Variant report

Variant	nsv976114
Chromosome Location	chr13:50935447-50940164
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	chr13:50940147-50940602	HepG2	liver:	n/a	n/a
2	ATF2	chr13:50939904-50940403	GM12878	blood:	n/a	n/a
3	ATF2	chr13:50939796-50940352	GM12878	blood:	n/a	n/a
4	BATF	chr13:50939878-50940334	GM12878	blood:	n/a	n/a
5	BATF	chr13:50939653-50940450	GM12878	blood:	n/a	n/a
6	BCL11A	chr13:50939815-50940358	GM12878	blood:	n/a	chr13:50940142-50940151
7	BCL11A	chr13:50939987-50940250	GM12878	blood:	n/a	chr13:50940142-50940151
8	CEBPB	chr13:50939983-50940528	HepG2	liver:	n/a	chr13:50940133-50940144
9	CEBPB	chr13:50939980-50940386	A549	lung:	n/a	chr13:50940133-50940144
10	CEBPB	chr13:50939897-50940526	MCF-7	breast:	n/a	chr13:50940133-50940144
11	CEBPB	chr13:50939852-50940578	MCF-7	breast:	n/a	chr13:50940133-50940144
12	CEBPB	chr13:50939898-50940662	A549	lung:	n/a	chr13:50940133-50940144
13	CEBPB	chr13:50939993-50940343	Hela-S3	cervix:	n/a	chr13:50940133-50940144
14	CEBPB	chr13:50940072-50940584	A549	lung:	n/a	chr13:50940133-50940144
15	EBF1	chr13:50939825-50940370	GM12878	blood:	n/a	n/a
16	EBF1	chr13:50940012-50940614	GM12878	blood:	n/a	n/a
17	EBF1	chr13:50940026-50940363	GM12878	blood:	n/a	n/a
18	ELF1	chr13:50939460-50939745	K562	blood:	n/a	chr13:50939619-50939632
19	EP300	chr13:50940131-50940699	A549	lung:	n/a	chr13:50940142-50940151
20	EP300	chr13:50940133-50940683	MCF-7	breast:	n/a	chr13:50940142-50940151
21	EP300	chr13:50940006-50940338	GM12878	blood:	n/a	chr13:50940142-50940151
22	EP300	chr13:50939939-50940679	A549	lung:	n/a	chr13:50940142-50940151
23	EP300	chr13:50939575-50941676	SK-N-SH	brain:	n/a	chr13:50940142-50940151
24	EP300	chr13:50939860-50940296	GM12878	blood:	n/a	chr13:50940142-50940151
25	EP300	chr13:50939837-50940684	T-47D	breast:	n/a	chr13:50940142-50940151
26	FOS	chr13:50940017-50940557	MCF10A-Er-Src	breast:	n/a	chr13:50940143-50940152 chr13:50940139-50940150 chr13:50940136-50940148
27	FOS	chr13:50940008-50940403	MCF10A-Er-Src	breast:	n/a	chr13:50940143-50940152 chr13:50940139-50940150 chr13:50940136-50940148
