Variant report

Variant	nsv902110
Chromosome Location	chr14:79624492-79998294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1262)
CpG islands
(count:1836)
Chromatin interactive
region (count:24)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1262 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:79892788-79893088	HepG2	liver:	n/a	n/a
2	ATF2	chr14:79844277-79844763	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr14:79844160-79844687	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr14:79981029-79981513	A549	lung:	n/a	n/a
5	ATF3	chr14:79836051-79836456	A549	lung:	n/a	n/a
6	BACH1	chr14:79831550-79831837	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:79746678-79746839	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:79745957-79746307	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:79745335-79745658	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:79744913-79745054	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr14:79995423-79995741	GM12878	blood:	n/a	n/a
12	BCL11A	chr14:79995484-79995633	GM12878	blood:	n/a	n/a
13	BCL11A	chr14:79995423-79995704	GM12878	blood:	n/a	n/a
14	BCL3	chr14:79949849-79950052	GM12878	blood:	n/a	n/a
15	BRCA1	chr14:79745642-79745842	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr14:79668038-79668544	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr14:79876061-79876235	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr14:79723742-79723963	K562	blood:	n/a	n/a
19	CBX3	chr14:79723711-79723919	K562	blood:	n/a	n/a
20	CEBPB	chr14:79885958-79886173	HepG2	liver:	n/a	chr14:79886023-79886034
21	CEBPB	chr14:79903160-79903330	HepG2	liver:	n/a	chr14:79903294-79903305 chr14:79903237-79903248
22	CEBPB	chr14:79694625-79694961	HepG2	liver:	n/a	chr14:79694792-79694803
23	CEBPB	chr14:79890808-79891203	IMR90	lung:	n/a	n/a
24	CEBPB	chr14:79640876-79641125	IMR90	lung:	n/a	chr14:79640950-79640963 chr14:79640950-79640963
25	CEBPB	chr14:79862419-79862716	HepG2	liver:	n/a	chr14:79862575-79862584 chr14:79862573-79862586 chr14:79862575-79862584 chr14:79862575-79862584 chr14:79862573-79862584 chr14:79862573-79862586
26	CEBPB	chr14:79980959-79981969	A549	lung:	n/a	n/a
27	CEBPB	chr14:79760802-79761387	IMR90	lung:	n/a	n/a
28	CEBPB	chr14:79977071-79977473	IMR90	lung:	n/a	n/a
29	CEBPB	chr14:79977257-79977423	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:79941838-79942149	IMR90	lung:	n/a	chr14:79941974-79941985
31	CEBPB	chr14:79836062-79836451	A549	lung:	n/a	chr14:79836365-79836377
32	CEBPB	chr14:79745881-79746154	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr14:79783756-79784053	IMR90	lung:	n/a	chr14:79783919-79783930
34	CEBPB	chr14:79981146-79981906	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr14:79941924-79942133	HepG2	liver:	n/a	chr14:79941974-79941985
36	CEBPB	chr14:79791437-79791882	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr14:79917462-79917502	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr14:79930899-79931227	IMR90	lung:	n/a	chr14:79931062-79931071 chr14:79931060-79931071
39	CEBPB	chr14:79890863-79891126	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr14:79818373-79818725	IMR90	lung:	n/a	chr14:79818558-79818569 chr14:79818556-79818569 chr14:79818380-79818393
41	CEBPB	chr14:79934306-79934586	IMR90	lung:	n/a	n/a
42	CEBPB	chr14:79800682-79800854	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr14:79667945-79668574	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr14:79885960-79886225	Hela-S3	cervix:	n/a	chr14:79886023-79886034
45	CEBPB	chr14:79862417-79862703	IMR90	lung:	n/a	chr14:79862575-79862584 chr14:79862573-79862586 chr14:79862575-79862584 chr14:79862575-79862584 chr14:79862573-79862584 chr14:79862573-79862586
46	CEBPB	chr14:79890911-79891175	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr14:79879725-79879843	A549	lung:	n/a	n/a
48	CEBPB	chr14:79862474-79862671	A549	lung:	n/a	chr14:79862575-79862584 chr14:79862573-79862586 chr14:79862575-79862584 chr14:79862575-79862584 chr14:79862573-79862584 chr14:79862573-79862586
49	CEBPB	chr14:79890870-79891175	A549	lung:	n/a	n/a
50	CEBPB	chr14:79942003-79942013	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1836 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:79968686-79968736	U87	brain:	n/a
