Variant report

Variant	rs6662683
Chromosome Location	chr1:84975387-84975388
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:84975272-84975504	MCF10A-Er-Src	breast:	n/a	n/a
2	POLR2A	chr1:84974723-84975710	K562	blood:	n/a	n/a

No data

(count:6 , 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	chr1:84975237..84977774-chr1:85017252..85019567,2	K562	blood:
4	chr1:84973183..84975597-chr1:85046521..85049495,2	K562	blood:
5	chr1:84974456..84976737-chr1:85018067..85020188,2	K562	blood:
6	chr1:84966614..84978118-chr1:85034515..85041986,38	K562	blood:

No data

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

Extended variants
information (count: 50 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10493754	0.85[ASN][1000 genomes]
rs10874449	0.85[ASN][1000 genomes]
rs11163973	0.91[ASN][1000 genomes]
rs11163974	0.84[ASN][1000 genomes]
rs11163975	0.91[ASN][1000 genomes]
rs11163976	0.91[ASN][1000 genomes]
rs11163982	1.00[ASN][1000 genomes]
rs11163985	1.00[ASN][1000 genomes]
rs11163986	0.85[ASN][1000 genomes]
rs11163987	1.00[ASN][1000 genomes]
rs11163993	0.85[ASN][1000 genomes]
rs11164001	0.85[ASN][1000 genomes]
rs12075532	0.85[ASN][1000 genomes]
rs12354394	0.85[ASN][1000 genomes]
rs13093	1.00[ASN][1000 genomes]
rs17110164	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17110485	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17110590	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17110949	0.85[ASN][1000 genomes]
rs1849880	0.82[AMR][1000 genomes]
rs3768247	0.84[ASN][1000 genomes]
rs56876287	1.00[ASN][1000 genomes]
rs6576712	0.85[ASN][1000 genomes]
rs6576714	0.82[ASN][1000 genomes]
rs6658034	0.91[ASN][1000 genomes]
rs6658974	1.00[ASN][1000 genomes]
rs6660306	0.85[ASN][1000 genomes]
rs6662644	1.00[ASN][1000 genomes]
rs6666052	0.91[ASN][1000 genomes]
rs6666572	0.91[ASN][1000 genomes]
rs6668752	1.00[ASN][1000 genomes]
rs6669593	0.85[ASN][1000 genomes]
rs6676502	0.96[ASN][1000 genomes]
rs6684882	1.00[ASN][1000 genomes]
rs6688208	0.85[ASN][1000 genomes]
rs6690906	0.82[ASN][1000 genomes]
rs6701280	1.00[ASN][1000 genomes]
rs6704452	1.00[ASN][1000 genomes]
rs72948416	0.88[ASN][1000 genomes]
rs7524576	1.00[ASN][1000 genomes]
rs7525512	0.82[AMR][1000 genomes]
rs7532298	0.82[ASN][1000 genomes]
rs7539413	1.00[ASN][1000 genomes]
rs7541850	0.92[ASN][1000 genomes]
rs7541909	1.00[ASN][1000 genomes]
rs7547208	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7551329	0.91[ASN][1000 genomes]
rs7555773	1.00[ASN][1000 genomes]
rs7555821	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6662683	CTBS	cis	Heart Left Ventricle	GTEx

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84973000-84976200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr1:84973000-84977000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr1:84973000-85003200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr1:84973200-84982200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:84973200-84982200	Weak transcription	NHDF-Ad	bronchial
6	chr1:84973200-85003200	Weak transcription	Adipose Nuclei	Adipose
7	chr1:84973400-84976000	Weak transcription	HUVEC	blood vessel
8	chr1:84973400-84991600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:84973400-84993800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:84973400-84994400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:84973400-84995200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr1:84973400-85002000	Weak transcription	Primary T cells from cord blood	blood
13	chr1:84973600-84976200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:84973600-84984600	Weak transcription	Fetal Heart	heart
15	chr1:84973800-84977200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr1:84974000-84982200	Weak transcription	Aorta	Aorta
17	chr1:84974200-84991400	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr1:84975000-84975800	ZNF genes & repeats	Fetal Intestine Small	intestine
19	chr1:84975200-84975400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:84975200-84975400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:84975200-84975400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:84975200-84975400	ZNF genes & repeats	Primary B cells from cord blood	blood
23	chr1:84975200-85019600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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