Variant report

Variant	rs10981867
Chromosome Location	chr9:116422072-116422073
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:116420295..116422298-chr9:116424343..116426140,2	MCF-7	breast:
2	chr9:116420136..116422934-chr9:116424938..116428259,3	K562	blood:
3	chr9:116419739..116422322-chr9:116424476..116427451,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1077072	0.84[CEU][hapmap];0.99[EUR][1000 genomes]
rs10817498	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10981865	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981866	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10981868	0.99[AFR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10981869	0.95[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10981870	0.95[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10981871	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10981872	0.95[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10981873	0.95[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10981874	0.95[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10981875	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16907657	0.88[CHB][hapmap];0.91[JPT][hapmap]
rs16907724	0.84[CEU][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2101069	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2622266	0.92[JPT][hapmap];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59286569	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59638505	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7031646	0.98[AFR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7031648	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7031666	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7047639	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7047776	0.90[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7048067	0.91[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs745730	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7854061	0.93[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs880205	0.89[EUR][1000 genomes];0.98[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	nsv530949	chr9:115821128-116487796	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv893749	chr9:116378759-116439749	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv466512	chr9:116413751-116446881	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv615220	chr9:116413751-116446881	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv3326886	chr9:116417931-116422229	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116416200-116422200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr9:116420200-116425800	Weak transcription	Psoas Muscle	Psoas
3	chr9:116420400-116425800	Weak transcription	Left Ventricle	heart
4	chr9:116420800-116427200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:116421000-116423800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr9:116421000-116425800	Weak transcription	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links