Variant report

Variant	nsv1027612
Chromosome Location	chr5:17409558-17432699
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:240)
CpG islands
(count:123)
Chromatin interactive
region (count:8)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:240 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:17413435-17413764	K562	blood:	n/a	n/a
2	ATF1	chr5:17415654-17415786	K562	blood:	n/a	n/a
3	ATF2	chr5:17425371-17425899	GM12878	blood:	n/a	n/a
4	ATF2	chr5:17426396-17426854	GM12878	blood:	n/a	n/a
5	ATF2	chr5:17425402-17425976	GM12878	blood:	n/a	n/a
6	BACH1	chr5:17413521-17413685	K562	blood:	n/a	chr5:17413586-17413600
7	BACH1	chr5:17415528-17415532	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr5:17413423-17413703	GM12878	blood:	n/a	chr5:17413589-17413600
9	BATF	chr5:17425526-17425766	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:17425193-17426019	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:17413400-17413989	K562	blood:	n/a	n/a
12	BHLHE40	chr5:17413480-17413606	GM12878	blood:	n/a	n/a
13	CCNT2	chr5:17413432-17413642	K562	blood:	n/a	n/a
14	CEBPB	chr5:17418170-17418517	MCF-7	breast:	n/a	n/a
15	CEBPB	chr5:17428888-17429095	IMR90	lung:	n/a	chr5:17429009-17429018 chr5:17429007-17429018 chr5:17429007-17429020
16	CEBPB	chr5:17418161-17418572	MCF-7	breast:	n/a	n/a
17	CEBPB	chr5:17428943-17429143	K562	blood:	n/a	chr5:17429009-17429018 chr5:17429007-17429018 chr5:17429007-17429020
18	CEBPB	chr5:17411605-17411851	A549	lung:	n/a	chr5:17411694-17411707 chr5:17411696-17411707 chr5:17411696-17411707 chr5:17411694-17411707
19	CEBPB	chr5:17428891-17429120	A549	lung:	n/a	chr5:17429009-17429018 chr5:17429007-17429018 chr5:17429007-17429020
20	CEBPB	chr5:17413506-17413705	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:17411531-17411914	IMR90	lung:	n/a	chr5:17411694-17411707 chr5:17411696-17411707 chr5:17411696-17411707 chr5:17411694-17411707
22	CHD2	chr5:17412805-17412837	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr5:17413030-17413073	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr5:17413500-17413736	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr5:17430191-17430254	HepG2	liver:	n/a	n/a
26	CHD2	chr5:17415552-17415775	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr5:17413522-17413555	GM12892	blood:	n/a	n/a
28	CTCF	chr5:17413327-17413703	GM12878	blood:	n/a	n/a
29	CTCF	chr5:17413420-17413570	NB4	blood:	n/a	n/a
30	CTCF	chr5:17413500-17413650	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:17413500-17413650	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr5:17413311-17413700	K562	blood:	n/a	n/a
33	CTCF	chr5:17413458-17413546	GM10248	blood:	n/a	n/a
34	CTCF	chr5:17413468-17413562	MCF-7	breast:	n/a	n/a
35	CTCF	chr5:17413560-17413710	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr5:17413556-17413561	GM12892	blood:	n/a	n/a
37	CTCF	chr5:17413488-17413604	GM19240	blood:	n/a	n/a
38	CTCF	chr5:17413478-17413547	GM13976	blood:	n/a	n/a
39	CTCF	chr5:17413458-17413538	K562	blood:	n/a	n/a
40	CTCF	chr5:17413524-17413588	GM12891	blood:	n/a	n/a
41	CTCF	chr5:17413360-17413510	GM12871	blood:	n/a	n/a
42	CTCF	chr5:17413457-17413559	GM12878	blood:	n/a	n/a
43	CTCF	chr5:17413455-17413533	GM13977	blood:	n/a	n/a
44	CTCF	chr5:17418850-17418888	GM13976	blood:	n/a	n/a
45	CTCF	chr5:17413496-17413561	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr5:17413420-17413570	GM12873	blood:	n/a	n/a
47	CUX1	chr5:17431261-17431531	K562	blood:	n/a	n/a
48	CUX1	chr5:17431450-17431455	GM12878	blood:	n/a	n/a
49	CUX1	chr5:17413396-17413744	K562	blood:	n/a	n/a
50	E2F6	chr5:17412723-17413277	H1-hESC	embryonic stem cell:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17427098-17427148	HIPEpiC	eye:	n/a
2	chr5:17427098-17427148	HIPEpiC	eye:	n/a
3	chr5:17414184-17414234	MCF-7	breast:	n/a
4	chr5:17414184-17414234	GM19239	blood:	n/a
5	chr5:17427098-17427148	HepG2	liver:	n/a
6	chr5:17414184-17414234	AoSMC	blood vessel:	n/a
7	chr5:17427098-17427148	AoSMC	blood vessel:	n/a
8	chr5:17414184-17414234	SKMC	muscle:	n/a
9	chr5:17414184-17414234	T-47D	breast:	n/a
10	chr5:17414184-17414234	Caco-2	colon:	n/a
11	chr5:17414184-17414234	NH-A	brain:	n/a
12	chr5:17414184-17414234	HNPCEpiC	eye:	n/a
13	chr5:17427098-17427148	Jurkat	blood:	n/a
14	chr5:17427098-17427148	ECC-1	luminal epithelium:	n/a
15	chr5:17427098-17427148	Caco-2	colon:	n/a
16	chr5:17427098-17427148	AG09319	gingival:	n/a
17	chr5:17414184-17414234	Jurkat	blood:	n/a
18	chr5:17427098-17427148	GM12892	blood:	n/a
19	chr5:17414184-17414234	A549	lung:	n/a
20	chr5:17414184-17414234	HRPEpiC	eye:	n/a
21	chr5:17427098-17427148	NHBE	bronchial:	n/a
22	chr5:17427098-17427148	Hepatocyte	liver:	n/a
23	chr5:17427098-17427148	PANC-1	pancreas:	n/a
24	chr5:17427098-17427148	BE2_C	brain:	n/a
25	chr5:17427098-17427148	CMK	blood:	n/a
26	chr5:17427098-17427148	NHDF-neo	bronchial:	n/a
27	chr5:17427098-17427148	GM19239	blood:	n/a
28	chr5:17427098-17427148	Hela-S3	cervix:	n/a
29	chr5:17414184-17414234	HCM	heart:	n/a
