Variant report

Variant	rs574737
Chromosome Location	chr1:10889464-10889465
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:10888572..10890725-chr1:10893676..10896099,3	K562	blood:
2	chr1:10882568..10884699-chr1:10885799..10889692,3	K562	blood:
3	chr1:10889433..10892912-chr1:10893269..10895457,3	MCF-7	breast:
4	chr1:10887422..10891418-chr1:10892933..10896099,4	K562	blood:

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12727463	0.99[ASN][1000 genomes]
rs12747228	0.96[ASN][1000 genomes]
rs34473345	0.99[ASN][1000 genomes]
rs35897090	0.99[ASN][1000 genomes]
rs634478	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs71645014	0.99[ASN][1000 genomes]
rs74052536	0.99[ASN][1000 genomes]
rs7534054	0.99[ASN][1000 genomes]
rs7555879	0.99[ASN][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	nsv870849	chr1:10694125-10894724	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv529981	chr1:10697093-11353487	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
3	esv2757723	chr1:10742502-11055147	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	esv2758921	chr1:10742502-11055147	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv871772	chr1:10832322-10894724	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv870589	chr1:10840905-10901994	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv871617	chr1:10858746-10935232	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv871155	chr1:10858746-10998509	Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	esv1825837	chr1:10887923-11093741	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10880200-10889800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:10883600-10902800	Weak transcription	Right Atrium	heart
3	chr1:10884400-10890000	Weak transcription	Fetal Heart	heart
4	chr1:10885000-10895600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:10886000-10890400	Weak transcription	Esophagus	oesophagus
6	chr1:10886200-10890200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr1:10886200-10890400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:10886200-10890400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:10886200-10890400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:10886200-10890400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:10886200-10890800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:10886200-10890800	Weak transcription	HMEC	breast
13	chr1:10886400-10890400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr1:10886400-10890400	Weak transcription	NHEK	skin
15	chr1:10887600-10890800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr1:10888400-10890000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:10888600-10890000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:10888800-10890400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:10889000-10895800	Weak transcription	Pancreas	Pancrea
20	chr1:10889200-10890200	Enhancers	Liver	Liver

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