Variant report

Variant	rs367665718
Chromosome Location	chr2:169606206-169606207
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:169599528..169602506-chr2:169604602..169606605,2	K562	blood:
2	chr2:169605248..169607017-chr2:169608764..169610767,2	K562	blood:

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

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915920	chr2:168851960-169696591	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	esv1983529	chr2:169605968-169606382	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3511947	chr2:169606010-169606295	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3511950	chr2:169606031-169606265	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3511953	chr2:169606045-169606250	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv4907	chr2:169606062-169606288	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3511949	chr2:169606073-169606257	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3335429	chr2:169606093-169606227	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3460660	chr2:169606116-169606215	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3511948	chr2:169606130-169606207	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv215317	chr2:169606132-169606207	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3460661	chr2:169606132-169606210	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3511954	chr2:169606132-169606210	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv1631379	chr2:169606133-169606209	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169565200-169622800	Weak transcription	Liver	Liver
2	chr2:169577600-169606400	Weak transcription	Thymus	Thymus
3	chr2:169577600-169613600	Weak transcription	Fetal Kidney	kidney
4	chr2:169579600-169610400	Weak transcription	HepG2	liver
5	chr2:169579600-169630200	Weak transcription	Aorta	Aorta
6	chr2:169579600-169630600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:169580400-169610600	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr2:169580800-169610600	Weak transcription	Primary B cells from cord blood	blood
9	chr2:169581000-169612000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:169581200-169606400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr2:169581600-169610400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr2:169583800-169613000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr2:169586000-169627600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:169586200-169607600	Weak transcription	Fetal Stomach	stomach
15	chr2:169586600-169606400	Weak transcription	GM12878-XiMat	blood
16	chr2:169587800-169623200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:169593400-169612400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr2:169594000-169611000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:169594400-169607600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:169595000-169608400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr2:169595000-169610600	Weak transcription	HMEC	breast
22	chr2:169595200-169621000	Weak transcription	Brain Germinal Matrix	brain
23	chr2:169595200-169622800	Weak transcription	NHEK	skin
24	chr2:169597200-169608600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr2:169597200-169635800	Weak transcription	Ovary	ovary
26	chr2:169597600-169613600	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr2:169598600-169622800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:169599200-169607400	Weak transcription	Fetal Intestine Large	intestine
29	chr2:169601400-169610600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr2:169601600-169625800	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr2:169602600-169609000	Weak transcription	Lung	lung
32	chr2:169602800-169610400	Weak transcription	Duodenum Mucosa	Duodenum
33	chr2:169603200-169608200	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr2:169603800-169608000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr2:169604200-169615200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr2:169604400-169606400	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr2:169604400-169606600	Enhancers	Fetal Heart	heart
38	chr2:169604400-169607200	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr2:169604400-169607400	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr2:169604400-169615400	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr2:169604600-169606600	Enhancers	Gastric	stomach
42	chr2:169604600-169606600	Enhancers	Psoas Muscle	Psoas
43	chr2:169604600-169606800	Enhancers	Primary T cells fromperipheralblood	blood
44	chr2:169604600-169607600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr2:169604600-169609200	Enhancers	Fetal Muscle Leg	muscle
46	chr2:169604600-169615800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr2:169604600-169616000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr2:169604800-169627600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr2:169605000-169606800	Enhancers	Fetal Muscle Trunk	muscle
50	chr2:169605000-169606800	Enhancers	Left Ventricle	heart

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