Variant report

Variant	rs10874811
Chromosome Location	chr1:94388143-94388144
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCLM-2	chr1:94388130-94389096	NONHSAT004559

Extended variants
information (count: 75 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10159000	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10489607	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10874809	0.84[CHB][hapmap]
rs10874812	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11165004	0.87[JPT][hapmap]
rs11165006	0.86[JPT][hapmap]
rs11165007	0.87[JPT][hapmap]
rs11165030	0.84[CHB][hapmap]
rs11165031	1.00[CHB][hapmap];0.95[CHD][hapmap];0.93[JPT][hapmap];0.95[ASN][1000 genomes]
rs11165034	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11165037	0.97[ASN][1000 genomes]
rs12068168	0.87[ASN][1000 genomes]
rs12068345	0.97[ASN][1000 genomes]
rs12089163	0.95[ASN][1000 genomes]
rs12122176	0.89[JPT][hapmap]
rs12122406	0.92[ASN][1000 genomes]
rs12125068	0.87[JPT][hapmap]
rs12129986	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12130623	0.93[ASN][1000 genomes]
rs12131163	0.92[ASN][1000 genomes]
rs12131247	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12134159	0.87[JPT][hapmap]
rs12135187	0.86[JPT][hapmap]
rs12135991	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12139561	0.87[JPT][hapmap]
rs12140014	0.87[JPT][hapmap]
rs12140097	0.97[ASN][1000 genomes]
rs12142384	0.87[JPT][hapmap]
rs12144277	0.80[JPT][hapmap]
rs12401354	0.89[ASN][1000 genomes]
rs12404613	0.82[CHB][hapmap]
rs12406885	0.87[JPT][hapmap]
rs12407732	0.87[JPT][hapmap]
rs12410342	0.87[JPT][hapmap]
rs12410985	0.84[CHB][hapmap]
rs1473711	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17100392	0.87[JPT][hapmap]
rs1852	0.90[CHB][hapmap]
rs1989020	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1989021	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2017736	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2092697	0.92[ASN][1000 genomes]
rs2143993	0.92[ASN][1000 genomes]
rs2273406	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2391324	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.93[JPT][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3170633	0.84[CHB][hapmap]
rs35674584	0.93[ASN][1000 genomes]
rs3761912	0.84[CHB][hapmap]
rs3827715	1.00[CHB][hapmap];0.91[CHD][hapmap];0.93[JPT][hapmap];0.98[ASN][1000 genomes]
rs41303970	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4573532	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4598495	0.95[ASN][1000 genomes]
rs57387172	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60120441	0.95[ASN][1000 genomes]
rs61667071	0.95[ASN][1000 genomes]
rs6680027	0.94[ASN][1000 genomes]
rs6681078	0.95[ASN][1000 genomes]
rs6687387	0.84[CHB][hapmap]
rs6688926	0.87[JPT][hapmap]
rs6696758	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6699912	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6700112	0.95[ASN][1000 genomes]
rs718873	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs718874	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs718875	1.00[CHB][hapmap];0.87[CHD][hapmap];0.93[JPT][hapmap];0.99[ASN][1000 genomes]
rs743119	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7517826	0.84[CHB][hapmap]
rs7533596	0.84[CHB][hapmap]
rs7536714	0.99[ASN][1000 genomes]
rs7544883	0.87[JPT][hapmap]
rs7546315	0.87[JPT][hapmap]
rs7549683	0.84[CHB][hapmap]
rs761889	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs769211	1.00[CHB][hapmap];0.91[CHD][hapmap];0.93[JPT][hapmap];0.95[ASN][1000 genomes]
rs960625	0.87[JPT][hapmap]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10874811	GCLM	cis	Thyroid	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94375600-94421200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:94386000-94390600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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