Variant report

Variant	nsv830674
Chromosome Location	chr6:64355412-64535801
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1826)
CpG islands
(count:367)
Chromatin interactive
region (count:105)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:1826 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:64467796-64467961	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:64474251-64474581	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:64373218-64373712	K562	blood:	n/a	n/a
4	ARID3A	chr6:64502828-64502906	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:64387165-64387637	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:64380929-64381340	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:64444667-64445117	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:64516019-64516583	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:64418724-64419399	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:64509356-64509581	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:64434630-64435248	HepG2	liver:	n/a	chr6:64434709-64434725
12	ARID3A	chr6:64512548-64512818	HepG2	liver:	n/a	n/a
13	ATF1	chr6:64387228-64387346	K562	blood:	n/a	n/a
14	ATF2	chr6:64392999-64393585	GM12878	blood:	n/a	n/a
15	ATF3	chr6:64516012-64516622	A549	lung:	n/a	n/a
16	BACH1	chr6:64405827-64405926	K562	blood:	n/a	n/a
17	BACH1	chr6:64373415-64373596	K562	blood:	n/a	n/a
18	BACH1	chr6:64415743-64415840	K562	blood:	n/a	n/a
19	BATF	chr6:64509823-64510050	GM12878	blood:	n/a	n/a
20	BCL3	chr6:64516097-64516650	A549	lung:	n/a	n/a
21	BCL3	chr6:64516032-64516762	A549	lung:	n/a	n/a
22	BHLHE40	chr6:64393154-64393440	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:64387255-64387507	HepG2	liver:	n/a	n/a
24	BHLHE40	chr6:64449181-64449495	HepG2	liver:	n/a	n/a
25	BHLHE40	chr6:64444906-64445178	HepG2	liver:	n/a	n/a
26	BHLHE40	chr6:64373459-64374038	K562	blood:	n/a	n/a
27	BHLHE40	chr6:64375030-64375331	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:64395340-64395806	GM12878	blood:	n/a	n/a
29	BRCA1	chr6:64474316-64474596	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr6:64515968-64516744	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr6:64516057-64516555	HCT-116	colon:	n/a	n/a
32	CBX3	chr6:64450448-64451115	HCT-116	colon:	n/a	n/a
33	CCNT2	chr6:64373424-64373624	K562	blood:	n/a	n/a
34	CEBPB	chr6:64474256-64474548	HepG2	liver:	n/a	chr6:64474412-64474423
35	CEBPB	chr6:64387238-64387610	K562	blood:	n/a	n/a
36	CEBPB	chr6:64516151-64516626	MCF-7	breast:	n/a	n/a
37	CEBPB	chr6:64504842-64504844	K562	blood:	n/a	n/a
38	CEBPB	chr6:64419031-64419394	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:64529773-64530065	Hela-S3	cervix:	n/a	chr6:64529929-64529940
40	CEBPB	chr6:64387185-64387633	A549	lung:	n/a	n/a
41	CEBPB	chr6:64387276-64387544	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:64387242-64387622	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:64512478-64512975	HepG2	liver:	n/a	chr6:64512893-64512904 chr6:64512891-64512904 chr6:64512539-64512548 chr6:64512695-64512708 chr6:64512537-64512550 chr6:64512539-64512550
44	CEBPB	chr6:64373212-64374152	Hela-S3	cervix:	n/a	chr6:64373996-64374007
45	CEBPB	chr6:64474381-64474479	Hela-S3	cervix:	n/a	chr6:64474412-64474423
46	CEBPB	chr6:64474248-64474584	IMR90	lung:	n/a	chr6:64474412-64474423
47	CEBPB	chr6:64373585-64374324	K562	blood:	n/a	chr6:64373996-64374007
48	CEBPB	chr6:64529788-64530058	A549	lung:	n/a	chr6:64529929-64529940
49	CEBPB	chr6:64373383-64374067	A549	lung:	n/a	chr6:64373996-64374007
50	CEBPB	chr6:64387213-64387616	MCF-7	breast:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:64515007-64515057	H1-hESC	embryonic stem cell:	embryo
2	chr6:64515007-64515057	H1-hESC	embryonic stem cell:	embryo
3	chr6:64390047-64390097	CMK	blood:	n/a
4	chr6:64356606-64356656	AG04450	lung:	fetal
5	chr6:64373226-64373276	U87	brain:	n/a
6	chr6:64527786-64527836	HUVEC	blood vessel:	n/a
7	chr6:64423797-64423847	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:64515007-64515057	AoSMC	blood vessel:	n/a
9	chr6:64390047-64390097	HepG2	liver:	n/a
10	chr6:64515007-64515057	T-47D	breast:	n/a
11	chr6:64390047-64390097	ProgFib	skin:	n/a
12	chr6:64515007-64515057	ECC-1	luminal epithelium:	n/a
13	chr6:64423797-64423847	AG09309	skin:	n/a
14	chr6:64527786-64527836	A549	lung:	n/a
15	chr6:64423797-64423847	AG04449	skin:	fetal
16	chr6:64527786-64527836	HRPEpiC	eye:	n/a
17	chr6:64527786-64527836	HAEpiC	amniotic membrane:	n/a
18	chr6:64390047-64390097	ovcar-3	ovarian:	n/a
19	chr6:64527786-64527836	HMEC	breast:	n/a
20	chr6:64423797-64423847	A549	lung:	n/a
21	chr6:64373226-64373276	ECC-1	luminal epithelium:	n/a
