Variant report

Variant	rs10019344
Chromosome Location	chr4:133047444-133047445
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10009200	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10033560	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10461212	0.81[AFR][1000 genomes]
rs11723078	0.85[AFR][1000 genomes]
rs11930158	0.86[ASN][1000 genomes]
rs13107581	0.96[AFR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13117543	0.94[ASN][1000 genomes]
rs13124410	0.86[AFR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13127678	0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13137404	0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13141865	0.91[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs13152802	0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1505407	0.82[AFR][1000 genomes]
rs17047796	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1827740	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59368900	0.95[ASN][1000 genomes]
rs6831366	0.91[ASN][1000 genomes]
rs6847338	0.84[AFR][1000 genomes]
rs7660282	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7660499	0.95[CHB][hapmap];0.86[JPT][hapmap];0.95[AFR][1000 genomes];0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7661243	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7661355	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7666320	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7680111	0.95[AFR][1000 genomes];0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7680265	0.91[ASN][1000 genomes]
rs9790555	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9990622	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9995917	0.82[AFR][1000 genomes]
rs9996530	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470073	chr4:132902055-133101094	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1031888	chr4:132903485-133355824	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv880002	chr4:132970231-133082999	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv595445	chr4:133022641-133338765	Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv880003	chr4:133047300-133513991	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:133045400-133047800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:133045400-133050000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:133046200-133050400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr4:133046400-133047800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:133046800-133047600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr4:133046800-133048200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:133047000-133047600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:133047000-133051600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr4:133047200-133047800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr4:133047400-133047600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:133047400-133047600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:133047400-133049200	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr4:133047400-133051800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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