Variant report

Variant	nsv534951
Chromosome Location	chr1:46910546-46948727
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:978)
CpG islands
(count:1711)
Chromatin interactive
region (count:89)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:46943131-46943340	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:46912670-46912849	K562	blood:	n/a	n/a
3	ATF1	chr1:46915195-46915537	K562	blood:	n/a	n/a
4	ATF1	chr1:46943125-46943434	K562	blood:	n/a	n/a
5	ATF2	chr1:46943067-46943482	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:46943040-46943492	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:46943144-46943445	GM12878	blood:	n/a	n/a
8	ATF2	chr1:46912456-46912963	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:46943136-46943492	K562	blood:	n/a	n/a
10	BACH1	chr1:46915958-46915961	K562	blood:	n/a	n/a
11	BACH1	chr1:46912590-46913154	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:46913840-46914419	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:46932275-46933189	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:46912939-46913043	K562	blood:	n/a	n/a
15	BHLHE40	chr1:46912540-46912810	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:46915476-46915511	K562	blood:	n/a	n/a
17	BHLHE40	chr1:46932631-46932725	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:46946768-46946909	K562	blood:	n/a	n/a
19	BHLHE40	chr1:46943192-46943438	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:46912559-46912851	K562	blood:	n/a	n/a
21	BHLHE40	chr1:46943072-46943393	K562	blood:	n/a	n/a
22	BRCA1	chr1:46912641-46912783	HepG2	liver:	n/a	n/a
23	BRCA1	chr1:46914188-46914362	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr1:46915629-46916097	K562	blood:	n/a	n/a
25	CBX3	chr1:46912478-46912904	K562	blood:	n/a	n/a
26	CCNT2	chr1:46913868-46913890	K562	blood:	n/a	n/a
27	CCNT2	chr1:46932162-46932180	K562	blood:	n/a	n/a
28	CCNT2	chr1:46932525-46932802	K562	blood:	n/a	n/a
29	CCNT2	chr1:46915843-46916115	K562	blood:	n/a	n/a
30	CEBPB	chr1:46943250-46943263	K562	blood:	n/a	n/a
31	CEBPB	chr1:46915858-46916177	K562	blood:	n/a	n/a
32	CEBPB	chr1:46932071-46932076	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:46913273-46913366	K562	blood:	n/a	n/a
34	CEBPB	chr1:46946743-46947109	H1-hESC	embryonic stem cell:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
35	CEBPB	chr1:46946751-46947121	IMR90	lung:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
36	CEBPB	chr1:46946808-46947122	ECC-1	luminal epithelium:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
37	CEBPB	chr1:46946737-46947125	HepG2	liver:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
38	CEBPB	chr1:46946729-46947117	MCF-7	breast:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
39	CEBPB	chr1:46946791-46946993	HepG2	liver:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
40	CEBPB	chr1:46946625-46947257	K562	blood:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
41	CEBPB	chr1:46946776-46947186	K562	blood:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
42	CEBPB	chr1:46912658-46912773	K562	blood:	n/a	n/a
43	CEBPB	chr1:46946685-46947049	HepG2	liver:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
44	CEBPB	chr1:46946693-46947182	A549	lung:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
45	CEBPB	chr1:46946750-46947133	HepG2	liver:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
46	CEBPB	chr1:46946760-46947114	A549	lung:	n/a	chr1:46946931-46946942 chr1:46946929-46946940 chr1:46946929-46946942 chr1:46946931-46946940 chr1:46946929-46946942
47	CEBPB	chr1:46943072-46943429	K562	blood:	n/a	n/a
48	CEBPB	chr1:46915852-46916183	K562	blood:	n/a	n/a
49	CEBPB	chr1:46922133-46922391	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:46913245-46913398	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:46914528-46914578	K562	blood:	n/a
2	chr1:46940516-46940566	RPTEC	kidney:	n/a
3	chr1:46939866-46939916	Hepatocyte	liver:	n/a
4	chr1:46914528-46914578	K562	blood:	n/a
5	chr1:46940516-46940566	RPTEC	kidney:	n/a
6	chr1:46939866-46939916	Hepatocyte	liver:	n/a
7	chr1:46921844-46921894	PrEC	prostate:	n/a
8	chr1:46914023-46914073	HRPEpiC	eye:	n/a
9	chr1:46932305-46932355	ProgFib	skin:	n/a
10	chr1:46910885-46910935	BE2_C	brain:	n/a
11	chr1:46932239-46932289	Hela-S3	cervix:	n/a
12	chr1:46914672-46914722	Caco-2	colon:	n/a
13	chr1:46932891-46932941	K562	blood:	n/a
14	chr1:46914033-46914083	GM12878	blood:	n/a
15	chr1:46934661-46934711	SAEC	small airway:	n/a
16	chr1:46914672-46914722	HUVEC	blood vessel:	n/a
17	chr1:46914528-46914578	Hela-S3	cervix:	n/a
18	chr1:46918254-46918304	T-47D	breast:	n/a
