Variant report

Variant	nsv510587
Chromosome Location	chr13:61979753-61994053
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:247)
CpG islands
(count:1102)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:247 , 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	BACH1	chr13:61989073-61989080	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr13:61988936-61989251	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr13:61991399-61991696	MCF-7	breast:	n/a	chr13:61991520-61991533 chr13:61991521-61991532 chr13:61991520-61991531 chr13:61991520-61991533
4	CEBPB	chr13:61991381-61991687	HepG2	liver:	n/a	chr13:61991520-61991533 chr13:61991521-61991532 chr13:61991520-61991531 chr13:61991520-61991533
5	CEBPB	chr13:61983510-61983698	HepG2	liver:	n/a	chr13:61983629-61983640
6	CHD2	chr13:61988785-61988924	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr13:61989233-61989545	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr13:61989057-61989987	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr13:61984860-61985010	HVMF	connective:	n/a	n/a
10	CTCF	chr13:61984920-61985070	HPF	lung:	n/a	n/a
11	CTCF	chr13:61984960-61985110	GM12875	blood:	n/a	n/a
12	CTCF	chr13:61984920-61985070	AG04449	skin:	n/a	n/a
13	CTCF	chr13:61984940-61985090	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr13:61984900-61985050	BJ	skin:	n/a	n/a
15	CTCF	chr13:61984924-61985121	GM12878	blood:	n/a	n/a
16	CTCF	chr13:61985320-61985470	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr13:61984920-61985070	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr13:61984880-61985030	AG04450	lung:	n/a	n/a
19	CTCF	chr13:61984960-61985110	NHEK	skin:	n/a	n/a
20	CTCF	chr13:61984940-61985090	GM12865	blood:	n/a	n/a
21	CTCF	chr13:61984940-61985090	BE2_C	brain:	n/a	n/a
22	CTCF	chr13:61984920-61985070	BJ	skin:	n/a	n/a
23	CTCF	chr13:61984843-61985179	K562	blood:	n/a	n/a
24	CTCF	chr13:61984940-61985090	AG04449	skin:	n/a	n/a
25	CTCF	chr13:61985286-61985397	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr13:61984877-61985144	ECC-1	luminal epithelium:	n/a	n/a
27	CTCF	chr13:61984940-61985090	AG10803	skin:	n/a	n/a
28	CTCF	chr13:61984967-61985110	K562	blood:	n/a	n/a
29	CTCF	chr13:61985000-61985150	GM12872	blood:	n/a	n/a
30	CTCF	chr13:61984816-61985107	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr13:61984960-61985110	HAc	cerebellar:	n/a	n/a
32	CTCF	chr13:61984920-61985070	AG09319	gingival:	n/a	n/a
33	CTCF	chr13:61984980-61985130	HCM	heart:	n/a	n/a
34	CTCF	chr13:61984920-61985070	HRE	kidney:	n/a	n/a
35	CTCF	chr13:61984920-61985070	GM12865	blood:	n/a	n/a
36	CTCF	chr13:61984940-61985090	GM12867	blood:	n/a	n/a
37	CTCF	chr13:61984894-61985147	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr13:61984914-61985263	MCF-7	breast:	n/a	n/a
39	CTCF	chr13:61984920-61985070	HMF	breast:	n/a	n/a
40	CTCF	chr13:61984960-61985110	GM12873	blood:	n/a	n/a
41	CTCF	chr13:61984771-61985165	SK-N-SH	brain:	n/a	n/a
42	CTCF	chr13:61984977-61985067	MCF-7	breast:	n/a	n/a
43	CTCF	chr13:61984970-61985054	ProgFib	skin:	n/a	n/a
44	CTCF	chr13:61984880-61985185	HepG2	liver:	n/a	n/a
45	CTCF	chr13:61984960-61985110	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr13:61984682-61984773	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr13:61984960-61985110	GM12874	blood:	n/a	n/a
48	CTCF	chr13:61984980-61985130	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr13:61984940-61985090	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr13:61984920-61985070	RPTEC	kidney:	n/a	n/a

