Variant report

Variant	rs6917261
Chromosome Location	chr6:144665357-144665358
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 143 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:139)

rs_ID	r²[population]
rs12660406	1.00[EUR][1000 genomes]
rs12660513	1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs12660531	1.00[EUR][1000 genomes]
rs12660596	1.00[EUR][1000 genomes]
rs12661781	1.00[EUR][1000 genomes]
rs12661969	0.92[CHB][hapmap];0.91[CHD][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12662267	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12662696	1.00[EUR][1000 genomes]
rs12662724	1.00[EUR][1000 genomes]
rs12662786	1.00[EUR][1000 genomes]
rs12662872	1.00[EUR][1000 genomes]
rs12662904	1.00[EUR][1000 genomes]
rs12663172	1.00[EUR][1000 genomes]
rs12663380	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12663605	1.00[EUR][1000 genomes]
rs12663851	1.00[EUR][1000 genomes]
rs12664200	1.00[EUR][1000 genomes]
rs12664245	1.00[EUR][1000 genomes]
rs12664298	1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs12664304	1.00[EUR][1000 genomes]
rs12665589	1.00[EUR][1000 genomes]
rs12665850	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17073442	1.00[EUR][1000 genomes]
rs17073463	1.00[EUR][1000 genomes]
rs17073482	1.00[EUR][1000 genomes]
rs17073498	1.00[EUR][1000 genomes]
rs17073506	1.00[EUR][1000 genomes]
rs17073524	1.00[EUR][1000 genomes]
rs17073528	1.00[EUR][1000 genomes]
rs17073529	1.00[EUR][1000 genomes]
rs17073544	1.00[EUR][1000 genomes]
rs17073571	1.00[EUR][1000 genomes]
rs17073580	1.00[EUR][1000 genomes]
rs17073598	1.00[EUR][1000 genomes]
rs17073602	1.00[EUR][1000 genomes]
rs17073610	1.00[EUR][1000 genomes]
rs17073623	1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs17073629	1.00[EUR][1000 genomes]
rs17073631	1.00[EUR][1000 genomes]
rs17073672	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17073678	1.00[EUR][1000 genomes]
rs17840301	1.00[EUR][1000 genomes]
rs1998367	1.00[EUR][1000 genomes]
rs34140249	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34502493	1.00[EUR][1000 genomes]
rs35325795	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35681372	1.00[EUR][1000 genomes]
rs36007040	1.00[EUR][1000 genomes]
rs3811097	1.00[EUR][1000 genomes]
rs4301321	1.00[EUR][1000 genomes]
rs4896714	1.00[EUR][1000 genomes]
rs4896715	1.00[EUR][1000 genomes]
rs4896717	1.00[EUR][1000 genomes]
rs55684976	1.00[EUR][1000 genomes]
rs56820385	1.00[EUR][1000 genomes]
rs56897751	1.00[EUR][1000 genomes]
rs57069580	1.00[EUR][1000 genomes]
rs57380483	1.00[EUR][1000 genomes]
rs57485302	1.00[EUR][1000 genomes]
rs57592921	1.00[EUR][1000 genomes]
rs57679521	1.00[EUR][1000 genomes]
rs57704478	1.00[EUR][1000 genomes]
rs57712072	1.00[EUR][1000 genomes]
rs57751197	1.00[EUR][1000 genomes]
rs58084770	1.00[EUR][1000 genomes]
rs58396690	1.00[EUR][1000 genomes]
rs58590469	1.00[EUR][1000 genomes]
rs58646546	0.85[ASN][1000 genomes]
rs58847604	1.00[EUR][1000 genomes]
rs58849686	1.00[EUR][1000 genomes]
rs58857193	1.00[EUR][1000 genomes]
rs59003501	1.00[EUR][1000 genomes]
rs59612420	1.00[EUR][1000 genomes]
rs59614628	1.00[EUR][1000 genomes]
rs59718967	1.00[EUR][1000 genomes]
rs59803839	1.00[EUR][1000 genomes]
rs59810504	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59892317	0.95[ASN][1000 genomes]
rs59936141	1.00[EUR][1000 genomes]
rs60053855	1.00[EUR][1000 genomes]
rs60188478	1.00[EUR][1000 genomes]
rs60234245	1.00[EUR][1000 genomes]
rs60345197	1.00[EUR][1000 genomes]
rs60439721	1.00[EUR][1000 genomes]
rs60484357	1.00[EUR][1000 genomes]
rs60559108	1.00[EUR][1000 genomes]
rs60634096	1.00[EUR][1000 genomes]
rs60762289	1.00[EUR][1000 genomes]
rs60811448	1.00[EUR][1000 genomes]
rs60857439	1.00[EUR][1000 genomes]
rs60859726	1.00[EUR][1000 genomes]
rs61087655	1.00[EUR][1000 genomes]
rs61211447	1.00[EUR][1000 genomes]
rs61249035	1.00[EUR][1000 genomes]
rs61327932	1.00[EUR][1000 genomes]
rs6903993	0.80[AMR][1000 genomes]
rs6911171	0.96[AMR][1000 genomes]
rs6914753	1.00[EUR][1000 genomes]
rs6915621	1.00[EUR][1000 genomes]
rs6916795	1.00[MEX][hapmap];0.84[AMR][1000 genomes]
rs6919115	0.96[AMR][1000 genomes]
rs6922109	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6922608	1.00[ASW][hapmap];0.92[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6924797	0.84[AMR][1000 genomes]
rs6927798	1.00[ASW][hapmap];1.00[GIH][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6941296	0.96[AMR][1000 genomes]
rs73588920	0.96[AMR][1000 genomes]
rs73589002	1.00[EUR][1000 genomes]
rs73591113	1.00[EUR][1000 genomes]
rs73594934	1.00[EUR][1000 genomes]
rs73594936	0.80[AMR][1000 genomes]
rs73594937	0.80[AMR][1000 genomes]
rs73780508	1.00[EUR][1000 genomes]
rs73780540	1.00[EUR][1000 genomes]
rs73780544	0.80[AMR][1000 genomes]
rs7741466	1.00[EUR][1000 genomes]
rs7743190	0.80[AMR][1000 genomes]
rs7745240	1.00[EUR][1000 genomes]
rs7745998	1.00[MEX][hapmap];0.84[AMR][1000 genomes]
rs7747486	1.00[EUR][1000 genomes]
