Variant report

Variant	rs59827083
Chromosome Location	chr10:5738044-5738045
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:5724274..5728540-chr10:5734829..5741563,8	MCF-7	breast:
2	chr10:5735790..5738712-chr10:5931841..5933412,2	MCF-7	breast:
3	chr10:5726410..5728417-chr10:5738015..5741917,3	MCF-7	breast:
4	chr10:5737326..5739856-chr10:5853864..5856173,2	MCF-7	breast:
5	chr10:5733360..5736300-chr10:5737628..5741126,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000134461	Chromatin interaction
ENSG00000057608	Chromatin interaction
ENSG00000272764	Chromatin interaction
ENSG00000108021	Chromatin interaction
ENSG00000134452	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11254115	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11254828	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11254898	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12257412	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12571055	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12572339	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1567708	0.81[ASN][1000 genomes]
rs2246268	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2275772	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2669133	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2669139	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2797490	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2797492	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2797497	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34404996	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3750636	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3793708	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3924378	0.83[ASN][1000 genomes]
rs57103262	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58502403	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7089693	0.82[ASN][1000 genomes]
rs7096328	0.94[ASN][1000 genomes]
rs73610559	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	esv2759729	chr10:5557024-5804780	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	esv2758209	chr10:5637111-5804780	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	esv1796213	chr10:5716555-5766165	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv522415	chr10:5721653-5768493	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
8	nsv1050663	chr10:5737979-5785918	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5728800-5746800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr10:5734800-5763400	Weak transcription	HSMM	muscle
3	chr10:5735200-5738800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr10:5735200-5739000	Weak transcription	Fetal Intestine Large	intestine
5	chr10:5735200-5739400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr10:5735200-5739400	Weak transcription	Lung	lung
7	chr10:5735200-5739400	Weak transcription	Pancreas	Pancrea
8	chr10:5735200-5739800	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr10:5735200-5743000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr10:5735200-5749000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr10:5735200-5750600	Weak transcription	Gastric	stomach
12	chr10:5735200-5767000	Weak transcription	Fetal Muscle Leg	muscle
13	chr10:5735400-5738200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr10:5735400-5738200	Weak transcription	Right Atrium	heart
15	chr10:5735400-5738400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr10:5735400-5738600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr10:5735400-5739200	Weak transcription	Fetal Heart	heart
18	chr10:5735400-5739200	Weak transcription	Fetal Intestine Small	intestine
19	chr10:5735400-5739400	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr10:5735400-5739400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr10:5735400-5739400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr10:5735400-5739600	Weak transcription	Colonic Mucosa	Colon
23	chr10:5735400-5744800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr10:5735400-5750800	Weak transcription	Spleen	Spleen
25	chr10:5735400-5761600	Weak transcription	NHEK	skin
26	chr10:5735400-5762000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr10:5735600-5739000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr10:5735800-5739000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr10:5735800-5741800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr10:5735800-5752800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr10:5736000-5739600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr10:5736200-5739200	Weak transcription	Thymus	Thymus
33	chr10:5736200-5739400	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr10:5736200-5739600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr10:5736200-5740000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr10:5736200-5740200	Weak transcription	A549	lung
37	chr10:5736200-5742600	Weak transcription	Brain Angular Gyrus	brain
38	chr10:5736200-5751600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:5736400-5738200	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr10:5736400-5738200	Weak transcription	Fetal Thymus	thymus
41	chr10:5736400-5738200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr10:5736400-5739000	Weak transcription	Duodenum Mucosa	Duodenum
43	chr10:5736400-5739200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr10:5736400-5741000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr10:5736400-5753000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr10:5736600-5738600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr10:5736600-5739000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr10:5736600-5741600	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr10:5736800-5738400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr10:5736800-5739400	Weak transcription	Primary B cells from peripheral blood	blood

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