28	FOS	chr13:50940019-50940491	MCF10A-Er-Src	breast:	n/a	chr13:50940143-50940152 chr13:50940139-50940150 chr13:50940136-50940148
29	FOS	chr13:50939956-50940502	MCF10A-Er-Src	breast:	n/a	chr13:50940143-50940152 chr13:50940139-50940150 chr13:50940136-50940148
30	FOS	chr13:50939409-50940688	HUVEC	blood vessel:	n/a	chr13:50939648-50939659 chr13:50940143-50940152 chr13:50940139-50940150 chr13:50940136-50940148
31	FOSL2	chr13:50939854-50940440	MCF-7	breast:	n/a	chr13:50940143-50940152 chr13:50940139-50940150 chr13:50940136-50940148
32	FOSL2	chr13:50939879-50940744	A549	lung:	n/a	chr13:50940143-50940152 chr13:50940139-50940150 chr13:50940136-50940148
33	FOSL2	chr13:50939915-50940503	MCF-7	breast:	n/a	chr13:50940143-50940152 chr13:50940139-50940150 chr13:50940136-50940148
34	FOXA1	chr13:50939978-50940728	T-47D	breast:	n/a	n/a
35	FOXA1	chr13:50939990-50940588	T-47D	breast:	n/a	n/a
36	FOXA1	chr13:50940162-50940601	HepG2	liver:	n/a	n/a
37	FOXA1	chr13:50940148-50940654	HepG2	liver:	n/a	n/a
38	FOXA1	chr13:50940065-50940606	HepG2	liver:	n/a	n/a
39	FOXA1	chr13:50940164-50940656	HepG2	liver:	n/a	n/a
40	FOXA2	chr13:50940154-50940853	A549	lung:	n/a	n/a
41	FOXA2	chr13:50940017-50940619	HepG2	liver:	n/a	n/a
42	FOXA2	chr13:50939862-50940831	A549	lung:	n/a	n/a
43	FOXM1	chr13:50939865-50940373	GM12878	blood:	n/a	chr13:50940112-50940120
44	GATA2	chr13:50939454-50940205	HUVEC	blood vessel:	n/a	chr13:50939654-50939668 chr13:50940144-50940153
45	GATA3	chr13:50939660-50940627	MCF-7	breast:	n/a	chr13:50940144-50940153
46	GATA3	chr13:50939818-50940830	MCF-7	breast:	n/a	chr13:50940144-50940153
47	GATA3	chr13:50939936-50940655	T-47D	breast:	n/a	chr13:50940144-50940153
48	GATA3	chr13:50939849-50940831	A549	lung:	n/a	chr13:50940144-50940153
49	HDAC2	chr13:50939796-50940339	MCF-7	breast:	n/a	n/a
50	IRF1	chr13:50940009-50940249	K562	blood:	n/a	chr13:50940169-50940182 chr13:50940170-50940183 chr13:50940172-50940183 chr13:50940169-50940182 chr13:50940163-50940183 chr13:50940168-50940182 chr13:50940167-50940181 chr13:50940169-50940182 chr13:50940169-50940182 chr13:50940171-50940182

