| Tag | Content |
|---|
EnhancerAtlas ID | HS050-31772 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr18:56428190-56430500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr18:56429316-56429327 | CCTTCCCGCCC | - | 6.62 | | MEF2A | MA0052.3 | chr18:56429066-56429078 | TCTATAAATAGA | + | 6.74 | | PLAG1 | MA0163.1 | chr18:56429892-56429906 | CCCCCTTGGGCCAC | - | 7.03 | | RUNX1 | MA0002.2 | chr18:56430298-56430309 | CTCTGTGGTTT | + | 6.14 | | ZNF263 | MA0528.1 | chr18:56430465-56430486 | GGGGGAAGGAGAGAGAAAGGG | + | 6.12 | | ZNF263 | MA0528.1 | chr18:56430469-56430490 | GAAGGAGAGAGAAAGGGGGGA | + | 7.03 |
|
| | 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 |
| GH18I058761 | chr18 | 56429001 | 56429150 |
|
Enhancer Sequence | TGACTTCAGG TGCTGCGGCA GGCAGGTGGC CCAGGGAGTA ACTGGGGAGT GAAAATGAGA 60
ATGCAGCACA TGGACCAACT CCTGTTGAGC CTCTTAGCAA AAGCCAGCCC TGTCCAGTAG 120
AGCATTTTCC AACTGTTGCA AAAATTACCC TATGAACACC TCTCTCCCCA GAGTTCAAAC 180
TCGCACCTTT GATGATACTG CTTCCTGCTG CCATTGCCTA TTCTGATGTC AGAGCAGCCA 240
TTCCCATGGA AAATGGAATG GAAAGCTAAA TGGAGAGTGA GTAGGGGTTA AGACTTCTCT 300
AAAATACCGC GGCTGCCAGG CAATTTCATT AAGGAGAAAC AGAGATGGAC AATGTCATAA 360
ACATTCTCCA GCCATCAGAA GAAACCACTT CCAGGAAAAG TAAATTTTGT GGTCGTAAAC 420
ACTCACAGCA AGGGCCAGGC CACAGGCAGC GTGGCACTGG CAGAGAGCAG TGGTTGAGGT 480
GAAAGTCACC CTGGGGCCCA GGTCTCAAAC TTACCCTGGC TAGACTGAAC CAGAACATTT 540
TTCCGTTTCT TTTCCGTAAA TTAATGTTTA AAAGTTCCCC TCCCCACATA ATCCCAATCT 600
CACTTTCAAG AGATAATGCT ATCTCTTCAG TGTATATTTC TTCCGGTTGT ATTATGCATA 660
TAAATCTCCA GACCATATGG ACACACACAC ACATATGCAC ACACACGTAT GAGTATTATA 720
CACATACATG TGTACAGATA TCTTTTATAC ATGTATACAC ACAGGTGTAC ACATATGTGC 780
ATATGTGAGA TCATGCTGAG CTCACCGTTT TCCAGTTCCT ACTTTCACTT CACAATAGCT 840
CTTGGCCATC TTCCACCACA GTGTATTTAG AGTGACTCTA TAAATAGAAC GATTTCTAAT 900
GCACCTTTCA GATTTCAACT CTTTAAATAA ATGCGACAAG GGCACATCTC GTGGTCCAAG 960
GTCGTGACTG CTAAGGCCCA GAGAACACAA CAAATTTGCT GGCTTCAGCC GTGCTGACCT 1020
GCTGGAAGAT GGGTACAGGC TCCTAAGTGG ATGCTGCCAT TTGTGCGCCT CCCAGCCACG 1080
CACCCCACCC TCATATACAC ACTATCCCTT GAGGAACATT TACCTTCCTT CCCGCCCCAG 1140
GTGTTTGTGA CTTGGTGGGT AGTGGGTGAC AGAGATGCAC CTGTGTCTTC AGAACACAGG 1200
CCACTGAAGG ACAGCAGGCC CGGGGCTGGT GGGGGCCTGA GCATGCCCTC CCTCACCAGG 1260
CTGACCAGGC TTGCATGCAG TGGGGCAGAG GCAGTGGAAC TATCCAGAAA ACATGCCCAT 1320
CCCCCCGCCC AAGCCATCAC AATGGGAGCT GAGTACAGGG TCACTAGGAC AAAGAGTGAA 1380
TGGAACCATC TTGAAAACAG CGGTGATGTT TCCTGTCTCC GCTGGCACAG GCCTCCGTGG 1440
AGCCCACGTT CTTTTCACAG AGTTCAAGTT GCTCAAAGAA ATAAGGAGAG GCCACTTGTG 1500
AGCAGTGGTC CTCCAGGTGA AACCCAGAGG GCGTCGGGAT GCCCACAGGT TCCTCAGGAA 1560
ACTCATGCGG GGAGACATGG GGGTGCCAGG GACACGCCTC CACCCCACCA TGGCTGCCCA 1620
TAGCAGGGTC CGTGGCAAAG GGACCAGGTG GCCCATGGGT TAGTGGGAGC AGATGCCCAA 1680
CCACCTCCTC CAGGCCCCAC TGCCCCCTTG GGCCACCACA GAGACCTCCA ACTTCTCCAT 1740
CCTCTCTGTC TCTCCCTCTC TCTCCCCACT TGCTCTCTTC CTCAAGGGCC CTTTCCCTGT 1800
CAACTACCAC TGGCACCCGG CTGGAGGAAC AGGGCAGGTT TGCCTGTTAG TACCTGCGGC 1860
AACTCATCCC CCAGCCCCTA ACTTTGAGGC GATCCCATTT TCCTCCTGTA TTCCCTGAGC 1920
TTGACACAGC TGAATGTGGA AGACCCCAGG GCAACAAGAG GCTTGGGAAG GAAGGTCACA 1980
CTGGAGTCGC GGGGGAAGGG TCACCCAGGC ACAGGTACTC AGCATAGACT GCAGATGCTG 2040
GCCAGCCAGT CCTACACCCA GCTTACTGCA GAGGCACGAC CACACTTCTG CTGCAAGGCT 2100
GGGGGAGACT CTGTGGTTTC GGTGAGGAAG AGGACAAGGA GGTGAGCGAG CCAGGAACAG 2160
CCCCCGCATG TCTCTTATCA CGCCTTCATT CCCCTCTCCC CGCAGCACTG AGCTTCTGTG 2220
TTTTCTTTCC CCCAAGACTG TTCTCTCGGC TGCTGGTGGC AAAGGAGAGG GCTGCGGGGG 2280
AAGGAGAGAG AAAGGGGGGA CCCCAGATGA 2310
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