Variant report

Variant	nsv1027745
Chromosome Location	chr9:495809-546734
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:552)
CpG islands
(count:368)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:504390-504746	K562	blood:	n/a	n/a
2	ARID3A	chr9:495829-496174	HepG2	liver:	n/a	n/a
3	BACH1	chr9:503516-503574	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:503882-504954	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:505331-505595	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr9:503842-504488	A549	lung:	n/a	chr9:504175-504184 chr9:504327-504340 chr9:504456-504469
7	BHLHE40	chr9:503924-504891	K562	blood:	n/a	chr9:504430-504446 chr9:504607-504623 chr9:504604-504620 chr9:504606-504622
8	BHLHE40	chr9:504376-504833	GM12878	blood:	n/a	chr9:504430-504446 chr9:504607-504623 chr9:504604-504620 chr9:504606-504622
9	BRCA1	chr9:504440-504580	HepG2	liver:	n/a	n/a
10	CCNT2	chr9:503997-505117	K562	blood:	n/a	chr9:504819-504828
11	CEBPB	chr9:530490-531138	HCT-116	colon:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
12	CEBPB	chr9:530695-530959	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr9:504299-504587	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:530652-530956	A549	lung:	n/a	n/a
15	CEBPB	chr9:530749-531005	A549	lung:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
16	CHD1	chr9:505142-505200	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr9:505550-505585	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr9:504063-504105	HepG2	liver:	n/a	n/a
19	CHD2	chr9:504310-504609	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr9:504194-504505	GM12878	blood:	n/a	n/a
21	CHD2	chr9:504693-504735	HepG2	liver:	n/a	n/a
22	CHD2	chr9:518207-518317	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr9:504228-504863	Hela-S3	cervix:	n/a	n/a
24	CREB1	chr9:503894-504982	HepG2	liver:	n/a	n/a
25	CREB1	chr9:504023-504978	A549	lung:	n/a	n/a
26	CTBP2	chr9:503852-505238	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr9:504300-504450	AG04450	lung:	n/a	chr9:504426-504439
28	CTCF	chr9:504333-504618	GM19239	blood:	n/a	chr9:504426-504439
29	CTCF	chr9:504420-504570	MCF-7	breast:	n/a	chr9:504426-504439
30	CTCF	chr9:504420-504570	AG04449	skin:	n/a	chr9:504426-504439
31	CTCF	chr9:504420-504570	GM12873	blood:	n/a	chr9:504426-504439
32	CTCF	chr9:504393-504558	GM13976	blood:	n/a	chr9:504426-504439
33	CTCF	chr9:504382-504585	SK-N-SH_RA	brain:	n/a	chr9:504426-504439
34	CTCF	chr9:504380-504530	Caco-2	colon:	n/a	chr9:504426-504439
35	CTCF	chr9:504400-504550	GM12864	blood:	n/a	chr9:504426-504439
36	CTCF	chr9:504372-504534	HUVEC	blood vessel:	n/a	chr9:504426-504439
37	CTCF	chr9:504380-504530	NHEK	skin:	n/a	chr9:504426-504439
38	CTCF	chr9:504400-504550	HCPEpiC	choroid plexus:	n/a	chr9:504426-504439
39	CTCF	chr9:504380-504530	HPAF	blood vessel:	n/a	chr9:504426-504439
40	CTCF	chr9:540000-540150	BJ	skin:	n/a	n/a
41	CTCF	chr9:504360-504510	HMEC	breast:	n/a	chr9:504426-504439
42	CTCF	chr9:504380-504530	WERI-Rb-1	eye:	n/a	chr9:504426-504439
43	CTCF	chr9:504040-504190	HMEC	breast:	n/a	chr9:504065-504073 chr9:504060-504073
44	CTCF	chr9:505860-506010	GM12869	blood:	n/a	n/a
45	CTCF	chr9:504269-504617	A549	lung:	n/a	chr9:504426-504439
46	CTCF	chr9:504340-504490	GM12873	blood:	n/a	chr9:504426-504439
47	CTCF	chr9:504380-504530	NHDF-neo	bronchial:	n/a	chr9:504426-504439
48	CTCF	chr9:504360-504510	GM12869	blood:	n/a	chr9:504426-504439
49	CTCF	chr9:505780-505930	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr9:504380-504530	HMEC	breast:	n/a	chr9:504426-504439

