Variant report

Variant	rs16970132
Chromosome Location	chr15:40281772-40281773
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11070241	0.83[JPT][hapmap]
rs12441486	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12591670	0.83[JPT][hapmap]
rs12901892	0.83[JPT][hapmap]
rs1436276	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1436278	0.87[JPT][hapmap];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1689605	0.85[GIH][hapmap];0.88[JPT][hapmap]
rs16970030	0.88[JPT][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16970033	1.00[GIH][hapmap];0.88[JPT][hapmap];0.90[MEX][hapmap];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16970098	0.87[JPT][hapmap];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16970164	1.00[CEU][hapmap]
rs16970168	0.94[JPT][hapmap]
rs2196470	0.88[JPT][hapmap];0.87[AMR][1000 genomes]
rs2279580	0.94[JPT][hapmap]
rs2291623	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2307102	1.00[CEU][hapmap]
rs2307105	1.00[GIH][hapmap];0.85[MEX][hapmap];0.83[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2307106	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2307107	0.83[JPT][hapmap];0.98[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2640645	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28369403	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28619481	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2898974	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs35390951	0.88[JPT][hapmap]
rs3765127	0.95[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4566130	0.84[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.93[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs472027	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs479500	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs503671	0.88[JPT][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs509200	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs510949	1.00[GIH][hapmap];0.85[MEX][hapmap];0.83[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs514152	1.00[GIH][hapmap];0.85[MEX][hapmap];0.83[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs518802	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs536503	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs548091	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7165105	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7170569	0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7174767	1.00[GIH][hapmap];0.85[MEX][hapmap];0.83[TSI][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7178419	0.83[JPT][hapmap]
rs72729459	0.87[AMR][1000 genomes]
rs72729462	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72729469	0.85[AMR][1000 genomes]
rs72729490	0.97[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72729494	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8029465	0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs8036381	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8036388	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9888665	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530816	chr15:40003136-40586792	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv428635	chr15:40274500-40436293	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40227400-40283400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:40228200-40323800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr15:40236600-40303000	Weak transcription	Small Intestine	intestine
4	chr15:40249000-40304800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr15:40250000-40294800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr15:40250200-40299600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr15:40260800-40303400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr15:40262600-40293800	Weak transcription	Stomach Mucosa	stomach
9	chr15:40266400-40281800	Weak transcription	K562	blood
10	chr15:40269000-40284800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr15:40269000-40293200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:40269000-40293200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr15:40269200-40282000	Weak transcription	Esophagus	oesophagus
14	chr15:40269200-40283000	Weak transcription	Psoas Muscle	Psoas
15	chr15:40269400-40283000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr15:40269600-40282400	Weak transcription	Fetal Brain Male	brain
17	chr15:40269600-40295600	Weak transcription	Fetal Heart	heart
18	chr15:40269800-40285400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr15:40270400-40282400	Weak transcription	Primary B cells from peripheral blood	blood
20	chr15:40276400-40295600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr15:40277600-40287400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:40277600-40288000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr15:40277600-40288000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:40277600-40288400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:40277600-40294600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr15:40277600-40303600	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr15:40277600-40303800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr15:40277600-40304400	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr15:40277800-40283800	Strong transcription	HUVEC	blood vessel
30	chr15:40277800-40284200	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr15:40277800-40285800	Strong transcription	Brain Cingulate Gyrus	brain
32	chr15:40277800-40286000	Strong transcription	Brain Anterior Caudate	brain
33	chr15:40277800-40286600	Strong transcription	Skeletal Muscle Male	skeletal muscle
34	chr15:40277800-40286600	Strong transcription	A549	lung
35	chr15:40277800-40286600	Strong transcription	Dnd41	blood
36	chr15:40277800-40286600	Strong transcription	HSMM	muscle
37	chr15:40277800-40286600	Strong transcription	NHDF-Ad	bronchial
38	chr15:40277800-40286600	Strong transcription	NHEK	skin
39	chr15:40277800-40286600	Strong transcription	Osteobl	bone
40	chr15:40277800-40286800	Strong transcription	Muscle Satellite Cultured Cells	--
41	chr15:40277800-40287000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr15:40277800-40287600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr15:40277800-40287800	Strong transcription	Rectal Smooth Muscle	rectum
44	chr15:40277800-40288000	Strong transcription	HMEC	breast
45	chr15:40277800-40288200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr15:40277800-40288400	Strong transcription	NH-A	brain
47	chr15:40277800-40288600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr15:40277800-40288800	Strong transcription	Placenta	Placenta
49	chr15:40277800-40288800	Strong transcription	Fetal Stomach	stomach
50	chr15:40277800-40290200	Strong transcription	Ovary	ovary

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