Variant report

Variant	rs2012614
Chromosome Location	chr2:116202767-116202768
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10221735	0.85[ASN][1000 genomes]
rs10496493	0.85[ASN][1000 genomes]
rs13014804	0.91[ASN][1000 genomes]
rs13401718	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13408150	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1375146	0.92[ASN][1000 genomes]
rs1375147	0.92[ASN][1000 genomes]
rs1448461	0.90[ASN][1000 genomes]
rs1597190	0.92[ASN][1000 genomes]
rs1597191	0.92[ASN][1000 genomes]
rs1628917	0.87[ASN][1000 genomes]
rs1666950	0.92[ASN][1000 genomes]
rs17044463	0.81[ASN][1000 genomes]
rs1712004	0.91[ASN][1000 genomes]
rs1839135	0.92[ASN][1000 genomes]
rs1839136	0.92[ASN][1000 genomes]
rs1839137	0.92[ASN][1000 genomes]
rs1850446	0.90[ASN][1000 genomes]
rs1955167	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2166905	0.92[ASN][1000 genomes]
rs2677296	0.90[ASN][1000 genomes]
rs2901335	0.92[ASN][1000 genomes]
rs4378817	0.85[ASN][1000 genomes]
rs4417722	0.92[ASN][1000 genomes]
rs4530380	0.91[ASN][1000 genomes]
rs55929901	0.84[ASN][1000 genomes]
rs61080124	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6542263	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6542264	0.92[ASN][1000 genomes]
rs6707490	0.85[ASN][1000 genomes]
rs6710379	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs708650	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs717522	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72959740	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7562993	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7565824	0.91[ASN][1000 genomes]
rs7573129	0.90[ASN][1000 genomes]
rs7595751	0.85[ASN][1000 genomes]
rs7600133	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs843384	0.93[ASN][1000 genomes]
rs843397	0.93[ASN][1000 genomes]
rs843407	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs843415	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs843427	0.89[ASN][1000 genomes]
rs843428	0.86[ASN][1000 genomes]
rs843429	0.89[ASN][1000 genomes]
rs843432	0.89[ASN][1000 genomes]
rs979519	0.90[ASN][1000 genomes]
rs979520	0.92[ASN][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	nsv874919	chr2:116130709-116219686	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1014859	chr2:116196951-116938584	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:116196600-116203400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:116196800-116203400	Weak transcription	Pancreas	Pancrea
3	chr2:116201600-116204600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
4	chr2:116201600-116205000	Weak transcription	Fetal Brain Male	brain
5	chr2:116201800-116203400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:116202200-116205000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:116202400-116204000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell

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