Variant report

Variant	rs2987836
Chromosome Location	chr10:25774337-25774338
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:25773471..25775405-chr10:25777171..25778749,2	K562	blood:
2	chr10:25766334..25768605-chr10:25771419..25774517,3	K562	blood:
3	chr10:25773088..25775353-chr10:25781192..25783925,2	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10508695	0.99[ASN][1000 genomes]
rs10508696	0.99[ASN][1000 genomes]
rs1069531	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11014576	0.99[ASN][1000 genomes]
rs12415532	0.90[ASN][1000 genomes]
rs12763436	0.95[ASN][1000 genomes]
rs12766947	0.99[ASN][1000 genomes]
rs12770449	0.95[ASN][1000 genomes]
rs12770880	0.95[ASN][1000 genomes]
rs12778509	0.99[ASN][1000 genomes]
rs1329255	0.83[ASN][1000 genomes]
rs1329256	0.83[ASN][1000 genomes]
rs1329257	0.84[ASN][1000 genomes]
rs1360123	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1361634	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1410931	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1590833	0.86[ASN][1000 genomes]
rs1592137	0.89[ASN][1000 genomes]
rs1620326	1.00[ASN][1000 genomes]
rs1773636	0.94[EUR][1000 genomes]
rs1773637	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1928365	0.83[ASN][1000 genomes]
rs2211344	0.88[EUR][1000 genomes]
rs2480348	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2480349	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2487819	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2987832	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987833	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987834	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987835	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987838	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987839	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987840	0.83[ASN][1000 genomes]
rs3005181	0.83[ASN][1000 genomes]
rs3005182	0.83[ASN][1000 genomes]
rs3005187	0.81[ASN][1000 genomes]
rs3005189	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3005191	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3005193	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3005194	0.94[EUR][1000 genomes]
rs3123901	0.83[ASN][1000 genomes]
rs34535236	0.99[ASN][1000 genomes]
rs36146927	0.94[ASN][1000 genomes]
rs4408231	0.93[EUR][1000 genomes]
rs4545439	0.86[ASN][1000 genomes]
rs4630196	0.85[EUR][1000 genomes]
rs57048226	0.99[ASN][1000 genomes]
rs66516873	0.99[ASN][1000 genomes]
rs67290477	0.99[ASN][1000 genomes]
rs67616835	0.99[ASN][1000 genomes]
rs702977	0.89[EUR][1000 genomes]
rs702980	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7075106	0.92[ASN][1000 genomes]
rs7084979	0.99[ASN][1000 genomes]
rs7085111	0.99[ASN][1000 genomes]
rs7086959	0.92[ASN][1000 genomes]
rs7089568	0.96[ASN][1000 genomes]
rs824588	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824589	0.87[EUR][1000 genomes]
rs824607	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824608	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824609	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824610	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[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	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25756800-25775000	Weak transcription	K562	blood
2	chr10:25765800-25782800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:25769600-25777800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr10:25770400-25774800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr10:25771000-25774600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr10:25772200-25774800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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