Variant report

Variant	rs59397913
Chromosome Location	chr19:40310058-40310059
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:40309497..40312112-chr19:40336240..40338482,2	MCF-7	breast:
2	chr19:40306242..40311061-chr19:40311644..40314932,5	K562	blood:
3	chr19:40306929..40308532-chr19:40309647..40311721,2	MCF-7	breast:
4	chr19:40309125..40311120-chr19:40323233..40324762,2	K562	blood:

Variant related genes	Relation type
ENSG00000105202	Chromatin interaction
ENSG00000105204	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs4621102	1.00[AMR][1000 genomes]
rs7247534	1.00[AMR][1000 genomes]
rs73930648	1.00[AMR][1000 genomes]
rs73930649	1.00[AMR][1000 genomes]
rs73930652	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057361	chr19:40123868-40310996	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1061361	chr19:40131820-40310996	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv579511	chr19:40132825-40310497	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1062394	chr19:40133229-40310186	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv544004	chr19:40133229-40310186	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	esv3329492	chr19:40198535-40437035	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
7	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
8	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
9	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

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40296200-40314200	Weak transcription	Right Ventricle	heart
2	chr19:40298800-40314200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr19:40299800-40313600	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr19:40300200-40314200	Weak transcription	Gastric	stomach
5	chr19:40300800-40313400	Weak transcription	Pancreas	Pancrea
6	chr19:40301600-40314200	Weak transcription	Ovary	ovary
7	chr19:40301600-40314400	Weak transcription	Primary B cells from cord blood	blood
8	chr19:40301600-40314400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr19:40302600-40314400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr19:40302800-40314200	Weak transcription	Brain Angular Gyrus	brain
11	chr19:40303000-40314200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr19:40303000-40314200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr19:40303200-40314200	Weak transcription	Duodenum Mucosa	Duodenum
14	chr19:40303800-40314200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr19:40304000-40313400	Weak transcription	Brain Germinal Matrix	brain
16	chr19:40304000-40314200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr19:40304600-40314200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr19:40304600-40314200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr19:40304600-40314200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr19:40305000-40314200	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr19:40305200-40314200	Weak transcription	Thymus	Thymus
22	chr19:40305200-40314200	Weak transcription	NHLF	lung
23	chr19:40305400-40310400	Strong transcription	Primary T cells from cord blood	blood
24	chr19:40305400-40314200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr19:40305400-40314200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr19:40305800-40314200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr19:40305800-40314400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr19:40306000-40314200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr19:40306000-40314200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr19:40306000-40314200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr19:40306000-40314400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr19:40306200-40313400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr19:40306200-40314200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr19:40306200-40314200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr19:40306200-40314200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr19:40306400-40314200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr19:40306600-40314200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr19:40306600-40314200	Weak transcription	HSMM	muscle
39	chr19:40306800-40311200	Strong transcription	Fetal Stomach	stomach
40	chr19:40306800-40313800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr19:40306800-40314200	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr19:40306800-40314400	Weak transcription	NHEK	skin
43	chr19:40307000-40313600	Weak transcription	Fetal Brain Male	brain
44	chr19:40307200-40314200	Weak transcription	Brain Hippocampus Middle	brain
45	chr19:40307200-40314200	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr19:40307400-40313600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:40307400-40314400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr19:40307600-40313600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr19:40307600-40314200	Weak transcription	Lung	lung
50	chr19:40307600-40314400	Weak transcription	Aorta	Aorta

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