Variant report

Variant	nsv873158
Chromosome Location	chr1:212610755-212646225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:763)
CpG islands
(count:366)
Chromatin interactive
region (count:75)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:212629322-212629574	HepG2	liver:	n/a	n/a
2	ATF1	chr1:212612248-212612603	K562	blood:	n/a	n/a
3	BHLHE40	chr1:212629244-212629542	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:212643471-212643619	K562	blood:	n/a	n/a
5	BHLHE40	chr1:212631302-212631304	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:212629194-212629545	K562	blood:	n/a	n/a
7	BHLHE40	chr1:212612245-212612610	K562	blood:	n/a	n/a
8	BHLHE40	chr1:212633871-212634123	K562	blood:	n/a	n/a
9	BHLHE40	chr1:212631181-212631342	K562	blood:	n/a	n/a
10	BRCA1	chr1:212629265-212629529	HepG2	liver:	n/a	n/a
11	BRCA1	chr1:212631178-212631403	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr1:212645114-212645188	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr1:212629383-212629449	GM12878	blood:	n/a	n/a
14	BRCA1	chr1:212629240-212629556	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr1:212632106-212632397	K562	blood:	n/a	n/a
16	CBX3	chr1:212611546-212612003	K562	blood:	n/a	n/a
17	CBX3	chr1:212631864-212632541	K562	blood:	n/a	n/a
18	CBX3	chr1:212612217-212612656	K562	blood:	n/a	n/a
19	CBX3	chr1:212630987-212631675	K562	blood:	n/a	n/a
20	CBX3	chr1:212631034-212631565	K562	blood:	n/a	n/a
21	CCNT2	chr1:212612290-212612513	K562	blood:	n/a	n/a
22	CEBPB	chr1:212610513-212610889	Hela-S3	cervix:	n/a	chr1:212610699-212610710
23	CEBPB	chr1:212633103-212633390	HepG2	liver:	n/a	chr1:212633237-212633248
24	CEBPB	chr1:212629412-212629414	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:212632814-212632947	K562	blood:	n/a	n/a
26	CEBPB	chr1:212610494-212610860	ECC-1	luminal epithelium:	n/a	chr1:212610699-212610710
27	CEBPB	chr1:212621885-212621976	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:212615023-212615146	K562	blood:	n/a	n/a
29	CEBPB	chr1:212610536-212610864	HepG2	liver:	n/a	chr1:212610699-212610710
30	CEBPB	chr1:212610455-212610858	ECC-1	luminal epithelium:	n/a	chr1:212610699-212610710
31	CEBPB	chr1:212610551-212610881	IMR90	lung:	n/a	chr1:212610699-212610710
32	CEBPB	chr1:212610534-212610875	A549	lung:	n/a	chr1:212610699-212610710
33	CEBPB	chr1:212610526-212610889	K562	blood:	n/a	chr1:212610699-212610710
34	CEBPB	chr1:212624413-212624665	A549	lung:	n/a	n/a
35	CEBPB	chr1:212621895-212621989	A549	lung:	n/a	n/a
36	CEBPB	chr1:212635624-212635668	HepG2	liver:	n/a	chr1:212635652-212635663
37	CEBPB	chr1:212643356-212643846	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:212643487-212643633	A549	lung:	n/a	n/a
39	CEBPB	chr1:212615585-212615715	Hela-S3	cervix:	n/a	chr1:212615679-212615690
40	CEBPB	chr1:212624460-212624597	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:212621868-212622076	HepG2	liver:	n/a	n/a
42	CEBPB	chr1:212610436-212610900	A549	lung:	n/a	chr1:212610699-212610710
43	CEBPB	chr1:212610508-212610902	K562	blood:	n/a	chr1:212610699-212610710
44	CEBPB	chr1:212621864-212622078	IMR90	lung:	n/a	n/a
45	CHD2	chr1:212631206-212631225	K562	blood:	n/a	n/a
46	CREB1	chr1:212643348-212643818	A549	lung:	n/a	n/a
47	CTCF	chr1:212631091-212631425	K562	blood:	n/a	n/a
48	CTCF	chr1:212629279-212629513	MCF-7	breast:	n/a	chr1:212629400-212629409 chr1:212629389-212629410 chr1:212629367-212629380 chr1:212629395-212629411 chr1:212629397-212629407 chr1:212629394-212629412 chr1:212629396-212629409
49	CTCF	chr1:212629250-212629539	Gliobla	brain:	n/a	chr1:212629400-212629409 chr1:212629389-212629410 chr1:212629367-212629380 chr1:212629395-212629411 chr1:212629397-212629407 chr1:212629394-212629412 chr1:212629396-212629409
50	CTCF	chr1:212629340-212629490	HVMF	connective:	n/a	chr1:212629400-212629409 chr1:212629389-212629410 chr1:212629367-212629380 chr1:212629395-212629411 chr1:212629397-212629407 chr1:212629394-212629412 chr1:212629396-212629409

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:212619763-212619813	HAEpiC	amniotic membrane:	n/a
2	chr1:212620748-212620798	U87	brain:	n/a
3	chr1:212619763-212619813	ProgFib	skin:	n/a
4	chr1:212626474-212626524	U87	brain:	n/a
5	chr1:212619763-212619813	ovcar-3	ovarian:	n/a
6	chr1:212619763-212619813	AG09309	skin:	n/a
7	chr1:212619380-212619430	HepG2	liver:	n/a
8	chr1:212620748-212620798	AG09309	skin:	n/a
9	chr1:212635804-212635854	HAEpiC	amniotic membrane:	n/a
10	chr1:212620748-212620798	SKMC	muscle:	n/a
11	chr1:212619763-212619813	CMK	blood:	n/a
12	chr1:212619763-212619813	HUVEC	blood vessel:	n/a
13	chr1:212620748-212620798	Jurkat	blood:	n/a
14	chr1:212626474-212626524	HCT-116	colon:	n/a
