Variant report

Variant	rs2366736
Chromosome Location	chr2:32392448-32392449
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:32392057-32392471	K562	blood:	n/a	n/a
2	POLR2A	chr2:32392122-32393066	HepG2	liver:	n/a	n/a
3	ZNF384	chr2:32392405-32392553	GM12878	blood:	n/a	n/a
4	ZNF384	chr2:32392286-32392677	K562	blood:	n/a	n/a
5	POLR2A	chr2:32390504-32392571	K562	blood:	n/a	n/a
6	CBX3	chr2:32392334-32393217	K562	blood:	n/a	n/a
7	POU2F2	chr2:32392343-32392780	GM12878	blood:	n/a	n/a
8	POLR2A	chr2:32392427-32393233	HepG2	liver:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:32263820..32266854-chr2:32389080..32393861,5	MCF-7	breast:
2	chr2:32391365..32393354-chr2:32406873..32408474,2	K562	blood:
3	chr2:32390024..32393805-chr2:32579476..32583220,6	K562	blood:
4	chr2:32286352..32290626-chr2:32388602..32393371,12	K562	blood:
5	chr2:32389583..32392652-chr2:32503120..32506003,3	K562	blood:
6	chr2:32338831..32341439-chr2:32391344..32393556,2	K562	blood:
7	chr2:32286363..32290764-chr2:32387862..32393371,13	K562	blood:
8	chr2:32287157..32290220-chr2:32389830..32392599,3	MCF-7	breast:
9	chr2:32235154..32237462-chr2:32390889..32392468,2	MCF-7	breast:
10	chr2:32233185..32238105-chr2:32388775..32395245,11	K562	blood:
11	chr2:32233077..32237611-chr2:32388376..32395245,10	K562	blood:
12	chr2:32206318..32208970-chr2:32391722..32393852,2	K562	blood:
13	chr2:32389277..32392458-chr2:32500839..32506003,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000272716	TF binding region
ENSG00000021574	Chromatin interaction
ENSG00000162961	Chromatin interaction
ENSG00000119820	Chromatin interaction
ENSG00000162959	Chromatin interaction
ENSG00000115760	Chromatin interaction

Extended variants
information (count: 103 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10172468	0.85[CEU][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10208246	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10490360	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs11124274	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs11124275	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs11124278	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11676475	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11676938	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs11678119	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs12465124	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12465351	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.97[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12474598	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12614686	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs12989936	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs12997026	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.87[YRI][hapmap];0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13017189	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs13022197	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs13427170	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs177083	0.96[CEU][hapmap];0.81[EUR][1000 genomes]
rs17767988	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs212679	0.96[JPT][hapmap]
rs212686	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs212687	1.00[CEU][hapmap];0.91[JPT][hapmap];0.93[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs212694	0.83[EUR][1000 genomes]
rs212703	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs212704	0.96[CEU][hapmap];0.80[EUR][1000 genomes]
rs212706	0.83[CEU][hapmap]
rs212707	0.81[CEU][hapmap]
rs212708	0.83[CEU][hapmap]
rs212713	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs212715	0.91[CHB][hapmap];0.96[JPT][hapmap]
rs212716	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs212717	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs212738	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs212739	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs212740	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs212741	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs212743	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs212744	1.00[CEU][hapmap];0.96[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs212745	0.95[JPT][hapmap]
rs212746	0.96[JPT][hapmap]
rs212748	1.00[CEU][hapmap];0.96[JPT][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs212749	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs212753	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs212755	1.00[CEU][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs212757	0.87[EUR][1000 genomes]
rs212760	0.96[JPT][hapmap]
rs212762	0.95[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs216544	0.83[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs2280967	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2280973	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2365555	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs3752916	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3752917	0.83[AMR][1000 genomes]
rs3769602	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs3769604	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs3769606	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs385076	0.83[CHB][hapmap]
rs3851308	0.86[AMR][1000 genomes]
rs4258846	0.82[ASN][1000 genomes]
rs435572	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4407291	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs443609	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4519572	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs467523	0.88[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs479333	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4952209	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4952248	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs4952250	1.00[CHB][hapmap];0.96[JPT][hapmap]
rs4952252	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55877106	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56208031	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62134021	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs659239	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6716179	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6717209	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.97[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6723154	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs6725184	0.87[CHB][hapmap]
rs6737500	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs6748621	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs6752375	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs6758024	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs6760105	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs6761417	0.83[AMR][1000 genomes]
rs72863940	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7561519	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs7566162	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs7572964	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs7573543	1.00[CHB][hapmap];0.96[JPT][hapmap]
rs7577696	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs7581340	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7581432	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7586448	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs7588883	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7601267	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs7605242	1.00[CHB][hapmap];0.92[JPT][hapmap]

