Variant report

Variant	rs73932300
Chromosome Location	chr19:55600369-55600370
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:55590464..55596493-chr19:55598673..55602443,7	MCF-7	breast:
2	chr19:55598098..55602192-chr19:55668353..55672028,4	K562	blood:
3	chr19:55599509..55600587-chr19:55671358..55672598,4	K562	blood:
4	chr19:55392520..55393347-chr19:55599997..55600552,2	K562	blood:
5	chr19:55591753..55593275-chr19:55598361..55600388,2	MCF-7	breast:
6	chr19:55599844..55600585-chr19:55657438..55658005,2	K562	blood:
7	chr19:55599701..55601283-chr19:55870959..55872935,2	K562	blood:

Variant related genes	Relation type
ENSG00000267110	Chromatin interaction
ENSG00000267577	Chromatin interaction
ENSG00000129991	Chromatin interaction
ENSG00000131037	Chromatin interaction
ENSG00000167646	Chromatin interaction
ENSG00000105048	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs8112233	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3319164	chr19:54983548-55605784	Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
2	esv3319165	chr19:54983548-55605784	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
3	esv3395724	chr19:54983577-55605784	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
4	esv3341592	chr19:54983611-55605750	Weak transcription Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
5	nsv534462	chr19:55028722-55683018	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
6	nsv1063666	chr19:55030439-55622780	Weak transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
7	nsv817874	chr19:55595687-55614923	Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv912449	chr19:55595687-55630425	Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
9	nsv912450	chr19:55595687-55633043	Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv912452	chr19:55595687-55644325	Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
11	nsv912451	chr19:55595687-55680746	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
12	esv20543	chr19:55600088-55600754	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55592600-55602400	Weak transcription	Hela-S3	cervix
2	chr19:55593800-55620400	Weak transcription	HMEC	breast
3	chr19:55594800-55606000	Weak transcription	HepG2	liver
4	chr19:55598000-55602000	Weak transcription	Dnd41	blood
5	chr19:55598800-55601400	Enhancers	Fetal Heart	heart
6	chr19:55599000-55603000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr19:55599200-55600400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr19:55599200-55600400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
9	chr19:55599200-55602000	Weak transcription	Brain Angular Gyrus	brain
10	chr19:55599200-55602400	Weak transcription	NHEK	skin
11	chr19:55599200-55626600	Weak transcription	Fetal Kidney	kidney
12	chr19:55599200-55627200	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr19:55599400-55600800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr19:55599400-55600800	Weak transcription	A549	lung
15	chr19:55599400-55601000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr19:55599400-55601200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr19:55599400-55601200	Weak transcription	Brain Substantia Nigra	brain
18	chr19:55599400-55601800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr19:55599400-55602000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr19:55599400-55602000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr19:55599400-55604800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr19:55599400-55614800	Weak transcription	GM12878-XiMat	blood
23	chr19:55599600-55600400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr19:55599600-55600600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
25	chr19:55599600-55600600	Enhancers	Left Ventricle	heart
26	chr19:55599600-55600800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr19:55599600-55601600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr19:55599600-55602000	Weak transcription	Gastric	stomach
29	chr19:55599800-55600400	Enhancers	Fetal Brain Female	brain
30	chr19:55599800-55600400	Genic enhancers	Fetal Stomach	stomach
31	chr19:55599800-55600600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
32	chr19:55599800-55600800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr19:55599800-55600800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr19:55599800-55601000	Weak transcription	Ovary	ovary
35	chr19:55599800-55601200	Enhancers	Stomach Smooth Muscle	stomach
36	chr19:55599800-55601400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr19:55599800-55601800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr19:55599800-55602000	Weak transcription	Brain Anterior Caudate	brain
39	chr19:55599800-55602000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr19:55599800-55602000	Weak transcription	Lung	lung
41	chr19:55599800-55602000	Weak transcription	Psoas Muscle	Psoas
42	chr19:55599800-55602000	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr19:55599800-55602000	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr19:55599800-55602200	Weak transcription	Small Intestine	intestine
45	chr19:55599800-55602400	Weak transcription	Pancreas	Pancrea
46	chr19:55599800-55626000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr19:55600000-55600400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr19:55600000-55600400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr19:55600000-55600400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr19:55600000-55600400	Enhancers	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links