Variant report

Variant	rs73404730
Chromosome Location	chr15:42808309-42808310
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:42808288..42811039-chr15:42812742..42814723,2	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10518766	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1060291	1.00[ASN][1000 genomes]
rs1060293	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11022	1.00[ASN][1000 genomes]
rs11070376	1.00[ASN][1000 genomes]
rs11636577	1.00[ASN][1000 genomes]
rs16973320	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17709180	1.00[ASN][1000 genomes]
rs17709377	1.00[ASN][1000 genomes]
rs17766532	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1900921	1.00[ASN][1000 genomes]
rs2899051	1.00[ASN][1000 genomes]
rs2899059	0.94[EUR][1000 genomes]
rs34359922	1.00[ASN][1000 genomes]
rs34643746	1.00[ASN][1000 genomes]
rs34792942	1.00[ASN][1000 genomes]
rs3986280	1.00[ASN][1000 genomes]
rs4923948	1.00[ASN][1000 genomes]
rs4924684	1.00[ASN][1000 genomes]
rs4924687	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56357092	1.00[ASN][1000 genomes]
rs56982416	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58042601	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58641431	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59697584	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59705032	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60380503	1.00[ASN][1000 genomes]
rs60584955	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60812675	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61489160	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022317	1.00[ASN][1000 genomes]
rs7180483	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73402783	1.00[ASN][1000 genomes]
rs73402785	1.00[ASN][1000 genomes]
rs73404714	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73404717	0.91[EUR][1000 genomes]
rs73404723	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73404763	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73406518	1.00[ASN][1000 genomes]
rs73406534	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73406545	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74009095	1.00[ASN][1000 genomes]
rs8033412	1.00[ASN][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	nsv1049445	chr15:42239738-42830484	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv542366	chr15:42239738-42830484	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	esv3334708	chr15:42664344-42827738	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv528725	chr15:42755555-43104406	Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42790800-42809800	Weak transcription	Spleen	Spleen
2	chr15:42790800-42810000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr15:42790800-42821400	Weak transcription	Right Ventricle	heart
4	chr15:42791200-42809800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr15:42793000-42809800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr15:42793000-42835600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr15:42793800-42837200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr15:42797400-42839800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr15:42797600-42822200	Weak transcription	Small Intestine	intestine
10	chr15:42797600-42839400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr15:42798600-42808400	Weak transcription	Gastric	stomach
12	chr15:42799200-42839400	Weak transcription	Stomach Mucosa	stomach
13	chr15:42801000-42809400	Weak transcription	Fetal Lung	lung
14	chr15:42802200-42812000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr15:42802400-42839200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:42802600-42811800	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr15:42802600-42817400	Strong transcription	Primary B cells from peripheral blood	blood
18	chr15:42802800-42817200	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr15:42803000-42810600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr15:42803200-42809000	Weak transcription	NHLF	lung
21	chr15:42803200-42837200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr15:42803600-42839400	Weak transcription	A549	lung
23	chr15:42803800-42808600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr15:42803800-42817600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr15:42804000-42810600	Strong transcription	NHEK	skin
26	chr15:42804000-42826800	Strong transcription	HUVEC	blood vessel
27	chr15:42804400-42814400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr15:42804600-42836400	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr15:42804800-42808600	Strong transcription	Osteobl	bone
30	chr15:42804800-42812200	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr15:42804800-42812400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr15:42804800-42814600	Strong transcription	Primary T cells from cord blood	blood
33	chr15:42804800-42817200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr15:42804800-42817400	Strong transcription	Adipose Nuclei	Adipose
35	chr15:42804800-42818000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr15:42804800-42818000	Strong transcription	Fetal Intestine Large	intestine
37	chr15:42804800-42825400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr15:42804800-42828800	Strong transcription	Placenta	Placenta
39	chr15:42804800-42836400	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr15:42804800-42836400	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr15:42805000-42811400	Strong transcription	HSMM	muscle
42	chr15:42805000-42812200	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr15:42805000-42814400	Strong transcription	Fetal Thymus	thymus
44	chr15:42805000-42814600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr15:42805000-42818400	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr15:42805000-42818800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr15:42805000-42818800	Strong transcription	NH-A	brain
48	chr15:42805200-42811000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr15:42805200-42812200	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr15:42805200-42812200	Strong transcription	Colon Smooth Muscle	Colon

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