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	nsv949102	chr2:32030307-33011548	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv833670	chr2:32295778-32481857	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS 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	25 gene(s)	inside rSNPs	diseases
3	nsv873778	chr2:32297984-32409007	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking 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	23 gene(s)	inside rSNPs	diseases
4	nsv817386	chr2:32332893-32724794	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1001038	chr2:32333378-32657112	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
6	nsv1009359	chr2:32333378-32725117	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv535613	chr2:32333378-32725117	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2366736	NLRC4	cis	Lymphoblastoid	GTEx

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:32389400-32392600	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr2:32389400-32392600	Active TSS	K562	blood
3	chr2:32391400-32401800	Weak transcription	Spleen	Spleen
4	chr2:32391400-32402000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:32391400-32402000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:32391600-32392800	Enhancers	Primary B cells from peripheral blood	blood
7	chr2:32391600-32392800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
8	chr2:32391600-32397200	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr2:32391600-32397400	Weak transcription	Left Ventricle	heart
10	chr2:32391600-32401800	Weak transcription	Gastric	stomach
11	chr2:32391600-32402000	Weak transcription	Esophagus	oesophagus
12	chr2:32391600-32402800	Weak transcription	Lung	lung
13	chr2:32391600-32403400	Weak transcription	Aorta	Aorta
14	chr2:32391600-32406600	Weak transcription	Small Intestine	intestine
15	chr2:32391600-32409600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr2:32391600-32426400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr2:32391600-32452800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr2:32391800-32392600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr2:32391800-32392800	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr2:32391800-32392800	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr2:32391800-32393000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr2:32391800-32393200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr2:32391800-32393200	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr2:32391800-32394600	Weak transcription	Right Atrium	heart
25	chr2:32391800-32396800	Weak transcription	Fetal Muscle Leg	muscle
26	chr2:32391800-32397200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr2:32391800-32397200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr2:32391800-32397600	Weak transcription	Fetal Thymus	thymus
29	chr2:32391800-32397600	Weak transcription	Ovary	ovary
30	chr2:32391800-32397800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr2:32391800-32400200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr2:32391800-32400200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr2:32391800-32401800	Weak transcription	Brain Substantia Nigra	brain
34	chr2:32391800-32409600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr2:32391800-32431400	Weak transcription	Stomach Mucosa	stomach
36	chr2:32391800-32453800	Weak transcription	Colonic Mucosa	Colon
37	chr2:32392000-32392600	Enhancers	NHDF-Ad	bronchial
38	chr2:32392000-32392800	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr2:32392000-32392800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr2:32392000-32393000	Genic enhancers	Brain Cingulate Gyrus	brain
41	chr2:32392000-32395600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:32392000-32397000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr2:32392000-32397000	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr2:32392000-32397000	Weak transcription	Primary T cells from cord blood	blood
45	chr2:32392000-32397000	Weak transcription	Fetal Brain Female	brain
46	chr2:32392000-32397000	Weak transcription	NH-A	brain
47	chr2:32392000-32397200	Weak transcription	Primary B cells from cord blood	blood
48	chr2:32392000-32397200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr2:32392000-32397200	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr2:32392000-32397400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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