Variant report

Variant	rs10115576
Chromosome Location	chr9:115617822-115617823
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:115616161..115618077-chr9:115630043..115631979,2	MCF-7	breast:
2	chr9:115615772..115618098-chr9:115620406..115622597,2	K562	blood:
3	chr9:115616179..115618234-chr9:115622844..115625535,2	K562	blood:

Extended variants
information (count: 97 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10115711	0.82[CEU][hapmap]
rs10124260	0.85[CEU][hapmap]
rs10124939	0.82[CEU][hapmap]
rs10124979	0.82[CEU][hapmap]
rs1041086	0.86[EUR][1000 genomes]
rs10481638	0.81[GIH][hapmap];0.83[LWK][hapmap];0.89[MKK][hapmap]
rs10732374	0.81[GIH][hapmap]
rs10733594	0.85[CEU][hapmap]
rs10733595	0.81[GIH][hapmap]
rs10733596	0.81[GIH][hapmap];0.83[LWK][hapmap]
rs10733597	0.81[LWK][hapmap]
rs10733598	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs10733599	1.00[CEU][hapmap]
rs10739370	0.82[CEU][hapmap]
rs10739371	0.81[GIH][hapmap]
rs10739373	0.85[CEU][hapmap];0.88[GIH][hapmap];0.87[TSI][hapmap]
rs10739376	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs10739378	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs10739379	0.80[EUR][1000 genomes]
rs10759590	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs10759596	0.81[GIH][hapmap];0.83[LWK][hapmap]
rs10759598	0.81[GIH][hapmap];0.83[LWK][hapmap]
rs10759601	0.80[AFR][1000 genomes]
rs10759603	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs10759604	0.80[EUR][1000 genomes]
rs10817381	1.00[CHB][hapmap]
rs10817398	0.81[GIH][hapmap]
rs10981529	0.98[ASN][1000 genomes]
rs11794827	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12684608	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs12685108	1.00[CHB][hapmap]
rs12686253	0.90[ASN][1000 genomes]
rs1324931	1.00[CEU][hapmap];0.88[GIH][hapmap];0.82[TSI][hapmap];0.81[EUR][1000 genomes]
rs1361720	0.85[CEU][hapmap]
rs1418409	0.85[CEU][hapmap]
rs1418410	0.88[TSI][hapmap]
rs1475293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.88[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1539338	0.85[CEU][hapmap]
rs1539341	0.81[LWK][hapmap]
rs1539342	0.81[GIH][hapmap];0.83[LWK][hapmap]
rs16917411	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1711744	0.88[TSI][hapmap]
rs1711747	0.82[TSI][hapmap]
rs1891402	0.85[CEU][hapmap]
rs1891403	0.85[CEU][hapmap];1.00[GIH][hapmap];0.94[TSI][hapmap]
rs1970528	0.83[LWK][hapmap]
rs2025544	1.00[CEU][hapmap];0.88[GIH][hapmap]
rs2153837	0.82[TSI][hapmap]
rs2645993	0.85[CEU][hapmap]
rs2645994	0.82[TSI][hapmap]
rs2796028	0.85[CEU][hapmap]
rs4246892	0.85[CEU][hapmap]
rs4304397	0.85[CEU][hapmap];0.88[GIH][hapmap];0.82[TSI][hapmap]
rs4978507	0.85[CEU][hapmap]
rs4978511	0.82[CEU][hapmap]
rs4979153	0.85[CEU][hapmap]
rs4979154	0.85[CEU][hapmap]
rs4979157	0.85[CEU][hapmap]
rs4979163	0.81[GIH][hapmap]
rs4979165	0.85[CEU][hapmap]
rs4979170	1.00[CEU][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.86[EUR][1000 genomes]
rs4979173	0.86[EUR][1000 genomes]
rs4979176	0.80[EUR][1000 genomes]
rs6477959	0.85[CEU][hapmap]
rs700122	0.85[CEU][hapmap]
rs7030795	0.85[CEU][hapmap]
rs7047914	0.84[EUR][1000 genomes]
rs7856199	0.81[GIH][hapmap]
rs7859175	0.85[CEU][hapmap]
rs7868830	0.85[CEU][hapmap]
rs786961	0.82[TSI][hapmap]
rs786968	0.82[TSI][hapmap]
rs786977	0.82[TSI][hapmap]
rs786978	0.88[TSI][hapmap]
rs787271	0.85[CEU][hapmap];1.00[GIH][hapmap];0.94[TSI][hapmap]
rs787274	1.00[GIH][hapmap];0.81[TSI][hapmap]
rs787276	0.85[CEU][hapmap]
rs787280	0.85[CEU][hapmap];1.00[GIH][hapmap];0.94[TSI][hapmap]
rs787284	0.85[CEU][hapmap]
rs787287	0.85[CEU][hapmap]
rs787294	0.85[CEU][hapmap]
rs787295	0.85[CEU][hapmap];1.00[GIH][hapmap];0.94[TSI][hapmap]
rs787297	0.85[CEU][hapmap];1.00[GIH][hapmap];0.94[TSI][hapmap]
rs787298	0.85[CEU][hapmap]
rs787299	0.85[CEU][hapmap];0.88[GIH][hapmap];0.87[TSI][hapmap]
rs787301	0.85[CEU][hapmap];1.00[GIH][hapmap];0.94[TSI][hapmap]
rs787302	0.85[CEU][hapmap]
rs7873289	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs813101	0.85[CEU][hapmap]
rs885387	0.85[CEU][hapmap]
rs9409123	0.85[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758198	chr9:115240454-116002951	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759710	chr9:115240454-116002951	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv893733	chr9:115397206-115712068	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	esv2422302	chr9:115550339-115656433	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	esv2757351	chr9:115600623-115632898	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1047000	chr9:115610445-115884038	ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	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
rs10115576	TXNDC8	cis	parietal	SCAN

