Variant report

Variant	nsv1039312
Chromosome Location	chr13:48898950-48925357
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	chr13:48908715-48909033	HepG2	liver:	n/a	n/a
2	CEBPB	chr13:48908140-48908467	IMR90	lung:	n/a	n/a
3	CEBPB	chr13:48919840-48920097	HepG2	liver:	n/a	chr13:48919969-48919978 chr13:48919968-48919979
4	CTCF	chr13:48908780-48908930	GM12865	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
5	CTCF	chr13:48908737-48908985	GM12878	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
6	CTCF	chr13:48908780-48908930	HMEC	breast:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
7	CTCF	chr13:48908780-48908930	GM12801	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
8	CTCF	chr13:48908760-48908910	HPF	lung:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
9	CTCF	chr13:48908740-48908890	HAc	cerebellar:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
10	CTCF	chr13:48908703-48908984	HepG2	liver:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
11	CTCF	chr13:48908760-48908910	HRE	kidney:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
12	CTCF	chr13:48908760-48908910	K562	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
13	CTCF	chr13:48908800-48908950	NB4	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
14	CTCF	chr13:48908881-48908884	GM20000	blood:	n/a	n/a
15	CTCF	chr13:48908760-48908910	GM12874	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
16	CTCF	chr13:48908760-48908910	HA-sp	spinal cord:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
17	CTCF	chr13:48908760-48908910	HL-60	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
18	CTCF	chr13:48908665-48909046	K562	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
19	CTCF	chr13:48908734-48908976	Lung_OC	lung:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
20	CTCF	chr13:48908340-48908490	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr13:48908760-48908910	GM12865	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
22	CTCF	chr13:48908597-48909016	MCF-7	breast:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
23	CTCF	chr13:48908660-48908810	GM12870	blood:	n/a	n/a
24	CTCF	chr13:48908736-48908983	Medullo	brain:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
25	CTCF	chr13:48908860-48909010	GM12870	blood:	n/a	n/a
26	CTCF	chr13:48908700-48908850	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr13:48908780-48908930	HUVEC	blood vessel:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
28	CTCF	chr13:48908730-48909018	K562	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
29	CTCF	chr13:48908642-48909082	GM12878	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
30	CTCF	chr13:48908800-48908950	BJ	skin:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
31	CTCF	chr13:48913201-48913305	MCF-7	breast:	n/a	n/a
32	CTCF	chr13:48908760-48908910	HFF	foreskin:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
33	CTCF	chr13:48908740-48908890	BJ	skin:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
34	CTCF	chr13:48908760-48908910	GM12869	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
35	CTCF	chr13:48908740-48908890	RPTEC	kidney:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
36	CTCF	chr13:48908700-48908850	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr13:48908761-48908937	GM13977	blood:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
38	CTCF	chr13:48908740-48908890	HRPEpiC	eye:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
39	CTCF	chr13:48908677-48909001	SK-N-SH_RA	brain:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
40	CTCF	chr13:48908760-48908910	HEEpiC	esophagus:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
41	CTCF	chr13:48908720-48908870	HFF-Myc	foreskin:	n/a	chr13:48908852-48908870
42	CTCF	chr13:48908760-48908910	MCF-7	breast:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
43	CTCF	chr13:48908760-48908910	HVMF	connective:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
44	CTCF	chr13:48908720-48908870	GM06990	blood:	n/a	chr13:48908852-48908870
45	CTCF	chr13:48908720-48908870	GM12864	blood:	n/a	chr13:48908852-48908870
46	CTCF	chr13:48908380-48908530	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr13:48908759-48909023	HCT-116	colon:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
48	CTCF	chr13:48908780-48908930	AG09319	gingival:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
49	CTCF	chr13:48908780-48908930	HRE	kidney:	n/a	chr13:48908854-48908875 chr13:48908852-48908870
50	CTCF	chr13:48908360-48908510	BJ	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:48908843..48909363-chr13:49153698..49154640,2	MCF-7	breast:
2	chr13:48904305..48906234-chr13:48906368..48908562,2	MCF-7	breast:
3	chr13:48877798..48879447-chr13:48917286..48919351,2	K562	blood:
4	chr13:48904305..48906234-chr13:48906368..48908562,2	MCF-7	breast:
5	chr13:48908385..48909298-chr13:49342938..49343582,2	MCF-7	breast:

Variant related genes	Relation type
PCNPP5	TF binding region
PPP1R26P1	TF binding region
ENSG00000139687	chromatin interactions

