Variant report

Variant	nsv428618
Chromosome Location	chr14:20500951-20660726
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:489)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20584982-20585271	K562	blood:	n/a	n/a
2	ARID3A	chr14:20512405-20512844	K562	blood:	n/a	n/a
3	ARID3A	chr14:20644582-20645133	K562	blood:	n/a	n/a
4	ARID3A	chr14:20645562-20646086	K562	blood:	n/a	n/a
5	ATF1	chr14:20584956-20585164	K562	blood:	n/a	n/a
6	ATF1	chr14:20645594-20645932	K562	blood:	n/a	n/a
7	ATF1	chr14:20608626-20608778	K562	blood:	n/a	n/a
8	ATF1	chr14:20561670-20561913	K562	blood:	n/a	n/a
9	ATF3	chr14:20645584-20645910	K562	blood:	n/a	n/a
10	ATF3	chr14:20584968-20585229	K562	blood:	n/a	n/a
11	ATF3	chr14:20512489-20512787	K562	blood:	n/a	n/a
12	ATF3	chr14:20638032-20638356	K562	blood:	n/a	n/a
13	BACH1	chr14:20584638-20585505	K562	blood:	n/a	n/a
14	BHLHE40	chr14:20653018-20653080	K562	blood:	n/a	n/a
15	BHLHE40	chr14:20645542-20646303	K562	blood:	n/a	n/a
16	CBX3	chr14:20645492-20645863	K562	blood:	n/a	n/a
17	CBX3	chr14:20632642-20632904	K562	blood:	n/a	n/a
18	CBX3	chr14:20584916-20585201	K562	blood:	n/a	n/a
19	CBX3	chr14:20586942-20587293	K562	blood:	n/a	n/a
20	CBX3	chr14:20586982-20587337	K562	blood:	n/a	n/a
21	CBX3	chr14:20632656-20632932	K562	blood:	n/a	n/a
22	CBX3	chr14:20645515-20645980	K562	blood:	n/a	n/a
23	CBX3	chr14:20512416-20512761	K562	blood:	n/a	n/a
24	CCNT2	chr14:20516381-20516636	K562	blood:	n/a	n/a
25	CCNT2	chr14:20645714-20646195	K562	blood:	n/a	n/a
26	CEBPB	chr14:20546411-20546602	K562	blood:	n/a	n/a
27	CEBPB	chr14:20578626-20578939	A549	lung:	n/a	n/a
28	CEBPB	chr14:20659170-20659372	K562	blood:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
29	CEBPB	chr14:20578635-20578967	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:20524789-20524910	A549	lung:	n/a	n/a
31	CEBPB	chr14:20584757-20585090	K562	blood:	n/a	n/a
32	CEBPB	chr14:20638926-20639276	K562	blood:	n/a	chr14:20639103-20639114
33	CEBPB	chr14:20522010-20522214	K562	blood:	n/a	chr14:20522084-20522095
34	CEBPB	chr14:20645573-20645988	K562	blood:	n/a	n/a
35	CEBPB	chr14:20639049-20639270	IMR90	lung:	n/a	chr14:20639103-20639114
36	CEBPB	chr14:20645527-20645985	K562	blood:	n/a	n/a
37	CEBPB	chr14:20618584-20618626	A549	lung:	n/a	n/a
38	CEBPB	chr14:20638951-20639274	A549	lung:	n/a	chr14:20639103-20639114
39	CEBPB	chr14:20638948-20639275	HepG2	liver:	n/a	chr14:20639103-20639114
40	CEBPB	chr14:20643233-20643506	K562	blood:	n/a	chr14:20643311-20643324
41	CEBPB	chr14:20522008-20522207	HepG2	liver:	n/a	chr14:20522084-20522095
42	CEBPB	chr14:20578612-20578943	IMR90	lung:	n/a	n/a
43	CEBPB	chr14:20622449-20622660	HepG2	liver:	n/a	chr14:20622561-20622572
44	CEBPB	chr14:20644548-20644852	K562	blood:	n/a	chr14:20644780-20644791 chr14:20644718-20644735 chr14:20644780-20644791
45	CEBPB	chr14:20659063-20659394	HepG2	liver:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
46	CEBPB	chr14:20652454-20652480	HepG2	liver:	n/a	n/a
47	CEBPB	chr14:20631110-20631224	HepG2	liver:	n/a	chr14:20631171-20631182
48	CEBPB	chr14:20578686-20578922	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr14:20578620-20578945	K562	blood:	n/a	n/a
50	CEBPB	chr14:20634808-20635061	HepG2	liver:	n/a	chr14:20634950-20634963 chr14:20634951-20634962 chr14:20634950-20634961 chr14:20634952-20634961

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20586367-20586417	AG04450	lung:	fetal
2	chr14:20586367-20586417	AG04450	lung:	fetal
3	chr14:20612220-20612270	HCM	heart:	n/a
4	chr14:20585753-20585803	AG09319	gingival:	n/a
5	chr14:20584239-20584289	HCF	heart:	n/a
6	chr14:20528812-20528862	AG09309	skin:	n/a
7	chr14:20585753-20585803	ECC-1	luminal epithelium:	n/a
8	chr14:20611779-20611829	Jurkat	blood:	n/a
9	chr14:20502658-20502708	LNCaP	prostate:	n/a
10	chr14:20585753-20585803	HEK293	kidney:	embryo
11	chr14:20502658-20502708	SKMC	muscle:	n/a
12	chr14:20584239-20584289	BJ	skin:	n/a
13	chr14:20584239-20584289	PrEC	prostate:	n/a
