Variant report

Variant	rs7573946
Chromosome Location	chr2:173577894-173577895
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:173576581..173579136-chr2:173580919..173583053,2	K562	blood:
2	chr2:173574519..173576819-chr2:173577534..173580369,2	MCF-7	breast:
3	chr2:173575339..173578126-chr2:173587981..173590920,2	MCF-7	breast:

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10166107	0.91[EUR][1000 genomes]
rs10172894	0.88[EUR][1000 genomes]
rs10178654	1.00[CHB][hapmap]
rs10180021	1.00[CHB][hapmap]
rs10190099	0.89[EUR][1000 genomes]
rs10198425	0.92[EUR][1000 genomes]
rs10198426	0.92[EUR][1000 genomes]
rs10198546	0.92[EUR][1000 genomes]
rs10199472	1.00[CHB][hapmap]
rs10201129	1.00[CHB][hapmap]
rs10202550	1.00[CHB][hapmap]
rs10205076	0.89[EUR][1000 genomes]
rs10205126	0.87[EUR][1000 genomes]
rs10208151	1.00[CHB][hapmap]
rs10210195	0.91[EUR][1000 genomes]
rs10210546	1.00[CHB][hapmap]
rs11887454	1.00[CHB][hapmap]
rs11887904	0.89[EUR][1000 genomes]
rs11888564	0.92[EUR][1000 genomes]
rs11890159	1.00[CHB][hapmap]
rs11891071	0.92[EUR][1000 genomes]
rs11894913	0.91[EUR][1000 genomes]
rs11895461	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs11897396	0.92[EUR][1000 genomes]
rs11898565	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[EUR][1000 genomes]
rs11899594	0.91[EUR][1000 genomes]
rs11902043	0.92[EUR][1000 genomes]
rs12328591	0.92[EUR][1000 genomes]
rs12328781	0.92[EUR][1000 genomes]
rs12329241	0.92[EUR][1000 genomes]
rs12693005	1.00[CHB][hapmap]
rs13007707	1.00[CHB][hapmap]
rs13384609	0.89[EUR][1000 genomes]
rs13385403	1.00[CHB][hapmap]
rs13387816	0.89[EUR][1000 genomes]
rs13389072	0.91[EUR][1000 genomes]
rs13392808	1.00[CHB][hapmap]
rs13394924	1.00[CHB][hapmap]
rs13400719	0.92[EUR][1000 genomes]
rs13408965	0.92[EUR][1000 genomes]
rs13411408	0.90[EUR][1000 genomes]
rs13415156	1.00[CHB][hapmap]
rs13417334	1.00[CHB][hapmap]
rs13417913	0.92[EUR][1000 genomes]
rs13420845	0.91[EUR][1000 genomes]
rs13422388	0.89[EUR][1000 genomes]
rs13423248	0.92[EUR][1000 genomes]
rs13425350	0.89[EUR][1000 genomes]
rs13427701	0.89[EUR][1000 genomes]
rs13427921	0.89[EUR][1000 genomes]
rs13428122	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13432176	0.91[EUR][1000 genomes]
rs1451447	0.92[EUR][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	0.92[EUR][1000 genomes]
rs28541707	0.92[EUR][1000 genomes]
rs28670307	0.89[EUR][1000 genomes]
rs28690076	0.93[EUR][1000 genomes]
rs3816536	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[EUR][1000 genomes]
rs57104776	0.89[EUR][1000 genomes]
rs59648896	0.90[EUR][1000 genomes]
rs62168072	0.92[EUR][1000 genomes]
rs62169319	0.89[EUR][1000 genomes]
rs62169322	0.92[EUR][1000 genomes]
rs62169323	0.85[EUR][1000 genomes]
rs62169324	0.92[EUR][1000 genomes]
rs62169325	0.92[EUR][1000 genomes]
rs62169326	0.84[EUR][1000 genomes]
rs6717366	0.92[EUR][1000 genomes]
rs6717851	0.87[EUR][1000 genomes]
rs6723872	1.00[CHB][hapmap]
rs6724116	0.92[EUR][1000 genomes]
rs6741433	0.92[EUR][1000 genomes]
rs6752257	1.00[CHB][hapmap]
rs6757567	0.90[EUR][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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173577000-173578600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:173577200-173578400	Enhancers	Right Ventricle	heart
3	chr2:173577400-173578400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr2:173577800-173578600	Enhancers	Adipose Nuclei	Adipose

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