Variant report

Variant	rs1414145
Chromosome Location	chr9:117955089-117955090
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	chr9:117953158..117955908-chr9:117957675..117960563,2	MCF-7	breast:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10817723	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1335343	0.93[YRI][hapmap]
rs1335349	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1335350	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1414146	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs4978627	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62577989	0.87[ASN][1000 genomes]
rs7024589	0.84[CEU][hapmap];0.92[JPT][hapmap];0.82[EUR][1000 genomes]
rs7032660	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7040243	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs7849266	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7851185	0.84[CEU][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7866695	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv831697	chr9:117860416-118023927	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv893769	chr9:117936903-117985886	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117930000-117964400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:117945600-117959400	Weak transcription	Fetal Kidney	kidney
3	chr9:117945800-117959600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:117953600-117955200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr9:117953800-117955400	Enhancers	Primary B cells from peripheral blood	blood
6	chr9:117953800-117955600	Enhancers	GM12878-XiMat	blood
7	chr9:117954000-117955200	Enhancers	Fetal Intestine Large	intestine
8	chr9:117954000-117955400	Enhancers	Duodenum Mucosa	Duodenum
9	chr9:117954000-117955400	Enhancers	Fetal Intestine Small	intestine
10	chr9:117954000-117955600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:117954000-117956400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr9:117954000-117956800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr9:117954000-117956800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr9:117954000-117956800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr9:117954000-117956800	Enhancers	Fetal Muscle Leg	muscle
16	chr9:117954200-117955600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr9:117954400-117955200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:117954400-117955200	Weak transcription	Placenta	Placenta
19	chr9:117954400-117957400	Enhancers	Colon Smooth Muscle	Colon
20	chr9:117954600-117955200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:117954600-117955400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr9:117954600-117955400	Weak transcription	Stomach Smooth Muscle	stomach
23	chr9:117954600-117957000	Enhancers	NHLF	lung
24	chr9:117954600-117957400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:117954600-117959400	Weak transcription	Rectal Smooth Muscle	rectum
26	chr9:117954800-117955200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr9:117954800-117955200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr9:117954800-117955800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr9:117954800-117956200	Enhancers	Fetal Lung	lung
30	chr9:117955000-117955600	Enhancers	Fetal Stomach	stomach
31	chr9:117955000-117955600	Enhancers	Spleen	Spleen
32	chr9:117955000-117956600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr9:117955000-117957400	Enhancers	NHDF-Ad	bronchial

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