Variant report

Variant	rs10018048
Chromosome Location	chr4:152807665-152807666
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10005715	1.00[AFR][1000 genomes]
rs10007840	1.00[AFR][1000 genomes]
rs10014252	1.00[AFR][1000 genomes]
rs10020124	1.00[AFR][1000 genomes]
rs10030443	1.00[AFR][1000 genomes]
rs28506896	1.00[AFR][1000 genomes]
rs28535054	1.00[AFR][1000 genomes]
rs9994738	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432644	chr4:152635395-153023402	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	esv2757086	chr4:152776271-152809738	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2759289	chr4:152776271-152809738	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv595731	chr4:152790580-152831309	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv432652	chr4:152791533-152818018	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1030328	chr4:152791533-152875666	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv1028836	chr4:152791680-152879097	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv10588	chr4:152807665-152809854	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152796400-152808200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:152803400-152809200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr4:152804000-152808800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr4:152804000-152809000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr4:152804200-152809400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr4:152805600-152808400	Weak transcription	Fetal Thymus	thymus
7	chr4:152806400-152809200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:152806800-152807800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:152806800-152808400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr4:152807000-152808000	Weak transcription	GM12878-XiMat	blood
11	chr4:152807000-152808200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:152807000-152808400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr4:152807000-152808600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:152807200-152808200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr4:152807400-152808200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr4:152807400-152808400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr4:152807400-152808400	Weak transcription	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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