Variant report

Variant	nsv1009290
Chromosome Location	chr1:189554045-189908459
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1782)
CpG islands
(count:122)
Chromatin interactive
region (count:53)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1782 , 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	chr1:189655218-189655237	K562	blood:	n/a	n/a
2	ARID3A	chr1:189743917-189744230	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:189576379-189576601	HepG2	liver:	n/a	n/a
4	ATF1	chr1:189849426-189849494	K562	blood:	n/a	n/a
5	ATF1	chr1:189645110-189645131	K562	blood:	n/a	n/a
6	ATF1	chr1:189692607-189692756	K562	blood:	n/a	n/a
7	ATF1	chr1:189759191-189759268	K562	blood:	n/a	n/a
8	ATF1	chr1:189869294-189869344	K562	blood:	n/a	n/a
9	ATF3	chr1:189624065-189624449	HCT-116	colon:	n/a	n/a
10	ATF3	chr1:189576142-189576647	A549	lung:	n/a	n/a
11	BACH1	chr1:189774960-189775194	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:189660033-189660067	K562	blood:	n/a	n/a
13	BATF	chr1:189565411-189565576	GM12878	blood:	n/a	chr1:189565508-189565518
14	BCL3	chr1:189575858-189576821	A549	lung:	n/a	n/a
15	BCL3	chr1:189650561-189651101	A549	lung:	n/a	n/a
16	BCL3	chr1:189743704-189744394	A549	lung:	n/a	chr1:189744338-189744347
17	BHLHE40	chr1:189821289-189821443	GM12878	blood:	n/a	n/a
18	BRCA1	chr1:189588843-189589197	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr1:189640354-189640407	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr1:189627431-189627982	HCT-116	colon:	n/a	n/a
21	CBX3	chr1:189828579-189828874	K562	blood:	n/a	n/a
22	CBX3	chr1:189588801-189589528	HCT-116	colon:	n/a	n/a
23	CBX3	chr1:189631288-189631734	HCT-116	colon:	n/a	n/a
24	CBX3	chr1:189828545-189828884	K562	blood:	n/a	n/a
25	CBX3	chr1:189588763-189589390	HCT-116	colon:	n/a	n/a
26	CBX3	chr1:189626762-189627309	HCT-116	colon:	n/a	n/a
27	CBX3	chr1:189631264-189631803	HCT-116	colon:	n/a	n/a
28	CEBPB	chr1:189631210-189631769	HCT-116	colon:	n/a	n/a
29	CEBPB	chr1:189731505-189731602	K562	blood:	n/a	chr1:189731575-189731586
30	CEBPB	chr1:189672613-189673256	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:189626830-189627327	MCF-7	breast:	n/a	chr1:189627200-189627217
32	CEBPB	chr1:189864108-189864385	IMR90	lung:	n/a	chr1:189864217-189864230 chr1:189864219-189864228 chr1:189864217-189864228 chr1:189864219-189864228 chr1:189864219-189864228 chr1:189864218-189864229 chr1:189864219-189864228
33	CEBPB	chr1:189650548-189650953	A549	lung:	n/a	n/a
34	CEBPB	chr1:189626895-189627312	Hela-S3	cervix:	n/a	chr1:189627200-189627217
35	CEBPB	chr1:189818364-189818608	A549	lung:	n/a	n/a
36	CEBPB	chr1:189606177-189606515	Hela-S3	cervix:	n/a	chr1:189606323-189606334
37	CEBPB	chr1:189626911-189627214	MCF-7	breast:	n/a	n/a
38	CEBPB	chr1:189553909-189554210	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:189623883-189624474	A549	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
40	CEBPB	chr1:189572754-189573023	HepG2	liver:	n/a	chr1:189572877-189572890 chr1:189572878-189572889 chr1:189572877-189572888 chr1:189572879-189572888
41	CEBPB	chr1:189576169-189576599	A549	lung:	n/a	n/a
42	CEBPB	chr1:189606035-189606521	A549	lung:	n/a	chr1:189606323-189606334
43	CEBPB	chr1:189689001-189689131	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:189688098-189688417	A549	lung:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
45	CEBPB	chr1:189604520-189604793	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:189623953-189624457	MCF-7	breast:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
47	CEBPB	chr1:189624021-189624372	A549	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
48	CEBPB	chr1:189627413-189628000	HCT-116	colon:	n/a	n/a
49	CEBPB	chr1:189626761-189627411	A549	lung:	n/a	chr1:189627200-189627217
50	CEBPB	chr1:189624017-189624416	A549	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:189722103-189722153	SK-N-SH	brain:	n/a
2	chr1:189722103-189722153	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:189722103-189722153	HRE	kidney:	n/a
4	chr1:189744005-189744055	BE2_C	brain:	n/a
5	chr1:189744005-189744055	Caco-2	colon:	n/a
6	chr1:189722103-189722153	NB4	blood:	n/a
7	chr1:189744005-189744055	NT2-D1	testis:	n/a
8	chr1:189722103-189722153	ovcar-3	ovarian:	n/a
9	chr1:189744005-189744055	RPTEC	kidney:	n/a
10	chr1:189722103-189722153	HRPEpiC	eye:	n/a
11	chr1:189744005-189744055	PANC-1	pancreas:	n/a
12	chr1:189744005-189744055	HCPEpiC	choroid plexus:	n/a
13	chr1:189722103-189722153	U87	brain:	n/a
14	chr1:189722103-189722153	PANC-1	pancreas:	n/a
15	chr1:189722103-189722153	NHBE	bronchial:	n/a