2	chr14:79745997-79746047	AG04449	skin:	fetal
3	chr14:79745154-79745204	NHBE	bronchial:	n/a
4	chr14:79748641-79748691	T-47D	breast:	n/a
5	chr14:79982284-79982334	Hela-S3	cervix:	n/a
6	chr14:79746780-79746830	HNPCEpiC	eye:	n/a
7	chr14:79968686-79968736	U87	brain:	n/a
8	chr14:79745997-79746047	AG04449	skin:	fetal
9	chr14:79745154-79745204	NHBE	bronchial:	n/a
10	chr14:79748641-79748691	T-47D	breast:	n/a
11	chr14:79982284-79982334	Hela-S3	cervix:	n/a
12	chr14:79746780-79746830	HNPCEpiC	eye:	n/a
13	chr14:79747774-79747824	PrEC	prostate:	n/a
14	chr14:79745579-79745629	ECC-1	luminal epithelium:	n/a
15	chr14:79745403-79745453	AG09319	gingival:	n/a
16	chr14:79880024-79880074	HCT-116	colon:	n/a
17	chr14:79808311-79808361	GM06990	blood:	n/a
18	chr14:79880024-79880074	HCPEpiC	choroid plexus:	n/a
19	chr14:79844568-79844618	NH-A	brain:	n/a
20	chr14:79808311-79808361	MCF10A-Er-Src	breast:	n/a
21	chr14:79745592-79745642	LNCaP	prostate:	n/a
22	chr14:79745579-79745629	T-47D	breast:	n/a
23	chr14:79744991-79745041	AG04449	skin:	fetal
24	chr14:79808311-79808361	ProgFib	skin:	n/a
25	chr14:79748641-79748691	MCF-7	breast:	n/a
26	chr14:79792615-79792665	PANC-1	pancreas:	n/a
27	chr14:79746627-79746677	NT2-D1	testis:	n/a
28	chr14:79745579-79745629	PANC-1	pancreas:	n/a
29	chr14:79747774-79747824	ovcar-3	ovarian:	n/a
30	chr14:79933641-79933691	HUVEC	blood vessel:	n/a
31	chr14:79840647-79840697	HepG2	liver:	n/a
32	chr14:79745471-79745521	AG09319	gingival:	n/a
33	chr14:79747774-79747824	Hepatocyte	liver:	n/a
34	chr14:79760047-79760097	HEK293	kidney:	embryo
35	chr14:79939536-79939586	HCF	heart:	n/a
36	chr14:79989467-79989517	H1-hESC	embryonic stem cell:	embryo
37	chr14:79745579-79745629	MCF-7	breast:	n/a
38	chr14:79744991-79745041	ProgFib	skin:	n/a
39	chr14:79745592-79745642	HCT-116	colon:	n/a
40	chr14:79968686-79968736	HIPEpiC	eye:	n/a
41	chr14:79745997-79746047	HRE	kidney:	n/a
42	chr14:79746780-79746830	ovcar-3	ovarian:	n/a
43	chr14:79746359-79746409	ECC-1	luminal epithelium:	n/a
44	chr14:79792615-79792665	U87	brain:	n/a
45	chr14:79792615-79792665	SAEC	small airway:	n/a
46	chr14:79808311-79808361	GM12891	blood:	n/a
47	chr14:79747774-79747824	GM12878	blood:	n/a
48	chr14:79760047-79760097	HCM	heart:	n/a
49	chr14:79744991-79745041	K562	blood:	n/a
50	chr14:79747774-79747824	HEK293	kidney:	embryo

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:79962362..79964375-chr14:79965844..79968447,2	K562	blood:
2	chr14:79899576..79901464-chr14:79902826..79905660,2	K562	blood:
3	chr14:79808364..79810054-chr14:79814203..79817029,2	K562	blood:
4	chr14:79879666..79880179-chr14:79981324..79981914,2	MCF-7	breast:
5	chr14:79875683..79878645-chr5:173629859..173632851,2	MCF-7	breast:
6	chr14:79633552..79635611-chr14:79637121..79639941,2	MCF-7	breast:
7	chr14:79792610..79795331-chr14:79808836..79811275,2	MCF-7	breast:
8	chr14:79793930..79796173-chr14:79801791..79803941,2	MCF-7	breast:
9	chr14:79792610..79795331-chr14:79808836..79811275,2	MCF-7	breast:
10	chr14:79879666..79880608-chr14:79981324..79981922,3	MCF-7	breast:
11	chr14:79952202..79952971-chr8:128747799..128748754,2	NB4	blood:
12	chr14:79962362..79964375-chr14:79965844..79968447,2	K562	blood:
13	chr14:79704504..79705275-chr6:56819303..56820074,2	HCT-116	colon:
14	chr14:79899576..79901464-chr14:79902826..79905660,2	K562	blood:
15	chr14:79633552..79635611-chr14:79637121..79639941,2	MCF-7	breast:
16	chr14:79792537..79795369-chr14:79800633..79803440,2	MCF-7	breast:
17	chr14:79946169..79946771-chr5:64323360..64323893,2	MCF-7	breast:
18	chr14:79793930..79796173-chr14:79801791..79803941,2	MCF-7	breast:
19	chr14:79879666..79880608-chr14:79981324..79981922,3	MCF-7	breast:
20	chr14:79808988..79811235-chr14:81320946..81323442,2	MCF-7	breast:
21	chr14:79808364..79810054-chr14:79814203..79817029,2	K562	blood:
22	chr14:79477398..79478037-chr14:79822214..79823031,2	MCF-7	breast:
23	chr14:79792537..79795369-chr14:79800633..79803440,2	MCF-7	breast:
24	chr14:79879666..79880179-chr14:79981324..79981914,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIO2-4	chr14:79713408-79713445	ENSG00000258662.1
2	lnc-DIO2-4	chr14:79713602-79713690	ENSG00000258662.1
3	lnc-ADCK1-1	chr14:79667377-79667975	ENSG00000258419.1
4	lnc-DIO2-4	chr14:79715265-79715366	ENSG00000258662.1