15	chr1:212619380-212619430	AG04450	lung:	fetal
16	chr1:212619763-212619813	ECC-1	luminal epithelium:	n/a
17	chr1:212643521-212643571	RPTEC	kidney:	n/a
18	chr1:212619380-212619430	MCF-7	breast:	n/a
19	chr1:212619763-212619813	SKMC	muscle:	n/a
20	chr1:212619763-212619813	HepG2	liver:	n/a
21	chr1:212643521-212643571	PrEC	prostate:	n/a
22	chr1:212626474-212626524	HUVEC	blood vessel:	n/a
23	chr1:212643521-212643571	HAEpiC	amniotic membrane:	n/a
24	chr1:212619763-212619813	MCF-7	breast:	n/a
25	chr1:212635804-212635854	HCM	heart:	n/a
26	chr1:212635804-212635854	T-47D	breast:	n/a
27	chr1:212626474-212626524	AG04449	skin:	fetal
28	chr1:212619380-212619430	CMK	blood:	n/a
29	chr1:212643521-212643571	ProgFib	skin:	n/a
30	chr1:212626474-212626524	GM19239	blood:	n/a
31	chr1:212643521-212643571	AoSMC	blood vessel:	n/a
32	chr1:212626474-212626524	AG09309	skin:	n/a
33	chr1:212619763-212619813	HCPEpiC	choroid plexus:	n/a
34	chr1:212626474-212626524	HRPEpiC	eye:	n/a
35	chr1:212619380-212619430	NB4	blood:	n/a
36	chr1:212619380-212619430	GM12878	blood:	n/a
37	chr1:212619763-212619813	HL-60	blood:	n/a
38	chr1:212643521-212643571	K562	blood:	n/a
39	chr1:212619380-212619430	ovcar-3	ovarian:	n/a
40	chr1:212635804-212635854	PrEC	prostate:	n/a
41	chr1:212635804-212635854	HL-60	blood:	n/a
42	chr1:212626474-212626524	T-47D	breast:	n/a
43	chr1:212643521-212643571	PFSK-1	brain:	n/a
44	chr1:212635804-212635854	PANC-1	pancreas:	n/a
45	chr1:212643521-212643571	HCF	heart:	n/a
46	chr1:212643521-212643571	ovcar-3	ovarian:	n/a
47	chr1:212635804-212635854	ProgFib	skin:	n/a
48	chr1:212643521-212643571	HIPEpiC	eye:	n/a
49	chr1:212619380-212619430	HUVEC	blood vessel:	n/a
50	chr1:212620748-212620798	HL-60	blood:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:212230913..212233313-chr1:212635726..212638248,2	K562	blood:
2	chr1:212641004..212645017-chr1:212780879..212784098,6	K562	blood:
3	chr1:212185000..212185952-chr1:212629353..212630011,4	K562	blood:
4	chr1:212541081..212541608-chr1:212629168..212629838,2	MCF-7	breast:
5	chr1:212639889..212643172-chr1:212795709..212798826,3	K562	blood:
6	chr1:212185098..212185653-chr1:212627594..212628123,2	K562	blood:
7	chr1:212623749..212625535-chr1:212782027..212783657,2	K562	blood:
8	chr1:212606882..212608476-chr1:212631103..212632696,2	MCF-7	breast:
9	chr1:212634490..212636091-chr1:212645524..212647172,2	K562	blood:
10	chr1:212645024..212669819-chr1:212778382..212791615,68	K562	blood:
11	chr1:212634490..212636091-chr1:212645524..212647172,2	K562	blood:
12	chr1:212645805..212648932-chr1:212650111..212654210,5	K562	blood:
13	chr1:212631286..212631786-chr1:212838659..212839233,2	K562	blood:
14	chr1:212630980..212631781-chr1:212955510..212956087,2	K562	blood:
15	chr1:211871766..211872437-chr1:212628934..212629488,2	K562	blood:
16	chr1:212548749..212550698-chr1:212631997..212633826,2	K562	blood:
17	chr1:212589362..212592084-chr1:212630605..212632407,2	K562	blood:
18	chr1:212630852..212631355-chr1:212641154..212641815,2	K562	blood:
19	chr1:212204655..212207528-chr1:212612348..212614666,2	K562	blood:
20	chr1:212592142..212594928-chr1:212610906..212612518,2	K562	blood:
21	chr1:212644101..212647867-chr1:212656026..212658886,3	K562	blood:
22	chr1:212622646..212625445-chr1:212627199..212631249,4	K562	blood:
23	chr1:212540816..212542855-chr1:212627781..212629569,2	K562	blood:
24	chr1:212626698..212637479-chr1:212779685..212784714,19	K562	blood:
25	chr1:212642565..212644909-chr1:212645772..212647720,2	K562	blood:
26	chr1:212646040..212648577-chr1:212802320..212804648,2	K562	blood:
27	chr1:212617519..212622581-chr1:212622841..212626048,6	K562	blood:
28	chr1:212606631..212609505-chr1:212609658..212612237,5	K562	blood:
29	chr1:212641150..212642930-chr1:212730817..212733456,2	MCF-7	breast:
30	chr1:211854193..211854711-chr1:212629143..212629667,2	K562	blood:
31	chr1:212313138..212314989-chr1:212629911..212632338,2	K562	blood:
32	chr1:212235956..212236900-chr1:212628594..212629549,5	K562	blood:
33	chr1:212611206..212613997-chr1:212623720..212626273,2	MCF-7	breast:
34	chr1:212622374..212624323-chr1:212736768..212739383,2	K562	blood:
35	chr1:212612620..212614790-chr1:212782003..212783590,2	K562	blood:
36	chr1:212630808..212631798-chr1:213168552..213169259,4	K562	blood:
37	chr1:212641004..212643308-chr1:212781641..212784619,3	K562	blood:
38	chr1:212639121..212641967-chr1:212780550..212783593,4	MCF-7	breast:
39	chr1:212635707..212638056-chr1:212640059..212642694,3	K562	blood:
40	chr1:212606261..212607831-chr1:212629678..212631842,2	K562	blood:
41	chr1:212634664..212637460-chr1:212638255..212640310,2	MCF-7	breast:
42	chr1:212604148..212606552-chr1:212621916..212623938,2	K562	blood:
43	chr1:212634664..212637460-chr1:212638255..212640310,2	MCF-7	breast:
44	chr1:212628946..212629890-chr1:212838453..212839228,2	K562	blood:
45	chr1:212540519..212541569-chr1:212628751..212630135,3	K562	blood:
46	chr1:212636838..212639720-chr1:212643460..212645324,2	K562	blood:
47	chr1:212636838..212639720-chr1:212643460..212645324,2	K562	blood:
48	chr1:212243790..212245029-chr1:212629216..212630156,6	K562	blood:
49	chr1:212561364..212563303-chr1:212611566..212613873,2	K562	blood:
50	chr1:212646206..212648127-chr1:212778382..212780130,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM206-2	chr1:212640158-212640439	XLOC_001193
2	lnc-TMEM206-2	chr1:212641009-212641085	XLOC_001193

No data

Variant related genes	Relation type
ENSG00000224535	TF binding region
ENSG00000224535	CpG island
ENSG00000264590	chromatin interactions
ENSG00000237980	chromatin interactions
ENSG00000162771	chromatin interactions
ENSG00000260805	chromatin interactions
ENSG00000162772	chromatin interactions
ENSG00000117691	chromatin interactions
ENSG00000224535	chromatin interactions

Extended variants
information (count: 1386 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1386 , 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	rs583058	chr1:212610755-212610756	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571593605	chr1:212610783-212610784	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs185167631	chr1:212610864-212610865	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528118169	chr1:212610907-212610908	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs527840	chr1:212611039-212611040	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs595066	chr1:212611054-212611055	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs532263369	chr1:212611077-212611078	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550776102	chr1:212611119-212611120	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs189927681	chr1:212611143-212611144	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs74138155	chr1:212611145-212611146	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs539318313	chr1:212611194-212611195	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs114110198	chr1:212611217-212611218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs199960728	chr1:212611218-212611219	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs386639116	chr1:212611238-212611239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs369203059	chr1:212611261-212611262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs377607902	chr1:212611276-212611277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139531131	chr1:212611288-212611289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144289657	chr1:212611311-212611312	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12041303	chr1:212611336-212611337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs578199747	chr1:212611418-212611419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs74140013	chr1:212611470-212611471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs182009750	chr1:212611480-212611481	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575782129	chr1:212611498-212611499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543220730	chr1:212611510-212611511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184702028	chr1:212611514-212611515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75258460	chr1:212611536-212611537	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs147729891	chr1:212611538-212611539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs60977696	chr1:212611544-212611545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs550639071	chr1:212611545-212611546	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562782974	chr1:212611630-212611631	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370356849	chr1:212611631-212611632	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs188173099	chr1:212611663-212611664	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs180708101	chr1:212611682-212611683	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571875639	chr1:212611723-212611724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567431442	chr1:212611755-212611756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554534599	chr1:212611850-212611851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552411252	chr1:212611988-212611989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565834362	chr1:212612026-212612027	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534749267	chr1:212612033-212612034	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs11119937	