Variant report

Variant	rs16958379
Chromosome Location	chr15:74133964-74133965
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:74127469..74129836-chr15:74131658..74134641,2	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10519015	0.99[ASN][1000 genomes]
rs10519016	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11636381	0.86[ASN][1000 genomes]
rs11636619	0.84[ASN][1000 genomes]
rs12592471	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16958297	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16958333	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16958334	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16958382	1.00[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1869177	1.00[AMR][1000 genomes]
rs35127778	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35809461	0.82[ASN][1000 genomes]
rs4996372	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57180956	0.92[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs58443873	1.00[AMR][1000 genomes]
rs58492359	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58594871	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs60302365	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs61319694	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61661320	1.00[AMR][1000 genomes]
rs74023570	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs746655	0.98[ASN][1000 genomes]
rs8023384	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8030364	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8030745	0.86[AFR][1000 genomes]
rs8031663	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs878322	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043335	chr15:74078689-74241186	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74131800-74136800	Weak transcription	Pancreas	Pancrea
2	chr15:74132200-74134000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr15:74132400-74134200	Weak transcription	Fetal Brain Female	brain
4	chr15:74132400-74146600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:74132800-74134000	Weak transcription	Fetal Brain Male	brain
6	chr15:74133800-74134200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:74133800-74134600	Enhancers	Right Atrium	heart

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