Variant report

Variant	nsv830292
Chromosome Location	chr1:77425571-77584307
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:777)
CpG islands
(count:549)
Chromatin interactive
region (count:22)
LncRNA
region (count:4)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:777 , 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	chr1:77570248-77570348	K562	blood:	n/a	n/a
2	ATF1	chr1:77566175-77566187	K562	blood:	n/a	n/a
3	ATF3	chr1:77505308-77505819	A549	lung:	n/a	n/a
4	BATF	chr1:77496981-77497309	GM12878	blood:	n/a	chr1:77497182-77497193
5	BCL3	chr1:77464210-77464710	A549	lung:	n/a	n/a
6	BHLHE40	chr1:77513573-77513780	GM12878	blood:	n/a	chr1:77513699-77513708 chr1:77513698-77513707 chr1:77513698-77513707
7	BHLHE40	chr1:77460734-77460763	GM12878	blood:	n/a	n/a
8	BRCA1	chr1:77454713-77454719	GM12878	blood:	n/a	n/a
9	CBX3	chr1:77464148-77464900	HCT-116	colon:	n/a	n/a
10	CBX3	chr1:77464191-77464739	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:77436437-77436719	HepG2	liver:	n/a	chr1:77436607-77436618
12	CEBPB	chr1:77490145-77490533	ECC-1	luminal epithelium:	n/a	chr1:77490333-77490350
13	CEBPB	chr1:77505304-77506057	HCT-116	colon:	n/a	chr1:77505660-77505673
14	CEBPB	chr1:77490227-77490440	HepG2	liver:	n/a	chr1:77490333-77490350
15	CEBPB	chr1:77471222-77471389	IMR90	lung:	n/a	chr1:77471303-77471314
16	CEBPB	chr1:77528352-77528666	IMR90	lung:	n/a	chr1:77528511-77528520 chr1:77528477-77528490 chr1:77528477-77528488 chr1:77528509-77528520 chr1:77528510-77528521
17	CEBPB	chr1:77484490-77484759	MCF-7	breast:	n/a	n/a
18	CEBPB	chr1:77490159-77490522	HepG2	liver:	n/a	chr1:77490333-77490350
19	CEBPB	chr1:77510978-77511306	IMR90	lung:	n/a	chr1:77511123-77511134
20	CEBPB	chr1:77490207-77490402	HepG2	liver:	n/a	chr1:77490333-77490350
21	CEBPB	chr1:77464090-77464915	HCT-116	colon:	n/a	n/a
22	CEBPB	chr1:77464107-77464848	HCT-116	colon:	n/a	n/a
23	CEBPB	chr1:77528341-77528657	HepG2	liver:	n/a	chr1:77528511-77528520 chr1:77528477-77528490 chr1:77528477-77528488 chr1:77528509-77528520 chr1:77528510-77528521
24	CEBPB	chr1:77514276-77514525	A549	lung:	n/a	chr1:77514387-77514398 chr1:77514407-77514418
25	CEBPB	chr1:77514280-77514532	IMR90	lung:	n/a	chr1:77514387-77514398 chr1:77514407-77514418
26	CEBPB	chr1:77584248-77584512	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:77552814-77553055	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:77464250-77464707	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:77471163-77471387	HepG2	liver:	n/a	chr1:77471303-77471314
30	CEBPB	chr1:77490203-77490483	ECC-1	luminal epithelium:	n/a	chr1:77490333-77490350
31	CEBPB	chr1:77484337-77484752	MCF-7	breast:	n/a	n/a
32	CEBPB	chr1:77505499-77505866	MCF-7	breast:	n/a	chr1:77505660-77505673
33	CEBPB	chr1:77490188-77490490	Hela-S3	cervix:	n/a	chr1:77490333-77490350
34	CEBPB	chr1:77511021-77511233	K562	blood:	n/a	chr1:77511123-77511134
35	CEBPB	chr1:77505424-77505864	A549	lung:	n/a	chr1:77505660-77505673
36	CEBPB	chr1:77464157-77464772	A549	lung:	n/a	n/a
37	CEBPB	chr1:77464273-77464568	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:77458850-77459070	H1-hESC	embryonic stem cell:	n/a	chr1:77458926-77458937
39	CEBPB	chr1:77458743-77459113	HepG2	liver:	n/a	chr1:77458926-77458937
40	CEBPB	chr1:77514327-77514487	H1-hESC	embryonic stem cell:	n/a	chr1:77514387-77514398 chr1:77514407-77514418
41	CEBPB	chr1:77505440-77505873	IMR90	lung:	n/a	chr1:77505660-77505673
42	CEBPB	chr1:77458762-77459085	A549	lung:	n/a	chr1:77458926-77458937
43	CEBPB	chr1:77484383-77484730	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr1:77505461-77505883	Hela-S3	cervix:	n/a	chr1:77505660-77505673
45	CEBPB	chr1:77490166-77490528	HepG2	liver:	n/a	chr1:77490333-77490350
46	CEBPB	chr1:77490047-77490654	HCT-116	colon:	n/a	chr1:77490333-77490350
47	CEBPB	chr1:77514261-77514576	HepG2	liver:	n/a	chr1:77514387-77514398 chr1:77514407-77514418
48	CEBPB	chr1:77458748-77459109	IMR90	lung:	n/a	chr1:77458926-77458937
49	CEBPB	chr1:77505335-77505973	A549	lung:	n/a	chr1:77505660-77505673
50	CEBPB	chr1:77505405-77505853	A549	lung:	n/a	chr1:77505660-77505673

