1620
AATACAAAAG TTAGCCAGGC ATGGTGAAGG GTGCCTGTAA TCCCAGCTAC TTGGGAGGCT 1680
GAGCCAGGAG AATCACTTGA ACCCAGGAGG CAGAAGTTGC AGTGAGTCGA GATCGAGCCA 1740
CTGCACCCCA GCCTGAGCAA CAGAGTGAGA CTCTGCCTGA AAAAAAAAAA AAAAAAAAAA 1800
AGAAGCTTTG AGGTAGACAA CCAACATGTG AATCATGAAT CACTTCTCCA TCATTTACTA 1860
GCACTGTGAC CTTGGGCAAG GCCCTTAAGC TCTATGAACC TCAGTTTCTT TATCTGCAAA 1920
ATGAGGATCA TAGAACCCAC CACAAAGGGT TCTTGAGAGC ATGACTGGAT GCTGGCTGGA 1980
TCGAAGCACA GCACAGGCTG AGCAAGCACA GAGGGACTTA AGTGGCTGGC AGAGGGCCAA 2040
GCACTTAATT GTAAACTTAA GTCAAAAGTG TGAACTGGAT GAAGCTAGGA GCTGGGGCAG 2100
AGGGCTGGCC AAAACATTCT GCTGCCCAGT TTCCCAAAAC ATAAATCACC CTGTACTAGG 2160
TATGTAAATG GTTACTCTCA CTAACTGTCT TAGATAAAAG AGCTCATATG TACATGCTTG 2220
TACAAACATG TCATGGCAGA GGGTACAACA GGCTCCTGTG TGTTGGACAC TCAGCATAAC 2280
AGTCACACAA CCTTACATGG CAGCTTTGTG 2310
|
