Variant report

Variant	rs192937358
Chromosome Location	chr4:48749489-48749490
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv1002674	chr4:48507608-49032909	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv537087	chr4:48507608-49032909	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1010923	chr4:48575156-49083089	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv537088	chr4:48575156-49083089	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS 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	18 gene(s)	inside rSNPs	diseases
5	nsv1013762	chr4:48580484-49032909	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv537089	chr4:48580484-49032909	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	esv1792683	chr4:48686817-48764009	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv1795181	chr4:48686817-48764009	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv1793455	chr4:48686817-48859142	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv1010381	chr4:48701525-49309842	Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
11	esv1792281	chr4:48719424-48764009	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	esv1794245	chr4:48719424-48764009	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	esv1794757	chr4:48719424-48764009	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv594137	chr4:48748305-48763163	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48731600-48751000	Weak transcription	Lung	lung
2	chr4:48731600-48779800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:48741000-48751200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:48742000-48758800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:48742000-48768400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr4:48742600-48751200	Weak transcription	Esophagus	oesophagus
7	chr4:48742600-48768200	Weak transcription	Pancreas	Pancrea
8	chr4:48742800-48753800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr4:48744400-48750400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr4:48744600-48750400	Weak transcription	Right Ventricle	heart
11	chr4:48744600-48751200	Weak transcription	Brain Substantia Nigra	brain
12	chr4:48744600-48752800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr4:48744600-48753000	Weak transcription	Osteobl	bone
14	chr4:48744800-48750800	Weak transcription	Fetal Heart	heart
15	chr4:48744800-48753600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr4:48745000-48750000	Weak transcription	Psoas Muscle	Psoas
17	chr4:48745000-48750600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr4:48745000-48751200	Weak transcription	Primary B cells from peripheral blood	blood
19	chr4:48745000-48751800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:48745000-48765200	Weak transcription	Primary B cells from cord blood	blood
21	chr4:48746800-48751200	Weak transcription	GM12878-XiMat	blood
22	chr4:48747200-48751400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr4:48747200-48754800	Weak transcription	Fetal Stomach	stomach
24	chr4:48747200-48777200	Weak transcription	Fetal Intestine Small	intestine
25	chr4:48747400-48767800	Weak transcription	Fetal Intestine Large	intestine
26	chr4:48748600-48749800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr4:48748600-48749800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:48748600-48750000	Enhancers	HMEC	breast
29	chr4:48748600-48750200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:48748600-48751000	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr4:48748600-48751800	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr4:48748600-48751800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr4:48748600-48756400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr4:48748800-48750000	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr4:48748800-48751400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr4:48748800-48751600	Enhancers	Dnd41	blood
37	chr4:48749000-48750400	Weak transcription	Left Ventricle	heart
38	chr4:48749000-48750400	Weak transcription	Right Atrium	heart
39	chr4:48749000-48751000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr4:48749000-48751000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:48749000-48751000	Weak transcription	Brain Hippocampus Middle	brain
42	chr4:48749000-48751000	Weak transcription	Spleen	Spleen
43	chr4:48749000-48751200	Weak transcription	Ovary	ovary
44	chr4:48749000-48751400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:48749000-48751400	Enhancers	Primary T cells from cord blood	blood
46	chr4:48749000-48757200	Weak transcription	Gastric	stomach
47	chr4:48749200-48749800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr4:48749200-48750000	Weak transcription	Fetal Thymus	thymus
49	chr4:48749200-48750000	Enhancers	NHEK	skin
50	chr4:48749200-48750400	Weak transcription	Brain Angular Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links