5	lnc-DIO2-4	chr14:79714940-79715028	ENSG00000258662.1
6	lnc-ADCK1-1	chr14:79666325-79666381	ENSG00000258419.1
7	lnc-DIO2-4	chr14:79713011-79713088	ENSG00000258662.1

No data

Variant related genes	Relation type
NRXN3	TF binding region
ENSG00000258419	TF binding region
ENSG00000258662	TF binding region
NRXN3	CpG island
ENSG00000258419	CpG island
ENSG00000258662	CpG island
ENSG00000151914	chromatin interactions
ENSG00000136997	chromatin interactions
ENSG00000151917	chromatin interactions

Extended variants
information (count: 11076 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:11076 , 50 per page) page: 1 2 3 4 5 6 7 ... 222

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569745191	chr14:79632013-79632014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375902050	chr14:79632038-79632039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113958957	chr14:79632039-79632040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549038925	chr14:79632097-79632098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180937377	chr14:79632193-79632194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377696159	chr14:79632220-79632221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79706052	chr14:79632221-79632222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554055246	chr14:79632232-79632233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570766435	chr14:79632247-79632248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370356919	chr14:79632264-79632265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73325806	chr14:79632326-79632327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556250147	chr14:79632328-79632329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576369680	chr14:79632355-79632356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561450515	chr14:79632377-79632378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12891595	chr14:79632397-79632398	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs563746086	chr14:79632449-79632450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184009253	chr14:79632478-79632479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189861914	chr14:79632485-79632486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141714196	chr14:79632493-79632494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533044274	chr14:79632494-79632495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543683665	chr14:79632500-79632501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563162052	chr14:79632565-79632566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528877603	chr14:79632662-79632663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370693723	chr14:79632704-79632705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541243086	chr14:79632764-79632765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs61992527	chr14:79632802-79632803	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs17108796	chr14:79632822-79632823	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs547560084	chr14:79632858-79632859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147090238	chr14:79632973-79632974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201443777	chr14:79632977-79632978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539779989	chr14:79632994-79632995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373725529	chr14:79632999-79633000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374710318	chr14:79633049-79633050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556795352	chr14:79633058-79633059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569999580	chr14:79633078-79633079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181456216	chr14:79633080-79633081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555899976	chr14:79633140-79633141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2199797	chr14:79633169-79633170	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs556829391	chr14:79641409-79641410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35100523	chr14:79641418-79641419	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs542169498	chr14:79641438-79641439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552673337	