Variant report

Variant	nsv1048316
Chromosome Location	chr14:47297113-47885723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1347)
CpG islands
(count:733)
Chromatin interactive
region (count:20)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:47872730-47872904	K562	blood:	n/a	n/a
2	ATF2	chr14:47513971-47514339	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:47354745-47355139	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:47804741-47804747	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:47840011-47840068	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr14:47354811-47355132	K562	blood:	n/a	n/a
7	BACH1	chr14:47827183-47827600	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:47858719-47859063	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:47555354-47555385	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr14:47356455-47356637	GM12878	blood:	n/a	chr14:47356567-47356578
11	BATF	chr14:47356425-47356723	GM12878	blood:	n/a	chr14:47356567-47356578
12	BCL11A	chr14:47514066-47514301	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr14:47514116-47514346	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr14:47657519-47657543	GM12878	blood:	n/a	n/a
15	BRCA1	chr14:47303861-47303947	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:47509696-47510005	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr14:47649201-47649458	K562	blood:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
18	CEBPB	chr14:47743152-47743532	IMR90	lung:	n/a	n/a
19	CEBPB	chr14:47649157-47649470	Hela-S3	cervix:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
20	CEBPB	chr14:47758513-47758743	A549	lung:	n/a	chr14:47758676-47758687 chr14:47758675-47758688
21	CEBPB	chr14:47773674-47773940	HepG2	liver:	n/a	chr14:47773834-47773847 chr14:47773812-47773823
22	CEBPB	chr14:47393718-47394047	IMR90	lung:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
23	CEBPB	chr14:47743099-47743552	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr14:47362102-47362436	HepG2	liver:	n/a	chr14:47362259-47362270
25	CEBPB	chr14:47303607-47303836	A549	lung:	n/a	chr14:47303681-47303692
26	CEBPB	chr14:47649141-47649487	IMR90	lung:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
27	CEBPB	chr14:47743152-47743531	K562	blood:	n/a	n/a
28	CEBPB	chr14:47617889-47618242	HepG2	liver:	n/a	chr14:47618074-47618085
29	CEBPB	chr14:47738831-47739429	HCT-116	colon:	n/a	chr14:47739390-47739403 chr14:47738862-47738879 chr14:47738864-47738876
30	CEBPB	chr14:47617899-47618250	IMR90	lung:	n/a	chr14:47618074-47618085
31	CEBPB	chr14:47586722-47586989	HepG2	liver:	n/a	chr14:47586859-47586870
32	CEBPB	chr14:47743181-47743550	HCT-116	colon:	n/a	n/a
33	CEBPB	chr14:47404933-47405117	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr14:47647084-47647297	A549	lung:	n/a	n/a
35	CEBPB	chr14:47743164-47743546	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:47509711-47510131	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr14:47834961-47835168	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:47743156-47743521	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr14:47670622-47670894	IMR90	lung:	n/a	chr14:47670750-47670761
40	CEBPB	chr14:47520035-47520324	A549	lung:	n/a	n/a
41	CEBPB	chr14:47617893-47618243	ECC-1	luminal epithelium:	n/a	chr14:47618074-47618085
42	CEBPB	chr14:47586722-47587018	A549	lung:	n/a	chr14:47586859-47586870
43	CEBPB	chr14:47380994-47381232	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:47366550-47366832	A549	lung:	n/a	chr14:47366671-47366680 chr14:47366671-47366682 chr14:47366669-47366682 chr14:47366669-47366680
45	CEBPB	chr14:47815725-47815829	H1-hESC	embryonic stem cell:	n/a	chr14:47815797-47815808
46	CEBPB	chr14:47485732-47485940	HepG2	liver:	n/a	chr14:47485846-47485857 chr14:47485886-47485898
47	CEBPB	chr14:47617920-47618180	H1-hESC	embryonic stem cell:	n/a	chr14:47618074-47618085
48	CEBPB	chr14:47434809-47435009	HepG2	liver:	n/a	chr14:47434916-47434933
49	CEBPB	chr14:47743201-47743510	A549	lung:	n/a	n/a
50	CEBPB	chr14:47624242-47624527	A549	lung:	n/a	chr14:47624388-47624399

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:47769981-47770031	NH-A	brain:	n/a
2	chr14:47769981-47770031	NH-A	brain:	n/a
3	chr14:47572921-47572971	HPAEpiC	pulmonary alveolar:	n/a
4	chr14:47311141-47311191	MCF-7	breast:	n/a
5	chr14:47872288-47872338	SK-N-SH	brain:	n/a
6	chr14:47311141-47311191	BE2_C	brain:	n/a
7	chr14:47834520-47834570	MCF-7	breast:	n/a