14	chr14:20528812-20528862	ovcar-3	ovarian:	n/a
15	chr14:20586367-20586417	AG09319	gingival:	n/a
16	chr14:20586367-20586417	PFSK-1	brain:	n/a
17	chr14:20502658-20502708	NHDF-neo	bronchial:	n/a
18	chr14:20528812-20528862	NHBE	bronchial:	n/a
19	chr14:20585753-20585803	HIPEpiC	eye:	n/a
20	chr14:20611696-20611746	HCM	heart:	n/a
21	chr14:20611779-20611829	ECC-1	luminal epithelium:	n/a
22	chr14:20586367-20586417	BE2_C	brain:	n/a
23	chr14:20586367-20586417	HCPEpiC	choroid plexus:	n/a
24	chr14:20586367-20586417	SAEC	small airway:	n/a
25	chr14:20585753-20585803	SK-N-MC	brain:	n/a
26	chr14:20528812-20528862	BJ	skin:	n/a
27	chr14:20528812-20528862	GM12892	blood:	n/a
28	chr14:20584239-20584289	Caco-2	colon:	n/a
29	chr14:20586367-20586417	GM06990	blood:	n/a
30	chr14:20611779-20611829	HRE	kidney:	n/a
31	chr14:20612220-20612270	GM12891	blood:	n/a
32	chr14:20612220-20612270	HEEpiC	esophagus:	n/a
33	chr14:20585753-20585803	LNCaP	prostate:	n/a
34	chr14:20586367-20586417	HEEpiC	esophagus:	n/a
35	chr14:20612220-20612270	U87	brain:	n/a
36	chr14:20585753-20585803	HCPEpiC	choroid plexus:	n/a
37	chr14:20611696-20611746	HRPEpiC	eye:	n/a
38	chr14:20585753-20585803	HCT-116	colon:	n/a
39	chr14:20612220-20612270	PrEC	prostate:	n/a
40	chr14:20611696-20611746	GM12878	blood:	n/a
41	chr14:20611779-20611829	HNPCEpiC	eye:	n/a
42	chr14:20585753-20585803	NB4	blood:	n/a
43	chr14:20611779-20611829	MCF10A-Er-Src	breast:	n/a
44	chr14:20585753-20585803	Hepatocyte	liver:	n/a
45	chr14:20528812-20528862	IMR90	lung:	fetal
46	chr14:20586367-20586417	K562	blood:	n/a
47	chr14:20611696-20611746	AG04450	lung:	fetal
48	chr14:20584239-20584289	HCT-116	colon:	n/a
49	chr14:20612220-20612270	AoSMC	blood vessel:	n/a
50	chr14:20528812-20528862	SAEC	small airway:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
2	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
3	chr14:20530040..20532845-chr14:20547946..20550280,2	K562	blood:
4	chr14:20623957..20624479-chr3:64655642..64656615,2	MCF-7	breast:
5	chr14:20642540..20645135-chr14:20796578..20798741,2	K562	blood:
6	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:
7	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
8	chr14:20645666..20648683-chr14:20649468..20653312,5	K562	blood:
9	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
10	chr14:20530040..20532845-chr14:20547946..20550280,2	K562	blood:
11	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
12	chr14:20645875..20648132-chr14:20651152..20653312,3	K562	blood:
13	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
14	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
15	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
16	chr14:20615947..20618319-chr14:20622650..20625486,3	K562	blood:
17	chr14:20615947..20618319-chr14:20622650..20625017,2	K562	blood:
18	chr14:20582658..20584245-chr14:20584576..20586426,2	K562	blood:
19	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
20	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
21	chr14:20583619..20586533-chr14:20649310..20650931,2	K562	blood:
22	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
23	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
24	chr14:20518924..20521802-chr14:20525808..20527615,2	K562	blood:
25	chr14:20518924..20521802-chr14:20525808..20527615,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4N5-1	chr14:20617391-20617904	NONHSAT035552

No data

Variant related genes	Relation type
ENSG00000265199	TF binding region
OR4T1P	TF binding region
OR11G2	TF binding region
OR4L1	TF binding region
RNA5SP380	TF binding region
OR4K13	TF binding region
OR4N5	TF binding region
OR4K17	TF binding region
OR4U1P	TF binding region
RNA5SP381	TF binding region
ENSG00000259095	TF binding region
OR11G1P	TF binding region
PSMB7P1	TF binding region
ENSG00000265199	CpG island
OR4T1P	CpG island
OR11G2	CpG island
OR4L1	CpG island
RNA5SP380	CpG island
OR4K13	CpG island
OR4N5	CpG island
