Variant report

Variant	rs375785535
Chromosome Location	chr1:209956725-209956726
allele	C/G
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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:209955222..209959394-chr1:210545816..210547914,4	K562	blood:
2	chr1:209940844..209943415-chr1:209955888..209958090,3	K562	blood:
3	chr1:209946631..209949857-chr1:209956266..209959109,3	MCF-7	breast:
4	chr1:209947385..209948947-chr1:209955247..209957526,2	MCF-7	breast:
5	chr1:209955520..209962214-chr1:209976009..209982555,8	K562	blood:
6	chr1:209955222..209958022-chr1:210545930..210547914,2	K562	blood:
7	chr1:209802370..209804993-chr1:209955747..209957464,2	K562	blood:
8	chr1:209950429..209953463-chr1:209956092..209959569,7	K562	blood:
9	chr1:209956517..209958141-chr1:209999783..210001469,2	MCF-7	breast:
10	chr1:209953015..209954990-chr1:209956352..209958315,2	MCF-7	breast:
11	chr1:209955602..209959674-chr1:209962858..209967873,6	MCF-7	breast:
12	chr1:209956289..209959543-chr1:209978892..209981541,4	K562	blood:
13	chr1:209921622..209924785-chr1:209954989..209957828,3	MCF-7	breast:
14	chr1:209935010..209937588-chr1:209955355..209957792,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000117595	Chromatin interaction
ENSG00000200972	Chromatin interaction
ENSG00000117597	Chromatin interaction
ENSG00000009790	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	nsv999901	chr1:209600631-210205379	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1014034	chr1:209759648-210501731	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv873139	chr1:209828955-210050794	Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1006632	chr1:209886202-209970355	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv4343	chr1:209929932-209974877	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv1067914	chr1:209955818-209972979	Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209942800-209956800	Weak transcription	Small Intestine	intestine
2	chr1:209942800-209957200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:209943800-209957000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:209943800-209957200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:209945000-209956800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:209945000-209956800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:209945200-209957200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:209946400-209956800	Strong transcription	Primary hematopoietic stem cells	blood
9	chr1:209949200-209957000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:209950000-209956800	Strong transcription	Primary T cells from cord blood	blood
11	chr1:209950200-209957400	Weak transcription	Aorta	Aorta
12	chr1:209951600-209956800	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr1:209952000-209957000	Weak transcription	HUVEC	blood vessel
14	chr1:209952800-209956800	Strong transcription	HMEC	breast
15	chr1:209953800-209956800	Weak transcription	Stomach Mucosa	stomach
16	chr1:209953800-209957400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr1:209954200-209956800	Weak transcription	Placenta	Placenta
18	chr1:209954200-209957000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:209954200-209957400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr1:209954400-209956800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr1:209954600-209956800	Genic enhancers	Fetal Intestine Large	intestine
22	chr1:209954600-209956800	Strong transcription	NHEK	skin
23	chr1:209954800-209956800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:209954800-209956800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr1:209954800-209956800	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr1:209955000-209956800	Weak transcription	A549	lung
27	chr1:209955200-209957200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr1:209955400-209957000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr1:209955600-209956800	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr1:209955800-209956800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:209956000-209956800	Genic enhancers	Brain Anterior Caudate	brain
32	chr1:209956000-209957000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr1:209956000-209957000	Enhancers	Fetal Heart	heart
34	chr1:209956000-209957000	Genic enhancers	Fetal Muscle Leg	muscle
35	chr1:209956000-209957200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr1:209956200-209956800	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr1:209956200-209956800	Genic enhancers	GM12878-XiMat	blood
38	chr1:209956200-209957000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr1:209956200-209957200	Genic enhancers	Fetal Stomach	stomach
40	chr1:209956400-209956800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:209956400-209956800	Enhancers	Gastric	stomach
42	chr1:209956400-209956800	Genic enhancers	Lung	lung
43	chr1:209956400-209956800	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr1:209956400-209956800	Enhancers	Spleen	Spleen
45	chr1:209956400-209957000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
46	chr1:209956400-209957000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
47	chr1:209956400-209957000	Enhancers	Fetal Muscle Trunk	muscle
48	chr1:209956400-209957000	Enhancers	HSMMtube	muscle
49	chr1:209956400-209957200	Enhancers	Left Ventricle	heart
50	chr1:209956400-209957400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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