Variant report

Variant	rs36104147
Chromosome Location	chr1:47068975-47068976
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:47054632..47056967-chr1:47067428..47069828,2	K562	blood:
2	chr1:47053775..47056193-chr1:47067460..47069823,2	MCF-7	breast:
3	chr1:47066512..47069474-chr1:47070954..47073416,4	K562	blood:
4	chr1:47068429..47072503-chr1:47081068..47085092,4	MCF-7	breast:
5	chr1:47068203..47069866-chr1:47187301..47190738,3	MCF-7	breast:
6	chr1:47053959..47056132-chr1:47066697..47069062,3	K562	blood:
7	chr1:47033343..47035201-chr1:47067108..47069992,2	K562	blood:
8	chr1:47041717..47044206-chr1:47067000..47069818,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000079277	Chromatin interaction
ENSG00000142961	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001455	chr1:46828004-47326539	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv534950	chr1:46828004-47326539	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1009193	chr1:46939999-47085667	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv1008246	chr1:47007844-47069845	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS 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	12 gene(s)	inside rSNPs	diseases
5	nsv870392	chr1:47040676-47095097	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv3409996	chr1:47068523-47068987	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47042600-47069000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr1:47046200-47069000	Weak transcription	Fetal Kidney	kidney
3	chr1:47048400-47069000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:47057000-47069000	Weak transcription	NH-A	brain
5	chr1:47057600-47069000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr1:47058600-47069200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:47059800-47069000	Weak transcription	HSMMtube	muscle
8	chr1:47060000-47069000	Weak transcription	Fetal Intestine Small	intestine
9	chr1:47060000-47069000	Weak transcription	Fetal Stomach	stomach
10	chr1:47060400-47069000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:47065800-47069000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr1:47065800-47069000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:47065800-47069200	Weak transcription	Small Intestine	intestine
14	chr1:47067000-47069000	Enhancers	Left Ventricle	heart
15	chr1:47067000-47069200	Enhancers	Lung	lung
16	chr1:47067000-47069400	Enhancers	Stomach Mucosa	stomach
17	chr1:47067200-47069000	Enhancers	Gastric	stomach
18	chr1:47067600-47069600	Enhancers	Spleen	Spleen
19	chr1:47068000-47069000	Enhancers	Primary T cells fromperipheralblood	blood
20	chr1:47068200-47069000	Enhancers	K562	blood
21	chr1:47068200-47069400	Flanking Active TSS	Pancreas	Pancrea
22	chr1:47068400-47069000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:47068400-47069000	Enhancers	Liver	Liver
24	chr1:47068400-47069000	Enhancers	Fetal Muscle Leg	muscle
25	chr1:47068400-47069000	Enhancers	Right Atrium	heart
26	chr1:47068400-47069200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:47068400-47069200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:47068400-47069200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr1:47068400-47069200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr1:47068400-47069200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr1:47068400-47069200	Enhancers	Aorta	Aorta
32	chr1:47068400-47069200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr1:47068400-47069200	Enhancers	Fetal Heart	heart
34	chr1:47068400-47069400	Flanking Active TSS	Duodenum Mucosa	Duodenum
35	chr1:47068400-47069600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr1:47068400-47069800	Flanking Active TSS	Fetal Thymus	thymus
37	chr1:47068400-47069800	Flanking Active TSS	Stomach Smooth Muscle	stomach
38	chr1:47068600-47069000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr1:47068600-47069000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr1:47068600-47069000	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr1:47068600-47069000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:47068600-47069000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:47068600-47069000	Enhancers	Brain Germinal Matrix	brain
44	chr1:47068600-47069000	Flanking Active TSS	Colonic Mucosa	Colon
45	chr1:47068600-47069000	Enhancers	Fetal Brain Male	brain
46	chr1:47068600-47069000	Enhancers	Fetal Lung	lung
47	chr1:47068600-47069000	Enhancers	Fetal Muscle Trunk	muscle
48	chr1:47068600-47069000	Enhancers	NHDF-Ad	bronchial
49	chr1:47068600-47069200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr1:47068600-47069200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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