Variant report

Variant	rs2295522
Chromosome Location	chr14:65220775-65220776
allele	A/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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:65219332..65221350-chr14:65225849..65228107,2	K562	blood:
2	chr14:65217187..65219069-chr14:65219788..65222108,2	MCF-7	breast:
3	chr14:65219449..65221733-chr14:65223947..65226345,2	MCF-7	breast:
4	chr14:65201615..65203157-chr14:65220105..65223085,2	K562	blood:
5	chr14:65168373..65176902-chr14:65220182..65231670,21	MCF-7	breast:
6	chr14:65168335..65178043-chr14:65220677..65234710,31	MCF-7	breast:
7	chr14:65212266..65214655-chr14:65220230..65222860,3	MCF-7	breast:
8	chr14:65218923..65222036-chr14:65223226..65227599,7	K562	blood:
9	chr14:65220335..65220855-chr2:133012578..133013363,2	MCF-7	breast:
10	chr14:65205002..65209276-chr14:65218300..65221160,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000070182	Chromatin interaction
ENSG00000126822	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs229656	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1818582	chr14:65172898-65256685	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1035833	chr14:65176371-65246181	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
3	esv1801406	chr14:65193725-65264416	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
4	nsv902023	chr14:65200821-65243885	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
5	nsv902024	chr14:65200821-65244950	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65201000-65221800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr14:65208600-65222400	Weak transcription	Stomach Mucosa	stomach
3	chr14:65209800-65223600	Weak transcription	Psoas Muscle	Psoas
4	chr14:65211200-65228800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr14:65212000-65224400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr14:65212800-65224200	Weak transcription	Aorta	Aorta
7	chr14:65213800-65222200	Weak transcription	Colon Smooth Muscle	Colon
8	chr14:65214000-65221600	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr14:65214000-65223600	Weak transcription	Right Atrium	heart
10	chr14:65214200-65221200	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr14:65214200-65224800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr14:65214400-65224200	Weak transcription	Fetal Lung	lung
13	chr14:65214400-65224400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr14:65214400-65224600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr14:65214400-65224600	Weak transcription	Fetal Kidney	kidney
16	chr14:65214600-65224600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr14:65214800-65222000	Strong transcription	Fetal Muscle Trunk	muscle
18	chr14:65214800-65224600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr14:65215000-65221200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr14:65215000-65222200	Weak transcription	NH-A	brain
21	chr14:65215000-65224800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr14:65215200-65224600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr14:65215200-65232400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr14:65215400-65220800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr14:65215400-65222200	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr14:65215400-65223600	Weak transcription	Gastric	stomach
27	chr14:65215400-65224600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr14:65215400-65224800	Weak transcription	Brain Substantia Nigra	brain
29	chr14:65215600-65221200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr14:65215600-65224600	Weak transcription	Brain Angular Gyrus	brain
31	chr14:65216200-65221200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr14:65216200-65224400	Weak transcription	Brain Anterior Caudate	brain
33	chr14:65216800-65221400	Weak transcription	Ovary	ovary
34	chr14:65216800-65221400	Weak transcription	Pancreas	Pancrea
35	chr14:65216800-65221400	Weak transcription	Spleen	Spleen
36	chr14:65216800-65222400	Weak transcription	Esophagus	oesophagus
37	chr14:65216800-65223400	Weak transcription	Left Ventricle	heart
38	chr14:65216800-65223600	Weak transcription	Right Ventricle	heart
39	chr14:65216800-65224000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr14:65216800-65224400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr14:65216800-65224600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr14:65216800-65224800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr14:65216800-65225000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr14:65217000-65221800	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr14:65217000-65222000	Weak transcription	A549	lung
46	chr14:65217000-65224400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr14:65217200-65221000	Weak transcription	NHEK	skin
48	chr14:65217200-65221400	Weak transcription	Hela-S3	cervix
49	chr14:65217200-65221800	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr14:65217400-65221600	Weak transcription	Fetal Intestine Large	intestine

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