Variant report

Variant	rs851198
Chromosome Location	chr1:223431864-223431865
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:223431564..223434363-chr1:223444284..223446683,2	MCF-7	breast:
2	chr1:223424612..223427154-chr1:223429985..223432180,2	MCF-7	breast:
3	chr1:223428944..223431971-chr1:223436003..223438459,3	K562	blood:
4	chr1:223431021..223433765-chr1:223535205..223536885,2	MCF-7	breast:
5	chr1:223427403..223430031-chr1:223430338..223431900,2	MCF-7	breast:
6	chr1:223398875..223400534-chr1:223430075..223432511,2	K562	blood:
7	chr1:223431095..223433282-chr1:223435699..223438633,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000143502	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17163754	1.00[EUR][1000 genomes]
rs712859	1.00[EUR][1000 genomes]
rs73122211	1.00[EUR][1000 genomes]
rs73122214	1.00[EUR][1000 genomes]
rs73122215	1.00[EUR][1000 genomes]
rs851195	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs851197	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs851200	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers 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 target site	48 gene(s)	inside rSNPs	diseases
2	nsv832659	chr1:223294767-223438487	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1000039	chr1:223429733-223527845	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	4 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	chr1:223423800-223439600	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr1:223424200-223438800	Weak transcription	Ovary	ovary
3	chr1:223427400-223442000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr1:223428400-223432200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:223430200-223432000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:223430200-223432000	Weak transcription	Esophagus	oesophagus
7	chr1:223430400-223432000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:223430400-223432000	Weak transcription	HMEC	breast
9	chr1:223431200-223432200	Weak transcription	Pancreas	Pancrea
10	chr1:223431400-223433000	Enhancers	A549	lung
11	chr1:223431400-223433600	Enhancers	Fetal Intestine Large	intestine
12	chr1:223431600-223432400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr1:223431800-223432200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:223431800-223432600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:223431800-223432600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:223431800-223432600	Enhancers	Stomach Mucosa	stomach
17	chr1:223431800-223432600	Enhancers	NHEK	skin
18	chr1:223431800-223433000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:223431800-223433200	Enhancers	Fetal Intestine Small	intestine
20	chr1:223431800-223433400	Weak transcription	Primary T cells from cord blood	blood

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