Variant report

Variant	rs6814542
Chromosome Location	chr4:187750561-187750562
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:187739285..187742127-chr4:187749398..187750937,2	K562	blood:
2	chr4:187749229..187751221-chr4:187752968..187755678,3	K562	blood:
3	chr4:187749305..187751343-chr4:187753363..187755921,2	MCF-7	breast:
4	chr4:187742199..187747517-chr4:187748005..187751181,4	K562	blood:
5	chr4:187749279..187751049-chr4:187752829..187754468,2	K562	blood:
6	chr4:187749742..187751497-chr4:187825991..187828310,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10000282	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10006400	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10019663	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1431930	1.00[ASN][1000 genomes]
rs1431933	1.00[CHB][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1431937	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1431938	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1560547	1.00[ASN][1000 genomes]
rs1821137	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2043204	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2060139	1.00[ASN][1000 genomes]
rs2375938	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs322408	1.00[CHB][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs322450	1.00[ASN][1000 genomes]
rs322455	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4241835	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4862739	1.00[ASN][1000 genomes]
rs62344821	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344822	0.96[EUR][1000 genomes]
rs62344826	1.00[ASN][1000 genomes]
rs62345960	1.00[ASN][1000 genomes]
rs62345966	1.00[ASN][1000 genomes]
rs62345967	1.00[ASN][1000 genomes]
rs62345968	1.00[ASN][1000 genomes]
rs6821756	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs919649	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025244	chr4:187419770-188284813	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv1034212	chr4:187437895-188030805	Weak transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv537438	chr4:187437895-188030805	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv532745	chr4:187471692-188205443	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv1022262	chr4:187475862-187848284	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv1024705	chr4:187534005-187849091	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv1026970	chr4:187537418-187913351	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv596440	chr4:187538133-187848075	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv1031603	chr4:187636716-188020741	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv880401	chr4:187668795-188047143	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv596441	chr4:187695564-187786316	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187741800-187751000	Weak transcription	Stomach Mucosa	stomach
2	chr4:187742000-187752600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:187742200-187750600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:187742200-187750600	Weak transcription	NHLF	lung
5	chr4:187742600-187750600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr4:187742600-187750600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr4:187747800-187750600	Weak transcription	Fetal Intestine Large	intestine
8	chr4:187747800-187750800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr4:187747800-187752600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:187748000-187750600	Weak transcription	Small Intestine	intestine
11	chr4:187748800-187750600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr4:187749800-187750800	Enhancers	K562	blood
13	chr4:187750000-187752000	Enhancers	Duodenum Mucosa	Duodenum
14	chr4:187750200-187751800	Enhancers	HepG2	liver
15	chr4:187750200-187752600	Enhancers	HUVEC	blood vessel
16	chr4:187750200-187753800	Enhancers	Hela-S3	cervix
17	chr4:187750400-187750600	Flanking Active TSS	A549	lung
18	chr4:187750400-187750600	Enhancers	Osteobl	bone
19	chr4:187750400-187752200	Enhancers	Fetal Intestine Small	intestine
20	chr4:187750400-187752800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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