Variant report

Variant	nsv882191
Chromosome Location	chr5:74478078-74554826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:891)
CpG islands
(count:672)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:891 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74522901-74522920	K562	blood:	n/a	n/a
2	ARID3A	chr5:74532687-74532790	K562	blood:	n/a	n/a
3	ARID3A	chr5:74532794-74533010	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:74510856-74511041	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:74485211-74485511	HepG2	liver:	n/a	n/a
6	ATF3	chr5:74532621-74532936	K562	blood:	n/a	chr5:74532787-74532796
7	ATF3	chr5:74532653-74532914	HepG2	liver:	n/a	chr5:74532787-74532796
8	BACH1	chr5:74493604-74493975	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:74493585-74493943	K562	blood:	n/a	n/a
10	BACH1	chr5:74532563-74533094	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:74532117-74532129	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:74532667-74533059	K562	blood:	n/a	n/a
13	BCLAF1	chr5:74532480-74533071	GM12878	blood:	n/a	chr5:74532712-74532725 chr5:74532807-74532816
14	BHLHE40	chr5:74519635-74519784	K562	blood:	n/a	n/a
15	BHLHE40	chr5:74532532-74533117	GM12878	blood:	n/a	chr5:74532785-74532801 chr5:74533055-74533071
16	BHLHE40	chr5:74532228-74533127	K562	blood:	n/a	chr5:74532785-74532801 chr5:74533055-74533071
17	BRCA1	chr5:74532830-74533048	GM12878	blood:	n/a	n/a
18	BRCA1	chr5:74532701-74532945	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr5:74532796-74532900	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr5:74535454-74536020	HCT-116	colon:	n/a	n/a
21	CBX3	chr5:74532596-74533042	K562	blood:	n/a	n/a
22	CCNT2	chr5:74493718-74493858	K562	blood:	n/a	n/a
23	CCNT2	chr5:74532202-74533086	K562	blood:	n/a	chr5:74532787-74532796
24	CEBPB	chr5:74513259-74513547	A549	lung:	n/a	chr5:74513393-74513404
25	CEBPB	chr5:74513309-74513508	K562	blood:	n/a	chr5:74513393-74513404
26	CEBPB	chr5:74536380-74536580	K562	blood:	n/a	chr5:74536486-74536495 chr5:74536486-74536497 chr5:74536484-74536495
27	CEBPB	chr5:74532392-74532649	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:74532284-74532970	K562	blood:	n/a	n/a
29	CEBPB	chr5:74513255-74513518	HepG2	liver:	n/a	chr5:74513393-74513404
30	CEBPB	chr5:74535558-74535876	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr5:74532317-74532937	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:74535627-74535883	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr5:74536462-74536614	HepG2	liver:	n/a	chr5:74536486-74536495 chr5:74536486-74536497 chr5:74536484-74536495
34	CEBPB	chr5:74535487-74535900	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr5:74532429-74532968	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr5:74496697-74496969	Hela-S3	cervix:	n/a	n/a
37	CHD1	chr5:74532572-74533033	GM12878	blood:	n/a	n/a
38	CHD1	chr5:74532821-74533331	H1-hESC	embryonic stem cell:	n/a	chr5:74533061-74533071
39	CHD2	chr5:74532399-74533116	GM12878	blood:	n/a	chr5:74533061-74533071
40	CHD2	chr5:74532585-74533034	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr5:74532256-74532974	K562	blood:	n/a	n/a
42	CHD2	chr5:74532393-74532938	HepG2	liver:	n/a	n/a
43	CHD2	chr5:74532296-74533083	Hela-S3	cervix:	n/a	chr5:74533061-74533071
44	CREB1	chr5:74532473-74533087	GM12878	blood:	n/a	n/a
45	CREB1	chr5:74532590-74532862	A549	lung:	n/a	n/a
46	CREB1	chr5:74532475-74533148	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr5:74532533-74533039	K562	blood:	n/a	n/a
48	CREB1	chr5:74532508-74533188	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr5:74532627-74533114	ECC-1	luminal epithelium:	n/a	n/a
50	CREB1	chr5:74532526-74533089	A549	lung:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74533279-74533329	CMK	blood:	n/a
2	chr5:74533279-74533329	CMK	blood:	n/a
3	chr5:74533066-74533116	BE2_C	brain:	n/a
4	chr5:74532880-74532930	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:74531185-74531235	Jurkat	blood:	n/a
6	chr5:74536793-74536843	Caco-2	colon:	n/a
7	chr5:74531185-74531235	HMEC	breast:	n/a
8	chr5:74532862-74532912	AG04450	lung:	fetal
9	chr5:74536793-74536843	Hela-S3	cervix:	n/a
10	chr5:74536793-74536843	AoSMC	blood vessel:	n/a
11	chr5:74532880-74532930	HRPEpiC	eye:	n/a
12	chr5:74536793-74536843	T-47D	breast:	n/a
13	chr5:74532862-74532912	HCT-116	colon:	n/a
14	chr5:74533066-74533116	AG10803	skin:	n/a
15	chr5:74532880-74532930	HCPEpiC	choroid plexus:	n/a
16	chr5:74532268-74532318	ovcar-3	ovarian:	n/a
17	chr5:74532835-74532885	NHDF-neo	bronchial:	n/a
18	chr5:74532880-74532930	K562	blood:	n/a
19	chr5:74531185-74531235	AoSMC	blood vessel:	n/a
20	chr5:74532862-74532912	ProgFib	skin:	n/a
21	chr5:74532862-74532912	SK-N-MC	brain:	n/a
22	chr5:74532894-74532944	NT2-D1	testis:	n/a
23	chr5:74533279-74533329	HEEpiC	esophagus:	n/a
24	chr5:74532835-74532885	SKMC	muscle:	n/a
25	chr5:74532852-74532902	H1-hESC	embryonic stem cell:	embryo
26	chr5:74531185-74531235	NHBE	bronchial:	n/a
27	chr5:74532894-74532944	CMK	blood:	n/a
28	chr5:74532862-74532912	GM19239	blood:	n/a
29	chr5:74532835-74532885	AG04449	skin:	fetal
30	chr5:74533066-74533116	RPTEC	kidney:	n/a
31	chr5:74533042-74533092	AG04450	lung:	fetal
