Variant report

Variant	rs559537332
Chromosome Location	chr5:80044403-80044404
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024844	chr5:79862428-80860430	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv882231	chr5:79984714-80187929	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv598747	chr5:79996632-80322712	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1016100	chr5:80023679-80254194	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1021784	chr5:80023679-80313586	ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv537787	chr5:80023679-80313586	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	esv1795990	chr5:80043404-80066135	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79964800-80057800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:79971800-80112400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr5:79985000-80100600	Weak transcription	Brain Germinal Matrix	brain
4	chr5:79998600-80051000	Weak transcription	Fetal Brain Male	brain
5	chr5:79998800-80109400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr5:80004000-80050400	Weak transcription	NHDF-Ad	bronchial
7	chr5:80016400-80050800	Weak transcription	Psoas Muscle	Psoas
8	chr5:80022800-80051200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:80024200-80046800	Weak transcription	Brain Angular Gyrus	brain
10	chr5:80032400-80045400	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr5:80033200-80051400	Weak transcription	HMEC	breast
12	chr5:80034200-80049400	Strong transcription	Primary T cells from cord blood	blood
13	chr5:80034800-80050600	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr5:80035000-80050400	Weak transcription	Stomach Mucosa	stomach
15	chr5:80037200-80049800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:80037200-80050600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr5:80037400-80045800	Strong transcription	Liver	Liver
18	chr5:80037400-80049000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:80037400-80050600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr5:80037600-80049000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr5:80037600-80050200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr5:80038400-80045800	Strong transcription	Adipose Nuclei	Adipose
23	chr5:80039200-80045000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr5:80039200-80050200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr5:80039200-80051200	Weak transcription	Colonic Mucosa	Colon
26	chr5:80039200-80075800	Weak transcription	HepG2	liver
27	chr5:80039400-80060200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr5:80040200-80073800	Weak transcription	Hela-S3	cervix
29	chr5:80040400-80048600	Strong transcription	Primary B cells from cord blood	blood
30	chr5:80040600-80047000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr5:80040600-80049600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr5:80041000-80045800	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr5:80041000-80050200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr5:80041200-80050200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr5:80041200-80050400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr5:80041200-80076000	Weak transcription	Small Intestine	intestine
37	chr5:80041200-80100400	Weak transcription	Gastric	stomach
38	chr5:80041400-80049400	Weak transcription	Colon Smooth Muscle	Colon
39	chr5:80041600-80045000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr5:80041600-80045800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr5:80041800-80055200	Weak transcription	Esophagus	oesophagus
42	chr5:80041800-80094200	Weak transcription	NHLF	lung
43	chr5:80042200-80048000	Weak transcription	Fetal Kidney	kidney
44	chr5:80042200-80049200	Weak transcription	Placenta	Placenta
45	chr5:80042200-80075800	Weak transcription	A549	lung
46	chr5:80042400-80045400	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr5:80042400-80050800	Weak transcription	Fetal Thymus	thymus
48	chr5:80042400-80051200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr5:80042400-80056800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr5:80042800-80044600	Enhancers	HUES64 Cell Line	embryonic stem cell

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