Variant report

Variant	rs10176681
Chromosome Location	chr2:58308159-58308160
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:58307014..58309268-chr2:58311845..58314843,2	K562	blood:
2	chr2:58272808..58275291-chr2:58306964..58308775,2	MCF-7	breast:
3	chr2:58304898..58306855-chr2:58308067..58311851,3	K562	blood:
4	chr2:58302165..58304819-chr2:58306974..58309943,3	K562	blood:

Variant related genes	Relation type
ENSG00000028116	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10165760	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs10174202	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10176942	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10178025	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10182762	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs10187411	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10203014	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1025755	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs11883874	0.90[YRI][hapmap];0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11891477	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs11892302	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs12104650	0.81[AFR][1000 genomes]
rs13382369	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13394820	0.98[AFR][1000 genomes]
rs13405281	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs13410500	0.92[YRI][hapmap];0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs13419989	0.96[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13431271	0.85[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1371213	0.89[AMR][1000 genomes]
rs17049333	1.00[ASN][1000 genomes]
rs17049337	1.00[ASN][1000 genomes]
rs17049338	1.00[ASN][1000 genomes]
rs17049414	1.00[ASN][1000 genomes]
rs2165100	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2165103	0.91[YRI][hapmap];0.95[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2312486	0.80[YRI][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28521626	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs4459722	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs57112138	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs57597086	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs58470176	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs60364084	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6718190	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs716758	0.89[AMR][1000 genomes]
rs72949131	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs72949137	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs72949158	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs72951042	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs72951048	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs72951056	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs73944804	0.94[AFR][1000 genomes]
rs7563312	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7569731	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7574578	0.91[YRI][hapmap];1.00[AMR][1000 genomes]
rs7574694	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7577402	1.00[ASN][1000 genomes]
rs7600213	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs9973345	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9973928	0.85[YRI][hapmap];0.95[AFR][1000 genomes];0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525988	chr2:58161520-58427786	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv999591	chr2:58214871-58316147	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv582097	chr2:58266099-58346966	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv874201	chr2:58269871-58350504	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv874202	chr2:58269871-58375688	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:58274800-58317400	Weak transcription	Fetal Muscle Trunk	muscle
2	chr2:58275000-58317400	Weak transcription	Colon Smooth Muscle	Colon
3	chr2:58275000-58321600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr2:58275000-58326600	Weak transcription	Pancreas	Pancrea
5	chr2:58275800-58316800	Weak transcription	HMEC	breast
6	chr2:58279000-58319000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:58279400-58315600	Weak transcription	Dnd41	blood
8	chr2:58282600-58350400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr2:58284200-58317600	Weak transcription	HepG2	liver
10	chr2:58284400-58325000	Weak transcription	NHEK	skin
11	chr2:58285200-58317000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr2:58286200-58317600	Weak transcription	K562	blood
13	chr2:58286400-58317600	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr2:58287200-58315800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr2:58288200-58311000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr2:58290400-58315800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr2:58291200-58316400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr2:58291600-58315600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr2:58291600-58316200	Weak transcription	HUVEC	blood vessel
20	chr2:58291600-58317800	Weak transcription	HSMM	muscle
21	chr2:58291600-58317800	Weak transcription	NH-A	brain
22	chr2:58291600-58319000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr2:58291600-58321800	Weak transcription	Fetal Thymus	thymus
24	chr2:58291600-58325000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr2:58291800-58318800	Weak transcription	Osteobl	bone
26	chr2:58292000-58316200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr2:58292200-58316200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr2:58292200-58319000	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr2:58292200-58319000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr2:58294200-58320800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr2:58297000-58316800	Weak transcription	Ovary	ovary
32	chr2:58297200-58311400	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr2:58297600-58319000	Weak transcription	Primary T cells from cord blood	blood
34	chr2:58297800-58316400	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr2:58297800-58317000	Weak transcription	Fetal Intestine Large	intestine
36	chr2:58298000-58315800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:58298000-58317600	Weak transcription	Left Ventricle	heart
38	chr2:58298200-58313400	Weak transcription	Liver	Liver
39	chr2:58298200-58315600	Weak transcription	Adipose Nuclei	Adipose
40	chr2:58298200-58316200	Weak transcription	Fetal Lung	lung
41	chr2:58298200-58317000	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr2:58301600-58319200	Weak transcription	Psoas Muscle	Psoas
43	chr2:58302400-58311200	Weak transcription	Primary B cells from cord blood	blood
44	chr2:58302400-58313400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr2:58302400-58315800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr2:58302400-58317200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:58302600-58310800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:58302600-58312600	Weak transcription	Primary B cells from peripheral blood	blood
49	chr2:58302600-58315200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:58302600-58315600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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