Variant report

Variant	rs4832257
Chromosome Location	chr2:86453919-86453920
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:86451560..86455569-chr2:86456212..86459487,3	K562	blood:
2	chr2:86452854..86455973-chr2:86457257..86460636,3	K562	blood:
3	chr2:86453452..86455586-chr2:86457167..86459065,2	MCF-7	breast:

Extended variants
information (count: 54 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1019592	0.91[MEX][hapmap]
rs1025104	0.91[MEX][hapmap]
rs1075622	0.91[MEX][hapmap]
rs11127017	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12622691	0.90[ASN][1000 genomes]
rs12622715	0.90[CHB][hapmap];0.81[JPT][hapmap];0.90[ASN][1000 genomes]
rs1424520	0.91[MEX][hapmap]
rs1559512	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1559515	0.91[MEX][hapmap]
rs1991106	0.91[MEX][hapmap]
rs2241436	0.91[MEX][hapmap]
rs2288118	0.91[MEX][hapmap]
rs2288120	0.91[MEX][hapmap]
rs2288121	0.83[CHB][hapmap]
rs2367202	0.91[MEX][hapmap]
rs311565	0.82[MEX][hapmap]
rs311567	0.80[CHD][hapmap]
rs311572	0.82[MEX][hapmap]
rs3770069	0.91[MEX][hapmap]
rs4832244	0.91[MEX][hapmap]
rs4832245	0.91[MEX][hapmap]
rs4832249	0.91[MEX][hapmap]
rs4832250	0.80[CHD][hapmap];0.91[MEX][hapmap]
rs4832255	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4832256	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57367442	0.90[ASN][1000 genomes]
rs6740228	0.91[MEX][hapmap]
rs6750581	0.91[MEX][hapmap]
rs749579	1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs749581	0.82[CEU][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7598787	0.91[MEX][hapmap]
rs7606421	0.91[MEX][hapmap]
rs918859	0.82[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751903	chr2:86253542-86505453	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv531380	chr2:86253552-86469217	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv1007474	chr2:86281967-86505453	Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv997563	chr2:86281967-86506132	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv1008924	chr2:86282722-86499402	Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
6	nsv999956	chr2:86285944-86505453	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	nsv1012768	chr2:86285944-86506132	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv1003207	chr2:86286314-86496732	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1000441	chr2:86286314-86508168	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
10	nsv535808	chr2:86286314-86508168	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
11	nsv1004442	chr2:86286480-86506132	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
12	nsv916616	chr2:86289130-86509326	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv458563	chr2:86292341-86507688	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	nsv582370	chr2:86292341-86507688	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
15	nsv1009140	chr2:86294939-86506132	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
16	nsv582371	chr2:86296566-86507688	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer 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 miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv531381	chr2:86301091-86478346	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers 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 miRNA target site	47 gene(s)	inside rSNPs	diseases
18	nsv1001157	chr2:86301440-86508168	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
19	esv3412938	chr2:86370969-86867936	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
20	nsv458574	chr2:86385728-86507688	Enhancers Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
21	nsv582372	chr2:86385728-86507688	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs4832257	POLR1A	cis	cerebellum	SCAN
rs4832257	PTCD3	cis	parietal	SCAN
rs4832257	POLR1A	cis	parietal	SCAN
rs4832257	IMMT	cis	parietal	SCAN
rs4832257	POLR1A	cis	Esophagus Muscularis	GTEx
rs4832257	MRPL35	cis	Artery Tibial	GTEx
rs4832257	VAMP5	cis	cerebellum	SCAN
rs4832257	MRPL35	cis	Esophagus Muscularis	GTEx
rs4832257	RNF181	cis	cerebellum	SCAN
rs4832257	MRPL35	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86448200-86454600	Enhancers	Fetal Muscle Leg	muscle
2	chr2:86448200-86454600	Enhancers	Left Ventricle	heart
3	chr2:86449000-86454200	Enhancers	Fetal Heart	heart
4	chr2:86450200-86458200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr2:86450800-86455200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:86450800-86455400	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr2:86450800-86457200	Weak transcription	Pancreas	Pancrea
8	chr2:86450800-86463400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:86450800-86476400	Weak transcription	Fetal Brain Male	brain
10	chr2:86451400-86458000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:86451600-86456200	Weak transcription	Fetal Intestine Large	intestine
12	chr2:86451600-86457200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr2:86451600-86458000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr2:86451800-86455400	Enhancers	Lung	lung
15	chr2:86451800-86457200	Enhancers	Primary B cells from cord blood	blood
16	chr2:86451800-86457200	Enhancers	Primary B cells from peripheral blood	blood
17	chr2:86451800-86459600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:86451800-86462400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:86452000-86456600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr2:86452000-86462200	Weak transcription	HSMMtube	muscle
21	chr2:86452200-86461800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr2:86452400-86458000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:86452400-86458000	Weak transcription	Fetal Lung	lung
24	chr2:86452400-86467400	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr2:86452400-86477400	Weak transcription	Brain Angular Gyrus	brain
26	chr2:86453000-86455200	Weak transcription	NHEK	skin
27	chr2:86453000-86456200	Weak transcription	Brain Anterior Caudate	brain
28	chr2:86453000-86456200	Weak transcription	Fetal Intestine Small	intestine
29	chr2:86453000-86461600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr2:86453000-86461600	Weak transcription	Colon Smooth Muscle	Colon
31	chr2:86453200-86454400	Enhancers	GM12878-XiMat	blood
32	chr2:86453200-86455200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr2:86453200-86455800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:86453200-86456200	Weak transcription	Fetal Muscle Trunk	muscle
35	chr2:86453200-86456200	Weak transcription	Fetal Thymus	thymus
36	chr2:86453200-86456600	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr2:86453200-86457600	Weak transcription	Fetal Stomach	stomach
38	chr2:86453200-86458200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:86453200-86459200	Weak transcription	Esophagus	oesophagus
40	chr2:86453200-86462200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr2:86453200-86467600	Weak transcription	Spleen	Spleen
42	chr2:86453200-86468400	Weak transcription	Gastric	stomach
43	chr2:86453200-86475800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr2:86453400-86454000	Weak transcription	Brain Hippocampus Middle	brain
45	chr2:86453400-86456200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr2:86453400-86457800	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr2:86453400-86461800	Weak transcription	Right Atrium	heart
48	chr2:86453400-86470400	Weak transcription	Aorta	Aorta
49	chr2:86453600-86454400	Weak transcription	Stomach Smooth Muscle	stomach
50	chr2:86453600-86455600	Strong transcription	Fetal Brain Female	brain

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