Variant report

Variant	rs2812212
Chromosome Location	chr13:50910525-50910526
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:50907927..50911991-chr13:50914729..50916836,3	K562	blood:
2	chr13:50910484..50912390-chr13:50913694..50915729,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASEH2B-3	chr13:50910372-50910540	NONHSAT033831
2	lnc-RNASEH2B-3	chr13:50910372-50910540	NONHSAT140130

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1149858	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1262865	0.85[EUR][1000 genomes]
rs1326125	1.00[CHB][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs1409279	0.82[CHB][hapmap];0.82[CHD][hapmap];0.86[JPT][hapmap]
rs2066684	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2109236	0.89[ASN][1000 genomes]
rs2159440	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2532966	0.89[ASN][1000 genomes]
rs2532967	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2532969	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2532970	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2580182	0.89[ASN][1000 genomes]
rs2580183	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740531	0.81[AFR][1000 genomes]
rs2740534	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2740535	0.85[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.84[YRI][hapmap];0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740538	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740540	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2762055	0.85[ASN][1000 genomes]
rs2762057	0.81[EUR][1000 genomes]
rs2762059	0.85[ASW][hapmap];0.81[CEU][hapmap];0.91[GIH][hapmap];0.88[TSI][hapmap];0.84[YRI][hapmap];0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2762061	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2762064	0.89[ASN][1000 genomes]
rs3990215	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs4942914	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs806352	0.82[CHB][hapmap];0.85[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035151	chr13:50513535-51167850	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1254 gene(s)	inside rSNPs	diseases
2	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
4	esv2752608	chr13:50550099-51054499	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1249 gene(s)	inside rSNPs	diseases
5	nsv900076	chr13:50710579-50912578	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv561632	chr13:50874346-50912578	Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50907000-50910600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr13:50908600-50911200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr13:50908800-50913800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr13:50909200-50910800	Weak transcription	Gastric	stomach
5	chr13:50909200-50918600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr13:50909400-50913800	Weak transcription	Fetal Intestine Small	intestine
7	chr13:50909400-50914200	Weak transcription	Fetal Heart	heart
8	chr13:50909400-50915200	Weak transcription	Fetal Kidney	kidney
9	chr13:50909600-50911000	Enhancers	K562	blood
10	chr13:50909600-50911600	Weak transcription	NH-A	brain
11	chr13:50909600-50912800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr13:50909600-50913200	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr13:50909800-50912200	Weak transcription	HepG2	liver
14	chr13:50909800-50914000	Weak transcription	Pancreas	Pancrea
15	chr13:50909800-50914400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr13:50909800-50915200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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