30	chr5:17427098-17427148	SK-N-SH	brain:	n/a
31	chr5:17427098-17427148	ovcar-3	ovarian:	n/a
32	chr5:17414184-17414234	HCT-116	colon:	n/a
33	chr5:17414184-17414234	Hepatocyte	liver:	n/a
34	chr5:17427098-17427148	AG04449	skin:	fetal
35	chr5:17414184-17414234	AG04450	lung:	fetal
36	chr5:17414184-17414234	AG09309	skin:	n/a
37	chr5:17414184-17414234	HEK293	kidney:	embryo
38	chr5:17427098-17427148	SK-N-SH_RA	brain:	n/a
39	chr5:17414184-17414234	HL-60	blood:	n/a
40	chr5:17427098-17427148	HL-60	blood:	n/a
41	chr5:17414184-17414234	HUVEC	blood vessel:	n/a
42	chr5:17414184-17414234	HRCEpiC	kidney:	n/a
43	chr5:17414184-17414234	AG10803	skin:	n/a
44	chr5:17414184-17414234	ovcar-3	ovarian:	n/a
45	chr5:17427098-17427148	ProgFib	skin:	n/a
46	chr5:17414184-17414234	PANC-1	pancreas:	n/a
47	chr5:17414184-17414234	RPTEC	kidney:	n/a
48	chr5:17414184-17414234	SK-N-SH_RA	brain:	n/a
49	chr5:17414184-17414234	NT2-D1	testis:	n/a
50	chr5:17414184-17414234	GM12891	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:17413771..17415306-chr5:17416901..17419149,2	MCF-7	breast:
2	chr5:17428609..17430151-chr5:17432039..17433769,2	MCF-7	breast:
3	chr5:17428609..17430151-chr5:17432039..17433769,2	MCF-7	breast:
4	chr5:17422805..17424378-chr5:17424436..17427431,2	MCF-7	breast:
5	chr5:17413771..17415306-chr5:17416901..17419149,2	MCF-7	breast:
6	chr5:17216329..17216875-chr5:17413138..17413983,2	MCF-7	breast:
7	chr5:17401084..17403430-chr5:17409103..17412028,2	K562	blood:
8	chr5:17422805..17424378-chr5:17424436..17427431,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO10-8	chr5:17432016-17433619	ucscGeneNc_uc003jga_2
2	lnc-BASP1-3	chr5:17412001-17412207	XLOC_004308
3	lnc-BASP1-3	chr5:17412000-17412207	NONHSAT100631
4	lnc-BASP1-3	chr5:17430053-17430082	XLOC_004308
5	lnc-BASP1-3	chr5:17430038-17430385	NONHSAT100631

No data

Variant related genes	Relation type
ENSG00000248455	TF binding region
ENSG00000248455	CpG island
GTF2I	miRNA target sites

Extended variants
information (count: 884 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:884 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10475105	chr5:17409558-17409559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577349717	chr5:17409620-17409621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199544060	chr5:17409634-17409635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529813956	chr5:17409635-17409636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs397885122	chr5:17409645-17409646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs397882416	chr5:17409646-17409647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545961862	chr5:17409658-17409659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546076082	chr5:17409678-17409679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35873344	chr5:17409761-17409762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs142420781	chr5:17409795-17409796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs207465644	chr5:17409797-17409798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562146871	chr5:17409861-17409862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527976894	chr5:17409869-17409870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151296801	chr5:17409924-17409925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559700553	chr5:17409932-17409933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192348528	chr5:17409979-17409980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183455935	chr5:17409982-17409983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77683291	chr5:17409987-17409988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11133899	chr5:17409998-17409999	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs187089838	chr5:17410008-17410009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139998775	chr5:17410009-17410010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568306495	chr5:17410032-17410033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534069422	chr5:17410072-17410073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554138128	chr5:17410081-17410082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191538925	chr5:17410109-17410110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145398100	chr5:17410132-17410133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556295094	chr5:17410188-17410189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576436006	chr5:17410197-17410198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542005820	chr5:17410248-17410249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12653054	chr5:17410261-17410262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572341300	chr5:17410288-17410289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541302789	chr5:17410332-17410333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142369265	chr5:17410344-17410345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528700568	