Variant report

Variant	rs114048884
Chromosome Location	chr4:15641206-15641207
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:15639836..15641917-chr4:15654767..15657580,3	K562	blood:
2	chr4:15639542..15641253-chr4:15682901..15685078,2	MCF-7	breast:
3	chr4:15638821..15642037-chr4:15654372..15658464,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000118564	Chromatin interaction
ENSG00000237765	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3448986	chr4:14928802-15805558	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv2757923	chr4:15444617-15749520	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv2759227	chr4:15444617-15749520	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv428439	chr4:15556961-15749520	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1012988	chr4:15597510-16091527	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv518830	chr4:15610771-15672200	Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv521183	chr4:15610771-15692136	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	esv3464800	chr4:15640253-15642440	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv3464801	chr4:15640301-15642414	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv3464802	chr4:15640316-15642413	Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15568400-15655600	Weak transcription	Gastric	stomach
2	chr4:15600800-15653000	Weak transcription	Colonic Mucosa	Colon
3	chr4:15601000-15651600	Weak transcription	Small Intestine	intestine
4	chr4:15602600-15655600	Weak transcription	Pancreas	Pancrea
5	chr4:15605800-15650200	Weak transcription	Stomach Mucosa	stomach
6	chr4:15618600-15651000	Weak transcription	Spleen	Spleen
7	chr4:15622200-15655400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:15622600-15645800	Weak transcription	Aorta	Aorta
9	chr4:15625200-15644800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr4:15625400-15643200	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr4:15625800-15642400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:15625800-15643400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:15625800-15643600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:15625800-15643600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr4:15625800-15643600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr4:15626400-15646000	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr4:15627400-15645800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr4:15627400-15650000	Weak transcription	Fetal Heart	heart
19	chr4:15627400-15651200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr4:15627400-15652400	Weak transcription	Fetal Brain Male	brain
21	chr4:15627600-15645600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr4:15627600-15646800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr4:15627600-15650200	Weak transcription	Right Ventricle	heart
24	chr4:15628000-15655600	Weak transcription	Lung	lung
25	chr4:15628200-15645800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr4:15629600-15650400	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr4:15631200-15644400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr4:15633400-15642000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr4:15633400-15643800	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr4:15633400-15643800	Strong transcription	Fetal Intestine Large	intestine
31	chr4:15633600-15643400	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr4:15633600-15643600	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr4:15633600-15646400	Strong transcription	Fetal Thymus	thymus
34	chr4:15633800-15642400	Strong transcription	Liver	Liver
35	chr4:15634000-15642400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr4:15634000-15643600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr4:15634000-15643800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:15634200-15644400	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr4:15634600-15642600	Strong transcription	Primary B cells from peripheral blood	blood
40	chr4:15634600-15642600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr4:15634600-15643400	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr4:15634600-15643600	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr4:15634600-15646600	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr4:15634800-15643600	Strong transcription	Fetal Muscle Leg	muscle
45	chr4:15635000-15644000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:15635000-15644400	Strong transcription	Osteobl	bone
47	chr4:15635000-15647000	Strong transcription	HSMM	muscle
48	chr4:15635200-15643800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr4:15635400-15643800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:15635600-15642800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links