Variant report

Variant	nsv974246
Chromosome Location	chr13:50798236-50805245
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:171)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:171 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50804624-50804820	HepG2	liver:	n/a	n/a
2	ATF2	chr13:50800468-50801255	GM12878	blood:	n/a	n/a
3	ATF2	chr13:50800453-50801302	GM12878	blood:	n/a	n/a
4	ATF2	chr13:50798526-50799130	GM12878	blood:	n/a	n/a
5	ATF2	chr13:50798444-50799091	GM12878	blood:	n/a	n/a
6	BATF	chr13:50800484-50801207	GM12878	blood:	n/a	n/a
7	BATF	chr13:50798656-50799051	GM12878	blood:	n/a	chr13:50798841-50798852
8	BATF	chr13:50800557-50801190	GM12878	blood:	n/a	n/a
9	BATF	chr13:50798577-50799094	GM12878	blood:	n/a	chr13:50798841-50798852
10	BCL11A	chr13:50798562-50799110	GM12878	blood:	n/a	n/a
11	BCL11A	chr13:50798676-50798969	GM12878	blood:	n/a	n/a
12	BCL11A	chr13:50800543-50801190	GM12878	blood:	n/a	n/a
13	BCL3	chr13:50798615-50798978	GM12878	blood:	n/a	n/a
14	BCL3	chr13:50798689-50798988	GM12878	blood:	n/a	n/a
15	BCLAF1	chr13:50798643-50799075	GM12878	blood:	n/a	n/a
16	BCLAF1	chr13:50798500-50799092	GM12878	blood:	n/a	n/a
17	BHLHE40	chr13:50798692-50798986	GM12878	blood:	n/a	n/a
18	CEBPB	chr13:50804451-50804979	A549	lung:	n/a	chr13:50804722-50804733
19	CEBPB	chr13:50804525-50804836	HepG2	liver:	n/a	chr13:50804722-50804733
20	CEBPB	chr13:50798701-50798908	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr13:50804509-50804901	Hela-S3	cervix:	n/a	chr13:50804722-50804733
22	CEBPB	chr13:50804531-50804851	HepG2	liver:	n/a	chr13:50804722-50804733
23	CEBPB	chr13:50804447-50804947	MCF-7	breast:	n/a	chr13:50804722-50804733
24	CEBPB	chr13:50804530-50804907	IMR90	lung:	n/a	chr13:50804722-50804733
25	CEBPB	chr13:50804642-50804763	H1-hESC	embryonic stem cell:	n/a	chr13:50804722-50804733
26	CEBPB	chr13:50798734-50799067	K562	blood:	n/a	chr13:50799023-50799034
27	CEBPB	chr13:50799005-50799075	HepG2	liver:	n/a	chr13:50799023-50799034
28	CEBPB	chr13:50804591-50804797	K562	blood:	n/a	chr13:50804722-50804733
29	CEBPB	chr13:50804519-50804917	MCF-7	breast:	n/a	chr13:50804722-50804733
30	CEBPB	chr13:50804560-50804859	A549	lung:	n/a	chr13:50804722-50804733
31	CEBPB	chr13:50804512-50804906	A549	lung:	n/a	chr13:50804722-50804733
32	CEBPB	chr13:50804484-50804919	HepG2	liver:	n/a	chr13:50804722-50804733
33	CEBPB	chr13:50804537-50804909	K562	blood:	n/a	chr13:50804722-50804733
34	CEBPB	chr13:50798646-50799033	GM12878	blood:	n/a	n/a
35	CEBPB	chr13:50804551-50804827	HepG2	liver:	n/a	chr13:50804722-50804733
36	CEBPB	chr13:50798495-50799140	GM12878	blood:	n/a	chr13:50799023-50799034
37	CEBPB	chr13:50804502-50804866	K562	blood:	n/a	chr13:50804722-50804733
38	CEBPD	chr13:50804564-50804804	HepG2	liver:	n/a	n/a
39	CREB1	chr13:50798590-50799124	GM12878	blood:	n/a	n/a
40	CREB1	chr13:50798691-50799097	GM12878	blood:	n/a	n/a
41	CTCF	chr13:50799540-50799690	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr13:50799965-50800043	LNCaP	prostate:	n/a	n/a
43	E2F4	chr13:50798727-50798939	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr13:50804610-50804770	MCF10A-Er-Src	breast:	n/a	n/a
45	EBF1	chr13:50800580-50801077	GM12878	blood:	n/a	chr13:50800874-50800885
46	EBF1	chr13:50798707-50798955	GM12878	blood:	n/a	n/a
47	EBF1	chr13:50800686-50801041	GM12878	blood:	n/a	chr13:50800874-50800885
48	EBF1	chr13:50800768-50801030	GM12878	blood:	n/a	chr13:50800874-50800885
49	ELF1	chr13:50804527-50804779	HepG2	liver:	n/a	n/a
50	EP300	chr13:50800716-50801021	GM12878	blood:	n/a	chr13:50800726-50800736

