Variant report

Variant	rs13201341
Chromosome Location	chr6:25822661-25822662
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:25800380..25802142-chr6:25822216..25823807,2	K562	blood:
2	chr6:25800380..25801917-chr6:25822307..25825107,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs13191296	0.80[CEU][hapmap]
rs13191445	1.00[CEU][hapmap]
rs13192365	0.83[CEU][hapmap]
rs13192713	0.91[CEU][hapmap]
rs13195279	0.83[CEU][hapmap]
rs13196552	0.83[CEU][hapmap]
rs13198474	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs13199775	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs13200921	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs13202688	1.00[CEU][hapmap]
rs13207673	0.83[CEU][hapmap]
rs13211947	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13212534	1.00[CEU][hapmap]
rs13213957	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs13214280	0.83[CEU][hapmap]
rs16891235	0.83[CEU][hapmap]
rs17526722	1.00[CEU][hapmap]
rs17586553	0.83[CEU][hapmap]
rs17587226	0.91[CEU][hapmap]
rs34043431	0.84[EUR][1000 genomes]
rs34351439	0.84[EUR][1000 genomes]
rs34493019	0.86[EUR][1000 genomes]
rs36014129	0.81[EUR][1000 genomes]
rs3734523	0.83[CEU][hapmap]
rs3734528	0.83[CEU][hapmap]
rs3884025	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3949215	0.89[CEU][hapmap]
rs41266779	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4236040	0.91[CEU][hapmap]
rs55912630	0.84[EUR][1000 genomes]
rs68006638	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6913795	0.81[EUR][1000 genomes]
rs6939997	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs6940007	0.83[CEU][hapmap]
rs6940698	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs7748167	0.83[CEU][hapmap]
rs9295675	0.83[CEU][hapmap]
rs9461216	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs9461219	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs9461222	0.83[CEU][hapmap]
rs9467600	0.81[EUR][1000 genomes]
rs9467603	0.81[EUR][1000 genomes]
rs9467606	0.81[EUR][1000 genomes]
rs9467607	0.81[EUR][1000 genomes]
rs9467609	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs9467613	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs9467621	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs9467622	0.91[CEU][hapmap]
rs9467626	0.91[CEU][hapmap]
rs9467635	0.83[CEU][hapmap]
rs972087	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv427747	chr6:25641380-25908218	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
5	esv3344159	chr6:25822340-25822670	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs13201341	BTN3A2	Cis_1M	lymphoblastoid	RTeQTL
rs13201341	BTN3A2///BTN3A3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25821800-25829600	Weak transcription	Liver	Liver
2	chr6:25822400-25822800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:25822400-25823000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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