Variant report

Variant	rs4918412
Chromosome Location	chr10:96345964-96345965
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1018602	0.80[EUR][1000 genomes]
rs10786168	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10786169	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10786170	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10882469	0.83[EUR][1000 genomes]
rs10882471	0.83[EUR][1000 genomes]
rs10882473	0.83[EUR][1000 genomes]
rs10882474	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10882477	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10882481	0.83[EUR][1000 genomes]
rs10882486	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11187980	0.80[EUR][1000 genomes]
rs11187996	0.81[EUR][1000 genomes]
rs11188009	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11188016	0.80[EUR][1000 genomes]
rs11188017	0.82[EUR][1000 genomes]
rs11188019	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11188026	0.82[EUR][1000 genomes]
rs11188030	0.82[EUR][1000 genomes]
rs11188038	0.83[EUR][1000 genomes]
rs11188039	0.83[EUR][1000 genomes]
rs11188040	0.83[EUR][1000 genomes]
rs11188041	0.83[EUR][1000 genomes]
rs11592354	0.82[EUR][1000 genomes]
rs11638	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12218213	0.84[EUR][1000 genomes]
rs12218216	0.84[EUR][1000 genomes]
rs12219906	0.82[EUR][1000 genomes]
rs12220588	0.84[EUR][1000 genomes]
rs12572040	0.84[EUR][1000 genomes]
rs1326838	0.80[EUR][1000 genomes]
rs1326839	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1359262	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1359263	0.82[EUR][1000 genomes]
rs1854035	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2148553	0.83[EUR][1000 genomes]
rs2274096	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2274417	0.83[EUR][1000 genomes]
rs2281791	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2860821	0.81[EUR][1000 genomes]
rs34814196	0.82[EUR][1000 genomes]
rs3740358	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3758522	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3758523	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3781262	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4421688	0.81[EUR][1000 genomes]
rs4918401	0.81[EUR][1000 genomes]
rs4918402	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4918404	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4918409	0.84[EUR][1000 genomes]
rs4918411	0.84[EUR][1000 genomes]
rs4918417	0.83[EUR][1000 genomes]
rs4918418	0.83[EUR][1000 genomes]
rs4918419	0.83[EUR][1000 genomes]
rs6583943	0.80[EUR][1000 genomes]
rs6583944	0.82[EUR][1000 genomes]
rs6583945	0.82[EUR][1000 genomes]
rs6583946	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs68046102	0.83[EUR][1000 genomes]
rs701885	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7068337	0.84[EUR][1000 genomes]
rs7078236	0.80[EUR][1000 genomes]
rs7078811	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7079934	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7083898	0.80[EUR][1000 genomes]
rs7100415	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7906843	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7906968	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv1819509	chr10:96064300-96361776	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1053747	chr10:96211618-96366396	Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
4	nsv517681	chr10:96343228-96387079	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96306400-96357200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr10:96306400-96365600	Weak transcription	Esophagus	oesophagus
3	chr10:96306400-96370400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr10:96306400-96370600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr10:96306400-96371000	Weak transcription	Ovary	ovary
6	chr10:96306600-96349800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr10:96306600-96353800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr10:96306600-96379200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:96306800-96348000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr10:96306800-96348200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr10:96306800-96348400	Weak transcription	Primary B cells from cord blood	blood
12	chr10:96306800-96349800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr10:96306800-96357200	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr10:96306800-96373000	Weak transcription	Primary T cells from cord blood	blood
15	chr10:96307000-96358200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr10:96307000-96375000	Weak transcription	Osteobl	bone
17	chr10:96307200-96371200	Weak transcription	Fetal Brain Male	brain
18	chr10:96307600-96356000	Weak transcription	NHDF-Ad	bronchial
19	chr10:96307600-96373200	Weak transcription	Brain Germinal Matrix	brain
20	chr10:96307800-96348200	Weak transcription	NHEK	skin
21	chr10:96307800-96373000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr10:96308000-96373200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:96309400-96354000	Weak transcription	K562	blood
24	chr10:96309600-96372800	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr10:96309600-96377000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr10:96312200-96354000	Weak transcription	Gastric	stomach
27	chr10:96312800-96372200	Strong transcription	Dnd41	blood
28	chr10:96314200-96373400	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr10:96315000-96369200	Weak transcription	Fetal Kidney	kidney
30	chr10:96316000-96371400	Weak transcription	Fetal Brain Female	brain
31	chr10:96316000-96374000	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr10:96316200-96357600	Weak transcription	Duodenum Mucosa	Duodenum
33	chr10:96316200-96373000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr10:96317000-96372600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr10:96317400-96348000	Weak transcription	NH-A	brain
36	chr10:96321000-96353200	Weak transcription	Fetal Intestine Large	intestine
37	chr10:96324000-96356600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr10:96324000-96376600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:96324200-96353800	Weak transcription	Primary B cells from peripheral blood	blood
40	chr10:96324200-96365600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr10:96325800-96348200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr10:96325800-96376000	Weak transcription	NHLF	lung
43	chr10:96327000-96347400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr10:96327800-96348000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr10:96330200-96348000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr10:96330600-96347800	Weak transcription	HUVEC	blood vessel
47	chr10:96331000-96377400	Weak transcription	Placenta	Placenta
48	chr10:96331200-96361800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:96332400-96359200	Weak transcription	Left Ventricle	heart
50	chr10:96332600-96348000	Weak transcription	HMEC	breast

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