Variant report

Variant	nsv826646
Chromosome Location	chr13:54355102-54423461
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	BHLHE40	chr13:54356605-54356862	GM12878	blood:	n/a	n/a
2	CEBPB	chr13:54356658-54356771	HepG2	liver:	n/a	n/a
3	CEBPB	chr13:54356591-54356893	K562	blood:	n/a	n/a
4	CEBPB	chr13:54361120-54361404	HepG2	liver:	n/a	chr13:54361258-54361269
5	CEBPB	chr13:54356561-54356901	HepG2	liver:	n/a	n/a
6	CEBPB	chr13:54356551-54356967	ECC-1	luminal epithelium:	n/a	chr13:54356928-54356936
7	CEBPB	chr13:54356576-54356912	IMR90	lung:	n/a	n/a
8	CEBPB	chr13:54356622-54356826	A549	lung:	n/a	n/a
9	CEBPB	chr13:54356561-54356898	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr13:54356588-54356906	A549	lung:	n/a	n/a
11	CEBPB	chr13:54356549-54356924	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr13:54376269-54376545	HepG2	liver:	n/a	chr13:54376521-54376534 chr13:54376318-54376331
13	CEBPB	chr13:54404485-54404673	HepG2	liver:	n/a	chr13:54404618-54404629
14	CEBPB	chr13:54356619-54356839	MCF-7	breast:	n/a	n/a
15	CTCF	chr13:54356600-54356750	HFF-Myc	foreskin:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
16	CTCF	chr13:54356640-54356790	HMF	breast:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
17	CTCF	chr13:54357000-54357049	GM12892	blood:	n/a	n/a
18	CTCF	chr13:54356575-54356892	HUVEC	blood vessel:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
19	CTCF	chr13:54356640-54356790	BJ	skin:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
20	CTCF	chr13:54356980-54357130	GM12874	blood:	n/a	n/a
21	CTCF	chr13:54356649-54356830	SK-N-SH_RA	brain:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
22	CTCF	chr13:54356660-54356810	HMEC	breast:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
23	CTCF	chr13:54356640-54356790	GM06990	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
24	CTCF	chr13:54356495-54356859	ECC-1	luminal epithelium:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
25	CTCF	chr13:54356670-54356839	GM19238	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
26	CTCF	chr13:54356660-54356810	GM12866	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
27	CTCF	chr13:54356600-54356750	HA-sp	spinal cord:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
28	CTCF	chr13:54356698-54356782	H1-hESC	embryonic stem cell:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
29	CTCF	chr13:54356690-54356808	GM12892	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
30	CTCF	chr13:54356660-54356810	GM12867	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
31	CTCF	chr13:54356200-54356350	BE2_C	brain:	n/a	chr13:54356250-54356266
32	CTCF	chr13:54356603-54356852	MCF-7	breast:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
33	CTCF	chr13:54356588-54356865	Lung_OC	lung:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
34	CTCF	chr13:54356240-54356390	GM06990	blood:	n/a	chr13:54356250-54356266
35	CTCF	chr13:54356534-54356897	K562	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
36	CTCF	chr13:54356340-54356490	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr13:54356660-54356810	GM12871	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
38	CTCF	chr13:54356026-54356986	MCF-7	breast:	n/a	chr13:54356716-54356737 chr13:54356250-54356266 chr13:54356714-54356732 chr13:54356715-54356731
39	CTCF	chr13:54356232-54356325	Gliobla	brain:	n/a	chr13:54356250-54356266
40	CTCF	chr13:54356660-54356810	AG04450	lung:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
41	CTCF	chr13:54356640-54356790	AoAF	blood vessel:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
42	CTCF	chr13:54356602-54356838	Pancreas_OC	pancreas:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
43	CTCF	chr13:54356680-54356830	GM12870	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
44	CTCF	chr13:54356660-54356810	HMF	breast:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
45	CTCF	chr13:54356600-54356750	GM12875	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
46	CTCF	chr13:54357787-54357917	MCF-7	breast:	n/a	n/a
47	CTCF	chr13:54356662-54356828	NHEK	skin:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
48	CTCF	chr13:54362480-54362630	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr13:54356465-54356915	HepG2	liver:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
50	CTCF	chr13:54356470-54356905	T-47D	breast:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:54422912-54422962	BJ	skin:	n/a
2	chr13:54422912-54422962	U87	brain:	n/a
3	chr13:54362844-54362894	MCF10A-Er-Src	breast:	n/a
4	chr13:54362844-54362894	BE2_C	brain:	n/a
5	chr13:54422912-54422962	SKMC	muscle:	n/a
6	chr13:54422912-54422962	GM06990	blood:	n/a
7	chr13:54422912-54422962	IMR90	lung:	fetal
8	chr13:54422912-54422962	HCPEpiC	choroid plexus:	n/a
9	chr13:54362844-54362894	LNCaP	prostate:	n/a
10	chr13:54422912-54422962	Caco-2	colon:	n/a
11	chr13:54422912-54422962	PFSK-1	brain:	n/a
12	chr13:54422912-54422962	HIPEpiC	eye:	n/a
13	chr13:54422912-54422962	HMEC	breast:	n/a
14	chr13:54362844-54362894	AG10803	skin:	n/a
15	chr13:54422912-54422962	HEK293	kidney:	embryo
16	chr13:54362844-54362894	A549	lung:	n/a
17	chr13:54422912-54422962	K562	blood:	n/a
18	chr13:54362844-54362894	PrEC	prostate:	n/a
19	chr13:54362844-54362894	HPAEpiC	pulmonary alveolar:	n/a
