Variant report

Variant	nsv871156
Chromosome Location	chr1:10690948-10750432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:929)
CpG islands
(count:6111)
Chromatin interactive
region (count:92)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:929 , 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	chr1:10739699-10740090	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:10739738-10739938	K562	blood:	n/a	n/a
3	ARID3A	chr1:10746020-10747010	HepG2	liver:	n/a	n/a
4	ATF1	chr1:10706410-10706754	K562	blood:	n/a	n/a
5	ATF2	chr1:10739666-10740097	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:10739634-10740012	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr1:10706380-10706785	K562	blood:	n/a	n/a
8	ATF3	chr1:10711894-10712078	K562	blood:	n/a	n/a
9	ATF3	chr1:10706374-10706728	K562	blood:	n/a	n/a
10	BACH1	chr1:10692955-10692981	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:10699434-10699676	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:10710049-10710152	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:10709033-10709307	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr1:10711172-10711384	GM12878	blood:	n/a	n/a
15	BCL3	chr1:10722391-10722933	GM12878	blood:	n/a	n/a
16	BCL3	chr1:10722400-10722952	GM12878	blood:	n/a	n/a
17	BCL3	chr1:10711104-10711370	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:10739818-10739897	K562	blood:	n/a	n/a
19	BHLHE40	chr1:10745752-10746071	K562	blood:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
20	BHLHE40	chr1:10745723-10746597	HepG2	liver:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
21	BHLHE40	chr1:10706431-10706689	K562	blood:	n/a	n/a
22	BHLHE40	chr1:10722323-10722716	K562	blood:	n/a	n/a
23	BHLHE40	chr1:10704722-10704778	K562	blood:	n/a	n/a
24	BHLHE40	chr1:10701393-10701600	HepG2	liver:	n/a	n/a
25	BRCA1	chr1:10737875-10737890	HepG2	liver:	n/a	n/a
26	CBX3	chr1:10706366-10706742	K562	blood:	n/a	n/a
27	CBX3	chr1:10739625-10740024	K562	blood:	n/a	n/a
28	CEBPB	chr1:10746636-10747091	HepG2	liver:	n/a	chr1:10746910-10746923
29	CEBPB	chr1:10706494-10706643	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:10711206-10711315	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:10739707-10739926	K562	blood:	n/a	n/a
32	CEBPB	chr1:10706393-10706782	K562	blood:	n/a	n/a
33	CEBPB	chr1:10695625-10695985	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:10739719-10739976	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:10704649-10704938	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:10695688-10695932	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:10706430-10706778	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:10737782-10737942	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr1:10706493-10706670	K562	blood:	n/a	n/a
40	CEBPB	chr1:10695597-10696010	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:10694733-10694869	Hela-S3	cervix:	n/a	chr1:10694745-10694758
42	CEBPB	chr1:10706457-10706718	A549	lung:	n/a	n/a
43	CEBPB	chr1:10706429-10706778	K562	blood:	n/a	n/a
44	CEBPB	chr1:10706418-10706752	IMR90	lung:	n/a	n/a
45	CEBPB	chr1:10739750-10739932	K562	blood:	n/a	n/a
46	CEBPD	chr1:10745991-10746333	HepG2	liver:	n/a	n/a
47	CHD1	chr1:10699506-10699568	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr1:10739793-10739993	HepG2	liver:	n/a	n/a
49	CHD2	chr1:10746764-10746893	K562	blood:	n/a	n/a
50	CHD2	chr1:10704633-10704864	Hela-S3	cervix:	n/a	n/a

(count:6111 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10692799-10692849	T-47D	breast:	n/a
2	chr1:10702712-10702762	HCPEpiC	choroid plexus:	n/a
3	chr1:10711695-10711745	IMR90	lung:	fetal
4	chr1:10696018-10696068	SK-N-SH	brain:	n/a
5	chr1:10732063-10732113	HCT-116	colon:	n/a
6	chr1:10698794-10698844	Hela-S3	cervix:	n/a
7	chr1:10709185-10709235	ovcar-3	ovarian:	n/a
8	chr1:10710847-10710897	HAEpiC	amniotic membrane:	n/a
9	chr1:10707454-10707504	AG09309	skin:	n/a
10	chr1:10714619-10714669	HRPEpiC	eye:	n/a
11	chr1:10697703-10697753	AG10803	skin:	n/a
12	chr1:10692799-10692849	T-47D	breast:	n/a
13	chr1:10702712-10702762	HCPEpiC	choroid plexus:	n/a
14	chr1:10711695-10711745	IMR90	lung:	fetal
15	chr1:10696018-10696068	SK-N-SH	brain:	n/a
16	chr1:10732063-10732113	HCT-116	colon:	n/a
17	chr1:10698794-10698844	Hela-S3	cervix:	n/a
18	chr1:10709185-10709235	ovcar-3	ovarian:	n/a
19	chr1:10710847-10710897	HAEpiC	amniotic membrane:	n/a
20	chr1:10707454-10707504	AG09309	skin:	n/a
21	chr1:10714619-10714669	HRPEpiC	eye:	n/a
22	chr1:10697703-10697753	AG10803	skin:	n/a
23	chr1:10720716-10720766	Jurkat	blood:	n/a
