Variant report

Variant	rs571970759
Chromosome Location	chr1:92712287-92712288
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv871508	chr1:92478130-92781579	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv830592	chr1:92669282-92805629	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv870667	chr1:92697188-92813741	Active TSS Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	esv1794222	chr1:92711407-92735359	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92705600-92726800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr1:92705800-92729200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr1:92707200-92764000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:92708200-92741200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:92709000-92717400	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr1:92709000-92718800	Weak transcription	Lung	lung
7	chr1:92709000-92737200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr1:92709000-92762800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr1:92709200-92718800	Weak transcription	Pancreas	Pancrea
10	chr1:92709400-92712400	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr1:92709400-92735800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr1:92709600-92730800	Weak transcription	Hela-S3	cervix
13	chr1:92710000-92717800	Weak transcription	Brain Germinal Matrix	brain
14	chr1:92710000-92737600	Weak transcription	HSMM	muscle
15	chr1:92710000-92745200	Weak transcription	Brain Hippocampus Middle	brain
16	chr1:92710200-92715000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr1:92710200-92717400	Weak transcription	Adipose Nuclei	Adipose
18	chr1:92710200-92717800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:92710200-92717800	Weak transcription	Placenta	Placenta
20	chr1:92710200-92718000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr1:92710200-92718800	Weak transcription	Left Ventricle	heart
22	chr1:92710200-92718800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:92710200-92739400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr1:92710400-92712800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:92710400-92713200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr1:92710400-92718600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr1:92710400-92724800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:92710600-92713000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:92710600-92715200	Weak transcription	K562	blood
30	chr1:92710600-92718400	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr1:92710600-92718400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr1:92710600-92718600	Weak transcription	Fetal Muscle Trunk	muscle
33	chr1:92710600-92718800	Weak transcription	Aorta	Aorta
34	chr1:92710600-92718800	Weak transcription	Fetal Intestine Small	intestine
35	chr1:92710600-92718800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr1:92710600-92719000	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr1:92710600-92725000	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr1:92710600-92726000	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr1:92710600-92726200	Weak transcription	Right Ventricle	heart
40	chr1:92710600-92726200	Weak transcription	Stomach Smooth Muscle	stomach
41	chr1:92710600-92726600	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr1:92710600-92753200	Weak transcription	Small Intestine	intestine
43	chr1:92710600-92762000	Weak transcription	Fetal Brain Male	brain
44	chr1:92710600-92763400	Weak transcription	Brain Angular Gyrus	brain
45	chr1:92710600-92764000	Weak transcription	Gastric	stomach
46	chr1:92710800-92717800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:92710800-92718800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr1:92710800-92726800	Weak transcription	NH-A	brain
49	chr1:92711000-92713600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
50	chr1:92711000-92713600	Strong transcription	Primary B cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links