Variant report

Variant	nsv901470
Chromosome Location	chr14:21203159-21244696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:229)
CpG islands
(count:795)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:229 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21226178-21226475	K562	blood:	n/a	n/a
2	ATF2	chr14:21235950-21236475	GM12878	blood:	n/a	n/a
3	BATF	chr14:21229113-21229415	GM12878	blood:	n/a	chr14:21229293-21229304
4	BATF	chr14:21236052-21236220	GM12878	blood:	n/a	n/a
5	BATF	chr14:21239931-21240176	GM12878	blood:	n/a	n/a
6	BATF	chr14:21236013-21236287	GM12878	blood:	n/a	n/a
7	BCLAF1	chr14:21236015-21236389	GM12878	blood:	n/a	n/a
8	CEBPB	chr14:21242556-21242653	K562	blood:	n/a	n/a
9	CEBPB	chr14:21224593-21224978	MCF-7	breast:	n/a	chr14:21224753-21224762 chr14:21224753-21224762 chr14:21224751-21224764 chr14:21224753-21224762 chr14:21224751-21224762 chr14:21224753-21224764 chr14:21224753-21224762
10	CEBPB	chr14:21242434-21242832	MCF-7	breast:	n/a	n/a
11	CEBPB	chr14:21224587-21224876	K562	blood:	n/a	chr14:21224753-21224762 chr14:21224753-21224762 chr14:21224751-21224764 chr14:21224753-21224762 chr14:21224751-21224762 chr14:21224753-21224764 chr14:21224753-21224762
12	CEBPB	chr14:21211686-21212171	MCF-7	breast:	n/a	n/a
13	CEBPB	chr14:21224644-21224920	HepG2	liver:	n/a	chr14:21224753-21224762 chr14:21224753-21224762 chr14:21224751-21224764 chr14:21224753-21224762 chr14:21224751-21224762 chr14:21224753-21224764 chr14:21224753-21224762
14	CEBPB	chr14:21211774-21212120	MCF-7	breast:	n/a	n/a
15	CTCF	chr14:21226240-21226382	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr14:21226220-21226370	HEK293	kidney:	n/a	n/a
17	CTCF	chr14:21226209-21226404	MCF-7	breast:	n/a	n/a
18	CTCF	chr14:21226190-21226385	GM12891	blood:	n/a	n/a
19	CTCF	chr14:21226161-21226431	HepG2	liver:	n/a	n/a
20	CTCF	chr14:21226196-21226453	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr14:21226220-21226370	HCT-116	colon:	n/a	n/a
22	CTCF	chr14:21242906-21242979	Lung_OC	lung:	n/a	n/a
23	CTCF	chr14:21226185-21226398	GM19238	blood:	n/a	n/a
24	CTCF	chr14:21226380-21226530	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr14:21226220-21226370	HRE	kidney:	n/a	n/a
26	CTCF	chr14:21226220-21226370	HMF	breast:	n/a	n/a
27	CTCF	chr14:21226280-21226430	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr14:21226240-21226390	SAEC	small airway:	n/a	n/a
29	CTCF	chr14:21226300-21226450	MCF-7	breast:	n/a	n/a
30	CTCF	chr14:21226227-21226360	MCF-7	breast:	n/a	n/a
31	CTCF	chr14:21226220-21226370	GM12868	blood:	n/a	n/a
32	CTCF	chr14:21226200-21226350	GM12872	blood:	n/a	n/a
33	CTCF	chr14:21226260-21226410	Caco-2	colon:	n/a	n/a
34	CTCF	chr14:21226240-21226390	A549	lung:	n/a	n/a
35	CTCF	chr14:21226220-21226370	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr14:21226300-21226450	BE2_C	brain:	n/a	n/a
37	CTCF	chr14:21226200-21226350	HepG2	liver:	n/a	n/a
38	CTCF	chr14:21226260-21226410	HepG2	liver:	n/a	n/a
39	CTCF	chr14:21226860-21227010	HepG2	liver:	n/a	n/a
40	CTCF	chr14:21226180-21226330	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr14:21226240-21226390	GM12873	blood:	n/a	n/a
42	CTCF	chr14:21226240-21226390	Caco-2	colon:	n/a	n/a
43	CTCF	chr14:21226122-21226865	K562	blood:	n/a	chr14:21226777-21226795 chr14:21226779-21226800
44	CTCF	chr14:21226280-21226430	GM12864	blood:	n/a	n/a
45	CTCF	chr14:21226220-21226370	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr14:21226280-21226430	GM12866	blood:	n/a	n/a
47	CTCF	chr14:21226721-21226851	K562	blood:	n/a	chr14:21226777-21226795 chr14:21226779-21226800
48	CTCF	chr14:21226234-21226414	HepG2	liver:	n/a	n/a
49	CTCF	chr14:21226200-21226350	GM12867	blood:	n/a	n/a
50	CTCF	chr14:21226107-21226502	K562	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21238111-21238161	SKMC	muscle:	n/a