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77484471-77484521	PANC-1	pancreas:	n/a
2	chr1:77477593-77477643	GM12891	blood:	n/a
3	chr1:77484471-77484521	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:77505574-77505624	AG09319	gingival:	n/a
5	chr1:77484471-77484521	AG10803	skin:	n/a
6	chr1:77529073-77529123	RPTEC	kidney:	n/a
7	chr1:77533592-77533642	K562	blood:	n/a
8	chr1:77477593-77477643	HL-60	blood:	n/a
9	chr1:77528748-77528798	Jurkat	blood:	n/a
10	chr1:77484471-77484521	HCM	heart:	n/a
11	chr1:77505574-77505624	HRCEpiC	kidney:	n/a
12	chr1:77525228-77525278	NB4	blood:	n/a
13	chr1:77492835-77492885	AG09319	gingival:	n/a
14	chr1:77533592-77533642	HEEpiC	esophagus:	n/a
15	chr1:77484471-77484521	PrEC	prostate:	n/a
16	chr1:77529073-77529123	ovcar-3	ovarian:	n/a
17	chr1:77529073-77529123	AG09309	skin:	n/a
18	chr1:77533592-77533642	HepG2	liver:	n/a
19	chr1:77492835-77492885	HCPEpiC	choroid plexus:	n/a
20	chr1:77533592-77533642	RPTEC	kidney:	n/a
21	chr1:77525228-77525278	T-47D	breast:	n/a
22	chr1:77528748-77528798	GM19239	blood:	n/a
23	chr1:77525228-77525278	NH-A	brain:	n/a
24	chr1:77492835-77492885	Jurkat	blood:	n/a
25	chr1:77525228-77525278	A549	lung:	n/a
26	chr1:77547505-77547555	SAEC	small airway:	n/a
27	chr1:77529073-77529123	H1-hESC	embryonic stem cell:	embryo
28	chr1:77492835-77492885	HAEpiC	amniotic membrane:	n/a
29	chr1:77528748-77528798	Caco-2	colon:	n/a
30	chr1:77505574-77505624	MCF10A-Er-Src	breast:	n/a
31	chr1:77547505-77547555	Hela-S3	cervix:	n/a
32	chr1:77529073-77529123	HRCEpiC	kidney:	n/a
33	chr1:77547505-77547555	LNCaP	prostate:	n/a
34	chr1:77505574-77505624	SK-N-SH_RA	brain:	n/a
35	chr1:77484471-77484521	K562	blood:	n/a
36	chr1:77492835-77492885	H1-hESC	embryonic stem cell:	embryo
37	chr1:77547505-77547555	AG09319	gingival:	n/a
38	chr1:77525228-77525278	GM12892	blood:	n/a
39	chr1:77533592-77533642	AG04450	lung:	fetal
40	chr1:77547505-77547555	NH-A	brain:	n/a
41	chr1:77492835-77492885	HRE	kidney:	n/a
42	chr1:77484471-77484521	H1-hESC	embryonic stem cell:	embryo
43	chr1:77529073-77529123	NT2-D1	testis:	n/a
