Variant report

Variant	rs16903459
Chromosome Location	chr5:37031416-37031417
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	chr5:37027894..37031584-chr5:37032093..37035843,4	K562	blood:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10512664	1.00[ASW][hapmap];0.87[GIH][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap]
rs12654646	0.81[ASN][1000 genomes]
rs12658479	1.00[ASW][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap]
rs13166829	0.86[AFR][1000 genomes]
rs13171061	0.86[AFR][1000 genomes]
rs13177573	0.86[AFR][1000 genomes]
rs13177875	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13181187	0.86[AFR][1000 genomes]
rs13183090	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13184464	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs13188136	0.86[AFR][1000 genomes]
rs151945	0.84[ASN][1000 genomes]
rs151946	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs151947	0.83[ASN][1000 genomes]
rs158410	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[ASN][1000 genomes]
rs158411	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs158412	0.84[ASN][1000 genomes]
rs158792	0.87[ASN][1000 genomes]
rs158793	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs158794	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs158797	0.87[ASN][1000 genomes]
rs158798	0.87[ASN][1000 genomes]
rs158799	0.87[ASN][1000 genomes]
rs158802	0.86[AFR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs159140	0.93[ASN][1000 genomes]
rs159141	0.93[ASN][1000 genomes]
rs167146	0.85[ASN][1000 genomes]
rs16903490	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16903531	1.00[ASW][hapmap];0.90[GIH][hapmap];1.00[LWK][hapmap];0.82[YRI][hapmap]
rs181755	0.84[ASN][1000 genomes]
rs245587	0.84[ASN][1000 genomes]
rs245588	0.86[AFR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs292160	0.81[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.89[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.88[ASN][1000 genomes]
rs292179	0.81[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.89[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs292180	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[ASN][1000 genomes]
rs292181	0.81[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[ASN][1000 genomes]
rs292186	0.96[ASN][1000 genomes]
rs292196	0.93[ASN][1000 genomes]
rs293746	0.87[ASN][1000 genomes]
rs293748	1.00[ASW][hapmap];0.81[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap];1.00[YRI][hapmap];0.88[ASN][1000 genomes]
rs293774	1.00[ASW][hapmap];0.93[CEU][hapmap];0.94[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs294695	0.81[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs34066351	0.90[ASN][1000 genomes]
rs34479946	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34525350	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs35011787	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35701604	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs468022	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56261529	0.82[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs59398009	0.86[AFR][1000 genomes]
rs61748200	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6861906	0.84[ASN][1000 genomes]
rs9632396	1.00[YRI][hapmap]
rs9637791	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492319	chr5:36570707-37061019	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv525478	chr5:36804225-37349895	Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	esv1793961	chr5:36866835-37361728	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
4	nsv530225	chr5:36886635-37331912	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1024051	chr5:36899712-37303001	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer 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	27 gene(s)	inside rSNPs	diseases
6	nsv537725	chr5:36899712-37303001	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv530226	chr5:36906377-37606367	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv1030883	chr5:36932448-37039857	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
9	esv1803659	chr5:36935129-37039857	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
10	nsv1033928	chr5:36947293-37039857	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
11	nsv917880	chr5:36948778-37115342	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
12	esv1802391	chr5:36958598-37242600	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
13	nsv597822	chr5:36997953-37147152	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
14	esv1803948	chr5:37016522-37047066	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36949600-37086800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:36969800-37065000	Weak transcription	Stomach Mucosa	stomach
3	chr5:36979800-37057800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr5:36991000-37064600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:36997600-37064600	Weak transcription	Esophagus	oesophagus
6	chr5:37001200-37066200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr5:37005200-37041800	Weak transcription	Lung	lung
8	chr5:37009200-37049200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr5:37010200-37043600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr5:37010800-37064600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr5:37011000-37054400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr5:37012400-37064600	Weak transcription	Gastric	stomach
13	chr5:37014000-37033000	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr5:37014200-37032600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr5:37014200-37032800	Strong transcription	Placenta	Placenta
16	chr5:37014200-37033000	Strong transcription	Liver	Liver
17	chr5:37014200-37033000	Strong transcription	Duodenum Mucosa	Duodenum
18	chr5:37014200-37034600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:37014200-37034800	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr5:37014200-37035400	Strong transcription	Dnd41	blood
21	chr5:37014200-37036000	Strong transcription	Adipose Nuclei	Adipose
22	chr5:37014200-37066200	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr5:37014200-37067200	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr5:37014400-37032000	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr5:37014400-37032400	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr5:37014600-37033000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:37014600-37036200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr5:37014800-37031600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:37014800-37032000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:37014800-37033000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr5:37014800-37033600	Strong transcription	Fetal Thymus	thymus
32	chr5:37014800-37036000	Strong transcription	Primary B cells from peripheral blood	blood
33	chr5:37016000-37032400	Strong transcription	Primary T helper cells PMA-I stimulated	--
34	chr5:37016800-37034600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:37016800-37034600	Weak transcription	Brain Substantia Nigra	brain
36	chr5:37016800-37037600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr5:37017000-37032200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr5:37017000-37032800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:37017000-37041200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:37017600-37033000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:37017800-37033000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr5:37018000-37032800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr5:37018400-37033000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr5:37018600-37032800	Strong transcription	Fetal Muscle Trunk	muscle
45	chr5:37019000-37032200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:37019200-37060000	Weak transcription	Psoas Muscle	Psoas
47	chr5:37021200-37035000	Weak transcription	Brain Angular Gyrus	brain
48	chr5:37022400-37063600	Weak transcription	NHEK	skin
49	chr5:37023800-37050600	Weak transcription	Fetal Heart	heart
50	chr5:37024600-37032200	Strong transcription	Fetal Muscle Leg	muscle

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