Variant report

Variant	rs9327347
Chromosome Location	chr5:124339525-124339526
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:124144207..124147001-chr5:124338580..124340102,2	K562	blood:

Variant related genes	Relation type
ENSG00000242814	Chromatin interaction

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

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

rs_ID	r²[population]
rs10043770	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10155594	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13357021	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13359555	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28620272	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28697281	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3936060	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4272129	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5027562	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6862525	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6888931	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7707465	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7708412	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7728062	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9327345	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9327346	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9327348	1.00[CHB][hapmap]

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	nsv882822	chr5:124250018-124449375	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830474	chr5:124263628-124431299	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124323400-124348600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:124326600-124342000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:124333000-124341000	Weak transcription	Brain Anterior Caudate	brain
4	chr5:124333400-124339600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr5:124333800-124341400	Weak transcription	Fetal Kidney	kidney
6	chr5:124336400-124341800	Enhancers	Dnd41	blood
7	chr5:124336800-124343000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:124337000-124343000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr5:124337000-124343000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr5:124337200-124341800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr5:124337200-124342000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:124337400-124341800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr5:124337600-124342600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr5:124337800-124342600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:124337800-124342800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr5:124338000-124343000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr5:124338400-124340000	Enhancers	H9 Cell Line	embryonic stem cell
18	chr5:124338400-124343000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:124338400-124343000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:124338600-124340400	Enhancers	H1 Cell Line	embryonic stem cell
21	chr5:124338600-124340600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:124338800-124342800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:124339000-124340200	Weak transcription	Primary B cells from cord blood	blood
24	chr5:124339000-124340400	Weak transcription	Primary B cells from peripheral blood	blood
25	chr5:124339200-124339600	Enhancers	Fetal Brain Female	brain
26	chr5:124339400-124339800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr5:124339400-124340600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr5:124339400-124340800	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr5:124339400-124341000	Weak transcription	GM12878-XiMat	blood

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