Variant report

Variant	rs1917881
Chromosome Location	chr1:73313762-73313763
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11210084	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11210085	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12025823	0.94[ASN][1000 genomes]
rs12129026	0.86[EUR][1000 genomes]
rs12129942	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12136682	0.80[EUR][1000 genomes]
rs1464952	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1525978	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1525979	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2841192	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2901713	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61774086	0.80[EUR][1000 genomes]
rs6656687	0.87[EUR][1000 genomes]
rs6689491	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7546928	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs940917	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv1013549	chr1:73209040-73408373	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1001105	chr1:73262558-73319499	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1014200	chr1:73310043-73345847	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73310800-73314000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr1:73311200-73313800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr1:73311600-73314200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr1:73311800-73313800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr1:73312400-73313800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr1:73312400-73313800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:73312800-73314400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr1:73313200-73313800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr1:73313400-73313800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr1:73313400-73314000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:73313600-73314000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:73313600-73317400	Weak transcription	H9 Cell Line	embryonic stem cell

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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

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