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50802085-50802135	SAEC	small airway:	n/a
2	chr13:50802085-50802135	GM12878	blood:	n/a
3	chr13:50802085-50802135	SKMC	muscle:	n/a
4	chr13:50802085-50802135	HRPEpiC	eye:	n/a
5	chr13:50802085-50802135	HIPEpiC	eye:	n/a
6	chr13:50802085-50802135	Hela-S3	cervix:	n/a
7	chr13:50802085-50802135	SK-N-SH_RA	brain:	n/a
8	chr13:50802085-50802135	SK-N-SH	brain:	n/a
9	chr13:50802085-50802135	HepG2	liver:	n/a
10	chr13:50802085-50802135	PANC-1	pancreas:	n/a
11	chr13:50802085-50802135	HEK293	kidney:	embryo
12	chr13:50802085-50802135	GM12892	blood:	n/a
13	chr13:50802085-50802135	IMR90	lung:	fetal
14	chr13:50802085-50802135	NH-A	brain:	n/a
15	chr13:50802085-50802135	Hepatocyte	liver:	n/a
16	chr13:50802085-50802135	A549	lung:	n/a
17	chr13:50802085-50802135	NHDF-neo	bronchial:	n/a
18	chr13:50802085-50802135	NT2-D1	testis:	n/a
19	chr13:50802085-50802135	MCF-7	breast:	n/a
20	chr13:50802085-50802135	U87	brain:	n/a
21	chr13:50802085-50802135	RPTEC	kidney:	n/a
22	chr13:50802085-50802135	HL-60	blood:	n/a
23	chr13:50802085-50802135	HEEpiC	esophagus:	n/a
24	chr13:50802085-50802135	HCF	heart:	n/a
25	chr13:50802085-50802135	AG09309	skin:	n/a
26	chr13:50802085-50802135	HCM	heart:	n/a
27	chr13:50802085-50802135	GM19239	blood:	n/a
28	chr13:50802085-50802135	HRCEpiC	kidney:	n/a
29	chr13:50802085-50802135	GM12891	blood:	n/a
30	chr13:50802085-50802135	CMK	blood:	n/a
31	chr13:50802085-50802135	HPAEpiC	pulmonary alveolar:	n/a
32	chr13:50802085-50802135	AG10803	skin:	n/a
33	chr13:50802085-50802135	Caco-2	colon:	n/a
34	chr13:50802085-50802135	ovcar-3	ovarian:	n/a
35	chr13:50802085-50802135	T-47D	breast:	n/a
36	chr13:50802085-50802135	AoSMC	blood vessel:	n/a
37	chr13:50802085-50802135	SK-N-MC	brain:	n/a
38	chr13:50802085-50802135	GM06990	blood:	n/a
39	chr13:50802085-50802135	ProgFib	skin:	n/a
40	chr13:50802085-50802135	HRE	kidney:	n/a
41	chr13:50802085-50802135	BJ	skin:	n/a
42	chr13:50802085-50802135	H1-hESC	embryonic stem cell:	embryo
43	chr13:50802085-50802135	AG09319	gingival:	n/a
44	chr13:50802085-50802135	NHBE	bronchial:	n/a
45	chr13:50802085-50802135	Jurkat	blood:	n/a
46	chr13:50802085-50802135	ECC-1	luminal epithelium:	n/a
47	chr13:50802085-50802135	HAEpiC	amniotic membrane:	n/a
48	chr13:50802085-50802135	AG04450	lung:	fetal
49	chr13:50802085-50802135	LNCaP	prostate:	n/a
50	chr13:50802085-50802135	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:50796637..50798644-chr13:50801798..50803965,2	MCF-7	breast:
2	chr13:50801110..50803059-chr13:50816334..50818261,2	MCF-7	breast:
3	chr13:50801740..50804287-chr13:50809039..50811026,2	K562	blood:
4	chr13:50795214..50796979-chr13:50798701..50801659,2	MCF-7	breast:
5	chr13:50788495..50791287-chr13:50799483..50801951,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPRYD7-5	chr13:50802555-50802588	NONHSAT033830
2	lnc-RNASEH2B-3	chr13:50798417-50798513	NONHSAT033833

No data

Variant related genes	Relation type
DLEU1	TF binding region
DLEU1	CpG island
ENSG00000176124	chromatin interactions

