Variant report

Variant	nsv530443
Chromosome Location	chr17:43751674-43975766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3731)
CpG islands
(count:3972)
Chromatin interactive
region (count:130)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3731 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:43931758-43931805	K562	blood:	n/a	n/a
2	ARID3A	chr17:43971626-43971843	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:43935417-43935673	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:43889560-43889800	HepG2	liver:	n/a	n/a
5	ARID3A	chr17:43954222-43954286	HepG2	liver:	n/a	n/a
6	ARID3A	chr17:43889519-43889725	K562	blood:	n/a	n/a
7	ARID3A	chr17:43930148-43930468	K562	blood:	n/a	n/a
8	ARID3A	chr17:43947549-43947645	K562	blood:	n/a	n/a
9	ATF1	chr17:43765896-43766163	K562	blood:	n/a	n/a
10	ATF1	chr17:43866141-43866180	K562	blood:	n/a	n/a
11	ATF1	chr17:43763629-43763990	K562	blood:	n/a	n/a
12	ATF1	chr17:43782928-43783062	K562	blood:	n/a	n/a
13	ATF2	chr17:43971458-43971860	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr17:43971648-43971983	K562	blood:	n/a	chr17:43971822-43971831 chr17:43971772-43971781 chr17:43971663-43971676
15	ATF3	chr17:43945110-43945378	K562	blood:	n/a	n/a
16	ATF3	chr17:43947408-43947615	K562	blood:	n/a	n/a
17	ATF3	chr17:43900474-43900705	K562	blood:	n/a	n/a
18	ATF3	chr17:43782856-43783016	K562	blood:	n/a	n/a
19	ATF3	chr17:43971597-43972321	HepG2	liver:	n/a	chr17:43971822-43971831 chr17:43971772-43971781 chr17:43971663-43971676
20	ATF3	chr17:43782647-43783165	A549	lung:	n/a	n/a
21	ATF3	chr17:43782784-43783128	K562	blood:	n/a	n/a
22	ATF3	chr17:43871433-43871593	K562	blood:	n/a	n/a
23	BACH1	chr17:43868220-43868229	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr17:43971380-43971981	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr17:43771258-43771432	K562	blood:	n/a	n/a
26	BACH1	chr17:43884496-43884682	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr17:43873478-43873526	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr17:43889499-43889875	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr17:43799650-43799799	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr17:43860630-43860920	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr17:43974981-43975074	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr17:43972737-43972937	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr17:43930251-43930449	K562	blood:	n/a	n/a
34	BACH1	chr17:43889524-43889762	K562	blood:	n/a	n/a
35	BACH1	chr17:43862427-43862819	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr17:43862140-43862214	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr17:43848419-43848593	H1-hESC	embryonic stem cell:	n/a	n/a
38	BCL3	chr17:43881004-43881323	GM12878	blood:	n/a	n/a
39	BCL3	chr17:43832325-43832616	GM12878	blood:	n/a	n/a
40	BCL3	chr17:43881027-43881318	GM12878	blood:	n/a	n/a
41	BCL3	chr17:43832364-43832691	GM12878	blood:	n/a	n/a
42	BCL3	chr17:43971312-43972099	A549	lung:	n/a	chr17:43971870-43971883 chr17:43971537-43971546 chr17:43971867-43971880 chr17:43971815-43971828
43	BCLAF1	chr17:43971647-43972007	GM12878	blood:	n/a	chr17:43971870-43971883 chr17:43971867-43971880 chr17:43971815-43971828
44	BCLAF1	chr17:43971573-43971931	K562	blood:	n/a	chr17:43971870-43971883 chr17:43971867-43971880 chr17:43971815-43971828
45	BHLHE40	chr17:43912498-43912641	K562	blood:	n/a	n/a
46	BHLHE40	chr17:43971589-43972011	HepG2	liver:	n/a	chr17:43971857-43971873 chr17:43971662-43971678
47	BHLHE40	chr17:43971463-43971932	K562	blood:	n/a	chr17:43971857-43971873 chr17:43971662-43971678
48	BHLHE40	chr17:43763607-43763996	K562	blood:	n/a	n/a
49	BHLHE40	chr17:43870501-43870686	K562	blood:	n/a	n/a
50	BHLHE40	chr17:43930197-43930312	K562	blood:	n/a	n/a

(count:3972 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:43969268-43969318	T-47D	breast:	n/a
2	chr17:43973146-43973196	NT2-D1	testis:	n/a
3	chr17:43862910-43862960	T-47D	breast:	n/a
