Variant report

Variant	rs9876021
Chromosome Location	chr3:121440339-121440340
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	chr3:121422713..121424587-chr3:121439673..121442209,2	MCF-7	breast:
2	chr3:121439769..121441731-chr3:121445734..121447295,2	MCF-7	breast:

Extended variants
information (count: 70 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10934560	0.81[EUR][1000 genomes]
rs12489511	0.82[EUR][1000 genomes]
rs12631824	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13067629	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1492177	0.89[EUR][1000 genomes]
rs1574655	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1574735	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17849995	0.82[EUR][1000 genomes]
rs1873645	0.91[EUR][1000 genomes]
rs1919552	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1919557	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1986351	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1986874	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2001390	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2001391	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2070179	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2840143	0.90[EUR][1000 genomes]
rs34920680	0.81[EUR][1000 genomes]
rs34980632	0.80[EUR][1000 genomes]
rs35295338	0.84[EUR][1000 genomes]
rs35713885	0.82[EUR][1000 genomes]
rs36022362	0.81[EUR][1000 genomes]
rs3772127	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4676684	0.89[EUR][1000 genomes]
rs4676685	0.91[EUR][1000 genomes]
rs4676686	0.90[EUR][1000 genomes]
rs4676690	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4676751	0.83[EUR][1000 genomes]
rs57420306	0.82[EUR][1000 genomes]
rs59740137	0.82[EUR][1000 genomes]
rs6438645	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6438660	0.82[EUR][1000 genomes]
rs6770719	0.81[EUR][1000 genomes]
rs6771716	0.81[EUR][1000 genomes]
rs6774164	0.82[EUR][1000 genomes]
rs6776703	0.83[EUR][1000 genomes]
rs6791896	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6792659	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6794341	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6794677	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6802033	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6803839	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6807711	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73179983	0.82[ASN][1000 genomes]
rs7375038	0.91[EUR][1000 genomes]
rs7429247	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7430165	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7611913	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7620842	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7646346	0.81[EUR][1000 genomes]
rs7646585	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9289172	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9289173	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9681209	0.82[EUR][1000 genomes]
rs9809114	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9812411	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9829053	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9832267	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9835182	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9854052	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9861992	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9864907	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][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	nsv591395	chr3:120970900-121501070	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv591396	chr3:120970900-121557533	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv591397	chr3:120977383-121505882	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv432480	chr3:121355723-121629928	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv432482	chr3:121364236-121629634	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv432481	chr3:121364236-121637178	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv829703	chr3:121383290-121534493	Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
8	nsv516233	chr3:121419301-121670405	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9876021	HCLS1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121386600-121447200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:121399000-121440400	Weak transcription	K562	blood
3	chr3:121411000-121442400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr3:121413400-121446200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:121418800-121442000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:121426200-121442600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr3:121426200-121443200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:121429000-121450000	Strong transcription	Rectal Mucosa Donor 29	rectum
9	chr3:121429400-121442800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:121429400-121448800	Strong transcription	Primary hematopoietic stem cells	blood
11	chr3:121429400-121449000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr3:121430200-121442400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:121430200-121450000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr3:121430400-121441400	Strong transcription	Osteobl	bone
15	chr3:121430600-121449000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr3:121430600-121449400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:121430600-121450000	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr3:121430800-121443600	Strong transcription	Placenta	Placenta
19	chr3:121430800-121448200	Strong transcription	Duodenum Smooth Muscle	Duodenum
20	chr3:121430800-121448800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr3:121430800-121448800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr3:121430800-121450000	Strong transcription	Fetal Intestine Large	intestine
23	chr3:121431000-121441000	Strong transcription	HepG2	liver
24	chr3:121431000-121442400	Strong transcription	GM12878-XiMat	blood
25	chr3:121431000-121444800	Strong transcription	Fetal Muscle Trunk	muscle
26	chr3:121431000-121448600	Strong transcription	Adipose Nuclei	Adipose
27	chr3:121431000-121449000	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr3:121431000-121449000	Strong transcription	Fetal Thymus	thymus
29	chr3:121431000-121449600	Strong transcription	Liver	Liver
30	chr3:121431000-121450000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:121431000-121450000	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr3:121431200-121448200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:121431400-121448800	Strong transcription	HUES6 Cell Line	embryonic stem cell
34	chr3:121431400-121449800	Strong transcription	Duodenum Mucosa	Duodenum
35	chr3:121431400-121450400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr3:121431600-121441800	Strong transcription	Placenta Amnion	Placenta Amnion
37	chr3:121431600-121446000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr3:121431600-121446600	Strong transcription	HSMMtube	muscle
39	chr3:121431600-121449000	Strong transcription	Rectal Mucosa Donor 31	rectum
40	chr3:121432000-121440800	Strong transcription	Brain Germinal Matrix	brain
41	chr3:121432000-121441000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr3:121432000-121442000	Strong transcription	Brain Inferior Temporal Lobe	brain
43	chr3:121432000-121444800	Strong transcription	Brain Anterior Caudate	brain
44	chr3:121432000-121444800	Strong transcription	Fetal Brain Female	brain
45	chr3:121432000-121448200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr3:121432000-121448400	Strong transcription	HSMM	muscle
47	chr3:121432000-121448800	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr3:121432000-121448800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chr3:121432000-121448800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr3:121432000-121448800	Strong transcription	NH-A	brain

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