chr5:17410406-17410407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35427720	chr5:17410429-17410430	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs115563324	chr5:17410433-17410434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562344790	chr5:17410446-17410447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10071892	chr5:17410452-17410453	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs548018810	chr5:17410495-17410496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184453327	chr5:17410511-17410512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150191757	chr5:17410543-17410544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547630577	chr5:17410601-17410602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570720749	chr5:17410602-17410603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539358032	chr5:17410609-17410610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532893424	chr5:17410632-17410633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2457758	chr5:17410655-17410656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs569993274	chr5:17410742-17410743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77822163	chr5:17410775-17410776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555467369	chr5:17410793-17410794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs58124586	chr5:17410883-17410884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	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
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17403000-17413000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:17404600-17411200	Weak transcription	Fetal Brain Male	brain
3	chr5:17407000-17413000	Weak transcription	Stomach Mucosa	stomach
4	chr5:17407200-17411200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:17407200-17411400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:17407200-17411400	Weak transcription	NHEK	skin
7	chr5:17407200-17411800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr5:17407200-17411800	Weak transcription	HMEC	breast
9	chr5:17407200-17412200	Weak transcription	NH-A	brain
10	chr5:17407800-17413200	Weak transcription	Hela-S3	cervix
11	chr5:17411200-17412400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr5:17411200-17416000	Enhancers	Fetal Brain Male	brain
13	chr5:17411400-17412000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr5:17411400-17412200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:17411400-17412600	Enhancers	NHEK	skin
16	chr5:17411600-17411800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr5:17411600-17411800	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr5:17411600-17412800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr5:17411600-17413000	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr5:17411800-17412000	Enhancers	Fetal Brain Female	brain
21	chr5:17411800-17412200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:17411800-17412200	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr5:17411800-17412200	Enhancers	HMEC	breast
24	chr5:17411800-17412200	Enhancers	Osteobl	bone
25	chr5:17411800-17412400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr5:17411800-17413000	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:17412000-17412200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr5:17412000-17412200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:17412000-17412200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr5:17412000-17412200	Enhancers	Fetal Kidney	kidney
31	chr5:17412000-17412800	Weak transcription	Fetal Brain Female	brain
32	chr5:17412000-17413200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr5:17412000-17415200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr5:17412200-17412400	Enhancers	Brain Germinal Matrix	brain
35	chr5:17412200-17412600	Enhancers	NH-A	brain
36	chr5:17412200-17413000	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr5:17412200-17413000	Weak transcription	Fetal Kidney	kidney
38	chr5:17412200-17413200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr5:17412200-17413400	Weak transcription	HMEC	breast
40	chr5:17412200-17413600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr5:17412200-17414400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:17412400-17412600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:17412400-17413200	Enhancers	Brain Cingulate Gyrus	brain
44	chr5:17412400-17413600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr5:17412400-17414400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr5:17412400-17416000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr5:17412600-17413600	Weak transcription	NHEK	skin
48	chr5:17412600-17415600	Weak transcription	NH-A	brain
49	chr5:17412600-17416000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:17412800-17413000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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