Variant report

Variant	nsv328038
Chromosome Location	chr5:52772280-52777292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:52774070-52775568	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:52772612-52773356	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:52774106-52774465	K562	blood:	n/a	n/a
4	ARID3A	chr5:52775928-52775935	HepG2	liver:	n/a	n/a
5	BACH1	chr5:52775685-52775828	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:52776389-52776678	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr5:52774544-52774977	HepG2	liver:	n/a	n/a
8	BHLHE40	chr5:52772843-52773312	HepG2	liver:	n/a	n/a
9	BRCA1	chr5:52775301-52775539	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr5:52775637-52775661	HepG2	liver:	n/a	n/a
11	BRCA1	chr5:52774161-52774586	H1-hESC	embryonic stem cell:	n/a	n/a
12	CCNT2	chr5:52776379-52776703	K562	blood:	n/a	n/a
13	CEBPB	chr5:52775311-52775509	HepG2	liver:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
14	CEBPB	chr5:52775163-52775606	A549	lung:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
15	CEBPB	chr5:52775145-52775612	ECC-1	luminal epithelium:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
16	CEBPB	chr5:52775122-52775638	MCF-7	breast:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
17	CEBPB	chr5:52775242-52775758	H1-hESC	embryonic stem cell:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
18	CEBPB	chr5:52775780-52775790	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:52775231-52775598	HepG2	liver:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
20	CEBPB	chr5:52775219-52775569	HepG2	liver:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
21	CEBPB	chr5:52772985-52773252	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:52775204-52775648	Hela-S3	cervix:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
23	CEBPB	chr5:52772769-52773331	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:52772736-52773320	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:52775079-52775658	A549	lung:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
26	CEBPB	chr5:52775228-52775559	K562	blood:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
27	CEBPB	chr5:52775177-52775524	ECC-1	luminal epithelium:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
28	CEBPB	chr5:52772828-52773255	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:52775257-52775487	K562	blood:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
30	CEBPB	chr5:52775182-52775612	MCF-7	breast:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
31	CEBPB	chr5:52775212-52775570	A549	lung:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
32	CEBPB	chr5:52775200-52775596	IMR90	lung:	n/a	chr5:52775386-52775397 chr5:52775385-52775398
33	CEBPD	chr5:52772920-52773253	HepG2	liver:	n/a	n/a
34	CEBPD	chr5:52775945-52776124	HepG2	liver:	n/a	n/a
35	CEBPD	chr5:52775893-52776567	HepG2	liver:	n/a	n/a
36	CEBPD	chr5:52772883-52773242	HepG2	liver:	n/a	n/a
37	CEBPD	chr5:52774528-52774913	HepG2	liver:	n/a	n/a
38	CHD1	chr5:52775159-52775927	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr5:52773963-52779659	IMR90	lung:	n/a	chr5:52776596-52776606 chr5:52777700-52777710 chr5:52776601-52776611
40	CHD1	chr5:52776600-52778067	H1-hESC	embryonic stem cell:	n/a	chr5:52777700-52777710 chr5:52776601-52776611
41	CHD1	chr5:52774236-52774872	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr5:52774124-52774479	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr5:52774158-52774628	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr5:52775433-52775960	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr5:52777238-52778083	Hela-S3	cervix:	n/a	chr5:52777700-52777710
46	CHD2	chr5:52775573-52776816	HepG2	liver:	n/a	chr5:52776596-52776606 chr5:52776601-52776611
47	CHD2	chr5:52776171-52776498	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr5:52774576-52774922	HepG2	liver:	n/a	n/a
49	CHD2	chr5:52775653-52775902	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr5:52775303-52776721	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:52774551-52774601	IMR90	lung:	fetal
2	chr5:52776694-52776744	NHBE	bronchial:	n/a
3	chr5:52774551-52774601	IMR90	lung:	fetal
4	chr5:52776694-52776744	NHBE	bronchial:	n/a
5	chr5:52776344-52776394	HIPEpiC	eye:	n/a
6	chr5:52776344-52776394	GM06990	blood:	n/a
7	chr5:52775681-52775731	PrEC	prostate:	n/a
8	chr5:52774812-52774862	GM06990	blood:	n/a
9	chr5:52776630-52776680	PrEC	prostate:	n/a
10	chr5:52773135-52773185	ovcar-3	ovarian:	n/a
11	chr5:52774551-52774601	Jurkat	blood:	n/a
12	chr5:52773135-52773185	AG09309	skin:	n/a
13	chr5:52776244-52776294	AoSMC	blood vessel:	n/a
14	chr5:52776344-52776394	LNCaP	prostate:	n/a
15	chr5:52775681-52775731	HCF	heart:	n/a
16	chr5:52776244-52776294	LNCaP	prostate:	n/a
17	chr5:52774812-52774862	HEK293	kidney:	embryo
18	chr5:52775681-52775731	Jurkat	blood:	n/a
19	chr5:52775681-52775731	H1-hESC	embryonic stem cell:	embryo
20	chr5:52773135-52773185	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:52776694-52776744	T-47D	breast:	n/a
22	chr5:52776694-52776744	CMK	blood:	n/a
23	chr5:52776344-52776394	HRPEpiC	eye:	n/a
24	chr5:52776344-52776394	HepG2	liver:	n/a
25	chr5:52776244-52776294	NH-A	brain:	n/a
26	chr5:52776694-52776744	Hepatocyte	liver:	n/a
