Variant report

Variant	rs9821807
Chromosome Location	chr3:85014750-85014751
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12714616	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12714617	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13066623	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13075494	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13075873	0.82[EUR][1000 genomes]
rs13082518	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13092125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13096651	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1691471	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1872552	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs2101344	0.82[JPT][hapmap]
rs2171143	0.92[CEU][hapmap];0.90[JPT][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2326225	1.00[CHB][hapmap]
rs28693686	0.83[AMR][1000 genomes]
rs4516626	1.00[CHB][hapmap]
rs4856554	0.82[EUR][1000 genomes]
rs6791363	0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7628129	0.82[JPT][hapmap]
rs7630382	0.82[JPT][hapmap]
rs7645633	0.82[EUR][1000 genomes]
rs9309967	0.89[CEU][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9647393	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9815258	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9818659	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9823454	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9828496	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9839708	0.84[EUR][1000 genomes]
rs9860513	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9870384	0.89[CEU][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9874302	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9876378	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9877460	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9878472	0.82[JPT][hapmap]
rs9878707	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9881257	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9883443	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	esv3381298	chr3:84689266-85030314	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1002058	chr3:84757044-85389876	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1001316	chr3:84773522-85071342	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv877091	chr3:84876250-85069287	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv482371	chr3:84880813-85031486	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv471620	chr3:84880814-85031486	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv1829788	chr3:84926769-85086403	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1010140	chr3:84997012-85034281	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85011200-85016600	Weak transcription	Psoas Muscle	Psoas
2	chr3:85011200-85016800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:85011200-85016800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr3:85011600-85016800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr3:85011600-85016800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr3:85011600-85018400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:85012000-85016800	Weak transcription	Brain Germinal Matrix	brain
8	chr3:85012800-85015400	Weak transcription	Fetal Brain Male	brain
9	chr3:85013400-85019200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:85013600-85016800	Weak transcription	Fetal Brain Female	brain
11	chr3:85013800-85014800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr3:85013800-85015000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr3:85013800-85016600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:85014000-85015400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr3:85014200-85015200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr3:85014200-85016200	Enhancers	Brain Substantia Nigra	brain
17	chr3:85014200-85016600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:85014400-85014800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr3:85014400-85014800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr3:85014400-85014800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:85014400-85014800	Flanking Active TSS	Brain Hippocampus Middle	brain
22	chr3:85014400-85014800	Enhancers	A549	lung
23	chr3:85014400-85015000	Enhancers	Brain Anterior Caudate	brain
24	chr3:85014400-85015200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:85014400-85016600	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr3:85014400-85016800	Enhancers	Brain Cingulate Gyrus	brain
27	chr3:85014400-85020000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:85014600-85014800	Active TSS	Brain Angular Gyrus	brain
29	chr3:85014600-85014800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
30	chr3:85014600-85015200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr3:85014600-85016800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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