8	chr14:47544244-47544294	GM19239	blood:	n/a
9	chr14:47572921-47572971	HCT-116	colon:	n/a
10	chr14:47544244-47544294	BE2_C	brain:	n/a
11	chr14:47812515-47812565	HCF	heart:	n/a
12	chr14:47769981-47770031	GM12878	blood:	n/a
13	chr14:47834520-47834570	NT2-D1	testis:	n/a
14	chr14:47670060-47670110	K562	blood:	n/a
15	chr14:47311141-47311191	HIPEpiC	eye:	n/a
16	chr14:47311141-47311191	HNPCEpiC	eye:	n/a
17	chr14:47411755-47411805	A549	lung:	n/a
18	chr14:47769981-47770031	AG09319	gingival:	n/a
19	chr14:47544244-47544294	HMEC	breast:	n/a
20	chr14:47310377-47310427	AoSMC	blood vessel:	n/a
21	chr14:47834520-47834570	BJ	skin:	n/a
22	chr14:47859275-47859325	AoSMC	blood vessel:	n/a
23	chr14:47812515-47812565	PANC-1	pancreas:	n/a
24	chr14:47310377-47310427	NHDF-neo	bronchial:	n/a
25	chr14:47769981-47770031	SKMC	muscle:	n/a
26	chr14:47544244-47544294	NHDF-neo	bronchial:	n/a
27	chr14:47544244-47544294	LNCaP	prostate:	n/a
28	chr14:47769981-47770031	BE2_C	brain:	n/a
29	chr14:47544244-47544294	AG10803	skin:	n/a
30	chr14:47513774-47513824	HPAEpiC	pulmonary alveolar:	n/a
31	chr14:47572921-47572971	AG10803	skin:	n/a
32	chr14:47859275-47859325	PANC-1	pancreas:	n/a
33	chr14:47310377-47310427	SK-N-MC	brain:	n/a
34	chr14:47812515-47812565	HRPEpiC	eye:	n/a
35	chr14:47311141-47311191	NB4	blood:	n/a
36	chr14:47513774-47513824	Hela-S3	cervix:	n/a
37	chr14:47812515-47812565	LNCaP	prostate:	n/a
38	chr14:47872288-47872338	HPAEpiC	pulmonary alveolar:	n/a
39	chr14:47834520-47834570	AG04450	lung:	fetal
40	chr14:47572921-47572971	HAEpiC	amniotic membrane:	n/a
41	chr14:47812515-47812565	NHBE	bronchial:	n/a
42	chr14:47769981-47770031	CMK	blood:	n/a
43	chr14:47572921-47572971	Jurkat	blood:	n/a
44	chr14:47812515-47812565	PrEC	prostate:	n/a
45	chr14:47670060-47670110	HMEC	breast:	n/a
46	chr14:47769981-47770031	NT2-D1	testis:	n/a
47	chr14:47411755-47411805	HL-60	blood:	n/a
48	chr14:47513774-47513824	HRCEpiC	kidney:	n/a
49	chr14:47544244-47544294	NH-A	brain:	n/a
50	chr14:47769981-47770031	PrEC	prostate:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:47584419..47587324-chr14:47587496..47590029,2	MCF-7	breast:
2	chr14:47525262..47526210-chr14:47747163..47747902,2	MCF-7	breast:
3	chr14:47825822..47827429-chr14:47839476..47841080,2	K562	blood:
4	chr14:47729955..47732269-chr14:47732563..47734465,2	MCF-7	breast:
5	chr14:47699505..47700030-chr20:46283707..46284523,2	MCF-7	breast:
6	chr14:47401862..47402382-chr2:190007804..190008571,2	MCF-7	breast:
7	chr14:47417689..47420302-chr14:47420799..47423183,3	MCF-7	breast:
8	chr12:54734855..54737428-chr14:47592677..47595618,2	MCF-7	breast:
9	chr14:47525262..47526210-chr14:47747163..47747902,2	MCF-7	breast:
10	chr14:47050056..47050875-chr14:47509400..47510237,2	MCF-7	breast:
11	chr14:47417689..47420302-chr14:47420799..47423183,3	MCF-7	breast:
12	chr14:47706399..47708616-chr14:47715847..47717651,2	MCF-7	breast:
13	chr14:47409007..47410877-chr14:47415123..47417216,2	K562	blood:
14	chr14:47706399..47708616-chr14:47715847..47717651,2	MCF-7	breast:
15	chr14:47811604..47813341-chr14:47823132..47825953,2	K562	blood:
16	chr14:47729955..47732269-chr14:47732563..47734465,2	MCF-7	breast:
17	chr14:47584419..47587324-chr14:47587496..47590029,2	MCF-7	breast:
18	chr14:47825822..47827429-chr14:47839476..47841080,2	K562	blood:
19	chr14:47409007..47410877-chr14:47415123..47417216,2	K562	blood:
20	chr14:47749473..47749973-chr5:68319722..68320581,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-12	chr14:47748394-47748994	l_979_chr14:47733075-47748994_testes
2	lnc-RPL10L-3	chr14:47775280-47775345	NONHSAT036687
3	lnc-RPL10L-3	chr14:47774434-47774526	NONHSAT036687
4	lnc-FANCM-12	chr14:47766804-47767153	l_979_chr14:47733075-47748994_testes
5	lnc-RPL10L-3	chr14:47812301-47812319	NONHSAT036687
6	lnc-RPL10L-2	chr14:47669778-47670307	NONHSAT036686
7	lnc-FANCM-12	chr14:47743855-47743971	l_979_chr14:47733075-47748994_testes
8	lnc-FANCM-12	chr14:47733076-47733185	l_979_chr14:47733075-47748994_testes
9	lnc-RPL10L-3	chr14:47798814-47799743	l_980_chr14:47772660-47799743_76bGuttman_hES
10	lnc-FANCM-12	chr14:47747104-47747220	l_979_chr14:47733075-47748994_testes
11	lnc-RPL10L-3	chr14:47768550-47768742	NONHSAT036687
12	lnc-FANCM-12	chr14:47765169-47765272	l_979_chr14:47733075-47748994_testes
13	lnc-FANCM-12	chr14:47751190-47751359	l_979_chr14:47733075-47748994_testes
14	lnc-FANCM-12	chr14:47752540-47752618	l_979_chr14:47733075-47748994_testes
15	lnc-RPL10L-3	chr14:47770614-47770753	NONHSAT036687
