Variant report

Variant	nsv968916
Chromosome Location	chr5:59944877-59962647
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	chr5:59945165-59945564	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:59945154-59945496	K562	blood:	n/a	n/a
3	BACH1	chr5:59948213-59948360	K562	blood:	n/a	n/a
4	BHLHE40	chr5:59945324-59945422	HepG2	liver:	n/a	n/a
5	CBX3	chr5:59949056-59949287	K562	blood:	n/a	n/a
6	CEBPB	chr5:59947986-59948470	HCT-116	colon:	n/a	chr5:59948192-59948203
7	CEBPB	chr5:59947859-59948500	A549	lung:	n/a	chr5:59948192-59948203
8	CEBPB	chr5:59947390-59948442	IMR90	lung:	n/a	chr5:59948192-59948203
9	CEBPB	chr5:59948015-59948330	K562	blood:	n/a	chr5:59948192-59948203
10	CEBPB	chr5:59947408-59947609	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:59947835-59948505	MCF-7	breast:	n/a	chr5:59948192-59948203
12	CEBPB	chr5:59947984-59948374	K562	blood:	n/a	chr5:59948192-59948203
13	CEBPB	chr5:59948006-59948383	A549	lung:	n/a	chr5:59948192-59948203
14	CEBPB	chr5:59947973-59948387	A549	lung:	n/a	chr5:59948192-59948203
15	CEBPB	chr5:59948016-59948391	Hela-S3	cervix:	n/a	chr5:59948192-59948203
16	CEBPB	chr5:59947994-59948374	K562	blood:	n/a	chr5:59948192-59948203
17	CEBPB	chr5:59948060-59948362	HepG2	liver:	n/a	chr5:59948192-59948203
18	CEBPB	chr5:59947819-59948439	MCF-7	breast:	n/a	chr5:59948192-59948203
19	CTCF	chr5:59945780-59945930	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr5:59945140-59945290	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr5:59945220-59945370	GM12865	blood:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
22	CTCF	chr5:59945213-59945388	SK-N-SH_RA	brain:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
23	CTCF	chr5:59945720-59945870	Caco-2	colon:	n/a	n/a
24	CTCF	chr5:59945209-59945427	GM10266	blood:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
25	CTCF	chr5:59945180-59945330	HRE	kidney:	n/a	n/a
26	CTCF	chr5:59945260-59945410	HRPEpiC	eye:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
27	CTCF	chr5:59945180-59945330	HAc	cerebellar:	n/a	n/a
28	CTCF	chr5:59945200-59945350	HEK293	kidney:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
29	CTCF	chr5:59945075-59945478	T-47D	breast:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
30	CTCF	chr5:59945220-59945370	GM12872	blood:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
31	CTCF	chr5:59945240-59945390	HUVEC	blood vessel:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
32	CTCF	chr5:59945110-59945415	T-47D	breast:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
33	CTCF	chr5:59945260-59945410	HEEpiC	esophagus:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
34	CTCF	chr5:59945220-59945370	HCT-116	colon:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
35	CTCF	chr5:59945151-59945460	HCT-116	colon:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
36	CTCF	chr5:59945220-59945370	GM12866	blood:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
37	CTCF	chr5:59945240-59945390	WERI-Rb-1	eye:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
38	CTCF	chr5:59945200-59945350	HL-60	blood:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
39	CTCF	chr5:59945219-59945463	Pancreas_OC	pancreas:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
40	CTCF	chr5:59945240-59945390	HMEC	breast:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
41	CTCF	chr5:59945182-59945456	HUVEC	blood vessel:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
42	CTCF	chr5:59945240-59945390	HRPEpiC	eye:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
43	CTCF	chr5:59944900-59945050	BJ	skin:	n/a	n/a
44	CTCF	chr5:59945194-59945497	GM10248	blood:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
45	CTCF	chr5:59945200-59945350	HEEpiC	esophagus:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
46	CTCF	chr5:59945161-59945427	MCF-7	breast:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
47	CTCF	chr5:59945188-59945403	MCF-7	breast:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
48	CTCF	chr5:59945170-59945463	GM12878	blood:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
49	CTCF	chr5:59945149-59945429	ECC-1	luminal epithelium:	n/a	chr5:59945316-59945337 chr5:59945323-59945336
50	CTCF	chr5:59945115-59945514	K562	blood:	n/a	chr5:59945316-59945337 chr5:59945323-59945336

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59947488-59947538	GM12892	blood:	n/a
2	chr5:59947488-59947538	ovcar-3	ovarian:	n/a
3	chr5:59947488-59947538	ECC-1	luminal epithelium:	n/a
4	chr5:59947488-59947538	ProgFib	skin:	n/a
5	chr5:59947488-59947538	HUVEC	blood vessel:	n/a
6	chr5:59947488-59947538	HCPEpiC	choroid plexus:	n/a
7	chr5:59947488-59947538	AoSMC	blood vessel:	n/a
8	chr5:59947488-59947538	HEEpiC	esophagus:	n/a
9	chr5:59947488-59947538	Jurkat	blood:	n/a
10	chr5:59947488-59947538	GM06990	blood:	n/a
11	chr5:59947488-59947538	HIPEpiC	eye:	n/a
12	chr5:59947488-59947538	BJ	skin:	n/a
13	chr5:59947488-59947538	PANC-1	pancreas:	n/a
14	chr5:59947488-59947538	HNPCEpiC	eye:	n/a
15	chr5:59947488-59947538	HL-60	blood:	n/a
16	chr5:59947488-59947538	AG04449	skin:	fetal
17	chr5:59947488-59947538	HepG2	liver:	n/a
18	chr5:59947488-59947538	PFSK-1	brain:	n/a
