Variant report

Variant	rs9289814
Chromosome Location	chr3:150215551-150215552
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:150127999..150131136-chr3:150212098..150216943,5	MCF-7	breast:
2	chr3:150214841..150217041-chr3:150221027..150224321,3	MCF-7	breast:
3	chr3:150110814..150113461-chr3:150215165..150218125,2	K562	blood:
4	chr3:150139889..150142772-chr3:150213958..150216741,2	K562	blood:
5	chr3:150146836..150150944-chr3:150211993..150216271,5	K562	blood:
6	chr3:150124804..150129560-chr3:150211663..150216825,11	K562	blood:
7	chr3:150124117..150127899-chr3:150211651..150217297,6	MCF-7	breast:
8	chr3:150214669..150217465-chr6:26198086..26200944,2	MCF-7	breast:
9	chr3:150004090..150004638-chr3:150215260..150215980,2	K562	blood:
10	chr3:150214882..150216583-chr3:150220861..150223172,3	K562	blood:
11	chr3:150214882..150218189-chr3:150218353..150222806,4	K562	blood:

No data

No data

No data

Variant related genes	Relation type
ENSG00000196428	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000197846	Chromatin interaction
ENSG00000196866	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10935804	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10935805	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28663502	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4277711	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4681624	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4681626	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4681627	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4681628	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55667242	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55788129	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56397117	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6440681	0.80[ASN][1000 genomes]
rs7634891	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9839876	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9866194	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9866525	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9881276	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];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	nsv532662	chr3:150180747-150633414	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150188200-150218800	Weak transcription	HSMM	muscle
2	chr3:150210600-150218600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr3:150213200-150215600	Weak transcription	NHEK	skin
4	chr3:150214000-150215600	Weak transcription	NHLF	lung
5	chr3:150214000-150233200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr3:150214800-150216200	Enhancers	K562	blood
7	chr3:150215000-150216800	Enhancers	Hela-S3	cervix
8	chr3:150215400-150215800	Enhancers	Osteobl	bone
9	chr3:150215400-150216000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:150215400-150216200	Enhancers	HUVEC	blood vessel

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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