Variant report

Variant	rs7843326
Chromosome Location	chr8:120873342-120873343
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:120867595..120870469-chr8:120870937..120874357,4	K562	blood:
2	chr8:120867595..120870172-chr8:120870937..120873708,3	K562	blood:
3	chr8:120867099..120869701-chr8:120870607..120873491,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136982	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10094587	1.00[YRI][hapmap]
rs10103058	1.00[YRI][hapmap]
rs10107579	1.00[YRI][hapmap]
rs10110216	0.84[AFR][1000 genomes]
rs10110223	0.84[AFR][1000 genomes]
rs10216503	1.00[YRI][hapmap]
rs10955941	1.00[YRI][hapmap]
rs11781657	0.88[ASW][hapmap];0.92[LWK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs12681402	1.00[YRI][hapmap]
rs12681623	0.88[ASW][hapmap];0.97[LWK][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap]
rs13257316	1.00[YRI][hapmap]
rs13260088	0.80[AFR][1000 genomes]
rs13260933	0.88[ASW][hapmap];0.97[LWK][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap]
rs13263296	0.81[AFR][1000 genomes]
rs13279398	1.00[YRI][hapmap]
rs13282901	0.90[YRI][hapmap]
rs1467044	0.95[LWK][hapmap];0.87[MKK][hapmap];0.81[YRI][hapmap]
rs17217893	0.82[CHD][hapmap];1.00[JPT][hapmap]
rs2037346	0.88[ASW][hapmap];0.90[LWK][hapmap];0.95[YRI][hapmap]
rs4073560	1.00[YRI][hapmap]
rs4871013	1.00[YRI][hapmap]
rs4871569	1.00[JPT][hapmap]
rs4871744	0.82[ASW][hapmap]
rs4871772	1.00[YRI][hapmap]
rs4871773	1.00[YRI][hapmap]
rs6469855	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6469861	1.00[YRI][hapmap]
rs6469863	1.00[YRI][hapmap]
rs6469867	1.00[YRI][hapmap]
rs6469868	1.00[YRI][hapmap]
rs6469871	1.00[YRI][hapmap]
rs6469872	1.00[YRI][hapmap]
rs6469878	1.00[YRI][hapmap]
rs6987580	0.88[ASW][hapmap];0.92[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap]
rs6988011	1.00[YRI][hapmap]
rs6995139	1.00[YRI][hapmap]
rs7002839	1.00[YRI][hapmap]
rs7003126	0.81[AFR][1000 genomes]
rs7015470	1.00[YRI][hapmap]
rs7387264	1.00[YRI][hapmap]
rs7387694	0.88[ASW][hapmap];0.97[LWK][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs7388508	1.00[YRI][hapmap]
rs7462250	1.00[YRI][hapmap]
rs7462302	0.88[ASW][hapmap];0.97[LWK][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap]
rs7465181	1.00[YRI][hapmap]
rs7814294	1.00[YRI][hapmap]
rs7824545	1.00[YRI][hapmap]
rs939241	1.00[YRI][hapmap]
rs9987332	0.88[ASW][hapmap];0.92[LWK][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534028	chr8:120348940-120906079	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv949368	chr8:120568034-121019872	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1021071	chr8:120589963-120968317	Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
5	nsv465789	chr8:120636850-120994394	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv612111	chr8:120636850-120994394	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv427826	chr8:120642181-120953395	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs7843326	DSCC1	cis	parietal	SCAN
rs7843326	TAF2	cis	cerebellum	SCAN
rs7843326	DSCC1	cis	cerebellum	SCAN
rs7843326	DSCC1	cis	Artery Tibial	GTEx
rs7843326	ENPP2	cis	cerebellum	SCAN
rs7843326	DEPDC6	cis	cerebellum	SCAN
rs7843326	DSCC1	cis	Esophagus Muscularis	GTEx

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120868800-120879200	Weak transcription	Stomach Mucosa	stomach
2	chr8:120868800-120885600	Weak transcription	Left Ventricle	heart
3	chr8:120869200-120875200	Weak transcription	A549	lung
4	chr8:120869600-120875400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr8:120869600-120885400	Weak transcription	Fetal Lung	lung
6	chr8:120870000-120875200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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