Variant report

Variant	esv3486915
Chromosome Location	chr14:21951462-21955760
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:15)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:15 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:21954795-21955377	IMR90	lung:	n/a	chr14:21955213-21955224 chr14:21955212-21955223
2	CEBPB	chr14:21955145-21955321	HepG2	liver:	n/a	chr14:21955213-21955224 chr14:21955212-21955223
3	MAFK	chr14:21951293-21951567	HepG2	liver:	n/a	n/a
4	MAFK	chr14:21951310-21951495	HepG2	liver:	n/a	n/a
5	MAZ	chr14:21954957-21954961	HepG2	liver:	n/a	n/a
6	POLR2A	chr14:21955731-21955827	A549	lung:	n/a	n/a
7	POLR2A	chr14:21955649-21955697	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr14:21955722-21955842	MCF-7	breast:	n/a	n/a
9	POLR2A	chr14:21955756-21955837	MCF-7	breast:	n/a	n/a
10	POLR2A	chr14:21951940-21951956	MCF-7	breast:	n/a	n/a
11	POLR2A	chr14:21955752-21955859	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr14:21953086-21953226	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr14:21951917-21952193	HepG2	liver:	n/a	n/a
14	STAT3	chr14:21955386-21955421	MCF10A-Er-Src	breast:	n/a	n/a
15	STAT3	chr14:21951773-21951804	MCF10A-Er-Src	breast:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr14:21941797..21947093-chr14:21954513..21961521,11	MCF-7	breast:
2	chr14:21942911..21947036-chr14:21948493..21952401,7	MCF-7	breast:
3	chr14:21950181..21952493-chr14:21954450..21957059,4	MCF-7	breast:
4	chr14:21945001..21948392-chr14:21948946..21951939,4	K562	blood:
5	chr14:21923120..21925863-chr14:21948762..21952189,3	MCF-7	breast:
6	chr14:21954693..21956685-chr14:21971149..21973765,2	MCF-7	breast:
7	chr14:21948837..21951421-chr14:21953212..21956640,4	MCF-7	breast:
8	chr14:21953304..21957637-chr14:21977622..21980273,4	K562	blood:

No data

Variant related genes	Relation type
TOX4	TF binding region
ENSG00000100888	chromatin interactions
ENSG00000129472	chromatin interactions
ENSG00000165819	chromatin interactions
ENSG00000092203	chromatin interactions

Extended variants
information (count: 147 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:147 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367949219	chr14:21951468-21951469	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs568981509	chr14:21951488-21951489	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs150535900	chr14:21951518-21951519	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs4982449	chr14:21951542-21951543	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs370433754	chr14:21951546-21951547	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs78112936	chr14:21951560-21951561	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs398024523	chr14:21951561-21951562	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs200033558	chr14:21951562-21951563	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs568152283	chr14:21951600-21951601	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs534129811	chr14:21951661-21951662	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs66771279	chr14:21951671-21951672	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs138419391	chr14:21951673-21951674	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs141651363	chr14:21951696-21951697	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs550243671	chr14:21951706-21951707	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs556090903	chr14:21951761-21951762	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs568539020	chr14:21951770-21951771	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs548317368	chr14:21951780-21951781	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs61973220	chr14:21951813-21951814	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs572523593	chr14:21951816-21951817	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs550923023	chr14:21951841-21951842	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs199879748	chr14:21951848-21951849	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs568293146	chr14:21951859-21951860	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs11156994	chr14:21951875-21951876	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs71887551	chr14:21951906-21951907	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs36072627	chr14:21951907-21951908	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs552213493	chr14:21951943-21951944	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs371752876	chr14:21951944-21951945	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs35731052	chr14:21951962-21951963	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs72206008	chr14:21951963-21951964	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs398117964	chr14:21951965-21951966	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs72220259	chr14:21951973-21951974	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs201473794	chr14:21951974-21951975	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs375381078	chr14:21951976-21951977	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs75258240	chr14:21951978-21951979	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs531481762	chr14:21951979-21951980	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs577918800	chr14:21951980-21951981	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs568280808	chr14:21951981-21951982	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs72684774	chr14:21952049-21952050	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs538371029	chr14:21952076-21952077	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs369052853	chr14:21952077-21952078	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs570656848	chr14:21952086-21952087	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs146111921	chr14:21952090-21952091	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs556177021	chr14:21952102-21952103	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs569709681	chr14:21952111-21952112	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs368876937	chr14:21952116-21952117	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs538799858	chr14:21952155-21952156	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs535579381	chr14:21952193-21952194	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs140141455	chr14:21952291-21952292	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572477747	chr14:21952303-21952304	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs554124009	chr14:21952311-21952312	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ewing''s sarcoma	18628472	CNVD
Rheumatoid arthritis	23223014	CNVD
Ependymoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21946000-21960600	Weak transcription	Small Intestine	intestine
2	chr14:21946200-21955600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:21946200-21955600	Weak transcription	Gastric	stomach
4	chr14:21946200-21955600	Weak transcription	Left Ventricle	heart
5	chr14:21946200-21955600	Weak transcription	Ovary	ovary
6	chr14:21946200-21955600	Weak transcription	Thymus	Thymus
7	chr14:21946200-21977600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr14:21946400-21952000	Weak transcription	Lung	lung
9	chr14:21946400-21952600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:21946400-21952800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:21946400-21955400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr14:21946400-21955600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr14:21946400-21958000	Weak transcription	Pancreas	Pancrea
14	chr14:21946400-21958800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr14:21946400-21960800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr14:21946400-21971400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:21946600-21954600	Weak transcription	HSMMtube	muscle
18	chr14:21946600-21954800	Weak transcription	Rectal Smooth Muscle	rectum
19	chr14:21946600-21954800	Weak transcription	K562	blood
20	chr14:21946600-21955000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr14:21946600-21955000	Weak transcription	Fetal Thymus	thymus
22	chr14:21946600-21955400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr14:21946600-21955400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr14:21946600-21955600	Weak transcription	Brain Germinal Matrix	brain
25	chr14:21946600-21955600	Weak transcription	Colonic Mucosa	Colon
26	chr14:21946600-21955600	Weak transcription	Fetal Muscle Leg	muscle
27	chr14:21946600-21955600	Weak transcription	Psoas Muscle	Psoas
28	chr14:21946600-21955600	Weak transcription	Right Ventricle	heart
29	chr14:21946600-21955600	Weak transcription	Spleen	Spleen
30	chr14:21946600-21955800	Weak transcription	Fetal Brain Female	brain
31	chr14:21946600-21958000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr14:21946600-21960400	Weak transcription	Stomach Mucosa	stomach
33	chr14:21946600-21960800	Weak transcription	Aorta	Aorta
34	chr14:21946800-21954600	Weak transcription	Brain Hippocampus Middle	brain
35	chr14:21946800-21954800	Weak transcription	Osteobl	bone
36	chr14:21946800-21955000	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr14:21946800-21955400	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr14:21946800-21955600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr14:21946800-21955600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr14:21946800-21955600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr14:21946800-21955600	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr14:21946800-21955600	Weak transcription	A549	lung
43	chr14:21946800-21955600	Weak transcription	GM12878-XiMat	blood
44	chr14:21946800-21955600	Weak transcription	NHEK	skin
45	chr14:21946800-21956200	Weak transcription	NH-A	brain
46	chr14:21946800-21956400	Weak transcription	Hela-S3	cervix
47	chr14:21946800-21956800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr14:21946800-21956800	Weak transcription	Brain Angular Gyrus	brain
49	chr14:21946800-21956800	Weak transcription	HMEC	breast
50	chr14:21946800-21959000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links