27	chr5:52776630-52776680	HCT-116	colon:	n/a
28	chr5:52774812-52774862	SK-N-SH	brain:	n/a
29	chr5:52774812-52774862	NB4	blood:	n/a
30	chr5:52775805-52775855	ProgFib	skin:	n/a
31	chr5:52775805-52775855	PrEC	prostate:	n/a
32	chr5:52773135-52773185	GM12878	blood:	n/a
33	chr5:52776244-52776294	HL-60	blood:	n/a
34	chr5:52776344-52776394	AG10803	skin:	n/a
35	chr5:52776694-52776744	HL-60	blood:	n/a
36	chr5:52774812-52774862	U87	brain:	n/a
37	chr5:52776344-52776394	Jurkat	blood:	n/a
38	chr5:52776244-52776294	HCT-116	colon:	n/a
39	chr5:52775805-52775855	HepG2	liver:	n/a
40	chr5:52775702-52775752	AG04449	skin:	fetal
41	chr5:52775702-52775752	HEEpiC	esophagus:	n/a
42	chr5:52775805-52775855	HEEpiC	esophagus:	n/a
43	chr5:52774551-52774601	AoSMC	blood vessel:	n/a
44	chr5:52776694-52776744	AG04450	lung:	fetal
45	chr5:52776694-52776744	MCF-7	breast:	n/a
46	chr5:52775805-52775855	HRCEpiC	kidney:	n/a
47	chr5:52775805-52775855	HPAEpiC	pulmonary alveolar:	n/a
48	chr5:52776344-52776394	SK-N-MC	brain:	n/a
49	chr5:52776694-52776744	AG04449	skin:	fetal
50	chr5:52776694-52776744	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:52388112..52388681-chr5:52772747..52773456,2	MCF-7	breast:
2	chr5:52773878..52774764-chr5:53524810..53525607,3	MCF-7	breast:
3	chr5:52772594..52773194-chr5:52899890..52900738,2	MCF-7	breast:
4	chr5:52772655..52773163-chr5:53952034..53952615,2	MCF-7	breast:
5	chr5:52774220..52774824-chr5:53287438..53288055,2	MCF-7	breast:
6	chr5:52774231..52774841-chr5:52855913..52856842,2	MCF-7	breast:
7	chr5:52619745..52620444-chr5:52772653..52773364,2	MCF-7	breast:
8	chr17:56735383..56737636-chr5:52775178..52776995,2	MCF-7	breast:
9	chr5:52384993..52385720-chr5:52772505..52773240,2	MCF-7	breast:
10	chr5:52634537..52635379-chr5:52772608..52773561,2	MCF-7	breast:
11	chr5:52773843..52774731-chr5:53166346..53167079,2	MCF-7	breast:
12	chr5:52772738..52773313-chr5:53455804..53456355,2	MCF-7	breast:
13	chr5:52774000..52774674-chr5:53166806..53167591,2	MCF-7	breast:
14	chr5:52774119..52774818-chr5:53166203..53166706,2	K562	blood:
15	chr5:52772745..52773247-chr5:53021978..53022710,2	MCF-7	breast:
16	chr5:52772632..52773163-chr5:53951902..53952615,3	MCF-7	breast:

Variant related genes	Relation type
FST	TF binding region
FST	CpG island
ENSG00000164258	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000272123	chromatin interactions

Extended variants
information (count: 185 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:185 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541279851	chr5:52772325-52772326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371303698	chr5:52772353-52772354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7732512	chr5:52772374-52772375	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs553561971	chr5:52772387-52772388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7733870	chr5:52772543-52772544	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs78827161	chr5:52772572-52772573	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs145333284	chr5:52772665-52772666	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs115994807	chr5:52772666-52772667	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs113191050	chr5:52772679-52772680	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs543701733	chr5:52772682-52772683	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs397883827	chr5:52772683-52772684	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs141358419	chr5:52772723-52772724	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs186801603	chr5:52772736-52772737	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs191584943	chr5:52772746-52772747	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs547258521	chr5:52772774-52772775	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs541505098	chr5:52772835-52772836	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs11743591	chr5:52772862-52772863	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs543456521	chr5:52772895-52772896	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs548277168	chr5:52772915-52772916	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs569671142	chr5:52772935-52772936	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs184107984	chr5:52772941-52772942	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs578065687	chr5:52772990-52772991	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs558795476	chr5:52773003-52773004	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs187256933	chr5:52773008-52773009	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535364935	chr5:52773012-52773013	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545200533	chr5:52773022-52773023	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs553285089	chr5:52773052-52773053	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs145148441	chr5:52773065-52773066	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542698342	chr5:52773072-52773073	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs554715110	chr5:52773080-52773081	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs576344686	chr5:52773107-52773108	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576074690	