No.	Distal block	Cell Line	Cell type
1	chr13:50698219..50700301-chr13:50938439..50940061,3	MCF-7	breast:
2	chr13:50931295..50934143-chr13:50939870..50941977,3	MCF-7	breast:
3	chr13:50697261..50699908-chr13:50935542..50937568,2	K562	blood:
4	chr13:50698526..50701372-chr13:50933812..50935948,3	MCF-7	breast:
5	chr13:50698177..50699740-chr13:50938730..50941309,2	MCF-7	breast:
6	chr13:50929441..50932225-chr13:50939480..50941358,2	MCF-7	breast:
7	chr13:50939370..50941845-chr13:50950043..50952232,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLEU7-9	chr13:50935546-50935899	NONHSAT033838

Variant related genes	Relation type
ENSG00000221198	TF binding region
RPL34P26	TF binding region
ENSG00000231607	chromatin interactions

Extended variants
information (count: 143 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535159110	chr13:50935501-50935502	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148058939	chr13:50935505-50935506	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550846461	chr13:50935559-50935560	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs2812215	chr13:50935593-50935594	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs180888707	chr13:50935655-50935656	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs558313609	chr13:50935679-50935680	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs566858679	chr13:50935700-50935701	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs185968260	chr13:50935733-50935734	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs555697676	chr13:50935785-50935786	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs373575923	chr13:50935791-50935792	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs9562961	chr13:50935841-50935842	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs17461017	chr13:50935855-50935856	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs562306163	chr13:50935885-50935886	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs12874278	chr13:50935922-50935923	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs374019540	chr13:50935925-50935926	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113196633	chr13:50935950-50935951	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141793441	chr13:50935959-50935960	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs527280230	chr13:50936028-50936029	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542259088	chr13:50936071-50936072	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145986139	chr13:50936084-50936085	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs60147627	chr13:50936129-50936130	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs551282355	chr13:50936214-50936215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189690877	chr13:50936221-50936222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370555473	chr13:50936242-50936243	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs143661387	chr13:50936280-50936281	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs373737604	chr13:50936336-50936337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs534291833	chr13:50936351-50936352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs555435441	chr13:50936364-50936365	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201498973	chr13:50936402-50936403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs537720755	chr13:50936415-50936416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs556448015	chr13:50936437-50936438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146328914	chr13:50936442-50936443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs544843298	chr13:50936462-50936463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553446075	chr13:50936512-50936513	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139321309	chr13:50936562-50936563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149982748	chr13:50936577-50936578	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs527917113	chr13:50936578-50936579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs59399754	chr13:50936606-50936607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs370488846	chr13:50936615-50936616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576019003	chr13:50936629-50936630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373935915	chr13:50936730-50936731	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181335292	chr13:50936756-50936757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185994063	chr13:50936800-50936801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs145216424	chr13:50936807-50936808	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543426933	chr13:50936818-50936819	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551958254	chr13:50936839-50936840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs35585374	chr13:50936851-50936852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116335921	chr13:50936872-50936873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563090147	chr13:50936883-50936884	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs149207423	chr13:50937021-50937022	Weak transcription	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
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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD

Chromatin state (count:134 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50930000-50935800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr13:50930200-50939200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr13:50930200-50939600	Weak transcription	Duodenum Mucosa	Duodenum
4	chr13:50931600-50939000	Weak transcription	HepG2	liver
5	chr13:50932000-50940800	Weak transcription	Small Intestine	intestine
6	chr13:50932400-50936200	Enhancers	Primary T cells fromperipheralblood	blood
7	chr13:50932400-50936200	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr13:50932400-50936400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr13:50932800-50935800	Weak transcription	Spleen	Spleen
10	chr13:50932800-50936200	Weak transcription	Fetal Brain Female	brain
11	chr13:50932800-50939400	Weak transcription	Gastric	stomach
12	chr13:50932800-50939400	Weak transcription	Pancreas	Pancrea
13	chr13:50932800-50939600	Weak transcription	Fetal Kidney	kidney
14	chr13:50933000-50935800	Weak transcription	Fetal Muscle Leg	muscle
15	chr13:50933000-50935800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr13:50933000-50936000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr13:50933200-50936600	Weak transcription	Fetal Heart	heart
18	chr13:50933200-50939200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr13:50933400-50939800	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr13:50933400-50944600	Weak transcription	Fetal Lung	lung
21	chr13:50933800-50944000	Weak transcription	Primary B cells from cord blood	blood
22	chr13:50934000-50935600	Weak transcription	Primary B cells from peripheral blood	blood
23	chr13:50934000-50939600	Weak transcription	Brain Germinal Matrix	brain
24	chr13:50934200-50935800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr13:50934600-50936000	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr13:50934600-50942000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr13:50934800-50935800	Enhancers	Dnd41	blood
28	chr13:50935000-50936000	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr13:50935000-50939400	Weak transcription	Fetal Thymus	thymus
30	chr13:50935200-50935600	Enhancers	Brain Anterior Caudate	brain
31	chr13:50935200-50936800	Enhancers	Liver	Liver
32	chr13:50935400-50935800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
33	chr13:50935400-50936200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr13:50935600-50935800	Bivalent Enhancer	GM12878-XiMat	blood
35	chr13:50935600-50936200	Enhancers	Primary B cells from peripheral blood	blood
36	chr13:50935800-50936000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
37	chr13:50935800-50936200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr13:50935800-50936200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr13:50935800-50936200	Enhancers	Spleen	Spleen
40	chr13:50935800-50936400	Enhancers	Fetal Muscle Leg	muscle
41	chr13:50935800-50936400	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr13:50936000-50936800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr13:50936000-50936800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr13:50936000-50939000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr13:50936000-50939000	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr13:50936200-50936400	Enhancers	Fetal Brain Female	brain
47	chr13:50936200-50938800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr13:50936200-50938800	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr13:50936200-50939000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr13:50936200-50939200	Weak transcription	Primary T cells fromperipheralblood	blood

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