Variant report

Variant	nsv830562
Chromosome Location	chr5:179555313-179622441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:427)
CpG islands
(count:2262)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:179601223-179601365	K562	blood:	n/a	n/a
2	ATF3	chr5:179563820-179563990	K562	blood:	n/a	n/a
3	BACH1	chr5:179561454-179561491	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr5:179601323-179601671	GM12878	blood:	n/a	n/a
5	BCL3	chr5:179601267-179601897	GM12878	blood:	n/a	chr5:179601663-179601676
6	BHLHE40	chr5:179604518-179604553	K562	blood:	n/a	n/a
7	BHLHE40	chr5:179601408-179601608	K562	blood:	n/a	n/a
8	BHLHE40	chr5:179569016-179569216	K562	blood:	n/a	chr5:179569061-179569082 chr5:179569068-179569077
9	BHLHE40	chr5:179563858-179564016	K562	blood:	n/a	n/a
10	BHLHE40	chr5:179600029-179600349	HepG2	liver:	n/a	n/a
11	CBX3	chr5:179563853-179564104	K562	blood:	n/a	n/a
12	CEBPB	chr5:179599936-179600312	HepG2	liver:	n/a	chr5:179600119-179600130
13	CEBPB	chr5:179583154-179583357	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:179599982-179600245	HepG2	liver:	n/a	chr5:179600119-179600130
15	CEBPB	chr5:179599930-179600309	HepG2	liver:	n/a	chr5:179600119-179600130
16	CEBPB	chr5:179604282-179604596	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:179600034-179600223	A549	lung:	n/a	chr5:179600119-179600130
18	CEBPB	chr5:179591922-179592067	A549	lung:	n/a	n/a
19	CEBPB	chr5:179599877-179600339	MCF-7	breast:	n/a	chr5:179600119-179600130
20	CEBPB	chr5:179599972-179600343	HepG2	liver:	n/a	chr5:179600119-179600130
21	CEBPB	chr5:179604308-179604523	HepG2	liver:	n/a	n/a
22	CEBPD	chr5:179599968-179600197	HepG2	liver:	n/a	n/a
23	CHD2	chr5:179604506-179604549	HepG2	liver:	n/a	n/a
24	CTCF	chr5:179589051-179589145	LNCaP	prostate:	n/a	n/a
25	CTCF	chr5:179589080-179589230	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr5:179589013-179589264	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:179589140-179589290	MCF-7	breast:	n/a	n/a
28	CTCF	chr5:179583173-179583324	Hela-S3	cervix:	n/a	chr5:179583211-179583224 chr5:179583260-179583269
29	CTCF	chr5:179588521-179588660	HepG2	liver:	n/a	n/a
30	CTCF	chr5:179589014-179589291	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr5:179560620-179560770	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:179556600-179556706	A549	lung:	n/a	n/a
33	CTCF	chr5:179589040-179589190	NB4	blood:	n/a	n/a
34	CTCF	chr5:179583140-179583290	Caco-2	colon:	n/a	chr5:179583211-179583224 chr5:179583260-179583269
35	CTCF	chr5:179583012-179583429	H1-hESC	embryonic stem cell:	n/a	chr5:179583211-179583224 chr5:179583260-179583269
36	CTCF	chr5:179583160-179583310	Caco-2	colon:	n/a	chr5:179583211-179583224 chr5:179583260-179583269
37	CTCF	chr5:179589123-179589131	ProgFib	skin:	n/a	n/a
38	CTCF	chr5:179561428-179561587	K562	blood:	n/a	chr5:179561463-179561481
39	CTCF	chr5:179589000-179589150	GM12875	blood:	n/a	n/a
40	CTCF	chr5:179599140-179599290	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr5:179588292-179589535	SK-N-SH	brain:	n/a	n/a
42	CTCF	chr5:179555400-179555442	Fibrobl	skin:	n/a	n/a
43	CTCF	chr5:179589020-179589264	K562	blood:	n/a	n/a
44	CTCF	chr5:179589040-179589190	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr5:179589080-179589230	AG04450	lung:	n/a	n/a
46	CTCF	chr5:179589080-179589230	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr5:179588520-179588670	Caco-2	colon:	n/a	n/a
48	CTCF	chr5:179555382-179555520	K562	blood:	n/a	n/a
49	CTCF	chr5:179561180-179561330	GM12866	blood:	n/a	n/a
50	CTCF	chr5:179588980-179589130	SAEC	small airway:	n/a	n/a

(count:2262 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179606623-179606673	GM06990	blood:	n/a
2	chr5:179564602-179564652	AG04450	lung:	fetal
3	chr5:179565362-179565412	ECC-1	luminal epithelium:	n/a
4	chr5:179597454-179597504	HEEpiC	esophagus:	n/a
5	chr5:179569548-179569598	NB4	blood:	n/a
6	chr5:179606623-179606673	GM06990	blood:	n/a
7	chr5:179564602-179564652	AG04450	lung:	fetal
8	chr5:179565362-179565412	ECC-1	luminal epithelium:	n/a
9	chr5:179597454-179597504	HEEpiC	esophagus:	n/a
10	chr5:179569548-179569598	NB4	blood:	n/a
