Variant report

Variant	rs978437
Chromosome Location	chr7:136614178-136614179
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10243944	0.95[YRI][hapmap]
rs1158586	0.96[CEU][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12155015	0.96[CEU][hapmap]
rs1364407	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1364409	1.00[CEU][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1378645	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1378646	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1378647	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1455857	0.91[CEU][hapmap];0.92[AMR][1000 genomes]
rs1455858	0.91[CEU][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1824024	0.92[CEU][hapmap];0.87[AMR][1000 genomes]
rs2350780	0.80[AMR][1000 genomes]
rs2350783	0.96[CEU][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6467695	0.96[CEU][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6467696	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6942627	0.83[AMR][1000 genomes]
rs6943950	0.81[AMR][1000 genomes]
rs6945230	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6947206	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs6952264	0.96[CEU][hapmap];0.83[AMR][1000 genomes]
rs6960707	0.96[CEU][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7782965	0.96[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7792449	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831147	chr7:136583444-136755741	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136607800-136638000	Weak transcription	NHLF	lung
2	chr7:136610800-136623400	Weak transcription	Colon Smooth Muscle	Colon
3	chr7:136611000-136616400	Weak transcription	Right Atrium	heart
4	chr7:136611000-136623200	Weak transcription	Left Ventricle	heart
5	chr7:136611800-136614600	Enhancers	Fetal Heart	heart
6	chr7:136612000-136614200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:136612000-136614200	Weak transcription	HUVEC	blood vessel
8	chr7:136613200-136614200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr7:136613400-136614400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:136613400-136614400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:136614000-136614200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links