Variant report

Variant	rs576265673
Chromosome Location	chr22:31456616-31456617
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:31363691..31369255-chr22:31456002..31460514,7	MCF-7	breast:
2	chr22:31363469..31366268-chr22:31450278..31456884,6	MCF-7	breast:
3	chr22:31455769..31462183-chr22:31475245..31482356,13	K562	blood:
4	chr22:31455775..31461842-chr22:31476267..31480955,13	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253352	Chromatin interaction
ENSG00000133422	Chromatin interaction
ENSG00000273387	Chromatin interaction
ENSG00000183963	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv9896	chr22:31369204-31513933	Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
2	nsv524366	chr22:31440703-31480069	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv829173	chr22:31450043-31543956	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
4	nsv964620	chr22:31452981-31465140	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv962852	chr22:31455516-31465140	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr22:31452000-31458000	Weak transcription	Adipose Nuclei	Adipose
2	chr22:31452800-31456800	Weak transcription	Hela-S3	cervix
3	chr22:31452800-31458200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr22:31455400-31458400	Enhancers	K562	blood
5	chr22:31455600-31457000	Enhancers	HepG2	liver
6	chr22:31455600-31457600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr22:31455800-31457400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr22:31455800-31458400	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr22:31456000-31458200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr22:31456000-31458200	Weak transcription	Fetal Muscle Trunk	muscle
11	chr22:31456000-31458200	Weak transcription	HMEC	breast
12	chr22:31456200-31456800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr22:31456200-31457000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr22:31456200-31460000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr22:31456200-31460000	Weak transcription	A549	lung
16	chr22:31456400-31456800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr22:31456400-31456800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr22:31456400-31458200	Weak transcription	Fetal Intestine Large	intestine
19	chr22:31456400-31458400	Weak transcription	Fetal Intestine Small	intestine
20	chr22:31456600-31457200	Enhancers	NHEK	skin
21	chr22:31456600-31461000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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