Variant report

Variant	rs2523982
Chromosome Location	chr6:30083070-30083071
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1034326	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1034327	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1541269	0.87[EUR][1000 genomes]
rs2239529	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2245420	0.83[EUR][1000 genomes]
rs2249099	0.83[EUR][1000 genomes]
rs2427749	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2517595	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2517596	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2517597	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2517598	0.83[EUR][1000 genomes]
rs2523976	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2523977	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2523979	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2523981	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2523983	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2523984	0.83[EUR][1000 genomes]
rs2523985	0.83[EUR][1000 genomes]
rs2523986	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2523987	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2523988	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2523989	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2523992	0.81[ASN][1000 genomes]
rs2844790	0.88[EUR][1000 genomes]
rs2844792	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2844793	0.88[AFR][1000 genomes];0.85[EUR][1000 genomes];0.84[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	nsv884055	chr6:30078275-30087776	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2523982	HLA-C	Cis_chr	lymphoblastoid	RTeQTL

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30082000-30089400	Weak transcription	Duodenum Mucosa	Duodenum
2	chr6:30082200-30083400	Weak transcription	GM12878-XiMat	blood
3	chr6:30082200-30086400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr6:30082200-30087400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr6:30082400-30087200	Weak transcription	Hela-S3	cervix
6	chr6:30082400-30091000	Weak transcription	HepG2	liver
7	chr6:30082600-30086400	Weak transcription	Stomach Mucosa	stomach
8	chr6:30082600-30086400	Weak transcription	A549	lung
9	chr6:30082800-30086200	Weak transcription	Fetal Intestine Large	intestine
10	chr6:30082800-30086200	Weak transcription	Fetal Intestine Small	intestine

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