Variant report

Variant	nsv883217
Chromosome Location	chr5:178099758-178193081
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:949)
CpG islands
(count:980)
Chromatin interactive
region (count:34)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:949 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178157633-178157957	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178110831-178111247	K562	blood:	n/a	n/a
3	ARID3A	chr5:178157786-178157877	K562	blood:	n/a	n/a
4	ATF1	chr5:178144690-178144749	K562	blood:	n/a	n/a
5	ATF1	chr5:178157668-178158241	K562	blood:	n/a	n/a
6	ATF1	chr5:178110850-178111124	K562	blood:	n/a	n/a
7	ATF2	chr5:178157616-178158016	GM12878	blood:	n/a	n/a
8	ATF3	chr5:178157635-178157861	GM12878	blood:	n/a	n/a
9	ATF3	chr5:178157537-178157936	K562	blood:	n/a	n/a
10	ATF3	chr5:178157671-178158035	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr5:178157554-178157898	HepG2	liver:	n/a	n/a
12	BACH1	chr5:178157309-178157437	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr5:178157607-178157972	GM12878	blood:	n/a	n/a
14	BCLAF1	chr5:178157439-178158032	GM12878	blood:	n/a	chr5:178157688-178157701 chr5:178157489-178157502 chr5:178157641-178157650 chr5:178157728-178157741
15	BCLAF1	chr5:178157395-178157998	GM12878	blood:	n/a	chr5:178157397-178157410 chr5:178157688-178157701 chr5:178157489-178157502 chr5:178157396-178157409 chr5:178157641-178157650 chr5:178157728-178157741
16	BHLHE40	chr5:178113315-178113354	K562	blood:	n/a	n/a
17	BHLHE40	chr5:178157347-178158015	GM12878	blood:	n/a	chr5:178157492-178157508 chr5:178157481-178157497 chr5:178157714-178157730
18	BHLHE40	chr5:178157553-178158038	K562	blood:	n/a	chr5:178157714-178157730
19	BHLHE40	chr5:178157604-178157987	HepG2	liver:	n/a	chr5:178157714-178157730
20	BRCA1	chr5:178157848-178157930	HepG2	liver:	n/a	n/a
21	BRCA1	chr5:178157660-178158042	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr5:178157542-178158014	K562	blood:	n/a	n/a
23	CBX3	chr5:178157429-178158086	HCT-116	colon:	n/a	n/a
24	CCNT2	chr5:178110768-178111204	K562	blood:	n/a	n/a
25	CCNT2	chr5:178157173-178157918	K562	blood:	n/a	chr5:178157712-178157721
26	CCNT2	chr5:178105126-178105232	K562	blood:	n/a	n/a
27	CEBPB	chr5:178110910-178111199	K562	blood:	n/a	n/a
28	CEBPB	chr5:178146340-178146571	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:178166821-178166835	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:178157795-178157995	K562	blood:	n/a	n/a
31	CEBPB	chr5:178157864-178157885	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:178129077-178129365	HepG2	liver:	n/a	chr5:178129231-178129242 chr5:178129230-178129243
33	CEBPB	chr5:178157548-178158121	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr5:178110786-178111163	K562	blood:	n/a	n/a
35	CEBPB	chr5:178117100-178117303	A549	lung:	n/a	chr5:178117211-178117222
36	CEBPB	chr5:178129092-178129318	K562	blood:	n/a	chr5:178129231-178129242 chr5:178129230-178129243
37	CEBPB	chr5:178117070-178117383	K562	blood:	n/a	chr5:178117211-178117222
38	CEBPB	chr5:178104526-178104750	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:178117156-178117377	HepG2	liver:	n/a	chr5:178117211-178117222
40	CEBPB	chr5:178133629-178133887	HepG2	liver:	n/a	chr5:178133746-178133757
41	CEBPD	chr5:178110778-178111152	K562	blood:	n/a	n/a
42	CEBPD	chr5:178110743-178111261	K562	blood:	n/a	n/a
43	CHD1	chr5:178157084-178158135	IMR90	lung:	n/a	n/a
44	CHD2	chr5:178157572-178157974	HepG2	liver:	n/a	n/a
45	CHD2	chr5:178157579-178157987	K562	blood:	n/a	n/a
46	CHD2	chr5:178157266-178157974	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr5:178157575-178157991	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr5:178157467-178157960	GM12878	blood:	n/a	n/a
49	CREB1	chr5:178157435-178158010	A549	lung:	n/a	n/a
50	CREB1	chr5:178157561-178158107	H1-hESC	embryonic stem cell:	n/a	n/a

(count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178157801-178157851	HEEpiC	esophagus:	n/a
2	chr5:178157956-178158006	T-47D	breast:	n/a
3	chr5:178153430-178153480	SK-N-MC	brain:	n/a
4	chr5:178157346-178157396	NHDF-neo	bronchial:	n/a
5	chr5:178157801-178157851	HEEpiC	esophagus:	n/a
6	chr5:178157956-178158006	T-47D	breast:	n/a
7	chr5:178153430-178153480	SK-N-MC	brain:	n/a
8	chr5:178157346-178157396	NHDF-neo	bronchial:	n/a
9	chr5:178157550-178157600	GM12891	blood:	n/a
10	chr5:178157809-178157859	Hela-S3	cervix:	n/a
11	chr5:178157346-178157396	AG09319	gingival:	n/a
12	chr5:178160252-178160302	HUVEC	blood vessel:	n/a
