Variant report

Variant	nsv882190
Chromosome Location	chr5:74463185-74554826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1037)
CpG islands
(count:671)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74463323-74463328	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74532687-74532790	K562	blood:	n/a	n/a
3	ARID3A	chr5:74522901-74522920	K562	blood:	n/a	n/a
4	ARID3A	chr5:74485211-74485511	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:74510856-74511041	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:74532794-74533010	HepG2	liver:	n/a	n/a
7	ATF3	chr5:74532621-74532936	K562	blood:	n/a	chr5:74532787-74532796
8	ATF3	chr5:74532653-74532914	HepG2	liver:	n/a	chr5:74532787-74532796
9	BACH1	chr5:74532117-74532129	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:74532563-74533094	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:74493604-74493975	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:74532667-74533059	K562	blood:	n/a	n/a
13	BACH1	chr5:74493585-74493943	K562	blood:	n/a	n/a
14	BCLAF1	chr5:74532480-74533071	GM12878	blood:	n/a	chr5:74532712-74532725 chr5:74532807-74532816
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	BHLHE40	chr5:74519635-74519784	K562	blood:	n/a	n/a
18	BRCA1	chr5:74532701-74532945	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr5:74532830-74533048	GM12878	blood:	n/a	n/a
20	BRCA1	chr5:74532796-74532900	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr5:74532596-74533042	K562	blood:	n/a	n/a
22	CBX3	chr5:74463153-74463586	HCT-116	colon:	n/a	n/a
23	CBX3	chr5:74535454-74536020	HCT-116	colon:	n/a	n/a
24	CCNT2	chr5:74493718-74493858	K562	blood:	n/a	n/a
25	CCNT2	chr5:74532202-74533086	K562	blood:	n/a	chr5:74532787-74532796
26	CEBPB	chr5:74536462-74536614	HepG2	liver:	n/a	chr5:74536486-74536495 chr5:74536486-74536497 chr5:74536484-74536495
27	CEBPB	chr5:74532317-74532937	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:74513259-74513547	A549	lung:	n/a	chr5:74513393-74513404
29	CEBPB	chr5:74466954-74467123	HepG2	liver:	n/a	chr5:74467037-74467048
30	CEBPB	chr5:74466982-74467091	K562	blood:	n/a	chr5:74467037-74467048
31	CEBPB	chr5:74536380-74536580	K562	blood:	n/a	chr5:74536486-74536495 chr5:74536486-74536497 chr5:74536484-74536495
32	CEBPB	chr5:74532284-74532970	K562	blood:	n/a	n/a
33	CEBPB	chr5:74496697-74496969	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr5:74535627-74535883	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr5:74535487-74535900	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr5:74535558-74535876	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr5:74513309-74513508	K562	blood:	n/a	chr5:74513393-74513404
38	CEBPB	chr5:74532392-74532649	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:74513255-74513518	HepG2	liver:	n/a	chr5:74513393-74513404
40	CEBPB	chr5:74532429-74532968	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr5:74532572-74533033	GM12878	blood:	n/a	n/a
42	CHD1	chr5:74532821-74533331	H1-hESC	embryonic stem cell:	n/a	chr5:74533061-74533071
43	CHD2	chr5:74532296-74533083	Hela-S3	cervix:	n/a	chr5:74533061-74533071
44	CHD2	chr5:74532393-74532938	HepG2	liver:	n/a	n/a
45	CHD2	chr5:74532256-74532974	K562	blood:	n/a	n/a
46	CHD2	chr5:74532585-74533034	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr5:74532399-74533116	GM12878	blood:	n/a	chr5:74533061-74533071
48	CREB1	chr5:74532526-74533089	A549	lung:	n/a	n/a
49	CREB1	chr5:74532533-74533039	K562	blood:	n/a	n/a
50	CREB1	chr5:74532508-74533188	H1-hESC	embryonic stem cell:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74532862-74532912	HNPCEpiC	eye:	n/a
2	chr5:74536793-74536843	HCM	heart:	n/a
3	chr5:74532862-74532912	BJ	skin:	n/a
4	chr5:74532852-74532902	HCF	heart:	n/a
5	chr5:74532852-74532902	PFSK-1	brain:	n/a
6	chr5:74533279-74533329	HRPEpiC	eye:	n/a
7	chr5:74532268-74532318	NB4	blood:	n/a
8	chr5:74532268-74532318	HCF	heart:	n/a
9	chr5:74532835-74532885	CMK	blood:	n/a
10	chr5:74532894-74532944	HIPEpiC	eye:	n/a
11	chr5:74536793-74536843	AG09309	skin:	n/a
12	chr5:74532852-74532902	HepG2	liver:	n/a
13	chr5:74531185-74531235	HAEpiC	amniotic membrane:	n/a
14	chr5:74531185-74531235	MCF10A-Er-Src	breast:	n/a
15	chr5:74533066-74533116	NH-A	brain:	n/a
16	chr5:74531185-74531235	SK-N-SH_RA	brain:	n/a
17	chr5:74533042-74533092	HUVEC	blood vessel:	n/a
18	chr5:74532268-74532318	RPTEC	kidney:	n/a
19	chr5:74532268-74532318	SKMC	muscle:	n/a
20	chr5:74533066-74533116	GM12891	blood:	n/a
21	chr5:74533066-74533116	HAEpiC	amniotic membrane:	n/a
22	chr5:74532852-74532902	AoSMC	blood vessel:	n/a
23	chr5:74533066-74533116	T-47D	breast:	n/a
24	chr5:74533066-74533116	Caco-2	colon:	n/a
25	chr5:74533042-74533092	HCF	heart:	n/a
26	chr5:74532862-74532912	HCT-116	colon:	n/a
27	chr5:74531185-74531235	HCF	heart:	n/a
28	chr5:74532862-74532912	SAEC	small airway:	n/a
29	chr5:74531185-74531235	HCT-116	colon:	n/a
30	chr5:74532852-74532902	HRPEpiC	eye:	n/a
31	chr5:74532835-74532885	HIPEpiC	eye:	n/a
32	chr5:74532268-74532318	K562	blood:	n/a
33	chr5:74532862-74532912	SK-N-SH	brain:	n/a
34	chr5:74533066-74533116	HCF	heart:	n/a
35	chr5:74533279-74533329	AG09319	gingival:	n/a
