Variant report

Variant	rs1776029
Chromosome Location	chr1:220080028-220080029
allele	A/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:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:220049654..220055066-chr1:220079311..220085497,6	K562	blood:
2	chr1:220072364..220075393-chr1:220077961..220082079,4	K562	blood:
3	chr1:220070443..220076054-chr1:220076970..220083388,8	K562	blood:
4	chr1:220056357..220058646-chr1:220078386..220080543,2	K562	blood:
5	chr1:220078897..220080422-chr1:220101936..220103801,2	K562	blood:
6	chr1:220065741..220068828-chr1:220078028..220081073,4	K562	blood:
7	chr1:220078373..220081113-chr1:220217284..220220035,3	K562	blood:

No data

No data

No data

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10863510	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10863511	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1694592	0.85[AMR][1000 genomes]
rs1694593	0.85[AMR][1000 genomes]
rs1694594	0.85[AMR][1000 genomes]
rs1694595	0.85[AMR][1000 genomes]
rs1776030	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1776043	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1776046	0.85[AMR][1000 genomes]
rs1776050	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1776052	0.85[AMR][1000 genomes]
rs2275707	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2378331	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6541114	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6541115	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7525274	0.85[AMR][1000 genomes]
rs947517	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006393	chr1:219925261-220126458	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1067840	chr1:219990803-220091941	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220077000-220080400	Weak transcription	HepG2	liver
2	chr1:220077400-220080600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr1:220077400-220086800	Weak transcription	Fetal Intestine Large	intestine
4	chr1:220077400-220088400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr1:220077400-220088600	Weak transcription	Fetal Intestine Small	intestine
6	chr1:220079200-220080200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr1:220079600-220081400	Flanking Active TSS	K562	blood
8	chr1:220080000-220080600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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