Variant report

Variant	rs74012839
Chromosome Location	chr15:50201358-50201359
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10519245	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16963036	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16963041	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16963042	0.96[AFR][1000 genomes]
rs16963049	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74012836	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74012840	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044277	chr15:49921547-50702386	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542380	chr15:49921547-50702386	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv833003	chr15:50100372-50273309	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr15:50161800-50210600	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr15:50196800-50201400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr15:50199400-50201400	Weak transcription	Gastric	stomach
4	chr15:50200000-50201800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
5	chr15:50200200-50202000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr15:50200400-50201800	Enhancers	Placenta	Placenta
7	chr15:50200400-50202200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr15:50200600-50201800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr15:50200800-50201600	ZNF genes & repeats	Spleen	Spleen
10	chr15:50200800-50201800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:50200800-50201800	Enhancers	Fetal Muscle Trunk	muscle
12	chr15:50200800-50202600	Strong transcription	Primary hematopoietic stem cells	blood
13	chr15:50201000-50209400	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr15:50201200-50201400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr15:50201200-50201800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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

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