rs7748278	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs7751351	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7751876	1.00[EUR][1000 genomes]
rs7754883	1.00[EUR][1000 genomes]
rs7761280	0.80[AMR][1000 genomes]
rs7766883	1.00[EUR][1000 genomes]
rs7768531	1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs7774175	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9321968	1.00[MEX][hapmap];0.96[AMR][1000 genomes]
rs9321969	1.00[MEX][hapmap];0.96[AMR][1000 genomes]
rs9484874	1.00[EUR][1000 genomes]
rs9496925	0.96[AMR][1000 genomes]
rs9496928	0.96[AMR][1000 genomes]
rs9496930	0.84[AMR][1000 genomes]
rs9496932	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9496935	1.00[ASW][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9496938	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9496944	0.92[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9496955	1.00[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	nsv830832	chr6:144572378-144759023	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2422260	chr6:144574591-144731630	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1031253	chr6:144599055-144883013	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv538461	chr6:144599055-144883013	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144648800-144672800	Weak transcription	Fetal Stomach	stomach
2	chr6:144652000-144668200	Weak transcription	Aorta	Aorta
3	chr6:144653200-144684600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:144656000-144668400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:144656000-144670600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:144657000-144670800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:144657800-144666400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:144658200-144668200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:144658400-144670400	Weak transcription	Fetal Lung	lung
10	chr6:144660000-144665400	Enhancers	Primary hematopoietic stem cells	blood
11	chr6:144660000-144667800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:144660200-144667600	Weak transcription	Placenta	Placenta
13	chr6:144660400-144668200	Weak transcription	Brain Hippocampus Middle	brain
14	chr6:144660400-144670800	Weak transcription	Colon Smooth Muscle	Colon
15	chr6:144660800-144665400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:144661000-144666600	Enhancers	Stomach Mucosa	stomach
17	chr6:144661600-144665400	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr6:144661600-144665400	Weak transcription	Rectal Smooth Muscle	rectum
19	chr6:144661600-144666400	Weak transcription	Spleen	Spleen
20	chr6:144661600-144670400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr6:144661600-144670800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr6:144661800-144670800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:144662600-144665400	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr6:144662800-144668000	Weak transcription	HSMMtube	muscle
25	chr6:144663000-144665600	Enhancers	Pancreas	Pancrea
26	chr6:144663200-144668200	Weak transcription	Brain Anterior Caudate	brain
27	chr6:144663200-144685800	Weak transcription	Brain Substantia Nigra	brain
28	chr6:144663400-144665600	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr6:144663400-144668200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr6:144663400-144675200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr6:144663600-144665400	Weak transcription	Right Ventricle	heart
32	chr6:144663600-144667400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:144663600-144667400	Weak transcription	Hela-S3	cervix
34	chr6:144663600-144667600	Weak transcription	NHLF	lung
35	chr6:144663600-144668400	Weak transcription	Gastric	stomach
36	chr6:144664000-144665400	Enhancers	Fetal Intestine Small	intestine
37	chr6:144664000-144666000	Enhancers	Liver	Liver
38	chr6:144664000-144667000	Flanking Active TSS	Primary B cells from cord blood	blood
39	chr6:144664000-144667000	Flanking Active TSS	Dnd41	blood
40	chr6:144664200-144665400	Weak transcription	Psoas Muscle	Psoas
41	chr6:144664200-144665800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
42	chr6:144664200-144666000	Enhancers	Fetal Kidney	kidney
43	chr6:144664200-144666600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr6:144664200-144667800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chr6:144664400-144665400	Weak transcription	Colonic Mucosa	Colon
46	chr6:144664400-144665600	Flanking Active TSS	Duodenum Mucosa	Duodenum
47	chr6:144664400-144665800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr6:144664400-144665800	Enhancers	Fetal Intestine Large	intestine
49	chr6:144664400-144666000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr6:144664400-144666400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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