4	chr17:43974975-43975025	U87	brain:	n/a
5	chr17:43863303-43863353	ovcar-3	ovarian:	n/a
6	chr17:43973311-43973361	HRPEpiC	eye:	n/a
7	chr17:43974975-43975025	AG09309	skin:	n/a
8	chr17:43969268-43969318	T-47D	breast:	n/a
9	chr17:43973146-43973196	NT2-D1	testis:	n/a
10	chr17:43862910-43862960	T-47D	breast:	n/a
11	chr17:43974975-43975025	U87	brain:	n/a
12	chr17:43863303-43863353	ovcar-3	ovarian:	n/a
13	chr17:43973311-43973361	HRPEpiC	eye:	n/a
14	chr17:43974975-43975025	AG09309	skin:	n/a
15	chr17:43923255-43923305	HCPEpiC	choroid plexus:	n/a
16	chr17:43866278-43866328	GM12878	blood:	n/a
17	chr17:43971177-43971227	PFSK-1	brain:	n/a
18	chr17:43862927-43862977	HMEC	breast:	n/a
19	chr17:43863356-43863406	PANC-1	pancreas:	n/a
20	chr17:43922240-43922290	BJ	skin:	n/a
21	chr17:43942128-43942178	HRE	kidney:	n/a
22	chr17:43878769-43878819	SK-N-SH	brain:	n/a
23	chr17:43922356-43922406	AoSMC	blood vessel:	n/a
24	chr17:43974804-43974854	SK-N-SH_RA	brain:	n/a
25	chr17:43942128-43942178	SK-N-SH	brain:	n/a
26	chr17:43973426-43973476	BE2_C	brain:	n/a
27	chr17:43974919-43974969	NT2-D1	testis:	n/a
28	chr17:43883072-43883122	GM12891	blood:	n/a
29	chr17:43973146-43973196	GM12878	blood:	n/a
30	chr17:43975063-43975113	AG09319	gingival:	n/a
31	chr17:43862032-43862082	SK-N-SH	brain:	n/a
32	chr17:43922122-43922172	ProgFib	skin:	n/a
33	chr17:43860691-43860741	HPAEpiC	pulmonary alveolar:	n/a
34	chr17:43973146-43973196	HUVEC	blood vessel:	n/a
35	chr17:43909151-43909201	HCM	heart:	n/a
36	chr17:43787766-43787816	BE2_C	brain:	n/a
37	chr17:43971461-43971511	HRCEpiC	kidney:	n/a
38	chr17:43974804-43974854	MCF10A-Er-Src	breast:	n/a
39	chr17:43922122-43922172	HAEpiC	amniotic membrane:	n/a
40	chr17:43922240-43922290	GM06990	blood:	n/a
41	chr17:43861682-43861732	T-47D	breast:	n/a
42	chr17:43861104-43861154	CMK	blood:	n/a
43	chr17:43971906-43971956	CMK	blood:	n/a
44	chr17:43787766-43787816	NHBE	bronchial:	n/a
45	chr17:43973146-43973196	HEK293	kidney:	embryo
46	chr17:43972969-43973019	A549	lung:	n/a
47	chr17:43972969-43973019	BJ	skin:	n/a
48	chr17:43863000-43863050	HUVEC	blood vessel:	n/a
49	chr17:43861668-43861718	HIPEpiC	eye:	n/a
50	chr17:43973146-43973196	HCT-116	colon:	n/a

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:43763764..43766264-chr17:43767602..43770243,2	K562	blood:
2	chr17:43739220..43741224-chr17:43749198..43751921,2	K562	blood:
3	chr17:43895221..43899496-chr17:43899685..43904015,5	K562	blood:
4	chr17:43807016..43807933-chr20:45946281..45947140,2	MCF-7	breast:
5	chr17:43799128..43800390-chr17:43929502..43930739,5	MCF-7	breast:
6	chr17:43867694..43870674-chr20:52481399..52483362,2	MCF-7	breast:
7	chr17:43797225..43798101-chr17:43871968..43872865,2	MCF-7	breast:
8	chr17:43962896..43965248-chr17:43965393..43967420,2	MCF-7	breast:
9	chr17:43780531..43783010-chr17:43795789..43798250,2	MCF-7	breast:
10	chr17:43791472..43793205-chr17:43796908..43798873,2	K562	blood:
11	chr17:43788529..43790856-chr17:43791588..43793113,2	K562	blood:
12	chr17:43717454..43718388-chr17:43905836..43906373,2	MCF-7	breast:
13	chr17:43915875..43918874-chr17:43921810..43923680,2	K562	blood:
14	chr17:43784544..43786909-chr17:43788749..43793221,4	K562	blood:
15	chr17:43783070..43786688-chr17:43789498..43793282,3	MCF-7	breast:
16	chr17:43900583..43902240-chr17:43902534..43906054,4	K562	blood:
17	chr17:43726189..43726690-chr17:43929745..43930647,2	K562	blood:
18	chr17:43962896..43965248-chr17:43965393..43967420,2	MCF-7	breast:
19	chr17:43967392..43969152-chr17:43971301..43972912,2	MCF-7	breast:
20	chr17:43778580..43779511-chr4:127075071..127075732,2	MCF-7	breast:
21	chr17:43887903..43889656-chr17:43897713..43900085,2	K562	blood:
22	chr17:43791472..43793205-chr17:43796908..43798873,2	K562	blood:
23	chr17:43935533..43937226-chr17:43938981..43941704,2	K562	blood:
24	chr17:43860223..43862667-chr17:43869286..43872505,3	K562	blood:
25	chr17:43900583..43902240-chr17:43902534..43906054,4	K562	blood:
26	chr17:43860147..43861189-chr17:43909188..43910157,4	K562	blood:
27	chr17:43912051..43914057-chr17:43916584..43918632,2	K562	blood:
28	chr17:43912051..43914057-chr17:43916584..43918632,2	K562	blood:
29	chr17:43966999..43969829-chr17:43969977..43971693,2	K562	blood:
30	chr17:43743554..43744059-chr17:43905812..43906447,2	MCF-7	breast:
31	chr17:43933126..43935030-chr17:43935790..43937473,2	K562	blood:
32	chr17:43783070..43786688-chr17:43789498..43793282,3	MCF-7	breast:
33	chr17:43965692..43967222-chr17:43969905..43972570,2	MCF-7	breast:
34	chr17:43880060..43882832-chr17:43907307..43909233,2	MCF-7	breast:
35	chr17:43912642..43917854-chr17:43921730..43925787,6	K562	blood:
36	chr17:43869487..43869987-chr7:218621..219124,2	Hela-S3	cervix:
37	chr11:102323272..102323836-chr17:43861612..43862112,2	HCT-116	colon:
38	chr17:43933126..43935030-chr17:43935790..43937473,2	K562	blood:
39	chr17:43797225..43798101-chr17:43871968..43872865,2	MCF-7	breast:
40	chr17:43789857..43791520-chr17:43798686..43801656,2	MCF-7	breast:
41	chr17:43817457..43820007-chr17:43824546..43827220,2	K562	blood:
42	chr17:43224534..43227319-chr17:43971403..43973410,2	MCF-7	breast:
43	chr17:43717401..43718123-chr17:43909177..43909809,3	MCF-7	breast:
44	chr1:23004679..23005482-chr17:43783141..43783641,2	NB4	blood:
45	chr17:43799305..43800192-chr17:43909160..43909723,3	K562	blood:
46	chr17:43930225..43931201-chr17:43971666..43972273,2	K562	blood:
47	chr17:43966999..43969829-chr17:43969977..43971693,2	K562	blood:
48	chr17:43929689..43931704-chr17:43969284..43972074,2	K562	blood:
49	chr17:43776056..43777807-chr17:43778898..43781028,2	K562	blood:
50	chr17:43799128..43800390-chr17:43929502..43930739,5	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC091132.2-1	chr17:43810069-43810343	ENSG00000265547.1
2	lnc-AC091132.2-2	chr17:43810719-43810892	ENSG00000265964.1
3	lnc-AC091132.2-2	chr17:43811650-43812035	ENSG00000265964.1
4	lnc-KIAA1267-3	chr17:43921235-43921527	NONHSAT054181
5	lnc-KIAA1267-3	chr17:43972846-43972966	ENSG00000264589.1
6	lnc-C17orf69-2	chr17:43893829-43893909	ENSG00000263715.1
7	lnc-KIAA1267-3	chr17:43921240-43921527	ENSG00000264589.1
8	lnc-KIAA1267-3	chr17:43922005-43922123	ENSG00000264589.1
9	lnc-C17orf69-2	chr17:43884376-43884463	ENSG00000263715.1
10	lnc-KIAA1267-3	chr17:43922005-43922143	NONHSAT054181
11	lnc-KIAA1267-3	chr17:43921017-43921527	ENSG00000264589.1
12	lnc-KIAA1267-3	chr17:43972846-43972879	NONHSAT054180
13	lnc-AC091132.2-1	chr17:43811650-43812020	NONHSAT054176
14	lnc-KIAA1267-3	chr17:43920722-43921527	NONHSAT054180
15	lnc-AC091132.2-1	chr17:43809068-43809310	NONHSAT054176
16	lnc-KIAA1267-3	chr17:43921352-43921527	ENSG00000264589.1
17	lnc-KIAA1267-3	chr17:43971978-43972879	ENSG00000264589.1
18	lnc-AC217771.1-2	chr17:43973149-43976164	NONHSAT054183
19	lnc-AC091132.2-1	chr17:43809069-43809310	ENSG00000265547.1

No data

Variant related genes	Relation type
SPPL2C	TF binding region
CRHR1	TF binding region
MAPT	TF binding region
ENSG00000265547	TF binding region
ENSG00000265964	TF binding region
MAPT-AS1	TF binding region
SPPL2C	CpG island
CRHR1	CpG island
MAPT	CpG island
ENSG00000265547	CpG island
ENSG00000265964	CpG island
MAPT-AS1	CpG island
ENSG00000186834	chromatin interactions
ENSG00000120088	chromatin interactions
ENSG00000265964	chromatin interactions
ENSG00000264589	chromatin interactions
ENSG00000152558	chromatin interactions
ENSG00000265547	chromatin interactions
ENSG00000159314	chromatin interactions
ENSG00000255337	chromatin interactions
ENSG00000185294	chromatin interactions
ENSG00000204650	chromatin interactions
ENSG00000186868	chromatin interactions

Extended variants