20	chr13:54422912-54422962	HPAEpiC	pulmonary alveolar:	n/a
21	chr13:54422912-54422962	HCF	heart:	n/a
22	chr13:54422912-54422962	SK-N-SH_RA	brain:	n/a
23	chr13:54362844-54362894	HUVEC	blood vessel:	n/a
24	chr13:54422912-54422962	Hepatocyte	liver:	n/a
25	chr13:54422912-54422962	SK-N-MC	brain:	n/a
26	chr13:54422912-54422962	AG09309	skin:	n/a
27	chr13:54362844-54362894	HL-60	blood:	n/a
28	chr13:54362844-54362894	CMK	blood:	n/a
29	chr13:54362844-54362894	Caco-2	colon:	n/a
30	chr13:54422912-54422962	AG04449	skin:	fetal
31	chr13:54422912-54422962	GM12891	blood:	n/a
32	chr13:54422912-54422962	GM12892	blood:	n/a
33	chr13:54422912-54422962	AG09319	gingival:	n/a
34	chr13:54362844-54362894	Hepatocyte	liver:	n/a
35	chr13:54362844-54362894	HRPEpiC	eye:	n/a
36	chr13:54422912-54422962	GM19239	blood:	n/a
37	chr13:54362844-54362894	MCF-7	breast:	n/a
38	chr13:54362844-54362894	Hela-S3	cervix:	n/a
39	chr13:54422912-54422962	LNCaP	prostate:	n/a
40	chr13:54362844-54362894	GM12878	blood:	n/a
41	chr13:54422912-54422962	HRPEpiC	eye:	n/a
42	chr13:54362844-54362894	AG04450	lung:	fetal
43	chr13:54422912-54422962	PANC-1	pancreas:	n/a
44	chr13:54362844-54362894	BJ	skin:	n/a
45	chr13:54362844-54362894	NH-A	brain:	n/a
46	chr13:54422912-54422962	NH-A	brain:	n/a
47	chr13:54362844-54362894	HCT-116	colon:	n/a
48	chr13:54422912-54422962	ECC-1	luminal epithelium:	n/a
49	chr13:54362844-54362894	HAEpiC	amniotic membrane:	n/a
50	chr13:54362844-54362894	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:53824183..53825128-chr13:54355772..54356571,3	MCF-7	breast:
2	chr13:54411879..54413790-chr13:54440349..54442010,2	K562	blood:
3	chr13:53824070..53825129-chr13:54355995..54357044,7	MCF-7	breast:
4	chr13:54359558..54362515-chr13:54378341..54380305,2	MCF-7	breast:
5	chr13:54359558..54362515-chr13:54378341..54380305,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM4-3	chr13:54414818-54414945	ENSG00000261517.1
2	lnc-OLFM4-3	chr13:54389554-54389628	ENSG00000261517.1
3	lnc-OLFM4-3	chr13:54418480-54418657	ENSG00000261517.1
4	lnc-OLFM4-3	chr13:54412874-54412924	ENSG00000261517.1

Variant related genes	Relation type
LINC00558	TF binding region
LINC00558	CpG island

Extended variants
information (count: 771 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533218249	chr13:54355113-54355114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187953307	chr13:54355120-54355121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1350457	chr13:54355150-54355151	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs531379460	chr13:54355241-54355242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1350458	chr13:54355270-54355271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191142968	chr13:54355323-54355324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1350459	chr13:54355328-54355329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141448728	chr13:54355379-54355380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184023665	chr13:54355417-54355418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557693322	chr13:54355424-54355425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188362637	chr13:54355467-54355468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540894371	chr13:54355504-54355505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554148762	chr13:54355541-54355542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192290647	chr13:54355565-54355566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185251743	chr13:54355570-54355571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552396356	chr13:54355583-54355584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs9568921	chr13:54355589-54355590	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs531649084	chr13:54355592-54355593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs138118244	chr13:54355621-54355622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531890819	chr13:54355625-54355626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550026925	chr13:54355678-54355679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141351752	chr13:54355684-54355685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190531205	chr13:54355686-54355687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78108574	chr13:54355692-54355693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563290317	chr13:54355719-54355720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547801776	chr13:54355730-54355731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182303451	chr13:54355740-54355741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115694414	chr13:54355761-54355762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549152175	chr13:54355816-54355817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569082058	chr13:54355817-54355818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537906916	chr13:54355827-54355828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557590497	chr13:54355892-54355893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571348873	chr13:54355911-54355912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533539496	chr13:54355944-54355945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553774165	chr13:54355958-54355959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553862912	