Variant report

Variant	rs13277305
Chromosome Location	chr8:126606895-126606896
allele	C/G
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:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:126589816..126592471-chr8:126605971..126608086,2	MCF-7	breast:
2	chr8:126551415..126553791-chr8:126604012..126607735,3	MCF-7	breast:
3	chr8:126440732..126445779-chr8:126600349..126612045,20	MCF-7	breast:
4	chr8:126584493..126586027-chr8:126604796..126607336,2	MCF-7	breast:
5	chr8:126606627..126608562-chr8:126611107..126612785,3	MCF-7	breast:
6	chr8:126455135..126457376-chr8:126604842..126607089,2	MCF-7	breast:
7	chr8:126585008..126593535-chr8:126599853..126611131,18	MCF-7	breast:
8	chr8:126605898..126607935-chr8:126618594..126621504,4	MCF-7	breast:
9	chr8:126507152..126508926-chr8:126605095..126607004,2	MCF-7	breast:
10	chr8:126606536..126608218-chr8:126626974..126628718,2	MCF-7	breast:
11	chr8:126605005..126607033-chr8:126613419..126615572,2	MCF-7	breast:
12	chr8:126440111..126444206-chr8:126606253..126610724,8	MCF-7	breast:
13	chr8:126605765..126606903-chr8:126656478..126657365,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000266452	Chromatin interaction
ENSG00000173334	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1015109	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11777118	0.86[EUR][1000 genomes]
rs11783267	0.86[EUR][1000 genomes]
rs11988437	0.86[EUR][1000 genomes]
rs11991475	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11995177	0.84[EUR][1000 genomes]
rs11996453	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11998450	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13255329	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13265324	0.84[EUR][1000 genomes]
rs13269369	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57078059	0.81[EUR][1000 genomes]
rs7016867	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7821956	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891437	chr8:126470817-126629328	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv6377	chr8:126579620-126639253	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv38	chr8:126593465-126639253	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1015513	chr8:126602536-126618074	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126602200-126608600	Enhancers	Placenta	Placenta
2	chr8:126602400-126607400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr8:126602800-126607400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr8:126603800-126607000	Enhancers	Esophagus	oesophagus
5	chr8:126603800-126607200	Enhancers	Pancreas	Pancrea
6	chr8:126604000-126608800	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr8:126604600-126607000	Enhancers	Placenta Amnion	Placenta Amnion
8	chr8:126605400-126608400	Enhancers	Fetal Intestine Large	intestine
9	chr8:126605400-126608400	Enhancers	Fetal Intestine Small	intestine
10	chr8:126605600-126607800	Enhancers	Hela-S3	cervix
11	chr8:126605600-126608800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr8:126605800-126608000	Weak transcription	HSMMtube	muscle
13	chr8:126606000-126607000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr8:126606000-126608200	Enhancers	Stomach Mucosa	stomach
15	chr8:126606200-126607200	Enhancers	Duodenum Mucosa	Duodenum
16	chr8:126606200-126607800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr8:126606200-126608200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr8:126606600-126608400	Enhancers	Colonic Mucosa	Colon
19	chr8:126606600-126608600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr8:126606600-126608600	Enhancers	Small Intestine	intestine
21	chr8:126606600-126613800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:126606800-126607000	Weak transcription	Left Ventricle	heart
23	chr8:126606800-126607200	Enhancers	A549	lung
24	chr8:126606800-126607600	Weak transcription	Right Ventricle	heart
25	chr8:126606800-126607800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:126606800-126607800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr8:126606800-126607800	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr8:126606800-126607800	Weak transcription	Gastric	stomach
29	chr8:126606800-126607800	Weak transcription	Psoas Muscle	Psoas
30	chr8:126606800-126608000	Weak transcription	Lung	lung
31	chr8:126606800-126608000	Weak transcription	Right Atrium	heart
32	chr8:126606800-126609000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr8:126606800-126609000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:126606800-126610400	Weak transcription	NHEK	skin
35	chr8:126606800-126610800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr8:126606800-126612800	Weak transcription	Spleen	Spleen
37	chr8:126606800-126613600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:126606800-126614800	Weak transcription	Osteobl	bone

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