36	chr5:74532852-74532902	GM06990	blood:	n/a
37	chr5:74531185-74531235	PFSK-1	brain:	n/a
38	chr5:74532835-74532885	RPTEC	kidney:	n/a
39	chr5:74532894-74532944	SK-N-SH	brain:	n/a
40	chr5:74531185-74531235	NH-A	brain:	n/a
41	chr5:74536793-74536843	HUVEC	blood vessel:	n/a
42	chr5:74531185-74531235	T-47D	breast:	n/a
43	chr5:74532852-74532902	GM12891	blood:	n/a
44	chr5:74532862-74532912	K562	blood:	n/a
45	chr5:74532880-74532930	SK-N-SH_RA	brain:	n/a
46	chr5:74533042-74533092	HEEpiC	esophagus:	n/a
47	chr5:74533279-74533329	Caco-2	colon:	n/a
48	chr5:74533279-74533329	HIPEpiC	eye:	n/a
49	chr5:74532880-74532930	CMK	blood:	n/a
50	chr5:74532852-74532902	NHDF-neo	bronchial:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:74527339..74529345-chr5:74531111..74533787,2	K562	blood:
2	chr5:74535747..74537406-chr5:74677465..74679427,2	K562	blood:
3	chr5:74481183..74484880-chr5:74486837..74490307,3	K562	blood:
4	chr5:74348653..74349615-chr5:74462874..74463564,2	MCF-7	breast:
5	chr5:74530643..74533204-chr5:74537611..74539237,3	K562	blood:
6	chr5:74491047..74493376-chr5:74495534..74497598,2	K562	blood:
7	chr5:74532153..74534047-chr5:74632305..74633924,2	MCF-7	breast:
8	chr5:74532409..74533382-chr5:74632361..74633307,2	Hela-S3	cervix:
9	chr5:74504360..74506170-chr5:74531534..74533618,3	K562	blood:
10	chr5:74491047..74493376-chr5:74495534..74497598,2	K562	blood:
11	chr5:74505529..74508894-chr5:74510527..74513977,3	K562	blood:
12	chr5:74518294..74520803-chr5:74529681..74531542,2	K562	blood:
13	chr5:74526525..74528959-chr5:74530851..74533698,2	MCF-7	breast:
14	chr5:74505529..74508894-chr5:74510527..74513977,3	K562	blood:
15	chr5:74504886..74507088-chr5:74507988..74510413,2	K562	blood:
16	chr5:74504886..74507088-chr5:74507988..74510413,2	K562	blood:
17	chr5:74490335..74492474-chr5:74495385..74497140,2	K562	blood:
18	chr5:74345728..74346291-chr5:74523458..74524224,2	MCF-7	breast:
19	chr5:74518294..74520803-chr5:74529681..74531542,2	K562	blood:
20	chr5:74481183..74484880-chr5:74486837..74490307,3	K562	blood:
21	chr5:74490335..74492474-chr5:74495385..74497140,2	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
ANKRD31	TF binding region
SUMO2P5	TF binding region
ANKRD31	CpG island
SUMO2P5	CpG island
ENSG00000113163	chromatin interactions
ENSG00000250889	chromatin interactions
ENSG00000145700	chromatin interactions
ENSG00000247372	chromatin interactions
ENSG00000113161	chromatin interactions

Extended variants
information (count: 2173 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2173 , 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	rs1363577	chr5:74463185-74463186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573949662	chr5:74463228-74463229	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs115443442	chr5:74463305-74463306	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116243965	chr5:74463320-74463321	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs16872434	chr5:74463387-74463388	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs148440038	chr5:74463406-74463407	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185146790	chr5:74463408-74463409	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs374537580	chr5:74463411-74463412	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558640200	chr5:74463412-74463413	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs16872436	chr5:74463442-74463443	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs16872437	chr5:74463464-74463465	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563473189	chr5:74463473-74463474	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs529158721	chr5:74463491-74463492	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560124380	chr5:74463500-74463501	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs542570990	chr5:74463511-74463512	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559679797	chr5:74463545-74463546	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs528513393	chr5:74463568-74463569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551846184	chr5:74463572-74463573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571457466	chr5:74463591-74463592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190078541	chr5:74463599-74463600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554760264	chr5:74463602-74463603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182212442	chr5:74463605-74463606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567536897	chr5:74463607-74463608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs16872438	chr5:74463812-74463813	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs143521714	chr5:74463863-74463864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371522168	chr5:74463865-74463866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565654358	chr5:74463897-74463898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534361243	chr5:74463911-74463912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs151218154	chr5:74463938-74463939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557883650	chr5:74464027-74464028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185597811	