11	chr5:179597454-179597504	A549	lung:	n/a
12	chr5:179588673-179588723	IMR90	lung:	fetal
13	chr5:179564602-179564652	NH-A	brain:	n/a
14	chr5:179621621-179621671	AG04450	lung:	fetal
15	chr5:179565544-179565594	SK-N-SH	brain:	n/a
16	chr5:179565362-179565412	GM06990	blood:	n/a
17	chr5:179588673-179588723	RPTEC	kidney:	n/a
18	chr5:179587950-179588000	IMR90	lung:	fetal
19	chr5:179569583-179569633	GM12892	blood:	n/a
20	chr5:179602982-179603032	GM12878	blood:	n/a
21	chr5:179597454-179597504	MCF-7	breast:	n/a
22	chr5:179569548-179569598	BE2_C	brain:	n/a
23	chr5:179563738-179563788	T-47D	breast:	n/a
24	chr5:179597454-179597504	NT2-D1	testis:	n/a
25	chr5:179597454-179597504	BE2_C	brain:	n/a
26	chr5:179564268-179564318	RPTEC	kidney:	n/a
27	chr5:179588838-179588888	SAEC	small airway:	n/a
28	chr5:179621162-179621212	SKMC	muscle:	n/a
29	chr5:179562118-179562168	AG04450	lung:	fetal
30	chr5:179597395-179597445	A549	lung:	n/a
31	chr5:179563896-179563946	HAEpiC	amniotic membrane:	n/a
32	chr5:179588440-179588490	HIPEpiC	eye:	n/a
33	chr5:179563866-179563916	NHDF-neo	bronchial:	n/a
34	chr5:179585198-179585248	MCF10A-Er-Src	breast:	n/a
35	chr5:179563738-179563788	GM12878	blood:	n/a
36	chr5:179588673-179588723	GM06990	blood:	n/a
37	chr5:179569583-179569633	ProgFib	skin:	n/a
38	chr5:179563839-179563889	GM12892	blood:	n/a
39	chr5:179569548-179569598	ECC-1	luminal epithelium:	n/a
40	chr5:179569548-179569598	GM06990	blood:	n/a
41	chr5:179597395-179597445	HCPEpiC	choroid plexus:	n/a
42	chr5:179588673-179588723	SK-N-SH_RA	brain:	n/a
43	chr5:179588440-179588490	MCF10A-Er-Src	breast:	n/a
44	chr5:179602982-179603032	HCM	heart:	n/a
45	chr5:179588551-179588601	BJ	skin:	n/a
46	chr5:179569583-179569633	HEEpiC	esophagus:	n/a
47	chr5:179588838-179588888	PANC-1	pancreas:	n/a
48	chr5:179569548-179569598	GM19239	blood:	n/a
49	chr5:179587950-179588000	MCF10A-Er-Src	breast:	n/a
50	chr5:179621621-179621671	HNPCEpiC	eye:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179598097..179600752-chr5:179603179..179605823,2	K562	blood:
2	chr5:179560653..179562263-chr5:179716326..179719288,2	MCF-7	breast:
3	chr5:179598082..179600622-chr5:179601152..179603406,2	K562	blood:
4	chr5:179562265..179564254-chr5:179568163..179570454,2	K562	blood:
5	chr5:179556597..179557163-chr5:179565658..179566414,2	MCF-7	breast:
6	chr5:179558293..179560674-chr5:179562402..179565370,2	MCF-7	breast:
7	chr5:179594862..179596612-chr5:179598475..179600165,2	MCF-7	breast:
8	chr5:179551929..179554732-chr5:179557989..179560690,2	K562	blood:
9	chr5:179556597..179557163-chr5:179565658..179566414,2	MCF-7	breast:
10	chr5:179598097..179600752-chr5:179603179..179605823,2	K562	blood:
11	chr5:179555641..179558112-chr5:179558686..179561172,2	K562	blood:
12	chr5:179546334..179548220-chr5:179553814..179555869,2	MCF-7	breast:
13	chr5:179588724..179589352-chr5:179627753..179628617,2	MCF-7	breast:
14	chr5:179554536..179556521-chr5:179716236..179718994,2	MCF-7	breast:
15	chr5:179598082..179600622-chr5:179601152..179603406,2	K562	blood:
16	chr5:179601654..179603372-chr5:179739320..179741770,2	MCF-7	breast:
17	chr5:179568439..179571185-chr5:179571573..179574464,2	K562	blood:
18	chr5:179551435..179553864-chr5:179559199..179562159,2	K562	blood:
19	chr5:179565014..179567523-chr5:179570668..179572800,2	K562	blood:
20	chr5:179561122..179566111-chr5:179566279..179570642,6	MCF-7	breast:
21	chr5:179568439..179571185-chr5:179571573..179574464,2	K562	blood:
22	chr5:179553164..179556296-chr5:179740039..179742529,3	MCF-7	breast:
23	chr5:179603344..179605727-chr5:179894143..179896109,2	K562	blood:
24	chr5:179616220..179617824-chr5:179714865..179717440,2	MCF-7	breast:
25	chr5:179594862..179596612-chr5:179598475..179600165,2	MCF-7	breast:
26	chr5:179555641..179558112-chr5:179558686..179561172,2	K562	blood:
27	chr5:179546163..179549028-chr5:179553453..179555820,2	K562	blood:

No data

Variant related genes	Relation type
RASGEF1C	TF binding region
RASGEF1C	CpG island
ENSG00000050748	chromatin interactions
ENSG00000146090	chromatin interactions

Extended variants
