Variant report

Variant	rs312396
Chromosome Location	chr1:84973945-84973946
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF384	chr1:84973416-84974018	K562	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84972325..84974748-chr1:85028304..85030920,3	K562	blood:
2	chr1:84969735..84979623-chr1:84983174..84994888,16	K562	blood:
3	chr1:84973180..84975531-chr1:85217909..85219916,2	K562	blood:
4	chr1:84973183..84975597-chr1:85046521..85049495,2	K562	blood:
5	chr1:84966614..84978118-chr1:85034515..85041986,38	K562	blood:
6	chr1:84966967..84974535-chr1:85036439..85041823,24	K562	blood:

No data

Variant related genes	Relation type
GNG5	TF binding region
ENSG00000117151	Chromatin interaction
ENSG00000122432	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1246156	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1246256	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1911157	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2135552	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2659168	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2911587	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2911596	1.00[AMR][1000 genomes]
rs2943667	0.81[AFR][1000 genomes]
rs2945154	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2945157	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2945159	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2994952	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3096444	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs312400	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs312402	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7511674	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830437	chr1:84837524-85001269	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84972600-84975200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:84972600-84975200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:84973000-84974000	Enhancers	Aorta	Aorta
4	chr1:84973000-84974600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:84973000-84974600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:84973000-84975200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:84973000-84976200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:84973000-84977000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr1:84973000-85003200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr1:84973200-84974200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:84973200-84974400	Enhancers	Fetal Intestine Large	intestine
12	chr1:84973200-84975000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:84973200-84982200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:84973200-84982200	Weak transcription	NHDF-Ad	bronchial
15	chr1:84973200-85003200	Weak transcription	Adipose Nuclei	Adipose
16	chr1:84973400-84974200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr1:84973400-84976000	Weak transcription	HUVEC	blood vessel
18	chr1:84973400-84991600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:84973400-84993800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:84973400-84994400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:84973400-84995200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr1:84973400-85002000	Weak transcription	Primary T cells from cord blood	blood
23	chr1:84973600-84974000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:84973600-84974000	Weak transcription	Liver	Liver
25	chr1:84973600-84974200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:84973600-84974400	Enhancers	Dnd41	blood
27	chr1:84973600-84975000	Weak transcription	Fetal Intestine Small	intestine
28	chr1:84973600-84975200	Weak transcription	Primary B cells from cord blood	blood
29	chr1:84973600-84976200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:84973600-84984600	Weak transcription	Fetal Heart	heart
31	chr1:84973800-84974000	Enhancers	Thymus	Thymus
32	chr1:84973800-84974000	Active TSS	K562	blood
33	chr1:84973800-84974400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:84973800-84974800	Enhancers	HepG2	liver
35	chr1:84973800-84977200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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