chr5:52773135-52773136	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs59812618	chr5:52773136-52773137	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564929169	chr5:52773146-52773147	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs373966752	chr5:52773167-52773168	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs11951354	chr5:52773279-52773280	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs139017945	chr5:52773317-52773318	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140739710	chr5:52773349-52773350	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs78241245	chr5:52773384-52773385	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs116342571	chr5:52773474-52773475	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs143653497	chr5:52773542-52773543	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs192945114	chr5:52773546-52773547	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs552139138	chr5:52773570-52773571	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs565841668	chr5:52773577-52773578	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs570868463	chr5:52773587-52773588	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs535007158	chr5:52773594-52773595	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs185487617	chr5:52773611-52773612	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs190411969	chr5:52773617-52773618	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs182551460	chr5:52773662-52773663	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs541035353	chr5:52773680-52773681	Weak transcription Enhancers	TF binding region	1 gene(s)	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	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
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52761600-52774400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:52766800-52772800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:52766800-52773000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:52766800-52774400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:52768000-52774200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:52768600-52772800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:52768600-52774000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:52769200-52774000	Enhancers	HepG2	liver
9	chr5:52769800-52772800	Weak transcription	HMEC	breast
10	chr5:52769800-52774000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr5:52770000-52774000	Weak transcription	NHEK	skin
12	chr5:52770800-52774200	Enhancers	Liver	Liver
13	chr5:52772000-52773000	Enhancers	Brain Anterior Caudate	brain
14	chr5:52772000-52773400	Enhancers	HSMM	muscle
15	chr5:52772200-52774000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:52772400-52772600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:52772400-52773200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:52772600-52772800	Enhancers	Brain Germinal Matrix	brain
19	chr5:52772600-52773400	Enhancers	Brain Substantia Nigra	brain
20	chr5:52772600-52774400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:52772800-52773000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr5:52772800-52773000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr5:52772800-52773200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:52772800-52773200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr5:52772800-52773200	Enhancers	H9 Cell Line	embryonic stem cell
26	chr5:52772800-52773200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr5:52772800-52773200	Enhancers	Hela-S3	cervix
28	chr5:52772800-52773200	Enhancers	HSMMtube	muscle
29	chr5:52772800-52773400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr5:52772800-52773400	Enhancers	Brain Cingulate Gyrus	brain
31	chr5:52772800-52773400	Enhancers	Brain Hippocampus Middle	brain
32	chr5:52772800-52773400	Enhancers	HMEC	breast
33	chr5:52772800-52774400	Weak transcription	Brain Germinal Matrix	brain
34	chr5:52773000-52773200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr5:52773000-52773200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:52773000-52773200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr5:52773000-52773200	Flanking Bivalent TSS/Enh	Brain Angular Gyrus	brain
38	chr5:52773000-52774000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr5:52773000-52774000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr5:52773000-52774000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr5:52773000-52774000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:52773000-52774000	Weak transcription	Brain Anterior Caudate	brain
43	chr5:52773200-52774000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr5:52773200-52774000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr5:52773200-52774000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:52773200-52774000	Weak transcription	Hela-S3	cervix
47	chr5:52773200-52774000	Weak transcription	HSMMtube	muscle
48	chr5:52773200-52774200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:52773200-52774400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr5:52773200-52774400	Weak transcription	H9 Cell Line	embryonic stem cell

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