Variant report

Variant	nsv872658
Chromosome Location	chr1:189069537-189675416
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2325)
CpG islands
(count:61)
Chromatin interactive
region (count:130)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2325 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:189118670-189118888	K562	blood:	n/a	n/a
2	ARID3A	chr1:189655218-189655237	K562	blood:	n/a	n/a
3	ARID3A	chr1:189398814-189399014	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:189576379-189576601	HepG2	liver:	n/a	n/a
5	ATF1	chr1:189118704-189119125	K562	blood:	n/a	n/a
6	ATF1	chr1:189202401-189202585	K562	blood:	n/a	n/a
7	ATF1	chr1:189645110-189645131	K562	blood:	n/a	n/a
8	ATF1	chr1:189500705-189500755	K562	blood:	n/a	n/a
9	ATF1	chr1:189204451-189204466	K562	blood:	n/a	n/a
10	ATF1	chr1:189495461-189495472	K562	blood:	n/a	n/a
11	ATF3	chr1:189576142-189576647	A549	lung:	n/a	n/a
12	ATF3	chr1:189624065-189624449	HCT-116	colon:	n/a	n/a
13	BACH1	chr1:189389331-189389475	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:189258605-189258799	K562	blood:	n/a	n/a
15	BACH1	chr1:189660033-189660067	K562	blood:	n/a	n/a
16	BATF	chr1:189565411-189565576	GM12878	blood:	n/a	chr1:189565508-189565518
17	BATF	chr1:189206204-189206354	GM12878	blood:	n/a	chr1:189206300-189206311
18	BCL3	chr1:189650561-189651101	A549	lung:	n/a	n/a
19	BCL3	chr1:189575858-189576821	A549	lung:	n/a	n/a
20	BCLAF1	chr1:189118637-189119186	K562	blood:	n/a	n/a
21	BHLHE40	chr1:189118889-189119095	K562	blood:	n/a	n/a
22	BRCA1	chr1:189588843-189589197	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr1:189640354-189640407	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr1:189631288-189631734	HCT-116	colon:	n/a	n/a
25	CBX3	chr1:189238133-189238458	K562	blood:	n/a	n/a
26	CBX3	chr1:189626762-189627309	HCT-116	colon:	n/a	n/a
27	CBX3	chr1:189627431-189627982	HCT-116	colon:	n/a	n/a
28	CBX3	chr1:189588763-189589390	HCT-116	colon:	n/a	n/a
29	CBX3	chr1:189238100-189238627	HCT-116	colon:	n/a	n/a
30	CBX3	chr1:189588801-189589528	HCT-116	colon:	n/a	n/a
31	CBX3	chr1:189118747-189119060	K562	blood:	n/a	n/a
32	CBX3	chr1:189094793-189095258	HCT-116	colon:	n/a	n/a
33	CBX3	chr1:189118641-189119561	K562	blood:	n/a	n/a
34	CBX3	chr1:189238189-189238535	K562	blood:	n/a	n/a
35	CBX3	chr1:189631264-189631803	HCT-116	colon:	n/a	n/a
36	CBX3	chr1:189238064-189238627	HCT-116	colon:	n/a	n/a
37	CCNT2	chr1:189330861-189331308	K562	blood:	n/a	n/a
38	CCNT2	chr1:189281785-189281923	K562	blood:	n/a	n/a
39	CEBPB	chr1:189623938-189624460	HCT-116	colon:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
40	CEBPB	chr1:189553909-189554210	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:189572710-189572977	IMR90	lung:	n/a	chr1:189572877-189572890 chr1:189572878-189572889 chr1:189572877-189572888 chr1:189572879-189572888
42	CEBPB	chr1:189624014-189624396	IMR90	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
43	CEBPB	chr1:189558442-189558746	A549	lung:	n/a	chr1:189558577-189558588
44	CEBPB	chr1:189305304-189305667	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:189572754-189573023	HepG2	liver:	n/a	chr1:189572877-189572890 chr1:189572878-189572889 chr1:189572877-189572888 chr1:189572879-189572888
46	CEBPB	chr1:189400481-189400821	MCF-7	breast:	n/a	chr1:189400690-189400701
47	CEBPB	chr1:189576038-189577215	A549	lung:	n/a	chr1:189576923-189576935
48	CEBPB	chr1:189166339-189166622	A549	lung:	n/a	n/a
49	CEBPB	chr1:189346049-189346081	H1-hESC	embryonic stem cell:	n/a	chr1:189346050-189346061
50	CEBPB	chr1:189626976-189627210	IMR90	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:189194949-189194999	BE2_C	brain:	n/a
2	chr1:189194949-189194999	NHBE	bronchial:	n/a
3	chr1:189194949-189194999	ECC-1	luminal epithelium:	n/a
4	chr1:189194949-189194999	BJ	skin:	n/a
5	chr1:189194949-189194999	HMEC	breast:	n/a
6	chr1:189194949-189194999	HCF	heart:	n/a
7	chr1:189194949-189194999	SK-N-MC	brain:	n/a
8	chr1:189194949-189194999	Jurkat	blood:	n/a
9	chr1:189194949-189194999	AG04449	skin:	fetal
10	chr1:189194949-189194999	A549	lung:	n/a
11	chr1:189194949-189194999	MCF10A-Er-Src	breast:	n/a
12	chr1:189194949-189194999	HL-60	blood:	n/a
13	chr1:189194949-189194999	HCM	heart:	n/a
14	chr1:189194949-189194999	NH-A	brain:	n/a
15	chr1:189194949-189194999	SAEC	small airway:	n/a
16	chr1:189194949-189194999	NB4	blood:	n/a
17	chr1:189194949-189194999	HIPEpiC	eye:	n/a
18	chr1:189194949-189194999	GM19239	blood:	n/a
19	chr1:189194949-189194999	SKMC	muscle:	n/a
20	chr1:189194949-189194999	HUVEC	blood vessel:	n/a
21	chr1:189194949-189194999	HRCEpiC	kidney:	n/a
