Variant report

Variant	rs28565083
Chromosome Location	chr15:40121121-40121122
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11070235	0.86[ASN][1000 genomes]
rs1166729	0.84[ASN][1000 genomes]
rs11854663	0.87[ASN][1000 genomes]
rs11855441	0.87[ASN][1000 genomes]
rs12438821	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12442442	0.87[ASN][1000 genomes]
rs1436274	0.86[ASN][1000 genomes]
rs1836850	0.97[ASN][1000 genomes]
rs1865754	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28401568	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35194933	0.95[ASN][1000 genomes]
rs3784392	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4923842	0.87[ASN][1000 genomes]
rs4923843	0.87[ASN][1000 genomes]
rs4924393	0.85[ASN][1000 genomes]
rs4924394	0.87[ASN][1000 genomes]
rs62002492	0.86[ASN][1000 genomes]
rs62002493	0.86[ASN][1000 genomes]
rs7181712	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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	nsv832979	chr15:40041928-40218407	Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv832983	chr15:40098766-40248839	Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40103000-40121400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:40110400-40129800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr15:40111600-40123400	Weak transcription	Aorta	Aorta
4	chr15:40112600-40121400	Weak transcription	Right Atrium	heart
5	chr15:40114400-40121400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr15:40116000-40122600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr15:40116200-40122600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr15:40116800-40125600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr15:40117000-40121200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr15:40118200-40121800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr15:40119800-40121600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr15:40120000-40121400	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr15:40120000-40123200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr15:40120200-40121200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:40120200-40121400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr15:40120200-40121600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr15:40120200-40123600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr15:40120200-40123600	Enhancers	NHLF	lung
19	chr15:40120400-40121400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr15:40120400-40121400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr15:40120400-40121600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:40120400-40121600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr15:40120400-40121600	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr15:40120400-40121600	Genic enhancers	HSMM	muscle
25	chr15:40120400-40121600	Enhancers	NH-A	brain
26	chr15:40120400-40121600	Enhancers	NHDF-Ad	bronchial
27	chr15:40120400-40121800	Enhancers	Osteobl	bone
28	chr15:40120400-40122000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr15:40120400-40122000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:40120400-40122000	Enhancers	HUVEC	blood vessel
31	chr15:40120400-40123800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr15:40120600-40121200	Enhancers	Adipose Nuclei	Adipose
33	chr15:40120600-40121600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr15:40120600-40121600	Enhancers	Liver	Liver
35	chr15:40120600-40121600	Enhancers	Spleen	Spleen
36	chr15:40120800-40122800	Enhancers	Muscle Satellite Cultured Cells	--
37	chr15:40120800-40125200	Weak transcription	HSMMtube	muscle
38	chr15:40120800-40125600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr15:40120800-40128000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr15:40121000-40121400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr15:40121000-40121400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr15:40121000-40121400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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