Variant report

Variant	rs7750221
Chromosome Location	chr6:167142542-167142543
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11964446	0.80[EUR][1000 genomes]
rs1810469	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2007901	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2007919	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6456110	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6456119	0.80[EUR][1000 genomes]
rs6932950	0.80[EUR][1000 genomes]
rs6933260	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6942153	0.80[EUR][1000 genomes]
rs7738499	0.80[EUR][1000 genomes]
rs7750004	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7750476	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7750983	0.80[EUR][1000 genomes]
rs7751129	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7754793	0.94[ASN][1000 genomes]
rs7757799	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7762526	0.80[EUR][1000 genomes]
rs7762789	0.80[EUR][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	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	nsv432984	chr6:167018915-167181613	Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	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
6	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
7	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
8	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

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167136600-167157600	Weak transcription	Brain Angular Gyrus	brain
2	chr6:167139000-167143200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:167140000-167147400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:167141000-167143800	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr6:167141600-167143000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:167141800-167142600	Enhancers	NH-A	brain
7	chr6:167141800-167143200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr6:167142000-167142600	Weak transcription	Lung	lung
9	chr6:167142000-167142800	Enhancers	Primary hematopoietic stem cells	blood
10	chr6:167142200-167142600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:167142200-167142800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:167142200-167142800	Enhancers	Pancreas	Pancrea
13	chr6:167142200-167143400	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr6:167142200-167143600	Enhancers	Fetal Thymus	thymus
15	chr6:167142200-167143600	Enhancers	Thymus	Thymus
16	chr6:167142400-167142600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr6:167142400-167142600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:167142400-167142800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr6:167142400-167142800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr6:167142400-167142800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:167142400-167143200	Enhancers	Primary T cells fromperipheralblood	blood
22	chr6:167142400-167143800	Enhancers	Primary T cells from cord blood	blood

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