Variant report

Variant	rs617527
Chromosome Location	chr18:9687622-9687623
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:9687090..9689506-chr18:9715021..9717452,2	MCF-7	breast:
2	chr18:9684743..9687685-chr18:9730508..9732228,2	K562	blood:
3	chr18:9686886..9688402-chr18:9740468..9742300,2	K562	blood:
4	chr18:9686215..9688324-chr18:9694336..9696864,2	K562	blood:
5	chr18:9686466..9688287-chr18:9706905..9709990,3	K562	blood:
6	chr18:9687164..9689155-chr18:9707518..9710077,2	MCF-7	breast:
7	chr18:9613899..9615643-chr18:9685662..9687979,2	MCF-7	breast:
8	chr18:9686824..9689922-chr18:9694336..9698483,3	K562	blood:
9	chr18:9687189..9690124-chr18:9701130..9704989,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000263627	Chromatin interaction
ENSG00000154845	Chromatin interaction
ENSG00000168461	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs583917	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs602911	0.94[ASN][1000 genomes]
rs606910	0.81[ASN][1000 genomes]
rs616583	0.94[ASN][1000 genomes]
rs617512	0.94[ASN][1000 genomes]
rs620726	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs621707	0.94[ASN][1000 genomes]
rs630467	0.93[ASN][1000 genomes]
rs679231	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs681114	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3693417	chr18:9512985-9693638	Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv458024	chr18:9558240-9828448	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv576448	chr18:9558240-9828448	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv576449	chr18:9623052-9700382	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv469897	chr18:9674498-9870517	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv482461	chr18:9674498-9870517	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9684000-9688000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr18:9684200-9688000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr18:9684200-9688000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr18:9684200-9688200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr18:9684200-9688200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr18:9684200-9688200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr18:9685200-9695200	Weak transcription	Spleen	Spleen
8	chr18:9685400-9688200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr18:9685600-9687800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr18:9685600-9688000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr18:9685600-9688000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr18:9685600-9688000	Weak transcription	Esophagus	oesophagus
13	chr18:9685600-9688200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr18:9685600-9688200	Weak transcription	HMEC	breast
15	chr18:9685600-9688200	Weak transcription	NH-A	brain
16	chr18:9685600-9695800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr18:9685600-9696800	Weak transcription	Right Atrium	heart
18	chr18:9685800-9688000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr18:9685800-9688200	Weak transcription	Osteobl	bone
20	chr18:9685800-9690600	Weak transcription	NHLF	lung
21	chr18:9685800-9690800	Weak transcription	Fetal Lung	lung
22	chr18:9685800-9695200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr18:9686000-9687800	Weak transcription	K562	blood
24	chr18:9686000-9688400	Weak transcription	Fetal Thymus	thymus
25	chr18:9686000-9690600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr18:9686000-9695400	Weak transcription	Fetal Muscle Leg	muscle
27	chr18:9686000-9695600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr18:9686400-9691000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr18:9686400-9693600	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr18:9686600-9688200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr18:9687600-9688000	Enhancers	NHEK	skin

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