Variant report

Variant	rs72782772
Chromosome Location	chr5:90047307-90047308
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:90045038..90047655-chr5:90049129..90051100,2	K562	blood:
2	chr5:90042349..90044397-chr5:90045490..90049083,3	K562	blood:
3	chr5:90046899..90048953-chr5:90056620..90058436,2	K562	blood:
4	chr5:90036431..90041664-chr5:90043469..90047392,6	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs55748173	1.00[AFR][1000 genomes]
rs55813746	1.00[AFR][1000 genomes]
rs72782737	1.00[AMR][1000 genomes]
rs72782753	1.00[AMR][1000 genomes]
rs72782758	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72782776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72782792	1.00[AFR][1000 genomes]
rs72784605	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
5	nsv882367	chr5:89956991-90209824	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv934323	chr5:89968158-90111853	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv1015449	chr5:89968626-90219398	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv1031718	chr5:89999033-90099868	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
9	nsv517049	chr5:90003131-90262475	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90022400-90074000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:90034600-90059600	Weak transcription	Brain Anterior Caudate	brain
3	chr5:90036200-90066000	Weak transcription	Pancreas	Pancrea
4	chr5:90036600-90059800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:90037200-90058600	Weak transcription	Fetal Brain Female	brain
6	chr5:90038200-90064400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:90039800-90082000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr5:90040800-90050200	Weak transcription	Fetal Brain Male	brain
9	chr5:90041800-90055200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr5:90042000-90053400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:90042800-90058600	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr5:90043000-90062400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr5:90043600-90054200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr5:90043600-90086800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr5:90044000-90048000	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:90044200-90059600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr5:90044800-90047400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:90044800-90048400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:90045200-90065200	Weak transcription	Brain Germinal Matrix	brain
20	chr5:90045600-90073000	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr5:90045800-90047400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
22	chr5:90045800-90051000	Strong transcription	K562	blood
23	chr5:90046400-90047400	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr5:90046800-90047400	Strong transcription	H9 Cell Line	embryonic stem cell
25	chr5:90047200-90047400	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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