Variant report

Variant	rs73179759
Chromosome Location	chr5:89900285-89900286
allele	A/T
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:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:89735291..89736086-chr5:89900052..89900990,6	MCF-7	breast:
2	chr5:89899238..89902193-chr5:89950994..89956361,5	K562	blood:
3	chr5:89735670..89736479-chr5:89900164..89900970,2	K562	blood:
4	chr5:89704196..89707423-chr5:89899106..89902473,4	K562	blood:
5	chr5:89853355..89855789-chr5:89900091..89901923,2	MCF-7	breast:
6	chr5:89898813..89900369-chr5:89978096..89979989,2	K562	blood:
7	chr5:89899642..89902183-chr5:89950994..89955309,3	K562	blood:
8	chr5:89825636..89826384-chr5:89900047..89900941,2	K562	blood:
9	chr5:89894691..89897119-chr5:89898075..89900513,3	K562	blood:
10	chr5:89767614..89772956-chr5:89898929..89905987,8	K562	blood:
11	chr5:89900245..89902488-chr5:89903253..89905685,5	K562	blood:
12	chr5:89737219..89738135-chr5:89899968..89900731,2	MCF-7	breast:
13	chr5:89823952..89826315-chr5:89899219..89901608,2	K562	blood:
14	chr5:89844169..89846312-chr5:89898402..89900420,2	K562	blood:
15	chr5:89897975..89900696-chr5:89937499..89939734,2	K562	blood:

No data

No data

No data

Variant related genes	Relation type
ENSG00000176055	Chromatin interaction
ENSG00000113356	Chromatin interaction
ENSG00000164199	Chromatin interaction
ENSG00000255647	Chromatin interaction
ENSG00000153140	Chromatin interaction
ENSG00000176018	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs60195623	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60513905	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6867812	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6868030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6889020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73179752	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73179753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73179756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73179757	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73179758	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73179761	1.00[AFR][1000 genomes];1.00[AMR][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	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv933668	chr5:89854253-89999672	Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv531965	chr5:89886550-90145002	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89892800-89909000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:89893000-89907800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr5:89893200-89902000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:89895000-89907400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr5:89899000-89900800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr5:89899200-89900800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:89899200-89901000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:89899400-89900400	Weak transcription	K562	blood
9	chr5:89899600-89900600	Weak transcription	GM12878-XiMat	blood
10	chr5:89899600-89902000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:89899800-89900800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr5:89900000-89900800	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr5:89900200-89900800	Enhancers	Brain Anterior Caudate	brain

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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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