16	lnc-RPL10L-3	chr14:47774384-47774574	l_980_chr14:47772660-47799743_76bGuttman_hES
17	lnc-FANCM-11	chr14:47465657-47466377	NONHSAT036685
18	lnc-RPL10L-3	chr14:47772661-47773179	l_980_chr14:47772660-47799743_76bGuttman_hES

No data

Variant related genes	Relation type
RPA2P1	TF binding region
RPL13AP2	TF binding region
ENSG00000251735	TF binding region
MDGA2	TF binding region
RPA2P1	CpG island
RPL13AP2	CpG island
ENSG00000251735	CpG island
MDGA2	CpG island
ENSG00000139915	chromatin interactions

Extended variants
information (count: 12419 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:12419 , 50 per page) page: 1 2 3 4 5 6 7 ... 249

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189571916	chr14:47297128-47297129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547282100	chr14:47297141-47297142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543549483	chr14:47297213-47297214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562139378	chr14:47297254-47297255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529233838	chr14:47297342-47297343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180869147	chr14:47297391-47297392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141172513	chr14:47297393-47297394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146918612	chr14:47297394-47297395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185269655	chr14:47297419-47297420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371847276	chr14:47297470-47297471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138548041	chr14:47297489-47297490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537199192	chr14:47297569-47297570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555149925	chr14:47297607-47297608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567288877	chr14:47297617-47297618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534618874	chr14:47297619-47297620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565485883	chr14:47297638-47297639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572780835	chr14:47297671-47297672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567024880	chr14:47297737-47297738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546509483	chr14:47297768-47297769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79117117	chr14:47297853-47297854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558376855	chr14:47297905-47297906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112548139	chr14:47297974-47297975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191160018	chr14:47297996-47297997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142602516	chr14:47298018-47298019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183427328	chr14:47298019-47298020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541026504	chr14:47298022-47298023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559279674	chr14:47298060-47298061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369852127	chr14:47298097-47298098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143352674	chr14:47298098-47298099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373189919	chr14:47298112-47298113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188313907	chr14:47298193-47298194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533099795	chr14:47298197-47298198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191987032	chr14:47298213-47298214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569863340	chr14:47298217-47298218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183279703	chr14:47298250-47298251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201347903	chr14:47298261-47298262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549129028	chr14:47298277-47298278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34688745	chr14:47298299-47298300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397852302	chr14:47298311-47298312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567392073	chr14:47298323-47298324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141517161	chr14:47298396-47298397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34612876	chr14:47298443-47298444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187934449	chr14:47298447-47298448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs397852530	chr14:47298450-47298451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150863937	chr14:47298453-47298454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375213426	chr14:47298464-47298465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548192888	chr14:47298490-47298491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35697587	chr14:47298505-47298506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs77895101	chr14:47298541-47298542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191246277	chr14:47298582-47298583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
