Variant report

Variant	rs58497131
Chromosome Location	chr6:167184519-167184520
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:167182263..167184637-chr6:167557115..167559460,2	K562	blood:
2	chr6:167173252..167177821-chr6:167180840..167184779,4	K562	blood:
3	chr6:167179347..167182239-chr6:167183994..167186208,2	K562	blood:
4	chr6:167172216..167176506-chr6:167180840..167185522,4	K562	blood:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16899435	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59966748	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6926309	1.00[AMR][1000 genomes]
rs73264991	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs733293	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73788141	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	nsv605260	chr6:166984094-167455139	Enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
4	nsv482478	chr6:167071366-167265821	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1019381	chr6:167090236-167558598	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
6	nsv538541	chr6:167090236-167558598	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1022866	chr6:167108740-167345629	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv482525	chr6:167151805-167324406	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv605326	chr6:167182277-167196032	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167173400-167189000	Weak transcription	Brain Anterior Caudate	brain
2	chr6:167180200-167186000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr6:167181000-167185200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:167182200-167218600	Weak transcription	Right Atrium	heart
5	chr6:167183400-167185000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:167183600-167184800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:167183600-167185000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr6:167183600-167185000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr6:167183800-167185000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr6:167183800-167185200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr6:167184000-167184800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr6:167184000-167184800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr6:167184000-167184800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr6:167184000-167185000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr6:167184200-167185000	Enhancers	Primary T cells from cord blood	blood
16	chr6:167184200-167185200	Enhancers	Fetal Thymus	thymus
17	chr6:167184200-167185400	Enhancers	Primary hematopoietic stem cells	blood
18	chr6:167184200-167189000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr6:167184400-167185000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr6:167184400-167185000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:167184400-167189000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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