13	chr5:178157518-178157568	HRPEpiC	eye:	n/a
14	chr5:178157792-178157842	ovcar-3	ovarian:	n/a
15	chr5:178157550-178157600	HCT-116	colon:	n/a
16	chr5:178157962-178158012	RPTEC	kidney:	n/a
17	chr5:178157772-178157822	ovcar-3	ovarian:	n/a
18	chr5:178158086-178158136	NHBE	bronchial:	n/a
19	chr5:178138736-178138786	Hepatocyte	liver:	n/a
20	chr5:178157518-178157568	GM12878	blood:	n/a
21	chr5:178158086-178158136	NH-A	brain:	n/a
22	chr5:178157792-178157842	IMR90	lung:	fetal
23	chr5:178157962-178158012	CMK	blood:	n/a
24	chr5:178157346-178157396	HL-60	blood:	n/a
25	chr5:178157518-178157568	RPTEC	kidney:	n/a
26	chr5:178158086-178158136	SK-N-SH	brain:	n/a
27	chr5:178153430-178153480	ECC-1	luminal epithelium:	n/a
28	chr5:178157346-178157396	IMR90	lung:	fetal
29	chr5:178157801-178157851	HNPCEpiC	eye:	n/a
30	chr5:178157809-178157859	BJ	skin:	n/a
31	chr5:178156304-178156354	ECC-1	luminal epithelium:	n/a
32	chr5:178160252-178160302	PANC-1	pancreas:	n/a
33	chr5:178157962-178158012	AG09309	skin:	n/a
34	chr5:178155817-178155867	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:178160252-178160302	RPTEC	kidney:	n/a
36	chr5:178157518-178157568	HEK293	kidney:	embryo
37	chr5:178138736-178138786	CMK	blood:	n/a
38	chr5:178157772-178157822	BE2_C	brain:	n/a
39	chr5:178157792-178157842	PFSK-1	brain:	n/a
40	chr5:178156304-178156354	BE2_C	brain:	n/a
41	chr5:178157550-178157600	HRE	kidney:	n/a
42	chr5:178157825-178157875	CMK	blood:	n/a
43	chr5:178157825-178157875	HEK293	kidney:	embryo
44	chr5:178157550-178157600	GM12878	blood:	n/a
45	chr5:178158086-178158136	HRCEpiC	kidney:	n/a
46	chr5:178157346-178157396	GM12892	blood:	n/a
47	chr5:178138736-178138786	GM12892	blood:	n/a
48	chr5:178155817-178155867	HMEC	breast:	n/a
49	chr5:178157801-178157851	AoSMC	blood vessel:	n/a
50	chr5:178160252-178160302	HL-60	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178135058..178137507-chr5:178144599..178147677,3	MCF-7	breast:
2	chr5:178189340..178191048-chr5:178195069..178197316,2	MCF-7	breast:
3	chr5:170259431..170263893-chr5:178180791..178183224,3	MCF-7	breast:
4	chr5:178154460..178156007-chr5:178156141..178157886,2	MCF-7	breast:
5	chr5:178124799..178126399-chr5:178156119..178159054,2	MCF-7	breast:
6	chr5:178042530..178044673-chr5:178156858..178158969,2	MCF-7	breast:
7	chr5:178152814..178155589-chr5:178155933..178157780,2	MCF-7	breast:
8	chr5:178049762..178051706-chr5:178156637..178158195,2	MCF-7	breast:
9	chr5:178135141..178137270-chr5:178138560..178140664,2	K562	blood:
10	chr5:178119500..178121494-chr5:178122164..178124985,2	MCF-7	breast:
11	chr5:178103410..178105385-chr5:178107182..178109270,2	MCF-7	breast:
12	chr5:178103410..178105385-chr5:178107182..178109270,2	MCF-7	breast:
13	chr5:178144858..178146405-chr5:178152270..178154350,2	MCF-7	breast:
14	chr5:178140402..178144156-chr5:178146582..178150587,3	MCF-7	breast:
15	chr5:178051446..178054153-chr5:178157357..178158910,2	MCF-7	breast:
16	chr5:178154802..178159439-chr5:178284936..178288781,7	MCF-7	breast:
17	chr5:178119500..178121494-chr5:178122164..178124985,2	MCF-7	breast:
18	chr5:178130386..178132471-chr5:178136423..178139272,2	K562	blood:
19	chr5:178156014..178158845-chr5:178285994..178289826,5	MCF-7	breast:
20	chr5:177663150..177665160-chr5:178157825..178159335,2	MCF-7	breast:
21	chr5:178130386..178132471-chr5:178136423..178139272,2	K562	blood:
22	chr5:178135141..178137270-chr5:178138560..178140664,2	K562	blood:
23	chr5:178145453..178147162-chr5:178151776..178154712,2	MCF-7	breast:
24	chr5:178135058..178137507-chr5:178144599..178147677,3	MCF-7	breast:
25	chr5:178152146..178155385-chr5:178293103..178294784,3	MCF-7	breast:
26	chr5:178144858..178146405-chr5:178152270..178154350,2	MCF-7	breast:
27	chr5:178097922..178100302-chr5:178156074..178157784,2	MCF-7	breast:
28	chr5:178052822..178055819-chr5:178156143..178158096,2	MCF-7	breast:
29	chr5:178140402..178144156-chr5:178146582..178150587,3	MCF-7	breast:
30	chr5:178145453..178147162-chr5:178151776..178154712,2	MCF-7	breast:
31	chr5:178157243..178158078-chr5:178286943..178287443,2	MCF-7	breast:
32	chr5:178056292..178058896-chr5:178156268..178158313,2	MCF-7	breast:
33	chr5:178157230..178157844-chr5:178286636..178287441,3	MCF-7	breast:
34	chr5:178135337..178138008-chr5:178419462..178422313,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF354A-1	chr5:178123098-178123182	XLOC_005102
2	lnc-ZNF354A-1	chr5:178124587-178124696	XLOC_005102
3	lnc-ZNF354A-3	chr5:178181044-178181218	NONHSAT105547
4	lnc-ZNF354A-2	chr5:178178077-178178301	NONHSAT105546
