Variant report

Variant	rs11895461
Chromosome Location	chr2:173551352-173551353
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SP1	chr2:173550953-173551398	K562	blood:	n/a	n/a
2	NFYB	chr2:173551156-173551424	GM12878	blood:	n/a	n/a
3	NFYB	chr2:173550960-173551444	K562	blood:	n/a	n/a
4	NFYA	chr2:173550973-173551356	K562	blood:	n/a	chr2:173551143-173551161 chr2:173551185-173551203

Variant related genes	Relation type
ENSG00000239041	TF binding region

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10166107	0.95[ASN][1000 genomes]
rs10172894	1.00[ASN][1000 genomes]
rs10178654	1.00[CHB][hapmap]
rs10180021	1.00[CHB][hapmap]
rs10188207	1.00[ASN][1000 genomes]
rs10188540	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10190099	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10198425	0.85[ASN][1000 genomes]
rs10198426	0.85[ASN][1000 genomes]
rs10198546	0.85[ASN][1000 genomes]
rs10199472	1.00[CHB][hapmap]
rs10201129	1.00[CHB][hapmap]
rs10202550	1.00[CHB][hapmap]
rs10205076	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10205126	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10208151	1.00[CHB][hapmap]
rs10209860	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10210195	1.00[ASN][1000 genomes]
rs10210546	1.00[CHB][hapmap]
rs11887454	1.00[CHB][hapmap]
rs11887904	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11888564	0.95[ASN][1000 genomes]
rs11890159	1.00[CHB][hapmap]
rs11891071	0.95[ASN][1000 genomes]
rs11894913	0.95[ASN][1000 genomes]
rs11897396	0.85[ASN][1000 genomes]
rs11898565	0.90[CEU][hapmap];1.00[CHB][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11899594	1.00[ASN][1000 genomes]
rs11902043	0.85[ASN][1000 genomes]
rs12328591	0.85[ASN][1000 genomes]
rs12328781	0.85[ASN][1000 genomes]
rs12329241	0.85[ASN][1000 genomes]
rs12693005	1.00[CHB][hapmap]
rs13007707	1.00[CHB][hapmap]
rs13384609	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13385403	1.00[CHB][hapmap]
rs13385676	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13387816	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13389072	0.95[ASN][1000 genomes]
rs13392808	1.00[CHB][hapmap]
rs13394924	1.00[CHB][hapmap]
rs13400719	0.85[ASN][1000 genomes]
rs13408965	0.85[ASN][1000 genomes]
rs13411408	0.85[ASN][1000 genomes]
rs13415156	1.00[CHB][hapmap]
rs13417334	1.00[CHB][hapmap]
rs13417913	0.85[ASN][1000 genomes]
rs13420845	1.00[ASN][1000 genomes]
rs13422388	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13423248	0.85[ASN][1000 genomes]
rs13425350	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13427701	0.90[ASN][1000 genomes]
rs13427921	0.90[ASN][1000 genomes]
rs13432176	1.00[ASN][1000 genomes]
rs1451447	0.95[ASN][1000 genomes]
rs16860696	1.00[CHB][hapmap]
rs16860697	1.00[CHB][hapmap]
rs17299956	1.00[CHB][hapmap]
rs17702263	1.00[CHB][hapmap]
rs17706710	1.00[CHB][hapmap]
rs1869922	1.00[CHB][hapmap]
rs2167374	0.85[ASN][1000 genomes]
rs28541707	0.85[ASN][1000 genomes]
rs28670307	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28690076	0.85[ASN][1000 genomes]
rs3816536	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs57104776	0.95[ASN][1000 genomes]
rs59648896	1.00[ASN][1000 genomes]
rs62168072	0.85[ASN][1000 genomes]
rs62169318	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62169319	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62169322	0.82[ASN][1000 genomes]
rs62169323	0.82[ASN][1000 genomes]
rs62169324	0.95[ASN][1000 genomes]
rs62169325	0.95[ASN][1000 genomes]
rs62169326	0.90[ASN][1000 genomes]
rs6712686	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6717366	0.95[ASN][1000 genomes]
rs6717851	0.95[ASN][1000 genomes]
rs6723872	1.00[CHB][hapmap]
rs6724116	0.85[ASN][1000 genomes]
rs6741433	0.95[ASN][1000 genomes]
rs6752257	1.00[CHB][hapmap]
rs6757567	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	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	esv2760591	chr2:173396905-173719520	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv583665	chr2:173460640-173643087	Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	esv274888	chr2:173550156-173559068	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173539600-173554200	Weak transcription	Primary T cells from cord blood	blood
2	chr2:173548600-173553000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:173549800-173557400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:173550400-173557200	Weak transcription	Fetal Heart	heart

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