Variant report

Variant	rs12811201
Chromosome Location	chr12:29544185-29544186
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:29543513..29545340-chr12:29551723..29553492,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10492383	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11608616	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11609540	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11610197	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11611420	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11613628	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12809493	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12810064	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12810315	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12811723	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12813520	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12813731	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12813789	0.83[ASN][1000 genomes]
rs12814180	0.92[ASN][1000 genomes]
rs12814930	0.84[ASN][1000 genomes]
rs12815222	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12817578	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12817825	0.82[ASN][1000 genomes]
rs12817985	0.84[ASN][1000 genomes]
rs12819896	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12821498	0.84[ASN][1000 genomes]
rs12821559	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12821708	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12823372	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12823485	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12824407	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12829666	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12830274	0.84[ASN][1000 genomes]
rs12830493	0.88[ASN][1000 genomes]
rs12830678	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12831730	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12832038	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12832263	0.88[ASN][1000 genomes]
rs1988943	0.88[ASN][1000 genomes]
rs35618989	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36126531	0.84[ASN][1000 genomes]
rs3764952	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7134744	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7295387	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7308372	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7314594	0.84[ASN][1000 genomes]
rs7979654	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv995123	chr12:29095272-29571558	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1053641	chr12:29268813-29854413	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv975466	chr12:29541892-29547802	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs12811201	RP11-996F15.2	cis	Artery Tibial	GTEx
rs12811201	RP11-996F15.2	cis	Esophagus Mucosa	GTEx
rs12811201	RP11-996F15.2	cis	Esophagus Muscularis	GTEx
rs12811201	RP11-996F15.2	cis	Adipose Subcutaneous	GTEx
rs12811201	RP11-996F15.2	cis	Skin Sun Exposed Lower leg	GTEx
rs12811201	RP11-996F15.2	cis	Nerve Tibial	GTEx
rs12811201	RP11-996F15.2	cis	Thyroid	GTEx
rs12811201	RP11-996F15.2	cis	lung	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29542600-29544200	Enhancers	Hela-S3	cervix
2	chr12:29542800-29544400	Enhancers	Primary T cells from cord blood	blood
3	chr12:29542800-29544400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr12:29542800-29544400	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr12:29542800-29544600	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr12:29543000-29544200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr12:29543000-29544200	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr12:29543400-29544200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr12:29543400-29545000	Enhancers	HepG2	liver
10	chr12:29543600-29544400	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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