19	chr5:59947488-59947538	Hela-S3	cervix:	n/a
20	chr5:59947488-59947538	SKMC	muscle:	n/a
21	chr5:59947488-59947538	GM12891	blood:	n/a
22	chr5:59947488-59947538	MCF10A-Er-Src	breast:	n/a
23	chr5:59947488-59947538	HRE	kidney:	n/a
24	chr5:59947488-59947538	SAEC	small airway:	n/a
25	chr5:59947488-59947538	HRPEpiC	eye:	n/a
26	chr5:59947488-59947538	NH-A	brain:	n/a
27	chr5:59947488-59947538	HRCEpiC	kidney:	n/a
28	chr5:59947488-59947538	T-47D	breast:	n/a
29	chr5:59947488-59947538	GM19239	blood:	n/a
30	chr5:59947488-59947538	HCT-116	colon:	n/a
31	chr5:59947488-59947538	A549	lung:	n/a
32	chr5:59947488-59947538	NB4	blood:	n/a
33	chr5:59947488-59947538	NHDF-neo	bronchial:	n/a
34	chr5:59947488-59947538	K562	blood:	n/a
35	chr5:59947488-59947538	BE2_C	brain:	n/a
36	chr5:59947488-59947538	AG04450	lung:	fetal
37	chr5:59947488-59947538	LNCaP	prostate:	n/a
38	chr5:59947488-59947538	AG09309	skin:	n/a
39	chr5:59947488-59947538	CMK	blood:	n/a
40	chr5:59947488-59947538	NT2-D1	testis:	n/a
41	chr5:59947488-59947538	PrEC	prostate:	n/a
42	chr5:59947488-59947538	MCF-7	breast:	n/a
43	chr5:59947488-59947538	GM12878	blood:	n/a
44	chr5:59947488-59947538	AG09319	gingival:	n/a
45	chr5:59947488-59947538	NHBE	bronchial:	n/a
46	chr5:59947488-59947538	HCF	heart:	n/a
47	chr5:59947488-59947538	IMR90	lung:	fetal
48	chr5:59947488-59947538	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:59947488-59947538	HEK293	kidney:	embryo
50	chr5:59947488-59947538	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:59944857..59945693-chr5:59972891..59974305,6	MCF-7	breast:
2	chr5:59942675..59945605-chr5:59945905..59947831,2	K562	blood:
3	chr5:59945171..59945833-chr5:59964252..59964826,2	MCF-7	breast:
4	chr5:59945219..59945730-chr5:59995159..59995998,2	MCF-7	breast:
5	chr5:59944972..59945763-chr5:59964296..59965220,3	MCF-7	breast:
6	chr5:59589888..59590741-chr5:59944874..59945467,2	MCF-7	breast:
7	chr5:59105772..59106332-chr5:59944917..59945827,2	MCF-7	breast:

Variant related genes	Relation type
DEPDC1B	TF binding region
ENSG00000256404	TF binding region
DEPDC1B	CpG island
ENSG00000256404	CpG island
ENSG00000035499	chromatin interactions

Extended variants
information (count: 656 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570911840	chr5:59944894-59944895	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs112037727	chr5:59944933-59944934	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs537985968	chr5:59944940-59944941	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs556497045	chr5:59944950-59944951	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs559063451	chr5:59945255-59945256	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs141168490	chr5:59945259-59945260	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs74553644	chr5:59945307-59945308	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs112840116	chr5:59945364-59945365	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs184359427	chr5:59945380-59945381	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs35338178	chr5:59945459-59945460	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs138301116	chr5:59945468-59945469	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs112229303	chr5:59945505-59945506	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs113427624	chr5:59945655-59945656	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192082265	chr5:59945666-59945667	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544895639	chr5:59945685-59945686	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs185039425	chr5:59945771-59945772	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs189503868	chr5:59945776-59945777	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs553870670	chr5:59945906-59945907	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554049080	chr5:59945943-59945944	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs547512763	chr5:59945954-59945955	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs572456239	chr5:59945956-59945957	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs55829289	chr5:59945971-59945972	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs201736541	chr5:59946002-59946003	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs199882987	chr5:59946003-59946004	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs398084153	chr5:59946006-59946007	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs373551390	chr5:59946007-59946008	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs367721380	chr5:59946008-59946009	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371594045	chr5:59946009-59946010	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs77280054	chr5:59946121-59946122	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs572129435	chr5:59946149-59946150	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376495310	chr5:59946153-59946154	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs570256973	chr5:59946191-59946192	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs142018832	chr5:59946219-59946220	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs558903100	chr5:59946305-59946306	