Variant report

Variant	rs6843444
Chromosome Location	chr4:81431685-81431686
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10009812	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs10033567	0.82[JPT][hapmap]
rs10857170	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11099248	1.00[ASN][1000 genomes]
rs11732671	0.98[ASN][1000 genomes]
rs11732964	0.98[ASN][1000 genomes]
rs12233833	0.95[ASN][1000 genomes]
rs12639952	0.95[ASN][1000 genomes]
rs12639967	0.95[ASN][1000 genomes]
rs12640833	0.81[ASN][1000 genomes]
rs12641282	0.91[ASN][1000 genomes]
rs12647975	0.86[ASN][1000 genomes]
rs12648193	0.98[ASN][1000 genomes]
rs12650756	1.00[ASN][1000 genomes]
rs13111397	1.00[ASN][1000 genomes]
rs13112370	1.00[ASN][1000 genomes]
rs13115510	0.83[ASN][1000 genomes]
rs13124220	0.87[ASN][1000 genomes]
rs13127693	0.87[ASN][1000 genomes]
rs13129636	1.00[ASN][1000 genomes]
rs13131230	0.85[ASN][1000 genomes]
rs13136894	0.95[ASN][1000 genomes]
rs13141796	0.95[ASN][1000 genomes]
rs13146627	1.00[ASN][1000 genomes]
rs13152141	0.93[ASN][1000 genomes]
rs1486023	0.95[ASN][1000 genomes]
rs1495484	0.84[ASN][1000 genomes]
rs1495490	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1531959	0.98[ASN][1000 genomes]
rs17004908	0.87[ASN][1000 genomes]
rs17004945	0.95[ASN][1000 genomes]
rs2172879	0.91[ASN][1000 genomes]
rs28494703	0.93[ASN][1000 genomes]
rs34636382	0.85[ASN][1000 genomes]
rs34890603	1.00[ASN][1000 genomes]
rs34938691	1.00[ASN][1000 genomes]
rs35308242	0.81[ASN][1000 genomes]
rs35466241	0.95[ASN][1000 genomes]
rs35565546	1.00[ASN][1000 genomes]
rs35990705	0.95[ASN][1000 genomes]
rs6820209	0.87[ASN][1000 genomes]
rs6829720	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6833553	0.93[ASN][1000 genomes]
rs6856538	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71596010	1.00[ASN][1000 genomes]
rs71596022	0.95[ASN][1000 genomes]
rs7672761	0.84[ASN][1000 genomes]
rs7678081	0.95[ASN][1000 genomes]
rs7684929	0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013945	chr4:81410029-81454166	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81430400-81434200	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr4:81430400-81434400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr4:81430600-81434200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr4:81431600-81431800	Flanking Active TSS	Pancreas	Pancrea

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