OR4K17	CpG island
OR4U1P	CpG island
RNA5SP381	CpG island
ENSG00000259095	CpG island
OR11G1P	CpG island
PSMB7P1	CpG island
ENSG00000184394	chromatin interactions
ENSG00000100814	chromatin interactions
ENSG00000258468	chromatin interactions
ENSG00000176230	chromatin interactions
ENSG00000259074	chromatin interactions

Extended variants
information (count: 2164 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2164 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540794720	chr14:20501209-20501210	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs139827649	chr14:20502235-20502236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146225521	chr14:20502242-20502243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139197151	chr14:20502267-20502268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368969142	chr14:20502270-20502271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149892824	chr14:20502285-20502286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs199844086	chr14:20502289-20502290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373091422	chr14:20502292-20502293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145005726	chr14:20502331-20502332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567573202	chr14:20502332-20502333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534566618	chr14:20502339-20502340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201972592	chr14:20502341-20502342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528478794	chr14:20502344-20502345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148655599	chr14:20502354-20502355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552941006	chr14:20502368-20502369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142233028	chr14:20502389-20502390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs202096230	chr14:20502409-20502410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376852073	chr14:20502414-20502415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147844931	chr14:20502442-20502443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141584254	chr14:20502466-20502467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370148123	chr14:20502468-20502469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192679665	chr14:20502472-20502473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576745694	chr14:20502477-20502478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113651738	chr14:20502481-20502482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373021760	chr14:20502502-20502503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140037435	chr14:20502506-20502507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199940502	chr14:20502512-20502513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370881689	chr14:20502517-20502518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562116163	chr14:20502531-20502532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147654583	chr14:20502538-20502539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574282025	chr14:20502553-20502554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541325547	chr14:20502556-20502557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149347818	chr14:20502567-20502568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76336343	chr14:20502602-20502603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377194294	chr14:20502603-20502604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200877569	chr14:20502608-20502609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563455180	chr14:20502610-20502611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116485278	chr14:20502614-20502615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549162154	chr14:20502629-20502630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184617178	chr14:20502633-20502634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138902767	