Variant report

Variant	rs62424479
Chromosome Location	chr6:132179464-132179465
allele	C/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:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	6:132176847-132180372..6:132514341-132516787	GM12878	blood:
2	6:132176847-132180372..6:132441471-132451441	K562	blood:
3	6:132176847-132180372..6:132286019-132296348	K562	blood:
4	6:132176847-132180372..6:132483283-132485040	GM12878	blood:
5	6:132176847-132180372..6:132547485-132550513	GM12878	blood:
6	6:132176847-132180372..6:132542770-132543792	Hela-S3	cervix:
7	6:132176847-132180372..6:132259484-132267655	GM12878	blood:
8	6:132176847-132180372..6:132506466-132514341	GM12878	blood:
9	6:132176847-132180372..6:132191683-132192688	GM12878	blood:
10	6:132176847-132180372..6:132232580-132243347	GM12878	blood:
11	6:132176847-132180372..6:132564401-132574898	K562	blood:
12	6:132176847-132180372..6:132204869-132216114	K562	blood:
13	6:132176847-132180372..6:132373869-132383497	K562	blood:
14	6:132176847-132180372..6:132550513-132556576	K562	blood:
15	6:132176847-132180372..6:132406656-132416065	K562	blood:

No data

Variant related genes	Relation type
ENSG00000236166	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10452622	1.00[EUR][1000 genomes]
rs41286150	1.00[EUR][1000 genomes]
rs55893997	1.00[EUR][1000 genomes]
rs55910745	1.00[EUR][1000 genomes]
rs56235303	1.00[EUR][1000 genomes]
rs56814151	1.00[EUR][1000 genomes]
rs59610382	1.00[EUR][1000 genomes]
rs60455745	1.00[EUR][1000 genomes]
rs61209790	1.00[EUR][1000 genomes]
rs62424475	1.00[EUR][1000 genomes]
rs62424476	0.93[EUR][1000 genomes]
rs62424477	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62424480	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62424481	1.00[EUR][1000 genomes]
rs62424482	1.00[EUR][1000 genomes]
rs62424483	1.00[EUR][1000 genomes]
rs62424484	1.00[EUR][1000 genomes]
rs62424485	1.00[EUR][1000 genomes]
rs62424486	1.00[EUR][1000 genomes]
rs62424489	1.00[EUR][1000 genomes]
rs62424493	1.00[EUR][1000 genomes]
rs62424495	1.00[EUR][1000 genomes]
rs62424513	1.00[EUR][1000 genomes]
rs62424514	1.00[EUR][1000 genomes]
rs66564329	1.00[EUR][1000 genomes]
rs67025760	1.00[EUR][1000 genomes]
rs67619761	0.93[EUR][1000 genomes]
rs72983672	0.93[EUR][1000 genomes]
rs7741198	0.93[EUR][1000 genomes]
rs7768555	0.93[EUR][1000 genomes]
rs9483345	0.93[EUR][1000 genomes]
rs9493110	1.00[EUR][1000 genomes]
rs9493114	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs997509	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv515476	chr6:131615425-132228577	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv7968	chr6:131917172-132321099	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv886670	chr6:132071193-132193395	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
4	nsv886671	chr6:132071193-132203432	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132147600-132199200	Weak transcription	Fetal Stomach	stomach
2	chr6:132151600-132182400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:132159600-132179800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr6:132160000-132180600	Weak transcription	Placenta	Placenta
5	chr6:132162200-132211000	Weak transcription	Fetal Kidney	kidney
6	chr6:132162600-132181000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:132163000-132181000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:132163000-132182600	Weak transcription	HSMMtube	muscle
9	chr6:132163000-132213600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:132163600-132183400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr6:132166000-132180000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:132166000-132185000	Weak transcription	Fetal Intestine Large	intestine
13	chr6:132166200-132179800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:132168800-132183800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr6:132169800-132181000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr6:132170600-132201800	Weak transcription	Left Ventricle	heart
17	chr6:132170800-132211200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr6:132171000-132180200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr6:132171200-132183800	Weak transcription	Stomach Mucosa	stomach
20	chr6:132171200-132209400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr6:132172400-132180000	Weak transcription	HSMM	muscle
22	chr6:132172400-132184600	Weak transcription	Fetal Muscle Leg	muscle
23	chr6:132172400-132196800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr6:132172600-132180800	Weak transcription	Aorta	Aorta
25	chr6:132172600-132184600	Weak transcription	Fetal Intestine Small	intestine
26	chr6:132172800-132198200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr6:132173000-132192600	Weak transcription	Adipose Nuclei	Adipose
28	chr6:132173200-132181000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr6:132176400-132179800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:132176800-132197000	Weak transcription	Fetal Muscle Trunk	muscle
31	chr6:132177000-132198200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:132177400-132181000	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr6:132177400-132181000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr6:132177400-132186200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr6:132179000-132180200	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr6:132179000-132180600	Genic enhancers	Liver	Liver
37	chr6:132179000-132187400	Strong transcription	HepG2	liver
38	chr6:132179000-132197000	Weak transcription	Ovary	ovary
39	chr6:132179200-132179800	Enhancers	NH-A	brain
40	chr6:132179200-132180400	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr6:132179200-132181200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr6:132179200-132181200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr6:132179200-132181200	Enhancers	NHDF-Ad	bronchial
44	chr6:132179200-132182000	Enhancers	NHLF	lung
45	chr6:132179200-132186600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr6:132179400-132181600	Enhancers	Osteobl	bone
47	chr6:132179400-132183000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:132179400-132183400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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