Tag | Content |
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EnhancerAtlas ID | HS050-70802 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:133796200-133798000 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr9:133796911-133796921 | GGGGATTTCC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 133796569 | 133797432 | chr9 | 133797514 | 133797564 |
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| Number: 2 | ID | Chromosome | Start | End |
GH09I130921 | chr9 | 133796921 | 133797070 | GH09I130922 | chr9 | 133797161 | 133797310 |
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Enhancer Sequence | CTCCCCATCC CTGGCACAAG TCGGCTTCCT TGTCCTTCTG TCCACCAGGC TGGGAGCCCG 60 CTGAGCTGTC TCGTCGCTGC TGACCTCCCT GACCCCGGCT TGCTTTAGGC ATTCAAGGTT 120 TGAACACAAG AATGAGCGTG TGCCACTGTG GGAGGCCTGG AGGCTGCTGG GTGACCTCGG 180 GCACATCCCT GGCCTTCTCT GAGGCTGCCC TGCCTGCCTC CAGGGATTGA AGGGCGCTGG 240 CGTGATGCCG GGGGTGGGGG GCAGGGGTGT ATGAACTGTA AAGTGGCCCT GGGGACAGGC 300 TGCTGAGTTG CACCCTTGCC CACACAGGTC CCTCCGGGAA GCAGGCTCTG GTGAGACTGT 360 CCAGCCCCAG GGTCTCGGGG CACAGTTCCA GGTGCCCTGT CCTCCAGGAA GGATCAGGTG 420 GCATTGGCGC TGAAGGCCTA GCAGTTCGGA CAGGGAGTCT AATGAGGATG GATGGTATCC 480 AGGGCTGGAG AGGTGGCAGC CAGCTCCTTC CCAAACAAAA ACTGAGTTTC TGACGGATTC 540 CATGTGGCGG GGGGTGATCC TGACAGATGT CGAGAGGTTC CTGGGAAAAG ATTGCTTCTG 600 ATGGAGGCCC AAATGGATAT TAATGCTCAC TGGCCAGGCA AGCACTTCTC AGATGAGAAT 660 GGCCTCTCTC CCAGGGCCCC CGGAACCGGG TGTCTGAGCG CCAGGGCTGG CGGGGATTTC 720 CTCATCGACT CCCCTCTAAT CGCCCCTGAA GCTGAGTCCG TCGGAATGAC CGGCCTCCCA 780 GCCCAAATCC TGATTGACTT CCCGGGAGAT TGGCTTCATG TCCACCAGAG TGGAAGACGC 840 ATGGCCCGCT CCGGCGTCCT GATCTTTCAT TAAGCCTGTC CTGACCCTGA ACTCTGATTT 900 CTGGGTTCGG CTGGTGCCTC CTCACTGTTC CGCCCGCCAA GGGGTTCCCA GAAGCAAATG 960 CCATAACTCA GACGTTCTTG GCGTTAGGAA AACAAAAGAG CTTTTATCCC CCAGACGCAG 1020 CTCCAGTACA TTTTTAAAAG CTCTCCTCTG GAGCTTGAAG ACAGGTTTAG AGATGTGTCT 1080 GTCTTTGGGG TCTTGTGGGG ATTCTCATCT GCGCACGCTG ACTCCTAACA TAGCAGGCTC 1140 TGCCTTGCTG GCGGACTCGT CCCTCCACCG GCCGCCTGTG CGGGCCTCCC CGCGTCCTGC 1200 CTCTGCTGGG GACCGCTGAC CCCTTTCAAA ACTGACCCAG GCTGCCTGCA CCCCTGCCTC 1260 CCCCAAAAAC TCCCCGCCAA GAGGCTTCCC TCTCTCCTGT TTCTCGGTCA CTTGTTTTGT 1320 CTGATGTTAA GCCCTTCCCC CAGATGTTTG TGGGCCTGGA CATCAATACA CCAAAAATAG 1380 TCAGCACCAA GATCCCAGGC GAGATGCGTC CCGCACTCAG TGGCAGCAGC CCTGGGGCGG 1440 TGGGGTTCTC ACCGGCCCAC CCCCGGGCCT GGTCTGGGGT CTCTGTTCCT GGCTAAGCAG 1500 GCCTGACTGG CATCGCCGGC CTCCCAGTCT CTCTCCAGCA CACTTCTTCT CAGCTGAGCC 1560 CCCCACTTTC TTGTGCTTGC AGTTAAGAGG TCTAAGGATG TAGGTGGGCA TCCCCGTTTC 1620 ACAGCTGAGG AAACGGGGGC TCAGAGAACC GAGGTAAGTT GCCCCAGGTC ACACAGCAGG 1680 ACTCAGAGCC ATGCCTGGGG CAGCCTGTGG ATGACAGGGC CAGAGCGTGG AACCTCCAGG 1740 CTCCCCGCCT CTCTGACATC TGCTGTCGGG GTCCCATCAT AGACCTGTGG ACTGAACGGT 1800
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