2	chr14:21214331-21214381	HCPEpiC	choroid plexus:	n/a
3	chr14:21238111-21238161	SKMC	muscle:	n/a
4	chr14:21214331-21214381	HCPEpiC	choroid plexus:	n/a
5	chr14:21214331-21214381	NHBE	bronchial:	n/a
6	chr14:21213898-21213948	ECC-1	luminal epithelium:	n/a
7	chr14:21214331-21214381	MCF10A-Er-Src	breast:	n/a
8	chr14:21238166-21238216	MCF10A-Er-Src	breast:	n/a
9	chr14:21213343-21213393	AG10803	skin:	n/a
10	chr14:21214331-21214381	AG09319	gingival:	n/a
11	chr14:21238166-21238216	GM12892	blood:	n/a
12	chr14:21212718-21212768	HCPEpiC	choroid plexus:	n/a
13	chr14:21238436-21238486	HRE	kidney:	n/a
14	chr14:21243205-21243255	Jurkat	blood:	n/a
15	chr14:21214078-21214128	A549	lung:	n/a
16	chr14:21243205-21243255	NHBE	bronchial:	n/a
17	chr14:21237111-21237161	AG04449	skin:	fetal
18	chr14:21213343-21213393	HUVEC	blood vessel:	n/a
19	chr14:21237111-21237161	T-47D	breast:	n/a
20	chr14:21238111-21238161	HUVEC	blood vessel:	n/a
21	chr14:21213898-21213948	T-47D	breast:	n/a
22	chr14:21212718-21212768	NH-A	brain:	n/a
23	chr14:21213343-21213393	T-47D	breast:	n/a
24	chr14:21214078-21214128	RPTEC	kidney:	n/a
25	chr14:21214331-21214381	HCM	heart:	n/a
26	chr14:21216325-21216375	HEK293	kidney:	embryo
27	chr14:21215971-21216021	BE2_C	brain:	n/a
28	chr14:21215971-21216021	SK-N-MC	brain:	n/a
29	chr14:21214078-21214128	HCM	heart:	n/a
30	chr14:21237111-21237161	NHBE	bronchial:	n/a
31	chr14:21243205-21243255	GM19239	blood:	n/a
32	chr14:21215971-21216021	Caco-2	colon:	n/a
33	chr14:21213898-21213948	NB4	blood:	n/a
34	chr14:21238166-21238216	GM12891	blood:	n/a
35	chr14:21213343-21213393	CMK	blood:	n/a
36	chr14:21238166-21238216	U87	brain:	n/a
37	chr14:21214078-21214128	SAEC	small airway:	n/a
38	chr14:21238111-21238161	HCF	heart:	n/a
39	chr14:21214078-21214128	BJ	skin:	n/a
40	chr14:21213343-21213393	PrEC	prostate:	n/a
41	chr14:21215971-21216021	AoSMC	blood vessel:	n/a
42	chr14:21215971-21216021	AG04449	skin:	fetal
43	chr14:21212718-21212768	AG04450	lung:	fetal
44	chr14:21238166-21238216	GM06990	blood:	n/a
45	chr14:21212718-21212768	HCT-116	colon:	n/a
46	chr14:21214078-21214128	K562	blood:	n/a
47	chr14:21215971-21216021	MCF10A-Er-Src	breast:	n/a
48	chr14:21238436-21238486	U87	brain:	n/a
49	chr14:21213898-21213948	HRPEpiC	eye:	n/a
50	chr14:21243205-21243255	Caco-2	colon:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21241814..21243843-chr14:21252003..21253571,2	K562	blood:
2	chr14:21214265..21215903-chr14:21220143..21221742,2	MCF-7	breast:
3	chr14:21216332..21218814-chr14:21219434..21221917,2	K562	blood:
4	chr14:21225835..21226856-chr14:21323577..21324461,4	K562	blood:
5	chr14:21221271..21223338-chr14:21227917..21230397,2	MCF-7	breast:
6	chr14:21216332..21218814-chr14:21219434..21221917,2	K562	blood:
7	chr14:21239033..21242293-chr14:21242606..21246239,4	K562	blood:
8	chr14:21165555..21167023-chr14:21225530..21226742,6	MCF-7	breast:
9	chr14:21228059..21231751-chr14:21231942..21234798,3	MCF-7	breast:
10	chr14:21203729..21206173-chr14:21222860..21224894,2	MCF-7	breast:
11	chr14:21228059..21231751-chr14:21231942..21234798,3	MCF-7	breast:
12	chr14:21214265..21215903-chr14:21220143..21221742,2	MCF-7	breast:
13	chr14:21237702..21239397-chr14:21274792..21276728,2	K562	blood:
14	chr14:21216402..21218717-chr14:21226211..21228244,2	MCF-7	breast:
15	chr14:21216402..21218717-chr14:21226211..21228244,2	MCF-7	breast:
16	chr14:21203729..21206173-chr14:21222860..21224894,2	MCF-7	breast:
17	chr14:21239033..21242293-chr14:21242606..21246239,4	K562	blood:
18	chr14:21231150..21232961-chr14:21456666..21458618,2	MCF-7	breast:
19	chr14:21221271..21223338-chr14:21227917..21230397,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EDDM3A-1	chr14:21203985-21204012	NONHSAT035608

