Variant report

Variant	rs17347436
Chromosome Location	chr7:120195356-120195357
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:120191134..120192918-chr7:120193814..120196411,2	K562	blood:
2	chr7:120185278..120187697-chr7:120193746..120195499,2	K562	blood:
3	chr7:120195175..120197471-chr7:120198217..120202322,3	K562	blood:
4	chr7:120191418..120193640-chr7:120194004..120197390,3	K562	blood:
5	chr7:120195090..120195825-chr7:120365406..120366067,2	MCF-7	breast:
6	chr7:118910007..118910665-chr7:120194855..120195659,2	MCF-7	breast:

Extended variants
information (count: 47 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10156125	1.00[EUR][1000 genomes]
rs10224280	1.00[EUR][1000 genomes]
rs10224891	1.00[EUR][1000 genomes]
rs10227379	0.95[EUR][1000 genomes]
rs10228326	1.00[EUR][1000 genomes]
rs10234674	0.97[EUR][1000 genomes]
rs10239065	1.00[EUR][1000 genomes]
rs10245675	1.00[EUR][1000 genomes]
rs10247657	1.00[EUR][1000 genomes]
rs10248007	1.00[EUR][1000 genomes]
rs10253512	1.00[EUR][1000 genomes]
rs10257987	1.00[EUR][1000 genomes]
rs10259436	1.00[EUR][1000 genomes]
rs10262476	1.00[EUR][1000 genomes]
rs10265695	1.00[EUR][1000 genomes]
rs10270560	1.00[EUR][1000 genomes]
rs10270911	1.00[EUR][1000 genomes]
rs10272979	1.00[EUR][1000 genomes]
rs10273127	1.00[EUR][1000 genomes]
rs10277086	1.00[EUR][1000 genomes]
rs10278264	1.00[EUR][1000 genomes]
rs10282150	1.00[EUR][1000 genomes]
rs10488302	1.00[EUR][1000 genomes]
rs11536582	1.00[EUR][1000 genomes]
rs12111645	1.00[EUR][1000 genomes]
rs12111791	1.00[EUR][1000 genomes]
rs12171571	1.00[EUR][1000 genomes]
rs13438753	1.00[EUR][1000 genomes]
rs1609181	0.95[EUR][1000 genomes]
rs16870516	1.00[EUR][1000 genomes]
rs17142844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17142852	1.00[EUR][1000 genomes]
rs17142856	1.00[EUR][1000 genomes]
rs17142860	1.00[EUR][1000 genomes]
rs17283053	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17355253	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2049643	1.00[EUR][1000 genomes]
rs28454884	0.95[EUR][1000 genomes]
rs60967957	1.00[EUR][1000 genomes]
rs6466749	1.00[EUR][1000 genomes]
rs6970111	0.97[EUR][1000 genomes]
rs73441852	1.00[EUR][1000 genomes]
rs7357256	1.00[EUR][1000 genomes]
rs9886093	1.00[EUR][1000 genomes]
rs9886190	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv516686	chr7:120015843-120223084	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv889117	chr7:120122040-120266458	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17347436	KCND2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120190800-120196200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:120191000-120196200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr7:120192200-120196200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr7:120192600-120196200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:120192800-120196000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr7:120192800-120196200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr7:120193000-120196200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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