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:505721-505771	AG09309	skin:	n/a
2	chr9:507411-507461	RPTEC	kidney:	n/a
3	chr9:505721-505771	AG09309	skin:	n/a
4	chr9:507411-507461	RPTEC	kidney:	n/a
5	chr9:504774-504824	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:505571-505621	HL-60	blood:	n/a
7	chr9:505571-505621	PrEC	prostate:	n/a
8	chr9:505235-505285	AG04449	skin:	fetal
9	chr9:507411-507461	HEEpiC	esophagus:	n/a
10	chr9:505235-505285	BE2_C	brain:	n/a
11	chr9:504774-504824	SK-N-SH_RA	brain:	n/a
12	chr9:505721-505771	H1-hESC	embryonic stem cell:	embryo
13	chr9:505235-505285	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:507411-507461	SAEC	small airway:	n/a
15	chr9:504774-504824	SKMC	muscle:	n/a
16	chr9:504774-504824	Jurkat	blood:	n/a
17	chr9:507411-507461	Jurkat	blood:	n/a
18	chr9:505571-505621	HEK293	kidney:	embryo
19	chr9:503937-503987	ECC-1	luminal epithelium:	n/a
20	chr9:505571-505621	HCF	heart:	n/a
21	chr9:507411-507461	HRE	kidney:	n/a
22	chr9:505571-505621	HPAEpiC	pulmonary alveolar:	n/a
23	chr9:505571-505621	IMR90	lung:	fetal
24	chr9:505571-505621	HIPEpiC	eye:	n/a
25	chr9:504774-504824	ovcar-3	ovarian:	n/a
26	chr9:504774-504824	BE2_C	brain:	n/a
27	chr9:507411-507461	SKMC	muscle:	n/a
28	chr9:505571-505621	T-47D	breast:	n/a
29	chr9:505721-505771	MCF-7	breast:	n/a
30	chr9:505571-505621	SK-N-MC	brain:	n/a
31	chr9:503937-503987	NH-A	brain:	n/a
32	chr9:507411-507461	AG09319	gingival:	n/a
33	chr9:505571-505621	ECC-1	luminal epithelium:	n/a
34	chr9:505571-505621	SK-N-SH	brain:	n/a
35	chr9:504774-504824	HCM	heart:	n/a
36	chr9:505571-505621	SK-N-SH_RA	brain:	n/a
37	chr9:505721-505771	HUVEC	blood vessel:	n/a
38	chr9:505571-505621	HepG2	liver:	n/a
39	chr9:505721-505771	A549	lung:	n/a
40	chr9:505721-505771	HEK293	kidney:	embryo
41	chr9:505721-505771	RPTEC	kidney:	n/a
42	chr9:504774-504824	HEK293	kidney:	embryo
43	chr9:507411-507461	HNPCEpiC	eye:	n/a
44	chr9:505235-505285	PrEC	prostate:	n/a
45	chr9:507411-507461	T-47D	breast:	n/a
46	chr9:505235-505285	HIPEpiC	eye:	n/a
47	chr9:505571-505621	HUVEC	blood vessel:	n/a
48	chr9:505571-505621	GM06990	blood:	n/a
49	chr9:503937-503987	HRE	kidney:	n/a
50	chr9:507411-507461	Caco-2	colon:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
2	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
3	chr9:385596..386468-chr9:546637..547164,2	MCF-7	breast:
4	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
5	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
6	chr9:490052..492255-chr9:502875..504712,2	MCF-7	breast:
7	chr9:468830..470676-chr9:503247..506779,4	MCF-7	breast:
8	chr9:512039..514160-chr9:515791..519174,3	K562	blood:
9	chr9:490701..492635-chr9:494682..497058,2	K562	blood:
10	chr9:500269..502662-chr9:502681..505040,2	MCF-7	breast:
11	chr9:494848..496689-chr9:501659..504144,2	MCF-7	breast:
12	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
13	chr9:469974..471479-chr9:511045..512830,2	K562	blood:
14	chr9:468995..471572-chr9:503851..506185,2	MCF-7	breast:
15	chr9:504296..504898-chr9:21802481..21802992,2	HCT-116	colon:
16	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
17	chr9:495605..498122-chr9:502386..505122,3	MCF-7	breast:
18	chr9:494848..496689-chr9:501659..504144,2	MCF-7	breast:
19	chr9:487771..490019-chr9:514331..516293,2	MCF-7	breast:
20	chr9:512039..514160-chr9:515791..519174,3	K562	blood:
21	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-7	chr9:503057-504746	NONHSAT129929
2	lnc-C9orf66-8	chr9:507258-507553	NONHSAT129930

No data

Variant related genes	Relation type
ENSG00000226403	TF binding region
RN7SL412P	TF binding region
ENSG00000227155	TF binding region
KANK1	TF binding region
ENSG00000226403	CpG island
RN7SL412P	CpG island
ENSG00000227155	CpG island
KANK1	CpG island
ENSG00000107104	chromatin interactions
ENSG00000099810	chromatin interactions
ENSG00000228115	chromatin interactions
ENSG00000227155	chromatin interactions
ENSG00000264545	chromatin interactions

