Variant report

Variant	nsv5202
Chromosome Location	chr6:12916229-12958517
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:305)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:12935689-12936376	GM12878	blood:	n/a	n/a
2	BACH1	chr6:12957431-12957748	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:12923933-12924174	GM12878	blood:	n/a	n/a
4	BATF	chr6:12923879-12924195	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:12923929-12924262	GM12878	blood:	n/a	n/a
6	CEBPB	chr6:12958104-12958304	HepG2	liver:	n/a	chr6:12958170-12958181 chr6:12958172-12958183
7	CEBPB	chr6:12957947-12958380	MCF-7	breast:	n/a	chr6:12958170-12958181 chr6:12958172-12958183
8	CEBPB	chr6:12918855-12919207	K562	blood:	n/a	chr6:12919143-12919152
9	CEBPB	chr6:12918769-12919264	HepG2	liver:	n/a	chr6:12919143-12919152
10	CEBPB	chr6:12929982-12930171	K562	blood:	n/a	n/a
11	CEBPB	chr6:12958039-12958289	Hela-S3	cervix:	n/a	chr6:12958170-12958181 chr6:12958172-12958183
12	CEBPB	chr6:12930015-12930180	MCF-7	breast:	n/a	n/a
13	CEBPB	chr6:12937513-12937763	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr6:12918793-12919224	IMR90	lung:	n/a	chr6:12919143-12919152
15	CEBPB	chr6:12918890-12919242	MCF-7	breast:	n/a	chr6:12919143-12919152
16	CEBPB	chr6:12958033-12958327	IMR90	lung:	n/a	chr6:12958170-12958181 chr6:12958172-12958183
17	CEBPB	chr6:12958022-12958302	K562	blood:	n/a	chr6:12958170-12958181 chr6:12958172-12958183
18	CEBPB	chr6:12918775-12919171	A549	lung:	n/a	chr6:12919143-12919152
19	CEBPB	chr6:12958079-12958337	H1-hESC	embryonic stem cell:	n/a	chr6:12958170-12958181 chr6:12958172-12958183
20	CEBPB	chr6:12929992-12930201	A549	lung:	n/a	n/a
21	CEBPB	chr6:12918774-12919295	H1-hESC	embryonic stem cell:	n/a	chr6:12919143-12919152
22	CEBPB	chr6:12918972-12919228	MCF-7	breast:	n/a	chr6:12919143-12919152
23	CEBPB	chr6:12929968-12930276	HepG2	liver:	n/a	n/a
24	CTCF	chr6:12948340-12948490	GM12871	blood:	n/a	chr6:12948431-12948438 chr6:12948394-12948412 chr6:12948396-12948417
25	CTCF	chr6:12948300-12948450	HEK293	kidney:	n/a	chr6:12948431-12948438 chr6:12948394-12948412 chr6:12948396-12948417
26	CTCF	chr6:12948280-12948430	GM12873	blood:	n/a	chr6:12948394-12948412 chr6:12948396-12948417
27	CTCF	chr6:12958040-12958190	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr6:12923920-12924070	GM12869	blood:	n/a	n/a
29	CTCF	chr6:12958109-12958205	ProgFib	skin:	n/a	n/a
30	CTCF	chr6:12957840-12957990	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr6:12958016-12958230	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr6:12923920-12924070	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:12958062-12958260	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr6:12958079-12958237	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr6:12923960-12924110	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr6:12957780-12957930	HRE	kidney:	n/a	n/a
37	CTCF	chr6:12958200-12958350	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr6:12958080-12958230	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr6:12958029-12958322	GM12878	blood:	n/a	n/a
40	CTCF	chr6:12958066-12958213	Lung_OC	lung:	n/a	n/a
41	CTCF	chr6:12948348-12948422	GM13976	blood:	n/a	chr6:12948394-12948412 chr6:12948396-12948417
42	CTCF	chr6:12948260-12948410	GM12872	blood:	n/a	n/a
43	CTCF	chr6:12957980-12958130	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr6:12948360-12948510	MCF-7	breast:	n/a	chr6:12948431-12948438 chr6:12948394-12948412 chr6:12948396-12948417