24	chr1:10732558-10732608	K562	blood:	n/a
25	chr1:10698794-10698844	BE2_C	brain:	n/a
26	chr1:10714675-10714725	NHDF-neo	bronchial:	n/a
27	chr1:10732333-10732383	ovcar-3	ovarian:	n/a
28	chr1:10712967-10713017	ProgFib	skin:	n/a
29	chr1:10698313-10698363	HCM	heart:	n/a
30	chr1:10732063-10732113	A549	lung:	n/a
31	chr1:10732900-10732950	HL-60	blood:	n/a
32	chr1:10709185-10709235	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:10699604-10699654	T-47D	breast:	n/a
34	chr1:10712967-10713017	MCF10A-Er-Src	breast:	n/a
35	chr1:10702712-10702762	AoSMC	blood vessel:	n/a
36	chr1:10724490-10724540	CMK	blood:	n/a
37	chr1:10699958-10700008	GM12878	blood:	n/a
38	chr1:10714160-10714210	GM12892	blood:	n/a
39	chr1:10732333-10732383	NB4	blood:	n/a
40	chr1:10707934-10707984	NH-A	brain:	n/a
41	chr1:10699831-10699881	AG10803	skin:	n/a
42	chr1:10725237-10725287	AG09319	gingival:	n/a
43	chr1:10739980-10740030	GM12892	blood:	n/a
44	chr1:10724490-10724540	AG04450	lung:	fetal
45	chr1:10728270-10728320	Hela-S3	cervix:	n/a
46	chr1:10743216-10743266	NHBE	bronchial:	n/a
47	chr1:10732063-10732113	LNCaP	prostate:	n/a
48	chr1:10734693-10734743	Jurkat	blood:	n/a
49	chr1:10732333-10732383	HEEpiC	esophagus:	n/a
50	chr1:10707934-10707984	ECC-1	luminal epithelium:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:10715834..10717814-chr1:10789112..10791954,2	K562	blood:
2	chr1:10573337..10575488-chr1:10723481..10725688,2	K562	blood:
3	chr1:10742610..10744196-chr1:10755434..10757046,2	K562	blood:
4	chr1:10730026..10731880-chr1:10732441..10734858,2	MCF-7	breast:
5	chr1:10574993..10577268-chr1:10694934..10697136,2	MCF-7	breast:
6	chr1:10738789..10740392-chr1:10741913..10744233,2	MCF-7	breast:
7	chr1:10744767..10746959-chr1:10754994..10757049,2	K562	blood:
8	chr1:10723769..10726210-chr1:10728292..10729827,2	MCF-7	breast:
9	chr1:10703902..10706642-chr1:10707587..10709773,5	K562	blood:
10	chr1:10717594..10722225-chr1:10722686..10725044,4	K562	blood:
11	chr1:10739929..10741898-chr1:10854079..10856532,2	MCF-7	breast:
12	chr1:10715958..10718705-chr1:10751486..10753340,2	K562	blood:
13	chr1:10731829..10734631-chr1:10737455..10739630,2	K562	blood:
14	chr1:10689513..10692457-chr1:10716597..10719078,2	K562	blood:
15	chr1:10732310..10734082-chr1:10748973..10751556,2	K562	blood:
16	chr1:10711257..10713486-chr1:10721428..10724018,2	MCF-7	breast:
17	chr1:10712754..10714859-chr1:10715847..10719174,3	MCF-7	breast:
18	chr1:10659595..10662178-chr1:10730395..10732793,2	MCF-7	breast:
19	chr1:10716711..10719662-chr1:10722945..10725596,2	MCF-7	breast:
20	chr1:10739770..10741770-chr1:10741804..10744517,2	K562	blood:
21	chr1:10738788..10740418-chr1:10744263..10746556,2	MCF-7	breast:
22	chr1:10567638..10569716-chr1:10700234..10702656,2	K562	blood:
23	chr1:10723769..10726210-chr1:10728292..10729827,2	MCF-7	breast:
24	chr1:10703132..10705545-chr1:10711056..10713011,2	K562	blood:
25	chr1:10736438..10738952-chr1:10740834..10743683,3	K562	blood:
26	chr1:10741683..10743188-chr1:10744761..10747734,2	MCF-7	breast:
27	chr1:10735100..10736602-chr1:10738947..10741483,2	MCF-7	breast:
28	chr1:10703574..10707168-chr1:10709558..10711927,3	MCF-7	breast:
29	chr1:10703132..10705545-chr1:10711056..10713011,2	K562	blood:
30	chr1:10685500..10687497-chr1:10695365..10698289,2	K562	blood:
31	chr1:10750259..10753196-chr1:10853460..10855878,3	MCF-7	breast:
32	chr1:10742297..10745036-chr1:10749705..10751341,3	MCF-7	breast:
33	chr1:10731586..10734308-chr1:10735752..10737991,2	MCF-7	breast:
34	chr1:10731829..10734631-chr1:10737455..10739630,2	K562	blood:
35	chr1:10730915..10733198-chr1:10740298..10742012,2	K562	blood:
36	chr1:10685463..10687143-chr1:10735500..10738364,2	K562	blood:
37	chr1:10746225..10747873-chr1:10749821..10751374,2	K562	blood:
38	chr1:10698341..10701476-chr1:10701646..10704585,3	MCF-7	breast:
39	chr1:10722706..10724721-chr1:10733970..10736738,2	MCF-7	breast:
40	chr1:10744408..10746422-chr1:10754548..10756295,2	MCF-7	breast:
41	chr1:10694311..10696932-chr1:10702215..10704200,2	K562	blood:
42	chr1:10739997..10741906-chr1:10786836..10789661,2	MCF-7	breast:
43	chr1:10703574..10707168-chr1:10709558..10711927,3	MCF-7	breast:
44	chr1:10746278..10748730-chr1:10764916..10766801,2	K562	blood:
45	chr1:10749491..10752032-chr1:10752294..10754052,2	K562	blood:
46	chr1:10728805..10730887-chr1:10732213..10735865,3	MCF-7	breast:
47	chr1:10725635..10727609-chr1:10737981..10739512,2	K562	blood:
48	chr1:10738789..10740392-chr1:10741913..10744233,2	MCF-7	breast:
49	chr1:10705750..10708723-chr1:10731868..10733988,2	K562	blood:
