Variant report

Variant	rs61333739
Chromosome Location	chr6:35326284-35326285
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:35322565..35326076-chr6:35326260..35332051,7	K562	blood:
2	chr6:35324260..35326770-chr6:35333364..35334972,2	K562	blood:
3	chr6:35315105..35319537-chr6:35325978..35330834,4	K562	blood:
4	chr6:35322565..35324918-chr6:35326260..35328073,2	K562	blood:
5	chr6:35319034..35321264-chr6:35325609..35328038,2	MCF-7	breast:
6	chr6:35319334..35322299-chr6:35325979..35329998,4	MCF-7	breast:
7	chr6:35322678..35326427-chr6:35328080..35332051,5	K562	blood:
8	chr6:35324260..35327105-chr6:35332379..35334972,3	K562	blood:

No data

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs13362808	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2284197	0.94[ASN][1000 genomes]
rs34474204	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57060566	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58114880	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59654131	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61280851	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6457813	0.94[ASN][1000 genomes]
rs6915410	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6939017	0.84[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs73411747	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7744392	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7758272	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7771323	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9470016	0.95[ASN][1000 genomes]
rs9658061	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9658067	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9658080	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9658125	0.95[ASN][1000 genomes]
rs9942488	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9942501	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830641	chr6:35282534-35440603	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
2	nsv885798	chr6:35318784-35329406	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35311400-35326800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:35311600-35327600	Weak transcription	A549	lung
3	chr6:35311800-35331000	Weak transcription	Hela-S3	cervix
4	chr6:35312000-35328200	Weak transcription	Stomach Mucosa	stomach
5	chr6:35312200-35326400	Weak transcription	Fetal Brain Female	brain
6	chr6:35312800-35326800	Weak transcription	Fetal Brain Male	brain
7	chr6:35312800-35327400	Strong transcription	Fetal Stomach	stomach
8	chr6:35313000-35335600	Weak transcription	Small Intestine	intestine
9	chr6:35314800-35327000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr6:35315200-35326800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr6:35316000-35328600	Strong transcription	Duodenum Mucosa	Duodenum
12	chr6:35316800-35326800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:35316800-35327000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr6:35316800-35327200	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr6:35316800-35330000	Strong transcription	Fetal Intestine Small	intestine
16	chr6:35317400-35333000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr6:35319000-35326600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:35319200-35326400	Strong transcription	Fetal Intestine Large	intestine
19	chr6:35319200-35326400	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr6:35319200-35329000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr6:35319400-35327200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:35319600-35327200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr6:35319600-35327600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:35320800-35326400	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr6:35321000-35342400	Weak transcription	Fetal Kidney	kidney
26	chr6:35321400-35330400	Weak transcription	Colonic Mucosa	Colon
27	chr6:35321600-35327600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:35321600-35328000	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr6:35322000-35336000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr6:35322200-35331600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr6:35323000-35326800	Strong transcription	Primary B cells from cord blood	blood
32	chr6:35323000-35326800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr6:35323200-35326800	Strong transcription	Primary B cells from peripheral blood	blood
34	chr6:35323200-35326800	Strong transcription	Muscle Satellite Cultured Cells	--
35	chr6:35323200-35327400	Strong transcription	HSMM	muscle
36	chr6:35323600-35327000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr6:35323800-35329200	Enhancers	Brain Angular Gyrus	brain
38	chr6:35323800-35331600	Enhancers	Psoas Muscle	Psoas
39	chr6:35324000-35328000	Enhancers	Right Atrium	heart
40	chr6:35324400-35326600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr6:35324400-35327400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr6:35324400-35327800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr6:35324400-35328000	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr6:35324400-35328800	Enhancers	Brain Substantia Nigra	brain
45	chr6:35324600-35327600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr6:35324800-35326800	Enhancers	Fetal Heart	heart
47	chr6:35324800-35327800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr6:35324800-35327800	Genic enhancers	Fetal Muscle Leg	muscle
49	chr6:35324800-35329200	Enhancers	Ovary	ovary
50	chr6:35324800-35331400	Enhancers	Brain Hippocampus Middle	brain

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