Variant report

Variant	rs17137519
Chromosome Location	chr5:114525484-114525485
allele	C/T
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:4)

rs_ID	r²[population]
rs17137603	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs73251597	1.00[AFR][1000 genomes]
rs73255464	0.81[AFR][1000 genomes]
rs73257443	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830453	chr5:114277261-114546536	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv462399	chr5:114445023-114526010	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv599477	chr5:114445023-114526010	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv830454	chr5:114453864-114607159	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 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	chr5:114522800-114543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:114523000-114526800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:114523400-114576200	Weak transcription	Psoas Muscle	Psoas
4	chr5:114525200-114526600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr5:114525400-114525600	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr5:114525400-114525800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr5:114525400-114526000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:114525400-114526200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr5:114525400-114526400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:114525400-114526400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr5:114525400-114526400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr5:114525400-114526400	Enhancers	Gastric	stomach
13	chr5:114525400-114526600	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr5:114525400-114527400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr5:114525400-114531400	Enhancers	Rectal Mucosa Donor 31	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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