Variant report

Variant	rs7755028
Chromosome Location	chr6:163890620-163890621
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:163890293..163893385-chr6:163894823..163897543,3	K562	blood:
2	chr6:163889319..163891540-chr6:163964872..163967579,2	K562	blood:
3	chr6:163888891..163890676-chr6:164024271..164026675,2	K562	blood:
4	chr6:163833418..163836921-chr6:163889565..163892236,3	K562	blood:
5	chr6:163887956..163890806-chr6:163903233..163905754,2	K562	blood:
6	chr6:163882705..163885341-chr6:163888682..163891213,3	K562	blood:

Variant related genes	Relation type
ENSG00000270419	Chromatin interaction
ENSG00000112531	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10484571	0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10484572	0.84[YRI][hapmap];1.00[AMR][1000 genomes]
rs10484573	0.92[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11962850	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11964510	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11964587	0.88[AFR][1000 genomes]
rs11964910	1.00[AMR][1000 genomes]
rs11965425	0.91[YRI][hapmap];1.00[AFR][1000 genomes]
rs11965709	0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11966710	0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11966885	0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11966919	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11966922	0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11966958	0.83[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11969530	0.92[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11970766	0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16888837	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs16895001	0.92[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895012	0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895056	0.91[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895066	0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895078	0.92[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895118	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs16895125	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895139	0.84[YRI][hapmap];1.00[AMR][1000 genomes]
rs3846780	0.92[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3903714	0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56702350	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57292071	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57394768	1.00[AMR][1000 genomes]
rs57952819	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59845233	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60965967	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61306342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs62428365	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6937286	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73784410	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73784416	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73787639	0.88[AFR][1000 genomes]
rs73787643	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73787648	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73787650	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7754815	0.91[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][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	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv534621	chr6:163731741-163950870	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv1797109	chr6:163834147-163908115	Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1019551	chr6:163842358-163965216	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1017495	chr6:163856399-163981095	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv523664	chr6:163858237-163907885	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163878800-163910200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:163879200-163891000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:163879200-163891200	Weak transcription	Fetal Kidney	kidney
4	chr6:163879400-163891000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:163880600-163890800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr6:163880600-163891000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:163880600-163891000	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:163880600-163896600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr6:163880600-163897600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:163880600-163903200	Weak transcription	Pancreas	Pancrea
11	chr6:163880600-163906600	Weak transcription	Gastric	stomach
12	chr6:163881800-163897600	Weak transcription	Ovary	ovary
13	chr6:163881800-163901000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:163881800-163910800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr6:163882000-163891000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr6:163882000-163899800	Weak transcription	Placenta	Placenta
17	chr6:163882000-163900000	Weak transcription	Fetal Thymus	thymus
18	chr6:163882000-163906600	Weak transcription	Thymus	Thymus
19	chr6:163882800-163890800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:163883000-163891000	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr6:163883000-163891000	Weak transcription	HUVEC	blood vessel
22	chr6:163883000-163895800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:163883000-163900800	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr6:163883000-163900800	Weak transcription	NH-A	brain
25	chr6:163883000-163906800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr6:163883800-163897000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr6:163884000-163895800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:163884200-163891000	Enhancers	Brain Angular Gyrus	brain
29	chr6:163884600-163890800	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr6:163884600-163891200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:163885200-163893000	Weak transcription	Right Ventricle	heart
32	chr6:163886600-163890800	Weak transcription	Fetal Muscle Leg	muscle
33	chr6:163887200-163891000	Enhancers	Brain Anterior Caudate	brain
34	chr6:163887200-163891000	Weak transcription	Fetal Lung	lung
35	chr6:163887200-163893000	Weak transcription	Psoas Muscle	Psoas
36	chr6:163887200-163900000	Weak transcription	Fetal Stomach	stomach
37	chr6:163887600-163891000	Enhancers	Fetal Heart	heart
38	chr6:163888000-163890800	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr6:163888200-163891000	Enhancers	Brain Germinal Matrix	brain
40	chr6:163888200-163891200	Weak transcription	NHLF	lung
41	chr6:163888400-163892200	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr6:163888400-163893200	Weak transcription	Left Ventricle	heart
43	chr6:163888400-163902800	Weak transcription	Right Atrium	heart
44	chr6:163888400-163908200	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr6:163888600-163890800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:163888600-163890800	Weak transcription	HSMM	muscle
47	chr6:163888600-163891400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:163888800-163890800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:163888800-163891000	Weak transcription	NHDF-Ad	bronchial
50	chr6:163889000-163891000	Enhancers	Fetal Brain Female	brain

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