Variant report

Variant	nsv873155
Chromosome Location	chr1:212449195-212502157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1798)
CpG islands
(count:1100)
Chromatin interactive
region (count:78)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1798 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:212464827-212465194	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:212457762-212458752	K562	blood:	n/a	n/a
3	ARID3A	chr1:212460768-212461026	K562	blood:	n/a	n/a
4	ARID3A	chr1:212489252-212489485	K562	blood:	n/a	n/a
5	ARID3A	chr1:212463498-212463782	K562	blood:	n/a	n/a
6	ARID3A	chr1:212466830-212467243	K562	blood:	n/a	n/a
7	ARID3A	chr1:212457787-212458782	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:212483372-212483625	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:212462583-212462904	K562	blood:	n/a	n/a
10	ATF1	chr1:212457990-212458855	K562	blood:	n/a	n/a
11	ATF1	chr1:212497635-212497677	K562	blood:	n/a	n/a
12	ATF1	chr1:212464037-212464197	K562	blood:	n/a	n/a
13	ATF1	chr1:212489306-212489436	K562	blood:	n/a	n/a
14	ATF1	chr1:212469803-212470088	K562	blood:	n/a	n/a
15	ATF2	chr1:212459287-212459766	GM12878	blood:	n/a	n/a
16	ATF2	chr1:212457963-212458478	GM12878	blood:	n/a	n/a
17	ATF2	chr1:212457991-212458501	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr1:212457939-212458972	GM12878	blood:	n/a	n/a
19	ATF3	chr1:212464032-212464340	K562	blood:	n/a	n/a
20	BACH1	chr1:212462631-212462671	K562	blood:	n/a	n/a
21	BACH1	chr1:212458020-212459011	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr1:212459447-212460104	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr1:212457955-212458451	K562	blood:	n/a	n/a
24	BATF	chr1:212464023-212464282	GM12878	blood:	n/a	chr1:212464173-212464184 chr1:212464174-212464184 chr1:212464170-212464180
25	BATF	chr1:212489356-212489694	GM12878	blood:	n/a	n/a
26	BATF	chr1:212476325-212476640	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:212458581-212458974	GM12878	blood:	n/a	chr1:212458846-212458859 chr1:212458625-212458634 chr1:212458622-212458631
28	BCL3	chr1:212457683-212458578	A549	lung:	n/a	n/a
29	BCL3	chr1:212458453-212459006	GM12878	blood:	n/a	chr1:212458846-212458859 chr1:212458625-212458634 chr1:212458622-212458631
30	BCL3	chr1:212457657-212458370	A549	lung:	n/a	n/a
31	BCL3	chr1:212459387-212460152	A549	lung:	n/a	n/a
32	BCL3	chr1:212458429-212458985	A549	lung:	n/a	chr1:212458846-212458859 chr1:212458625-212458634 chr1:212458622-212458631
33	BCLAF1	chr1:212459279-212460105	GM12878	blood:	n/a	n/a
34	BCLAF1	chr1:212458542-212459094	GM12878	blood:	n/a	chr1:212459024-212459037 chr1:212458846-212458859 chr1:212458625-212458634 chr1:212458622-212458631
35	BCLAF1	chr1:212457873-212459111	GM12878	blood:	n/a	chr1:212459094-212459107 chr1:212459024-212459037 chr1:212458846-212458859 chr1:212458625-212458634 chr1:212458622-212458631
36	BCLAF1	chr1:212459219-212460145	GM12878	blood:	n/a	chr1:212459230-212459243
37	BHLHE40	chr1:212457930-212459050	GM12878	blood:	n/a	n/a
38	BHLHE40	chr1:212457785-212460059	K562	blood:	n/a	chr1:212459393-212459409
39	BHLHE40	chr1:212457940-212459093	HepG2	liver:	n/a	n/a
40	BHLHE40	chr1:212464922-212465128	HepG2	liver:	n/a	n/a
41	BRCA1	chr1:212458248-212458608	GM12878	blood:	n/a	n/a
42	BRCA1	chr1:212459559-212461049	Hela-S3	cervix:	n/a	chr1:212460300-212460307
43	BRCA1	chr1:212457751-212458543	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr1:212457846-212458969	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr1:212458099-212458876	HepG2	liver:	n/a	n/a
46	CBX3	chr1:212457562-212458992	K562	blood:	n/a	n/a
47	CBX3	chr1:212459342-212460181	K562	blood:	n/a	n/a
48	CCNT2	chr1:212460719-212460884	K562	blood:	n/a	n/a
49	CCNT2	chr1:212457631-212460019	K562	blood:	n/a	chr1:212458617-212458626 chr1:212458221-212458230 chr1:212458830-212458839
50	CEBPB	chr1:212501619-212501892	IMR90	lung:	n/a	chr1:212501765-212501776

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:212458738-212458788	HMEC	breast:	n/a