19	chr1:46921746-46921796	HRPEpiC	eye:	n/a
20	chr1:46913787-46913837	AG04450	lung:	fetal
21	chr1:46940516-46940566	NHDF-neo	bronchial:	n/a
22	chr1:46939866-46939916	U87	brain:	n/a
23	chr1:46930731-46930781	SK-N-MC	brain:	n/a
24	chr1:46945595-46945645	PFSK-1	brain:	n/a
25	chr1:46940420-46940470	NHBE	bronchial:	n/a
26	chr1:46940325-46940375	LNCaP	prostate:	n/a
27	chr1:46921844-46921894	HRPEpiC	eye:	n/a
28	chr1:46943714-46943764	PrEC	prostate:	n/a
29	chr1:46913787-46913837	HMEC	breast:	n/a
30	chr1:46932891-46932941	Hela-S3	cervix:	n/a
31	chr1:46913532-46913582	AG10803	skin:	n/a
32	chr1:46913787-46913837	CMK	blood:	n/a
33	chr1:46914023-46914073	BJ	skin:	n/a
34	chr1:46918254-46918304	HRPEpiC	eye:	n/a
35	chr1:46940516-46940566	NHBE	bronchial:	n/a
36	chr1:46932239-46932289	HL-60	blood:	n/a
37	chr1:46937902-46937952	PFSK-1	brain:	n/a
38	chr1:46940420-46940470	NHDF-neo	bronchial:	n/a
39	chr1:46938281-46938331	ECC-1	luminal epithelium:	n/a
40	chr1:46911983-46912033	MCF10A-Er-Src	breast:	n/a
41	chr1:46913787-46913837	HRE	kidney:	n/a
42	chr1:46932305-46932355	AoSMC	blood vessel:	n/a
43	chr1:46910885-46910935	AG10803	skin:	n/a
44	chr1:46940420-46940470	MCF10A-Er-Src	breast:	n/a
45	chr1:46921844-46921894	H1-hESC	embryonic stem cell:	embryo
46	chr1:46911983-46912033	ECC-1	luminal epithelium:	n/a
47	chr1:46947998-46948048	CMK	blood:	n/a
48	chr1:46932239-46932289	MCF-7	breast:	n/a
49	chr1:46932239-46932289	BE2_C	brain:	n/a
50	chr1:46913787-46913837	GM19239	blood:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:46925041..46927646-chr1:46928942..46933160,4	K562	blood:
2	chr1:46941343..46943305-chr1:46947938..46949564,2	K562	blood:
3	chr1:46943865..46944889-chr1:46993729..46994414,5	K562	blood:
4	chr1:46946915..46950728-chr1:46952343..46956054,5	K562	blood:
5	chr1:46917777..46919850-chr1:47011713..47013770,2	K562	blood:
6	chr1:46943126..46948119-chr1:46990723..46995697,9	K562	blood:
7	chr1:46942850..46943359-chr1:47013489..47014125,2	MCF-7	breast:
8	chr1:46942594..46944791-chr1:46952601..46954652,2	K562	blood:
9	chr1:46911496..46912061-chr1:46993397..46994029,2	MCF-7	breast:
10	chr1:46945764..46947413-chr1:47015063..47017944,2	K562	blood:
11	chr1:46925013..46927188-chr1:46930375..46933280,2	K562	blood:
12	chr1:46937967..46940531-chr1:46945842..46949034,3	K562	blood:
13	chr1:46943014..46945161-chr1:46980372..46982820,2	MCF-7	breast:
14	chr1:46945269..46946167-chr1:46993663..46994349,2	K562	blood:
15	chr1:46922290..46924854-chr1:46955635..46957608,2	K562	blood:
16	chr1:46945298..46948604-chr1:46953497..46956097,3	K562	blood:
17	chr1:46941691..46945346-chr1:46978586..46981286,3	K562	blood:
18	chr1:46935975..46938759-chr1:46941514..46943307,2	K562	blood:
19	chr1:46946474..46949627-chr1:46956674..46960959,4	K562	blood:
20	chr1:46912494..46913218-chr1:47000111..47001290,4	MCF-7	breast:
21	chr1:46925530..46928308-chr1:46985086..46986885,2	K562	blood:
22	chr1:46911278..46913612-chr1:46993367..46994439,12	MCF-7	breast:
23	chr1:46937967..46940531-chr1:46945842..46949034,3	K562	blood:
24	chr1:46938517..46940978-chr1:46993315..46995791,2	K562	blood:
25	chr1:46911310..46914050-chr1:46990566..46993135,2	MCF-7	breast:
26	chr1:46908155..46911848-chr1:46987375..46989961,4	K562	blood:
27	chr1:46912182..46913197-chr1:47190618..47191791,5	K562	blood:
28	chr1:46908179..46910338-chr1:46912412..46913923,2	K562	blood:
29	chr1:46942784..46943686-chr1:47190606..47191545,4	K562	blood:
30	chr1:46937960..46939481-chr1:46992013..46994117,2	K562	blood:
31	chr1:46907713..46908466-chr1:46942834..46943730,2	MCF-7	breast:
32	chr1:46948519..46951026-chr1:47010382..47012141,2	K562	blood:
33	chr1:46925013..46927188-chr1:46930375..46933280,2	K562	blood:
34	chr1:46912642..46915291-chr1:46916388..46919723,5	K562	blood:
35	chr1:46907167..46909679-chr1:46911926..46913949,3	K562	blood:
36	chr1:46908155..46911848-chr1:46987375..46989663,3	K562	blood:
37	chr1:46934483..46937169-chr1:46941614..46943173,2	MCF-7	breast:
38	chr1:46942860..46943709-chr1:47000567..47001413,4	MCF-7	breast:
39	chr1:46916965..46919039-chr1:46986661..46989583,2	K562	blood:
40	chr1:46910308..46913456-chr1:46992468..46994457,29	K562	blood:
41	chr1:46917028..46919676-chr1:46953546..46955125,2	MCF-7	breast:
42	chr1:46919780..46922314-chr1:46942777..46944737,2	K562	blood:
43	chr1:46908793..46911524-chr1:46938182..46940912,2	K562	blood:
44	chr1:46943210..46943796-chr1:46988470..46989208,2	K562	blood:
45	chr1:46910009..46912181-chr1:46914839..46917874,3	K562	blood:
46	chr1:46931207..46934381-chr1:46934694..46938368,4	K562	blood:
47	chr1:46930701..46932786-chr1:46941797..46943421,2	K562	blood:
48	chr1:46911763..46912358-chr1:46937871..46938393,2	K562	blood:
49	chr1:46905639..46908191-chr1:46929446..46931823,2	K562	blood:
50	chr1:46912478..46913032-chr1:46942779..46943728,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KNCN-1	chr1:46912474-46912817	NONHSAT003015
2	lnc-FAAH-1	chr1:46910871-46911374	NR_045483
3	lnc-KNCN-1	chr1:46913124-46913561	XLOC_000818
4	lnc-KNCN-1	chr1:46915159-46915376	XLOC_000818
5	lnc-KNCN-1	chr1:46913124-46913704	NONHSAT003015
6	lnc-DMBX1-1	chr1:46947882-46948147	XLOC_000170
7	lnc-FAAH-1	chr1:46910888-46910993	NONHSAT003013
8	lnc-KNCN-1	chr1:46912345-46912817	XLOC_000818
9	lnc-DMBX1-1	chr1:46921495-46921582	XLOC_000170

No data

Variant related genes	Relation type
LINC00505	TF binding region
ENSG00000224863	TF binding region
LINC00505	CpG island
ENSG00000224863	CpG island
ENSG00000162456	chromatin interactions
ENSG00000224863	chromatin interactions
ENSG00000225667	chromatin interactions
ENSG00000232022	chromatin interactions

Extended variants
information (count: 1387 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1387 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545133844	chr1:46910554-46910555	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs79195591	chr1:46910565-46910566	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs530587858	chr1:46910566-46910567	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs549203182	chr1:46910567-46910568	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs186483598	chr1:46910579-46910580	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528413785	chr1:46910680-46910681	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs546903511	chr1:46910779-46910780	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs558164606	chr1:46910797-46910798	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142625412	chr1:46910830-46910831	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs538654910	chr1:46910872-46910873	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs146043005	chr1:46910886-46910887	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs190445264	chr1:46910889-46910890	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs547581	chr1:46910892-46910893	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs114127808	chr1:46910970-46910971	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs573085046	chr1:46910989-46910990	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs536747466	chr1:46911022-46911023	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs534248987	chr1:46911049-46911050	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs2281775	chr1:46911060-46911061	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183036616	chr1:46911099-46911100	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs544688844	chr1:46911120-46911121	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs563250258	chr1:46911145-46911146	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs74227913	chr1:46911150-46911151	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs74227914	chr1:46911156-46911157	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs573078232	chr1:46911189-46911190	Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs2281774	chr1:46911290-46911291	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs577726214	chr1:46911341-46911342	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs546964684	chr1:46911377-46911378	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565027249	chr1:46911378-46911379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79830553	chr1:46911398-46911399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530666022	chr1:46911400-46911401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs550719744	chr1:46911408-46911409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs114022477	chr1:46911444-46911445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs117056215	chr1:46911450-46911451	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543952044	chr1:46911457-46911458	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566770536	chr1:46911474-46911475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534115270	chr1:46911542-46911543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs558684080	chr1:46911562-46911563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs138210854	chr1:46911652-46911653	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs577471601	chr1:46911723-46911724	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560599494	chr1:46911724-46911725	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs187756796	