Variant report

Variant	rs4849143
Chromosome Location	chr2:113787356-113787357
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:113780916..113783936-chr2:113784891..113788063,3	K562	blood:
2	chr2:113778463..113780634-chr2:113785926..113787939,2	K562	blood:
3	chr2:113778463..113783936-chr2:113784891..113788081,5	K562	blood:

Extended variants
information (count: 67 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10187916	0.83[EUR][1000 genomes]
rs11123156	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11123158	0.84[CEU][hapmap];0.80[TSI][hapmap];0.82[EUR][1000 genomes]
rs12475423	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.90[TSI][hapmap];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12614012	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1374285	0.82[ASN][1000 genomes]
rs1374286	0.82[ASN][1000 genomes]
rs1446508	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1446521	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.80[EUR][1000 genomes]
rs1530548	0.82[ASN][1000 genomes]
rs1530550	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1530551	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1530552	0.82[ASN][1000 genomes]
rs1530553	0.82[ASN][1000 genomes]
rs1530554	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1813048	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1867832	0.83[EUR][1000 genomes]
rs1867833	0.83[EUR][1000 genomes]
rs1900287	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];0.95[MKK][hapmap];0.90[TSI][hapmap];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1900288	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1900289	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2100071	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MKK][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs2197578	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.90[TSI][hapmap];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2218557	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2251872	0.82[ASN][1000 genomes]
rs2252007	0.82[ASN][1000 genomes]
rs2441375	0.82[ASN][1000 genomes]
rs2441376	0.82[ASN][1000 genomes]
rs2472187	0.82[ASN][1000 genomes]
rs2515394	0.82[ASN][1000 genomes]
rs2515395	0.82[ASN][1000 genomes]
rs2515396	0.82[ASN][1000 genomes]
rs2515397	0.82[ASN][1000 genomes]
rs2515398	0.82[ASN][1000 genomes]
rs2515399	0.82[ASN][1000 genomes]
rs2515400	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2515404	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MKK][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs2862775	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2862776	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2862853	0.88[CEU][hapmap];0.88[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs315921	1.00[ASW][hapmap]
rs4848311	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4848312	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4849144	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.90[TSI][hapmap]
rs4849147	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6542110	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6724667	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.93[MKK][hapmap];0.90[TSI][hapmap];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6728769	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6733859	0.82[ASN][1000 genomes]
rs6748448	0.82[ASN][1000 genomes]
rs7557928	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7567108	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7569284	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.90[TSI][hapmap]
rs7570058	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7570159	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7570267	0.81[CHB][hapmap]
rs7570483	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7599662	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MKK][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs9678578	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MKK][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs990524	0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[MKK][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532471	chr2:113682449-113862981	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv997348	chr2:113688093-113986508	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1007254	chr2:113726982-113887782	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv535894	chr2:113726982-113887782	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv961339	chr2:113772508-113796318	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv874885	chr2:113783671-113807021	Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv874886	chr2:113786504-113792776	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4849143	IL36B	cis	Esophagus Mucosa	GTEx
rs4849143	LOC654433	cis	parietal	SCAN
rs4849143	IL36B	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113765600-113797400	Weak transcription	Gastric	stomach
2	chr2:113785800-113787400	Enhancers	K562	blood

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