Variant report

Variant	rs617145
Chromosome Location	chr19:21448123-21448124
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10416988	0.83[EUR][1000 genomes]
rs10417249	0.84[EUR][1000 genomes]
rs10422057	0.84[EUR][1000 genomes]
rs12611085	0.84[EUR][1000 genomes]
rs12611135	0.84[EUR][1000 genomes]
rs12976375	0.81[EUR][1000 genomes]
rs1445847	0.84[EUR][1000 genomes]
rs1620157	0.85[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs1645791	0.81[EUR][1000 genomes]
rs1645804	0.84[EUR][1000 genomes]
rs1781860	0.81[EUR][1000 genomes]
rs1781861	0.81[EUR][1000 genomes]
rs1781862	0.81[EUR][1000 genomes]
rs1781879	0.82[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1781880	0.84[EUR][1000 genomes]
rs1937811	0.81[EUR][1000 genomes]
rs2021432	0.82[EUR][1000 genomes]
rs2042985	0.82[EUR][1000 genomes]
rs2081183	0.81[EUR][1000 genomes]
rs2081186	0.81[EUR][1000 genomes]
rs2081187	0.81[EUR][1000 genomes]
rs2081188	0.81[EUR][1000 genomes]
rs2113136	0.86[EUR][1000 genomes]
rs2259655	0.84[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs250003	0.88[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap]
rs29727	0.84[CEU][hapmap]
rs29730	0.84[CEU][hapmap]
rs388229	0.83[CHB][hapmap]
rs4121277	0.83[EUR][1000 genomes]
rs4305209	0.82[EUR][1000 genomes]
rs4411627	0.82[EUR][1000 genomes]
rs4468754	0.90[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs4482412	0.80[EUR][1000 genomes]
rs4485500	0.82[EUR][1000 genomes]
rs4493182	0.82[EUR][1000 genomes]
rs4560042	0.82[EUR][1000 genomes]
rs4606860	0.82[EUR][1000 genomes]
rs4609982	0.82[EUR][1000 genomes]
rs57740	0.86[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap]
rs584725	0.84[EUR][1000 genomes]
rs594638	0.85[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs625209	0.83[EUR][1000 genomes]
rs634249	0.84[EUR][1000 genomes]
rs634661	0.84[EUR][1000 genomes]
rs636752	0.84[EUR][1000 genomes]
rs637308	0.84[EUR][1000 genomes]
rs6511209	0.81[EUR][1000 genomes]
rs6511210	0.80[EUR][1000 genomes]
rs6511211	0.81[EUR][1000 genomes]
rs6511212	0.81[EUR][1000 genomes]
rs6511214	0.84[EUR][1000 genomes]
rs6511215	0.84[EUR][1000 genomes]
rs660551	0.82[EUR][1000 genomes]
rs661267	0.84[EUR][1000 genomes]
rs663416	0.84[EUR][1000 genomes]
rs665561	0.84[EUR][1000 genomes]
rs669038	0.84[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs673889	0.84[EUR][1000 genomes]
rs675130	0.84[EUR][1000 genomes]
rs689249	0.84[EUR][1000 genomes]
rs7245597	0.84[EUR][1000 genomes]
rs7246432	0.81[EUR][1000 genomes]
rs7247871	0.82[EUR][1000 genomes]
rs7247882	0.82[EUR][1000 genomes]
rs7248088	0.82[EUR][1000 genomes]
rs7250372	1.00[CEU][hapmap];0.94[CHB][hapmap];0.83[JPT][hapmap];0.84[EUR][1000 genomes]
rs7251075	0.84[EUR][1000 genomes]
rs7254835	0.81[EUR][1000 genomes]
rs7254957	0.81[EUR][1000 genomes]
rs7257208	0.81[EUR][1000 genomes]
rs7259520	0.84[CEU][hapmap]
rs7260451	0.81[EUR][1000 genomes]
rs72620580	0.83[ASN][1000 genomes]
rs72620581	0.81[ASN][1000 genomes]
rs8111169	0.81[EUR][1000 genomes]
rs9630897	0.84[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3385528	chr19:21030777-21495566	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	esv3414204	chr19:21301761-21839451	ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
5	nsv911414	chr19:21355473-21454672	Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv578950	chr19:21388995-21477431	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv911415	chr19:21388995-21487170	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv911416	chr19:21388995-21548211	Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv911417	chr19:21388995-21564001	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv911418	chr19:21390608-21454672	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv911419	chr19:21391844-21487170	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv978788	chr19:21403145-21458328	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region lncRNA	3 gene(s)	inside rSNPs	diseases
13	esv3325271	chr19:21445407-21792817	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs617145	ZNF708	cis	Muscle Skeletal	GTEx

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21447600-21448200	ZNF genes & repeats	Gastric	stomach
2	chr19:21447600-21448200	Genic enhancers	Ovary	ovary
3	chr19:21448000-21448200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links