| Tag | Content |
|---|
EnhancerAtlas ID | HS185-00022 |
Organism | Homo sapiens |
Tissue/cell | T98G |
Coordinate | chr1:7530800-7532330 |
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 |
|
| | 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 | TGCCCCACCT TTGTAGCCTC AGTTCAGTGG CCGCCTCCTG CCGGCCCACT GTGAACTCGC 60
TCCTGCCCTC TGAGATGCTC CAGCTGATGT CACCCAAGGC CACTTAGCAC TTAGTGGGCA 120
CGTCTGCCTA TGTTGGCCTC GATTTTCCTC TCCAACTAGT CAGCTCCCAA GGGAGAGACA 180
TGAATTCCTG TCTCCCCTGA GTGCCCAGCC CAGAGCCACA GCCACCACAG GGCAGGAGCC 240
AGCATTTGGG AGAGCCATGT TCTGCTGTGG TGACGTATCC ACCCCGGGGC GGGAATGAGC 300
AGGCCTCGCA GACTCGGGGC CTGGAGCTCA GGATTGGTGC CAAGATTTAC AGAGAAGGGC 360
CTGAGTTGAC GTGGCACGTA AGCTTCTGAG TCATCGGGCT TTCAGGGGAG GGTGCTACCT 420
CTCTGTCTGT GTCTGTCTGT CTGTCTTTCA GGCTCTCTGT CTCTCTCTGC GTCTCTCTCT 480
GTCATGTTCT CCCTCCCCAT CTCTCCATTG CTGACAAATA TTCTATTAGG CTATGAGCGA 540
GGAGACGGGC AGGGAGCCTC TCACAGGCAG GGCACTAGAG CCCATGTGGC CCATAGGCTC 600
ATAAAGCCAT TGGCATGACC AGTAACCACC ATGTGAGGTC ACCAGGACAG CTGGGGAGGG 660
ACCAGATGAC CTGAGCTCAG CCCACTCCAG CTGGGCAGGG CCAGAGCCAT GACCTGGAAG 720
AGGCCACCTC TTCCCCTCTG CTGGTGGCAC CCATCCTCAG CATTGCTGGG GGCTCTGTGT 780
CACAGCTGAC AGGGCCTTCA GGCTCCCCTG AGCCTACCCA GTGCATTTTC TAGAAGGATT 840
TCTGAGACCC AGCGAGAGCA GGGCCAGGCC CAGGTCACCC AGTGGGTCAG GGGAGGAGCA 900
GGCAGTGCTC CGTTCTCCCG ATGCCTTGGC CTCTGCCCCT ACCGCCTGAT GTGGGTGTCA 960
CTGCAGCCGC AGGACCCTGA GCCTCGTGAG GTAGAGGAGG CATGAAGGGG TGAGCTGGAC 1020
AGAGCGGTCC CTCCTGTTTG GGATTTTCTG ATGGTTTCGA GGGGTAGGCA GCAGAGGTTC 1080
AGGGCCCCCT GACCTCCTCA TGTGCCCCTT TCTCCTGGTC CTCCACCTTC CGTCCTTCTC 1140
TGCATTCTCC GCCTGCCCCC GCAGGGGACC AGGCCCCCAT TCCAGGCCAG ACTTCCCTGC 1200
AGATTCTGTA TGGCTCATTT GGAAACTATT TCTGCTTCTA ATGAGTGTTT TCCTTTGTGC 1260
CCTTGTCCTC TAAAATGCTT AATGACTGCT TTCCGTGCTC GAGTGAAGCG GGGGTGTGTC 1320
CCCGCATGGC TGCCATTGCC AGGCCGGAGC TGTTTGGCTG CCAAGCCCGG CTTGCTTGGG 1380
TGGAGGCAGC GGGGGGTCCT TCCTGGCCCA CGCTGGCAGC ACAGACCAAG CCTGTGGGGG 1440
CAAGAGCACG GCTGCGGGGA GACGAGGACC CTGGGGCCTT AGGAGACCAC AGGACAGGGT 1500
GGCAGTGCAG GTCGGGGCTC CCACATCACT 1530
|