chr5:74464041-74464042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147141355	chr5:74464065-74464066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576516753	chr5:74464101-74464102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113293247	chr5:74464166-74464167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573774670	chr5:74464244-74464245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545512720	chr5:74464260-74464261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190807371	chr5:74464265-74464266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2335149	chr5:74464276-74464277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371878223	chr5:74464358-74464359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560404282	chr5:74464411-74464412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1422696	chr5:74464415-74464416	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs545031295	chr5:74464465-74464466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112686605	chr5:74464520-74464521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530879394	chr5:74464546-74464547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550684611	chr5:74464552-74464553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199687056	chr5:74464561-74464562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75784944	chr5:74464568-74464569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562316331	chr5:74464575-74464576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531404001	chr5:74464627-74464628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567500127	chr5:74464639-74464640	Enhancers 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	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74458200-74463400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:74462000-74464200	Enhancers	Fetal Intestine Small	intestine
3	chr5:74462400-74465000	Enhancers	Fetal Intestine Large	intestine
4	chr5:74463000-74465800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:74463200-74463400	Enhancers	Gastric	stomach
6	chr5:74463200-74463800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:74463200-74464000	Enhancers	Duodenum Mucosa	Duodenum
8	chr5:74463200-74464400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr5:74463400-74463800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:74463400-74464200	Weak transcription	Gastric	stomach
11	chr5:74463600-74464000	Enhancers	Ovary	ovary
12	chr5:74463600-74464200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:74464000-74464800	Weak transcription	Duodenum Mucosa	Duodenum
14	chr5:74464000-74465200	Weak transcription	Ovary	ovary
15	chr5:74464200-74464600	Weak transcription	Fetal Intestine Small	intestine
16	chr5:74464600-74465400	Enhancers	Fetal Intestine Small	intestine
17	chr5:74464800-74465400	Enhancers	HSMM	muscle
18	chr5:74464800-74465600	Enhancers	Duodenum Mucosa	Duodenum
19	chr5:74465200-74465400	Enhancers	Ovary	ovary
20	chr5:74465200-74465600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr5:74465200-74465600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr5:74471600-74472400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
23	chr5:74479800-74497000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr5:74485000-74485800	Enhancers	HepG2	liver
25	chr5:74489200-74489400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr5:74493400-74493800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr5:74493600-74494000	Enhancers	K562	blood
28	chr5:74493600-74494200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:74493800-74495000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr5:74494000-74495000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr5:74494000-74496200	Enhancers	Duodenum Mucosa	Duodenum
32	chr5:74494200-74496200	Enhancers	Fetal Intestine Small	intestine
33	chr5:74494600-74495000	Enhancers	Gastric	stomach
34	chr5:74494600-74495000	Enhancers	Small Intestine	intestine
35	chr5:74494600-74495200	Enhancers	Fetal Intestine Large	intestine
36	chr5:74494600-74495200	Enhancers	Stomach Mucosa	stomach
37	chr5:74495000-74495200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr5:74495000-74495800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr5:74495000-74496000	Weak transcription	Gastric	stomach
40	chr5:74495000-74498800	Weak transcription	Small Intestine	intestine
41	chr5:74495200-74495600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr5:74495200-74498400	Weak transcription	Fetal Intestine Large	intestine
43	chr5:74495200-74498400	Weak transcription	Stomach Mucosa	stomach
44	chr5:74495600-74496000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr5:74495800-74496000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:74495800-74496200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:74496000-74496200	Enhancers	Gastric	stomach
48	chr5:74496000-74497600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr5:74496200-74498600	Weak transcription	Fetal Intestine Small	intestine
50	chr5:74496200-74498800	Weak transcription	Gastric	stomach

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