Variant report

Variant	rs17138233
Chromosome Location	chr7:17766429-17766430
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	chr7:17756594..17759569-chr7:17765843..17768676,2	K562	blood:

Extended variants
information (count: 84 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1003578	0.97[ASN][1000 genomes]
rs10241453	0.83[ASN][1000 genomes]
rs10241686	0.83[ASN][1000 genomes]
rs10256609	0.83[ASN][1000 genomes]
rs10256974	0.83[ASN][1000 genomes]
rs10257171	0.87[ASN][1000 genomes]
rs10264457	0.87[ASN][1000 genomes]
rs10488473	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs10488474	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs10950675	0.87[ASN][1000 genomes]
rs11762060	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11763522	0.81[ASN][1000 genomes]
rs11764183	0.87[ASN][1000 genomes]
rs11766639	0.81[ASN][1000 genomes]
rs11766640	0.81[ASN][1000 genomes]
rs11767183	0.85[ASN][1000 genomes]
rs11767212	0.85[ASN][1000 genomes]
rs11767614	0.87[ASN][1000 genomes]
rs11767702	0.87[ASN][1000 genomes]
rs11767707	0.87[ASN][1000 genomes]
rs11770723	0.83[ASN][1000 genomes]
rs11770758	0.83[ASN][1000 genomes]
rs11770975	0.87[ASN][1000 genomes]
rs11772381	0.87[ASN][1000 genomes]
rs12155308	0.87[ASN][1000 genomes]
rs12333540	0.82[ASN][1000 genomes]
rs12333542	0.82[ASN][1000 genomes]
rs12333670	0.83[ASN][1000 genomes]
rs12333818	0.82[ASN][1000 genomes]
rs13226195	0.93[ASN][1000 genomes]
rs13229595	0.91[ASN][1000 genomes]
rs13238802	0.83[CHB][hapmap];0.93[CHD][hapmap]
rs13239316	0.92[CHB][hapmap];0.81[ASN][1000 genomes]
rs13245576	0.97[ASN][1000 genomes]
rs2010992	0.80[ASN][1000 genomes]
rs2041589	0.83[ASN][1000 genomes]
rs2041590	0.83[ASN][1000 genomes]
rs2041591	0.83[ASN][1000 genomes]
rs2041592	0.87[ASN][1000 genomes]
rs2098223	0.83[ASN][1000 genomes]
rs2192066	0.87[ASN][1000 genomes]
rs2192067	0.94[ASN][1000 genomes]
rs2215683	0.90[ASN][1000 genomes]
rs2389836	0.83[ASN][1000 genomes]
rs2389837	0.83[ASN][1000 genomes]
rs2389838	0.87[ASN][1000 genomes]
rs2537566	0.94[ASN][1000 genomes]
rs2723579	0.94[ASN][1000 genomes]
rs2723586	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs34061308	0.94[ASN][1000 genomes]
rs34085905	0.87[ASN][1000 genomes]
rs34267616	0.94[ASN][1000 genomes]
rs34487278	0.82[ASN][1000 genomes]
rs34581548	0.87[ASN][1000 genomes]
rs34757903	0.94[ASN][1000 genomes]
rs34835564	0.94[ASN][1000 genomes]
rs34924739	0.87[ASN][1000 genomes]
rs35037338	0.81[ASN][1000 genomes]
rs35057721	0.94[ASN][1000 genomes]
rs35285005	0.97[ASN][1000 genomes]
rs35575660	0.94[ASN][1000 genomes]
rs35699364	0.83[ASN][1000 genomes]
rs3919527	0.87[ASN][1000 genomes]
rs3919528	0.83[ASN][1000 genomes]
rs4272251	0.83[ASN][1000 genomes]
rs5021389	0.87[ASN][1000 genomes]
rs5021390	0.84[ASN][1000 genomes]
rs62447458	0.94[ASN][1000 genomes]
rs6461346	0.83[ASN][1000 genomes]
rs6979914	0.83[ASN][1000 genomes]
rs71524220	0.83[ASN][1000 genomes]
rs7456348	0.87[ASN][1000 genomes]
rs7787725	0.97[ASN][1000 genomes]
rs7793320	0.83[ASN][1000 genomes]
rs9969319	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869352	chr7:17237983-17932878	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv1021524	chr7:17251148-17963307	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1021289	chr7:17254117-17873816	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv538754	chr7:17254117-17873816	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv534309	chr7:17254118-17932878	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv533938	chr7:17254118-18040301	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv887804	chr7:17571140-17885468	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv1024398	chr7:17630148-18545073	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
9	nsv538764	chr7:17630148-18545073	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs17138233	SOSTDC1	cis	parietal	SCAN
rs17138233	ABCB5	cis	parietal	SCAN
rs17138233	TWISTNB	cis	cerebellum	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17765800-17766600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:17765800-17770600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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