Variant report

Variant	rs10067251
Chromosome Location	chr5:36449612-36449613
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:36391426..36394057-chr5:36449010..36450884,2	K562	blood:
2	chr5:36438756..36441045-chr5:36448106..36450259,2	MCF-7	breast:
3	chr5:36448840..36449624-chr7:156724028..156724917,2	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10056349	1.00[AMR][1000 genomes]
rs10056352	1.00[AMR][1000 genomes]
rs10056466	1.00[AMR][1000 genomes]
rs10058111	1.00[AMR][1000 genomes]
rs10058115	1.00[AMR][1000 genomes]
rs10058314	1.00[AMR][1000 genomes]
rs10058422	1.00[AMR][1000 genomes]
rs10058564	1.00[AMR][1000 genomes]
rs10061999	1.00[AMR][1000 genomes]
rs10064305	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10070419	1.00[AMR][1000 genomes]
rs10073164	1.00[AMR][1000 genomes]
rs10073279	1.00[AMR][1000 genomes]
rs10077206	1.00[AMR][1000 genomes]
rs10085047	1.00[AMR][1000 genomes]
rs10085102	1.00[AMR][1000 genomes]
rs13354988	1.00[AMR][1000 genomes]
rs13359394	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2455284	0.84[ASN][1000 genomes]
rs2455285	0.84[ASN][1000 genomes]
rs2468534	0.84[ASN][1000 genomes]
rs28479598	1.00[AMR][1000 genomes]
rs28505610	1.00[AMR][1000 genomes]
rs28523559	1.00[AMR][1000 genomes]
rs28647761	1.00[AMR][1000 genomes]
rs4443438	0.84[ASN][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	nsv597817	chr5:36433782-36460075	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv597818	chr5:36440940-36460462	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv597819	chr5:36445458-36472990	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1023545	chr5:36448895-36461331	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1016667	chr5:36448895-36464362	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2763449	chr5:36448895-36464374	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36444400-36451800	Weak transcription	Fetal Kidney	kidney
2	chr5:36445000-36450400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr5:36445000-36451000	Weak transcription	HSMMtube	muscle
4	chr5:36445200-36450200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr5:36445400-36450400	Weak transcription	HSMM	muscle
6	chr5:36445400-36450400	Weak transcription	NH-A	brain
7	chr5:36445600-36449800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:36445600-36450200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr5:36445600-36450400	Weak transcription	Osteobl	bone
10	chr5:36445800-36450600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr5:36445800-36452400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr5:36445800-36462800	Weak transcription	Esophagus	oesophagus
13	chr5:36446400-36452000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr5:36446600-36452400	Weak transcription	Placenta	Placenta
15	chr5:36447800-36450600	Enhancers	NHEK	skin
16	chr5:36448000-36452600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr5:36448000-36453800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr5:36448600-36450200	Weak transcription	Hela-S3	cervix
19	chr5:36448800-36449800	Weak transcription	Stomach Mucosa	stomach
20	chr5:36449200-36452200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr5:36449200-36452800	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links