2	chr1:212459293-212459343	Hepatocyte	liver:	n/a
3	chr1:212458738-212458788	HMEC	breast:	n/a
4	chr1:212459293-212459343	Hepatocyte	liver:	n/a
5	chr1:212457424-212457474	SK-N-MC	brain:	n/a
6	chr1:212463238-212463288	SAEC	small airway:	n/a
7	chr1:212458738-212458788	T-47D	breast:	n/a
8	chr1:212463238-212463288	HCF	heart:	n/a
9	chr1:212483036-212483086	LNCaP	prostate:	n/a
10	chr1:212458138-212458188	AG09309	skin:	n/a
11	chr1:212459693-212459743	NHDF-neo	bronchial:	n/a
12	chr1:212463238-212463288	A549	lung:	n/a
13	chr1:212458726-212458776	HepG2	liver:	n/a
14	chr1:212458162-212458212	HNPCEpiC	eye:	n/a
15	chr1:212460169-212460219	SK-N-SH	brain:	n/a
16	chr1:212482804-212482854	SK-N-MC	brain:	n/a
17	chr1:212459290-212459340	HCM	heart:	n/a
18	chr1:212458138-212458188	ovcar-3	ovarian:	n/a
19	chr1:212460169-212460219	ProgFib	skin:	n/a
20	chr1:212457968-212458018	SAEC	small airway:	n/a
21	chr1:212459293-212459343	AG09309	skin:	n/a
22	chr1:212460169-212460219	ECC-1	luminal epithelium:	n/a
23	chr1:212459293-212459343	A549	lung:	n/a
24	chr1:212482804-212482854	HCF	heart:	n/a
25	chr1:212458736-212458786	HEEpiC	esophagus:	n/a
26	chr1:212459693-212459743	H1-hESC	embryonic stem cell:	embryo
27	chr1:212459293-212459343	ovcar-3	ovarian:	n/a
28	chr1:212482804-212482854	HCT-116	colon:	n/a
29	chr1:212455336-212455386	SAEC	small airway:	n/a
30	chr1:212483036-212483086	AG04449	skin:	fetal
31	chr1:212459693-212459743	ProgFib	skin:	n/a
32	chr1:212458726-212458776	NH-A	brain:	n/a
33	chr1:212458726-212458776	HEK293	kidney:	embryo
34	chr1:212464932-212464982	MCF10A-Er-Src	breast:	n/a
35	chr1:212458726-212458776	SK-N-SH	brain:	n/a
36	chr1:212483036-212483086	AoSMC	blood vessel:	n/a
37	chr1:212482804-212482854	U87	brain:	n/a
38	chr1:212459693-212459743	HepG2	liver:	n/a
39	chr1:212457968-212458018	GM12878	blood:	n/a
40	chr1:212458138-212458188	HCPEpiC	choroid plexus:	n/a
41	chr1:212457424-212457474	HUVEC	blood vessel:	n/a
42	chr1:212459029-212459079	NB4	blood:	n/a
43	chr1:212458138-212458188	IMR90	lung:	fetal
44	chr1:212483036-212483086	Hela-S3	cervix:	n/a
45	chr1:212459293-212459343	ECC-1	luminal epithelium:	n/a
46	chr1:212458726-212458776	LNCaP	prostate:	n/a
47	chr1:212459693-212459743	RPTEC	kidney:	n/a
48	chr1:212459029-212459079	Jurkat	blood:	n/a
49	chr1:212459693-212459743	MCF10A-Er-Src	breast:	n/a
50	chr1:212457915-212457965	SK-N-SH_RA	brain:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:212458567..212461041-chr1:212484616..212487117,2	MCF-7	breast:
2	chr1:212243775..212244788-chr1:212464563..212465496,5	K562	blood:
3	chr1:212458268..212458855-chr3:156873776..156874390,2	Hela-S3	cervix:
4	chr1:212458179..212461162-chr1:212476171..212477846,2	K562	blood:
5	chr1:212458597..212460542-chr1:212586367..212588357,2	MCF-7	breast:
6	chr1:212247974..212251489-chr1:212456327..212461743,5	MCF-7	breast:
7	chr1:212464978..212469431-chr1:212471345..212474474,8	K562	blood:
8	chr1:212412059..212414771-chr1:212457141..212460408,3	K562	blood:
9	chr1:212207316..212210086-chr1:212486077..212488983,2	MCF-7	breast:
10	chr1:212487148..212489947-chr1:212490208..212492615,2	K562	blood:
11	chr1:212457668..212459740-chr1:212480446..212483252,3	MCF-7	breast:
12	chr1:212244030..212244967-chr1:212464567..212465438,3	MCF-7	breast:
13	chr1:212235954..212236485-chr1:212466879..212467454,2	MCF-7	breast:
14	chr1:212207393..212212126-chr1:212456103..212460187,5	K562	blood:
15	chr1:212459145..212461703-chr1:212522964..212525110,2	K562	blood:
16	chr1:212413989..212416642-chr1:212457205..212458849,2	K562	blood:
17	chr1:212427390..212429185-chr1:212456996..212458799,2	K562	blood:
18	chr1:212413271..212416807-chr1:212458908..212461742,4	K562	blood:
19	chr1:212242593..212244252-chr1:212455169..212456960,2	MCF-7	breast:
20	chr1:212464233..212466790-chr1:212482649..212484293,2	K562	blood:
21	chr1:212467247..212471909-chr1:212472711..212476183,6	K562	blood:
22	chr1:212185459..212186004-chr1:212466665..212467621,2	K562	blood:
23	chr1:212317380..212319977-chr1:212460933..212463499,2	K562	blood:
24	chr1:212424523..212427087-chr1:212457087..212458716,2	K562	blood:
25	chr1:212458786..212460373-chr1:212467150..212468979,2	MCF-7	breast:
26	chr1:212497077..212499015-chr1:212500342..212502392,2	K562	blood:
27	chr1:212243541..212244748-chr1:212466553..212467549,3	MCF-7	breast:
28	chr1:212486882..212489433-chr1:212500849..212503303,2	K562	blood:
29	chr1:212447955..212449600-chr1:212455738..212457416,2	MCF-7	breast:
30	chr1:212241980..212244693-chr1:212464884..212466569,2	K562	blood:
31	chr1:212449889..212451870-chr1:212452202..212454178,2	K562	blood:
32	chr1:212206622..212210088-chr1:212456790..212460936,6	K562	blood:
33	chr1:212355708..212357502-chr1:212455747..212457374,2	K562	blood:
34	chr1:212222561..212225557-chr1:212458329..212459830,2	K562	blood:
35	chr1:212445933..212447648-chr1:212451138..212453935,2	K562	blood:
36	chr1:212456717..212458394-chr1:212483325..212485097,2	MCF-7	breast:
37	chr1:212340300..212343079-chr1:212458755..212460683,2	K562	blood:
38	chr1:212487148..212489947-chr1:212490208..212492615,2	K562	blood:
39	chr1:210546975..210548886-chr1:212457780..212460319,2	MCF-7	breast:
40	chr1:212457668..212459740-chr1:212480446..212483252,3	MCF-7	breast:
41	chr1:212456717..212458394-chr1:212483325..212485097,2	MCF-7	breast:
42	chr1:212348711..212350970-chr1:212462639..212464212,2	K562	blood:
43	chr1:212459558..212461570-chr1:212482463..212485190,2	K562	blood:
44	chr1:212446148..212447711-chr1:212451138..212453205,2	K562	blood:
45	chr1:212459054..212459554-chr3:186500797..186501438,2	Hela-S3	cervix:
46	chr1:212456696..212458579-chr1:212781101..212782934,2	K562	blood:
47	chr1:212497277..212499052-chr1:212502846..212504617,2	K562	blood:
48	chr1:212464978..212469431-chr1:212471345..212474474,8	K562	blood:
49	chr1:212458637..212459338-chr17:43138641..43139566,2	Hela-S3	cervix:
50	chr1:212497077..212499015-chr1:212500342..212502392,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM206-3	chr1:212472837-212472967	ENSG00000234915.1
2	lnc-TMEM206-3	chr1:212497766-212502930	l_184_chr1:212497765-212519010_heart
3	lnc-TMEM206-5	chr1:212458321-212458414	XLOC_001191
4	lnc-NENF-2	chr1:212470790-212471143	ENSG00000230063.1
5	lnc-NENF-4	chr1:212492719-212492894	NONHSAT009363
6	lnc-NENF-2	chr1:212472626-212472921	ENSG00000230063.1
7	lnc-NENF-4	chr1:212475205-212475434	NONHSAT009362
8	lnc-NENF-4	chr1:212492719-212492887	NONHSAT009362
9	lnc-NENF-4	chr1:212485015-212485041	NONHSAT009363

No data

Variant related genes	Relation type
ENSG00000225338	TF binding region
PPP2R5A	TF binding region
ENSG00000230063	TF binding region
ENSG00000225338	CpG island
PPP2R5A	CpG island
ENSG00000230063	CpG island
ENSG00000162772	chromatin interactions
ENSG00000136448	chromatin interactions
ENSG00000143493	chromatin interactions
ENSG00000229983	chromatin interactions
ENSG00000226251	chromatin interactions
ENSG00000074621	chromatin interactions
ENSG00000266552	chromatin interactions
ENSG00000066027	chromatin interactions
ENSG00000220749	chromatin interactions
ENSG00000138614	chromatin interactions
ENSG00000156976	chromatin interactions
ENSG00000252879	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000065600	chromatin interactions
ENSG00000264358	chromatin interactions
ENSG00000167468	chromatin interactions
ENSG00000104472	chromatin interactions
ENSG00000143476	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000100523	chromatin interactions
ENSG00000230063	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000258731	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000225338	chromatin interactions
ENSG00000022840	chromatin interactions
ENSG00000162231	chromatin interactions

Extended variants
