Variant report

Variant	rs529021797
Chromosome Location	chr13:40238965-40238966
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054600	chr13:39801283-40545027	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1054797	chr13:40198744-40618428	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
3	nsv541755	chr13:40198744-40618428	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
4	nsv832586	chr13:40222880-40379063	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	6 gene(s)	inside rSNPs	diseases
5	nsv870429	chr13:40235061-40265634	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	esv33028	chr13:40238180-40239010	Weak transcription Strong transcription Genic enhancers Enhancers	miRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40230600-40252200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:40230600-40254600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:40230600-40254600	Weak transcription	Lung	lung
4	chr13:40230600-40254800	Weak transcription	Aorta	Aorta
5	chr13:40230600-40263800	Weak transcription	Spleen	Spleen
6	chr13:40230800-40239400	Weak transcription	HSMMtube	muscle
7	chr13:40230800-40239600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr13:40230800-40239800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr13:40230800-40240000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr13:40230800-40246600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr13:40230800-40254600	Weak transcription	Left Ventricle	heart
12	chr13:40230800-40254600	Weak transcription	Psoas Muscle	Psoas
13	chr13:40230800-40254800	Weak transcription	Fetal Thymus	thymus
14	chr13:40230800-40256400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr13:40230800-40258400	Weak transcription	Colonic Mucosa	Colon
16	chr13:40230800-40262000	Weak transcription	Thymus	Thymus
17	chr13:40230800-40275000	Weak transcription	Right Ventricle	heart
18	chr13:40231000-40239200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr13:40231000-40241600	Weak transcription	Hela-S3	cervix
20	chr13:40231000-40243800	Weak transcription	Fetal Heart	heart
21	chr13:40231000-40252200	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr13:40231000-40252800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr13:40231000-40254400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr13:40231000-40254400	Weak transcription	Stomach Smooth Muscle	stomach
25	chr13:40231000-40254600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr13:40231000-40254600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr13:40231000-40254600	Weak transcription	NHLF	lung
28	chr13:40231000-40256400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr13:40231000-40256400	Weak transcription	NHEK	skin
30	chr13:40231000-40257200	Weak transcription	HMEC	breast
31	chr13:40231000-40261800	Weak transcription	Brain Substantia Nigra	brain
32	chr13:40231000-40266200	Weak transcription	Rectal Smooth Muscle	rectum
33	chr13:40231000-40270800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr13:40231000-40286000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr13:40231200-40239600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr13:40231200-40254400	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr13:40231200-40254600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr13:40231200-40254800	Weak transcription	Fetal Stomach	stomach
39	chr13:40231400-40253600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr13:40231400-40254600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr13:40231400-40264200	Weak transcription	Esophagus	oesophagus
42	chr13:40231400-40268000	Weak transcription	Small Intestine	intestine
43	chr13:40231600-40239800	Weak transcription	GM12878-XiMat	blood
44	chr13:40231600-40254400	Weak transcription	Fetal Brain Male	brain
45	chr13:40231600-40270200	Weak transcription	Gastric	stomach
46	chr13:40231800-40252000	Weak transcription	Brain Angular Gyrus	brain
47	chr13:40232000-40239800	Weak transcription	Brain Germinal Matrix	brain
48	chr13:40232000-40251600	Weak transcription	Brain Cingulate Gyrus	brain
49	chr13:40232000-40252800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr13:40232000-40253200	Weak transcription	Primary T helper naive cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links