Variant report

Variant	rs558979918
Chromosome Location	chr5:36928656-36928657
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:36926669..36929078-chr5:36937999..36941125,3	MCF-7	breast:
2	chr5:36927710..36929639-chr5:36961627..36963604,2	MCF-7	breast:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492319	chr5:36570707-37061019	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv525478	chr5:36804225-37349895	Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	esv1793961	chr5:36866835-37361728	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
4	nsv530225	chr5:36886635-37331912	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv830264	chr5:36887002-36941494	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1024051	chr5:36899712-37303001	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS 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	27 gene(s)	inside rSNPs	diseases
7	nsv537725	chr5:36899712-37303001	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS 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	27 gene(s)	inside rSNPs	diseases
8	nsv530226	chr5:36906377-37606367	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
9	nsv1033562	chr5:36927652-36994811	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv1023362	chr5:36927652-37010749	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
11	nsv1017947	chr5:36927652-37017180	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
12	nsv1029936	chr5:36927652-37025871	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
13	nsv1029319	chr5:36928654-37017180	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36907400-36938200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:36913800-36931400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr5:36919600-36931400	Weak transcription	Left Ventricle	heart
4	chr5:36919600-36938200	Weak transcription	Pancreas	Pancrea
5	chr5:36919800-36953000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr5:36919800-36961600	Weak transcription	K562	blood
7	chr5:36920400-36951400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr5:36921600-36929200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr5:36921600-36931600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:36923400-36931400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr5:36923600-36943600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr5:36924600-36943600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr5:36924800-36931000	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr5:36924800-36933000	Weak transcription	Aorta	Aorta
15	chr5:36924800-36939000	Weak transcription	Fetal Thymus	thymus
16	chr5:36924800-36955200	Weak transcription	Dnd41	blood
17	chr5:36925000-36929000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr5:36925200-36929200	Weak transcription	Fetal Heart	heart
19	chr5:36925400-36933800	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr5:36925600-36935200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr5:36926000-36936800	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr5:36926600-36928800	Weak transcription	Primary T cells from cord blood	blood
23	chr5:36926600-36931600	Weak transcription	GM12878-XiMat	blood
24	chr5:36926600-36939400	Weak transcription	Fetal Intestine Small	intestine
25	chr5:36926800-36934200	Weak transcription	Colon Smooth Muscle	Colon
26	chr5:36927600-36929000	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr5:36927600-36929000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr5:36927600-36929800	Enhancers	NHDF-Ad	bronchial
29	chr5:36927600-36961600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr5:36928000-36928800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:36928000-36929000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr5:36928000-36929000	Enhancers	Liver	Liver
33	chr5:36928000-36929400	Enhancers	Small Intestine	intestine
34	chr5:36928000-36929800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr5:36928200-36929200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr5:36928200-36929800	Enhancers	Osteobl	bone
37	chr5:36928200-36930200	Enhancers	HUVEC	blood vessel
38	chr5:36928200-36930800	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr5:36928200-36931200	Enhancers	Hela-S3	cervix
40	chr5:36928200-36931400	Weak transcription	Psoas Muscle	Psoas
41	chr5:36928200-36935200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr5:36928200-36935400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr5:36928400-36930200	Enhancers	Muscle Satellite Cultured Cells	--
44	chr5:36928400-36931400	Weak transcription	Ovary	ovary
45	chr5:36928600-36928800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:36928600-36929000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:36928600-36929000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr5:36928600-36929000	Enhancers	A549	lung
49	chr5:36928600-36929600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr5:36928600-36929600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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