information (count: 1817 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1817 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11119900	chr1:212449195-212449196	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78869470	chr1:212449230-212449231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540037283	chr1:212449341-212449342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551159622	chr1:212449354-212449355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370401645	chr1:212449372-212449373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112807567	chr1:212449373-212449374	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
7	rs536634072	chr1:212449388-212449389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554984074	chr1:212449396-212449397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs351418	chr1:212449403-212449404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs534566843	chr1:212449467-212449468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553249216	chr1:212449530-212449531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191242012	chr1:212449563-212449564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545217507	chr1:212449664-212449665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183530624	chr1:212449672-212449673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576651360	chr1:212449721-212449722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543837566	chr1:212449735-212449736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs562019013	chr1:212449797-212449798	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188530255	chr1:212449847-212449848	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141659439	chr1:212449889-212449890	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546526746	chr1:212449900-212449901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs72752367	chr1:212449977-212449978	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557494979	chr1:212450072-212450073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs533340636	chr1:212450097-212450098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375399230	chr1:212450141-212450142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs377727690	chr1:212450214-212450215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs351417	chr1:212450216-212450217	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs536797271	chr1:212450217-212450218	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs78479073	chr1:212450264-212450265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79261779	chr1:212450266-212450267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs77835133	chr1:212450276-212450277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs76569869	chr1:212450277-212450278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs548671235	chr1:212450330-212450331	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566888199	chr1:212450368-212450369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs75661031	chr1:212450392-212450393	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs12562618	chr1:212450399-212450400	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs192102153	chr1:212450406-212450407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569135144	chr1:212450409-212450410	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs114639177	chr1:212450516-212450517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575516763	chr1:212450536-212450537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368353117	chr1:212450550-212450551	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs77055446	chr1:212450617-212450618	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs78087693	chr1:212450626-212450627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369524505	chr1:212450667-212450668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs376202498	chr1:212450668-212450669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs397861575	chr1:212450681-212450682	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs372100536	chr1:212450726-212450727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573559030	chr1:212450745-212450746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562177012	chr1:212450751-212450752	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573920456	chr1:212450757-212450758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs541441830	chr1:212450767-212450768	Weak transcription	Chromatin interactive region	1 gene(s)	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1850 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212446000-212457000	Weak transcription	Stomach Mucosa	stomach
