| Tag | Content |
|---|
EnhancerAtlas ID | HS146-10375 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr3:53117570-53118990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr3:53117603-53117618 | GCACCCCTGGGGTCC | - | 7.8 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 53117674 | 53117903 | | chr3 | 53118007 | 53118685 | | chr3 | 53118046 | 53118214 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I053083 | chr3 | 53117568 | 53118295 |
|
Enhancer Sequence | GATGGTGCAG ATGGAAGAAG TGCTGAACAC AGGGCACCCC TGGGGTCCTT CCACCCAGGG 60
CCCGGCGCTT GGCCCTGTGC TTGCAGATCT GCGGCAGGCA GAGCTGAGAG CAGGCAAAGA 120
CAAGTCACCA CTGTGCTTGG GCATCCTGCC CACCAGCCCC ACCGGGCAGC CAGAGCTCCA 180
CATGGTTTCC ATCATGGTTA CAAAATAAAC AAATGCAAGT CACTCTGTCC CTTCTGTGGC 240
CCCCCACAGC CCGACATCTG CACATCTGCG AGAACATTCT CTCGTCATTA GAGAGATGCC 300
ACTTGGGGAT CTCAGAAGCC ATGTGGGGAA GACAGAAACC TTCAGCTCTA GTTCAGGAAC 360
ATTAAACACA CCATGCTATC CCAGTTTGTT CATAAAATTC TTGTGTTAAT GTCCTAGGGG 420
AAACAAAAAG GATAGCTATT TTAGCAGCAT TCTCTAGTTT GGTTGGGATT CTGTGTGGAG 480
AAGAGCTCTG TTTTCCTTCT GGCTGCAATG TCTTGATTCT CTGGGTCTTT GTGGTTCTCC 540
CTGCATGGCC CTGCCGGGCT CTGGTGAGGG AAGATAAGAG TGTGCTCCAA GGCTGGCGAG 600
GCTGGGGTTT TCGTCTGCAC CTGGTGAAAG GACTGGCTCC TACATCACCA GCTTCCCTCT 660
GAATATTTTC AGAATTCTCC TGGGAACAGT GGTGGACAAC AAAAGCCTTC TGAAAGAGGT 720
CCTCTGGCAC CCCTTATGCC ATTCCCCTGG TGTTACCTTT TGTGATTTTC AAATGAAAGG 780
GCAAAGAAGT GAGGAGTAGA TGAGCCGGGA ACAAAACTGG CGCTGCCCGC AGACAGTCAT 840
GCTTTCATTT CAGGCTCCCC CTGCTCTCCC ACCCCACATG GCCACGTGGA AGCCGCACAC 900
TATTAGTTCC ACATAATTGG AAAGGGTGTC AGGATCTCCC AGACATTAAC CAGAAACATG 960
CTGCTCAGTT GTCACCTCCA ATGTGACTAA TGCAGCCGTG TCTTAATTAG TCACTGCTCA 1020
CTGACTGCGA TGACAGCTCC CGAGCCTGTT CCAAGGCCCC AACCTGTGAT GGGGCACTGC 1080
AGAGCAGATT AAAGGTGAGA GGCCGCTGGG AAGGAAGGAC CAGGAGTTGC CAGTTTTTCA 1140
GGTCTCTTTC CCACTGAGCA CTGTGAACCC AGGTGGCCTC TGCCAAACCC CTTTGTCAAC 1200
ATTGTGACAG TAGAGTCAAT AGGGTCATAA CATTGGGACA CATTTATTGG AGGGAGAGAA 1260
GAAATGTGAC AGGGAAATGG TCTAGAAGAT TCCTTCACAA GTCAGCTGTT ATGTCACGGG 1320
TCCCCATGCA GCTCCCTGGG GAAGGGGCGA TGAGGGATGA ACCGTGCCAC TCTGACTGGC 1380
CTACACCTAG CAAATGCTGC TCAGGCCAGG GTGGCCCATC 1420
|
