Variant report

Variant	rs2007835
Chromosome Location	chr17:63127165-63127166
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1530351	0.93[CEU][hapmap];0.82[EUR][1000 genomes]
rs1533336	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs186167	0.88[ASN][1000 genomes]
rs1867212	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1867213	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2585859	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs299820	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs299821	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs299824	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs299834	0.82[JPT][hapmap];0.94[ASN][1000 genomes]
rs299837	0.94[ASN][1000 genomes]
rs299838	0.94[ASN][1000 genomes]
rs299842	1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs414341	1.00[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4790958	0.82[JPT][hapmap];0.86[EUR][1000 genomes]
rs4791230	0.82[EUR][1000 genomes]
rs510199	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8079386	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530764	chr17:62939944-63278472	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv527042	chr17:63123532-63128261	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:63119800-63133600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr17:63124000-63132600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr17:63126200-63127200	Enhancers	Primary hematopoietic stem cells	blood
4	chr17:63126200-63127600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr17:63126400-63127800	Enhancers	K562	blood
6	chr17:63126600-63127400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr17:63126800-63127400	Enhancers	GM12878-XiMat	blood
8	chr17:63126800-63127400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
9	chr17:63126800-63127600	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr17:63126800-63128200	Enhancers	Fetal Intestine Large	intestine
11	chr17:63126800-63129000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr17:63126800-63129000	Enhancers	Fetal Intestine Small	intestine
13	chr17:63127000-63127200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
14	chr17:63127000-63127400	Enhancers	Duodenum Mucosa	Duodenum
15	chr17:63127000-63127600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr17:63127000-63127800	Enhancers	Spleen	Spleen
17	chr17:63127000-63128000	Enhancers	HepG2	liver
18	chr17:63127000-63128200	Enhancers	Liver	Liver
19	chr17:63127000-63129000	Enhancers	NHDF-Ad	bronchial

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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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