Variant report

Variant	rs7181238
Chromosome Location	chr15:43062820-43062821
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10467975	0.93[ASW][hapmap];0.86[MEX][hapmap];1.00[MKK][hapmap];0.85[YRI][hapmap]
rs11070377	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11070378	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs11070380	0.94[CHB][hapmap]
rs11070382	0.93[ASW][hapmap];0.84[CHD][hapmap];0.81[YRI][hapmap]
rs11632809	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11853250	0.86[ASW][hapmap];0.86[MEX][hapmap];0.97[MKK][hapmap]
rs11854550	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12323990	0.84[LWK][hapmap];0.84[YRI][hapmap]
rs12591415	0.93[ASW][hapmap];0.92[LWK][hapmap];0.95[YRI][hapmap];0.81[AFR][1000 genomes]
rs12592573	1.00[ASW][hapmap];0.97[LWK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs12594325	0.86[AFR][1000 genomes]
rs12594600	0.93[ASW][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs12594696	0.93[ASW][hapmap];0.97[LWK][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs12594699	0.84[AFR][1000 genomes]
rs12594725	0.83[AFR][1000 genomes]
rs12594765	1.00[ASW][hapmap];0.94[LWK][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs16957031	0.85[YRI][hapmap]
rs16957037	0.84[LWK][hapmap];0.84[YRI][hapmap]
rs16957055	0.86[ASW][hapmap];0.83[LWK][hapmap];0.90[YRI][hapmap]
rs16957061	0.86[ASW][hapmap];0.81[LWK][hapmap];0.83[YRI][hapmap]
rs16957063	0.86[ASW][hapmap];0.86[LWK][hapmap];0.90[YRI][hapmap]
rs16957120	0.95[YRI][hapmap];0.85[AFR][1000 genomes]
rs16957165	0.87[ASW][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];0.86[MEX][hapmap];0.94[MKK][hapmap];0.90[YRI][hapmap];0.84[ASN][1000 genomes]
rs16957167	0.81[MEX][hapmap]
rs16957244	0.92[ASW][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.81[YRI][hapmap]
rs2139655	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs2682073	1.00[ASW][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.87[LWK][hapmap];0.86[YRI][hapmap]
rs28437884	0.88[AFR][1000 genomes]
rs28542286	0.83[AFR][1000 genomes]
rs28661826	0.84[AFR][1000 genomes]
rs28722903	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34302400	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35554267	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3742992	0.90[YRI][hapmap]
rs3742995	0.86[ASW][hapmap];0.86[LWK][hapmap];0.90[YRI][hapmap]
rs4334272	0.93[ASW][hapmap];0.94[LWK][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes]
rs4924696	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs55927779	0.81[ASN][1000 genomes]
rs56046122	0.84[AFR][1000 genomes]
rs58548142	0.88[AFR][1000 genomes]
rs60723187	0.81[AFR][1000 genomes]
rs6493065	0.86[ASW][hapmap];1.00[CEU][hapmap];0.92[JPT][hapmap];0.89[LWK][hapmap];0.86[MEX][hapmap];1.00[MKK][hapmap];0.95[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7169231	0.82[AFR][1000 genomes]
rs7174028	0.93[ASW][hapmap];0.84[CHD][hapmap]
rs7178567	0.86[ASW][hapmap];0.82[CHB][hapmap]
rs73410923	0.81[AFR][1000 genomes]
rs73410927	0.83[AFR][1000 genomes]
rs73410937	0.85[AFR][1000 genomes]
rs73410940	0.83[AFR][1000 genomes]
rs73410959	0.82[AFR][1000 genomes]
rs73410961	0.85[AFR][1000 genomes]
rs73410969	0.83[AFR][1000 genomes]
rs73410971	0.87[AFR][1000 genomes]
rs73410972	0.87[AFR][1000 genomes]
rs73410973	0.87[AFR][1000 genomes]
rs8024266	1.00[CEU][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8028167	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8028365	0.81[AFR][1000 genomes]
rs8028699	0.90[YRI][hapmap];0.81[AFR][1000 genomes]
rs8030696	0.83[EUR][1000 genomes]
rs8031767	0.93[ASW][hapmap];0.81[YRI][hapmap]
rs8033336	1.00[ASW][hapmap];0.97[LWK][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs8042738	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8042980	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9920092	0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9920562	0.93[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9920624	0.81[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.90[LWK][hapmap];0.94[MKK][hapmap];0.81[TSI][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9920935	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.89[LWK][hapmap];0.86[MEX][hapmap];1.00[MKK][hapmap];0.86[TSI][hapmap];0.90[YRI][hapmap];0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]

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	nsv528725	chr15:42755555-43104406	Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv427959	chr15:42931181-43207353	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats 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	10 gene(s)	inside rSNPs	diseases
3	nsv977054	chr15:43015821-43171355	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1050128	chr15:43056145-43262736	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv542368	chr15:43056145-43262736	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats 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	7 gene(s)	inside rSNPs	diseases
6	nsv525461	chr15:43062548-43482127	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7181238	EIF3J	cis	parietal	SCAN
rs7181238	CCNDBP1	cis	multi-tissue	Pritchard

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43029800-43071000	Weak transcription	Pancreas	Pancrea
2	chr15:43030000-43066200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr15:43030000-43067200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr15:43030000-43093600	Weak transcription	Colonic Mucosa	Colon
5	chr15:43038400-43067400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr15:43044800-43066400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr15:43045000-43065600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr15:43045400-43068000	Weak transcription	Fetal Heart	heart
9	chr15:43045600-43074400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr15:43045800-43064800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr15:43051800-43064000	Weak transcription	Left Ventricle	heart
12	chr15:43051800-43064400	Weak transcription	Fetal Stomach	stomach
13	chr15:43051800-43065200	Weak transcription	Placenta	Placenta
14	chr15:43051800-43066200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr15:43051800-43069400	Weak transcription	Gastric	stomach
16	chr15:43051800-43070600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:43051800-43074600	Weak transcription	Right Ventricle	heart
18	chr15:43051800-43075000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr15:43051800-43083800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr15:43052000-43063800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr15:43052000-43065800	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr15:43052000-43065800	Weak transcription	Thymus	Thymus
23	chr15:43052000-43066000	Weak transcription	Spleen	Spleen
24	chr15:43052000-43066600	Weak transcription	Ovary	ovary
25	chr15:43052000-43074600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr15:43053600-43112200	Weak transcription	Rectal Smooth Muscle	rectum
27	chr15:43053800-43066400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr15:43054000-43064400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr15:43054000-43066000	Weak transcription	Brain Angular Gyrus	brain
30	chr15:43054000-43066200	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr15:43054000-43066400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr15:43054000-43074600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr15:43054000-43080200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr15:43054400-43064000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr15:43054600-43064200	Weak transcription	Liver	Liver
36	chr15:43054600-43067200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr15:43054600-43068600	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr15:43054800-43063600	Weak transcription	Primary B cells from cord blood	blood
39	chr15:43054800-43064000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr15:43054800-43064000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr15:43054800-43064000	Weak transcription	Dnd41	blood
42	chr15:43054800-43064600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr15:43054800-43066400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr15:43054800-43067200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr15:43054800-43146000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr15:43055000-43064000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr15:43055000-43064000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr15:43055000-43064200	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr15:43055200-43063600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr15:43055200-43066600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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