Variant report

Variant	rs543511813
Chromosome Location	chr18:9208951-9208952
allele	-/TTAT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:9136075..9138683-chr18:9207289..9209442,2	K562	blood:
2	chr18:9195939..9198043-chr18:9208433..9210321,2	K562	blood:
3	chr18:9204077..9208041-chr18:9208940..9212355,4	K562	blood:

Variant related genes	Relation type
ENSG00000101745	Chromatin interaction
ENSG00000266053	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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	nsv916373	chr18:9026803-9592201	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv431971	chr18:9081185-9326852	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv1056407	chr18:9144345-9553764	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1055696	chr18:9191679-9309805	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv576446	chr18:9206003-9211269	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv961150	chr18:9207844-9212017	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv2570981	chr18:9208951-9208954	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv2223004	chr18:9208951-9208955	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9172000-9216200	Weak transcription	Fetal Brain Female	brain
2	chr18:9174600-9233600	Weak transcription	Spleen	Spleen
3	chr18:9174800-9211000	Weak transcription	Hela-S3	cervix
4	chr18:9174800-9233600	Weak transcription	Pancreas	Pancrea
5	chr18:9178000-9221800	Weak transcription	Fetal Heart	heart
6	chr18:9180200-9214200	Weak transcription	A549	lung
7	chr18:9181600-9214200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr18:9183400-9211400	Weak transcription	Brain Germinal Matrix	brain
9	chr18:9183800-9225600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr18:9184600-9233800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr18:9185200-9233800	Weak transcription	Right Ventricle	heart
12	chr18:9185400-9214200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr18:9185400-9223400	Weak transcription	Stomach Mucosa	stomach
14	chr18:9185600-9211000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr18:9185600-9232400	Weak transcription	Colonic Mucosa	Colon
16	chr18:9185800-9215200	Weak transcription	Small Intestine	intestine
17	chr18:9186000-9214400	Weak transcription	Brain Angular Gyrus	brain
18	chr18:9187000-9221800	Weak transcription	Fetal Brain Male	brain
19	chr18:9188400-9214400	Weak transcription	Brain Anterior Caudate	brain
20	chr18:9188400-9233600	Weak transcription	Esophagus	oesophagus
21	chr18:9188600-9233600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr18:9188800-9211600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr18:9188800-9218200	Weak transcription	Thymus	Thymus
24	chr18:9189200-9233800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr18:9189400-9215000	Weak transcription	Aorta	Aorta
26	chr18:9192200-9210400	Weak transcription	Left Ventricle	heart
27	chr18:9192200-9215400	Weak transcription	Psoas Muscle	Psoas
28	chr18:9192200-9233600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr18:9192200-9284000	Weak transcription	NHEK	skin
30	chr18:9192400-9211600	Weak transcription	HMEC	breast
31	chr18:9192400-9214400	Weak transcription	Fetal Muscle Leg	muscle
32	chr18:9193000-9211400	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr18:9193200-9211200	Weak transcription	Stomach Smooth Muscle	stomach
34	chr18:9193400-9224800	Weak transcription	Lung	lung
35	chr18:9193400-9230600	Weak transcription	Fetal Stomach	stomach
36	chr18:9193800-9211600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr18:9194200-9211400	Weak transcription	NH-A	brain
38	chr18:9194800-9219400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr18:9195200-9214400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr18:9195800-9211600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr18:9195800-9214400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr18:9196000-9209800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr18:9196400-9211000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr18:9196400-9211400	Weak transcription	HUVEC	blood vessel
45	chr18:9197400-9211200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr18:9199200-9224800	Weak transcription	Fetal Intestine Small	intestine
47	chr18:9200400-9214600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr18:9200800-9214200	Weak transcription	HepG2	liver
49	chr18:9201000-9211000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr18:9201000-9211200	Weak transcription	Fetal Kidney	kidney

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links