| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00326 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:7530560-7532650 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZIC3 | MA0697.1 | chr1:7532183-7532198 | AGGCAGCGGGGGGTC | - | 6.09 | | ZIC4 | MA0751.1 | chr1:7532183-7532198 | AGGCAGCGGGGGGTC | - | 6.13 | | ZNF263 | MA0528.1 | chr1:7531906-7531927 | CCTTTCTCCTGGTCCTCCACC | - | 6.09 | | ZNF263 | MA0528.1 | chr1:7530737-7530758 | GGAGGAAGGAAAGGAAGAAGT | + | 6.33 | | ZNF263 | MA0528.1 | chr1:7530726-7530747 | GGAGGAAAGAGGGAGGAAGGA | + | 6.36 | | ZNF263 | MA0528.1 | chr1:7530734-7530755 | GAGGGAGGAAGGAAAGGAAGA | + | 7.83 |
|
| | 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 |
| GH01I007468 | chr1 | 7528671 | 7533504 |
|
Enhancer Sequence | CAGGGCAGTG CCCATGTTGG GAGCTGAGGA AGGAGGCTGC TCAGATGCCA GCCCCGAGCC 60
AGCCTGGTCC TCTGAATGCA GGAGGCACTA GGAAAGGGAG TGATGGGCTG GCCATGCTCT 120
CTCAGCCCCC TGCAGGGGGT GAGCCTTCTA GAAAGGTAAG GGCATTGGAG GAAAGAGGGA 180
GGAAGGAAAG GAAGAAGTGC TTCTGGAAAA AGGAGACTTT CTCCAAGGAA TAGCACCCAC 240
TGCCCCACCT TTGTAGCCTC AGTTCAGTGG CCGCCTCCTG CCGGCCCACT GTGAACTCGC 300
TCCTGCCCTC TGAGATGCTC CAGCTGATGT CACCCAAGGC CACTTAGCAC TTAGTGGGCA 360
CGTCTGCCTA TGTTGGCCTC GATTTTCCTC TCCAACTAGT CAGCTCCCAA GGGAGAGACA 420
TGAATTCCTG TCTCCCCTGA GTGCCCAGCC CAGAGCCACA GCCACCACAG GGCAGGAGCC 480
AGCATTTGGG AGAGCCATGT TCTGCTGTGG TGACGTATCC ACCCCGGGGC GGGAATGAGC 540
AGGCCTCGCA GACTCGGGGC CTGGAGCTCA GGATTGGTGC CAAGATTTAC AGAGAAGGGC 600
CTGAGTTGAC GTGGCACGTA AGCTTCTGAG TCATCGGGCT TTCAGGGGAG GGTGCTACCT 660
CTCTGTCTGT GTCTGTCTGT CTGTCTTTCA GGCTCTCTGT CTCTCTCTGC GTCTCTCTCT 720
GTCATGTTCT CCCTCCCCAT CTCTCCATTG CTGACAAATA TTCTATTAGG CTATGAGCGA 780
GGAGACGGGC AGGGAGCCTC TCACAGGCAG GGCACTAGAG CCCATGTGGC CCATAGGCTC 840
ATAAAGCCAT TGGCATGACC AGTAACCACC ATGTGAGGTC ACCAGGACAG CTGGGGAGGG 900
ACCAGATGAC CTGAGCTCAG CCCACTCCAG CTGGGCAGGG CCAGAGCCAT GACCTGGAAG 960
AGGCCACCTC TTCCCCTCTG CTGGTGGCAC CCATCCTCAG CATTGCTGGG GGCTCTGTGT 1020
CACAGCTGAC AGGGCCTTCA GGCTCCCCTG AGCCTACCCA GTGCATTTTC TAGAAGGATT 1080
TCTGAGACCC AGCGAGAGCA GGGCCAGGCC CAGGTCACCC AGTGGGTCAG GGGAGGAGCA 1140
GGCAGTGCTC CGTTCTCCCG ATGCCTTGGC CTCTGCCCCT ACCGCCTGAT GTGGGTGTCA 1200
CTGCAGCCGC AGGACCCTGA GCCTCGTGAG GTAGAGGAGG CATGAAGGGG TGAGCTGGAC 1260
AGAGCGGTCC CTCCTGTTTG GGATTTTCTG ATGGTTTCGA GGGGTAGGCA GCAGAGGTTC 1320
AGGGCCCCCT GACCTCCTCA TGTGCCCCTT TCTCCTGGTC CTCCACCTTC CGTCCTTCTC 1380
TGCATTCTCC GCCTGCCCCC GCAGGGGACC AGGCCCCCAT TCCAGGCCAG ACTTCCCTGC 1440
AGATTCTGTA TGGCTCATTT GGAAACTATT TCTGCTTCTA ATGAGTGTTT TCCTTTGTGC 1500
CCTTGTCCTC TAAAATGCTT AATGACTGCT TTCCGTGCTC GAGTGAAGCG GGGGTGTGTC 1560
CCCGCATGGC TGCCATTGCC AGGCCGGAGC TGTTTGGCTG CCAAGCCCGG CTTGCTTGGG 1620
TGGAGGCAGC GGGGGGTCCT TCCTGGCCCA CGCTGGCAGC ACAGACCAAG CCTGTGGGGG 1680
CAAGAGCACG GCTGCGGGGA GACGAGGACC CTGGGGCCTT AGGAGACCAC AGGACAGGGT 1740
GGCAGTGCAG GTCGGGGCTC CCACATCACT GGAACAGGCA GATCTTTGAG CCTGAGTTCT 1800
AGGAGTTGAG CTCCTTGGGG GACTCTGGAT TCAGAGTCTG AGGAGCTGGA TTCCAGCTCT 1860
GCCTGGACCT ACCTGAGCAC CAGGAGCGGT GACCATGCCA CTGGACACCT CTGGTGCTGA 1920
CTCCTGGCTG GGCAGTGAGC CTCCACCACG CACCACACTT CACCTGGGAG AAAACAGCCT 1980
CCGAGAAGCT CCACAGTTGC TCAGTCAATA GGGGGCAACC ATCGCTGCCC TCCGCTGCCT 2040
CCCCTGGGGG CACCACCATC ACCCCTGTTT ATAGATGAGG CATTTGAGAA 2090
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