Variant report

Variant	rs8038148
Chromosome Location	chr15:42027000-42027001
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10152332	0.84[ASN][1000 genomes]
rs10152364	0.84[ASN][1000 genomes]
rs10775122	1.00[JPT][hapmap]
rs10775123	0.88[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10775124	0.84[ASN][1000 genomes]
rs11070345	0.84[ASN][1000 genomes]
rs11070347	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11632100	0.84[ASN][1000 genomes]
rs11634840	0.82[ASN][1000 genomes]
rs11855017	0.80[ASN][1000 genomes]
rs11856550	0.92[AMR][1000 genomes]
rs1197768	0.87[ASN][1000 genomes]
rs1197769	0.87[ASN][1000 genomes]
rs1197772	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12148330	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12441249	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12915325	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12916992	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1867416	0.81[ASN][1000 genomes]
rs1867417	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1880937	0.90[ASN][1000 genomes]
rs1880938	0.90[ASN][1000 genomes]
rs1899819	1.00[JPT][hapmap]
rs1899820	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1899821	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1918314	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2141141	0.84[ASN][1000 genomes]
rs2178004	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2250964	0.87[ASN][1000 genomes]
rs2577947	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2577950	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2577951	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2577953	0.87[ASN][1000 genomes]
rs2577954	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2577955	0.87[ASN][1000 genomes]
rs2577958	0.90[ASN][1000 genomes]
rs2577959	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2605570	0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs2695162	0.90[ASN][1000 genomes]
rs2695163	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2695164	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2695166	0.90[ASN][1000 genomes]
rs2695168	0.89[ASN][1000 genomes]
rs2695169	0.90[ASN][1000 genomes]
rs2918051	0.87[ASN][1000 genomes]
rs2925337	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2950446	0.83[ASN][1000 genomes]
rs3743028	0.88[ASN][1000 genomes]
rs4371125	0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs4465584	1.00[JPT][hapmap]
rs4923908	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4924568	0.84[ASN][1000 genomes]
rs4924571	0.84[ASN][1000 genomes]
rs4924572	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs62002069	0.84[ASN][1000 genomes]
rs7164209	0.84[ASN][1000 genomes]
rs7169496	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7169668	0.84[ASN][1000 genomes]
rs7177911	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7178205	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs8027390	0.84[ASN][1000 genomes]
rs8028886	0.80[ASN][1000 genomes]
rs8034261	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs8038783	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs8039440	1.00[JPT][hapmap];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049514	chr15:41958482-42081210	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1048655	chr15:41978391-42049360	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
4	nsv1036086	chr15:42004962-42091451	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv1041861	chr15:42016097-42062287	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1054671	chr15:42016097-42098896	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv1044347	chr15:42023805-42049360	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41972400-42065200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:41984200-42034800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:41989000-42041600	Weak transcription	Fetal Brain Male	brain
4	chr15:41996200-42034800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:42002200-42028400	Weak transcription	Pancreas	Pancrea
6	chr15:42003600-42027000	Weak transcription	Brain Germinal Matrix	brain
7	chr15:42003600-42028400	Weak transcription	Aorta	Aorta
8	chr15:42003800-42027200	Weak transcription	Spleen	Spleen
9	chr15:42003800-42028400	Weak transcription	Gastric	stomach
10	chr15:42003800-42028400	Weak transcription	Small Intestine	intestine
11	chr15:42003800-42056000	Weak transcription	Colonic Mucosa	Colon
12	chr15:42004000-42027000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr15:42005400-42027000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr15:42005400-42028400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr15:42005600-42027200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr15:42005600-42027400	Weak transcription	NHDF-Ad	bronchial
17	chr15:42005800-42027000	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr15:42005800-42028400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr15:42006000-42028400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr15:42006200-42027200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr15:42006200-42027200	Weak transcription	Colon Smooth Muscle	Colon
22	chr15:42006200-42034800	Weak transcription	A549	lung
23	chr15:42006400-42041400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr15:42006600-42027200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr15:42006800-42027400	Weak transcription	NHEK	skin
26	chr15:42009800-42056800	Weak transcription	Fetal Heart	heart
27	chr15:42016000-42028400	Weak transcription	Psoas Muscle	Psoas
28	chr15:42017400-42062600	Strong transcription	Primary T cells fromperipheralblood	blood
29	chr15:42019000-42037000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr15:42019200-42037200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr15:42019400-42032800	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr15:42019400-42036800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr15:42019400-42037000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr15:42019400-42060600	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr15:42020000-42036200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr15:42020400-42036200	Strong transcription	Fetal Thymus	thymus
37	chr15:42020600-42037000	Strong transcription	Hela-S3	cervix
38	chr15:42020800-42032600	Strong transcription	Fetal Muscle Trunk	muscle
39	chr15:42020800-42033000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr15:42021000-42036800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr15:42021200-42029000	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr15:42021200-42032600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr15:42021200-42032800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr15:42021800-42027000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr15:42021800-42028400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr15:42022000-42027000	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr15:42022200-42027200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr15:42022200-42028000	Weak transcription	HUVEC	blood vessel
49	chr15:42022400-42036800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr15:42022600-42027200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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