22	chr6:64515007-64515057	HEK293	kidney:	embryo
23	chr6:64373226-64373276	SKMC	muscle:	n/a
24	chr6:64390047-64390097	K562	blood:	n/a
25	chr6:64356606-64356656	HepG2	liver:	n/a
26	chr6:64515007-64515057	HUVEC	blood vessel:	n/a
27	chr6:64390047-64390097	HRE	kidney:	n/a
28	chr6:64356606-64356656	GM12892	blood:	n/a
29	chr6:64423797-64423847	AG10803	skin:	n/a
30	chr6:64373226-64373276	Jurkat	blood:	n/a
31	chr6:64527786-64527836	HCPEpiC	choroid plexus:	n/a
32	chr6:64515007-64515057	NT2-D1	testis:	n/a
33	chr6:64515007-64515057	GM19239	blood:	n/a
34	chr6:64515007-64515057	MCF10A-Er-Src	breast:	n/a
35	chr6:64527786-64527836	PANC-1	pancreas:	n/a
36	chr6:64515007-64515057	HCM	heart:	n/a
37	chr6:64423797-64423847	HNPCEpiC	eye:	n/a
38	chr6:64515007-64515057	HCF	heart:	n/a
39	chr6:64373226-64373276	SK-N-MC	brain:	n/a
40	chr6:64373226-64373276	HEK293	kidney:	embryo
41	chr6:64390047-64390097	Jurkat	blood:	n/a
42	chr6:64356606-64356656	ECC-1	luminal epithelium:	n/a
43	chr6:64527786-64527836	GM12878	blood:	n/a
44	chr6:64356606-64356656	NHBE	bronchial:	n/a
45	chr6:64390047-64390097	PFSK-1	brain:	n/a
46	chr6:64373226-64373276	Hela-S3	cervix:	n/a
47	chr6:64356606-64356656	HUVEC	blood vessel:	n/a
48	chr6:64390047-64390097	HPAEpiC	pulmonary alveolar:	n/a
49	chr6:64373226-64373276	GM12878	blood:	n/a
50	chr6:64423797-64423847	Jurkat	blood:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:64427838..64430410-chr6:64430505..64432521,2	K562	blood:
2	chr6:64362965..64366305-chr6:64371528..64374240,3	K562	blood:
3	chr6:64400258..64402209-chr6:64406199..64408000,2	K562	blood:
4	chr6:64352758..64355671-chr6:64367534..64370058,2	MCF-7	breast:
5	chr6:64357247..64360199-chr6:64361226..64363943,3	K562	blood:
6	chr6:64308255..64308783-chr6:64512237..64512792,2	MCF-7	breast:
7	chr6:64282565..64284253-chr6:64473647..64475499,2	K562	blood:
8	chr6:64362965..64366305-chr6:64371528..64374240,3	K562	blood:
9	chr6:64383782..64385638-chr6:64388338..64390794,2	K562	blood:
10	chr6:64380808..64382949-chr6:64384365..64385905,2	K562	blood:
11	chr6:64347337..64350491-chr6:64374830..64379357,4	K562	blood:
12	chr6:64356578..64359502-chr6:64361226..64363296,2	K562	blood:
13	chr6:64061712..64062525-chr6:64473904..64474743,3	MCF-7	breast:
14	chr6:64344073..64346131-chr6:64394565..64396308,2	K562	blood:
15	chr6:64344821..64347444-chr6:64375995..64378797,3	MCF-7	breast:
16	chr6:64308123..64308904-chr6:64474005..64474974,3	MCF-7	breast:
17	chr6:64369626..64372438-chr6:64376058..64378974,3	K562	blood:
18	chr6:64345767..64348847-chr6:64379987..64384270,3	K562	blood:
19	chr6:64344971..64347047-chr6:64415769..64418263,2	K562	blood:
20	chr6:64386744..64388275-chr6:64400257..64402696,2	K562	blood:
21	chr6:64503767..64506389-chr6:64511361..64513457,2	K562	blood:
22	chr6:64308218..64308885-chr6:64473955..64474904,2	K562	blood:
23	chr6:64281048..64283887-chr6:64413696..64416630,3	K562	blood:
24	chr6:64281916..64284591-chr6:64376493..64379119,2	MCF-7	breast:
25	chr6:64281737..64284624-chr6:64398462..64401172,2	MCF-7	breast:
26	chr6:64344529..64346659-chr6:64375006..64377744,2	K562	blood:
27	chr6:64344696..64348675-chr6:64358265..64360185,4	MCF-7	breast:
28	chr6:64348462..64350491-chr6:64377129..64380030,3	K562	blood:
29	chr6:64345547..64349156-chr6:64414533..64419389,4	K562	blood:
30	chr6:64366176..64368183-chr6:64370722..64372913,2	MCF-7	breast:
31	chr6:64462199..64464077-chr6:64470696..64472692,2	K562	blood:
32	chr6:64281819..64283796-chr6:64507632..64510704,3	MCF-7	breast:
33	chr6:64356578..64359502-chr6:64361226..64363296,2	K562	blood:
34	chr6:64369626..64372438-chr6:64376058..64378974,3	K562	blood:
35	chr6:64281613..64283644-chr6:64370499..64373275,2	MCF-7	breast:
36	chr6:64375915..64378129-chr6:64385885..64387947,2	MCF-7	breast:
37	chr6:64400258..64402209-chr6:64406199..64408000,2	K562	blood:
38	chr6:64375038..64377882-chr6:64378142..64379826,2	K562	blood:
39	chr6:64427028..64430486-chr6:64433539..64436384,3	K562	blood:
40	chr6:64479830..64482628-chr6:64484239..64486624,2	MCF-7	breast:
41	chr6:64281948..64284181-chr6:64510881..64512793,2	MCF-7	breast:
42	chr6:64282160..64284462-chr6:64395012..64398209,3	MCF-7	breast:
43	chr6:64347461..64349165-chr6:64396342..64398673,2	K562	blood:
44	chr6:64289813..64292111-chr6:64473996..64476108,2	K562	blood:
45	chr6:64380808..64382949-chr6:64384365..64385905,2	K562	blood:
46	chr6:64344337..64347250-chr6:64361782..64364684,2	MCF-7	breast:
47	chr6:64427028..64430486-chr6:64433539..64436384,3	K562	blood:
48	chr6:64062640..64063526-chr6:64474143..64474904,3	MCF-7	breast:
49	chr6:64366148..64368901-chr6:64374684..64376667,2	MCF-7	breast:
50	chr6:64062103..64065068-chr6:64510364..64512443,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF3-6	chr6:64507082-64507924	NONHSAT113355
2	lnc-PHF3-5	chr6:64487498-64488136	NONHSAT113354
3	lnc-PHF3-1	chr6:64531133-64532535	ENSG00000236345.1
4	lnc-PHF3-1	chr6:64516729-64516779	ENSG00000236345.1
5	lnc-PHF3-5	chr6:64489031-64489229	NONHSAT113354
6	lnc-PHF3-1	chr6:64527231-64527298	NONHSAT113357
7	lnc-PHF3-1	chr6:64531133-64532559	NONHSAT113357

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PHF3	hsa-miR-130b-3p	chr6:64424016-64424022
2	PHF3	hsa-miR-101-3p	chr6:64424284-64424290
3	PHF3	hsa-miR-130b-3p	chr6:64424003-64424023
4	PHF3	hsa-miR-101-3p	chr6:64424270-64424290
5	PHF3	hsa-miR-130b-3p	chr6:64424139-64424158

Variant related genes	Relation type
ENSG00000236345	TF binding region
EYS	TF binding region
ENSG00000218813	TF binding region
PHF3	TF binding region
ENSG00000236345	CpG island
EYS	CpG island
ENSG00000218813	CpG island
PHF3	CpG island
ENSG00000112245	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000118482	chromatin interactions
ENSG00000229117	chromatin interactions
ENSG00000266680	chromatin interactions
ENSG00000218813	chromatin interactions

Extended variants
information (count: 5821 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5821 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536105971	chr6:64355469-64355470	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs535683870	chr6:64355480-64355481	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs554167491	chr6:64355520-64355521	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs575981962	chr6:64355550-64355551	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs368737344	chr6:64355580-64355581	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs2225595	chr6:64355587-64355588	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558410006	chr6:64355616-64355617	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs562015956	chr6:64355673-64355674	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs148240234	chr6:64355681-64355682	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs372673017	chr6:64355690-64355691	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs560629939	chr6:64355709-64355710	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs528009380	chr6:64355715-64355716	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs141276192	chr6:64355735-64355736	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs561608915	chr6:64355770-64355771	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs539632138	chr6:64355788-64355789	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs56030400	chr6:64355796-64355797	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs550142200	chr6:64355837-64355838	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs565237107	chr6:64355866-64355867	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs571593916	chr6:64355879-64355880	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs200597978	chr6:64355892-64355893	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs551566778	chr6:64355908-64355909	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs532596552	chr6:64356012-64356013	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs112817052	chr6:64356128-64356129	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs527765375	chr6:64356163-64356164	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs565508459	chr6:64356170-64356171	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs150735581	chr6:64356215-64356216	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs548113922	chr6:64356243-64356244	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs4599615	chr6:64356277-64356278	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs558051745	chr6:64356314-64356315	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs375804081	chr6:64356570-64356571	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs536697221	chr6:64356572-64356573	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs150797375	chr6:64356606-64356607	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs201393499	chr6:64356688-64356689	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs148954717	chr6:64356707-64356708	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs556440760	chr6:64356710-64356711	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs11285703	chr6:64356712-64356713	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs398001804	chr6:64356733-64356734	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs372929712	chr6:64356750-64356751	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs576877394	