Variant report

Variant	rs6922765
Chromosome Location	chr6:150557060-150557061
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	chr6:150553894..150555591-chr6:150556253..150558267,2	K562	blood:
2	chr6:150555928..150559365-chr6:150559823..150562005,4	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11962230	1.00[ASN][1000 genomes]
rs11963544	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11966866	1.00[ASN][1000 genomes]
rs17079418	0.83[ASN][1000 genomes]
rs17079444	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17079447	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17079450	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17079463	1.00[CEU][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17079471	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28675173	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56000249	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56244054	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57214329	0.83[ASN][1000 genomes]
rs59288040	1.00[ASN][1000 genomes]
rs60476674	0.83[ASN][1000 genomes]
rs6557374	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6910142	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6926969	1.00[ASN][1000 genomes]
rs6935244	1.00[ASN][1000 genomes]
rs72995381	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73007978	1.00[ASN][1000 genomes]
rs73009855	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73009883	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73009887	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73009893	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73009895	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011604	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011614	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011616	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011621	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011630	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011655	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011658	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7744115	1.00[ASN][1000 genomes]
rs7747964	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7755328	1.00[ASN][1000 genomes]
rs7758014	1.00[ASN][1000 genomes]
rs7758186	1.00[ASN][1000 genomes]
rs7763851	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9479943	0.83[ASN][1000 genomes]
rs9479970	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9479978	1.00[CEU][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9480034	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9885695	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830843	chr6:150517411-150691173	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150550000-150558600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr6:150551200-150558800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:150552400-150557600	Weak transcription	Right Atrium	heart
4	chr6:150552400-150558600	Weak transcription	Fetal Brain Female	brain
5	chr6:150552600-150557400	Weak transcription	Fetal Lung	lung
6	chr6:150552600-150559400	Weak transcription	Lung	lung
7	chr6:150553000-150557400	Weak transcription	Fetal Brain Male	brain
8	chr6:150554400-150557200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:150554400-150559000	Weak transcription	Osteobl	bone
10	chr6:150554400-150559200	Weak transcription	K562	blood
11	chr6:150555200-150557600	Weak transcription	Pancreas	Pancrea
12	chr6:150555200-150561400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:150555400-150558600	Weak transcription	HMEC	breast
14	chr6:150555400-150559800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:150555600-150557200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:150555800-150558600	Weak transcription	NHEK	skin
17	chr6:150556200-150557600	Enhancers	Primary T cells fromperipheralblood	blood
18	chr6:150556200-150557600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr6:150556200-150557600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr6:150556200-150557600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr6:150556400-150558000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:150556400-150558600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:150556400-150559800	Enhancers	Left Ventricle	heart
24	chr6:150556400-150560000	Enhancers	Fetal Heart	heart
25	chr6:150556600-150557400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr6:150556600-150557600	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr6:150556600-150557600	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr6:150556600-150557600	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr6:150556600-150560400	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr6:150556800-150557800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr6:150557000-150557800	Enhancers	Adipose Nuclei	Adipose
32	chr6:150557000-150560000	Enhancers	Right Ventricle	heart
33	chr6:150557000-150560400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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