2	chr1:212446000-212457600	Weak transcription	Fetal Brain Female	brain
3	chr1:212446200-212454000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:212446400-212457200	Weak transcription	Fetal Heart	heart
5	chr1:212454000-212454200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:212454200-212457200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:212454600-212455400	Enhancers	Fetal Lung	lung
8	chr1:212455000-212455200	Enhancers	Hela-S3	cervix
9	chr1:212455000-212455200	Enhancers	NHLF	lung
10	chr1:212455000-212455400	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr1:212455000-212455400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:212455000-212455400	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr1:212455000-212455800	Enhancers	NHDF-Ad	bronchial
14	chr1:212455200-212455400	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr1:212455200-212455400	Enhancers	A549	lung
16	chr1:212455200-212457200	Weak transcription	Hela-S3	cervix
17	chr1:212455200-212457200	Weak transcription	NHLF	lung
18	chr1:212455400-212455600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:212455400-212456400	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr1:212455400-212457000	Weak transcription	Fetal Lung	lung
21	chr1:212455400-212457200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr1:212455400-212457200	Weak transcription	A549	lung
23	chr1:212455400-212457400	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr1:212455600-212457200	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr1:212455600-212457400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:212455800-212457400	Weak transcription	NHDF-Ad	bronchial
27	chr1:212456400-212457000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr1:212456600-212457200	Enhancers	Primary B cells from cord blood	blood
29	chr1:212456800-212457000	Enhancers	Primary T cells from cord blood	blood
30	chr1:212456800-212457000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr1:212456800-212457000	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr1:212456800-212457000	Enhancers	K562	blood
33	chr1:212456800-212457200	Enhancers	HepG2	liver
34	chr1:212456800-212457400	Enhancers	Primary T cells fromperipheralblood	blood
35	chr1:212457000-212457200	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr1:212457000-212457200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr1:212457000-212457200	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr1:212457000-212457200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr1:212457000-212457200	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr1:212457000-212457200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:212457000-212457200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr1:212457000-212457200	Enhancers	Adipose Nuclei	Adipose
43	chr1:212457000-212457200	Enhancers	Liver	Liver
44	chr1:212457000-212457200	Enhancers	Fetal Intestine Small	intestine
45	chr1:212457000-212457200	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr1:212457000-212457200	Enhancers	Stomach Mucosa	stomach
47	chr1:212457000-212457200	Enhancers	Dnd41	blood
48	chr1:212457000-212457400	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr1:212457000-212457600	Enhancers	Fetal Lung	lung
50	chr1:212457000-212457600	Flanking Active TSS	K562	blood

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