5	lnc-ZNF354A-2	chr5:178176203-178176293	NONHSAT105546
6	lnc-ZNF354A-3	chr5:178178352-178178894	NONHSAT105547
7	lnc-ZNF354A-1	chr5:178121721-178121948	XLOC_005102
8	lnc-ZNF354A-1	chr5:178133940-178134039	XLOC_005102
9	lnc-ZNF354A-1	chr5:178122288-178122599	XLOC_005102

No data

Variant related genes	Relation type
ZNF354A	TF binding region
ZNF354A	CpG island
ENSG00000113240	chromatin interactions
ENSG00000178338	chromatin interactions
ENSG00000169131	chromatin interactions
ENSG00000113262	chromatin interactions

Extended variants
information (count: 4163 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:4163 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11739297	chr5:178099758-178099759	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs386695479	chr5:178099770-178099771	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs6885081	chr5:178099771-178099772	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs570466708	chr5:178099786-178099787	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs6889262	chr5:178099806-178099807	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs184185470	chr5:178099809-178099810	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs12187838	chr5:178099833-178099834	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs72810671	chr5:178099851-178099852	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs553554431	chr5:178099888-178099889	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531567625	chr5:178099901-178099902	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565700245	chr5:178099907-178099908	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs151081344	chr5:178099908-178099909	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139920275	chr5:178099947-178099948	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577198828	chr5:178100039-178100040	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559671626	chr5:178100135-178100136	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556561065	chr5:178100154-178100155	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs6889811	chr5:178100162-178100163	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs568584771	chr5:178100197-178100198	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs575229784	chr5:178100243-178100244	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs72810672	chr5:178100294-178100295	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs560747197	chr5:178100317-178100318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572538055	chr5:178100397-178100398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11740168	chr5:178100442-178100443	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs368759567	chr5:178100443-178100444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573837903	chr5:178100452-178100453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539769155	chr5:178100485-178100486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188170364	chr5:178100492-178100493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549389117	chr5:178100499-178100500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372399367	chr5:178100501-178100502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375826600	chr5:178100539-178100540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529160032	chr5:178100579-178100580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547368016	chr5:178100607-178100608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180913272	chr5:178100621-178100622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369126626	chr5:178100660-178100661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72810673	chr5:178100686-178100687	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs371334114	chr5:178100695-178100696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570971392	chr5:178100721-178100722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147601532	chr5:178100724-178100725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556597926	chr5:178100725-178100726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142072089	chr5:178100729-178100730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116018602	chr5:178100730-178100731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536089065	chr5:178100737-178100738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555680642	chr5:178100738-178100739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116331018	