Variant report

Variant	rs2192435
Chromosome Location	chr12:9880479-9880480
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	chr12:9876110..9878240-chr12:9880296..9883371,3	K562	blood:
2	chr12:9874964..9878982-chr12:9880296..9882811,3	K562	blood:

Variant related genes	Relation type
ENSG00000184293	Chromatin interaction

Extended variants
information (count: 113 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs1008611	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10743820	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10743821	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10743822	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10772104	0.81[ASN][1000 genomes]
rs10844418	0.83[ASN][1000 genomes]
rs10844424	0.84[ASN][1000 genomes]
rs10844429	0.84[ASN][1000 genomes]
rs10844449	0.84[ASN][1000 genomes]
rs10844457	0.84[ASN][1000 genomes]
rs10844476	0.84[ASN][1000 genomes]
rs10844676	0.81[ASN][1000 genomes]
rs11052305	0.83[ASN][1000 genomes]
rs11052311	0.83[ASN][1000 genomes]
rs11052327	0.83[ASN][1000 genomes]
rs11052342	0.83[ASN][1000 genomes]
rs11052366	0.83[ASN][1000 genomes]
rs11052367	0.83[ASN][1000 genomes]
rs11052430	0.84[ASN][1000 genomes]
rs11052431	0.84[ASN][1000 genomes]
rs11052434	0.84[ASN][1000 genomes]
rs11052718	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11052771	0.81[ASN][1000 genomes]
rs11052785	1.00[ASN][1000 genomes]
rs11519377	0.83[ASN][1000 genomes]
rs11524523	0.83[ASN][1000 genomes]
rs12309762	0.83[ASN][1000 genomes]
rs12320830	0.84[ASN][1000 genomes]
rs12368445	0.89[ASN][1000 genomes]
rs12369995	0.83[ASN][1000 genomes]
rs12370579	0.83[ASN][1000 genomes]
rs12371503	0.83[ASN][1000 genomes]
rs12371981	0.83[ASN][1000 genomes]
rs12371982	0.83[ASN][1000 genomes]
rs12578698	1.00[ASN][1000 genomes]
rs12578928	0.84[ASN][1000 genomes]
rs12582616	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12809752	0.83[ASN][1000 genomes]
rs12810851	0.84[ASN][1000 genomes]
rs12812783	0.83[ASN][1000 genomes]
rs12814560	0.83[ASN][1000 genomes]
rs12815393	0.84[ASN][1000 genomes]
rs12816660	0.83[ASN][1000 genomes]
rs12817365	0.83[ASN][1000 genomes]
rs12817550	0.83[ASN][1000 genomes]
rs12817743	0.83[ASN][1000 genomes]
rs12818179	0.83[ASN][1000 genomes]
rs12819865	0.83[ASN][1000 genomes]
rs12820674	0.83[ASN][1000 genomes]
rs12823653	0.83[ASN][1000 genomes]
rs12823699	0.84[ASN][1000 genomes]
rs12825507	0.84[ASN][1000 genomes]
rs12828602	0.84[ASN][1000 genomes]
rs12828773	0.84[ASN][1000 genomes]
rs12830448	0.83[ASN][1000 genomes]
rs12830867	0.83[ASN][1000 genomes]
rs12830878	0.83[ASN][1000 genomes]
rs12831453	0.84[ASN][1000 genomes]
rs1861089	0.83[ASN][1000 genomes]
rs1990533	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2080207	0.83[ASN][1000 genomes]
rs2114872	0.84[ASN][1000 genomes]
rs2114873	0.84[ASN][1000 genomes]
rs2192433	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2192434	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2192439	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2401396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3136577	0.89[ASN][1000 genomes]
rs3176804	0.89[ASN][1000 genomes]
rs3176807	0.89[ASN][1000 genomes]
rs3176808	0.89[ASN][1000 genomes]
rs34201389	1.00[ASN][1000 genomes]
rs34279883	0.89[ASN][1000 genomes]
rs34826829	0.83[ASN][1000 genomes]
rs35078787	0.83[ASN][1000 genomes]
rs35237063	0.83[ASN][1000 genomes]
rs35494990	0.89[ASN][1000 genomes]
rs35512621	0.83[ASN][1000 genomes]
rs4763264	0.83[ASN][1000 genomes]
rs4763280	0.83[ASN][1000 genomes]
rs4763814	0.83[ASN][1000 genomes]
rs4763819	0.83[ASN][1000 genomes]
rs4763835	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4763865	0.81[ASN][1000 genomes]
rs4763867	0.81[ASN][1000 genomes]
rs61913428	1.00[ASN][1000 genomes]
rs6488109	0.83[ASN][1000 genomes]
rs6488122	0.84[ASN][1000 genomes]
rs66725265	0.83[ASN][1000 genomes]
rs67429242	0.83[ASN][1000 genomes]
rs71441764	0.83[ASN][1000 genomes]
rs7297324	0.81[ASN][1000 genomes]
rs7310897	0.84[ASN][1000 genomes]
rs7312624	0.81[ASN][1000 genomes]
rs7485402	0.83[ASN][1000 genomes]
rs7954062	0.95[ASN][1000 genomes]
rs7961812	0.83[ASN][1000 genomes]
rs7961903	0.83[ASN][1000 genomes]
rs7969074	0.83[ASN][1000 genomes]
rs7971721	0.81[ASN][1000 genomes]
rs7972035	0.83[ASN][1000 genomes]
rs7974554	0.83[ASN][1000 genomes]
rs7975557	0.83[ASN][1000 genomes]
rs7975865	0.83[ASN][1000 genomes]
rs7979758	0.84[ASN][1000 genomes]
rs9630264	0.84[ASN][1000 genomes]
rs9630265	0.84[ASN][1000 genomes]
rs9668568	0.83[ASN][1000 genomes]
rs982511	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758293	chr12:9371595-9923529	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
2	esv2759878	chr12:9371595-9923529	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
3	nsv983235	chr12:9852218-9893776	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv2757490	chr12:9855958-9888553	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2192435	LOC374443	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9861600-9882400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr12:9864600-9883800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr12:9874400-9881400	Enhancers	Primary B cells from cord blood	blood
4	chr12:9875000-9881200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr12:9878600-9881000	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr12:9878600-9882600	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr12:9878600-9886000	Active TSS	GM12878-XiMat	blood
8	chr12:9879200-9882800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr12:9880000-9880800	Enhancers	HUVEC	blood vessel
10	chr12:9880000-9880800	Enhancers	NHEK	skin
11	chr12:9880200-9880600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:9880400-9880800	Enhancers	Muscle Satellite Cultured Cells	--

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