Variant report

Variant	nsv974700
Chromosome Location	chr15:30325318-30351989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr15:30348379-30348447	K562	blood:	n/a	n/a
2	BRCA1	chr15:30333944-30334068	GM12878	blood:	n/a	n/a
3	CEBPB	chr15:30343011-30343208	HepG2	liver:	n/a	n/a
4	CEBPB	chr15:30331155-30331602	Hela-S3	cervix:	n/a	chr15:30331295-30331307
5	CHD1	chr15:30347814-30348022	GM12878	blood:	n/a	n/a
6	CHD1	chr15:30335445-30335601	GM12878	blood:	n/a	n/a
7	CHD1	chr15:30330953-30331153	GM12878	blood:	n/a	n/a
8	CHD2	chr15:30331324-30331787	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr15:30338134-30338199	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr15:30335611-30335683	Spleen_OC	spleen:	n/a	n/a
11	CTCF	chr15:30335291-30335859	HCT-116	colon:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
12	CTCF	chr15:30333650-30333708	GM20000	blood:	n/a	n/a
13	CTCF	chr15:30335526-30335733	LNCaP	prostate:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
14	CTCF	chr15:30335520-30335670	HFF	foreskin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
15	CTCF	chr15:30335500-30335650	NHLF	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
16	CTCF	chr15:30335382-30335820	HCT-116	colon:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
17	CTCF	chr15:30335570-30335690	SK-N-SH_RA	brain:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
18	CTCF	chr15:30335500-30335650	NHDF-neo	bronchial:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
19	CTCF	chr15:30335576-30335719	Gliobla	brain:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
20	CTCF	chr15:30338100-30338250	NHEK	skin:	n/a	n/a
21	CTCF	chr15:30335560-30335710	AG04450	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
22	CTCF	chr15:30335520-30335670	HUVEC	blood vessel:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
23	CTCF	chr15:30335500-30335650	AG09309	skin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
24	CTCF	chr15:30335418-30335830	IMR90	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
25	CTCF	chr15:30348780-30348930	HCT-116	colon:	n/a	chr15:30348836-30348857 chr15:30348841-30348859
26	CTCF	chr15:30335473-30335759	GM12878	blood:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
27	CTCF	chr15:30335569-30335696	Pancreas_OC	pancreas:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
28	CTCF	chr15:30335499-30335724	HUVEC	blood vessel:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
29	CTCF	chr15:30338071-30338223	MCF-7	breast:	n/a	n/a
30	CTCF	chr15:30335560-30335710	AG04449	skin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
31	CTCF	chr15:30335500-30335650	HRPEpiC	eye:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
32	CTCF	chr15:30335520-30335670	HRPEpiC	eye:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
33	CTCF	chr15:30335500-30335650	NHEK	skin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
34	CTCF	chr15:30338000-30338150	RPTEC	kidney:	n/a	n/a
35	CTCF	chr15:30335470-30335744	A549	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
36	CTCF	chr15:30335377-30335724	A549	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
37	CTCF	chr15:30335560-30335710	HRE	kidney:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
38	CTCF	chr15:30335460-30335610	HVMF	connective:	n/a	n/a
39	CTCF	chr15:30335395-30335799	A549	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
40	CTCF	chr15:30341502-30341583	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr15:30338160-30338310	HRE	kidney:	n/a	n/a
42	CTCF	chr15:30341480-30341630	A549	lung:	n/a	n/a
43	CTCF	chr15:30335640-30335790	MCF-7	breast:	n/a	n/a
44	CTCF	chr15:30335640-30335790	HRE	kidney:	n/a	n/a
45	CTCF	chr15:30335560-30335710	HPAF	blood vessel:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
46	CTCF	chr15:30335540-30335690	HPF	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
47	CTCF	chr15:30335480-30335630	HEEpiC	esophagus:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
48	CTCF	chr15:30335680-30335830	HAc	cerebellar:	n/a	n/a
49	CTCF	chr15:30335458-30335841	K562	blood:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
50	CTCF	chr15:30335540-30335690	AG10803	skin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30334898-30334948	SK-N-MC	brain:	n/a
2	chr15:30334898-30334948	SK-N-MC	brain:	n/a
3	chr15:30337875-30337925	NHBE	bronchial:	n/a
4	chr15:30337018-30337068	HAEpiC	amniotic membrane:	n/a
5	chr15:30334898-30334948	NH-A	brain:	n/a
6	chr15:30337018-30337068	AG09309	skin:	n/a
7	chr15:30334898-30334948	AG04450	lung:	fetal
8	chr15:30337018-30337068	NT2-D1	testis:	n/a
9	chr15:30337366-30337416	GM19239	blood:	n/a
10	chr15:30333911-30333961	ECC-1	luminal epithelium:	n/a
11	chr15:30336678-30336728	Hepatocyte	liver:	n/a
12	chr15:30334898-30334948	A549	lung:	n/a
13	chr15:30336915-30336965	BE2_C	brain:	n/a
14	chr15:30337366-30337416	NHDF-neo	bronchial:	n/a
15	chr15:30337018-30337068	PANC-1	pancreas:	n/a
16	chr15:30336940-30336990	HepG2	liver:	n/a
17	chr15:30337875-30337925	AG09319	gingival:	n/a
18	chr15:30337875-30337925	IMR90	lung:	fetal