chr5:178100740-178100741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114639187	chr5:178100767-178100768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147638133	chr5:178100780-178100781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368913042	chr5:178100781-178100782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564675398	chr5:178100797-178100798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575736845	chr5:178100818-178100819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187331856	chr5:178100827-178100828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Thoracic aortic aneurysm	21092924	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
small cell lung cancer	20016488	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
Breast cancer	21990379	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178095000-178101000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:178098400-178101400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr5:178099800-178102200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:178101000-178101200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:178101000-178101200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:178101000-178101200	Enhancers	Fetal Muscle Leg	muscle
7	chr5:178101200-178102000	Enhancers	Placenta	Placenta
8	chr5:178101200-178102600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:178101400-178101600	Enhancers	HMEC	breast
10	chr5:178101400-178103400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr5:178101600-178103000	Weak transcription	HMEC	breast
12	chr5:178102400-178102600	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr5:178102600-178103800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:178102600-178104000	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr5:178103000-178103600	Enhancers	HMEC	breast
16	chr5:178103400-178103800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:178103400-178104000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr5:178104000-178104400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr5:178104000-178104600	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr5:178104200-178105400	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr5:178104400-178105400	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr5:178104400-178105400	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr5:178104600-178105000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr5:178105000-178105400	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr5:178105400-178109400	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr5:178105400-178109800	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:178108600-178108800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:178109400-178110800	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr5:178109800-178110800	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr5:178110200-178113200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr5:178110400-178111800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr5:178110800-178111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:178110800-178111600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr5:178110800-178111800	Enhancers	K562	blood
35	chr5:178110800-178112000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr5:178111600-178113400	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr5:178112000-178115400	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr5:178112200-178112800	Enhancers	Placenta	Placenta
39	chr5:178112800-178113400	Flanking Active TSS	Placenta	Placenta
40	chr5:178113200-178115200	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr5:178113400-178113800	Enhancers	Placenta	Placenta
42	chr5:178113400-178115000	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr5:178115000-178115400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr5:178115200-178116400	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr5:178115400-178116000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr5:178115400-178116200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr5:178115400-178116400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr5:178115400-178117200	Enhancers	HMEC	breast
49	chr5:178115400-178118000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr5:178116000-178117200	Enhancers	Primary neutrophils fromperipheralblood	blood

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