Variant report

Variant	rs476390
Chromosome Location	chr1:197253267-197253268
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:197245308..197247584-chr1:197251530..197254404,2	K562	blood:
2	chr1:197249603..197251809-chr1:197252307..197255280,2	MCF-7	breast:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10429911	1.00[CEU][hapmap]
rs10732295	1.00[CEU][hapmap]
rs10732296	1.00[CEU][hapmap]
rs10754219	1.00[CEU][hapmap];0.83[YRI][hapmap];0.85[AMR][1000 genomes]
rs12677	0.87[CEU][hapmap]
rs1332662	0.87[CEU][hapmap]
rs1332663	0.87[CEU][hapmap]
rs1415214	0.81[YRI][hapmap]
rs1415217	1.00[CEU][hapmap]
rs1556763	1.00[CEU][hapmap]
rs1571964	0.87[CEU][hapmap]
rs1764622	0.82[YRI][hapmap]
rs1764623	0.88[YRI][hapmap]
rs1764629	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1764786	0.84[YRI][hapmap]
rs1764796	0.81[EUR][1000 genomes]
rs1764800	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2026429	0.87[CEU][hapmap]
rs2151134	1.00[CEU][hapmap]
rs2786114	0.91[EUR][1000 genomes]
rs4244141	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4342879	1.00[CEU][hapmap]
rs4350226	1.00[CEU][hapmap]
rs482526	0.85[YRI][hapmap]
rs4915337	0.87[CEU][hapmap]
rs4915378	1.00[CEU][hapmap]
rs4915379	1.00[CEU][hapmap]
rs510135	1.00[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs518149	1.00[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs550098	0.88[YRI][hapmap]
rs552708	0.89[AMR][1000 genomes]
rs568757	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs570845	0.86[YRI][hapmap]
rs571106	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs580067	0.82[YRI][hapmap]
rs615647	1.00[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs616675	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6428390	0.83[EUR][1000 genomes]
rs643025	0.88[YRI][hapmap]
rs658409	0.80[YRI][hapmap]
rs6656448	1.00[CEU][hapmap]
rs6656858	0.87[CEU][hapmap]
rs6677082	0.87[CEU][hapmap]
rs6678066	0.94[EUR][1000 genomes]
rs668590	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6703400	0.87[CEU][hapmap]
rs7513826	1.00[CEU][hapmap];0.85[AMR][1000 genomes]
rs7520503	1.00[CEU][hapmap]
rs7523013	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs7534353	0.87[CEU][hapmap]
rs7542397	0.87[CEU][hapmap]
rs7554995	0.85[AMR][1000 genomes]
rs877897	0.87[CEU][hapmap]

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	nsv528460	chr1:196542567-197446702	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197246800-197256600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr1:197250800-197253600	Weak transcription	Brain Substantia Nigra	brain
3	chr1:197251000-197253600	Weak transcription	Brain Anterior Caudate	brain
4	chr1:197251000-197257000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr1:197252400-197254600	Weak transcription	Primary T cells from cord blood	blood
6	chr1:197253200-197253400	Enhancers	Brain Angular Gyrus	brain
7	chr1:197253200-197255400	Enhancers	Stomach Mucosa	stomach

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