Variant report

Variant	rs73929358
Chromosome Location	chr2:47254922-47254923
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:47252397..47254046-chr2:47254810..47257644,2	K562	blood:
2	chr2:47227819..47229844-chr2:47253559..47255515,2	K562	blood:
3	chr2:47249673..47251618-chr2:47253667..47255571,2	MCF-7	breast:
4	chr2:47253562..47255469-chr2:47401214..47402778,2	K562	blood:
5	chr2:47252113..47260352-chr2:47399089..47405669,11	MCF-7	breast:
6	chr2:47239533..47242401-chr2:47254885..47256539,3	MCF-7	breast:
7	chr2:47246499..47248286-chr2:47253507..47255645,2	MCF-7	breast:
8	chr2:47252232..47263251-chr2:47397787..47406051,20	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000143933	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10495942	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11884118	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11890603	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11901122	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13353361	1.00[AMR][1000 genomes]
rs13423726	1.00[AMR][1000 genomes]
rs17036138	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17541155	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17541307	0.84[AMR][1000 genomes]
rs56200787	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 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
5	nsv524970	chr2:47162739-47302095	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv1000377	chr2:47189386-47344029	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv525197	chr2:47210747-47297973	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv518312	chr2:47224927-47262137	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv984532	chr2:47237908-47270533	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv581751	chr2:47243124-47255723	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv581752	chr2:47248111-47262137	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv521030	chr2:47249239-47255059	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv525855	chr2:47249239-47259467	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv457363	chr2:47249239-47263232	Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv581753	chr2:47249239-47263232	Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv528091	chr2:47249239-47273732	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47213600-47256400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:47214000-47262000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr2:47222000-47260600	Weak transcription	Small Intestine	intestine
4	chr2:47230200-47302800	Strong transcription	Dnd41	blood
5	chr2:47232000-47265000	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr2:47232400-47257000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:47234400-47283600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr2:47236000-47278600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr2:47236600-47259200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:47236600-47259200	Weak transcription	Fetal Kidney	kidney
11	chr2:47237000-47260400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr2:47240200-47256000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr2:47243800-47260200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr2:47243800-47260400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr2:47243800-47260800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr2:47243800-47261000	Weak transcription	K562	blood
17	chr2:47244000-47256000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:47244000-47256800	Strong transcription	Osteobl	bone
19	chr2:47244000-47257200	Weak transcription	HUVEC	blood vessel
20	chr2:47244000-47258800	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr2:47244000-47260600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr2:47244200-47261200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr2:47244400-47257000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:47244600-47257000	Strong transcription	NHLF	lung
25	chr2:47244600-47258800	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr2:47244800-47256200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:47244800-47256800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr2:47244800-47258800	Strong transcription	Placenta	Placenta
29	chr2:47245000-47255600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:47245800-47255000	Genic enhancers	Fetal Thymus	thymus
31	chr2:47245800-47268600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr2:47246000-47260400	Strong transcription	Primary B cells from cord blood	blood
33	chr2:47246000-47260800	Strong transcription	Primary B cells from peripheral blood	blood
34	chr2:47246000-47260800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:47246000-47261800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr2:47246000-47283800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr2:47246200-47261400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr2:47246800-47281600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr2:47247000-47259800	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr2:47247200-47257000	Genic enhancers	Fetal Muscle Trunk	muscle
41	chr2:47247400-47263000	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr2:47248200-47258000	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr2:47248600-47258000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:47248800-47256600	Strong transcription	Muscle Satellite Cultured Cells	--
45	chr2:47248800-47256800	Genic enhancers	Fetal Muscle Leg	muscle
46	chr2:47249000-47258800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr2:47249000-47259600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
48	chr2:47249200-47258200	Strong transcription	Pancreas	Pancrea
49	chr2:47249200-47259200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:47249200-47259200	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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