information (count: 8288 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:8288 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148936142	chr17:43751687-43751688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534382073	chr17:43751754-43751755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114197538	chr17:43751759-43751760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1635291	chr17:43751913-43751914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs544351130	chr17:43751960-43751961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573551966	chr17:43751985-43751986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531088571	chr17:43751995-43751996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs36047274	chr17:43751996-43751997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111623230	chr17:43751997-43751998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35942966	chr17:43752020-43752021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546242144	chr17:43752030-43752031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62055661	chr17:43752039-43752040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs111572315	chr17:43752073-43752074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545316032	chr17:43752122-43752123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148064146	chr17:43752145-43752146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527525264	chr17:43752146-43752147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556684411	chr17:43752155-43752156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548778697	chr17:43752185-43752186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560705774	chr17:43752190-43752191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531318402	chr17:43752244-43752245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117536416	chr17:43752305-43752306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184400063	chr17:43752320-43752321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538251486	chr17:43752367-43752368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565659745	chr17:43752382-43752383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186907812	chr17:43752420-43752421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539280845	chr17:43752421-43752422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536124915	chr17:43752453-43752454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371694084	chr17:43752477-43752478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554836540	chr17:43752485-43752486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534447509	chr17:43752510-43752511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs62055662	chr17:43752566-43752567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs572775071	chr17:43752614-43752615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140813520	chr17:43752665-43752666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538370807	chr17:43752704-43752705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537049603	chr17:43752788-43752789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115277086	chr17:43752795-43752796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369464419	chr17:43752797-43752798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555435423	chr17:43752813-43752814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578007644	chr17:43752831-43752832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544334312	chr17:43752860-43752861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573982261	chr17:43752863-43752864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544379949	chr17:43752867-43752868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114322578	chr17:43752871-43752872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150437646	chr17:43752910-43752911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563014101	chr17:43752943-43752944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138206821	chr17:43753134-43753135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115818923	chr17:43753168-43753169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149626292	chr17:43753172-43753173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542475755	chr17:43753179-43753180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146660756	chr17:43753191-43753192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	19156837	CNVD
