Variant report

Variant	rs6790187
Chromosome Location	chr3:99807358-99807359
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:99806279..99809036-chr3:99909487..99911239,2	K562	blood:
2	chr3:99802054..99805861-chr3:99806768..99808957,3	K562	blood:
3	chr3:99789802..99792121-chr3:99804695..99807400,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16842034	1.00[EUR][1000 genomes]
rs17313676	1.00[EUR][1000 genomes]
rs17314245	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17314280	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17314977	1.00[EUR][1000 genomes]
rs17338576	1.00[EUR][1000 genomes]
rs17392822	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17393080	1.00[EUR][1000 genomes]
rs17397949	1.00[EUR][1000 genomes]
rs17779605	1.00[EUR][1000 genomes]
rs36005744	1.00[EUR][1000 genomes]
rs41272629	1.00[EUR][1000 genomes]
rs41272631	1.00[EUR][1000 genomes]
rs41272633	1.00[EUR][1000 genomes]
rs41444055	0.89[AFR][1000 genomes]
rs41477051	0.89[AFR][1000 genomes]
rs62636640	1.00[EUR][1000 genomes]
rs62636641	1.00[EUR][1000 genomes]
rs6762809	1.00[EUR][1000 genomes]
rs6762871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6764470	0.89[AFR][1000 genomes]
rs6765822	0.89[AFR][1000 genomes]
rs6768684	1.00[EUR][1000 genomes]
rs6778756	0.89[AFR][1000 genomes]
rs6781780	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6784150	1.00[EUR][1000 genomes]
rs6787184	0.89[AFR][1000 genomes]
rs6788807	1.00[EUR][1000 genomes]
rs6789840	0.89[AFR][1000 genomes]
rs6791426	0.89[AFR][1000 genomes]
rs6794130	1.00[EUR][1000 genomes]
rs6794365	1.00[EUR][1000 genomes]
rs6807137	1.00[EUR][1000 genomes]
rs6807615	1.00[EUR][1000 genomes]
rs72936590	0.83[EUR][1000 genomes]
rs7611313	1.00[EUR][1000 genomes]
rs7619738	1.00[EUR][1000 genomes]
rs7626310	1.00[EUR][1000 genomes]
rs7628458	1.00[EUR][1000 genomes]
rs7646221	1.00[EUR][1000 genomes]
rs7648943	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7652596	1.00[EUR][1000 genomes]
rs766777	1.00[EUR][1000 genomes]
rs768527	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817478	chr3:99474086-99955548	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv916476	chr3:99478229-100124625	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv869848	chr3:99652246-99904276	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv932634	chr3:99660690-99888854	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1010579	chr3:99660754-99901817	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1008483	chr3:99660754-99903769	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1010897	chr3:99660754-99904783	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1001529	chr3:99661758-99892654	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
9	nsv536665	chr3:99661758-99892654	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
10	nsv591148	chr3:99774720-99905803	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99793800-99809800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr3:99795800-99866600	Weak transcription	Primary T cells from cord blood	blood
3	chr3:99796200-99807400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr3:99796600-99808800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr3:99796800-99808600	Weak transcription	Ovary	ovary
6	chr3:99796800-99808800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:99796800-99808800	Weak transcription	Left Ventricle	heart
8	chr3:99798000-99808800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr3:99800000-99808800	Weak transcription	Aorta	Aorta
10	chr3:99803200-99808800	Weak transcription	Fetal Intestine Small	intestine
11	chr3:99804000-99808800	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr3:99804000-99809000	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr3:99804200-99807800	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr3:99804200-99808600	Weak transcription	Primary hematopoietic stem cells	blood
15	chr3:99804400-99807400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr3:99804600-99807800	Weak transcription	K562	blood
17	chr3:99804600-99808800	Weak transcription	Fetal Muscle Leg	muscle
18	chr3:99804800-99807800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr3:99804800-99808600	Weak transcription	Fetal Kidney	kidney
20	chr3:99804800-99808600	Weak transcription	Psoas Muscle	Psoas
21	chr3:99805000-99807400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr3:99805000-99809600	Enhancers	Muscle Satellite Cultured Cells	--
23	chr3:99805600-99808200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:99805800-99807600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:99806000-99807400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr3:99806000-99807400	Weak transcription	A549	lung
27	chr3:99806000-99808800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr3:99806000-99808800	Weak transcription	Small Intestine	intestine
29	chr3:99806200-99807400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr3:99806200-99807400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr3:99806200-99807800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:99806200-99807800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr3:99806200-99807800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr3:99806200-99809800	Enhancers	NHDF-Ad	bronchial
35	chr3:99806200-99816000	Weak transcription	Rectal Smooth Muscle	rectum
36	chr3:99806200-99818600	Weak transcription	HSMM	muscle
37	chr3:99806400-99807400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:99806600-99807600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr3:99806600-99808400	Weak transcription	Osteobl	bone
40	chr3:99806600-99808600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr3:99806600-99808600	Weak transcription	NH-A	brain
42	chr3:99806600-99808600	Weak transcription	NHLF	lung
43	chr3:99806600-99812600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:99806800-99808800	Weak transcription	Fetal Intestine Large	intestine
45	chr3:99806800-99809400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr3:99806800-99809600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr3:99806800-99809800	Enhancers	HepG2	liver
48	chr3:99807000-99807400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr3:99807000-99809800	Enhancers	H1 Cell Line	embryonic stem cell
50	chr3:99807000-99809800	Enhancers	HUES48 Cell Line	embryonic stem cell

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