19	chr15:30336678-30336728	ECC-1	luminal epithelium:	n/a
20	chr15:30337018-30337068	PrEC	prostate:	n/a
21	chr15:30333911-30333961	Hepatocyte	liver:	n/a
22	chr15:30336915-30336965	HCM	heart:	n/a
23	chr15:30333911-30333961	NHBE	bronchial:	n/a
24	chr15:30337018-30337068	SKMC	muscle:	n/a
25	chr15:30336940-30336990	AoSMC	blood vessel:	n/a
26	chr15:30336915-30336965	RPTEC	kidney:	n/a
27	chr15:30336940-30336990	ProgFib	skin:	n/a
28	chr15:30337366-30337416	BE2_C	brain:	n/a
29	chr15:30339875-30339925	LNCaP	prostate:	n/a
30	chr15:30339875-30339925	GM12892	blood:	n/a
31	chr15:30337366-30337416	AG10803	skin:	n/a
32	chr15:30339875-30339925	NHBE	bronchial:	n/a
33	chr15:30337018-30337068	Hela-S3	cervix:	n/a
34	chr15:30339875-30339925	HIPEpiC	eye:	n/a
35	chr15:30339875-30339925	ProgFib	skin:	n/a
36	chr15:30339875-30339925	IMR90	lung:	fetal
37	chr15:30337366-30337416	HEEpiC	esophagus:	n/a
38	chr15:30336915-30336965	HRCEpiC	kidney:	n/a
39	chr15:30337366-30337416	AG09319	gingival:	n/a
40	chr15:30336678-30336728	SK-N-SH_RA	brain:	n/a
41	chr15:30333911-30333961	HCM	heart:	n/a
42	chr15:30337875-30337925	T-47D	breast:	n/a
43	chr15:30339875-30339925	BE2_C	brain:	n/a
44	chr15:30334898-30334948	IMR90	lung:	fetal
45	chr15:30336678-30336728	AG04450	lung:	fetal
46	chr15:30333911-30333961	SK-N-MC	brain:	n/a
47	chr15:30336940-30336990	CMK	blood:	n/a
48	chr15:30337366-30337416	MCF10A-Er-Src	breast:	n/a
49	chr15:30337018-30337068	Caco-2	colon:	n/a
50	chr15:30333911-30333961	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:30234442..30235027-chr15:30335180..30335724,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TJP1-1	chr15:30337914-30338051	ENSG00000259647.1

Variant related genes	Relation type
ENSG00000259647	TF binding region
ENSG00000260174	TF binding region
ENSG00000259647	CpG island
ENSG00000260174	CpG island

Extended variants
information (count: 950 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:950 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535079336	chr15:30325327-30325328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554966603	chr15:30325390-30325391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568338125	chr15:30325398-30325399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537433191	chr15:30325411-30325412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186569770	chr15:30325434-30325435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74631996	chr15:30325477-30325478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546032976	chr15:30325484-30325485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553100887	chr15:30325504-30325505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565321616	chr15:30325508-30325509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142454869	chr15:30325509-30325510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541525969	chr15:30325522-30325523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561744851	chr15:30325549-30325550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28414702	chr15:30325639-30325640	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs537876600	chr15:30325647-30325648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151258371	chr15:30325671-30325672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533216572	chr15:30325718-30325719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191710246	chr15:30325771-30325772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532362083	chr15:30325783-30325784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10220767	chr15:30325798-30325799	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528610599	chr15:30325807-30325808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76019133	chr15:30325818-30325819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200893540	chr15:30325902-30325903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537089062	chr15:30325928-30325929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76763103	chr15:30325940-30325941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4534821	chr15:30325949-30325950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570809660	chr15:30325966-30325967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78890210	chr15:30326021-30326022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553166233	chr15:30326047-30326048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549610584	chr15:30326069-30326070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370525686	chr15:30326099-30326100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201893302	chr15:30326145-30326146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542386237	chr15:30326159-30326160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4553604	chr15:30326188-30326189	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184698574	chr15:30326207-30326208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543868621	chr15:30326221-30326222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28605701	