Variant report

Variant	rs9810986
Chromosome Location	chr3:93819128-93819129
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:93781003..93783537-chr3:93816052..93819340,3	MCF-7	breast:
2	chr3:93818192..93820955-chr3:93826379..93828481,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000178700	Chromatin interaction
ENSG00000178694	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11927165	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13094371	0.87[ASN][1000 genomes]
rs13095871	0.87[ASN][1000 genomes]
rs28372461	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28479320	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6765330	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][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]
rs6795524	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.89[EUR][1000 genomes]
rs6809958	0.83[EUR][1000 genomes]
rs72929719	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7615950	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7644176	0.84[ASW][hapmap];1.00[CEU][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8178587	0.83[EUR][1000 genomes]
rs9815634	0.89[EUR][1000 genomes]
rs9826711	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs9869941	0.81[ASN][1000 genomes]
rs9990106	0.84[ASW][hapmap];1.00[CEU][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869241	chr3:93527675-94504491	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv998173	chr3:93575084-94427403	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv536644	chr3:93575084-94427403	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers 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	23 gene(s)	inside rSNPs	diseases
4	nsv1008711	chr3:93575284-94427264	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv536646	chr3:93575284-94427264	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv491829	chr3:93575285-94427263	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	esv1795060	chr3:93602038-93848525	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh 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	18 gene(s)	inside rSNPs	n/a
8	esv1791740	chr3:93602927-93849247	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	n/a
9	esv2755326	chr3:93605126-93882750	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats 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	19 gene(s)	inside rSNPs	n/a
10	nsv1013107	chr3:93654100-94102212	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
11	nsv536648	chr3:93654100-94102212	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv1004176	chr3:93654100-94502551	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
13	nsv877162	chr3:93779664-94278078	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv877163	chr3:93795972-94047775	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:93782800-93848200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:93782800-93849400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr3:93783200-93824600	Weak transcription	NHEK	skin
4	chr3:93783200-93851600	Weak transcription	HMEC	breast
5	chr3:93783400-93833000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr3:93783600-93837800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr3:93784800-93820200	Weak transcription	Hela-S3	cervix
8	chr3:93785600-93834400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr3:93786200-93834600	Weak transcription	Brain Substantia Nigra	brain
10	chr3:93786400-93830800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:93786800-93849800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr3:93791400-93841200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr3:93792200-93833200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr3:93795600-93822000	Weak transcription	HSMMtube	muscle
15	chr3:93795600-93847000	Weak transcription	Osteobl	bone
16	chr3:93796000-93857800	Weak transcription	Fetal Brain Male	brain
17	chr3:93799000-93851600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr3:93800000-93830800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr3:93800200-93851000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:93802200-93830800	Weak transcription	Fetal Kidney	kidney
21	chr3:93802400-93849600	Weak transcription	Stomach Mucosa	stomach
22	chr3:93802600-93851800	Weak transcription	Small Intestine	intestine
23	chr3:93802800-93830800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr3:93803000-93826600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr3:93803400-93835800	Weak transcription	Psoas Muscle	Psoas
26	chr3:93804400-93834600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr3:93804800-93833000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:93805000-93825800	Weak transcription	Fetal Intestine Small	intestine
29	chr3:93806400-93819600	Strong transcription	Sigmoid Colon	Sigmoid Colon
30	chr3:93806400-93820800	Weak transcription	HSMM	muscle
31	chr3:93806400-93834800	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr3:93807400-93819800	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr3:93808000-93819400	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr3:93808400-93849600	Weak transcription	Fetal Heart	heart
35	chr3:93808600-93830800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr3:93809600-93819400	Strong transcription	Primary B cells from peripheral blood	blood
37	chr3:93809600-93819600	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr3:93809800-93819400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr3:93810000-93819400	Strong transcription	Primary T cells from cord blood	blood
40	chr3:93811000-93820400	Strong transcription	GM12878-XiMat	blood
41	chr3:93811200-93819200	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr3:93811400-93832800	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr3:93812200-93821600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:93812200-93826800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr3:93812400-93852200	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr3:93812800-93820200	Strong transcription	Liver	Liver
47	chr3:93813000-93819600	Strong transcription	Adipose Nuclei	Adipose
48	chr3:93813000-93823400	Strong transcription	Dnd41	blood
49	chr3:93813000-93824600	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr3:93813200-93819400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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