Variant report

Variant	rs1801334
Chromosome Location	chr6:161781225-161781226
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:161774851..161778239-chr6:161778707..161783071,5	K562	blood:
2	chr6:161695256..161697012-chr6:161781193..161782822,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10455880	1.00[ASW][hapmap]
rs11966738	1.00[ASN][1000 genomes]
rs12198438	1.00[ASN][1000 genomes]
rs12208181	1.00[ASW][hapmap];1.00[ASN][1000 genomes]
rs12210160	1.00[ASW][hapmap]
rs12211065	1.00[ASN][1000 genomes]
rs12213394	1.00[ASN][1000 genomes]
rs12213397	1.00[ASN][1000 genomes]
rs12215325	1.00[ASN][1000 genomes]
rs12215774	1.00[ASN][1000 genomes]
rs13206689	1.00[ASN][1000 genomes]
rs13207820	1.00[ASN][1000 genomes]
rs13216830	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13217906	1.00[ASW][hapmap]
rs13220090	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs16892499	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35184046	1.00[ASN][1000 genomes]
rs35280474	1.00[ASN][1000 genomes]
rs35812310	1.00[ASN][1000 genomes]
rs35996169	1.00[ASN][1000 genomes]
rs66471370	1.00[ASN][1000 genomes]
rs6920768	1.00[GIH][hapmap]
rs71567607	1.00[ASN][1000 genomes]
rs73021269	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73021292	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73023258	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886817	chr6:161371621-161846654	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3381361	chr6:161373617-161864101	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv949397	chr6:161592100-161812932	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv2752091	chr6:161592100-161855785	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv1029727	chr6:161607680-161814295	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1030623	chr6:161611170-161796985	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv538494	chr6:161611170-161796985	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv481931	chr6:161647026-161961906	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv1031234	chr6:161676768-162250726	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv869611	chr6:161690974-161817564	Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv1025168	chr6:161702621-161831885	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv886819	chr6:161712035-162520133	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv886820	chr6:161712880-162184932	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv830854	chr6:161739926-161927515	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
15	nsv5577	chr6:161775026-161819733	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	1 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	chr6:161763400-161782000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr6:161775200-161784200	Weak transcription	Brain Anterior Caudate	brain
3	chr6:161775400-161781800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr6:161777400-161782600	Weak transcription	Pancreas	Pancrea
5	chr6:161777800-161786800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:161778400-161781400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:161780200-161781400	Enhancers	HSMMtube	muscle
8	chr6:161780200-161781600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:161780200-161781800	Enhancers	Fetal Heart	heart
10	chr6:161780200-161782200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr6:161780400-161782200	Enhancers	Left Ventricle	heart
12	chr6:161780600-161835800	Weak transcription	Right Atrium	heart
13	chr6:161780800-161781400	Enhancers	Osteobl	bone
14	chr6:161780800-161781800	Weak transcription	K562	blood
15	chr6:161780800-161782200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr6:161781000-161781400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:161781200-161781400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:161781200-161783800	Weak transcription	Right Ventricle	heart
19	chr6:161781200-161784000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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