(count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:61988802-61988852	A549	lung:	n/a
2	chr13:61988153-61988203	HepG2	liver:	n/a
3	chr13:61989724-61989774	NH-A	brain:	n/a
4	chr13:61989726-61989776	SK-N-SH	brain:	n/a
5	chr13:61988802-61988852	A549	lung:	n/a
6	chr13:61988153-61988203	HepG2	liver:	n/a
7	chr13:61989724-61989774	NH-A	brain:	n/a
8	chr13:61989726-61989776	SK-N-SH	brain:	n/a
9	chr13:61988802-61988852	GM06990	blood:	n/a
10	chr13:61989203-61989253	HPAEpiC	pulmonary alveolar:	n/a
11	chr13:61989475-61989525	MCF10A-Er-Src	breast:	n/a
12	chr13:61988153-61988203	HIPEpiC	eye:	n/a
13	chr13:61989037-61989087	HRCEpiC	kidney:	n/a
14	chr13:61989817-61989867	HRE	kidney:	n/a
15	chr13:61990741-61990791	HRPEpiC	eye:	n/a
16	chr13:61989037-61989087	Hela-S3	cervix:	n/a
17	chr13:61989475-61989525	MCF-7	breast:	n/a
18	chr13:61989770-61989820	MCF10A-Er-Src	breast:	n/a
19	chr13:61987935-61987985	RPTEC	kidney:	n/a
20	chr13:61989203-61989253	AG09319	gingival:	n/a
21	chr13:61989475-61989525	AG10803	skin:	n/a
22	chr13:61989737-61989787	SK-N-MC	brain:	n/a
23	chr13:61989724-61989774	GM12892	blood:	n/a
24	chr13:61988910-61988960	Caco-2	colon:	n/a
25	chr13:61989859-61989909	HRE	kidney:	n/a
26	chr13:61988802-61988852	ProgFib	skin:	n/a
27	chr13:61990741-61990791	A549	lung:	n/a
28	chr13:61987935-61987985	NHBE	bronchial:	n/a
29	chr13:61989412-61989462	MCF10A-Er-Src	breast:	n/a
30	chr13:61989737-61989787	ProgFib	skin:	n/a
31	chr13:61988802-61988852	MCF-7	breast:	n/a
32	chr13:61989726-61989776	HCT-116	colon:	n/a
33	chr13:61989475-61989525	HEEpiC	esophagus:	n/a
34	chr13:61989037-61989087	HEK293	kidney:	embryo
35	chr13:61988153-61988203	SKMC	muscle:	n/a
36	chr13:61989412-61989462	NT2-D1	testis:	n/a
37	chr13:61989726-61989776	NHBE	bronchial:	n/a
38	chr13:61989412-61989462	PFSK-1	brain:	n/a
39	chr13:61987935-61987985	GM06990	blood:	n/a
40	chr13:61988153-61988203	PFSK-1	brain:	n/a
41	chr13:61989724-61989774	Hepatocyte	liver:	n/a
42	chr13:61990025-61990075	HEK293	kidney:	embryo
43	chr13:61989817-61989867	NH-A	brain:	n/a
44	chr13:61989724-61989774	AG04450	lung:	fetal
45	chr13:61989770-61989820	HEK293	kidney:	embryo
46	chr13:61989724-61989774	HL-60	blood:	n/a
47	chr13:61989597-61989647	HRCEpiC	kidney:	n/a
48	chr13:61989859-61989909	NHBE	bronchial:	n/a
49	chr13:61989737-61989787	LNCaP	prostate:	n/a
50	chr13:61988802-61988852	HRCEpiC	kidney:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:61200993..61201900-chr13:61984142..61985108,2	MCF-7	breast:
2	chr13:61980884..61982584-chr13:61984499..61986608,2	K562	blood:
3	chr13:61985804..61987884-chr13:62010090..62011843,2	K562	blood:
4	chr13:61984597..61985106-chr13:62259471..62259973,2	MCF-7	breast:
5	chr13:61200948..61201884-chr13:61984819..61985392,2	K562	blood:
6	chr13:61980884..61982584-chr13:61984499..61986608,2	K562	blood:
7	chr13:61860028..61861070-chr13:61984556..61985605,8	MCF-7	breast:

No data

Variant related genes	Relation type
PCDH20	TF binding region
PCDH20	CpG island

Extended variants
information (count: 590 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563709010	chr13:61980026-61980027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs180799606	chr13:61980053-61980054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572944718	chr13:61980094-61980095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540243196	chr13:61980100-61980101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564892374	chr13:61980104-61980105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533081981	chr13:61980105-61980106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545250456	chr13:61980106-61980107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533219048	chr13:61980133-61980134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546850874	chr13:61980167-61980168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147350788	chr13:61980193-61980194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113918721	chr13:61980213-61980214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117151153	chr13:61980230-61980231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567344320	chr13:61980339-61980340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554018658	chr13:61980342-61980343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs80230259	chr13:61980476-61980477	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs546621603	chr13:61980484-61980485	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs139483691	chr13:61980517-61980518	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs75338317	chr13:61980549-61980550	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs150057119	chr13:61980597-61980598	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs183892014	chr13:61980603-61980604	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs536845401	chr13:61980604-61980605	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs188351620	chr13:61980630-61980631	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs573007166	chr13:61980649-61980650	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs534004247	chr13:61980650-61980651	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs549219774	chr13:61980659-61980660	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs181130539	chr13:61980676-61980677	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs576808170	chr13:61980687-61980688	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs545001342	chr13:61980692-61980693	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs563594284	chr13:61980704-61980705	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs111737085	chr13:61980709-61980710	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs575388877	chr13:61980712-61980713	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs568924025	chr13:61980825-61980826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570727920	chr13:61980839-61980840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs17059755	chr13:61980843-61980844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs561018213	chr13:61980855-61980856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537947486	chr13:61980862-61980863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528216293	chr13:61980863-61980864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546703414	chr13:61980891-61980892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186361037	chr13:61980902-61980903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191834483	chr13:61980932-61980933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551032642	chr13:61980935-61980936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569545578	chr13:61980947-61980948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145415139	chr13:61980964-61980965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148762654	chr13:61981008-61981009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539633131	chr13:61981032-61981033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73484426	chr13:61981050-61981051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142405517	chr13:61981127-61981128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17059756	chr13:61981185-61981186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181888672	chr13:61981211-61981212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538227132	chr13:61981251-61981252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Esophageal squamous carcinoma	20200074	CNVD
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Bipolar disorder	19214233	CNVD
Prostate cancer	22341455	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61980000-61980400	Enhancers	Fetal Heart	heart
2	chr13:61980000-61980600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:61980400-61980800	Flanking Active TSS	Fetal Heart	heart
4	chr13:61980600-61984000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr13:61980800-61982200	Weak transcription	Fetal Heart	heart
6	chr13:61982000-61982600	Enhancers	Brain Germinal Matrix	brain
7	chr13:61982000-61984600	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr13:61982200-61983200	Enhancers	Fetal Heart	heart
9	chr13:61982600-61983000	Weak transcription	Brain Germinal Matrix	brain
10	chr13:61982800-61983200	Enhancers	Brain Anterior Caudate	brain
11	chr13:61983000-61983200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr13:61983000-61983200	Enhancers	Fetal Brain Female	brain
13	chr13:61983200-61983400	Enhancers	Brain Germinal Matrix	brain
14	chr13:61983200-61985200	Weak transcription	Fetal Heart	heart
15	chr13:61983200-61987400	Weak transcription	Brain Anterior Caudate	brain
16	chr13:61983800-61984800	Enhancers	Fetal Brain Male	brain
17	chr13:61984000-61984800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr13:61984200-61984400	Enhancers	Fetal Lung	lung
19	chr13:61984200-61984800	Enhancers	Fetal Kidney	kidney
20	chr13:61984400-61984600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr13:61984400-61984600	Enhancers	Brain Cingulate Gyrus	brain
22	chr13:61984400-61984600	Enhancers	Fetal Brain Female	brain
23	chr13:61984600-61984800	Enhancers	Brain Angular Gyrus	brain
24	chr13:61985200-61985600	Enhancers	Fetal Heart	heart
25	chr13:61985400-61985600	Enhancers	Aorta	Aorta
26	chr13:61985400-61987200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr13:61985600-61985800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr13:61985600-61985800	Flanking Active TSS	Fetal Heart	heart
29	chr13:61985600-61986000	Active TSS	Brain Angular Gyrus	brain
30	chr13:61985600-61987600	Weak transcription	Aorta	Aorta
31	chr13:61985800-61986200	Enhancers	Fetal Heart	heart
32	chr13:61985800-61987400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr13:61986200-61986400	Flanking Active TSS	Fetal Heart	heart
34	chr13:61986400-61986800	Enhancers	Fetal Heart	heart
35	chr13:61986800-61987600	Genic enhancers	Fetal Heart	heart
36	chr13:61987200-61987600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr13:61987200-61987800	Enhancers	Right Atrium	heart
38	chr13:61987200-61988000	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
39	chr13:61987200-61989000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
40	chr13:61987200-61990200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
41	chr13:61987200-61990200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
42	chr13:61987400-61987600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr13:61987400-61987600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr13:61987400-61987600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr13:61987400-61987600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr13:61987400-61987600	Flanking Bivalent TSS/Enh	Brain Angular Gyrus	brain
47	chr13:61987400-61987600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
48	chr13:61987400-61987600	Bivalent/Poised TSS	Brain Substantia Nigra	brain
49	chr13:61987400-61987600	Enhancers	Colon Smooth Muscle	Colon
50	chr13:61987400-61987600	Bivalent Enhancer	Fetal Lung	lung

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