Variant report

Variant	rs61078734
Chromosome Location	chr19:53089469-53089470
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:53089314-53089498	GM12878	blood:	n/a	n/a
2	POLR2A	chr19:53089246-53089592	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:53085553..53087688-chr19:53089270..53091312,2	MCF-7	breast:
2	chr19:53087080..53089827-chr19:53090383..53092275,2	K562	blood:

Variant related genes	Relation type
ZNF137P	TF binding region
ENSG00000268886	TF binding region
ENSG00000123870	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs57517025	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57910852	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58021489	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8106591	1.00[AFR][1000 genomes];1.00[AMR][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	nsv1057296	chr19:52950339-53396986	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv510772	chr19:53037211-53103470	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1065584	chr19:53043126-53127459	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS 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	11 gene(s)	inside rSNPs	diseases
4	nsv833874	chr19:53058014-53257875	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv458743	chr19:53065661-53114267	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv580027	chr19:53065661-53114267	Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv912304	chr19:53071155-53114267	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	esv3385321	chr19:53086990-53090388	ZNF genes & repeats Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53074600-53103600	Weak transcription	Fetal Brain Male	brain
2	chr19:53075400-53089600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr19:53075400-53092200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr19:53075400-53092400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr19:53075400-53092400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
6	chr19:53076400-53096000	Strong transcription	Dnd41	blood
7	chr19:53079200-53092200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr19:53079400-53090400	ZNF genes & repeats	Liver	Liver
9	chr19:53079400-53092200	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
10	chr19:53079400-53094200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
11	chr19:53079400-53096000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
12	chr19:53079600-53089600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr19:53079600-53091800	ZNF genes & repeats	Thymus	Thymus
14	chr19:53079800-53091000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr19:53081600-53090200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
16	chr19:53083200-53091000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr19:53083400-53090400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
18	chr19:53083400-53091000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr19:53083600-53090400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr19:53083600-53090800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
21	chr19:53083600-53092400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr19:53083800-53092400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
23	chr19:53084600-53091200	ZNF genes & repeats	Colonic Mucosa	Colon
24	chr19:53085400-53091200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr19:53086800-53090000	ZNF genes & repeats	Lung	lung
26	chr19:53087200-53091000	ZNF genes & repeats	Spleen	Spleen
27	chr19:53087400-53091000	ZNF genes & repeats	Fetal Intestine Small	intestine
28	chr19:53087400-53091000	ZNF genes & repeats	Fetal Thymus	thymus
29	chr19:53087400-53095200	Weak transcription	Brain Anterior Caudate	brain
30	chr19:53087400-53103600	Weak transcription	Brain Substantia Nigra	brain
31	chr19:53087600-53089600	ZNF genes & repeats	Fetal Intestine Large	intestine
32	chr19:53087600-53089800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr19:53087600-53089800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr19:53087600-53090400	ZNF genes & repeats	Gastric	stomach
35	chr19:53087600-53091600	Weak transcription	Fetal Lung	lung
36	chr19:53087600-53095000	Weak transcription	Brain Cingulate Gyrus	brain
37	chr19:53087600-53095400	Weak transcription	Fetal Kidney	kidney
38	chr19:53087600-53095400	Weak transcription	NHLF	lung
39	chr19:53087600-53099000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr19:53087600-53099000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr19:53087600-53099000	Weak transcription	NHDF-Ad	bronchial
42	chr19:53087600-53099400	Weak transcription	Brain Angular Gyrus	brain
43	chr19:53087600-53103600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr19:53087800-53090800	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr19:53087800-53092200	Weak transcription	Brain Hippocampus Middle	brain
46	chr19:53087800-53095200	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr19:53087800-53095200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr19:53087800-53095200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr19:53087800-53095400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr19:53087800-53095400	Weak transcription	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links