44	chr1:77484471-77484521	NB4	blood:	n/a
45	chr1:77477593-77477643	AoSMC	blood vessel:	n/a
46	chr1:77529073-77529123	PrEC	prostate:	n/a
47	chr1:77528748-77528798	HIPEpiC	eye:	n/a
48	chr1:77547505-77547555	HEEpiC	esophagus:	n/a
49	chr1:77492835-77492885	HMEC	breast:	n/a
50	chr1:77547505-77547555	HRE	kidney:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:77469704..77471590-chr1:77474727..77477300,2	K562	blood:
2	chr1:77366800..77367486-chr1:77496947..77497587,3	MCF-7	breast:
3	chr1:77560743..77563432-chr1:77569835..77572448,2	K562	blood:
4	chr1:77577767..77579951-chr1:77584279..77585797,2	K562	blood:
5	chr1:77510838..77513802-chr1:77514493..77517850,4	K562	blood:
6	chr1:77577767..77579951-chr1:77584279..77585797,2	K562	blood:
7	chr1:77560724..77561244-chr4:118889670..118890190,2	MCF-7	breast:
8	chr1:77578497..77580194-chr1:77590857..77592378,2	K562	blood:
9	chr1:77495560..77497572-chr1:77499811..77501669,2	K562	blood:
10	chr1:77553476..77555257-chr1:77556294..77558834,2	K562	blood:
11	chr1:77584058..77586581-chr1:77589256..77592005,2	MCF-7	breast:
12	chr1:77510838..77513802-chr1:77514493..77517850,4	K562	blood:
13	chr1:77560743..77563432-chr1:77569835..77572448,2	K562	blood:
14	chr1:77469704..77471590-chr1:77474727..77477300,2	K562	blood:
15	chr1:77510838..77513708-chr1:77516057..77517850,2	K562	blood:
16	chr1:77495560..77497572-chr1:77499811..77501669,2	K562	blood:
17	chr1:77553476..77555257-chr1:77556294..77558834,2	K562	blood:
18	chr1:77579749..77582722-chr1:77596983..77598740,2	K562	blood:
19	chr1:76619661..76620511-chr1:77549962..77550737,2	MCF-7	breast:
20	chr1:77558452..77561081-chr1:77564506..77566487,2	K562	blood:
21	chr1:77510838..77513708-chr1:77516057..77517850,2	K562	blood:
22	chr1:77558452..77561081-chr1:77564506..77566487,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST6GALNAC5-1	chr1:77544025-77544167	XLOC_000262
2	lnc-ST6GALNAC5-1	chr1:77534421-77534528	XLOC_000262
3	lnc-ST6GALNAC5-1	chr1:77533769-77533932	XLOC_000262
4	lnc-ST6GALNAC5-1	chr1:77533605-77533686	XLOC_000262

