Variant report

Variant	rs564668416
Chromosome Location	chr19:37821450-37821451
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:37808606..37810203-chr19:37820197..37822284,2	MCF-7	breast:
2	chr19:37808613..37811422-chr19:37818380..37821776,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000181666	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv918028	chr19:37020645-38014526	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv2757695	chr19:37794850-38051606	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	esv2758759	chr19:37794850-38051606	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv978812	chr19:37821277-37824004	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37809200-37824800	Weak transcription	Stomach Mucosa	stomach
2	chr19:37809400-37825000	Weak transcription	Fetal Thymus	thymus
3	chr19:37809400-37825000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr19:37809600-37824400	Weak transcription	NHDF-Ad	bronchial
5	chr19:37809600-37825000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr19:37810000-37825000	Weak transcription	Hela-S3	cervix
7	chr19:37810200-37821800	ZNF genes & repeats	A549	lung
8	chr19:37810400-37821600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr19:37810600-37824400	Weak transcription	Small Intestine	intestine
10	chr19:37810600-37824800	Weak transcription	Fetal Heart	heart
11	chr19:37810800-37824200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr19:37811600-37825000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr19:37811800-37821600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr19:37813200-37821800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr19:37813400-37821600	Strong transcription	Fetal Muscle Trunk	muscle
16	chr19:37813400-37821600	Strong transcription	Skeletal Muscle Female	skeletal muscle
17	chr19:37813400-37821600	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr19:37813800-37821600	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr19:37813800-37821800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr19:37813800-37821800	Strong transcription	Fetal Intestine Large	intestine
21	chr19:37814000-37821600	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr19:37814400-37821600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr19:37815000-37824800	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr19:37815800-37821600	Strong transcription	Rectal Mucosa Donor 31	rectum
25	chr19:37816800-37825000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr19:37817000-37825000	Weak transcription	Gastric	stomach
27	chr19:37817200-37824800	Weak transcription	Psoas Muscle	Psoas
28	chr19:37818600-37821800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr19:37818800-37821600	ZNF genes & repeats	Liver	Liver
30	chr19:37819200-37821600	Strong transcription	Brain Anterior Caudate	brain
31	chr19:37819200-37824800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr19:37819400-37821600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr19:37819400-37821600	Strong transcription	NHEK	skin
34	chr19:37819400-37824800	Weak transcription	Fetal Intestine Small	intestine
35	chr19:37819600-37821600	Strong transcription	Aorta	Aorta
36	chr19:37819800-37821600	Strong transcription	Muscle Satellite Cultured Cells	--
37	chr19:37820000-37821600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr19:37820000-37821600	Strong transcription	Right Ventricle	heart
39	chr19:37820000-37825200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr19:37820200-37821600	Genic enhancers	Dnd41	blood
41	chr19:37820200-37824800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr19:37820200-37824800	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr19:37820400-37824400	Weak transcription	Colonic Mucosa	Colon
44	chr19:37820400-37824800	Weak transcription	Esophagus	oesophagus
45	chr19:37820400-37824800	Weak transcription	Fetal Brain Female	brain
46	chr19:37820400-37825000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr19:37820400-37825000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr19:37820400-37825000	Weak transcription	Fetal Lung	lung
49	chr19:37820600-37821800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr19:37820600-37821800	Enhancers	Primary T cells from cord blood	blood

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