chr15:30326254-30326255	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570241362	chr15:30326260-30326261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533281182	chr15:30326303-30326304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147029155	chr15:30326410-30326411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560460916	chr15:30326413-30326414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs5027258	chr15:30326484-30326485	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs571232259	chr15:30326486-30326487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549153737	chr15:30326490-30326491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190416812	chr15:30326554-30326555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181627680	chr15:30326555-30326556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77548153	chr15:30326589-30326590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550569028	chr15:30326634-30326635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547483272	chr15:30326635-30326636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570478284	chr15:30326642-30326643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539765298	chr15:30326673-30326674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Autism	20531469	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	19843651	CNVD
Schizophrenia	19843651	CNVD
Autism	22543975	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30324800-30325400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
2	chr15:30324800-30325600	Enhancers	Brain Angular Gyrus	brain
3	chr15:30324800-30326400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:30324800-30326400	Enhancers	Brain Anterior Caudate	brain
5	chr15:30324800-30326400	Enhancers	Brain Cingulate Gyrus	brain
6	chr15:30324800-30326400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr15:30324800-30326400	Enhancers	Brain Substantia Nigra	brain
8	chr15:30324800-30326600	Enhancers	Brain Hippocampus Middle	brain
9	chr15:30325000-30326400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr15:30325400-30327600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr15:30325600-30325800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr15:30325600-30327600	Weak transcription	Brain Angular Gyrus	brain
13	chr15:30326400-30327600	Weak transcription	Brain Cingulate Gyrus	brain
14	chr15:30326400-30327800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr15:30326400-30328000	Weak transcription	Brain Anterior Caudate	brain
16	chr15:30326400-30328200	Weak transcription	Brain Substantia Nigra	brain
17	chr15:30326600-30328200	Weak transcription	Brain Hippocampus Middle	brain
18	chr15:30327600-30328200	Enhancers	Brain Angular Gyrus	brain
19	chr15:30327600-30328400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr15:30327600-30328800	Enhancers	Brain Cingulate Gyrus	brain
21	chr15:30327600-30329800	Enhancers	Fetal Brain Male	brain
22	chr15:30327800-30328400	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr15:30327800-30328400	Enhancers	Fetal Brain Female	brain
24	chr15:30327800-30329000	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr15:30328000-30328200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr15:30328000-30328200	Enhancers	Brain Anterior Caudate	brain
27	chr15:30328200-30328400	Flanking Active TSS	Brain Anterior Caudate	brain
28	chr15:30328200-30328400	Enhancers	Brain Substantia Nigra	brain
29	chr15:30328200-30328600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr15:30328200-30328600	Enhancers	Brain Hippocampus Middle	brain
31	chr15:30328200-30331200	Weak transcription	Brain Angular Gyrus	brain
32	chr15:30328400-30328800	Active TSS	Brain Anterior Caudate	brain
33	chr15:30328400-30328800	Active TSS	Fetal Brain Female	brain
34	chr15:30328400-30331000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr15:30328400-30331200	Weak transcription	Brain Substantia Nigra	brain
36	chr15:30328400-30333600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr15:30328600-30331200	Weak transcription	Brain Hippocampus Middle	brain
38	chr15:30328800-30329200	Enhancers	Fetal Brain Female	brain
39	chr15:30328800-30331200	Weak transcription	Brain Anterior Caudate	brain
40	chr15:30328800-30333400	Weak transcription	Brain Cingulate Gyrus	brain
41	chr15:30329000-30331200	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr15:30329400-30329600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr15:30329600-30337400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr15:30329800-30330800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr15:30330400-30332400	Enhancers	Liver	Liver
46	chr15:30330600-30331800	Enhancers	Colonic Mucosa	Colon
47	chr15:30330600-30331800	Enhancers	Hela-S3	cervix
48	chr15:30330600-30332000	Enhancers	Duodenum Mucosa	Duodenum
49	chr15:30330800-30331200	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr15:30330800-30332000	Enhancers	Adipose Nuclei	Adipose

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