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7156-3p	chr1:77525865-77525887	MIMAT0028223
hsa-miR-7156-5p	chr1:77525828-77525850	MIMAT0028222

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ST6GALNAC5	hsa-miR-148b-3p	chr1:77509889-77509906
2	ST6GALNAC5	hsa-miR-148b-3p	chr1:77515977-77515998

Variant related genes	Relation type
ENSG00000230498	TF binding region
ENSG00000221720	TF binding region
ST6GALNAC5	TF binding region
ENSG00000230498	CpG island
ENSG00000221720	CpG island
ST6GALNAC5	CpG island

Extended variants
information (count: 5833 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:5833 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567677875	chr1:77425574-77425575	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527810617	chr1:77425625-77425626	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146461822	chr1:77425632-77425633	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374970807	chr1:77425640-77425641	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569224704	chr1:77425667-77425668	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375190975	chr1:77425769-77425770	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139027403	chr1:77425811-77425812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369808178	chr1:77425812-77425813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113971076	chr1:77425839-77425840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7555422	chr1:77425863-77425864	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs184161305	chr1:77425873-77425874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76574725	chr1:77425939-77425940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141963196	chr1:77425958-77425959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539534216	chr1:77425971-77425972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557622872	chr1:77425977-77425978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531629604	chr1:77426025-77426026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569879956	chr1:77426037-77426038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537334269	chr1:77426085-77426086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551521165	chr1:77426122-77426123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150661241	chr1:77426131-77426132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536681371	chr1:77426158-77426159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188496635	chr1:77426169-77426170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs180907443	chr1:77426170-77426171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10443170	chr1:77426171-77426172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184163426	chr1:77426230-77426231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369254150	chr1:77426246-77426247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533910781	chr1:77426256-77426257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564519514	chr1:77426266-77426267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547882367	chr1:77426277-77426278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543689292	chr1:77426297-77426298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562071972	chr1:77426298-77426299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190722578	chr1:77426305-77426306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546953834	chr1:77426334-77426335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565678813	chr1:77426365-77426366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567378319	chr1:77426371-77426372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs3925576	chr1:77426387-77426388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532884073	chr1:77426408-77426409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551495223	chr1:77426410-77426411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142444959	chr1:77426411-77426412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145956796	chr1:77426442-77426443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs858601	chr1:77426459-77426460	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs113026344	chr1:77426463-77426464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182004591	chr1:77426464-77426465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187100771	chr1:77426474-77426475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556336151	chr1:77426494-77426495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545969986	chr1:77426497-77426498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145642117	chr1:77426511-77426512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190449532	chr1:77426546-77426547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543581272	chr1:77426567-77426568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561959973	chr1:77426597-77426598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:936 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77393400-77429000	Weak transcription	Aorta	Aorta
2	chr1:77405400-77427000	Weak transcription	Fetal Stomach	stomach
3	chr1:77412200-77427000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:77416400-77427000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:77421600-77434600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:77423600-77425600	Enhancers	Fetal Brain Male	brain
7	chr1:77424000-77425600	Strong transcription	Cortex derived primary cultured neurospheres	brain
8	chr1:77424000-77425600	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr1:77424200-77425800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:77424600-77425800	Enhancers	NHDF-Ad	bronchial
11	chr1:77425000-77425600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:77425000-77425600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:77425000-77425800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:77425000-77427800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr1:77425200-77425600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr1:77425200-77425600	Enhancers	Osteobl	bone
17	chr1:77425200-77425800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr1:77425200-77425800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:77425200-77426600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr1:77425400-77425600	Enhancers	HSMM	muscle
21	chr1:77425400-77425800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:77425600-77426800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:77425600-77426800	Weak transcription	Osteobl	bone
24	chr1:77425600-77427000	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr1:77425600-77427000	Weak transcription	HSMM	muscle
26	chr1:77425600-77428800	Weak transcription	Fetal Brain Male	brain
27	chr1:77425800-77427000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr1:77425800-77427000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr1:77425800-77427000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:77425800-77427000	Weak transcription	NHDF-Ad	bronchial
31	chr1:77425800-77427200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:77426400-77427400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr1:77426800-77427000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr1:77426800-77427200	Enhancers	Osteobl	bone
35	chr1:77427000-77427200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr1:77427000-77427200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:77427000-77427400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:77427000-77427400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:77427000-77427800	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr1:77427000-77427800	Enhancers	HSMM	muscle
41	chr1:77427000-77427800	Enhancers	HSMMtube	muscle
42	chr1:77427000-77428200	Enhancers	NHDF-Ad	bronchial
43	chr1:77427200-77427400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr1:77427200-77427400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:77427200-77427600	Enhancers	Muscle Satellite Cultured Cells	--
46	chr1:77427200-77428000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:77427200-77428800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:77427400-77427600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr1:77427800-77428800	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr1:77428800-77429400	Enhancers	Fetal Brain Male	brain

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