Variant report

Variant	rs13262020
Chromosome Location	chr8:62671972-62671973
allele	A/C
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:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:62662413..62665090-chr8:62669593..62672242,2	K562	blood:
2	chr8:62671965..62673776-chr8:62679437..62680960,2	MCF-7	breast:
3	chr8:62671674..62674406-chr8:62692816..62694496,2	K562	blood:
4	chr8:62637876..62640545-chr8:62671155..62672770,2	K562	blood:
5	chr8:62618042..62628934-chr8:62666240..62683608,38	K562	blood:
6	chr1:146555118..146557644-chr8:62670729..62672845,2	K562	blood:
7	chr8:62616378..62628548-chr8:62667442..62677691,25	K562	blood:
8	chr8:62656958..62658937-chr8:62671143..62673593,2	K562	blood:
9	chr8:62646741..62649839-chr8:62670597..62672576,3	K562	blood:
10	chr8:62643774..62646108-chr8:62669331..62672229,2	K562	blood:
11	chr8:62649158..62652161-chr8:62671715..62675125,3	K562	blood:
12	chr8:62596550..62600642-chr8:62671938..62674240,3	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASPH-1	chr8:62671660-62674323	XLOC_007098
2	lnc-ASPH-1	chr8:62671653-62674323	ENSG00000251127

No data

Variant related genes	Relation type
ENSG00000198363	Chromatin interaction
ENSG00000230832	Chromatin interaction
ENSG00000264408	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10504333	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13248406	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13249337	0.82[GIH][hapmap]
rs13252124	0.97[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13258801	0.97[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13266959	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13275357	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.89[MEX][hapmap];0.88[MKK][hapmap];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13277217	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024432	chr8:62086247-62898782	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv932198	chr8:62336705-62914562	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv2761430	chr8:62517980-62873803	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription 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 miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1015216	chr8:62517980-62873803	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv436576	chr8:62666494-62673163	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62669000-62672000	Enhancers	HepG2	liver
2	chr8:62669400-62672000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:62669400-62672000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr8:62669400-62672200	Weak transcription	Esophagus	oesophagus
5	chr8:62669400-62672200	Weak transcription	Pancreas	Pancrea
6	chr8:62669400-62672200	Weak transcription	NHLF	lung
7	chr8:62669400-62672400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:62669400-62672400	Weak transcription	Fetal Muscle Trunk	muscle
9	chr8:62669400-62672600	Weak transcription	Lung	lung
10	chr8:62669400-62672600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr8:62669400-62672800	Weak transcription	Fetal Lung	lung
12	chr8:62669400-62672800	Weak transcription	Fetal Muscle Leg	muscle
13	chr8:62669400-62672800	Weak transcription	Gastric	stomach
14	chr8:62669600-62672000	Weak transcription	Adipose Nuclei	Adipose
15	chr8:62669800-62672000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:62669800-62672000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr8:62669800-62672000	Weak transcription	NHDF-Ad	bronchial
18	chr8:62669800-62672800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:62670800-62672200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr8:62671000-62675200	Flanking Active TSS	A549	lung
21	chr8:62671400-62672000	Enhancers	NH-A	brain
22	chr8:62671600-62672000	Enhancers	Hela-S3	cervix
23	chr8:62671600-62672400	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr8:62671800-62672000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr8:62671800-62672000	Enhancers	Osteobl	bone
26	chr8:62671800-62672200	Enhancers	Muscle Satellite Cultured Cells	--
27	chr8:62671800-62672200	Enhancers	K562	blood
28	chr8:62671800-62672400	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr8:62671800-62672800	Flanking Active TSS	HUVEC	blood vessel
30	chr8:62671800-62674200	Enhancers	Stomach Mucosa	stomach

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