Variant report

Variant	rs537447985
Chromosome Location	chr5:94954319-94954320
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	chr5:94953437..94955411-chr5:95066946..95068798,2	K562	blood:
2	chr5:94953878..94956024-chr5:94981084..94983825,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPATA9-2	chr5:94946081-94955781	NONHSAT102852

Variant related genes	Relation type
ENSG00000175449	Chromatin interaction
ENSG00000250240	Chromatin interaction
ENSG00000164292	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv598955	chr5:94903453-95136019	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	esv3421596	chr5:94954196-94958694	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94938200-94954400	Weak transcription	Primary T cells from cord blood	blood
2	chr5:94949000-94955000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:94949800-94955000	Weak transcription	Primary B cells from cord blood	blood
4	chr5:94951000-94955400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr5:94952200-94954600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr5:94952200-94955400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr5:94952400-94954600	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr5:94953000-94954400	Weak transcription	Pancreas	Pancrea
9	chr5:94953000-94955200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:94953200-94954400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:94953200-94954600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:94953200-94954600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:94953200-94954600	Weak transcription	HUVEC	blood vessel
14	chr5:94953200-94955000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr5:94953200-94955000	Weak transcription	NH-A	brain
16	chr5:94953200-94955200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr5:94953200-94955200	Weak transcription	GM12878-XiMat	blood
18	chr5:94953200-94955200	Weak transcription	Osteobl	bone
19	chr5:94953200-94955400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr5:94953200-94955400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr5:94953200-94955600	Enhancers	NHEK	skin
22	chr5:94953800-94955000	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr5:94953800-94955800	Weak transcription	HMEC	breast
24	chr5:94954000-94955000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr5:94954200-94954800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr5:94954200-94955200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr5:94954200-94955400	Enhancers	Primary T helper naive cells from peripheral blood	blood

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