information (count: 2791 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2791 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552586858	chr5:179555331-179555332	Active TSS Enhancers Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs571050738	chr5:179555340-179555341	Active TSS Enhancers Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538036673	chr5:179555357-179555358	Active TSS Enhancers Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201059437	chr5:179555367-179555368	Active TSS Enhancers Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370615313	chr5:179555377-179555378	Active TSS Enhancers Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375796499	chr5:179555389-179555390	Active TSS Enhancers Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368232404	chr5:179555402-179555403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184111969	chr5:179555403-179555404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs13354066	chr5:179555407-179555408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs553759260	chr5:179555418-179555419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs368535017	chr5:179555419-179555420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371799192	chr5:179555483-179555484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200583000	chr5:179555509-179555510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374919030	chr5:179555515-179555516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150580442	chr5:179555521-179555522	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539767479	chr5:179555549-179555550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs199522302	chr5:179555557-179555558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188445387	chr5:179555604-179555605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371588039	chr5:179555631-179555632	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375231921	chr5:179555639-179555640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs57188777	chr5:179555652-179555653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs6895192	chr5:179555654-179555655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs368641728	chr5:179555718-179555719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561837434	chr5:179555746-179555747	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs573786115	chr5:179555755-179555756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375251612	chr5:179555870-179555871	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559434041	chr5:179555891-179555892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs13172734	chr5:179555900-179555901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573002515	chr5:179555918-179555919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs552866997	chr5:179555971-179555972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs544797558	chr5:179556004-179556005	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564639397	chr5:179556029-179556030	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546676181	chr5:179556045-179556046	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs532001623	chr5:179556059-179556060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549962317	chr5:179556082-179556083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs115749035	chr5:179556122-179556123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs200871270	chr5:179556152-179556153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs575755960	chr5:179556178-179556179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568274340	chr5:179556179-179556180	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535593332	chr5:179556213-179556214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547480917	chr5:179556222-179556223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75819605	chr5:179556260-179556261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539435599	chr5:179556277-179556278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191415692	chr5:179556303-179556304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576281030	chr5:179556339-179556340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs11249670	chr5:179556352-179556353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs117201959	chr5:179556434-179556435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573873702	chr5:179556447-179556448	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541176014	chr5:179556470-179556471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184929424	chr5:179556510-179556511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	20808228	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179548000-179558800	Weak transcription	Fetal Brain Female	brain