16	chr1:189744005-189744055	NH-A	brain:	n/a
17	chr1:189722103-189722153	AG09309	skin:	n/a
18	chr1:189722103-189722153	AG10803	skin:	n/a
19	chr1:189722103-189722153	HMEC	breast:	n/a
20	chr1:189744005-189744055	GM12892	blood:	n/a
21	chr1:189722103-189722153	MCF-7	breast:	n/a
22	chr1:189744005-189744055	MCF10A-Er-Src	breast:	n/a
23	chr1:189744005-189744055	ECC-1	luminal epithelium:	n/a
24	chr1:189744005-189744055	HRCEpiC	kidney:	n/a
25	chr1:189744005-189744055	Jurkat	blood:	n/a
26	chr1:189722103-189722153	MCF10A-Er-Src	breast:	n/a
27	chr1:189722103-189722153	HL-60	blood:	n/a
28	chr1:189744005-189744055	Hepatocyte	liver:	n/a
29	chr1:189722103-189722153	HIPEpiC	eye:	n/a
30	chr1:189744005-189744055	T-47D	breast:	n/a
31	chr1:189722103-189722153	BJ	skin:	n/a
32	chr1:189722103-189722153	SAEC	small airway:	n/a
33	chr1:189744005-189744055	MCF-7	breast:	n/a
34	chr1:189744005-189744055	HIPEpiC	eye:	n/a
35	chr1:189722103-189722153	AG04449	skin:	fetal
36	chr1:189722103-189722153	GM06990	blood:	n/a
37	chr1:189744005-189744055	H1-hESC	embryonic stem cell:	embryo
38	chr1:189744005-189744055	AG09319	gingival:	n/a
39	chr1:189744005-189744055	AG10803	skin:	n/a
40	chr1:189744005-189744055	GM19239	blood:	n/a
41	chr1:189744005-189744055	K562	blood:	n/a
42	chr1:189722103-189722153	HEEpiC	esophagus:	n/a
43	chr1:189744005-189744055	CMK	blood:	n/a
44	chr1:189722103-189722153	IMR90	lung:	fetal
45	chr1:189722103-189722153	LNCaP	prostate:	n/a
46	chr1:189744005-189744055	ProgFib	skin:	n/a
47	chr1:189722103-189722153	HCM	heart:	n/a
48	chr1:189722103-189722153	HNPCEpiC	eye:	n/a
49	chr1:189722103-189722153	AoSMC	blood vessel:	n/a
50	chr1:189744005-189744055	HRPEpiC	eye:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:189790429..189793066-chr1:189800961..189802500,2	MCF-7	breast:
2	chr1:189740038..189741669-chr1:189745873..189748337,2	K562	blood:
3	chr1:189677420..189678491-chr1:190289916..190290952,3	MCF-7	breast:
4	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
5	chr1:189627826..189630498-chr1:189636599..189639267,2	MCF-7	breast:
6	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
7	chr1:189705156..189706947-chr1:189708552..189710958,2	K562	blood:
8	chr1:189853792..189857239-chr1:189857756..189861653,3	MCF-7	breast:
9	chr1:189646033..189647879-chr5:175874488..175876371,2	MCF-7	breast:
10	chr1:189778329..189781313-chr1:189784587..189786793,2	MCF-7	breast:
11	chr1:189588020..189590795-chr1:189591484..189594244,3	MCF-7	breast:
12	chr1:189398440..189399083-chr1:189642226..189643036,4	MCF-7	breast:
13	chr1:189627801..189630516-chr1:189640573..189642596,2	MCF-7	breast:
14	chr1:189740038..189741669-chr1:189745873..189748337,2	K562	blood:
15	chr1:189398408..189399387-chr1:189661985..189662829,2	MCF-7	breast:
16	chr1:189627801..189630516-chr1:189640573..189642596,2	MCF-7	breast:
17	chr1:189581455..189584315-chr1:189585168..189587493,2	K562	blood:
18	chr1:189709848..189710556-chr1:189743646..189744501,3	MCF-7	breast:
19	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
20	chr1:189617058..189619904-chr1:189621793..189623517,2	MCF-7	breast:
21	chr1:189588020..189590795-chr1:189591484..189594244,3	MCF-7	breast:
22	chr1:189709848..189710556-chr1:189743646..189744501,3	MCF-7	breast:
23	chr1:189790429..189793066-chr1:189800961..189802500,2	MCF-7	breast:
24	chr1:189608651..189610421-chr1:189613616..189615684,2	K562	blood:
25	chr1:189853792..189857239-chr1:189857756..189861653,3	MCF-7	breast:
26	chr1:189813747..189815721-chr1:189850350..189852733,2	K562	blood:
27	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
28	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
29	chr1:189778329..189781313-chr1:189784587..189786793,2	MCF-7	breast:
30	chr1:189828427..189829123-chr1:190093339..190093859,2	MCF-7	breast:
31	chr1:189589226..189590045-chr1:189662088..189662866,2	MCF-7	breast:
32	chr1:189117678..189120245-chr1:189847842..189850269,2	K562	blood:
33	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
34	chr1:189630297..189631878-chr1:189633078..189635794,2	K562	blood:
35	chr1:189844299..189845892-chr1:189850457..189852405,2	MCF-7	breast:
36	chr1:189581455..189584315-chr1:189585168..189587493,2	K562	blood:
37	chr1:189398509..189399144-chr1:189660311..189661261,2	MCF-7	breast:
38	chr1:189746682..189748361-chr1:189748606..189750164,2	MCF-7	breast:
39	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
40	chr1:189813747..189815721-chr1:189850350..189852733,2	K562	blood:
41	chr1:189589226..189590045-chr1:189662088..189662866,2	MCF-7	breast:
42	chr1:189677502..189678569-chr1:190053452..190054228,3	MCF-7	breast:
43	chr1:189746682..189748361-chr1:189748606..189750164,2	MCF-7	breast:
44	chr1:189898658..189901236-chr1:189902072..189905289,4	MCF-7	breast:
45	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
46	chr1:189898658..189901236-chr1:189902072..189905289,4	MCF-7	breast:
47	chr1:189617058..189619904-chr1:189621793..189623517,2	MCF-7	breast:
48	chr1:189897967..189900169-chr1:190054489..190056512,2	MCF-7	breast:
49	chr1:189899347..189901205-chr1:189918005..189920869,2	MCF-7	breast:
50	chr1:189627826..189630498-chr1:189636599..189639267,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-7	chr1:189744595-189744695	XLOC_000503
2	lnc-RGS18-7	chr1:189746390-189746467	XLOC_000503
3	lnc-RGS18-7	chr1:189760709-189760893	XLOC_000503
4	lnc-RGS18-7	chr1:189783962-189784048	XLOC_000503
5	lnc-FAM5C-1	chr1:189837131-189837342	XLOC_001130
6	lnc-FAM5C-1	chr1:189837457-189837658	XLOC_001130

No data

Variant related genes	Relation type
RNA5SP73	TF binding region
ENSG00000232212	TF binding region
ENSG00000238270	TF binding region
RNA5SP73	CpG island
ENSG00000232212	CpG island
ENSG00000238270	CpG island
ENSG00000113194	chromatin interactions
ENSG00000252553	chromatin interactions
SOX13	miRNA target sites
SOX11	miRNA target sites
SOX2	miRNA target sites

Extended variants
information (count: 4660 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4660 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372861736	chr1:189555232-189555233	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs375605148	chr1:189555233-189555234	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs12042405	chr1:189555246-189555247	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs141962381	chr1:189555257-189555258	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs143653314	chr1:189555264-189555265	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs550143474	chr1:189555268-189555269	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs61818929	chr1:189555272-189555273	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs558441798	chr1:189555274-189555275	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs201175930	chr1:189555275-189555276	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs61818930	chr1:189555276-189555277	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs140761902	chr1:189555280-189555281	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs61818931	chr1:189555286-189555287	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs35556590	chr1:189555290-189555291	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs66696237	chr1:189555291-189555292	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs140734289	chr1:189555298-189555299	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs571820160	chr1:189555301-189555302	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs537727119	chr1:189555310-189555311	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs71127688	chr1:189555313-189555314	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs557424437	chr1:189555314-189555315	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs113282356	chr1:189555317-189555318	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs186201345	chr1:189555325-189555326	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs139686274	chr1:189555330-189555331	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs112285077	chr1:189555343-189555344	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs143592346	chr1:189555344-189555345	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs78252542	chr1:189555361-189555362	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs553134887	chr1:189565299-189565300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540468453	chr1:189565331-189565332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs202042679	chr1:189565342-189565343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200113222	chr1:189565344-189565345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560380508	chr1:189565415-189565416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569038543	chr1:189565421-189565422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544064213	chr1:189565450-189565451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545523464	chr1:189565476-189565477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532698374	chr1:189565501-189565502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73049511	chr1:189565504-189565505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111517650	