22	chr1:189194949-189194999	T-47D	breast:	n/a
23	chr1:189194949-189194999	RPTEC	kidney:	n/a
24	chr1:189194949-189194999	GM12891	blood:	n/a
25	chr1:189194949-189194999	PrEC	prostate:	n/a
26	chr1:189194949-189194999	AG04450	lung:	fetal
27	chr1:189194949-189194999	HCT-116	colon:	n/a
28	chr1:189194949-189194999	HAEpiC	amniotic membrane:	n/a
29	chr1:189194949-189194999	CMK	blood:	n/a
30	chr1:189194949-189194999	HNPCEpiC	eye:	n/a
31	chr1:189194949-189194999	SK-N-SH_RA	brain:	n/a
32	chr1:189194949-189194999	PFSK-1	brain:	n/a
33	chr1:189194949-189194999	HEEpiC	esophagus:	n/a
34	chr1:189194949-189194999	MCF-7	breast:	n/a
35	chr1:189194949-189194999	NT2-D1	testis:	n/a
36	chr1:189194949-189194999	U87	brain:	n/a
37	chr1:189194949-189194999	AG09319	gingival:	n/a
38	chr1:189194949-189194999	Hela-S3	cervix:	n/a
39	chr1:189194949-189194999	HCPEpiC	choroid plexus:	n/a
40	chr1:189194949-189194999	ovcar-3	ovarian:	n/a
41	chr1:189194949-189194999	GM06990	blood:	n/a
42	chr1:189194949-189194999	K562	blood:	n/a
43	chr1:189194949-189194999	AoSMC	blood vessel:	n/a
44	chr1:189194949-189194999	NHDF-neo	bronchial:	n/a
45	chr1:189194949-189194999	ProgFib	skin:	n/a
46	chr1:189194949-189194999	HRE	kidney:	n/a
47	chr1:189194949-189194999	IMR90	lung:	fetal
48	chr1:189194949-189194999	HepG2	liver:	n/a
49	chr1:189194949-189194999	LNCaP	prostate:	n/a
50	chr1:189194949-189194999	GM12892	blood:	n/a

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:189109069..189111895-chr1:189118017..189120459,2	K562	blood:
2	chr1:189581455..189584315-chr1:189585168..189587493,2	K562	blood:
3	chr1:189456998..189459312-chr1:189462983..189466310,3	MCF-7	breast:
4	chr1:189398245..189398855-chr3:191237330..191238213,2	MCF-7	breast:
5	chr1:189117897..189121261-chr1:189121594..189126238,14	K562	blood:
6	chr1:189117456..189122192-chr1:189126377..189132093,10	K562	blood:
7	chr1:189416774..189418507-chr1:189422911..189425482,2	K562	blood:
8	chr1:189424671..189426547-chr1:189428199..189429967,2	K562	blood:
9	chr1:189118996..189121109-chr1:189287929..189290792,2	K562	blood:
10	chr1:188902220..188904596-chr1:189118871..189120838,2	K562	blood:
11	chr1:189116028..189120237-chr1:189160506..189163276,3	K562	blood:
12	chr1:189170367..189172924-chr1:189189578..189192081,2	K562	blood:
13	chr1:189493316..189495330-chr8:119780090..119782266,2	MCF-7	breast:
14	chr1:189148880..189151522-chr1:189151849..189154466,3	K562	blood:
15	chr1:189627801..189630516-chr1:189640573..189642596,2	MCF-7	breast:
16	chr1:189117472..189119445-chr1:189184383..189186495,2	K562	blood:
17	chr1:89355507..89357311-chr1:189270012..189271532,3	K562	blood:
18	chr1:189630297..189631878-chr1:189633078..189635794,2	K562	blood:
19	chr1:189174928..189177287-chr1:189180109..189182692,2	K562	blood:
20	chr1:189166300..189168058-chr1:189173903..189175630,2	MCF-7	breast:
21	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
22	chr1:189167872..189169675-chr1:189171676..189174219,2	K562	blood:
23	chr1:189275475..189276987-chr1:189302090..189304788,2	K562	blood:
24	chr1:189627826..189630498-chr1:189636599..189639267,2	MCF-7	breast:
25	chr1:189398256..189399319-chr1:190290193..190290907,3	MCF-7	breast:
26	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
27	chr1:189588020..189590795-chr1:189591484..189594244,3	MCF-7	breast:
28	chr1:189608651..189610421-chr1:189613616..189615684,2	K562	blood:
29	chr1:189121464..189123287-chr1:189388904..189390413,2	K562	blood:
30	chr1:189617058..189619904-chr1:189621793..189623517,2	MCF-7	breast:
31	chr1:189408828..189411419-chr1:189412082..189414422,2	K562	blood:
32	chr1:188751072..188751772-chr1:189118548..189119200,2	MCF-7	breast:
33	chr1:189119463..189122039-chr1:189394507..189396400,2	K562	blood:
34	chr1:189399166..189401720-chr1:189433273..189435659,2	K562	blood:
35	chr1:189398509..189399144-chr1:189660311..189661261,2	MCF-7	breast:
36	chr1:189119463..189122039-chr1:189394507..189396400,2	K562	blood:
37	chr1:189249441..189251122-chr1:189253559..189256297,2	K562	blood:
38	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
39	chr1:189475496..189478003-chr1:189479734..189481835,2	K562	blood:
40	chr1:189588020..189590795-chr1:189591484..189594244,3	MCF-7	breast:
41	chr1:189424671..189426547-chr1:189428199..189429967,2	K562	blood:
42	chr1:189608651..189610421-chr1:189613616..189615684,2	K562	blood:
43	chr1:189248572..189251429-chr1:189254137..189256255,2	MCF-7	breast:
44	chr1:189121464..189123287-chr1:189388904..189390413,2	K562	blood:
45	chr1:188762438..188765055-chr1:189455240..189458166,2	MCF-7	breast:
46	chr1:189275886..189277793-chr1:189279568..189282291,2	K562	blood:
47	chr1:189055283..189057511-chr1:189118631..189120197,2	K562	blood:
48	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
49	chr1:189112586..189116347-chr1:189117211..189120686,6	K562	blood:
50	chr1:189534638..189536257-chr1:189546205..189548519,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLA2G4A-7	chr1:189119673-189119860	XLOC_000502
2	lnc-PLA2G4A-7	chr1:189276860-189277008	NONHSAT008484
3	lnc-PLA2G4A-7	chr1:189119674-189119918	NONHSAT008484
4	lnc-PLA2G4A-18	chr1:189464076-189464220	NONHSAT008485
5	lnc-PLA2G4A-7	chr1:189118917-189119007	XLOC_000502
6	lnc-PLA2G4A-18	chr1:189456912-189457065	NONHSAT008485

No data

Variant related genes	Relation type
ENSG00000226196	TF binding region
RNA5SP73	TF binding region
ENSG00000226196	CpG island
RNA5SP73	CpG island
ENSG00000252553	chromatin interactions
ENSG00000113194	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000137947	chromatin interactions
ENSG00000202077	chromatin interactions

Extended variants
information (count: 5152 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5152 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192562728	chr1:189091022-189091023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6702671	chr1:189091127-189091128	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs553808094	chr1:189091206-189091207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570411657	chr1:189091223-189091224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139129727	chr1:189091246-189091247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556194006	chr1:189091254-189091255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576205246	chr1:189091330-189091331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574195332	chr1:189091331-189091332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532767006	chr1:189091339-189091340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182451142	chr1:189091416-189091417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555989931	chr1:189091458-189091459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572728031	chr1:189091462-189091463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541690352	chr1:189091465-189091466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187775937	chr1:189091467-189091468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192453637	chr1:189091481-189091482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143638573	chr1:189091579-189091580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563395781	chr1:189091580-189091581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78876673	chr1:189091585-189091586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184848806	chr1:189091649-189091650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561524404	chr1:189091674-189091675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114795474	chr1:189091693-189091694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148278648	chr1:189091711-189091712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188730915	chr1:189091720-189091721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570675088	chr1:189091752-189091753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73055167	chr1:189091844-189091845	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs549518381	chr1:189091859-189091860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191895726	chr1:189091870-189091871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535543829	chr1:189091874-189091875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373562621	chr1:189091877-189091878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76770093	chr1:189091906-189091907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554938018	chr1:189091925-189091926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111601178	chr1:189091941-189091942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112207404	chr1:189091962-189091963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113553457	chr1:189091971-189091972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141528827	chr1:189098000-189098001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143725351	chr1:189098051-189098052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs193154536	chr1:189098057-189098058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547463794	chr1:189098058-189098059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201335677	chr1:189098076-189098077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552075302	