Variant report

Variant	rs372475534
Chromosome Location	chr22:34151247-34151248
allele	A/G
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	nsv934109	chr22:33722066-34339500	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1055791	chr22:33822226-34159536	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	esv2763261	chr22:33831348-34288389	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1057450	chr22:33928913-34849012	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv914990	chr22:34090440-34373293	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1055203	chr22:34098417-34196685	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv914991	chr22:34106384-34293516	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv459878	chr22:34106745-34226592	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv588936	chr22:34106745-34226592	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1056553	chr22:34116979-34286191	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv914992	chr22:34135007-34283144	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv588937	chr22:34144823-34156607	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv524156	chr22:34145596-34260738	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv529885	chr22:34150132-34182300	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34123200-34152000	Weak transcription	Aorta	Aorta
2	chr22:34124800-34171000	Weak transcription	Ovary	ovary
3	chr22:34126200-34176200	Weak transcription	Spleen	Spleen
4	chr22:34131000-34154200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr22:34134400-34164800	Weak transcription	Brain Anterior Caudate	brain
6	chr22:34136200-34152800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr22:34136200-34152800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr22:34136400-34152600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr22:34136800-34152600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr22:34137400-34152600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr22:34137800-34152800	Weak transcription	Colon Smooth Muscle	Colon
12	chr22:34138000-34152600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr22:34138000-34152800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr22:34138000-34160800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr22:34140800-34152600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr22:34141600-34152600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr22:34141800-34152400	Weak transcription	Fetal Stomach	stomach
18	chr22:34141800-34153200	Weak transcription	Psoas Muscle	Psoas
19	chr22:34142800-34152600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr22:34143400-34160000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr22:34145000-34154000	Weak transcription	Primary B cells from peripheral blood	blood
22	chr22:34145200-34152600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr22:34146000-34151400	Weak transcription	Fetal Heart	heart
24	chr22:34146000-34152600	Weak transcription	Right Ventricle	heart
25	chr22:34146400-34152600	Weak transcription	Gastric	stomach
26	chr22:34146400-34152600	Weak transcription	Left Ventricle	heart
27	chr22:34147400-34158400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr22:34147400-34168600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr22:34147600-34154600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr22:34148800-34152800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr22:34149200-34167000	Weak transcription	Brain Angular Gyrus	brain
32	chr22:34149400-34153400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr22:34149800-34151800	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr22:34149800-34152000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr22:34149800-34152400	Weak transcription	Fetal Muscle Leg	muscle
36	chr22:34150200-34152200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr22:34150800-34154800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr22:34150800-34155000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr22:34151000-34151600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr22:34151000-34151800	Enhancers	Fetal Intestine Large	intestine
41	chr22:34151000-34152000	Enhancers	Fetal Intestine Small	intestine
42	chr22:34151000-34155000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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