Variant report

Variant	rs9497098
Chromosome Location	chr6:145170824-145170825
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:145166979..145168602-chr6:145169324..145170941,2	MCF-7	breast:
2	chr6:145168696..145171336-chr6:145172610..145175556,2	K562	blood:
3	chr6:145164758..145167653-chr6:145170294..145172652,2	K562	blood:
4	chr6:145169081..145170847-chr6:145177041..145178659,2	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs12111267	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28599831	1.00[AMR][1000 genomes]
rs4526210	0.90[AFR][1000 genomes]
rs6925418	1.00[AMR][1000 genomes]
rs6927968	1.00[AMR][1000 genomes]
rs6930763	1.00[AMR][1000 genomes]
rs6933210	0.88[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6933387	0.88[YRI][hapmap]
rs6939199	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6941932	1.00[AMR][1000 genomes]
rs7759926	1.00[AMR][1000 genomes]
rs7765793	1.00[AMR][1000 genomes]
rs7771184	1.00[AMR][1000 genomes]
rs9390234	0.81[LWK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs9484903	1.00[AMR][1000 genomes]
rs9484906	1.00[AMR][1000 genomes]
rs9484907	0.85[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484910	1.00[AMR][1000 genomes]
rs9484911	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497062	1.00[AMR][1000 genomes]
rs9497067	1.00[AMR][1000 genomes]
rs9497071	1.00[AMR][1000 genomes]
rs9497072	1.00[AMR][1000 genomes]
rs9497073	1.00[AMR][1000 genomes]
rs9497074	1.00[ASW][hapmap];0.88[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs9497075	1.00[AMR][1000 genomes]
rs9497076	1.00[AMR][1000 genomes]
rs9497077	1.00[AMR][1000 genomes]
rs9497078	1.00[ASW][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs9497079	1.00[AMR][1000 genomes]
rs9497080	1.00[AMR][1000 genomes]
rs9497082	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497083	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497084	0.82[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497085	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497086	0.88[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497099	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497129	1.00[AMR][1000 genomes]
rs9767429	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv830833	chr6:145001310-145201143	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv886740	chr6:145105354-145199259	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145117400-145175200	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr6:145130800-145172200	Weak transcription	NH-A	brain
3	chr6:145137400-145176800	Weak transcription	Fetal Heart	heart
4	chr6:145137800-145175800	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr6:145141400-145172000	Weak transcription	Brain Substantia Nigra	brain
6	chr6:145141400-145175200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:145142000-145171400	Weak transcription	HMEC	breast
8	chr6:145143000-145173600	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr6:145154200-145175200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr6:145154400-145173400	Strong transcription	Primary B cells from peripheral blood	blood
11	chr6:145154400-145175000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:145154400-145175200	Strong transcription	Dnd41	blood
13	chr6:145154800-145175200	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr6:145155800-145171800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr6:145157400-145173400	Weak transcription	Fetal Brain Male	brain
16	chr6:145157800-145176400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:145158600-145176800	Weak transcription	Esophagus	oesophagus
18	chr6:145158800-145173600	Weak transcription	Psoas Muscle	Psoas
19	chr6:145158800-145174800	Weak transcription	Placenta	Placenta
20	chr6:145159200-145173800	Weak transcription	GM12878-XiMat	blood
21	chr6:145159200-145176600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:145159400-145171600	Weak transcription	Fetal Kidney	kidney
23	chr6:145159400-145177400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr6:145159600-145175200	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr6:145161000-145174400	Weak transcription	Right Ventricle	heart
26	chr6:145161000-145176000	Weak transcription	Pancreas	Pancrea
27	chr6:145161000-145179000	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr6:145162200-145171600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr6:145162400-145172400	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr6:145162400-145173200	Weak transcription	Colonic Mucosa	Colon
31	chr6:145162600-145171200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr6:145162600-145173800	Weak transcription	Stomach Smooth Muscle	stomach
33	chr6:145162600-145176400	Weak transcription	Fetal Intestine Large	intestine
34	chr6:145162800-145176600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:145163800-145176200	Weak transcription	Fetal Intestine Small	intestine
36	chr6:145164200-145174800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr6:145164400-145175800	Strong transcription	Primary B cells from cord blood	blood
38	chr6:145164600-145172200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr6:145165400-145171600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:145165400-145171800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:145165800-145176600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr6:145166000-145175400	Weak transcription	Small Intestine	intestine
43	chr6:145166200-145176400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr6:145166400-145171600	Weak transcription	NHLF	lung
45	chr6:145166600-145174000	Strong transcription	Liver	Liver
46	chr6:145166600-145175000	Strong transcription	Adipose Nuclei	Adipose
47	chr6:145166600-145175200	Strong transcription	Primary T cells from cord blood	blood
48	chr6:145166800-145172400	Strong transcription	Fetal Muscle Leg	muscle
49	chr6:145167200-145171400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr6:145167200-145173400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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