| Tag | Content |
|---|
EnhancerAtlas ID | HS176-00052 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:7530420-7532330 |
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 | TAATGATGCT GTGGCCAGGT TTAATTTCTC TGATGTTAAA TAGGAAAGAA GCCATGAGTT 60
ACTGGCTCAG ATGGAAATTG GCTCAAGTGT GTCTCTGACA CCAATTACCA AGAAAAAGGA 120
TTAGGTGGGG TCCAAGGTGT CAGGGCAGTG CCCATGTTGG GAGCTGAGGA AGGAGGCTGC 180
TCAGATGCCA GCCCCGAGCC AGCCTGGTCC TCTGAATGCA GGAGGCACTA GGAAAGGGAG 240
TGATGGGCTG GCCATGCTCT CTCAGCCCCC TGCAGGGGGT GAGCCTTCTA GAAAGGTAAG 300
GGCATTGGAG GAAAGAGGGA GGAAGGAAAG GAAGAAGTGC TTCTGGAAAA AGGAGACTTT 360
CTCCAAGGAA TAGCACCCAC TGCCCCACCT TTGTAGCCTC AGTTCAGTGG CCGCCTCCTG 420
CCGGCCCACT GTGAACTCGC TCCTGCCCTC TGAGATGCTC CAGCTGATGT CACCCAAGGC 480
CACTTAGCAC TTAGTGGGCA CGTCTGCCTA TGTTGGCCTC GATTTTCCTC TCCAACTAGT 540
CAGCTCCCAA GGGAGAGACA TGAATTCCTG TCTCCCCTGA GTGCCCAGCC CAGAGCCACA 600
GCCACCACAG GGCAGGAGCC AGCATTTGGG AGAGCCATGT TCTGCTGTGG TGACGTATCC 660
ACCCCGGGGC GGGAATGAGC AGGCCTCGCA GACTCGGGGC CTGGAGCTCA GGATTGGTGC 720
CAAGATTTAC AGAGAAGGGC CTGAGTTGAC GTGGCACGTA AGCTTCTGAG TCATCGGGCT 780
TTCAGGGGAG GGTGCTACCT CTCTGTCTGT GTCTGTCTGT CTGTCTTTCA GGCTCTCTGT 840
CTCTCTCTGC GTCTCTCTCT GTCATGTTCT CCCTCCCCAT CTCTCCATTG CTGACAAATA 900
TTCTATTAGG CTATGAGCGA GGAGACGGGC AGGGAGCCTC TCACAGGCAG GGCACTAGAG 960
CCCATGTGGC CCATAGGCTC ATAAAGCCAT TGGCATGACC AGTAACCACC ATGTGAGGTC 1020
ACCAGGACAG CTGGGGAGGG ACCAGATGAC CTGAGCTCAG CCCACTCCAG CTGGGCAGGG 1080
CCAGAGCCAT GACCTGGAAG AGGCCACCTC TTCCCCTCTG CTGGTGGCAC CCATCCTCAG 1140
CATTGCTGGG GGCTCTGTGT CACAGCTGAC AGGGCCTTCA GGCTCCCCTG AGCCTACCCA 1200
GTGCATTTTC TAGAAGGATT TCTGAGACCC AGCGAGAGCA GGGCCAGGCC CAGGTCACCC 1260
AGTGGGTCAG GGGAGGAGCA GGCAGTGCTC CGTTCTCCCG ATGCCTTGGC CTCTGCCCCT 1320
ACCGCCTGAT GTGGGTGTCA CTGCAGCCGC AGGACCCTGA GCCTCGTGAG GTAGAGGAGG 1380
CATGAAGGGG TGAGCTGGAC AGAGCGGTCC CTCCTGTTTG GGATTTTCTG ATGGTTTCGA 1440
GGGGTAGGCA GCAGAGGTTC AGGGCCCCCT GACCTCCTCA TGTGCCCCTT TCTCCTGGTC 1500
CTCCACCTTC CGTCCTTCTC TGCATTCTCC GCCTGCCCCC GCAGGGGACC AGGCCCCCAT 1560
TCCAGGCCAG ACTTCCCTGC AGATTCTGTA TGGCTCATTT GGAAACTATT TCTGCTTCTA 1620
ATGAGTGTTT TCCTTTGTGC CCTTGTCCTC TAAAATGCTT AATGACTGCT TTCCGTGCTC 1680
GAGTGAAGCG GGGGTGTGTC CCCGCATGGC TGCCATTGCC AGGCCGGAGC TGTTTGGCTG 1740
CCAAGCCCGG CTTGCTTGGG TGGAGGCAGC GGGGGGTCCT TCCTGGCCCA CGCTGGCAGC 1800
ACAGACCAAG CCTGTGGGGG CAAGAGCACG GCTGCGGGGA GACGAGGACC CTGGGGCCTT 1860
AGGAGACCAC AGGACAGGGT GGCAGTGCAG GTCGGGGCTC CCACATCACT 1910
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