chr6:64356762-64356763	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs376861534	chr6:64356774-64356775	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs369018233	chr6:64356781-64356782	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs374422240	chr6:64356789-64356790	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs553081130	chr6:64356793-64356794	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs187245323	chr6:64356796-64356797	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs11755640	chr6:64356847-64356848	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs113157963	chr6:64356871-64356872	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs113652281	chr6:64356872-64356873	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs116731725	chr6:64356917-64356918	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs139579722	chr6:64356967-64356968	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs191619179	chr6:64357021-64357022	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164920	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2589 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64347000-64370600	Weak transcription	Left Ventricle	heart
2	chr6:64347000-64383200	Weak transcription	Esophagus	oesophagus
3	chr6:64347000-64422400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:64347200-64356400	Weak transcription	Aorta	Aorta
5	chr6:64347400-64357000	Weak transcription	Placenta	Placenta
6	chr6:64347400-64358400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr6:64347400-64359600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:64347400-64370800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:64347600-64365200	Weak transcription	Fetal Stomach	stomach
10	chr6:64347600-64381000	Weak transcription	Fetal Thymus	thymus
11	chr6:64347800-64357000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:64347800-64358400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr6:64347800-64361400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr6:64347800-64370600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:64347800-64386400	Weak transcription	Colonic Mucosa	Colon
16	chr6:64348000-64356600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr6:64348600-64355800	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr6:64349400-64356200	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr6:64349400-64370600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr6:64350000-64363000	Weak transcription	Brain Germinal Matrix	brain
21	chr6:64350200-64359800	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr6:64350200-64374400	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr6:64350200-64381200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:64350200-64382800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr6:64350400-64358000	Weak transcription	Fetal Kidney	kidney
26	chr6:64350400-64359200	Weak transcription	Stomach Mucosa	stomach
27	chr6:64350400-64368400	Weak transcription	Fetal Brain Male	brain
28	chr6:64350400-64369600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:64350600-64359200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:64350600-64359200	Weak transcription	HSMMtube	muscle
31	chr6:64350600-64373200	Weak transcription	HSMM	muscle
32	chr6:64351000-64359000	Weak transcription	NHLF	lung
33	chr6:64351000-64359200	Weak transcription	Fetal Lung	lung
34	chr6:64351000-64360000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr6:64351000-64373200	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr6:64351200-64356400	Weak transcription	Fetal Intestine Large	intestine
37	chr6:64351200-64357000	Weak transcription	Small Intestine	intestine
38	chr6:64351200-64358200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr6:64351200-64359200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr6:64351200-64359200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr6:64351200-64385000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr6:64351200-64405000	Weak transcription	Thymus	Thymus
43	chr6:64351400-64356600	Weak transcription	Psoas Muscle	Psoas
44	chr6:64351400-64359000	Weak transcription	Liver	Liver
45	chr6:64351400-64359200	Weak transcription	Duodenum Mucosa	Duodenum
46	chr6:64351400-64369400	Weak transcription	Fetal Heart	heart
47	chr6:64352200-64362200	Weak transcription	Fetal Muscle Leg	muscle
48	chr6:64352200-64365600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:64352400-64355800	Enhancers	Colon Smooth Muscle	Colon
50	chr6:64352400-64356200	Weak transcription	Monocytes-CD14+_RO01746	blood

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