Variant report

Variant	rs72507584
Chromosome Location	chr8:99372287-99372288
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:99371126..99375307-chr8:99376656..99381075,4	K562	blood:
2	chr8:99364130..99368810-chr8:99369067..99373271,6	MCF-7	breast:
3	chr8:99304426..99306642-chr8:99371126..99373408,3	MCF-7	breast:
4	chr8:99370597..99373057-chr8:99386585..99389317,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000104361	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs16896877	0.85[EUR][1000 genomes]
rs4446701	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59622499	0.89[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	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv831406	chr8:99290745-99482076	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv891217	chr8:99346537-99391285	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99363600-99373800	Weak transcription	Pancreas	Pancrea
2	chr8:99367400-99377000	Enhancers	Fetal Lung	lung
3	chr8:99368200-99372600	Enhancers	NHDF-Ad	bronchial
4	chr8:99369800-99373400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:99370400-99372600	Enhancers	Left Ventricle	heart
6	chr8:99370800-99374000	Weak transcription	Fetal Stomach	stomach
7	chr8:99370800-99374200	Weak transcription	Gastric	stomach
8	chr8:99371000-99373400	Weak transcription	Right Atrium	heart
9	chr8:99371000-99373800	Weak transcription	Ovary	ovary
10	chr8:99371000-99373800	Weak transcription	Right Ventricle	heart
11	chr8:99371000-99374000	Weak transcription	Esophagus	oesophagus
12	chr8:99371000-99374000	Weak transcription	Stomach Mucosa	stomach
13	chr8:99371000-99374000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr8:99371000-99374200	Weak transcription	Lung	lung
15	chr8:99371000-99375400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr8:99371000-99376400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr8:99371000-99376800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr8:99371000-99376800	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr8:99371200-99372400	Weak transcription	Fetal Heart	heart
20	chr8:99371200-99373000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr8:99371200-99373800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr8:99371200-99374000	Weak transcription	Fetal Muscle Leg	muscle
23	chr8:99371200-99374200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:99371200-99375000	Weak transcription	GM12878-XiMat	blood
25	chr8:99371200-99377000	Weak transcription	Aorta	Aorta
26	chr8:99371400-99372400	Enhancers	Osteobl	bone
27	chr8:99371400-99373800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:99371400-99373800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr8:99371400-99373800	Weak transcription	HMEC	breast
30	chr8:99371400-99374000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr8:99371400-99374000	Weak transcription	Adipose Nuclei	Adipose
32	chr8:99371400-99374200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:99371400-99374200	Weak transcription	NH-A	brain
34	chr8:99371400-99374400	Weak transcription	Placenta	Placenta
35	chr8:99371400-99374600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:99371400-99374600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr8:99371400-99376400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:99371400-99376400	Weak transcription	NHEK	skin
39	chr8:99371400-99376600	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr8:99371600-99372400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:99371600-99373800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr8:99372000-99373200	Enhancers	K562	blood
43	chr8:99372200-99373600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr8:99372200-99373800	Weak transcription	NHLF	lung

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