Variant report

Variant	rs6910121
Chromosome Location	chr6:166862844-166862845
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:166858354..166860474-chr6:166862060..166863705,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10806850	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10806851	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10806852	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10806853	0.91[EUR][1000 genomes]
rs12153873	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12191994	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2072828	0.82[YRI][hapmap]
rs2281052	0.83[CEU][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes]
rs2294330	0.90[CEU][hapmap];0.89[CHB][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3752927	0.83[AFR][1000 genomes]
rs4710049	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4710050	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4710051	0.95[CEU][hapmap];0.87[MKK][hapmap];0.92[TSI][hapmap];0.95[YRI][hapmap];0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6913835	0.91[EUR][1000 genomes]
rs6915132	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6932660	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6941841	0.84[EUR][1000 genomes]
rs73033724	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7739961	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7741232	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9295346	0.86[EUR][1000 genomes]
rs9355580	0.90[CEU][hapmap];0.89[CHB][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9355581	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[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	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	nsv886937	chr6:166830696-166922813	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv886938	chr6:166859725-166904398	Genic enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv886939	chr6:166859725-166922813	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv3441231	chr6:166861012-166863510	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166808200-166911800	Weak transcription	Psoas Muscle	Psoas
2	chr6:166824000-166901400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr6:166825200-166875800	Weak transcription	Colonic Mucosa	Colon
4	chr6:166827000-166873400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:166827600-166867200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr6:166830000-166866600	Weak transcription	Fetal Intestine Large	intestine
7	chr6:166833200-166864400	Weak transcription	Fetal Kidney	kidney
8	chr6:166833200-166879000	Weak transcription	NH-A	brain
9	chr6:166833400-166879000	Weak transcription	HSMM	muscle
10	chr6:166834000-166866400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:166834200-166863800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:166834200-166879400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:166843000-166865200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:166844200-166865200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr6:166845800-166863400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr6:166846000-166863200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr6:166846000-166881000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:166848800-166865200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr6:166850200-166863400	Weak transcription	Stomach Mucosa	stomach
20	chr6:166850200-166865200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:166850200-166870000	Weak transcription	Right Atrium	heart
22	chr6:166854000-166864200	Weak transcription	HUVEC	blood vessel
23	chr6:166855200-166864800	Strong transcription	Pancreas	Pancrea
24	chr6:166855400-166863200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:166855400-166864600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr6:166855600-166864600	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr6:166855800-166864800	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chr6:166856200-166864800	Strong transcription	Brain Anterior Caudate	brain
29	chr6:166857400-166863200	Strong transcription	Brain Hippocampus Middle	brain
30	chr6:166857800-166863000	Strong transcription	Fetal Stomach	stomach
31	chr6:166857800-166863200	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr6:166857800-166865200	Strong transcription	Fetal Muscle Trunk	muscle
33	chr6:166858000-166863400	Strong transcription	Stomach Smooth Muscle	stomach
34	chr6:166858000-166864800	Strong transcription	Gastric	stomach
35	chr6:166858000-166865000	Strong transcription	Skeletal Muscle Male	skeletal muscle
36	chr6:166858000-166865200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr6:166858200-166863200	Weak transcription	Fetal Brain Male	brain
38	chr6:166858200-166864200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr6:166858200-166864800	Strong transcription	NHLF	lung
40	chr6:166858600-166863200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr6:166859000-166863600	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr6:166859200-166863000	Strong transcription	Right Ventricle	heart
43	chr6:166860000-166863000	Strong transcription	Brain Germinal Matrix	brain
44	chr6:166860200-166864200	Strong transcription	Brain Cingulate Gyrus	brain
45	chr6:166860400-166863000	Strong transcription	H1 Cell Line	embryonic stem cell
46	chr6:166860400-166863400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:166860600-166865000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr6:166860600-166865200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:166861000-166865000	Strong transcription	Fetal Lung	lung
50	chr6:166861200-166864800	Strong transcription	Brain Angular Gyrus	brain

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