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs531413576	chr5:59946308-59946309	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs566299861	chr5:59946375-59946376	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs535211245	chr5:59946440-59946441	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs181012673	chr5:59946479-59946480	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs76705107	chr5:59946481-59946482	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs550908551	chr5:59946530-59946531	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs367679950	chr5:59946531-59946532	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs79988462	chr5:59946534-59946535	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs74785192	chr5:59946560-59946561	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs576272902	chr5:59946592-59946593	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs545320081	chr5:59946596-59946597	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs542409068	chr5:59946657-59946658	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565010935	chr5:59946731-59946732	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs572250996	chr5:59946850-59946851	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs114567370	chr5:59946884-59946885	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs139508506	chr5:59947078-59947079	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
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
Prostate cancer	21965145	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
adenomatous polyposis	22470819	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
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	21272361	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59920600-59947800	Weak transcription	HUVEC	blood vessel
2	chr5:59925200-59947200	Weak transcription	Pancreas	Pancrea
3	chr5:59926400-59967800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:59926600-59946200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:59929400-59947400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr5:59929400-59954600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:59929600-59948000	Weak transcription	NHEK	skin
8	chr5:59933400-59965200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr5:59933600-59981000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr5:59934800-59947600	Weak transcription	HMEC	breast
11	chr5:59936600-59961400	Weak transcription	Thymus	Thymus
12	chr5:59936800-59961800	Weak transcription	Fetal Thymus	thymus
13	chr5:59937000-59945800	Weak transcription	GM12878-XiMat	blood
14	chr5:59938600-59945200	Weak transcription	Fetal Kidney	kidney
15	chr5:59940400-59947800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr5:59940400-59947800	Weak transcription	HSMM	muscle
17	chr5:59940600-59945000	Weak transcription	Fetal Intestine Large	intestine
18	chr5:59940600-59947400	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr5:59940600-59947600	Weak transcription	A549	lung
20	chr5:59940600-59948000	Weak transcription	K562	blood
21	chr5:59940600-59950200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr5:59941000-59947200	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr5:59941200-59946600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr5:59941200-59947600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr5:59942200-59945400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr5:59942600-59947400	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:59942800-59952000	Weak transcription	Dnd41	blood
28	chr5:59942800-59961600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:59943400-59947600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:59943400-59947800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr5:59943400-59952400	Weak transcription	Placenta	Placenta
32	chr5:59943400-59977000	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr5:59943600-59945000	Enhancers	HepG2	liver
34	chr5:59943800-59945400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr5:59943800-59952600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr5:59944400-59952400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:59945000-59961800	Weak transcription	HepG2	liver
38	chr5:59946200-59946400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:59946400-59952400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:59946800-59947800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr5:59947000-59947800	Enhancers	NHLF	lung
42	chr5:59947200-59948600	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr5:59947400-59947800	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr5:59947400-59947800	Enhancers	NH-A	brain
45	chr5:59947400-59947800	Enhancers	NHDF-Ad	bronchial
46	chr5:59947400-59947800	Enhancers	Osteobl	bone
47	chr5:59947400-59948400	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr5:59947400-59948800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr5:59947400-59949000	Enhancers	Muscle Satellite Cultured Cells	--
50	chr5:59947600-59947800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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