Extended variants
information (count: 196 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:196 , 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	rs17074018	chr13:50798328-50798329	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547182016	chr13:50798329-50798330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565576190	chr13:50798349-50798350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142130558	chr13:50798353-50798354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184471549	chr13:50798373-50798374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569667466	chr13:50798522-50798523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187757716	chr13:50798537-50798538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558271494	chr13:50798542-50798543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs578195046	chr13:50798583-50798584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539375144	chr13:50798600-50798601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554385257	chr13:50798601-50798602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191524707	chr13:50798619-50798620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs151139134	chr13:50798648-50798649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538211919	chr13:50798667-50798668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561389896	chr13:50798684-50798685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576460042	chr13:50798709-50798710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557294129	chr13:50798729-50798730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs2580188	chr13:50798730-50798731	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs546071431	chr13:50798744-50798745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565172723	chr13:50798893-50798894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544817954	chr13:50798911-50798912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs140109153	chr13:50798944-50798945	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs147003004	chr13:50798945-50798946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186455954	chr13:50798973-50798974	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184059976	chr13:50798987-50798988	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559333882	chr13:50799060-50799061	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529808164	chr13:50799091-50799092	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs548092562	chr13:50799122-50799123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs116395277	chr13:50799185-50799186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188794545	chr13:50799196-50799197	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs552141743	chr13:50799223-50799224	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs1149846	chr13:50799247-50799248	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs181479856	chr13:50799274-50799275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554471209	chr13:50799296-50799297	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138207725	chr13:50799298-50799299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541560065	chr13:50799315-50799316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370256244	chr13:50799366-50799367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs575423094	chr13:50799385-50799386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs80314237	chr13:50799409-50799410	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184425396	chr13:50799476-50799477	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs558892195	chr13:50799480-50799481	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs190619137	chr13:50799521-50799522	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368288101	chr13:50799525-50799526	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs559182947	chr13:50799541-50799542	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs529942060	chr13:50799569-50799570	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542006724	chr13:50799570-50799571	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs182300726	chr13:50799598-50799599	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530447400	chr13:50799613-50799614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs185920346	chr13:50799623-50799624	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190796659	chr13:50799624-50799625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	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
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
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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	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
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Sezary syndrome	18413736	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50790400-50799400	Weak transcription	HepG2	liver
2	chr13:50793600-50799200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr13:50795400-50799600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr13:50795800-50800600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr13:50795800-50801000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr13:50796200-50804000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr13:50796800-50799400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr13:50797000-50804200	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr13:50797200-50799000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr13:50797200-50799600	Enhancers	HMEC	breast
11	chr13:50797200-50801600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr13:50797200-50801600	Weak transcription	Fetal Muscle Trunk	muscle
13	chr13:50797200-50802600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr13:50797200-50802800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr13:50797400-50798800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr13:50797400-50798800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr13:50797400-50799000	Enhancers	NHDF-Ad	bronchial
18	chr13:50797400-50799200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr13:50797400-50799600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr13:50797400-50799800	Enhancers	Osteobl	bone
21	chr13:50797400-50800000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr13:50797400-50800200	Weak transcription	Brain Cingulate Gyrus	brain
23	chr13:50797600-50798600	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr13:50797600-50798600	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr13:50797600-50798800	Weak transcription	HSMM	muscle
26	chr13:50797600-50798800	Weak transcription	NH-A	brain
27	chr13:50797600-50798800	Weak transcription	NHLF	lung
28	chr13:50797600-50799000	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr13:50797600-50799400	Weak transcription	Brain Hippocampus Middle	brain
30	chr13:50797600-50801400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr13:50797600-50802200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr13:50797800-50799800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr13:50798000-50798600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr13:50798000-50799200	Weak transcription	HSMMtube	muscle
35	chr13:50798000-50799400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr13:50798200-50799000	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr13:50798200-50799000	Weak transcription	Fetal Muscle Leg	muscle
38	chr13:50798200-50799200	Weak transcription	Brain Anterior Caudate	brain
39	chr13:50798200-50801800	Enhancers	GM12878-XiMat	blood
40	chr13:50798400-50798800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr13:50798600-50799200	Enhancers	Muscle Satellite Cultured Cells	--
42	chr13:50798600-50800600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr13:50798800-50799000	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr13:50798800-50799200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr13:50798800-50799200	Enhancers	NHLF	lung
46	chr13:50798800-50799400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr13:50798800-50799400	Enhancers	NH-A	brain
48	chr13:50799000-50799200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr13:50799000-50799200	Enhancers	HSMM	muscle
50	chr13:50799000-50799800	Enhancers	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links