Variant report

Variant	rs4907218
Chromosome Location	chr2:96553772-96553773
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 3 )

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3416818	chr2:96072529-96680708	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv874660	chr2:96091132-96669134	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv516044	chr2:96150959-96683378	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
4	nsv1003371	chr2:96326106-96684876	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv874662	chr2:96334397-96578621	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv874665	chr2:96370571-96596515	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv874666	chr2:96370571-96691125	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv1004482	chr2:96408987-96596717	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv428054	chr2:96438238-96627125	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv961832	chr2:96453677-96671971	Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv874667	chr2:96465201-96596515	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv874668	chr2:96465201-96600569	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
13	esv1826589	chr2:96468292-96583910	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
14	esv1826305	chr2:96468492-96583710	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
15	esv1848259	chr2:96477989-96583252	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region lncRNA	3 gene(s)	inside rSNPs	diseases
16	nsv834304	chr2:96493545-96667472	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv10093	chr2:96524159-96583335	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
18	esv1847850	chr2:96532929-96582175	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
19	nsv508154	chr2:96534336-96609925	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
20	esv1849015	chr2:96534572-96581975	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
21	nsv1004486	chr2:96544604-96684876	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
22	esv1847704	chr2:96545150-96583452	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
23	esv3506800	chr2:96545563-96588565	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
24	esv3506801	chr2:96545563-96588565	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
25	nsv874669	chr2:96547820-96691125	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
26	esv1010947	chr2:96549314-96586310	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
27	esv1797061	chr2:96550572-96582175	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
28	esv1793058	chr2:96553765-96583121	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4907218	ADRA2B	cis	Nerve Tibial	GTEx
rs4907218	ASTL	cis	Esophagus Mucosa	GTEx
rs4907218	ADRA2B	cis	Thyroid	GTEx

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96502600-96561400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr2:96502800-96555200	Weak transcription	Ovary	ovary
3	chr2:96502800-96585000	Weak transcription	Left Ventricle	heart
4	chr2:96502800-96616600	Weak transcription	Fetal Stomach	stomach
5	chr2:96503000-96563600	Weak transcription	Brain Hippocampus Middle	brain
6	chr2:96506600-96562000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:96521800-96555600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr2:96526600-96555200	Weak transcription	Fetal Muscle Leg	muscle
9	chr2:96526800-96555200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr2:96526800-96557600	Weak transcription	NHDF-Ad	bronchial
11	chr2:96527800-96554000	Weak transcription	HUVEC	blood vessel
12	chr2:96528600-96555600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr2:96528600-96560000	Weak transcription	Fetal Intestine Large	intestine
14	chr2:96530600-96555200	Weak transcription	Fetal Brain Female	brain
15	chr2:96531200-96557800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr2:96533000-96558000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:96536000-96576800	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr2:96541000-96555200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:96541000-96555800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr2:96541000-96582000	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr2:96541000-96595400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr2:96541200-96559800	Weak transcription	HMEC	breast
23	chr2:96541600-96595200	Weak transcription	Fetal Brain Male	brain
24	chr2:96542400-96557200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr2:96542600-96558400	Weak transcription	Brain Substantia Nigra	brain
26	chr2:96543000-96555200	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr2:96543800-96596200	Weak transcription	K562	blood
28	chr2:96544000-96555800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr2:96544600-96561800	Weak transcription	Colon Smooth Muscle	Colon
30	chr2:96544800-96557200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr2:96545000-96559600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr2:96545000-96576400	Weak transcription	Brain Germinal Matrix	brain
33	chr2:96546000-96555600	Weak transcription	Fetal Lung	lung
34	chr2:96546000-96577400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr2:96546400-96559800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:96546600-96554000	Weak transcription	HSMM	muscle
37	chr2:96546800-96562200	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr2:96547000-96555800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr2:96547000-96586400	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr2:96547200-96555600	Weak transcription	Fetal Heart	heart
41	chr2:96547200-96555600	Weak transcription	NH-A	brain
42	chr2:96547200-96558200	Weak transcription	HepG2	liver
43	chr2:96547400-96557200	Weak transcription	Aorta	Aorta
44	chr2:96547600-96575800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr2:96547800-96554000	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr2:96547800-96560200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:96548000-96563000	Weak transcription	Right Ventricle	heart
48	chr2:96548200-96555600	Weak transcription	GM12878-XiMat	blood
49	chr2:96548200-96557400	Weak transcription	NHEK	skin
50	chr2:96548200-96564200	Weak transcription	A549	lung

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