Variant report

Variant	rs59926068
Chromosome Location	chr4:149221320-149221321
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs57841317	1.00[AFR][1000 genomes]
rs72655278	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027263	chr4:149127120-149320135	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537296	chr4:149127120-149320135	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1031815	chr4:149172485-149282928	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1028105	chr4:149199913-149284620	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv537297	chr4:149199913-149284620	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1016966	chr4:149209467-149341037	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:149206400-149231600	Weak transcription	Right Ventricle	heart
2	chr4:149215200-149232800	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr4:149215400-149222200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr4:149215400-149224600	Weak transcription	Small Intestine	intestine
5	chr4:149216800-149226800	Weak transcription	Left Ventricle	heart
6	chr4:149216800-149238000	Weak transcription	Lung	lung
7	chr4:149217000-149224800	Weak transcription	Psoas Muscle	Psoas
8	chr4:149217000-149225600	Weak transcription	Pancreas	Pancrea
9	chr4:149220000-149221600	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr4:149220400-149225600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr4:149220600-149221400	Enhancers	Colonic Mucosa	Colon
12	chr4:149220600-149221400	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr4:149221000-149232000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr4:149221200-149221400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:149221200-149221400	Weak transcription	Rectal Smooth Muscle	rectum

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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