Variant report

Variant	rs529641811
Chromosome Location	chr13:49949039-49949040
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:49948746..49951030-chr13:49963060..49965178,2	K562	blood:
2	chr13:49937629..49939824-chr13:49947316..49949983,2	MCF-7	breast:

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900069	chr13:49815405-49976393	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer 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
2	nsv1047311	chr13:49895019-50224227	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv430558	chr13:49914393-50059354	Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv430559	chr13:49930369-50059354	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv430560	chr13:49930643-50059354	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv430562	chr13:49930643-50067246	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv430561	chr13:49930643-50089844	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv430564	chr13:49945247-50059354	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
9	nsv430566	chr13:49945247-50089844	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	esv997002	chr13:49948395-49955191	Enhancers Weak transcription Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49922800-49951400	Weak transcription	Gastric	stomach
2	chr13:49923200-49951200	Weak transcription	Pancreas	Pancrea
3	chr13:49929400-49950000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr13:49934200-49957400	Weak transcription	Left Ventricle	heart
5	chr13:49938600-49961000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:49942800-49952800	Weak transcription	Aorta	Aorta
7	chr13:49944400-49951400	Enhancers	Fetal Heart	heart
8	chr13:49945000-49952000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr13:49945200-49950200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr13:49945200-49973000	Weak transcription	Brain Substantia Nigra	brain
11	chr13:49946000-49949400	Enhancers	Hela-S3	cervix
12	chr13:49946200-49950400	Enhancers	Osteobl	bone
13	chr13:49946600-49949600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr13:49946800-49950600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr13:49946800-49950600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr13:49946800-49950600	Weak transcription	Fetal Intestine Small	intestine
17	chr13:49946800-49961400	Weak transcription	Brain Hippocampus Middle	brain
18	chr13:49946800-49961400	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr13:49946800-49962600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr13:49946800-49964000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr13:49947000-49949600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr13:49947000-49952200	Weak transcription	Fetal Stomach	stomach
23	chr13:49947600-49949200	Enhancers	Colon Smooth Muscle	Colon
24	chr13:49947600-49949200	Enhancers	Rectal Smooth Muscle	rectum
25	chr13:49947600-49949600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr13:49947600-49949600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr13:49947800-49949200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr13:49947800-49949400	Enhancers	NHDF-Ad	bronchial
29	chr13:49947800-49950200	Enhancers	Primary B cells from peripheral blood	blood
30	chr13:49948000-49949200	Enhancers	NH-A	brain
31	chr13:49948000-49949200	Enhancers	NHLF	lung
32	chr13:49948000-49949400	Enhancers	NHEK	skin
33	chr13:49948000-49950000	Weak transcription	Adipose Nuclei	Adipose
34	chr13:49948000-49950800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr13:49948000-49952800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr13:49948200-49949800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr13:49948200-49951200	Weak transcription	Stomach Mucosa	stomach
38	chr13:49948200-49961000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr13:49948200-49961200	Weak transcription	Brain Angular Gyrus	brain
40	chr13:49948200-49961600	Weak transcription	Ovary	ovary
41	chr13:49948600-49949600	Enhancers	Primary B cells from cord blood	blood
42	chr13:49948600-49953000	Weak transcription	Liver	Liver
43	chr13:49948800-49949200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr13:49948800-49949200	Enhancers	Brain Anterior Caudate	brain
45	chr13:49948800-49949200	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr13:49948800-49949200	Flanking Active TSS	GM12878-XiMat	blood
47	chr13:49949000-49949400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr13:49949000-49950000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr13:49949000-49950000	Weak transcription	HMEC	breast
50	chr13:49949000-49950800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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