Variant report

Variant	rs61413463
Chromosome Location	chr19:40484705-40484706
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:40483935-40485111	K562	blood:	n/a	n/a
2	POLR2A	chr19:40483895-40484854	SK-N-MC	brain:	n/a	n/a
3	POLR2A	chr19:40472172-40495393	PANC-1	pancreas:	n/a	n/a
4	POLR2A	chr19:40484371-40485687	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:40473089..40482317-chr19:40483091..40492558,21	K562	blood:
2	chr19:40475779..40479202-chr19:40484390..40487184,3	MCF-7	breast:

Variant related genes	Relation type
PSMC4	TF binding region
ENSG00000013275	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs16973959	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs173062	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234335	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234336	1.00[ASN][1000 genomes]
rs234337	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234344	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234345	1.00[ASN][1000 genomes]
rs234347	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234348	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234349	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234351	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234362	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234363	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234364	1.00[ASN][1000 genomes]
rs234366	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234367	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234369	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234373	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2542325	1.00[ASN][1000 genomes]
rs2542328	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs376630	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs378554	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs512360	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58294889	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59616965	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60025633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7249398	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7255173	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8113194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs913212	1.00[EUR][1000 genomes];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	esv2758498	chr19:40227904-40521130	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv2758760	chr19:40227904-40521130	Genic enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv428022	chr19:40227904-40521130	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv917321	chr19:40403192-40694875	Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40477800-40501800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:40478000-40485600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr19:40478200-40488200	Strong transcription	Thymus	Thymus
4	chr19:40478200-40488400	Strong transcription	Fetal Stomach	stomach
5	chr19:40478200-40489200	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr19:40478200-40489200	Strong transcription	Primary B cells from cord blood	blood
7	chr19:40478200-40489400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr19:40478200-40489400	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr19:40478200-40489600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr19:40478400-40488000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr19:40478400-40488200	Strong transcription	Fetal Muscle Trunk	muscle
12	chr19:40478400-40488200	Strong transcription	Fetal Muscle Leg	muscle
13	chr19:40478400-40488400	Strong transcription	Brain Anterior Caudate	brain
14	chr19:40478400-40488800	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr19:40478400-40488800	Strong transcription	Adipose Nuclei	Adipose
16	chr19:40478400-40489000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr19:40478400-40489000	Strong transcription	NH-A	brain
18	chr19:40478400-40489200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
19	chr19:40478400-40489200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr19:40478400-40489200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr19:40478400-40489400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr19:40478400-40489400	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr19:40478400-40489400	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr19:40478400-40489400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr19:40478400-40490000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr19:40478400-40490400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr19:40478400-40491000	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr19:40478400-40491200	Weak transcription	Fetal Heart	heart
29	chr19:40478600-40485600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr19:40478600-40488400	Strong transcription	Left Ventricle	heart
31	chr19:40478600-40488800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr19:40478600-40489200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr19:40478600-40489200	Strong transcription	Fetal Intestine Small	intestine
34	chr19:40478600-40489600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr19:40478600-40489600	Strong transcription	Liver	Liver
36	chr19:40478600-40489600	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr19:40478600-40489800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr19:40478600-40490000	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr19:40478600-40501800	Weak transcription	Right Atrium	heart
40	chr19:40479000-40488400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr19:40479000-40490200	Strong transcription	HSMMtube	muscle
42	chr19:40479200-40485800	Strong transcription	Ovary	ovary
43	chr19:40479200-40488400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr19:40479200-40490200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr19:40479600-40490200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr19:40480400-40489600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr19:40480800-40485600	Weak transcription	Aorta	Aorta
48	chr19:40480800-40488200	Strong transcription	Gastric	stomach
49	chr19:40481200-40488200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr19:40481800-40485400	Weak transcription	Skeletal Muscle Male	skeletal muscle

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