Variant report

Variant	rs73537247
Chromosome Location	chr19:19756051-19756052
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:19755845-19756152	K562	blood:	n/a	n/a
2	POLR2A	chr19:19755836-19756518	HL-60	blood:	n/a	n/a
3	POLR2A	chr19:19755915-19756155	K562	blood:	n/a	n/a
4	POLR2A	chr19:19755773-19756450	SK-N-MC	brain:	n/a	n/a

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:19751893..19756920-chr19:19758472..19762276,9	K562	blood:
2	chr19:19751259..19758144-chr19:19770384..19776332,14	K562	blood:
3	chr19:19752450..19756333-chr19:19763709..19769200,7	K562	blood:
4	chr19:19753961..19756109-chr19:19770427..19773007,2	MCF-7	breast:
5	chr19:19746005..19749139-chr19:19754452..19756751,3	K562	blood:
6	chr19:19751259..19757786-chr19:19771999..19776232,8	K562	blood:
7	chr19:19752883..19756107-chr19:19759212..19764518,8	MCF-7	breast:
8	chr19:19625550..19627956-chr19:19752305..19756076,5	MCF-7	breast:
9	chr19:19752144..19756505-chr19:19773208..19775858,7	MCF-7	breast:
10	chr19:19635157..19637400-chr19:19754505..19756149,2	K562	blood:
11	chr19:19754487..19757148-chr19:19764604..19766993,2	K562	blood:
12	chr19:19755727..19757407-chr19:19763663..19765667,2	MCF-7	breast:
13	chr19:19755704..19761642-chr19:19771468..19774473,6	MCF-7	breast:
14	chr19:19754977..19756747-chr19:19789710..19792104,2	K562	blood:
15	chr19:19746514..19749043-chr19:19754284..19756520,2	MCF-7	breast:

No data

Variant related genes	Relation type
GMIP	TF binding region
ENSG00000258674	Chromatin interaction
ENSG00000105726	Chromatin interaction
ENSG00000089639	Chromatin interaction
ENSG00000186010	Chromatin interaction
ENSG00000178093	Chromatin interaction
ENSG00000181896	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11878966	1.00[EUR][1000 genomes]
rs11879251	1.00[EUR][1000 genomes]
rs11880104	1.00[EUR][1000 genomes]
rs11882164	1.00[EUR][1000 genomes]
rs11883102	1.00[EUR][1000 genomes]
rs17378427	1.00[EUR][1000 genomes]
rs34087491	1.00[EUR][1000 genomes]
rs57474361	1.00[EUR][1000 genomes]
rs58294398	1.00[EUR][1000 genomes]
rs60101043	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60133934	1.00[EUR][1000 genomes]
rs60610603	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61489113	1.00[EUR][1000 genomes]
rs7247366	1.00[EUR][1000 genomes]
rs7248802	1.00[EUR][1000 genomes]
rs7250144	1.00[EUR][1000 genomes]
rs7253515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7257247	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7258865	1.00[EUR][1000 genomes]
rs73537262	1.00[EUR][1000 genomes]
rs73537266	1.00[EUR][1000 genomes]
rs73539233	1.00[EUR][1000 genomes]
rs73539261	1.00[EUR][1000 genomes]
rs73541334	1.00[EUR][1000 genomes]
rs73541344	1.00[EUR][1000 genomes]
rs73541360	1.00[EUR][1000 genomes]
rs73541377	1.00[EUR][1000 genomes]
rs8105557	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8111841	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8112744	1.00[EUR][1000 genomes]
rs8113100	1.00[EUR][1000 genomes]
rs9676945	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1828240	chr19:19591146-19900900	Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv1063273	chr19:19591146-20061367	ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription 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	67 gene(s)	inside rSNPs	diseases
3	nsv911309	chr19:19727042-19784891	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv911310	chr19:19753882-19784891	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
5	esv3330851	chr19:19755507-19852881	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 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	chr19:19754800-19756200	Weak transcription	Aorta	Aorta
2	chr19:19754800-19756200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr19:19754800-19756400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:19754800-19756400	Weak transcription	Psoas Muscle	Psoas
5	chr19:19754800-19756400	Weak transcription	HMEC	breast
6	chr19:19754800-19756400	Weak transcription	HSMMtube	muscle
7	chr19:19754800-19756600	Weak transcription	Brain Substantia Nigra	brain
8	chr19:19754800-19757600	Weak transcription	NH-A	brain
9	chr19:19754800-19757800	Weak transcription	NHDF-Ad	bronchial
10	chr19:19754800-19761400	Weak transcription	HSMM	muscle
11	chr19:19754800-19763600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr19:19754800-19764200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr19:19754800-19767200	Weak transcription	Fetal Brain Male	brain
14	chr19:19754800-19769000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr19:19754800-19772400	Weak transcription	Right Atrium	heart
16	chr19:19755000-19756800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr19:19755000-19757000	Weak transcription	Stomach Mucosa	stomach
18	chr19:19755000-19759000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr19:19755000-19759000	Strong transcription	Cortex derived primary cultured neurospheres	brain
20	chr19:19755000-19759000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr19:19755000-19761800	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr19:19755000-19765600	Weak transcription	Hela-S3	cervix
23	chr19:19755000-19769600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr19:19755000-19770800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr19:19755000-19771000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr19:19755000-19771200	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr19:19755000-19771200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
28	chr19:19755000-19772000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr19:19755000-19772000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr19:19755000-19772200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr19:19755200-19756600	Weak transcription	HepG2	liver
32	chr19:19755200-19756800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr19:19755200-19757000	Weak transcription	Colon Smooth Muscle	Colon
34	chr19:19755200-19757000	Strong transcription	K562	blood
35	chr19:19755200-19758600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr19:19755200-19758600	Strong transcription	Brain Angular Gyrus	brain
37	chr19:19755200-19759000	Strong transcription	Brain Hippocampus Middle	brain
38	chr19:19755200-19760200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr19:19755200-19761000	Strong transcription	Fetal Muscle Trunk	muscle
40	chr19:19755200-19761200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr19:19755200-19761200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr19:19755200-19761200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr19:19755200-19761400	Strong transcription	Fetal Muscle Leg	muscle
44	chr19:19755200-19761600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr19:19755200-19761600	Strong transcription	Brain Anterior Caudate	brain
46	chr19:19755200-19761800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr19:19755200-19761800	Strong transcription	Brain Cingulate Gyrus	brain
48	chr19:19755200-19763400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr19:19755200-19763400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr19:19755200-19763800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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