Variant report

Variant	rs17150961
Chromosome Location	chr7:78157207-78157208
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10271370	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1030013	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11773635	0.91[CEU][hapmap];0.90[EUR][1000 genomes]
rs13244963	0.88[EUR][1000 genomes]
rs17150934	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17371672	0.86[CEU][hapmap];0.87[EUR][1000 genomes]
rs28626666	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4470960	1.00[JPT][hapmap]
rs58289607	0.90[ASN][1000 genomes]
rs60845180	0.92[ASN][1000 genomes]
rs6466259	1.00[CEU][hapmap];0.86[YRI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6466265	0.81[CEU][hapmap];0.87[EUR][1000 genomes]
rs67367279	0.86[EUR][1000 genomes]
rs725555	0.86[CEU][hapmap];0.87[EUR][1000 genomes]
rs7778097	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9692191	1.00[CHB][hapmap];0.90[ASN][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	nsv1022764	chr7:77911072-78316607	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78128800-78158400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:78138400-78161800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:78144200-78160000	Weak transcription	Brain Hippocampus Middle	brain
4	chr7:78144400-78158200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr7:78144400-78158600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr7:78151600-78158400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:78153400-78159600	Weak transcription	Brain Angular Gyrus	brain
8	chr7:78153800-78157600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr7:78153800-78158000	Weak transcription	Osteobl	bone
10	chr7:78154000-78157600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:78155800-78159400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:78156400-78160000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr7:78156600-78157400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr7:78156800-78157400	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr7:78156800-78160400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr7:78157000-78158000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr7:78157000-78172000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:78157200-78157400	Enhancers	H9 Cell Line	embryonic stem cell

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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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