Variant report

Variant	rs74074918
Chromosome Location	chr1:57784550-57784551
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs12404869	0.90[AFR][1000 genomes]
rs12411278	0.90[AFR][1000 genomes]
rs12725140	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12737167	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12737593	0.90[AFR][1000 genomes]
rs12741031	0.90[AFR][1000 genomes]
rs12743986	0.95[AFR][1000 genomes]
rs12756218	0.95[AFR][1000 genomes]
rs1557223	0.95[AFR][1000 genomes]
rs17422457	1.00[ASN][1000 genomes]
rs17457585	0.90[AFR][1000 genomes]
rs34339837	0.90[AFR][1000 genomes]
rs34349049	0.90[AFR][1000 genomes]
rs34374446	0.90[AFR][1000 genomes]
rs34458695	1.00[AFR][1000 genomes]
rs34475805	0.91[AFR][1000 genomes]
rs34553708	0.95[AFR][1000 genomes]
rs34591213	0.90[AFR][1000 genomes]
rs34707135	0.90[AFR][1000 genomes]
rs34725826	0.90[AFR][1000 genomes]
rs35120429	0.95[AFR][1000 genomes]
rs35321467	0.95[AFR][1000 genomes]
rs35335448	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35344722	0.90[AFR][1000 genomes]
rs35404211	0.90[AFR][1000 genomes]
rs35511416	0.90[AFR][1000 genomes]
rs3908772	0.90[AFR][1000 genomes]
rs56096668	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56156700	0.90[AFR][1000 genomes]
rs58075307	0.95[AFR][1000 genomes]
rs71642115	0.90[AFR][1000 genomes]
rs71642118	0.90[AFR][1000 genomes]
rs74074913	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs74074976	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs74074978	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461628	chr1:57463326-57816489	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv546305	chr1:57463326-57816489	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv871943	chr1:57784144-57855876	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57773200-57790200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr1:57776600-57790200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:57779800-57784800	Weak transcription	Fetal Intestine Large	intestine
4	chr1:57779800-57784800	Weak transcription	Fetal Intestine Small	intestine
5	chr1:57780400-57784600	Weak transcription	Brain Angular Gyrus	brain
6	chr1:57780400-57787000	Weak transcription	Fetal Brain Male	brain
7	chr1:57782000-57784600	Weak transcription	Fetal Brain Female	brain
8	chr1:57784000-57785000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr1:57784000-57785400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links