No data

Variant related genes	Relation type
EDDM3A	TF binding region
EDDM3B	TF binding region
RNASE6	TF binding region
EDDM3A	CpG island
EDDM3B	CpG island
RNASE6	CpG island
ENSG00000258810	chromatin interactions
ENSG00000165792	chromatin interactions

Extended variants
information (count: 1765 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1765 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9671539	chr14:21203159-21203160	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117031746	chr14:21203166-21203167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570523779	chr14:21203196-21203197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12892436	chr14:21203216-21203217	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs9671506	chr14:21203217-21203218	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs574413282	chr14:21203221-21203222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9671507	chr14:21203264-21203265	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs555330955	chr14:21203267-21203268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528740230	chr14:21203277-21203278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138270676	chr14:21203278-21203279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9671547	chr14:21203332-21203333	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs565496815	chr14:21203338-21203339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs59919763	chr14:21203361-21203362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377540595	chr14:21203369-21203370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75060697	chr14:21203390-21203391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17308520	chr14:21203404-21203405	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs117121769	chr14:21203415-21203416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554735323	chr14:21203439-21203440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187815802	chr14:21203440-21203441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527602848	chr14:21203477-21203478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569741858	chr14:21203505-21203506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs8018673	chr14:21203519-21203520	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs117148296	chr14:21203570-21203571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144667151	chr14:21203622-21203623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11271085	chr14:21203623-21203624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs386775332	chr14:21203624-21203625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs57527927	chr14:21203625-21203626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72661332	chr14:21203627-21203628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568042455	chr14:21203663-21203664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146310628	chr14:21203669-21203670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374451247	chr14:21203677-21203678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558488502	chr14:21203730-21203731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191571951	chr14:21203735-21203736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184445840	chr14:21203751-21203752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2873977	chr14:21203826-21203827	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs142862402	chr14:21203853-21203854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144767283	chr14:21203857-21203858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577408176	chr14:21203887-21203888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544477953	chr14:21203892-21203893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189780929	chr14:21203898-21203899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574607229	chr14:21203907-21203908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541892007	chr14:21203925-21203926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74720157	chr14:21203943-21203944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2319444	chr14:21203950-21203951	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs74791268	chr14:21203956-21203957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181380803	chr14:21203984-21203985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74411294	chr14:21203992-21203993	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs138719292	chr14:21204002-21204003	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs113193832	chr14:21204169-21204170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568214310	chr14:21204211-21204212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21195400-21209400	Weak transcription	Gastric	stomach
2	chr14:21199000-21203800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:21200600-21204000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:21201400-21203200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr14:21203000-21203200	Enhancers	Pancreas	Pancrea
6	chr14:21203000-21203200	Enhancers	Right Atrium	heart
7	chr14:21203000-21204000	Weak transcription	Right Ventricle	heart
8	chr14:21204000-21204200	Enhancers	Right Ventricle	heart
9	chr14:21208400-21212800	Enhancers	Placenta	Placenta
10	chr14:21209400-21210800	Enhancers	Gastric	stomach
11	chr14:21210000-21210600	Enhancers	Primary B cells from cord blood	blood
12	chr14:21210200-21211000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:21210600-21211000	Enhancers	Stomach Mucosa	stomach
14	chr14:21211000-21214000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr14:21212800-21213800	Weak transcription	Placenta	Placenta
16	chr14:21213800-21214000	Enhancers	Placenta	Placenta
17	chr14:21214000-21214600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr14:21214200-21214400	Enhancers	Lung	lung
19	chr14:21215600-21216800	Enhancers	Duodenum Mucosa	Duodenum
20	chr14:21215800-21216600	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr14:21216000-21216400	Enhancers	Lung	lung
22	chr14:21216400-21216600	Weak transcription	Lung	lung
23	chr14:21216600-21217000	Enhancers	Lung	lung
24	chr14:21219800-21221200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
25	chr14:21220000-21220800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
26	chr14:21220000-21221200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr14:21220000-21221200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:21220000-21221600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:21220800-21221400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr14:21221200-21229000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:21221400-21241800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:21221600-21223800	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr14:21221800-21223200	Enhancers	Left Ventricle	heart
34	chr14:21222400-21223200	Enhancers	Liver	Liver
35	chr14:21222600-21223200	Enhancers	Pancreas	Pancrea
36	chr14:21223000-21223600	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr14:21223200-21224800	Enhancers	Gastric	stomach
38	chr14:21223200-21236200	Weak transcription	Left Ventricle	heart
39	chr14:21226000-21226800	Enhancers	Brain Hippocampus Middle	brain
40	chr14:21226200-21227000	Enhancers	Brain Cingulate Gyrus	brain
41	chr14:21226400-21227000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr14:21226400-21227000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr14:21226400-21227200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr14:21226400-21227200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr14:21226400-21227200	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr14:21226400-21227200	Enhancers	Primary hematopoietic stem cells	blood
47	chr14:21226400-21227400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr14:21226400-21227400	Enhancers	K562	blood
49	chr14:21226600-21226800	Enhancers	Right Atrium	heart
50	chr14:21226600-21226800	Enhancers	GM12878-XiMat	blood

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