45	CTCF	chr6:12958020-12958170	HRE	kidney:	n/a	n/a
46	CTCF	chr6:12952200-12952350	GM12866	blood:	n/a	n/a
47	CTCF	chr6:12923960-12924110	GM12875	blood:	n/a	n/a
48	CTCF	chr6:12958045-12958261	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:12958104-12958173	GM19240	blood:	n/a	n/a
50	CTCF	chr6:12958099-12958206	GM12892	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:12957918-12957968	CMK	blood:	n/a
2	chr6:12958080-12958130	NHDF-neo	bronchial:	n/a
3	chr6:12957651-12957701	HRPEpiC	eye:	n/a
4	chr6:12957697-12957747	ECC-1	luminal epithelium:	n/a
5	chr6:12957651-12957701	K562	blood:	n/a
6	chr6:12958080-12958130	Jurkat	blood:	n/a
7	chr6:12957697-12957747	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:12957651-12957701	SK-N-SH	brain:	n/a
9	chr6:12958080-12958130	GM06990	blood:	n/a
10	chr6:12957800-12957850	SK-N-SH	brain:	n/a
11	chr6:12957918-12957968	RPTEC	kidney:	n/a
12	chr6:12958080-12958130	ECC-1	luminal epithelium:	n/a
13	chr6:12957651-12957701	NB4	blood:	n/a
14	chr6:12957800-12957850	SKMC	muscle:	n/a
15	chr6:12957651-12957701	U87	brain:	n/a
16	chr6:12957651-12957701	T-47D	breast:	n/a
17	chr6:12958080-12958130	NB4	blood:	n/a
18	chr6:12957697-12957747	HCPEpiC	choroid plexus:	n/a
19	chr6:12957697-12957747	PFSK-1	brain:	n/a
20	chr6:12957800-12957850	HRE	kidney:	n/a
21	chr6:12958080-12958130	SK-N-SH	brain:	n/a
22	chr6:12957918-12957968	HepG2	liver:	n/a
23	chr6:12957697-12957747	Jurkat	blood:	n/a
24	chr6:12957697-12957747	MCF10A-Er-Src	breast:	n/a
25	chr6:12957800-12957850	NB4	blood:	n/a
26	chr6:12957800-12957850	U87	brain:	n/a
27	chr6:12957697-12957747	HepG2	liver:	n/a
28	chr6:12957651-12957701	HCM	heart:	n/a
29	chr6:12957651-12957701	H1-hESC	embryonic stem cell:	embryo
30	chr6:12957697-12957747	AG09319	gingival:	n/a
31	chr6:12957918-12957968	HAEpiC	amniotic membrane:	n/a
32	chr6:12958080-12958130	GM12892	blood:	n/a
33	chr6:12957697-12957747	GM12878	blood:	n/a
34	chr6:12957651-12957701	BE2_C	brain:	n/a
35	chr6:12957800-12957850	AoSMC	blood vessel:	n/a
36	chr6:12957697-12957747	NT2-D1	testis:	n/a
37	chr6:12957918-12957968	ECC-1	luminal epithelium:	n/a
38	chr6:12957800-12957850	NHDF-neo	bronchial:	n/a
39	chr6:12957918-12957968	MCF10A-Er-Src	breast:	n/a
40	chr6:12957651-12957701	PANC-1	pancreas:	n/a
41	chr6:12957651-12957701	AoSMC	blood vessel:	n/a
42	chr6:12957697-12957747	GM12892	blood:	n/a
43	chr6:12957651-12957701	AG04450	lung:	fetal
44	chr6:12957918-12957968	HCF	heart:	n/a
45	chr6:12957800-12957850	SAEC	small airway:	n/a
46	chr6:12957918-12957968	Jurkat	blood:	n/a
47	chr6:12957697-12957747	ProgFib	skin:	n/a
48	chr6:12958080-12958130	HPAEpiC	pulmonary alveolar:	n/a
49	chr6:12957800-12957850	MCF-7	breast:	n/a
50	chr6:12957800-12957850	HNPCEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:12936966..12939245-chr6:12942026..12943632,2	K562	blood:
2	chr6:12927202..12927897-chr6:13148834..13149408,2	MCF-7	breast:
3	chr6:12944669..12946335-chr6:12951774..12953726,2	K562	blood:
4	chr6:12936966..12940457-chr6:12942026..12944192,3	K562	blood:
5	chr6:12925983..12927810-chr6:12928390..12930957,2	K562	blood:
6	chr6:12917516..12920384-chr6:12920626..12922714,2	K562	blood:
7	chr6:12925983..12927810-chr6:12928390..12930957,2	K562	blood:
8	chr6:12944669..12946335-chr6:12951774..12953726,2	K562	blood:
9	chr6:12936966..12939245-chr6:12942026..12943632,2	K562	blood:
10	chr6:12917516..12920384-chr6:12920626..12922714,2	K562	blood:
11	chr6:12915914..12916714-chr6:13328445..13329423,2	MCF-7	breast:
12	chr6:12936966..12940457-chr6:12942026..12944192,3	K562	blood:

No data

Variant related genes	Relation type
PHACTR1	TF binding region
PHACTR1	CpG island
ENSG00000145979	chromatin interactions

Extended variants
information (count: 1603 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1603 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79323775	chr6:12916229-12916230	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs374582491	chr6:12916256-12916257	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs116723443	chr6:12916294-12916295	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546616912	chr6:12916295-12916296	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189111582	chr6:12916318-12916319	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535959476	chr6:12916345-12916346	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554422477	chr6:12916358-12916359	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs574585572	chr6:12916373-12916374	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368002102	chr6:12916385-12916386	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs9472955	chr6:12916393-12916394	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs181557454	chr6:12916432-12916433	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs577240697	chr6:12916438-12916439	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs79139907	chr6:12916439-12916440	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371828417	chr6:12916459-12916460	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553022094	chr6:12916483-12916484	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547956425	chr6:12916495-12916496	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374872694	chr6:12916554-12916555	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376170152	chr6:12916580-12916581	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568183820	chr6:12916590-12916591	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562099775	chr6:12916662-12916663	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186086724	chr6:12916673-12916674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs368867690	chr6:12916714-12916715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs9472958	chr6:12916730-12916731	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs67725562	chr6:12916773-12916774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556024476	chr6:12916774-12916775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs398000509	chr6:12916788-12916789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375309478	chr6:12916825-12916826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190440501	chr6:12916836-12916837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114840465	chr6:12916856-12916857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533479747	chr6:12916873-12916874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372115401	chr6:12916919-12916920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11964523	chr6:12916948-12916949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs74861293	chr6:12916976-12916977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529328623	chr6:12917009-12917010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180817343	chr6:12917080-12917081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536602035	chr6:12917115-12917116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537231046	chr6:12917137-12917138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186102117	chr6:12917152-12917153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191391889	chr6:12917156-12917157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200872024	chr6:12917159-12917160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539768439	chr6:12917214-12917215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191267649	chr6:12917265-12917266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72820830	chr6:12917286-12917287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs185719367	chr6:12917322-12917323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116507203	chr6:12917406-12917407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555436299	chr6:12917423-12917424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190484000	chr6:12917437-12917438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544383608	chr6:12917447-12917448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551998913	chr6:12917476-12917477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140925799	chr6:12917510-12917511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Cancer	21183584	CNVD
Acute myeloid leukemia	18000384	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Metastatic melanoma	18483359	CNVD
Breast cancer	21990379	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:12911200-12918000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:12912200-12929800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr6:12914200-12918200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:12914200-12918200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr6:12914600-12916800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr6:12915800-12916800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr6:12916000-12916600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr6:12916000-12916800	Enhancers	Primary hematopoietic stem cells	blood
9	chr6:12916000-12916800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:12916200-12916600	Enhancers	Primary B cells from cord blood	blood
11	chr6:12916200-12916600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:12918000-12918400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:12918200-12919000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:12918200-12919000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:12918400-12922600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:12919000-12922600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr6:12922600-12923000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:12922600-12923000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:12922600-12923400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr6:12923800-12924400	Enhancers	HUVEC	blood vessel
21	chr6:12927000-12927200	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr6:12927200-12927400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr6:12927400-12931800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr6:12929200-12930600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:12929400-12930000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr6:12929600-12930000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr6:12929600-12930400	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr6:12929600-12930800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr6:12929800-12930000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr6:12929800-12930000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr6:12929800-12930000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:12929800-12930400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:12930000-12930600	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr6:12930000-12931400	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr6:12930000-12931400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr6:12930000-12931600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr6:12930000-12931800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:12930400-12930800	Enhancers	Brain Anterior Caudate	brain
39	chr6:12930400-12951800	Weak transcription	Fetal Brain Female	brain
40	chr6:12930800-12941600	Weak transcription	Brain Anterior Caudate	brain
41	chr6:12931400-12932400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:12931400-12932400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:12931600-12932000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr6:12931600-12932400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr6:12931600-12932400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr6:12931800-12932000	Enhancers	H9 Cell Line	embryonic stem cell
47	chr6:12931800-12932400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr6:12931800-12932400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:12932400-12941400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:12933200-12944200	Weak transcription	Brain Germinal Matrix	brain

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