chr13:54356005-54356006	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573993678	chr13:54356009-54356010	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542919528	chr13:54356030-54356031	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547913928	chr13:54356037-54356038	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs367642985	chr13:54356061-54356062	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556299738	chr13:54356099-54356100	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187089203	chr13:54356100-54356101	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149653108	chr13:54356150-54356151	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189528080	chr13:54356198-54356199	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527823187	chr13:54356253-54356254	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs541062838	chr13:54356260-54356261	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs180671573	chr13:54356307-54356308	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs567803253	chr13:54356345-54356346	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs532147889	chr13:54356458-54356459	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185873115	chr13:54356477-54356478	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
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
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
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
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	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
Urothelial carcinoma	21177765	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54352600-54356000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:54353200-54356800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:54355400-54356200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:54355600-54355800	Enhancers	Fetal Brain Male	brain
5	chr13:54355600-54356200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:54355600-54356200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr13:54355600-54356400	Enhancers	Fetal Heart	heart
8	chr13:54355600-54356800	Enhancers	Fetal Brain Female	brain
9	chr13:54355800-54356000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr13:54355800-54356200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr13:54355800-54356200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr13:54355800-54356200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr13:54355800-54356800	Weak transcription	Fetal Brain Male	brain
14	chr13:54356000-54356200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr13:54356000-54356400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:54356000-54356800	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr13:54356000-54358800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr13:54356200-54356400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:54356200-54356400	Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr13:54356200-54356600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr13:54356200-54356600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr13:54356200-54356600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr13:54356200-54356600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr13:54356200-54356600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr13:54356200-54356600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
26	chr13:54356200-54356600	Active TSS	Fetal Muscle Leg	muscle
27	chr13:54356200-54356800	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr13:54356200-54356800	Enhancers	Fetal Lung	lung
29	chr13:54356200-54357000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr13:54356200-54357200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr13:54356400-54356600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr13:54356400-54356600	Flanking Active TSS	Fetal Heart	heart
33	chr13:54356400-54356800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr13:54356400-54356800	Active TSS	Fetal Kidney	kidney
35	chr13:54356400-54357200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr13:54356600-54356800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr13:54356600-54356800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr13:54356600-54356800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr13:54356600-54356800	Active TSS	Adipose Nuclei	Adipose
40	chr13:54356600-54356800	Enhancers	Brain Anterior Caudate	brain
41	chr13:54356600-54356800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr13:54356600-54356800	Enhancers	Colon Smooth Muscle	Colon
43	chr13:54356600-54356800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr13:54356600-54356800	Enhancers	Fetal Heart	heart
45	chr13:54356600-54356800	Enhancers	Fetal Muscle Leg	muscle
46	chr13:54356600-54356800	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr13:54356600-54357000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr13:54356600-54357000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr13:54356600-54357000	Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr13:54356600-54357200	Enhancers	HUES64 Cell Line	embryonic stem cell

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