Variant report

Variant	rs3780442
Chromosome Location	chr9:101077653-101077654
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:101077531..101078224-chr9:101537912..101538518,3	MCF-7	breast:
2	chr9:101070579..101073591-chr9:101076842..101079263,3	MCF-7	breast:
3	chr9:101076029..101078815-chr9:101516431..101518577,2	MCF-7	breast:
4	chr9:101077545..101078479-chr9:101537869..101538795,4	K562	blood:
5	chr9:101077361..101079468-chr9:101293328..101295468,2	K562	blood:
6	chr9:101076714..101079334-chr9:101138741..101140975,3	K562	blood:
7	chr9:101075867..101078208-chr9:101080022..101082370,2	K562	blood:
8	chr9:101077608..101078459-chr9:101336024..101336612,2	MCF-7	breast:
9	chr9:101077537..101078267-chr9:101507908..101508672,2	MCF-7	breast:
10	chr9:101077617..101078489-chr9:101558428..101559307,2	MCF-7	breast:
11	chr9:101077395..101078268-chr9:101530249..101530829,3	MCF-7	breast:
12	chr9:101076038..101079314-chr9:101086093..101088880,3	K562	blood:
13	chr9:101077513..101078805-chr9:101536863..101538719,11	MCF-7	breast:
14	chr9:101076603..101078214-chr9:101139182..101140975,2	K562	blood:
15	chr9:101077202..101078311-chr9:101536603..101537623,3	MCF-7	breast:
16	chr9:101077617..101078376-chr9:101246635..101247206,2	MCF-7	breast:
17	chr9:101077561..101078510-chr9:101535798..101536902,3	K562	blood:
18	chr9:101077527..101078492-chr9:101298829..101299830,3	K562	blood:
19	chr9:101077049..101078493-chr9:101285520..101286892,8	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000165138	Chromatin interaction

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

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

rs_ID	r²[population]
rs10985795	1.00[CEU][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10985799	0.81[JPT][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10985800	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10985811	0.90[JPT][hapmap]
rs13286336	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13290518	0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13300613	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1415111	0.84[JPT][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34283833	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35126377	0.97[EUR][1000 genomes]
rs3780440	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3780441	1.00[CEU][hapmap];0.94[JPT][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3780443	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56220486	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7022133	0.96[EUR][1000 genomes]
rs7850445	0.84[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831663	chr9:100941048-101109492	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1045780	chr9:100943318-101080389	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv540180	chr9:100943318-101080389	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv831664	chr9:101024862-101205637	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv519818	chr9:101024887-101092316	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101061600-101083400	Weak transcription	Brain Angular Gyrus	brain
2	chr9:101062000-101078000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr9:101069000-101085800	Weak transcription	Right Atrium	heart
4	chr9:101070800-101078000	Weak transcription	Fetal Brain Male	brain
5	chr9:101072000-101078000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr9:101075400-101082200	Enhancers	K562	blood
7	chr9:101076200-101078000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr9:101076400-101077800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:101076400-101078200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:101076400-101078200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr9:101076400-101078600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr9:101076400-101078600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:101076400-101079800	Enhancers	Placenta	Placenta
14	chr9:101076600-101077800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr9:101076600-101078200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr9:101076600-101078400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr9:101076800-101078000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr9:101076800-101078400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:101076800-101078400	Enhancers	NHDF-Ad	bronchial
20	chr9:101077000-101077800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr9:101077000-101078000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr9:101077000-101078000	Weak transcription	NHLF	lung
23	chr9:101077000-101078400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:101077000-101078400	Enhancers	Fetal Intestine Large	intestine
25	chr9:101077000-101078400	Enhancers	Lung	lung
26	chr9:101077200-101077800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr9:101077200-101078000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr9:101077200-101078000	Enhancers	Hela-S3	cervix
29	chr9:101077200-101078200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr9:101077200-101078400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:101077400-101078000	Enhancers	Stomach Mucosa	stomach
32	chr9:101077400-101079200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr9:101077400-101081200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:101077600-101078000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr9:101077600-101078000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr9:101077600-101080400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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