Variant report

Variant	rs9383732
Chromosome Location	chr6:150552214-150552215
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:150525124..150527770-chr6:150549822..150552808,2	K562	blood:
2	chr6:150549533..150552708-chr6:150557386..150559321,3	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs12662622	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2880661	1.00[AMR][1000 genomes]
rs3734729	0.90[CHB][hapmap]
rs4870404	1.00[AMR][1000 genomes]
rs6557375	0.86[ASN][1000 genomes]
rs6557376	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6922326	0.93[ASN][1000 genomes]
rs6936990	1.00[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs7741317	0.92[JPT][hapmap]
rs7749005	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs926930	0.84[JPT][hapmap]
rs9322253	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9322254	0.90[CHB][hapmap];1.00[AMR][1000 genomes]
rs9371362	0.90[CHB][hapmap]
rs9371830	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9371831	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9371833	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9371834	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9371843	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9371844	1.00[CHB][hapmap];0.91[JPT][hapmap];0.97[ASN][1000 genomes]
rs9371852	0.90[CHB][hapmap]
rs9384259	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9384261	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9384262	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9384264	1.00[CHB][hapmap];0.91[JPT][hapmap];0.97[ASN][1000 genomes]
rs9384270	1.00[AMR][1000 genomes]
rs9397206	0.92[JPT][hapmap]
rs9397229	1.00[AMR][1000 genomes]
rs9397234	1.00[AMR][1000 genomes]
rs9397777	0.90[CHB][hapmap];1.00[AMR][1000 genomes]
rs9397780	1.00[AMR][1000 genomes]
rs9478585	0.84[JPT][hapmap]
rs9885696	0.92[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830843	chr6:150517411-150691173	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150546600-150553000	Enhancers	Fetal Brain Male	brain
2	chr6:150548800-150553000	Enhancers	Fetal Heart	heart
3	chr6:150549800-150554000	Weak transcription	Psoas Muscle	Psoas
4	chr6:150549800-150556400	Weak transcription	Left Ventricle	heart
5	chr6:150550000-150556600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr6:150550000-150558600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr6:150550600-150552400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr6:150550600-150553000	Enhancers	NH-A	brain
9	chr6:150550600-150553200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:150550800-150552600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr6:150550800-150552600	Enhancers	K562	blood
12	chr6:150550800-150552800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:150550800-150553800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:150550800-150554800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:150550800-150555400	Enhancers	HMEC	breast
16	chr6:150551000-150552400	Enhancers	Right Atrium	heart
17	chr6:150551000-150552600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:150551000-150552600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:150551000-150552600	Enhancers	Placenta Amnion	Placenta Amnion
20	chr6:150551000-150552600	Enhancers	NHDF-Ad	bronchial
21	chr6:150551000-150552800	Enhancers	HSMM	muscle
22	chr6:150551000-150555000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:150551200-150552400	Enhancers	Right Ventricle	heart
24	chr6:150551200-150552400	Weak transcription	NHLF	lung
25	chr6:150551200-150552600	Enhancers	Fetal Muscle Leg	muscle
26	chr6:150551200-150553400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:150551200-150558800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:150551400-150553600	Enhancers	Osteobl	bone
29	chr6:150551600-150554000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:150551800-150552800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
31	chr6:150552200-150552400	Enhancers	Fetal Brain Female	brain
32	chr6:150552200-150552600	Flanking Active TSS	HSMMtube	muscle
33	chr6:150552200-150553000	Flanking Active TSS	NHEK	skin

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