chr1:212612048-212612049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs370309991	chr1:212612119-212612120	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs554868410	chr1:212612122-212612123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs571515689	chr1:212612160-212612161	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs539007853	chr1:212612208-212612209	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557396853	chr1:212612306-212612307	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs576003625	chr1:212612308-212612309	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536884380	chr1:212612331-212612332	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs6676744	chr1:212612354-212612355	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs186444429	chr1:212612411-212612412	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs191322006	chr1:212612412-212612413	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:922 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212607000-212614000	Weak transcription	Gastric	stomach
2	chr1:212607000-212623400	Weak transcription	HSMMtube	muscle
3	chr1:212607200-212617400	Weak transcription	Fetal Intestine Large	intestine
4	chr1:212607200-212617600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr1:212607400-212614000	Weak transcription	Fetal Kidney	kidney
6	chr1:212607400-212617600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:212607400-212617600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr1:212607400-212618800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr1:212607400-212622800	Weak transcription	Primary B cells from cord blood	blood
10	chr1:212607400-212625800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr1:212607400-212626000	Weak transcription	Colonic Mucosa	Colon
12	chr1:212607400-212629200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr1:212607600-212614000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr1:212607600-212617600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:212607600-212617600	Weak transcription	Placenta	Placenta
16	chr1:212607600-212617800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:212607600-212618000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:212607600-212618000	Weak transcription	Primary B cells from peripheral blood	blood
19	chr1:212607600-212619000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr1:212607600-212619000	Weak transcription	Thymus	Thymus
21	chr1:212607600-212619200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:212607600-212620600	Weak transcription	HMEC	breast
23	chr1:212607600-212621800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr1:212607600-212624000	Weak transcription	Fetal Brain Male	brain
25	chr1:212607600-212625800	Weak transcription	Stomach Mucosa	stomach
26	chr1:212607600-212626000	Weak transcription	NH-A	brain
27	chr1:212607800-212613800	Weak transcription	Psoas Muscle	Psoas
28	chr1:212607800-212614000	Weak transcription	Right Atrium	heart
29	chr1:212607800-212616800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:212607800-212617400	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr1:212607800-212617400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr1:212607800-212617600	Weak transcription	Primary T cells from cord blood	blood
33	chr1:212607800-212617600	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr1:212607800-212617600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr1:212607800-212617600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr1:212607800-212617600	Weak transcription	Right Ventricle	heart
37	chr1:212607800-212617800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:212607800-212617800	Weak transcription	Adipose Nuclei	Adipose
39	chr1:212607800-212618800	Weak transcription	Brain Germinal Matrix	brain
40	chr1:212607800-212619200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:212607800-212619200	Weak transcription	Fetal Thymus	thymus
42	chr1:212607800-212620000	Weak transcription	Osteobl	bone
43	chr1:212607800-212623400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr1:212607800-212624400	Weak transcription	NHEK	skin
45	chr1:212607800-212625800	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr1:212607800-212625800	Weak transcription	NHLF	lung
47	chr1:212607800-212629400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:212608000-212612200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr1:212608000-212613800	Weak transcription	Esophagus	oesophagus
50	chr1:212608000-212613800	Weak transcription	Skeletal Muscle Female	skeletal muscle

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