Variant report

Variant	rs28465613
Chromosome Location	chr2:47127061-47127062
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:46654722..46656648-chr2:47126320..47128240,2	K562	blood:
2	chr2:47126738..47129144-chr2:47143021..47145167,2	K562	blood:

Variant related genes	Relation type
ENSG00000180398	Chromatin interaction
ENSG00000068724	Chromatin interaction
ENSG00000187600	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10084332	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10164756	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10165085	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10181411	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10186980	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11897050	0.80[EUR][1000 genomes]
rs13391660	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13398748	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13406024	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13407588	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13409489	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13417753	0.80[EUR][1000 genomes]
rs13424086	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13430346	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13430703	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17035878	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17035912	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28405928	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28529158	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs28612371	0.80[EUR][1000 genomes]
rs28770495	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4300885	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4314044	0.85[AMR][1000 genomes]
rs4583513	0.85[AMR][1000 genomes]
rs6729569	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6755386	0.85[AMR][1000 genomes]
rs73926967	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73926970	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73926978	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73926980	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73926983	0.81[EUR][1000 genomes]
rs73926986	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73926988	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7577816	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7603884	0.81[EUR][1000 genomes]
rs9973769	0.85[AMR][1000 genomes];0.81[EUR][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	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv457352	chr2:47004788-47325973	Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv581749	chr2:47004788-47325973	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47106400-47131000	Weak transcription	Esophagus	oesophagus
2	chr2:47113200-47131200	Weak transcription	Aorta	Aorta
3	chr2:47116000-47133200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:47116200-47127400	Weak transcription	Fetal Stomach	stomach
5	chr2:47116200-47128200	Weak transcription	HSMM	muscle
6	chr2:47116200-47128400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr2:47116200-47128400	Weak transcription	NH-A	brain
8	chr2:47116200-47133000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr2:47116600-47128000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr2:47116600-47128200	Weak transcription	Fetal Thymus	thymus
11	chr2:47116600-47129600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:47116600-47129800	Weak transcription	Osteobl	bone
13	chr2:47116600-47131000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:47116600-47131200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:47116600-47131800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr2:47116600-47132200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr2:47116600-47132400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr2:47116600-47132400	Weak transcription	NHEK	skin
19	chr2:47116800-47131000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr2:47117400-47133200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr2:47117800-47131200	Weak transcription	Fetal Muscle Trunk	muscle
22	chr2:47119600-47140800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:47120000-47130800	Weak transcription	Left Ventricle	heart
24	chr2:47120000-47133200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:47120800-47133000	Weak transcription	Pancreas	Pancrea
26	chr2:47121000-47132200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr2:47121000-47132400	Weak transcription	Hela-S3	cervix
28	chr2:47121000-47132400	Weak transcription	NHDF-Ad	bronchial
29	chr2:47121200-47129800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:47121400-47127200	Weak transcription	K562	blood
31	chr2:47121600-47127600	Weak transcription	Primary T cells from cord blood	blood
32	chr2:47123600-47131000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:47124200-47131000	Weak transcription	Fetal Muscle Leg	muscle
34	chr2:47124400-47129600	Weak transcription	Primary B cells from cord blood	blood
35	chr2:47124400-47131000	Weak transcription	Fetal Intestine Small	intestine
36	chr2:47124800-47132400	Weak transcription	Fetal Lung	lung
37	chr2:47124800-47132800	Weak transcription	NHLF	lung
38	chr2:47125200-47131000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:47125200-47132200	Weak transcription	Dnd41	blood
40	chr2:47125400-47129800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr2:47125400-47132400	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr2:47125400-47133000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:47125600-47129600	Weak transcription	A549	lung
44	chr2:47125600-47130400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr2:47125600-47131200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:47125800-47133200	Weak transcription	Spleen	Spleen
47	chr2:47126000-47128200	Weak transcription	Stomach Smooth Muscle	stomach
48	chr2:47126000-47129600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:47126000-47130200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr2:47126000-47131400	Weak transcription	Adipose Nuclei	Adipose

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