Variant report

Variant	rs71573031
Chromosome Location	chr1:171321420-171321421
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:171289560..171292319-chr1:171321362..171324920,3	K562	blood:

Variant related genes	Relation type
ENSG00000076258	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10157634	0.90[ASN][1000 genomes]
rs1024171	0.90[ASN][1000 genomes]
rs1024173	0.88[ASN][1000 genomes]
rs1042772	0.82[ASN][1000 genomes]
rs10912810	0.89[ASN][1000 genomes]
rs10912830	0.88[ASN][1000 genomes]
rs10912833	0.83[ASN][1000 genomes]
rs12057885	0.86[ASN][1000 genomes]
rs12064618	0.88[ASN][1000 genomes]
rs12121479	0.89[ASN][1000 genomes]
rs12564530	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12735239	0.90[ASN][1000 genomes]
rs12736204	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12737633	0.89[ASN][1000 genomes]
rs12747017	0.90[ASN][1000 genomes]
rs1963273	0.90[ASN][1000 genomes]
rs2011345	0.84[ASN][1000 genomes]
rs2011548	0.90[ASN][1000 genomes]
rs2143090	0.86[ASN][1000 genomes]
rs2179375	0.86[ASN][1000 genomes]
rs2223477	0.86[ASN][1000 genomes]
rs2235508	0.89[ASN][1000 genomes]
rs2235509	0.89[ASN][1000 genomes]
rs2235510	0.89[ASN][1000 genomes]
rs2235511	0.89[ASN][1000 genomes]
rs34668298	0.89[ASN][1000 genomes]
rs35062585	0.90[ASN][1000 genomes]
rs36112567	0.89[ASN][1000 genomes]
rs4615872	0.86[ASN][1000 genomes]
rs6425167	0.86[ASN][1000 genomes]
rs6425192	0.86[ASN][1000 genomes]
rs6425194	0.86[ASN][1000 genomes]
rs6656117	0.88[ASN][1000 genomes]
rs6656219	0.88[ASN][1000 genomes]
rs6662297	0.90[ASN][1000 genomes]
rs6667507	0.89[ASN][1000 genomes]
rs6670432	0.84[ASN][1000 genomes]
rs6670627	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6688317	0.90[ASN][1000 genomes]
rs67595287	0.90[ASN][1000 genomes]
rs7518648	0.89[ASN][1000 genomes]
rs7519001	0.90[ASN][1000 genomes]
rs7548166	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7555359	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs980120	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001228	chr1:170885787-171452579	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
2	esv14617	chr1:171016086-171726961	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv10193	chr1:171128845-171414611	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv831882	chr1:171166224-171326083	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1002423	chr1:171294384-171376936	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv548188	chr1:171308832-171371998	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171315400-171324800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:171315600-171322400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:171319800-171322000	Enhancers	Liver	Liver

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