Variant report

Variant	rs10963786
Chromosome Location	chr9:18826610-18826611
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF263	chr9:18826225-18826685	HEK293-T-REx	kidney:	n/a	n/a
2	CTCF	chr9:18826460-18826610	MCF-7	breast:	n/a	n/a
3	CTCF	chr9:18826500-18826650	HBMEC	blood vessel:	n/a	n/a
4	CTCF	chr9:18826328-18826656	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:18826203..18828034-chr9:18832223..18834749,2	MCF-7	breast:

Variant related genes	Relation type
ADAMTSL1	TF binding region

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10156461	0.90[CHB][hapmap];0.84[CHD][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs10811041	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.89[EUR][1000 genomes]
rs10811043	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10963783	0.92[AFR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10963784	0.89[ASW][hapmap];0.90[CHB][hapmap];0.87[CHD][hapmap];0.93[JPT][hapmap];0.93[LWK][hapmap];0.83[MKK][hapmap];0.91[YRI][hapmap];0.96[AFR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10963785	1.00[CEU][hapmap];0.86[CHB][hapmap];0.87[CHD][hapmap];0.96[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10963789	0.82[ASN][1000 genomes]
rs10963791	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12551997	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.84[CHD][hapmap];0.86[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1433812	0.93[JPT][hapmap]
rs7019871	0.85[AFR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs718452	0.87[JPT][hapmap]
rs7869531	0.81[EUR][1000 genomes]
rs7874702	0.81[CHB][hapmap];1.00[JPT][hapmap];0.82[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	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1029449	chr9:18414752-18829127	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats 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 miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv540077	chr9:18414752-18829127	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1030931	chr9:18414752-18903530	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv892692	chr9:18519699-19045502	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv949111	chr9:18758205-18994588	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18815400-18829200	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr9:18818000-18845200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:18818200-18828800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr9:18822000-18826800	Enhancers	Fetal Heart	heart
5	chr9:18823000-18834400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr9:18824000-18827400	Enhancers	Primary T cells from cord blood	blood
7	chr9:18824000-18827800	Enhancers	Fetal Thymus	thymus
8	chr9:18825200-18827800	Strong transcription	NH-A	brain
9	chr9:18825400-18827400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:18825400-18828200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:18825400-18829800	Weak transcription	Aorta	Aorta
12	chr9:18825400-18829800	Weak transcription	Psoas Muscle	Psoas
13	chr9:18825400-18833000	Strong transcription	HSMM	muscle
14	chr9:18825400-18833400	Weak transcription	Right Ventricle	heart
15	chr9:18825400-18845200	Weak transcription	HSMMtube	muscle
16	chr9:18825400-18857200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr9:18825600-18830200	Weak transcription	NHLF	lung
18	chr9:18825600-18833600	Strong transcription	NHDF-Ad	bronchial
19	chr9:18825600-18857400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr9:18825800-18827800	Weak transcription	Adipose Nuclei	Adipose
21	chr9:18825800-18828600	Strong transcription	Osteobl	bone
22	chr9:18825800-18829800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:18825800-18829800	Weak transcription	Fetal Muscle Leg	muscle
24	chr9:18826000-18826800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr9:18826000-18827600	Strong transcription	Fetal Stomach	stomach
26	chr9:18826000-18827800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:18826000-18832600	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr9:18826200-18827800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr9:18826200-18827800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr9:18826200-18833600	Weak transcription	HUVEC	blood vessel
31	chr9:18826400-18826800	Enhancers	Gastric	stomach
32	chr9:18826400-18827200	Strong transcription	Fetal Muscle Trunk	muscle
33	chr9:18826400-18827600	Enhancers	Dnd41	blood
34	chr9:18826600-18830400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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