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
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
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	19907438	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Osteosarcoma	21215367	CNVD
Gastric cancer	18160780	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47294200-47298600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr14:47294600-47298600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:47298600-47299000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:47298600-47299000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:47302800-47303000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:47305400-47306600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:47307600-47307800	Enhancers	Brain Germinal Matrix	brain
8	chr14:47307800-47309200	Weak transcription	Brain Germinal Matrix	brain
9	chr14:47309200-47310400	Enhancers	Brain Germinal Matrix	brain
10	chr14:47309600-47310000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr14:47309600-47310000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:47309800-47310000	Enhancers	Brain Anterior Caudate	brain
13	chr14:47309800-47311200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:47309800-47311600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr14:47310000-47310200	Flanking Active TSS	Brain Anterior Caudate	brain
16	chr14:47310000-47310200	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr14:47310000-47310400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr14:47310000-47310400	Active TSS	Brain Hippocampus Middle	brain
19	chr14:47310000-47310600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr14:47310000-47310600	Active TSS	Brain Cingulate Gyrus	brain
21	chr14:47310000-47310800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr14:47310000-47310800	Active TSS	Brain Angular Gyrus	brain
23	chr14:47310000-47311000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr14:47310000-47311200	Active TSS	Brain Substantia Nigra	brain
25	chr14:47310200-47310400	Enhancers	Fetal Brain Female	brain
26	chr14:47310200-47310600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr14:47310200-47310600	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr14:47310200-47311200	Active TSS	Brain Anterior Caudate	brain
29	chr14:47310400-47310800	Flanking Active TSS	Brain Germinal Matrix	brain
30	chr14:47310400-47310800	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr14:47310400-47310800	Flanking Active TSS	Fetal Brain Female	brain
32	chr14:47310400-47311200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr14:47310400-47311200	Enhancers	Fetal Brain Male	brain
34	chr14:47310400-47311800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr14:47310600-47310800	Flanking Active TSS	Brain Cingulate Gyrus	brain
36	chr14:47310600-47311200	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr14:47310600-47312000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr14:47310800-47311200	Enhancers	Brain Germinal Matrix	brain
39	chr14:47310800-47311200	Enhancers	Brain Hippocampus Middle	brain
40	chr14:47310800-47311200	Enhancers	Fetal Brain Female	brain
41	chr14:47310800-47311400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:47311200-47311400	Enhancers	Brain Anterior Caudate	brain
43	chr14:47311800-47312200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr14:47312200-47312800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:47312800-47317800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr14:47317800-47318000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr14:47319400-47320400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr14:47319600-47320200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr14:47328200-47328600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
50	chr14:47337600-47339800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links