Variant report

Variant	rs902619
Chromosome Location	chr8:48251154-48251155
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10086987	0.81[EUR][1000 genomes]
rs10102598	0.81[EUR][1000 genomes]
rs1038797	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs10808752	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs10957074	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11774001	0.95[EUR][1000 genomes]
rs11775514	0.91[EUR][1000 genomes]
rs11775628	0.91[EUR][1000 genomes]
rs11779308	0.92[CEU][hapmap];0.93[TSI][hapmap];0.82[EUR][1000 genomes]
rs11779423	0.89[ASW][hapmap];0.92[CEU][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes]
rs11781727	1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[TSI][hapmap];0.94[EUR][1000 genomes]
rs11783141	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11784823	1.00[ASW][hapmap];0.82[CHB][hapmap];0.89[CHD][hapmap];0.94[JPT][hapmap];0.95[LWK][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap]
rs11785228	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12541086	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12543823	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12547513	0.94[EUR][1000 genomes]
rs12550067	0.81[EUR][1000 genomes]
rs12680669	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12682269	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs13259872	0.89[ASW][hapmap];0.92[CEU][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes]
rs13259913	0.95[EUR][1000 genomes]
rs16926260	1.00[YRI][hapmap]
rs2087656	1.00[CEU][hapmap];0.87[CHD][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes]
rs2130879	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2172121	1.00[CEU][hapmap];0.87[CHD][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs2362554	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34099416	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35045730	0.93[EUR][1000 genomes]
rs35235599	0.81[EUR][1000 genomes]
rs4242439	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs4388466	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.83[JPT][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.84[EUR][1000 genomes]
rs4495437	0.81[EUR][1000 genomes]
rs4498545	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4536257	0.89[CHD][hapmap];0.94[JPT][hapmap]
rs4872957	0.92[CEU][hapmap];0.91[TSI][hapmap];0.83[EUR][1000 genomes]
rs4873102	1.00[ASW][hapmap];1.00[CEU][hapmap];0.87[CHD][hapmap];0.91[LWK][hapmap];0.86[MKK][hapmap];0.95[TSI][hapmap];0.97[EUR][1000 genomes]
rs4873106	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4873292	0.83[ASN][1000 genomes]
rs4873293	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4873368	0.82[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap]
rs4873477	1.00[YRI][hapmap]
rs6472229	0.93[EUR][1000 genomes]
rs6981790	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6990123	0.96[EUR][1000 genomes]
rs6994218	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7002441	1.00[YRI][hapmap]
rs7012341	0.94[EUR][1000 genomes]
rs7819806	0.92[CEU][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes]
rs7826284	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7839134	0.93[EUR][1000 genomes]
rs876915	0.82[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028036	chr8:47531749-48256108	Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv1019289	chr8:47536056-48251883	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
3	nsv539591	chr8:47536056-48251883	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
4	nsv1015347	chr8:47698082-48318579	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	nsv539593	chr8:47698082-48318579	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
6	esv3693377	chr8:47824261-48582964	Genic enhancers Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	nsv491863	chr8:48053825-48586176	Strong transcription Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS 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	20 gene(s)	inside rSNPs	diseases
8	esv2758155	chr8:48188989-48321308	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv2759610	chr8:48188989-48321308	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	esv1817304	chr8:48205314-48321308	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs902619	KIAA0146	cis	parietal	SCAN
rs902619	MCM4	cis	cerebellum	SCAN

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48207400-48258000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr8:48209400-48266000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr8:48216200-48252400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:48223400-48252600	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr8:48228200-48251200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:48228200-48254400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr8:48228200-48256000	Weak transcription	Left Ventricle	heart
8	chr8:48228600-48265800	Weak transcription	K562	blood
9	chr8:48230000-48252400	Weak transcription	Lung	lung
10	chr8:48230400-48252200	Weak transcription	Fetal Stomach	stomach
11	chr8:48230400-48256200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr8:48230400-48267400	Weak transcription	Spleen	Spleen
13	chr8:48230600-48252800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:48236400-48252800	Weak transcription	Pancreas	Pancrea
15	chr8:48237600-48256000	Weak transcription	Esophagus	oesophagus
16	chr8:48238800-48274600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:48239000-48255200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:48239000-48265800	Weak transcription	Aorta	Aorta
19	chr8:48239600-48254200	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr8:48240600-48253400	Weak transcription	Placenta	Placenta
21	chr8:48244000-48251400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr8:48244200-48255800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:48244200-48255800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:48244200-48256000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr8:48244200-48256000	Weak transcription	Fetal Lung	lung
26	chr8:48244200-48256200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr8:48245800-48251200	Weak transcription	NHDF-Ad	bronchial
28	chr8:48245800-48254400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr8:48247800-48276400	Weak transcription	Colonic Mucosa	Colon
30	chr8:48248800-48309600	Weak transcription	Thymus	Thymus
31	chr8:48249200-48252200	Weak transcription	Primary T cells from cord blood	blood
32	chr8:48249200-48253000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:48249200-48253800	Weak transcription	Fetal Intestine Small	intestine
34	chr8:48249200-48254200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:48249200-48256000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:48249200-48256000	Weak transcription	NHEK	skin
37	chr8:48249200-48265600	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr8:48249200-48282000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr8:48249400-48254800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:48249600-48252400	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr8:48249600-48252800	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr8:48249600-48252800	Weak transcription	A549	lung
43	chr8:48249600-48255800	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr8:48249600-48256000	Weak transcription	Primary B cells from peripheral blood	blood
45	chr8:48249800-48252800	Weak transcription	Dnd41	blood
46	chr8:48249800-48254400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:48249800-48266000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr8:48249800-48267200	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr8:48249800-48277400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr8:48249800-48277800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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