Variant report

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10214468	0.88[JPT][hapmap]
rs1165158	1.00[JPT][hapmap]
rs1165159	1.00[JPT][hapmap]
rs1165161	1.00[JPT][hapmap]
rs1165162	1.00[JPT][hapmap]
rs1165164	1.00[JPT][hapmap]
rs1165165	1.00[JPT][hapmap]
rs1165167	1.00[JPT][hapmap]
rs1165168	1.00[JPT][hapmap]
rs1165187	1.00[JPT][hapmap]
rs1165189	1.00[JPT][hapmap]
rs1177441	1.00[JPT][hapmap]
rs1179087	1.00[JPT][hapmap]
rs1182814	1.00[JPT][hapmap]
rs1184498	1.00[JPT][hapmap]
rs13200784	1.00[JPT][hapmap]
rs1324082	1.00[JPT][hapmap]
rs1408268	1.00[JPT][hapmap]
rs1575534	1.00[JPT][hapmap]
rs1780969	1.00[JPT][hapmap]
rs2296199	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3778275	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3799346	1.00[JPT][hapmap]
rs3823151	0.88[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs3823155	0.82[EUR][1000 genomes]
rs4576235	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes]
rs56777435	0.80[ASN][1000 genomes]
rs57739734	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58366507	0.80[ASN][1000 genomes]
rs629444	1.00[JPT][hapmap]
rs6456703	1.00[JPT][hapmap]
rs6909187	1.00[CHB][hapmap]
rs6913879	1.00[JPT][hapmap]
rs7753366	1.00[JPT][hapmap]
rs942377	1.00[JPT][hapmap]
rs942378	1.00[JPT][hapmap]
rs9467604	1.00[JPT][hapmap]
rs9467610	1.00[JPT][hapmap]
rs972086	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes]
rs972087	0.86[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv969355	chr6:25733459-25779530	Genic enhancers Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3799341	TRIM38	cis	lymphoblastoid	seeQTL

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25758600-25764200	Weak transcription	Pancreas	Pancrea
2	chr6:25758600-25777200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr6:25759400-25763800	Weak transcription	Fetal Intestine Small	intestine
4	chr6:25762200-25764000	Strong transcription	Rectal Mucosa Donor 31	rectum
5	chr6:25762200-25780400	Strong transcription	Liver	Liver
6	chr6:25762800-25765600	Strong transcription	Duodenum Mucosa	Duodenum
7	chr6:25763000-25764800	Strong transcription	Rectal Mucosa Donor 29	rectum
8	chr6:25763200-25764800	Strong transcription	Fetal Intestine Large	intestine

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