| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00208 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:7530380-7532460 |
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 | CTCAGGGCAA TTTGTTCTGG TGCTAATTAC AACACCAGGA TAATGATGCT GTGGCCAGGT 60
TTAATTTCTC TGATGTTAAA TAGGAAAGAA GCCATGAGTT ACTGGCTCAG ATGGAAATTG 120
GCTCAAGTGT GTCTCTGACA CCAATTACCA AGAAAAAGGA TTAGGTGGGG TCCAAGGTGT 180
CAGGGCAGTG CCCATGTTGG GAGCTGAGGA AGGAGGCTGC TCAGATGCCA GCCCCGAGCC 240
AGCCTGGTCC TCTGAATGCA GGAGGCACTA GGAAAGGGAG TGATGGGCTG GCCATGCTCT 300
CTCAGCCCCC TGCAGGGGGT GAGCCTTCTA GAAAGGTAAG GGCATTGGAG GAAAGAGGGA 360
GGAAGGAAAG GAAGAAGTGC TTCTGGAAAA AGGAGACTTT CTCCAAGGAA TAGCACCCAC 420
TGCCCCACCT TTGTAGCCTC AGTTCAGTGG CCGCCTCCTG CCGGCCCACT GTGAACTCGC 480
TCCTGCCCTC TGAGATGCTC CAGCTGATGT CACCCAAGGC CACTTAGCAC TTAGTGGGCA 540
CGTCTGCCTA TGTTGGCCTC GATTTTCCTC TCCAACTAGT CAGCTCCCAA GGGAGAGACA 600
TGAATTCCTG TCTCCCCTGA GTGCCCAGCC CAGAGCCACA GCCACCACAG GGCAGGAGCC 660
AGCATTTGGG AGAGCCATGT TCTGCTGTGG TGACGTATCC ACCCCGGGGC GGGAATGAGC 720
AGGCCTCGCA GACTCGGGGC CTGGAGCTCA GGATTGGTGC CAAGATTTAC AGAGAAGGGC 780
CTGAGTTGAC GTGGCACGTA AGCTTCTGAG TCATCGGGCT TTCAGGGGAG GGTGCTACCT 840
CTCTGTCTGT GTCTGTCTGT CTGTCTTTCA GGCTCTCTGT CTCTCTCTGC GTCTCTCTCT 900
GTCATGTTCT CCCTCCCCAT CTCTCCATTG CTGACAAATA TTCTATTAGG CTATGAGCGA 960
GGAGACGGGC AGGGAGCCTC TCACAGGCAG GGCACTAGAG CCCATGTGGC CCATAGGCTC 1020
ATAAAGCCAT TGGCATGACC AGTAACCACC ATGTGAGGTC ACCAGGACAG CTGGGGAGGG 1080
ACCAGATGAC CTGAGCTCAG CCCACTCCAG CTGGGCAGGG CCAGAGCCAT GACCTGGAAG 1140
AGGCCACCTC TTCCCCTCTG CTGGTGGCAC CCATCCTCAG CATTGCTGGG GGCTCTGTGT 1200
CACAGCTGAC AGGGCCTTCA GGCTCCCCTG AGCCTACCCA GTGCATTTTC TAGAAGGATT 1260
TCTGAGACCC AGCGAGAGCA GGGCCAGGCC CAGGTCACCC AGTGGGTCAG GGGAGGAGCA 1320
GGCAGTGCTC CGTTCTCCCG ATGCCTTGGC CTCTGCCCCT ACCGCCTGAT GTGGGTGTCA 1380
CTGCAGCCGC AGGACCCTGA GCCTCGTGAG GTAGAGGAGG CATGAAGGGG TGAGCTGGAC 1440
AGAGCGGTCC CTCCTGTTTG GGATTTTCTG ATGGTTTCGA GGGGTAGGCA GCAGAGGTTC 1500
AGGGCCCCCT GACCTCCTCA TGTGCCCCTT TCTCCTGGTC CTCCACCTTC CGTCCTTCTC 1560
TGCATTCTCC GCCTGCCCCC GCAGGGGACC AGGCCCCCAT TCCAGGCCAG ACTTCCCTGC 1620
AGATTCTGTA TGGCTCATTT GGAAACTATT TCTGCTTCTA ATGAGTGTTT TCCTTTGTGC 1680
CCTTGTCCTC TAAAATGCTT AATGACTGCT TTCCGTGCTC GAGTGAAGCG GGGGTGTGTC 1740
CCCGCATGGC TGCCATTGCC AGGCCGGAGC TGTTTGGCTG CCAAGCCCGG CTTGCTTGGG 1800
TGGAGGCAGC GGGGGGTCCT TCCTGGCCCA CGCTGGCAGC ACAGACCAAG CCTGTGGGGG 1860
CAAGAGCACG GCTGCGGGGA GACGAGGACC CTGGGGCCTT AGGAGACCAC AGGACAGGGT 1920
GGCAGTGCAG GTCGGGGCTC CCACATCACT GGAACAGGCA GATCTTTGAG CCTGAGTTCT 1980
AGGAGTTGAG CTCCTTGGGG GACTCTGGAT TCAGAGTCTG AGGAGCTGGA TTCCAGCTCT 2040
GCCTGGACCT ACCTGAGCAC CAGGAGCGGT GACCATGCCA 2080
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