50	chr1:10709667..10713053-chr1:10713684..10716975,4	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PEX14-4	chr1:10703938-10704151	uc_5_+
2	lnc-DFFA-7	chr1:10717708-10718008	uc_6_-
3	lnc-PEX14-6	chr1:10717708-10718008	uc_6_+
4	lnc-DFFA-6	chr1:10710541-10710812	NONHSAT000867
5	lnc-DFFA-4	chr1:10697178-10697465	NONHSAT000866
6	lnc-DFFA-6	chr1:10710998-10711157	NONHSAT000867
7	lnc-DFFA-5	chr1:10703938-10704151	uc_5_-
8	lnc-DFFA-4	chr1:10698772-10698820	NONHSAT000866

No data

Variant related genes	Relation type
CASZ1	TF binding region
ENSG00000272078	TF binding region
CASZ1	CpG island
ENSG00000272078	CpG island
ENSG00000130940	chromatin interactions
ENSG00000272078	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 2775 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2775 , 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	rs17035482	chr1:10690948-10690949	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559353258	chr1:10690970-10690971	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs530025567	chr1:10690971-10690972	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs548107860	chr1:10690979-10690980	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs569295293	chr1:10690994-10690995	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs115817625	chr1:10691014-10691015	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs565046680	chr1:10691067-10691068	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs146945696	chr1:10691095-10691096	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538821822	chr1:10691099-10691100	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs547990685	chr1:10691108-10691109	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs566168186	chr1:10691112-10691113	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552396669	chr1:10691130-10691131	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536928141	chr1:10691141-10691142	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555340796	chr1:10691154-10691155	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs570721758	chr1:10691206-10691207	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531745263	chr1:10691224-10691225	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs537447945	chr1:10691239-10691240	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs558743794	chr1:10691247-10691248	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs368593223	chr1:10691260-10691261	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs577284998	chr1:10691274-10691275	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs540841905	chr1:10691299-10691300	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs550470531	chr1:10691370-10691371	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568623449	chr1:10691373-10691374	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs559479364	chr1:10691408-10691409	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs143386624	chr1:10691425-10691426	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs77603828	chr1:10691441-10691442	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs553467509	chr1:10691455-10691456	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147146399	chr1:10691529-10691530	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs530385556	chr1:10691530-10691531	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs72858506	chr1:10691554-10691555	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs563997168	chr1:10691557-10691558	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs371331378	chr1:10691578-10691579	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs528166862	chr1:10691589-10691590	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs546409937	chr1:10691689-10691690	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs138397599	chr1:10691728-10691729	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs284302	chr1:10691730-10691731	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs77123950	chr1:10691747-10691748	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs367933460	chr1:10691769-10691770	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs375292453	chr1:10691786-10691787	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs530949478	chr1:10691789-10691790	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs555893015	chr1:10691821-10691822	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs537410764	chr1:10691828-10691829	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs75229699	chr1:10691829-10691830	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577198349	chr1:10691911-10691912	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370906660	chr1:10691921-10691922	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149319329	chr1:10691930-10691931	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs79076237	chr1:10691937-10691938	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs183345721	chr1:10691946-10691947	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs541631897	chr1:10691991-10691992	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs151278750	chr1:10692006-10692007	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	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
