Variant report

Variant	rs7321314
Chromosome Location	chr13:75988283-75988284
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:75988028..75990689-chr13:75994977..75997792,3	K562	blood:
2	chr13:75987894..75988452-chr13:76055971..76056871,2	MCF-7	breast:
3	chr13:75987952..75988694-chr13:76056057..76056871,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136111	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17064351	0.92[AFR][1000 genomes]
rs59522855	0.97[AFR][1000 genomes]
rs59760682	0.87[AFR][1000 genomes]
rs60321479	0.83[AFR][1000 genomes]
rs7326818	0.86[AFR][1000 genomes]
rs7328556	0.86[AFR][1000 genomes]
rs73535658	0.81[AFR][1000 genomes]
rs7986697	0.92[AFR][1000 genomes]
rs7995247	0.94[AFR][1000 genomes]
rs9593074	0.85[AMR][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	nsv498067	chr13:75178898-76012362	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	esv2761803	chr13:75943309-76161774	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv455987	chr13:75972846-76090084	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv562346	chr13:75972846-76090084	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:75977400-75990600	Weak transcription	Brain Anterior Caudate	brain
2	chr13:75979800-75989400	Weak transcription	HSMM	muscle
3	chr13:75980800-75989200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr13:75981000-75990600	Weak transcription	Fetal Muscle Leg	muscle
5	chr13:75981200-75990800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:75982000-75988400	Weak transcription	Psoas Muscle	Psoas
7	chr13:75984600-75990600	Weak transcription	Lung	lung
8	chr13:75984600-75990600	Weak transcription	Right Atrium	heart
9	chr13:75985200-75991800	Enhancers	HepG2	liver
10	chr13:75985600-75994400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr13:75986600-75988400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr13:75986600-75989400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr13:75986600-75990600	Weak transcription	Right Ventricle	heart
14	chr13:75986800-75989800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr13:75987000-75988600	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr13:75987000-75990600	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr13:75987200-75989400	Weak transcription	Adipose Nuclei	Adipose
18	chr13:75987200-75989600	Weak transcription	HMEC	breast
19	chr13:75987200-75989800	Weak transcription	Liver	Liver
20	chr13:75987200-75990600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr13:75987200-75990600	Weak transcription	Left Ventricle	heart
22	chr13:75987800-75988800	Enhancers	Gastric	stomach
23	chr13:75987800-75994000	Enhancers	Fetal Heart	heart
24	chr13:75988000-75989000	Enhancers	Ovary	ovary
25	chr13:75988000-75990800	Enhancers	Hela-S3	cervix
26	chr13:75988200-75988400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr13:75988200-75988400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr13:75988200-75988400	Enhancers	Aorta	Aorta
29	chr13:75988200-75988400	Enhancers	Spleen	Spleen
30	chr13:75988200-75988600	Enhancers	Pancreas	Pancrea
31	chr13:75988200-75988600	Enhancers	K562	blood
32	chr13:75988200-75988800	Enhancers	A549	lung
33	chr13:75988200-75988800	Flanking Active TSS	GM12878-XiMat	blood
34	chr13:75988200-75990200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr13:75988200-75991200	Enhancers	Fetal Kidney	kidney

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