32	chr5:74532862-74532912	GM06990	blood:	n/a
33	chr5:74533279-74533329	PFSK-1	brain:	n/a
34	chr5:74532880-74532930	HIPEpiC	eye:	n/a
35	chr5:74532835-74532885	ECC-1	luminal epithelium:	n/a
36	chr5:74533042-74533092	MCF10A-Er-Src	breast:	n/a
37	chr5:74533279-74533329	AG04450	lung:	fetal
38	chr5:74532835-74532885	PFSK-1	brain:	n/a
39	chr5:74536793-74536843	MCF10A-Er-Src	breast:	n/a
40	chr5:74533042-74533092	HCF	heart:	n/a
41	chr5:74531185-74531235	GM12891	blood:	n/a
42	chr5:74532862-74532912	HCF	heart:	n/a
43	chr5:74532852-74532902	HUVEC	blood vessel:	n/a
44	chr5:74532894-74532944	ProgFib	skin:	n/a
45	chr5:74532268-74532318	NHDF-neo	bronchial:	n/a
46	chr5:74533279-74533329	LNCaP	prostate:	n/a
47	chr5:74536793-74536843	A549	lung:	n/a
48	chr5:74532268-74532318	ProgFib	skin:	n/a
49	chr5:74532894-74532944	HepG2	liver:	n/a
50	chr5:74532880-74532930	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:74518294..74520803-chr5:74529681..74531542,2	K562	blood:
2	chr5:74527339..74529345-chr5:74531111..74533787,2	K562	blood:
3	chr5:74491047..74493376-chr5:74495534..74497598,2	K562	blood:
4	chr5:74504886..74507088-chr5:74507988..74510413,2	K562	blood:
5	chr5:74535747..74537406-chr5:74677465..74679427,2	K562	blood:
6	chr5:74345728..74346291-chr5:74523458..74524224,2	MCF-7	breast:
7	chr5:74504360..74506170-chr5:74531534..74533618,3	K562	blood:
8	chr5:74505529..74508894-chr5:74510527..74513977,3	K562	blood:
9	chr5:74504886..74507088-chr5:74507988..74510413,2	K562	blood:
10	chr5:74490335..74492474-chr5:74495385..74497140,2	K562	blood:
11	chr5:74481183..74484880-chr5:74486837..74490307,3	K562	blood:
12	chr5:74532153..74534047-chr5:74632305..74633924,2	MCF-7	breast:
13	chr5:74532409..74533382-chr5:74632361..74633307,2	Hela-S3	cervix:
14	chr5:74526525..74528959-chr5:74530851..74533698,2	MCF-7	breast:
15	chr5:74505529..74508894-chr5:74510527..74513977,3	K562	blood:
16	chr5:74518294..74520803-chr5:74529681..74531542,2	K562	blood:
17	chr5:74491047..74493376-chr5:74495534..74497598,2	K562	blood:
18	chr5:74530643..74533204-chr5:74537611..74539237,3	K562	blood:
19	chr5:74490335..74492474-chr5:74495385..74497140,2	K562	blood:
20	chr5:74481183..74484880-chr5:74486837..74490307,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGCR-3	chr5:74521249-74521493	NONHSAT102199

No data

Variant related genes	Relation type
SUMO2P5	TF binding region
ANKRD31	TF binding region
SUMO2P5	CpG island
ANKRD31	CpG island
ENSG00000247372	chromatin interactions
ENSG00000113161	chromatin interactions
ENSG00000113163	chromatin interactions
ENSG00000145700	chromatin interactions

Extended variants
information (count: 2029 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2029 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113880768	chr5:74479813-74479814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs117072945	chr5:74479821-74479822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372906729	chr5:74479826-74479827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565993777	chr5:74479838-74479839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs58869372	chr5:74479846-74479847	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538854868	chr5:74479974-74479975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142910529	chr5:74479980-74479981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191553494	chr5:74479992-74479993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1903838	chr5:74479999-74480000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs146670571	chr5:74480045-74480046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556340850	chr5:74480063-74480064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182545823	chr5:74480086-74480087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74471017	chr5:74480147-74480148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555614330	chr5:74480162-74480163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572340381	chr5:74480189-74480190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369182032	chr5:74480224-74480225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564304577	chr5:74480259-74480260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs578003442	chr5:74480268-74480269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543551771	chr5:74480283-74480284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4704187	chr5:74480288-74480289	Weak transcription	n/a	n/a	Overlapped CNVs	disease
