Variant report

Variant	rs312395
Chromosome Location	chr1:84974960-84974961
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SETDB1	chr1:84974585-84975056	U2OS	brain:	n/a	n/a
2	ZNF384	chr1:84974782-84974975	GM12878	blood:	n/a	n/a
3	POLR2A	chr1:84974723-84975710	K562	blood:	n/a	n/a
4	KAP1	chr1:84974151-84975096	K562	blood:	n/a	n/a
5	ZNF384	chr1:84974717-84975032	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84969735..84979623-chr1:84983174..84994888,16	K562	blood:
2	chr1:84973180..84975531-chr1:85217909..85219916,2	K562	blood:
3	chr1:84973183..84975597-chr1:85046521..85049495,2	K562	blood:
4	chr1:84974456..84976737-chr1:85018067..85020188,2	K562	blood:
5	chr1:84966614..84978118-chr1:85034515..85041986,38	K562	blood:

No data

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

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11163971	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11163972	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11163980	0.81[CHB][hapmap]
rs11163981	0.81[CHB][hapmap]
rs11163992	1.00[ASN][1000 genomes]
rs1123981	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1144276	0.81[CHB][hapmap]
rs11578494	0.85[CHB][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs11586006	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12071149	0.81[CHB][hapmap]
rs12123381	1.00[ASN][1000 genomes]
rs12124568	1.00[ASN][1000 genomes]
rs12124731	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12126584	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12126924	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12128801	0.81[CHB][hapmap]
rs12136756	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12137559	1.00[ASN][1000 genomes]
rs12140555	1.00[ASN][1000 genomes]
rs12143652	0.93[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs12145405	0.98[ASN][1000 genomes]
rs1246159	0.81[CHB][hapmap]
rs1395416	1.00[ASN][1000 genomes]
rs1395417	1.00[ASN][1000 genomes]
rs1506707	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17109982	0.93[ASN][1000 genomes]
rs17110030	0.98[ASN][1000 genomes]
rs17110519	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1911159	0.81[CHB][hapmap]
rs2271620	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2292808	0.99[ASN][1000 genomes]
rs2659173	0.81[CHB][hapmap]
rs2794218	0.81[CHB][hapmap]
rs312397	0.81[CHB][hapmap]
rs3813605	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3813607	0.96[ASN][1000 genomes]
rs3922538	0.94[ASN][1000 genomes]
rs4906995	0.81[CHB][hapmap]
rs4907076	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4907077	1.00[ASN][1000 genomes]
rs4907078	0.81[CHB][hapmap]
rs56212819	1.00[ASN][1000 genomes]
rs57245302	1.00[ASN][1000 genomes]
rs57442052	1.00[ASN][1000 genomes]
rs6704211	0.81[CHB][hapmap]
rs74095416	0.93[ASN][1000 genomes]
rs74095424	1.00[ASN][1000 genomes]
rs74095432	1.00[ASN][1000 genomes]
rs74095436	1.00[ASN][1000 genomes]
rs7512922	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7513490	1.00[ASN][1000 genomes]
rs7514763	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7519606	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7535445	0.93[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs7536988	0.91[ASN][1000 genomes]
rs925740	1.00[ASN][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:25 , 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	chr1:84973000-84975200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:84973000-84976200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr1:84973000-84977000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr1:84973000-85003200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:84973200-84975000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:84973200-84982200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr1:84973200-84982200	Weak transcription	NHDF-Ad	bronchial
10	chr1:84973200-85003200	Weak transcription	Adipose Nuclei	Adipose
11	chr1:84973400-84976000	Weak transcription	HUVEC	blood vessel
12	chr1:84973400-84991600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:84973400-84993800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:84973400-84994400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr1:84973400-84995200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr1:84973400-85002000	Weak transcription	Primary T cells from cord blood	blood
17	chr1:84973600-84975000	Weak transcription	Fetal Intestine Small	intestine
18	chr1:84973600-84975200	Weak transcription	Primary B cells from cord blood	blood
19	chr1:84973600-84976200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:84973600-84984600	Weak transcription	Fetal Heart	heart
21	chr1:84973800-84977200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr1:84974000-84982200	Weak transcription	Aorta	Aorta
23	chr1:84974200-84975000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:84974200-84991400	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr1:84974600-84975200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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