Williams-beuren syndrome	18553513	CNVD
Mental retardation	17847001	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
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22817714	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:2045 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:43749800-43759000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr17:43754200-43754600	Enhancers	Fetal Brain Male	brain
3	chr17:43754600-43755000	Weak transcription	Fetal Brain Male	brain
4	chr17:43755000-43755200	Enhancers	Fetal Brain Male	brain
5	chr17:43755200-43755600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr17:43755200-43755600	Enhancers	Fetal Brain Female	brain
7	chr17:43755200-43757000	Weak transcription	Fetal Brain Male	brain
8	chr17:43755600-43757200	Weak transcription	Fetal Brain Female	brain
9	chr17:43757000-43758000	Enhancers	Fetal Brain Male	brain
10	chr17:43757200-43758000	Enhancers	Fetal Brain Female	brain
11	chr17:43758000-43758800	Weak transcription	Fetal Brain Male	brain
12	chr17:43758000-43764800	Weak transcription	Fetal Brain Female	brain
13	chr17:43758600-43758800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr17:43758800-43759000	Enhancers	Fetal Brain Male	brain
15	chr17:43758800-43759200	Enhancers	Brain Cingulate Gyrus	brain
16	chr17:43759000-43759800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr17:43759000-43760000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr17:43759000-43765000	Weak transcription	Fetal Brain Male	brain
19	chr17:43759200-43760000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr17:43759400-43759800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr17:43759400-43760000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr17:43759600-43759800	Enhancers	H9 Cell Line	embryonic stem cell
23	chr17:43759600-43760000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr17:43759800-43760400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr17:43761400-43762000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr17:43762000-43765200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr17:43762600-43763600	Enhancers	K562	blood
28	chr17:43763200-43763400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr17:43763600-43764000	Flanking Active TSS	K562	blood
30	chr17:43764000-43764800	Enhancers	K562	blood
31	chr17:43764800-43765400	Weak transcription	K562	blood
32	chr17:43764800-43768400	Enhancers	Fetal Brain Female	brain
33	chr17:43765000-43765400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr17:43765000-43768600	Enhancers	Fetal Brain Male	brain
35	chr17:43765200-43765600	Enhancers	Brain Angular Gyrus	brain
36	chr17:43765200-43766200	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr17:43765200-43766400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr17:43765200-43766400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr17:43765400-43766200	Enhancers	Fetal Muscle Leg	muscle
40	chr17:43765400-43766400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr17:43765400-43766400	Enhancers	K562	blood
42	chr17:43765400-43766600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr17:43765600-43765800	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr17:43765600-43765800	Enhancers	Brain Cingulate Gyrus	brain
45	chr17:43765600-43766000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr17:43765600-43766400	Enhancers	Brain Hippocampus Middle	brain
47	chr17:43766200-43766600	Bivalent Enhancer	Fetal Muscle Leg	muscle
48	chr17:43767600-43767800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
49	chr17:43767600-43768800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr17:43768000-43768200	Enhancers	Brain Inferior Temporal Lobe	brain

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