Variant report

Variant	rs2291064
Chromosome Location	chr15:33381286-33381287
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:33368160..33370967-chr15:33379580..33382279,2	K562	blood:
2	chr15:33374615..33377190-chr15:33380884..33382943,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1026752	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10519781	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10519788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10775202	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10851823	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11072170	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11072175	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11072187	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11636433	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11639303	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12439012	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12440002	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17235533	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17235547	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17816711	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2219159	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2291065	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2291066	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2306278	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28510826	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28551066	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28576977	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28603193	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28718544	0.96[ASN][1000 genomes]
rs345794	0.93[ASN][1000 genomes]
rs4779604	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4779605	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4779606	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4780074	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8033302	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8039005	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs922510	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs922511	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv903979	chr15:33144202-33550256	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1052966	chr15:33149753-33541951	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv542340	chr15:33149753-33541951	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv903981	chr15:33207082-33550256	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv568918	chr15:33244672-33446971	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv903982	chr15:33282844-33616150	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2291064	FMN1	cis	Esophagus Mucosa	GTEx

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33372600-33384200	Weak transcription	Brain Angular Gyrus	brain
2	chr15:33375800-33382200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr15:33376200-33382600	Weak transcription	Esophagus	oesophagus
4	chr15:33376800-33384600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr15:33376800-33384600	Weak transcription	NH-A	brain
6	chr15:33377200-33384200	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr15:33379200-33382200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr15:33379200-33382800	Weak transcription	Fetal Kidney	kidney
9	chr15:33379400-33381400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr15:33379400-33381400	Weak transcription	HSMMtube	muscle
11	chr15:33379400-33381400	Weak transcription	Osteobl	bone
12	chr15:33379400-33381600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr15:33379400-33381800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr15:33379400-33382000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr15:33379400-33382000	Weak transcription	HMEC	breast
16	chr15:33379400-33382000	Weak transcription	NHEK	skin
17	chr15:33379400-33382200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr15:33379400-33383200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr15:33379400-33384200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr15:33379400-33386200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:33379600-33381400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr15:33379600-33381400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr15:33379600-33381400	Weak transcription	NHDF-Ad	bronchial
24	chr15:33379600-33381800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr15:33379600-33382000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr15:33379600-33382000	Weak transcription	HSMM	muscle
27	chr15:33379600-33382400	Weak transcription	Fetal Thymus	thymus
28	chr15:33379800-33381400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr15:33380400-33381400	Weak transcription	Colonic Mucosa	Colon
30	chr15:33380600-33382400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr15:33380600-33383000	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr15:33380600-33387200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr15:33380800-33381400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:33380800-33381400	Genic enhancers	NHLF	lung
35	chr15:33380800-33382200	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr15:33380800-33382400	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr15:33381000-33381400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:33381000-33381400	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr15:33381000-33381600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr15:33381000-33381600	Enhancers	Fetal Muscle Leg	muscle
41	chr15:33381000-33381600	Enhancers	Psoas Muscle	Psoas
42	chr15:33381000-33382400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr15:33381000-33382600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr15:33381000-33382800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr15:33381000-33383000	Enhancers	Stomach Smooth Muscle	stomach
46	chr15:33381000-33383600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr15:33381000-33384800	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr15:33381200-33383000	Enhancers	Hela-S3	cervix
49	chr15:33381200-33383200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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