Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:30926791..30929464-chr13:30933560..30935693,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1275179	0.84[CEU][hapmap];0.85[EUR][1000 genomes]
rs1275180	0.86[EUR][1000 genomes]
rs1275181	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1291150	0.86[EUR][1000 genomes]
rs1621497	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs1754937	0.96[CEU][hapmap];0.96[EUR][1000 genomes]
rs17589894	0.80[EUR][1000 genomes]
rs202102	0.80[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs2077011	0.80[CEU][hapmap]
rs2149852	0.86[EUR][1000 genomes]
rs2149853	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2152945	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2183284	0.98[EUR][1000 genomes]
rs2185008	0.92[CEU][hapmap];0.94[JPT][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2185009	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7997259	0.85[EUR][1000 genomes]
rs9550555	0.81[AMR][1000 genomes]
rs9578163	0.86[EUR][1000 genomes]
rs9578165	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9579558	0.89[CEU][hapmap];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530602	chr13:30911025-31404272	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv455853	chr13:30911531-30951514	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv561394	chr13:30911531-30951514	Enhancers Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30920600-30929400	Weak transcription	Spleen	Spleen
2	chr13:30921400-30927200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr13:30921400-30928600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr13:30922200-30928800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr13:30922200-30937800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr13:30922800-30928400	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr13:30923200-30927200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr13:30924600-30940000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr13:30926400-30927800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr13:30926600-30927400	ZNF genes & repeats	Fetal Thymus	thymus
11	chr13:30926800-30927200	ZNF genes & repeats	Aorta	Aorta
12	chr13:30926800-30927600	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
13	chr13:30927000-30927200	Weak transcription	Thymus	Thymus
14	chr13:30927000-30927600	ZNF genes & repeats	Primary B cells from cord blood	blood
15	chr13:30927000-30927800	ZNF genes & repeats	Dnd41	blood

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