Variant report

Variant	rs9401081
Chromosome Location	chr6:118985502-118985503
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:118984312..118986553-chr6:119029407..119031346,2	K562	blood:

Variant related genes	Relation type
ENSG00000111860	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10457344	0.81[ASN][1000 genomes]
rs12530169	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1318050	0.83[ASN][1000 genomes]
rs13213527	0.80[ASN][1000 genomes]
rs17080423	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1808098	0.83[ASN][1000 genomes]
rs1891712	0.83[ASN][1000 genomes]
rs1936059	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2096265	0.81[ASN][1000 genomes]
rs2187945	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2356184	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2356502	0.80[ASN][1000 genomes]
rs3862828	0.80[ASN][1000 genomes]
rs4027728	0.80[ASN][1000 genomes]
rs422312	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4412243	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs482910	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs485416	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs492562	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4946351	0.80[ASN][1000 genomes]
rs516212	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs516463	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs541442	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6569023	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6569026	0.84[ASN][1000 genomes]
rs6909211	0.82[ASN][1000 genomes]
rs6923686	0.82[ASN][1000 genomes]
rs6928957	0.83[ASN][1000 genomes]
rs7749356	0.83[ASN][1000 genomes]
rs7754272	0.82[ASN][1000 genomes]
rs9285430	0.84[ASN][1000 genomes]
rs933257	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9372506	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9374735	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9374736	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9387586	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9387596	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9401073	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9481840	0.80[ASN][1000 genomes]
rs9489478	0.80[ASN][1000 genomes]
rs9489486	0.83[ASN][1000 genomes]
rs9489487	0.83[ASN][1000 genomes]
rs9689896	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532051	chr6:118551027-119044197	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1025456	chr6:118669672-119058789	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
5	nsv1027444	chr6:118687556-119121660	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv538428	chr6:118687556-119121660	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic 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	10 gene(s)	inside rSNPs	diseases
7	nsv949321	chr6:118692304-119137658	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active 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	10 gene(s)	inside rSNPs	diseases
8	nsv432958	chr6:118692307-119010307	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv1034448	chr6:118698169-119016383	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
10	nsv1025097	chr6:118699752-119058789	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
11	nsv532052	chr6:118711850-119057295	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
12	nsv432959	chr6:118716318-119010307	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
13	nsv604556	chr6:118722589-119065365	Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
14	nsv949416	chr6:118772508-119033063	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
15	nsv948980	chr6:118772508-119137658	Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription 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 miRNA target site	10 gene(s)	inside rSNPs	diseases
16	nsv604559	chr6:118786486-119113317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
17	nsv1022865	chr6:118786586-119058789	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic 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	8 gene(s)	inside rSNPs	diseases
18	nsv1020405	chr6:118786586-119241006	ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9401081	SSXP10	cis	Artery Tibial	GTEx

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118973400-118988800	Weak transcription	NH-A	brain
2	chr6:118973600-118989000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:118978200-118985600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:118978200-118989800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr6:118981400-118985600	Weak transcription	Small Intestine	intestine
6	chr6:118981600-118985600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr6:118981600-118985600	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr6:118981600-118985600	Weak transcription	Right Atrium	heart
9	chr6:118981600-118985600	Weak transcription	HSMMtube	muscle
10	chr6:118981600-118985800	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr6:118981600-118986200	Weak transcription	Pancreas	Pancrea
12	chr6:118981600-118988800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:118981600-118989600	Weak transcription	Left Ventricle	heart
14	chr6:118981800-118988000	Weak transcription	Fetal Lung	lung
15	chr6:118982000-118985600	Weak transcription	Fetal Muscle Leg	muscle
16	chr6:118982000-118985600	Weak transcription	Thymus	Thymus
17	chr6:118982000-118989000	Weak transcription	K562	blood
18	chr6:118983400-118985600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr6:118983400-118985600	Weak transcription	Dnd41	blood
20	chr6:118983600-118990200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr6:118984800-118985600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr6:118985000-118985600	Weak transcription	HMEC	breast
23	chr6:118985000-118986400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr6:118985200-118985600	Genic enhancers	Primary T cells from cord blood	blood
25	chr6:118985200-118985600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr6:118985200-118985800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:118985200-118985800	Enhancers	Psoas Muscle	Psoas
28	chr6:118985200-118986400	Genic enhancers	Fetal Thymus	thymus
29	chr6:118985200-118986400	Enhancers	Spleen	Spleen
30	chr6:118985200-118987000	Enhancers	Primary B cells from peripheral blood	blood
31	chr6:118985200-118987200	Enhancers	Stomach Mucosa	stomach
32	chr6:118985400-118985600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:118985400-118985600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
34	chr6:118985400-118985600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
35	chr6:118985400-118985600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr6:118985400-118985600	Active TSS	Muscle Satellite Cultured Cells	--
37	chr6:118985400-118985600	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr6:118985400-118985800	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
39	chr6:118985400-118985800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr6:118985400-118985800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr6:118985400-118985800	Flanking Active TSS	GM12878-XiMat	blood
42	chr6:118985400-118986000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr6:118985400-118986000	Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr6:118985400-118986000	Active TSS	HSMM	muscle
45	chr6:118985400-118986200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:118985400-118986200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr6:118985400-118986200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
48	chr6:118985400-118986200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr6:118985400-118986200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr6:118985400-118986200	Active TSS	Ovary	ovary

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