Extended variants
information (count: 2847 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2847 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529707889	chr9:495823-495824	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs543512490	chr9:495836-495837	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs539118998	chr9:495840-495841	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs188012675	chr9:495860-495861	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs532379801	chr9:495904-495905	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs139750711	chr9:495950-495951	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs144219531	chr9:495959-495960	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs372868154	chr9:495968-495969	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs33961058	chr9:495969-495970	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146539575	chr9:495978-495979	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs192485437	chr9:496041-496042	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs548576708	chr9:496049-496050	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs114814776	chr9:496056-496057	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs537111688	chr9:496105-496106	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs557470662	chr9:496121-496122	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs570954058	chr9:496124-496125	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs539675038	chr9:496131-496132	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549850614	chr9:496201-496202	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553237487	chr9:496202-496203	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs183190991	chr9:496214-496215	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs573171635	chr9:496224-496225	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs535748846	chr9:496262-496263	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569696200	chr9:496292-496293	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554226491	chr9:496299-496300	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs574411655	chr9:496324-496325	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs543146367	chr9:496329-496330	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs280233	chr9:496336-496337	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs166801	chr9:496342-496343	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs535073603	chr9:496361-496362	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs2094679	chr9:496412-496413	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs367894600	chr9:496434-496435	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187350502	chr9:496441-496442	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs141000229	chr9:496512-496513	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs528350184	chr9:496528-496529	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs192728699	chr9:496541-496542	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561925893	chr9:496573-496574	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs375546754	chr9:496584-496585	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs184742865	chr9:496751-496752	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs189255103	chr9:496867-496868	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs10815100	chr9:496919-496920	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs192768426	chr9:496932-496933	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs375536881	chr9:496939-496940	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs183580365	chr9:496946-496947	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs149787838	chr9:496953-496954	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs535737465	chr9:496983-496984	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs556069237	chr9:497007-497008	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs534621195	chr9:497016-497017	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs574326797	chr9:497066-497067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs145002508	chr9:497109-497110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189486269	chr9:497127-497128	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:1382 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:489600-503200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr9:494400-496200	Enhancers	A549	lung
3	chr9:494400-496200	Enhancers	HepG2	liver
4	chr9:494400-496400	Enhancers	Stomach Mucosa	stomach
5	chr9:494600-496200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:494600-496400	Enhancers	Pancreas	Pancrea
7	chr9:495000-496200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:495200-496200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:495400-496000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr9:495400-496200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:495400-496200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr9:495600-496200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:495800-496200	Enhancers	Gastric	stomach
14	chr9:495800-503200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr9:496200-496400	Bivalent Enhancer	HepG2	liver
16	chr9:496200-503200	Weak transcription	Gastric	stomach
17	chr9:496200-503200	Weak transcription	A549	lung
18	chr9:496400-497200	Weak transcription	Pancreas	Pancrea
19	chr9:496400-497200	Weak transcription	Stomach Mucosa	stomach
20	chr9:497200-497400	Enhancers	Pancreas	Pancrea
21	chr9:497200-497400	Enhancers	Stomach Mucosa	stomach
22	chr9:497400-502800	Weak transcription	Stomach Mucosa	stomach
23	chr9:497400-503400	Weak transcription	Pancreas	Pancrea
24	chr9:501400-501800	Enhancers	Fetal Heart	heart
25	chr9:501800-502800	Weak transcription	Fetal Heart	heart
26	chr9:502000-503200	Weak transcription	Fetal Intestine Small	intestine
27	chr9:502600-503400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr9:502800-503000	Enhancers	Fetal Heart	heart
29	chr9:502800-503000	Enhancers	Fetal Intestine Large	intestine
30	chr9:502800-503200	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr9:502800-503200	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr9:502800-503800	Enhancers	Stomach Mucosa	stomach
33	chr9:503000-503200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr9:503000-503200	Enhancers	Duodenum Mucosa	Duodenum
35	chr9:503000-503200	Bivalent Enhancer	Fetal Intestine Large	intestine
36	chr9:503000-503400	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr9:503000-503400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr9:503000-503600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr9:503000-504200	Flanking Active TSS	Fetal Heart	heart
40	chr9:503200-503400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
41	chr9:503200-503400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr9:503200-503400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
43	chr9:503200-503400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
44	chr9:503200-503400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr9:503200-503400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr9:503200-503400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr9:503200-503400	Flanking Active TSS	Colon Smooth Muscle	Colon
48	chr9:503200-503400	Enhancers	Fetal Intestine Small	intestine
49	chr9:503200-503400	Bivalent Enhancer	Fetal Thymus	thymus
50	chr9:503200-503400	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum

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