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	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
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	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
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2312 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10632600-10698000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:10651600-10715800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr1:10654800-10691600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:10658200-10694400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr1:10658400-10691600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:10660200-10697600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr1:10661800-10692000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:10662200-10694400	Weak transcription	HSMM	muscle
9	chr1:10662400-10694400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr1:10664400-10698000	Weak transcription	Primary B cells from cord blood	blood
11	chr1:10672600-10694800	Strong transcription	Fetal Intestine Small	intestine
12	chr1:10676000-10691600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr1:10676200-10691600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr1:10676400-10691800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:10676400-10691800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr1:10676600-10691800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:10676800-10691000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr1:10680400-10693800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr1:10680400-10694400	Weak transcription	HSMMtube	muscle
20	chr1:10681200-10697600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr1:10681600-10691600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr1:10681800-10691800	Strong transcription	Primary T cells from cord blood	blood
23	chr1:10682000-10692600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:10682200-10694000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:10682200-10694600	Strong transcription	Fetal Intestine Large	intestine
26	chr1:10682600-10693000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:10684600-10694600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:10685000-10692000	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr1:10685000-10695200	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr1:10685200-10691600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:10685200-10693000	Weak transcription	Brain Substantia Nigra	brain
32	chr1:10685200-10693600	Weak transcription	HMEC	breast
33	chr1:10685200-10695200	Weak transcription	Brain Angular Gyrus	brain
34	chr1:10685200-10699400	Weak transcription	Aorta	Aorta
35	chr1:10685400-10692000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr1:10685400-10692000	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr1:10685800-10694000	Weak transcription	NHEK	skin
38	chr1:10685800-10694200	Weak transcription	Osteobl	bone
39	chr1:10686200-10698000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:10686400-10692600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:10686600-10694600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr1:10686800-10691600	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr1:10686800-10694000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr1:10686800-10694400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:10686800-10695200	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr1:10687400-10691000	Weak transcription	Stomach Mucosa	stomach
47	chr1:10687600-10698000	Weak transcription	Small Intestine	intestine
48	chr1:10688000-10694800	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr1:10688400-10691400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr1:10688400-10691400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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