Variant report

Variant	rs2675957
Chromosome Location	chr2:233754364-233754365
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	chr2:233746656..233750390-chr2:233751961..233755416,5	K562	blood:
2	chr2:233748378..233751543-chr2:233754163..233756692,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000066248	Chromatin interaction

Extended variants
information (count: 63 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10933411	0.91[ASN][1000 genomes]
rs10933412	0.91[ASN][1000 genomes]
rs11676216	0.91[ASN][1000 genomes]
rs12694917	0.91[ASN][1000 genomes]
rs1446310	0.81[ASN][1000 genomes]
rs1446311	0.91[ASN][1000 genomes]
rs1562288	0.82[AFR][1000 genomes]
rs1867778	0.81[ASN][1000 genomes]
rs1947105	0.93[ASN][1000 genomes]
rs2044449	0.93[ASN][1000 genomes]
rs2100053	0.93[ASN][1000 genomes]
rs2166441	0.86[AFR][1000 genomes]
rs2250654	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2250665	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2305137	0.91[ASN][1000 genomes]
rs2305141	0.81[ASN][1000 genomes]
rs2592102	0.94[ASN][1000 genomes]
rs2592113	0.81[ASN][1000 genomes]
rs2592115	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2592116	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2592117	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2592121	0.82[AFR][1000 genomes]
rs2592126	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2674839	0.81[ASN][1000 genomes]
rs2675966	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2675967	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2675971	0.94[ASN][1000 genomes]
rs2675973	0.91[ASN][1000 genomes]
rs2675974	0.91[ASN][1000 genomes]
rs283466	0.81[ASN][1000 genomes]
rs3816334	0.91[ASN][1000 genomes]
rs4973053	0.81[ASN][1000 genomes]
rs4973054	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4973055	0.91[ASN][1000 genomes]
rs4973056	0.90[ASN][1000 genomes]
rs4973561	0.81[ASN][1000 genomes]
rs6437074	0.91[ASN][1000 genomes]
rs6719061	0.83[ASN][1000 genomes]
rs709933	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs709934	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs709938	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7558609	0.83[ASN][1000 genomes]
rs7573208	0.83[ASN][1000 genomes]
rs7587309	0.91[ASN][1000 genomes]
rs7589201	0.94[ASN][1000 genomes]
rs778338	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs778339	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs778340	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs778368	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs809639	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs812383	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs895430	0.94[ASN][1000 genomes]
rs991873	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948470	chr2:233166262-233886732	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1005123	chr2:233227729-233920152	Enhancers Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv536173	chr2:233227729-233920152	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv834570	chr2:233639160-233805067	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1009825	chr2:233709566-233763470	Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv984452	chr2:233725452-233762965	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv999116	chr2:233733352-233759864	Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1007029	chr2:233733352-233760519	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv536179	chr2:233735380-233757170	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	esv3375822	chr2:233750908-233755306	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2675957	C2orf82	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:233726800-233755600	Weak transcription	HSMMtube	muscle
2	chr2:233742400-233755600	Weak transcription	Fetal Intestine Large	intestine
3	chr2:233742800-233755600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr2:233743000-233755800	Weak transcription	Brain Hippocampus Middle	brain
5	chr2:233743200-233759600	Strong transcription	Duodenum Mucosa	Duodenum
6	chr2:233744600-233755400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:233745200-233755600	Weak transcription	Brain Angular Gyrus	brain
8	chr2:233745200-233755800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr2:233745600-233759800	Strong transcription	Liver	Liver
10	chr2:233749200-233755600	Weak transcription	NHLF	lung
11	chr2:233749400-233766000	Weak transcription	A549	lung
12	chr2:233750000-233755600	Weak transcription	Brain Germinal Matrix	brain
13	chr2:233750600-233755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr2:233750600-233759800	Strong transcription	HepG2	liver
15	chr2:233750800-233761000	Weak transcription	Stomach Mucosa	stomach
16	chr2:233751000-233755600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr2:233751000-233766000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr2:233751200-233755400	Weak transcription	Pancreas	Pancrea
19	chr2:233751200-233755600	Weak transcription	Fetal Brain Female	brain
20	chr2:233751200-233755600	Weak transcription	Gastric	stomach
21	chr2:233751200-233758400	Weak transcription	Fetal Brain Male	brain
22	chr2:233751800-233755800	Weak transcription	Right Atrium	heart
23	chr2:233752400-233754400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:233753200-233754800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr2:233753200-233755400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr2:233753200-233755400	Weak transcription	Colonic Mucosa	Colon
27	chr2:233753200-233755600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr2:233753200-233757200	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr2:233753400-233754400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr2:233753400-233754400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr2:233753400-233755200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:233753400-233755400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:233753400-233755400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:233753400-233755600	Weak transcription	Esophagus	oesophagus
35	chr2:233753400-233755800	Weak transcription	Brain Anterior Caudate	brain
36	chr2:233753400-233756400	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr2:233754200-233755600	Weak transcription	Fetal Intestine Small	intestine

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