Variant report

Variant	rs4422825
Chromosome Location	chr9:95832650-95832651
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:95818455..95825266-chr9:95831322..95836031,9	K562	blood:
2	chr9:95825270..95827646-chr9:95832621..95835628,3	K562	blood:
3	chr9:95832455..95836206-chr9:95854622..95857563,3	K562	blood:
4	chr9:95821315..95824272-chr9:95832580..95834111,2	K562	blood:

Variant related genes	Relation type
ENSG00000157303	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs57847437	1.00[EUR][1000 genomes]
rs60167811	1.00[EUR][1000 genomes]
rs61245995	1.00[EUR][1000 genomes]
rs7018579	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7020936	1.00[EUR][1000 genomes]
rs7026691	1.00[EUR][1000 genomes]
rs73651354	1.00[EUR][1000 genomes]

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	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1054767	chr9:95738134-95875977	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1035230	chr9:95770249-95934982	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv893575	chr9:95781040-95854013	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer 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
5	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	esv1824329	chr9:95811604-95921347	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv893577	chr9:95812707-95872216	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv893578	chr9:95818641-95887320	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95822000-95834200	Weak transcription	Esophagus	oesophagus
2	chr9:95822000-95834200	Weak transcription	Right Atrium	heart
3	chr9:95822600-95834400	Weak transcription	Brain Hippocampus Middle	brain
4	chr9:95824000-95833800	Weak transcription	Ovary	ovary
5	chr9:95824600-95854000	Weak transcription	Gastric	stomach
6	chr9:95824800-95833200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr9:95825200-95834000	Weak transcription	Liver	Liver
8	chr9:95827600-95833600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
9	chr9:95827600-95839800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
10	chr9:95828000-95834200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr9:95828200-95834400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr9:95828200-95841600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr9:95828400-95833400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr9:95828400-95833800	Weak transcription	Spleen	Spleen
15	chr9:95828400-95834600	Weak transcription	Adipose Nuclei	Adipose
16	chr9:95828400-95834600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr9:95828400-95834600	Weak transcription	Fetal Intestine Small	intestine
18	chr9:95828400-95834600	Weak transcription	Lung	lung
19	chr9:95828400-95840000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr9:95828600-95840000	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr9:95828600-95845000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr9:95828800-95833400	Weak transcription	Primary B cells from cord blood	blood
23	chr9:95829400-95834200	Strong transcription	Primary B cells from peripheral blood	blood
24	chr9:95829600-95834400	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr9:95829800-95833400	Weak transcription	K562	blood
26	chr9:95830600-95840200	Weak transcription	Primary hematopoietic stem cells	blood
27	chr9:95830800-95834200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr9:95830800-95836200	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr9:95831000-95834400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr9:95831400-95833000	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr9:95831400-95833000	Strong transcription	GM12878-XiMat	blood
32	chr9:95831400-95836400	Genic enhancers	Primary T cells fromperipheralblood	blood
33	chr9:95831800-95832800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr9:95831800-95834000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr9:95831800-95834800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr9:95831800-95837400	Strong transcription	Primary T cells from cord blood	blood
37	chr9:95832200-95833000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr9:95832200-95833000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr9:95832400-95834000	Strong transcription	Fetal Thymus	thymus
40	chr9:95832600-95833200	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr9:95832600-95834000	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr9:95832600-95834000	Strong transcription	Thymus	Thymus
43	chr9:95832600-95834200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links