Variant report

Variant	rs4253376
Chromosome Location	chr4:187172420-187172421
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:187111874..187113781-chr4:187171263..187172793,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269302	Chromatin interaction
ENSG00000145476	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs4253373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4253387	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4253856	1.00[AMR][1000 genomes]
rs72646238	1.00[AMR][1000 genomes]
rs72646242	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028146	chr4:186503899-187338335	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv530178	chr4:186659940-187478310	Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv931977	chr4:186912987-187364756	Active TSS Strong transcription Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv869299	chr4:186958290-187192748	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv1033203	chr4:186990348-187333476	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv537431	chr4:186990348-187333476	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv461864	chr4:187006806-187257004	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv596392	chr4:187006806-187257004	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv461865	chr4:187072383-187366649	Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv596401	chr4:187072383-187366649	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
11	nsv1022059	chr4:187082701-187183953	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
12	nsv881472	chr4:187152142-187187005	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187131800-187181600	Weak transcription	Brain Hippocampus Middle	brain
2	chr4:187146400-187172800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr4:187148000-187173000	Weak transcription	Psoas Muscle	Psoas
4	chr4:187148200-187179200	Weak transcription	Lung	lung
5	chr4:187148400-187172600	Weak transcription	Brain Anterior Caudate	brain
6	chr4:187148400-187179400	Weak transcription	Pancreas	Pancrea
7	chr4:187149800-187181600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr4:187149800-187186800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr4:187150200-187187200	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr4:187151000-187187200	Weak transcription	Colon Smooth Muscle	Colon
11	chr4:187151800-187173000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr4:187152000-187179400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr4:187154000-187182000	Weak transcription	Primary T cells from cord blood	blood
14	chr4:187156800-187179200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr4:187158000-187173000	Weak transcription	Left Ventricle	heart
16	chr4:187158400-187181400	Weak transcription	Fetal Intestine Large	intestine
17	chr4:187159800-187172600	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr4:187168600-187173000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr4:187168600-187173000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:187169200-187173600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:187170000-187179800	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr4:187170000-187180200	Weak transcription	Brain Angular Gyrus	brain
23	chr4:187170200-187175000	Weak transcription	Rectal Smooth Muscle	rectum
24	chr4:187170200-187179200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr4:187170400-187172600	Enhancers	Liver	Liver
26	chr4:187170400-187173000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr4:187170400-187173200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:187170600-187173000	Weak transcription	Brain Substantia Nigra	brain
29	chr4:187170800-187174400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:187170800-187182000	Weak transcription	Right Ventricle	heart
31	chr4:187171000-187172600	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr4:187171200-187182000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr4:187171400-187182000	Weak transcription	Spleen	Spleen
34	chr4:187171600-187179200	Weak transcription	Fetal Intestine Small	intestine
35	chr4:187171600-187182000	Weak transcription	Gastric	stomach
36	chr4:187171800-187181000	Weak transcription	Stomach Smooth Muscle	stomach
37	chr4:187172000-187172600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr4:187172000-187172800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr4:187172000-187182000	Weak transcription	Adipose Nuclei	Adipose
40	chr4:187172200-187173000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr4:187172200-187173200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr4:187172200-187182000	Weak transcription	Esophagus	oesophagus
43	chr4:187172400-187172800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:187172400-187173400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr4:187172400-187173600	Enhancers	HUES64 Cell Line	embryonic stem cell

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