chr14:20502652-20502653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149397731	chr14:20502653-20502654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs202200696	chr14:20502659-20502660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374416343	chr14:20502670-20502671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78395085	chr14:20502681-20502682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200605568	chr14:20502694-20502695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368560253	chr14:20502714-20502715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372694547	chr14:20502723-20502724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376242424	chr14:20502743-20502744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113736645	chr14:20502757-20502758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20502200-20502400	Enhancers	Pancreas	Pancrea
2	chr14:20502400-20504200	Weak transcription	Pancreas	Pancrea
3	chr14:20512200-20512400	Enhancers	K562	blood
4	chr14:20512400-20512800	Flanking Active TSS	K562	blood
5	chr14:20512800-20513200	Enhancers	K562	blood
6	chr14:20513200-20515800	Weak transcription	K562	blood
7	chr14:20514600-20515000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:20515000-20517000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr14:20515800-20517600	Enhancers	K562	blood
10	chr14:20520400-20521400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
11	chr14:20533000-20533400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
12	chr14:20542800-20543400	Active TSS	Fetal Heart	heart
13	chr14:20561600-20562000	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr14:20574400-20574600	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr14:20580400-20580800	Enhancers	K562	blood
16	chr14:20580800-20584200	Weak transcription	K562	blood
17	chr14:20584200-20584600	Enhancers	K562	blood
18	chr14:20584600-20585000	Flanking Active TSS	K562	blood
19	chr14:20585000-20585200	Enhancers	K562	blood
20	chr14:20585200-20585400	Flanking Active TSS	K562	blood
21	chr14:20585400-20585600	Enhancers	K562	blood
22	chr14:20585400-20585800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr14:20585600-20585800	ZNF genes & repeats	K562	blood
24	chr14:20585800-20586400	Genic enhancers	K562	blood
25	chr14:20586200-20586600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:20586400-20586600	Enhancers	K562	blood
27	chr14:20611200-20612600	Enhancers	K562	blood
28	chr14:20612400-20612800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:20613200-20613400	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr14:20613600-20621000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr14:20622200-20622400	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr14:20623000-20624000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr14:20630600-20630800	ZNF genes & repeats	Pancreas	Pancrea
34	chr14:20638000-20638800	Enhancers	K562	blood
35	chr14:20638400-20638600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr14:20638400-20638800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr14:20638800-20643000	Weak transcription	K562	blood
38	chr14:20643000-20644000	Enhancers	K562	blood
39	chr14:20643400-20643600	Enhancers	Pancreas	Pancrea
40	chr14:20643400-20643800	Enhancers	Stomach Mucosa	stomach
41	chr14:20643800-20645200	Weak transcription	Pancreas	Pancrea
42	chr14:20644000-20644200	Flanking Active TSS	K562	blood
43	chr14:20644200-20644400	Enhancers	Stomach Mucosa	stomach
44	chr14:20644200-20644600	Enhancers	K562	blood
45	chr14:20644600-20644800	Flanking Active TSS	K562	blood
46	chr14:20644800-20645000	Enhancers	K562	blood
47	chr14:20645000-20645200	Flanking Active TSS	K562	blood
48	chr14:20645200-20645800	Enhancers	K562	blood
49	chr14:20645200-20646400	Enhancers	Pancreas	Pancrea
50	chr14:20645800-20646400	Flanking Active TSS	K562	blood

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