Variant report

Variant	rs55646136
Chromosome Location	chr9:136723270-136723271
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:136721577..136724425-chr9:136727514..136729956,2	K562	blood:
2	chr9:136722305..136724047-chr9:136856724..136858703,2	MCF-7	breast:
3	chr9:136719836..136721567-chr9:136722658..136724295,2	MCF-7	breast:
4	chr9:136720764..136723622-chr9:136736992..136740613,4	MCF-7	breast:
5	chr9:136711109..136713982-chr9:136718065..136723456,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000160293	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10821526	0.90[ASN][1000 genomes]
rs10993820	0.96[ASN][1000 genomes]
rs10993822	1.00[ASN][1000 genomes]
rs10993823	1.00[ASN][1000 genomes]
rs10993824	1.00[ASN][1000 genomes]
rs10993826	1.00[ASN][1000 genomes]
rs10993828	1.00[ASN][1000 genomes]
rs10993829	1.00[ASN][1000 genomes]
rs10993830	1.00[ASN][1000 genomes]
rs10993832	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12000549	0.98[ASN][1000 genomes]
rs12005762	0.98[ASN][1000 genomes]
rs12341505	0.88[ASN][1000 genomes]
rs12377799	1.00[ASN][1000 genomes]
rs1557679	0.90[ASN][1000 genomes]
rs17663678	1.00[ASN][1000 genomes]
rs2073928	0.90[ASN][1000 genomes]
rs2073929	1.00[ASN][1000 genomes]
rs2073930	0.98[ASN][1000 genomes]
rs2156323	1.00[ASN][1000 genomes]
rs2260095	0.93[ASN][1000 genomes]
rs2261150	0.90[ASN][1000 genomes]
rs2428123	0.90[ASN][1000 genomes]
rs2428124	1.00[ASN][1000 genomes]
rs2428126	0.90[ASN][1000 genomes]
rs2428129	0.90[ASN][1000 genomes]
rs2486350	0.90[ASN][1000 genomes]
rs2486351	0.90[ASN][1000 genomes]
rs2502765	0.90[ASN][1000 genomes]
rs2510254	0.90[ASN][1000 genomes]
rs28436700	0.90[ASN][1000 genomes]
rs35711919	1.00[ASN][1000 genomes]
rs35776936	1.00[ASN][1000 genomes]
rs3819500	1.00[ASN][1000 genomes]
rs3819502	0.90[ASN][1000 genomes]
rs3819503	0.88[ASN][1000 genomes]
rs3819504	1.00[ASN][1000 genomes]
rs3819505	1.00[ASN][1000 genomes]
rs55939286	0.93[ASN][1000 genomes]
rs56745684	0.90[ASN][1000 genomes]
rs56868628	0.88[ASN][1000 genomes]
rs58816065	0.90[ASN][1000 genomes]
rs67484139	1.00[ASN][1000 genomes]
rs72762854	1.00[ASN][1000 genomes]
rs72762864	1.00[ASN][1000 genomes]
rs7853626	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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

No data

Chromatin state (count:86 , 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	chr9:136714600-136729400	Weak transcription	NHEK	skin
17	chr9:136715200-136725600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:136717200-136728600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr9:136717800-136724600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr9:136718200-136726400	Strong transcription	Primary B cells from peripheral blood	blood
21	chr9:136718400-136727400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr9:136719000-136724000	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr9:136719000-136724400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr9:136719000-136725600	Weak transcription	Gastric	stomach
25	chr9:136719400-136725600	Weak transcription	Aorta	Aorta
26	chr9:136719400-136728200	Weak transcription	NHDF-Ad	bronchial
27	chr9:136719600-136727400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr9:136719600-136727800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr9:136720000-136726200	Weak transcription	Fetal Brain Female	brain
30	chr9:136720600-136724200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr9:136720600-136726200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:136720600-136727800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr9:136721200-136725800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr9:136721200-136727400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr9:136721200-136727600	Weak transcription	Right Ventricle	heart
36	chr9:136721200-136728000	Weak transcription	Right Atrium	heart
37	chr9:136721200-136728600	Weak transcription	HSMMtube	muscle
38	chr9:136721200-136729800	Weak transcription	A549	lung
39	chr9:136721400-136724000	Weak transcription	Fetal Muscle Leg	muscle
40	chr9:136721400-136724400	Weak transcription	Spleen	Spleen
41	chr9:136721400-136725600	Weak transcription	Osteobl	bone
42	chr9:136721400-136727600	Weak transcription	Left Ventricle	heart
43	chr9:136721400-136728400	Weak transcription	Fetal Lung	lung
44	chr9:136721400-136738600	Weak transcription	HUVEC	blood vessel
45	chr9:136721600-136725600	Weak transcription	HSMM	muscle
46	chr9:136721600-136726000	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr9:136721600-136726000	Weak transcription	Fetal Thymus	thymus
48	chr9:136721600-136726600	Weak transcription	Adipose Nuclei	Adipose
49	chr9:136721600-136727200	Weak transcription	Colonic Mucosa	Colon
50	chr9:136721600-136728400	Weak transcription	Colon Smooth Muscle	Colon

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