Variant report

Variant	rs73555909
Chromosome Location	chr9:136721064-136721065
allele	A/G
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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:136719836..136721567-chr9:136722658..136724295,2	MCF-7	breast:
2	chr9:136707416..136709082-chr9:136718802..136721246,2	MCF-7	breast:
3	chr9:136713073..136715436-chr9:136719455..136721835,2	K562	blood:
4	chr9:136720347..136721280-chrX:15692525..15693445,2	Hela-S3	cervix:
5	chr9:136720764..136723622-chr9:136736992..136740613,4	MCF-7	breast:
6	chr9:136646541..136648587-chr9:136720513..136723174,2	MCF-7	breast:
7	chr9:136716723..136719526-chr9:136720633..136722987,2	MCF-7	breast:
8	chr9:136708244..136711057-chr9:136719535..136721439,2	MCF-7	breast:
9	chr9:136718031..136721993-chr9:136856767..136859513,3	MCF-7	breast:
10	chr9:136711109..136713982-chr9:136718065..136723456,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000186312	Chromatin interaction
ENSG00000160293	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10114727	1.00[EUR][1000 genomes]
rs10217159	1.00[EUR][1000 genomes]
rs11998957	1.00[EUR][1000 genomes]
rs12339322	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12342989	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12353234	1.00[EUR][1000 genomes]
rs2428122	1.00[EUR][1000 genomes]
rs60329120	1.00[EUR][1000 genomes]
rs7048686	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73550009	1.00[EUR][1000 genomes]
rs73553983	1.00[EUR][1000 genomes]
rs73555907	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73555919	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv894114	chr9:136538798-136779153	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv831745	chr9:136593702-136780273	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv831746	chr9:136607829-136750740	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv894122	chr9:136632662-136760639	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1035272	chr9:136665308-136772256	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv894123	chr9:136682408-136852501	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv894124	chr9:136716399-136870787	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	esv3401000	chr9:136717131-136721429	Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136675200-136728400	Weak transcription	Esophagus	oesophagus
2	chr9:136705400-136726800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:136705800-136724400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr9:136705800-136726000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr9:136705800-136729400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr9:136706000-136726400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr9:136707200-136726600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:136709000-136728600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:136710000-136727400	Weak transcription	Brain Substantia Nigra	brain
10	chr9:136710600-136727200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr9:136710800-136725600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:136710800-136728600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:136711000-136725800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr9:136711400-136737800	Weak transcription	NH-A	brain
15	chr9:136711600-136727400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr9:136712200-136721400	Strong transcription	Fetal Stomach	stomach
17	chr9:136714600-136721200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr9:136714600-136722800	Weak transcription	HMEC	breast
19	chr9:136714600-136729400	Weak transcription	NHEK	skin
20	chr9:136715200-136725600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr9:136715400-136723000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:136716600-136722000	Weak transcription	GM12878-XiMat	blood
23	chr9:136717200-136721200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr9:136717200-136728600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr9:136717600-136722600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr9:136717800-136724600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:136718200-136723000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr9:136718200-136726400	Strong transcription	Primary B cells from peripheral blood	blood
29	chr9:136718400-136727400	Weak transcription	Brain Cingulate Gyrus	brain
30	chr9:136718600-136722400	Genic enhancers	Fetal Intestine Small	intestine
31	chr9:136719000-136724000	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr9:136719000-136724400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr9:136719000-136725600	Weak transcription	Gastric	stomach
34	chr9:136719200-136721200	Genic enhancers	Pancreas	Pancrea
35	chr9:136719200-136721400	Enhancers	Fetal Kidney	kidney
36	chr9:136719200-136722200	Weak transcription	Brain Hippocampus Middle	brain
37	chr9:136719400-136723000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr9:136719400-136725600	Weak transcription	Aorta	Aorta
39	chr9:136719400-136728200	Weak transcription	NHDF-Ad	bronchial
40	chr9:136719600-136722400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr9:136719600-136727400	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr9:136719600-136727800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr9:136719800-136722200	Weak transcription	Brain Germinal Matrix	brain
44	chr9:136719800-136722200	Enhancers	Placenta	Placenta
45	chr9:136720000-136721200	Enhancers	Duodenum Mucosa	Duodenum
46	chr9:136720000-136721600	Weak transcription	Fetal Brain Male	brain
47	chr9:136720000-136722000	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr9:136720000-136722200	Genic enhancers	Primary B cells from cord blood	blood
49	chr9:136720000-136722400	Flanking Active TSS	Hela-S3	cervix
50	chr9:136720000-136726200	Weak transcription	Fetal Brain Female	brain

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