Variant report

Variant	rs28538332
Chromosome Location	chr10:27087395-27087396
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:27085060..27087648-chr10:27098555..27100631,2	K562	blood:
2	chr10:27087122..27088975-chr10:27089037..27091906,2	MCF-7	breast:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10159978	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10764642	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10764644	0.92[AFR][1000 genomes]
rs10764645	0.85[AFR][1000 genomes]
rs10829055	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10829056	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10829057	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10829059	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10829061	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10829062	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10829068	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10829069	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10829072	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10829073	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10829074	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10829079	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10829083	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10829085	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10829088	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10829107	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11015262	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11015266	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs11015267	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs11015276	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs11015283	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015298	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11015300	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015308	1.00[EUR][1000 genomes]
rs11015313	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015340	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11015343	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12243481	0.92[AFR][1000 genomes]
rs12247684	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12256219	0.87[AFR][1000 genomes]
rs12265625	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12267091	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12358409	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1408530	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16927341	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7082503	0.86[EUR][1000 genomes]
rs718827	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3415799	chr10:26929831-27233591	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv933544	chr10:27005220-27111998	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv831812	chr10:27061506-27234267	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv971858	chr10:27066006-27157708	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27070800-27091800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr10:27071200-27089000	Weak transcription	Lung	lung
3	chr10:27071200-27089600	Weak transcription	Spleen	Spleen
4	chr10:27071400-27088600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr10:27073000-27088200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr10:27074800-27091600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr10:27074800-27091800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr10:27075000-27089400	Weak transcription	Left Ventricle	heart
9	chr10:27075000-27091600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr10:27075000-27104600	Weak transcription	Esophagus	oesophagus
11	chr10:27075200-27088400	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr10:27079800-27091800	Weak transcription	Fetal Heart	heart
13	chr10:27079800-27092200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr10:27080800-27092000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr10:27082200-27088400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr10:27082200-27105400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr10:27082600-27091600	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr10:27082600-27094000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr10:27082800-27087600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr10:27082800-27088400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr10:27083400-27087800	ZNF genes & repeats	GM12878-XiMat	blood
22	chr10:27083600-27089800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr10:27083600-27094800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr10:27085000-27088400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr10:27085200-27088400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr10:27085600-27119000	Weak transcription	Fetal Lung	lung
27	chr10:27085800-27088200	Weak transcription	Primary hematopoietic stem cells	blood
28	chr10:27085800-27095600	Enhancers	Primary B cells from peripheral blood	blood
29	chr10:27086000-27087600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr10:27086000-27090400	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr10:27086000-27093400	Weak transcription	Fetal Intestine Small	intestine
32	chr10:27086200-27087600	Weak transcription	Primary T cells from cord blood	blood
33	chr10:27086200-27087800	Enhancers	Primary B cells from cord blood	blood
34	chr10:27086200-27096600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr10:27086400-27088000	Enhancers	Brain Anterior Caudate	brain
36	chr10:27086400-27088200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr10:27086400-27088400	Enhancers	Brain Cingulate Gyrus	brain
38	chr10:27086600-27089200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr10:27086600-27089600	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr10:27086600-27110400	Weak transcription	Fetal Intestine Large	intestine
41	chr10:27086800-27088200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr10:27086800-27089400	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr10:27086800-27092000	Weak transcription	A549	lung
44	chr10:27087000-27087600	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr10:27087000-27087800	Enhancers	Fetal Thymus	thymus
46	chr10:27087000-27088000	Enhancers	Thymus	Thymus
47	chr10:27087000-27088000	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr10:27087000-27088600	Enhancers	Brain Substantia Nigra	brain
49	chr10:27087000-27089400	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr10:27087000-27097000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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