Variant report

Variant	rs73181642
Chromosome Location	chr5:89941488-89941489
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr5:89823962..89827222-chr5:89937926..89943647,5	K562	blood:
2	chr5:89706235..89707904-chr5:89940605..89942496,2	K562	blood:
3	chr5:89768693..89770262-chr5:89940512..89942172,2	MCF-7	breast:
4	chr5:89703250..89710229-chr5:89936398..89944611,13	K562	blood:
5	chr5:89731732..89734444-chr5:89940233..89942146,2	K562	blood:
6	chr5:89938077..89942103-chr5:90675427..90679817,6	K562	blood:
7	chr5:89938681..89942307-chr5:90675773..90680271,6	K562	blood:
8	chr5:89842756..89845213-chr5:89939588..89942557,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000164199	Chromatin interaction
ENSG00000255647	Chromatin interaction
ENSG00000113356	Chromatin interaction
ENSG00000113369	Chromatin interaction
ENSG00000176055	Chromatin interaction
ENSG00000176018	Chromatin interaction
ENSG00000153140	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12108970	1.00[AMR][1000 genomes]
rs12109253	1.00[AMR][1000 genomes]
rs1504986	1.00[AMR][1000 genomes]
rs1504997	1.00[AMR][1000 genomes]
rs16868834	1.00[AMR][1000 genomes]
rs16868842	1.00[AMR][1000 genomes]
rs16868848	1.00[AMR][1000 genomes]
rs16868851	1.00[AMR][1000 genomes]
rs16868853	1.00[AMR][1000 genomes]
rs16868854	1.00[AMR][1000 genomes]
rs41304890	1.00[AMR][1000 genomes]
rs56926055	1.00[AMR][1000 genomes]
rs61740119	1.00[AMR][1000 genomes]
rs73173989	0.83[AFR][1000 genomes]
rs73177840	0.83[AFR][1000 genomes]
rs73179766	1.00[AMR][1000 genomes]
rs73179768	1.00[AMR][1000 genomes]
rs73179771	1.00[AMR][1000 genomes]
rs73179774	1.00[AMR][1000 genomes]
rs73179777	1.00[AMR][1000 genomes]
rs73179793	1.00[AMR][1000 genomes]
rs73181603	1.00[AMR][1000 genomes]
rs73181604	1.00[AMR][1000 genomes]
rs73181609	1.00[AMR][1000 genomes]
rs73181619	1.00[AMR][1000 genomes]
rs73181634	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73181640	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73181647	1.00[AMR][1000 genomes]
rs73181653	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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
6	nsv933161	chr5:89939500-89954066	Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
7	nsv1029970	chr5:89940489-89986831	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	nsv1032225	chr5:89940489-89999954	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89918000-89950600	Weak transcription	Pancreas	Pancrea
2	chr5:89929000-89948600	Weak transcription	Brain Anterior Caudate	brain
3	chr5:89936600-89949000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:89936600-89951000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:89936800-89948600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr5:89936800-89951000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:89936800-89994200	Weak transcription	Brain Germinal Matrix	brain
8	chr5:89937000-89948600	Weak transcription	Fetal Brain Female	brain
9	chr5:89937200-89943000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr5:89939600-89941600	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:89939800-89943000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:89940000-89941600	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr5:89940200-89942400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:89940400-89941800	Genic enhancers	HUES48 Cell Line	embryonic stem cell
15	chr5:89940400-89941800	Flanking Active TSS	K562	blood
16	chr5:89940800-89941600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr5:89941200-89942800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr5:89941400-89941600	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr5:89941400-89941600	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr5:89941400-89942400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr5:89941400-89942400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:89941400-89942400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:89941400-89948600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr5:89941400-89957400	Strong transcription	HUES64 Cell Line	embryonic stem cell

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