Variant report

Variant	rs227815
Chromosome Location	chr6:44672434-44672435
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1283921	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1283922	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1283924	1.00[ASN][1000 genomes]
rs1293597	1.00[ASN][1000 genomes]
rs1296351	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1298942	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17335164	1.00[ASN][1000 genomes]
rs1767800	0.81[EUR][1000 genomes]
rs190137	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227804	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227805	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227807	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227809	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227810	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227811	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227816	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227820	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227821	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227822	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227823	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227825	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs227826	0.81[EUR][1000 genomes]
rs227856	1.00[ASN][1000 genomes]
rs2461016	1.00[ASN][1000 genomes]
rs2817118	0.81[EUR][1000 genomes]
rs489448	0.81[EUR][1000 genomes]
rs489757	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs491590	1.00[ASN][1000 genomes]
rs504907	1.00[ASN][1000 genomes]
rs545441	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs546936	0.82[EUR][1000 genomes]
rs551817	1.00[ASN][1000 genomes]
rs552919	1.00[ASN][1000 genomes]
rs552972	1.00[ASN][1000 genomes]
rs554682	1.00[ASN][1000 genomes]
rs567297	1.00[ASN][1000 genomes]
rs570778	1.00[ASN][1000 genomes]
rs581216	1.00[ASN][1000 genomes]
rs613208	1.00[ASN][1000 genomes]
rs613948	1.00[ASN][1000 genomes]
rs625595	1.00[ASN][1000 genomes]
rs626965	1.00[ASN][1000 genomes]
rs631320	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs641011	1.00[ASN][1000 genomes]
rs641340	1.00[ASN][1000 genomes]
rs660643	1.00[ASN][1000 genomes]
rs666652	1.00[ASN][1000 genomes]
rs672098	1.00[ASN][1000 genomes]
rs6907056	0.92[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1817071	chr6:44670110-44698829	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44665600-44673800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:44667200-44691000	Weak transcription	Right Atrium	heart
3	chr6:44670200-44672600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr6:44670400-44679200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:44670400-44679600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:44670800-44673800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:44671400-44672800	Enhancers	GM12878-XiMat	blood
8	chr6:44671600-44673200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:44671800-44672800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr6:44672400-44672600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood

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