2	chr5:179553800-179556800	Enhancers	Brain Cingulate Gyrus	brain
3	chr5:179554000-179555800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:179554000-179556800	Enhancers	Brain Anterior Caudate	brain
5	chr5:179554000-179557000	Enhancers	Brain Hippocampus Middle	brain
6	chr5:179554000-179557000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr5:179554000-179557200	Enhancers	Brain Substantia Nigra	brain
8	chr5:179554600-179556800	Enhancers	Brain Angular Gyrus	brain
9	chr5:179554600-179557600	Enhancers	Fetal Muscle Leg	muscle
10	chr5:179554800-179555400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:179554800-179557200	Enhancers	Fetal Muscle Trunk	muscle
12	chr5:179554800-179557800	Weak transcription	Fetal Brain Male	brain
13	chr5:179555000-179555400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:179555000-179555600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr5:179555400-179556800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:179555400-179560800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr5:179555400-179571000	Weak transcription	Right Atrium	heart
18	chr5:179555600-179557000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr5:179556400-179556600	Enhancers	Placenta	Placenta
20	chr5:179556600-179556800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr5:179556800-179557000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr5:179556800-179560000	Weak transcription	Placenta	Placenta
23	chr5:179556800-179562400	Weak transcription	Brain Cingulate Gyrus	brain
24	chr5:179556800-179566600	Weak transcription	Brain Angular Gyrus	brain
25	chr5:179557000-179557200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:179557000-179562000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr5:179557000-179562200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr5:179557200-179562000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:179557800-179560200	Enhancers	Fetal Brain Male	brain
30	chr5:179558800-179559000	Enhancers	Fetal Brain Female	brain
31	chr5:179559000-179559400	Weak transcription	Fetal Brain Female	brain
32	chr5:179559000-179560200	Enhancers	Fetal Muscle Leg	muscle
33	chr5:179559000-179560400	Bivalent Enhancer	Fetal Stomach	stomach
34	chr5:179559200-179559600	Enhancers	Stomach Smooth Muscle	stomach
35	chr5:179559200-179560400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr5:179559400-179559600	Enhancers	Fetal Brain Female	brain
37	chr5:179559600-179565800	Weak transcription	Fetal Brain Female	brain
38	chr5:179560000-179561400	Enhancers	Placenta	Placenta
39	chr5:179560800-179561200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr5:179561200-179562200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr5:179561800-179562200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:179561800-179562800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr5:179561800-179563000	Enhancers	Osteobl	bone
44	chr5:179561800-179563200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr5:179561800-179563200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr5:179562000-179562200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:179562000-179562400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr5:179562000-179562600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr5:179562000-179562600	Enhancers	Primary hematopoietic stem cells	blood
50	chr5:179562000-179562600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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