chr1:189565570-189565571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75718774	chr1:189565653-189565654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548290098	chr1:189565658-189565659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79799345	chr1:189565689-189565690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183626483	chr1:189565694-189565695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7549115	chr1:189565695-189565696	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs570705140	chr1:189565713-189565714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539746829	chr1:189565717-189565718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556398258	chr1:189565729-189565730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141516615	chr1:189565742-189565743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188961908	chr1:189565745-189565746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541828224	chr1:189565800-189565801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs193134130	chr1:189565861-189565862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147066599	chr1:189565868-189565869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541534839	chr1:189565876-189565877	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	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
Hepatocellular carcinoma	18803288	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
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:189555200-189555400	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:189565200-189566800	Enhancers	HUVEC	blood vessel
3	chr1:189566400-189566800	Active TSS	A549	lung
4	chr1:189574200-189575400	Enhancers	A549	lung
5	chr1:189574200-189576600	Enhancers	Hela-S3	cervix
6	chr1:189574200-189577200	Enhancers	HMEC	breast
7	chr1:189574400-189574600	Enhancers	Muscle Satellite Cultured Cells	--
8	chr1:189574800-189575800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr1:189575200-189575600	Enhancers	Fetal Brain Male	brain
10	chr1:189575400-189576200	Flanking Active TSS	A549	lung
11	chr1:189575800-189576800	Enhancers	NH-A	brain
12	chr1:189575800-189578800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr1:189576000-189576800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:189576200-189576400	Active TSS	A549	lung
15	chr1:189576400-189576600	Flanking Active TSS	A549	lung
16	chr1:189576600-189576800	Active TSS	A549	lung
17	chr1:189576600-189577000	Enhancers	Osteobl	bone
18	chr1:189576800-189577400	Flanking Active TSS	A549	lung
19	chr1:189577400-189578200	Enhancers	A549	lung
20	chr1:189578000-189578600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:189578000-189578800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:189578200-189578600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:189578200-189578600	Genic enhancers	A549	lung
24	chr1:189578600-189585000	Weak transcription	A549	lung
25	chr1:189585000-189587000	Enhancers	A549	lung
26	chr1:189585600-189587000	Enhancers	Muscle Satellite Cultured Cells	--
27	chr1:189586000-189586400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:189586000-189586400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:189586000-189586400	Enhancers	HMEC	breast
30	chr1:189586000-189586600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:189586400-189588800	Weak transcription	HMEC	breast
32	chr1:189586400-189589000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr1:189586600-189588600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:189587000-189588200	Weak transcription	A549	lung
35	chr1:189587000-189588600	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr1:189588200-189588800	Enhancers	A549	lung
37	chr1:189588600-189589600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr1:189588600-189589600	Enhancers	HUVEC	blood vessel
39	chr1:189588600-189589800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:189588800-189589000	Active TSS	A549	lung
41	chr1:189588800-189589400	Enhancers	NHEK	skin
42	chr1:189588800-189589800	Enhancers	HMEC	breast
43	chr1:189589000-189589400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr1:189589000-189589400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:189589000-189589400	Flanking Active TSS	A549	lung
46	chr1:189589000-189589400	Enhancers	Hela-S3	cervix
47	chr1:189589000-189589400	Enhancers	NH-A	brain
48	chr1:189589000-189589400	Enhancers	Osteobl	bone
49	chr1:189589400-189589800	Enhancers	A549	lung
50	chr1:189589400-189593200	Weak transcription	Hela-S3	cervix

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