chr1:189098079-189098080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571612143	chr1:189098139-189098140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537387150	chr1:189098143-189098144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs59296151	chr1:189098174-189098175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556931883	chr1:189098189-189098190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1912900	chr1:189098195-189098196	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs542736647	chr1:189098199-189098200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548530469	chr1:189098203-189098204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553447718	chr1:189098232-189098233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201898349	chr1:189098234-189098235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371521234	chr1:189098294-189098295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Chronic lymphocytic leukemia	21546498	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	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:189091000-189092000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:189091200-189091800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr1:189098000-189102000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:189106200-189110600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:189110400-189111000	ZNF genes & repeats	Pancreas	Pancrea
6	chr1:189110600-189111000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:189111000-189118800	Weak transcription	Pancreas	Pancrea
8	chr1:189115600-189116600	Enhancers	Brain Germinal Matrix	brain
9	chr1:189118400-189120000	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr1:189118800-189119200	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr1:189118800-189119200	Active TSS	Liver	Liver
12	chr1:189118800-189119200	Active TSS	Gastric	stomach
13	chr1:189118800-189119400	Active TSS	Duodenum Mucosa	Duodenum
14	chr1:189118800-189119400	Active TSS	Fetal Intestine Large	intestine
15	chr1:189118800-189119400	ZNF genes & repeats	Pancreas	Pancrea
16	chr1:189118800-189119400	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr1:189118800-189120200	Active TSS	A549	lung
18	chr1:189118800-189121800	Active TSS	K562	blood
19	chr1:189127200-189127600	Active TSS	K562	blood
20	chr1:189152000-189152400	Enhancers	Fetal Heart	heart
21	chr1:189154000-189154600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:189154000-189154800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr1:189154000-189155000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr1:189154200-189154800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr1:189154200-189155200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:189154400-189155000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:189165000-189165200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr1:189165600-189167200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr1:189174200-189174800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr1:189175000-189175400	Enhancers	A549	lung
31	chr1:189181800-189182600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:189182000-189182800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:189194000-189194800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:189194600-189194800	ZNF genes & repeats	Gastric	stomach
35	chr1:189196000-189196400	Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr1:189237000-189237200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
37	chr1:189237000-189237400	ZNF genes & repeats	Liver	Liver
38	chr1:189237200-189237800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
39	chr1:189237200-189238800	ZNF genes & repeats	Adipose Nuclei	Adipose
40	chr1:189280800-189281600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:189281000-189281200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr1:189281000-189281200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr1:189281000-189281400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr1:189281000-189282200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:189281000-189283400	Enhancers	K562	blood
46	chr1:189281200-189281600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:189281200-189282200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr1:189281400-189281600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr1:189281400-189281800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:189281400-189282400	Weak transcription	HUES64 Cell Line	embryonic stem cell

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