Extended variants
information (count: 966 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:966 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575423557	chr13:48898975-48898976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376734455	chr13:48898980-48898981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7319732	chr13:48898986-48898987	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
4	rs150575722	chr13:48898987-48898988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372154845	chr13:48898989-48898990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540608662	chr13:48898990-48898991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374890023	chr13:48898998-48898999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190949097	chr13:48899011-48899012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540964121	chr13:48899053-48899054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371330370	chr13:48899085-48899086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554056559	chr13:48899121-48899122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs59792871	chr13:48899138-48899139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574204757	chr13:48899146-48899147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11309586	chr13:48899215-48899216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184043194	chr13:48899232-48899233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542728400	chr13:48899308-48899309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78982912	chr13:48899318-48899319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146127081	chr13:48899329-48899330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569308200	chr13:48899414-48899415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533584662	chr13:48899468-48899469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551029290	chr13:48899626-48899627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189123209	chr13:48899646-48899647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533671014	chr13:48899664-48899665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531690203	chr13:48899788-48899789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs367732583	chr13:48899826-48899827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542855644	chr13:48899827-48899828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192390744	chr13:48899847-48899848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570762806	chr13:48899856-48899857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182902813	chr13:48899861-48899862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537746808	chr13:48899893-48899894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556430149	chr13:48899922-48899923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187244698	chr13:48900028-48900029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538858031	chr13:48900045-48900046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565320038	chr13:48900098-48900099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574906019	chr13:48900108-48900109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191858522	chr13:48900217-48900218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539739851	chr13:48900244-48900245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183969380	chr13:48900262-48900263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189274094	chr13:48900329-48900330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369220317	chr13:48900343-48900344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs198600	chr13:48900453-48900454	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573978335	chr13:48900633-48900634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544541421	chr13:48900634-48900635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138922218	chr13:48900661-48900662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533338734	chr13:48900673-48900674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116358361	chr13:48900728-48900729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs199686727	chr13:48900751-48900752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368809750	chr13:48900766-48900767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112226810	chr13:48900769-48900770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142248890	chr13:48900861-48900862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Ovarian cancer	22355333	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	21750150	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Phyllodes tumor	17334353	CNVD
Retinoblastoma	22278416	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung adenocarcinoma	21151896	CNVD
Breast cancer	21518781	CNVD
Mantle cell lymphoma	21518781	CNVD
Ovarian cancer	21518781	CNVD
Retinoblastoma	21518781	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Osteosarcoma	21215367	CNVD
Bipolar disorder	19214233	CNVD
Chronic myeloid leukemia	21384125	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:48880200-48913200	Weak transcription	Aorta	Aorta
2	chr13:48880600-48924600	Weak transcription	Psoas Muscle	Psoas
3	chr13:48892600-48927800	Weak transcription	HUVEC	blood vessel
4	chr13:48894400-48906400	Weak transcription	Pancreas	Pancrea
5	chr13:48894400-48913800	Weak transcription	HSMM	muscle
6	chr13:48894600-48919200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr13:48894800-48907600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr13:48894800-48913200	Weak transcription	Lung	lung
9	chr13:48895200-48916800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr13:48895200-48923600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr13:48895200-48924600	Weak transcription	HSMMtube	muscle
12	chr13:48895400-48902800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr13:48895400-48908200	Weak transcription	Small Intestine	intestine
14	chr13:48895400-48912800	Weak transcription	Fetal Thymus	thymus
15	chr13:48895400-48924800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr13:48895600-48913400	Weak transcription	Ovary	ovary
17	chr13:48895800-48919600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr13:48895800-48920400	Weak transcription	Right Ventricle	heart
19	chr13:48895800-48926600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr13:48896000-48902600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr13:48896000-48913000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr13:48896000-48913000	Weak transcription	Left Ventricle	heart
23	chr13:48896000-48913000	Weak transcription	Thymus	Thymus
24	chr13:48896000-48919800	Weak transcription	Primary T cells from cord blood	blood
25	chr13:48896200-48907600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr13:48896200-48908000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr13:48896600-48902400	Weak transcription	Primary B cells from cord blood	blood
28	chr13:48896600-48913000	Weak transcription	Fetal Lung	lung
29	chr13:48896800-48902200	Weak transcription	Dnd41	blood
30	chr13:48896800-48902400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr13:48897000-48900800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr13:48897000-48903600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr13:48897000-48907800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr13:48897000-48917000	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr13:48897200-48907600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr13:48897400-48899000	Weak transcription	GM12878-XiMat	blood
37	chr13:48897400-48903600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr13:48897400-48904600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr13:48897400-48909800	Weak transcription	Primary B cells from peripheral blood	blood
40	chr13:48899200-48900800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr13:48899600-48900200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr13:48899600-48902200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr13:48900000-48900400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr13:48900200-48913000	Weak transcription	Fetal Intestine Large	intestine
45	chr13:48900800-48905200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr13:48902200-48903800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr13:48902200-48904000	Strong transcription	Dnd41	blood
48	chr13:48902400-48902800	Strong transcription	Primary B cells from cord blood	blood
49	chr13:48902400-48904000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr13:48902600-48903000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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