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115577600-115630400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr9:115582400-115630000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr9:115591400-115623200	Weak transcription	Fetal Heart	heart
4	chr9:115594200-115620400	Weak transcription	Thymus	Thymus
5	chr9:115594200-115634400	Weak transcription	NH-A	brain
6	chr9:115594400-115626800	Weak transcription	Colon Smooth Muscle	Colon
7	chr9:115599000-115623200	Weak transcription	Right Ventricle	heart
8	chr9:115599400-115623600	Weak transcription	Right Atrium	heart
9	chr9:115599400-115625200	Weak transcription	Colonic Mucosa	Colon
10	chr9:115601200-115641200	Weak transcription	Fetal Brain Male	brain
11	chr9:115601600-115620600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:115602000-115620600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:115602600-115626600	Weak transcription	Brain Germinal Matrix	brain
14	chr9:115602600-115626800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr9:115604000-115626600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr9:115604200-115621200	Weak transcription	HepG2	liver
17	chr9:115607400-115643400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr9:115607600-115620800	Strong transcription	Fetal Intestine Small	intestine
19	chr9:115607600-115630200	Weak transcription	NHEK	skin
20	chr9:115609400-115623200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr9:115611400-115628600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr9:115611400-115634600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr9:115611600-115619000	Weak transcription	Fetal Lung	lung
24	chr9:115611600-115626800	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr9:115611600-115630200	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr9:115611600-115634200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr9:115611800-115630200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr9:115612000-115620600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr9:115612000-115634600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr9:115612200-115620400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr9:115613400-115623800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr9:115613600-115625400	Weak transcription	Aorta	Aorta
33	chr9:115613600-115628200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr9:115613600-115642600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr9:115613800-115623400	Weak transcription	Left Ventricle	heart
36	chr9:115613800-115626600	Weak transcription	Ovary	ovary
37	chr9:115614000-115620600	Weak transcription	Primary hematopoietic stem cells	blood
38	chr9:115614000-115626800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr9:115614000-115632600	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr9:115614200-115620400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr9:115614200-115630200	Weak transcription	Fetal Brain Female	brain
42	chr9:115614800-115619800	Enhancers	Fetal Muscle Leg	muscle
43	chr9:115615000-115622800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr9:115615200-115623800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr9:115615200-115630200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:115615400-115618000	Enhancers	HSMM	muscle
47	chr9:115615600-115620200	Weak transcription	Primary B cells from cord blood	blood
48	chr9:115615600-115623600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr9:115615600-115626400	Weak transcription	Brain Anterior Caudate	brain
50	chr9:115615600-115626400	Weak transcription	Rectal Mucosa Donor 31	rectum

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