chr14:79641443-79641444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541081176	chr14:79641457-79641458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559769506	chr14:79641484-79641485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550478813	chr14:79641485-79641486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547884096	chr14:79641538-79641539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533299947	chr14:79641807-79641808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs8019477	chr14:79641808-79641809	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs527414208	chr14:79641814-79641815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565919340	chr14:79641819-79641820	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1736 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79632000-79633200	Enhancers	HUVEC	blood vessel
2	chr14:79641400-79641600	Enhancers	Fetal Brain Male	brain
3	chr14:79641800-79642000	Enhancers	Brain Cingulate Gyrus	brain
4	chr14:79642000-79642200	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr14:79642000-79642400	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr14:79642000-79642400	Active TSS	Brain Cingulate Gyrus	brain
7	chr14:79642000-79642400	Enhancers	Brain Substantia Nigra	brain
8	chr14:79642000-79642400	Active TSS	Colon Smooth Muscle	Colon
9	chr14:79642000-79642400	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr14:79642000-79642400	Active TSS	Stomach Smooth Muscle	stomach
11	chr14:79642000-79642600	Enhancers	Fetal Brain Female	brain
12	chr14:79642200-79642400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr14:79642200-79642400	Enhancers	Brain Hippocampus Middle	brain
14	chr14:79642200-79642400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
15	chr14:79642200-79644200	Enhancers	Fetal Brain Male	brain
16	chr14:79642200-79644200	Enhancers	Fetal Lung	lung
17	chr14:79642400-79642600	Enhancers	Brain Cingulate Gyrus	brain
18	chr14:79642400-79642600	Flanking Active TSS	Colon Smooth Muscle	Colon
19	chr14:79642400-79642600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
20	chr14:79642400-79642600	Flanking Active TSS	Stomach Smooth Muscle	stomach
21	chr14:79642400-79643000	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr14:79643600-79644000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:79643800-79644200	Enhancers	Fetal Brain Female	brain
24	chr14:79644200-79644400	Weak transcription	Fetal Lung	lung
25	chr14:79644400-79644800	Enhancers	Fetal Lung	lung
26	chr14:79648000-79652800	Weak transcription	HSMMtube	muscle
27	chr14:79652600-79653400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr14:79652600-79653600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr14:79652600-79653600	Enhancers	HSMM	muscle
30	chr14:79652800-79653400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr14:79652800-79653400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr14:79652800-79653400	Enhancers	HSMMtube	muscle
33	chr14:79653000-79653400	Enhancers	Fetal Lung	lung
34	chr14:79653000-79653400	Enhancers	Placenta Amnion	Placenta Amnion
35	chr14:79653000-79653800	Enhancers	NHLF	lung
36	chr14:79654800-79655000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr14:79660800-79661000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:79661000-79662400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr14:79661400-79662000	Enhancers	Placenta Amnion	Placenta Amnion
40	chr14:79662400-79664200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr14:79663400-79664200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr14:79663600-79664400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr14:79667400-79668000	Enhancers	Fetal Intestine Small	intestine
44	chr14:79667400-79668800	Enhancers	Fetal Intestine Large	intestine
45	chr14:79667800-79668200	Enhancers	Duodenum Mucosa	Duodenum
46	chr14:79668000-79668400	Enhancers	Fetal Lung	lung
47	chr14:79668400-79671200	Weak transcription	Fetal Lung	lung
48	chr14:79671200-79672400	Enhancers	Fetal Lung	lung
49	chr14:79673200-79673800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr14:79673400-79673800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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