Variant report

Variant	rs7248757
Chromosome Location	chr19:53161161-53161162
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11084175	0.84[EUR][1000 genomes]
rs11882437	0.86[EUR][1000 genomes]
rs12462353	0.84[EUR][1000 genomes]
rs12609383	0.84[EUR][1000 genomes]
rs189082	0.93[ASN][1000 genomes]
rs193039	0.85[ASN][1000 genomes]
rs329941	0.95[ASN][1000 genomes]
rs329952	0.94[ASN][1000 genomes]
rs329958	0.95[ASN][1000 genomes]
rs329959	0.92[ASN][1000 genomes]
rs329960	0.95[ASN][1000 genomes]
rs329961	0.94[ASN][1000 genomes]
rs329962	0.94[ASN][1000 genomes]
rs329963	0.93[ASN][1000 genomes]
rs3745105	0.98[ASN][1000 genomes]
rs3745106	0.98[ASN][1000 genomes]
rs406232	0.84[ASN][1000 genomes]
rs410857	0.85[ASN][1000 genomes]
rs472389	0.94[ASN][1000 genomes]
rs475188	0.94[ASN][1000 genomes]
rs476955	0.94[ASN][1000 genomes]
rs4801925	0.86[EUR][1000 genomes]
rs4801928	0.84[EUR][1000 genomes]
rs484919	0.87[ASN][1000 genomes]
rs619872	0.95[ASN][1000 genomes]
rs681090	0.95[ASN][1000 genomes]
rs7255536	0.97[ASN][1000 genomes]
rs7255970	0.97[ASN][1000 genomes]
rs7256179	0.98[ASN][1000 genomes]
rs7259344	0.97[ASN][1000 genomes]
rs7259397	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057296	chr19:52950339-53396986	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv833874	chr19:53058014-53257875	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv912305	chr19:53092465-53349850	Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv912306	chr19:53092465-53400760	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv912307	chr19:53092465-53433054	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv912308	chr19:53092465-53436337	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv912309	chr19:53092465-53440653	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	nsv912310	chr19:53092465-53451291	Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv912311	chr19:53103875-53212361	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
10	nsv912312	chr19:53103875-53296371	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
11	nsv912313	chr19:53103875-53436337	ZNF genes & repeats Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv912317	chr19:53105547-53440653	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
13	nsv1066762	chr19:53112568-53552217	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
14	nsv912318	chr19:53118278-53451291	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
15	nsv458744	chr19:53120559-53236331	Genic enhancers Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
16	nsv580028	chr19:53120559-53236331	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
17	esv3489404	chr19:53121944-53391394	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
18	esv3489405	chr19:53121944-53391394	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
19	nsv580029	chr19:53137583-53164172	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS 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	3 gene(s)	inside rSNPs	diseases
20	nsv961238	chr19:53144650-53221094	Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers 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 target site	8 gene(s)	inside rSNPs	diseases
21	nsv432072	chr19:53144788-53554388	Strong transcription ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
22	esv3401212	chr19:53151131-53482063	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
23	nsv912319	chr19:53152923-53241107	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53149400-53166000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr19:53150800-53166200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr19:53152200-53166800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr19:53152200-53172000	Weak transcription	Psoas Muscle	Psoas
5	chr19:53152400-53168600	Strong transcription	Dnd41	blood
6	chr19:53153400-53161400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr19:53153400-53163400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr19:53153600-53184200	Weak transcription	Colonic Mucosa	Colon
9	chr19:53153800-53164000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr19:53154000-53164400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr19:53154000-53166200	Strong transcription	Stomach Smooth Muscle	stomach
12	chr19:53154200-53164000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr19:53154200-53166000	Strong transcription	Primary T cells from cord blood	blood
14	chr19:53154400-53166000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr19:53154400-53166400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr19:53154600-53164200	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr19:53154600-53164600	Strong transcription	Fetal Muscle Leg	muscle
18	chr19:53154600-53168600	Strong transcription	Fetal Stomach	stomach
19	chr19:53154800-53161400	Weak transcription	HepG2	liver
20	chr19:53154800-53163600	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr19:53154800-53165400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr19:53155000-53163600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr19:53155000-53191400	Weak transcription	Colon Smooth Muscle	Colon
24	chr19:53155200-53164200	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr19:53155200-53165000	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr19:53155400-53165200	Strong transcription	Fetal Thymus	thymus
27	chr19:53155600-53162200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr19:53155600-53163800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr19:53155800-53166000	Strong transcription	Placenta	Placenta
30	chr19:53156000-53165400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr19:53156200-53162600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
32	chr19:53156200-53168000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr19:53156400-53161800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr19:53156400-53165000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr19:53156800-53162000	Weak transcription	Brain Hippocampus Middle	brain
36	chr19:53157000-53161400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr19:53157000-53162200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:53157000-53162200	Strong transcription	Thymus	Thymus
39	chr19:53157000-53167200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr19:53157000-53167600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr19:53157000-53176600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr19:53157200-53162000	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr19:53157200-53165000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr19:53157200-53165200	Weak transcription	Brain Cingulate Gyrus	brain
45	chr19:53157200-53165600	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr19:53157200-53167200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr19:53157200-53167600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr19:53157200-53167800	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr19:53157200-53168000	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr19:53157200-53191600	Weak transcription	Rectal Smooth Muscle	rectum

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