21	rs140220221	chr5:74480293-74480294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542780406	chr5:74480298-74480299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs80011239	chr5:74480378-74480379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565306512	chr5:74480464-74480465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533006691	chr5:74480490-74480491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145218266	chr5:74480523-74480524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188223341	chr5:74480532-74480533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570349434	chr5:74480571-74480572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80044650	chr5:74480577-74480578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551079972	chr5:74480578-74480579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375532651	chr5:74480619-74480620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139160060	chr5:74480631-74480632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549810435	chr5:74480632-74480633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142781073	chr5:74480654-74480655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370927986	chr5:74480722-74480723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566422665	chr5:74480772-74480773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149109924	chr5:74480778-74480779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543558087	chr5:74480855-74480856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200695362	chr5:74480861-74480862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34982542	chr5:74480920-74480921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78436544	chr5:74480951-74480952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528858260	chr5:74480954-74480955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143158192	chr5:74480982-74480983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548845289	chr5:74480988-74480989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577864397	chr5:74481013-74481014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377664428	chr5:74481041-74481042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543374651	chr5:74481115-74481116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556952351	chr5:74481116-74481117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527628916	chr5:74481139-74481140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185361327	chr5:74481145-74481146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74479800-74497000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:74485000-74485800	Enhancers	HepG2	liver
3	chr5:74489200-74489400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr5:74493400-74493800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:74493600-74494000	Enhancers	K562	blood
6	chr5:74493600-74494200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:74493800-74495000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:74494000-74495000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:74494000-74496200	Enhancers	Duodenum Mucosa	Duodenum
10	chr5:74494200-74496200	Enhancers	Fetal Intestine Small	intestine
11	chr5:74494600-74495000	Enhancers	Gastric	stomach
12	chr5:74494600-74495000	Enhancers	Small Intestine	intestine
13	chr5:74494600-74495200	Enhancers	Fetal Intestine Large	intestine
14	chr5:74494600-74495200	Enhancers	Stomach Mucosa	stomach
15	chr5:74495000-74495200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr5:74495000-74495800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr5:74495000-74496000	Weak transcription	Gastric	stomach
18	chr5:74495000-74498800	Weak transcription	Small Intestine	intestine
19	chr5:74495200-74495600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr5:74495200-74498400	Weak transcription	Fetal Intestine Large	intestine
21	chr5:74495200-74498400	Weak transcription	Stomach Mucosa	stomach
22	chr5:74495600-74496000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr5:74495800-74496000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr5:74495800-74496200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:74496000-74496200	Enhancers	Gastric	stomach
26	chr5:74496000-74497600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr5:74496200-74498600	Weak transcription	Fetal Intestine Small	intestine
28	chr5:74496200-74498800	Weak transcription	Gastric	stomach
29	chr5:74496600-74497400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr5:74496800-74497200	Enhancers	NHEK	skin
31	chr5:74497000-74497600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:74497000-74497600	Enhancers	HMEC	breast
33	chr5:74497000-74497800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:74497600-74497800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr5:74498400-74499000	Enhancers	Fetal Intestine Large	intestine
36	chr5:74498400-74499000	Enhancers	Stomach Mucosa	stomach
37	chr5:74498600-74499000	Enhancers	Fetal Intestine Small	intestine
38	chr5:74498800-74499000	Enhancers	Gastric	stomach
39	chr5:74498800-74499000	Enhancers	Small Intestine	intestine
40	chr5:74500600-74531400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr5:74505600-74506200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:74508600-74511200	Enhancers	Fetal Intestine Large	intestine
43	chr5:74509000-74509200	Enhancers	Fetal Intestine Small	intestine
44	chr5:74509200-74509400	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr5:74509200-74509800	Weak transcription	Fetal Intestine Small	intestine
46	chr5:74509400-74510400	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr5:74509800-74511200	Enhancers	Fetal Intestine Small	intestine
48	chr5:74510200-74510600	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr5:74510200-74511400	Enhancers	Duodenum Mucosa	Duodenum
50	chr5:74510400-74510600	Enhancers	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links