chr1:46911771-46911772	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563275330	chr1:46911776-46911777	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs74072347	chr1:46911800-46911801	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs529634613	chr1:46911801-46911802	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs1158942	chr1:46911921-46911922	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs542775727	chr1:46911922-46911923	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566002042	chr1:46911979-46911980	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs192493151	chr1:46912014-46912015	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573118016	chr1:46912061-46912062	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs4660929	chr1:46912066-46912067	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:943 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46908800-46912800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:46908800-46913400	Weak transcription	Spleen	Spleen
3	chr1:46909000-46910600	Enhancers	K562	blood
4	chr1:46909000-46911800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:46909000-46911800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:46909000-46912400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr1:46909000-46912600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr1:46909000-46913400	Weak transcription	Gastric	stomach
9	chr1:46909000-46913600	Weak transcription	Pancreas	Pancrea
10	chr1:46909000-46913800	Weak transcription	Right Atrium	heart
11	chr1:46910600-46912200	Weak transcription	K562	blood
12	chr1:46911000-46911200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:46911600-46911800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
14	chr1:46911600-46911800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:46911600-46912400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
16	chr1:46911800-46912000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
17	chr1:46911800-46912000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:46911800-46912800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
19	chr1:46911800-46912800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
20	chr1:46911800-46912800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:46911800-46913000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
22	chr1:46911800-46913000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:46911800-46913800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr1:46912000-46912400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
25	chr1:46912000-46912400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
26	chr1:46912000-46913400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr1:46912000-46913400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:46912200-46913200	Enhancers	K562	blood
29	chr1:46912400-46912600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
30	chr1:46912400-46912800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
31	chr1:46912400-46912800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr1:46912400-46913000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
33	chr1:46912400-46913200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
34	chr1:46912400-46914600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
35	chr1:46912400-46915200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr1:46912600-46912800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
37	chr1:46912600-46912800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:46912600-46912800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:46912600-46912800	Enhancers	Brain Hippocampus Middle	brain
40	chr1:46912600-46913200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
41	chr1:46912600-46913400	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
42	chr1:46912600-46914000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
43	chr1:46912600-46914400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
44	chr1:46912600-46914600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
45	chr1:46912600-46914600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:46912800-46913000	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr1:46912800-46913000	Bivalent Enhancer	Brain Germinal Matrix	brain
48	chr1:46912800-46913000	Bivalent Enhancer	Fetal Lung	lung
49	chr1:46912800-46913200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
50	chr1:46912800-46913200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood

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