Variant report

Variant	nsv965862
Chromosome Location	chr20:23654636-23757320
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	CEBPB	chr20:23710539-23710875	A549	lung:	n/a	chr20:23710701-23710712
2	CEBPB	chr20:23687994-23688164	IMR90	lung:	n/a	chr20:23688059-23688070
3	CEBPB	chr20:23655411-23655454	HepG2	liver:	n/a	n/a
4	CEBPB	chr20:23715136-23715338	IMR90	lung:	n/a	chr20:23715271-23715282
5	CEBPB	chr20:23710603-23710866	H1-hESC	embryonic stem cell:	n/a	chr20:23710701-23710712
6	CEBPB	chr20:23687946-23688194	A549	lung:	n/a	chr20:23688059-23688070
7	CEBPB	chr20:23710656-23710785	K562	blood:	n/a	chr20:23710701-23710712
8	CEBPB	chr20:23715133-23715386	HepG2	liver:	n/a	chr20:23715271-23715282
9	CEBPB	chr20:23710550-23710870	IMR90	lung:	n/a	chr20:23710701-23710712
10	CEBPB	chr20:23747142-23747274	K562	blood:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
11	CEBPB	chr20:23715126-23715326	A549	lung:	n/a	chr20:23715271-23715282
12	CEBPB	chr20:23684405-23684588	HepG2	liver:	n/a	chr20:23684504-23684515 chr20:23684504-23684517 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684517 chr20:23684506-23684515
13	CEBPB	chr20:23747045-23747345	HepG2	liver:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
14	CEBPB	chr20:23684500-23684595	A549	lung:	n/a	chr20:23684504-23684515 chr20:23684504-23684517 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684517 chr20:23684506-23684515
15	CEBPB	chr20:23710540-23710875	HepG2	liver:	n/a	chr20:23710701-23710712
16	CEBPB	chr20:23687909-23688202	HepG2	liver:	n/a	chr20:23688059-23688070
17	CEBPB	chr20:23747026-23747352	A549	lung:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747029-23747041 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
18	CTCF	chr20:23704420-23704570	WERI-Rb-1	eye:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
19	CTCF	chr20:23667760-23667910	A549	lung:	n/a	n/a
20	CTCF	chr20:23667840-23667990	HEK293	kidney:	n/a	n/a
21	CTCF	chr20:23756700-23756850	AG04449	skin:	n/a	chr20:23756767-23756780
22	CTCF	chr20:23704339-23704616	HepG2	liver:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
23	CTCF	chr20:23686920-23686977	GM10266	blood:	n/a	n/a
24	CTCF	chr20:23729640-23729790	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr20:23704724-23704864	GM13976	blood:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
26	CTCF	chr20:23704340-23704490	AG04449	skin:	n/a	n/a
27	CTCF	chr20:23704440-23704590	WERI-Rb-1	eye:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
28	CTCF	chr20:23703627-23703734	MCF-7	breast:	n/a	n/a
29	CTCF	chr20:23704130-23704247	GM10266	blood:	n/a	n/a
30	CTCF	chr20:23756660-23756810	A549	lung:	n/a	chr20:23756767-23756780
31	CTCF	chr20:23735500-23735650	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr20:23659995-23660064	MCF-7	breast:	n/a	n/a
33	CTCF	chr20:23704340-23704490	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr20:23704340-23704490	HMEC	breast:	n/a	n/a
35	CTCF	chr20:23704360-23704510	AG09319	gingival:	n/a	chr20:23704496-23704505
36	CTCF	chr20:23704380-23704530	HMEC	breast:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
37	CTCF	chr20:23668792-23668824	MCF-7	breast:	n/a	n/a
38	CTCF	chr20:23704357-23704831	GM12892	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
39	CTCF	chr20:23703638-23703722	MCF-7	breast:	n/a	n/a
40	CTCF	chr20:23715700-23715850	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr20:23704260-23704920	A549	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
42	CTCF	chr20:23677891-23677951	GM20000	blood:	n/a	n/a
43	CTCF	chr20:23704640-23704790	MCF-7	breast:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704740-23704758
44	CTCF	chr20:23704133-23705074	A549	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
45	CTCF	chr20:23704880-23705030	HCT-116	colon:	n/a	n/a
46	CTCF	chr20:23704360-23704510	AG09309	skin:	n/a	chr20:23704496-23704505
47	CTCF	chr20:23703820-23703970	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr20:23704320-23704470	HAc	cerebellar:	n/a	n/a
49	CTCF	chr20:23704381-23704601	Lung_OC	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
50	CTCF	chr20:23704284-23704889	A549	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23670089-23670139	GM12878	blood:	n/a
2	chr20:23670047-23670097	NHBE	bronchial:	n/a
3	chr20:23669470-23669520	NH-A	brain:	n/a
4	chr20:23728814-23728864	SK-N-SH_RA	brain:	n/a
5	chr20:23728432-23728482	BE2_C	brain:	n/a
6	chr20:23731367-23731417	HRCEpiC	kidney:	n/a
7	chr20:23731367-23731417	ProgFib	skin:	n/a
8	chr20:23728814-23728864	K562	blood:	n/a
9	chr20:23728432-23728482	AG09319	gingival:	n/a
10	chr20:23666505-23666555	HCM	heart:	n/a
11	chr20:23731367-23731417	NB4	blood:	n/a
12	chr20:23728432-23728482	GM12892	blood:	n/a
13	chr20:23671108-23671158	ECC-1	luminal epithelium:	n/a
14	chr20:23728814-23728864	ECC-1	luminal epithelium:	n/a
15	chr20:23666505-23666555	GM06990	blood:	n/a
16	chr20:23669470-23669520	HNPCEpiC	eye:	n/a
17	chr20:23671108-23671158	IMR90	lung:	fetal
18	chr20:23728432-23728482	NT2-D1	testis:	n/a
19	chr20:23728432-23728482	HEEpiC	esophagus:	n/a
20	chr20:23671108-23671158	GM19239	blood:	n/a
21	chr20:23671108-23671158	NHBE	bronchial:	n/a
22	chr20:23732873-23732923	Jurkat	blood:	n/a
23	chr20:23670047-23670097	HPAEpiC	pulmonary alveolar:	n/a
24	chr20:23732873-23732923	HL-60	blood:	n/a
25	chr20:23669241-23669291	HCT-116	colon:	n/a
26	chr20:23728432-23728482	AG04450	lung:	fetal
27	chr20:23728432-23728482	SKMC	muscle:	n/a
28	chr20:23669241-23669291	AG09319	gingival:	n/a
29	chr20:23669470-23669520	MCF10A-Er-Src	breast:	n/a
30	chr20:23731367-23731417	NT2-D1	testis:	n/a
31	chr20:23670047-23670097	HIPEpiC	eye:	n/a
32	chr20:23728432-23728482	AoSMC	blood vessel:	n/a
33	chr20:23669470-23669520	BJ	skin:	n/a
34	chr20:23728814-23728864	Jurkat	blood:	n/a
35	chr20:23666505-23666555	K562	blood:	n/a
36	chr20:23666505-23666555	PANC-1	pancreas:	n/a
37	chr20:23670047-23670097	HEEpiC	esophagus:	n/a
38	chr20:23728814-23728864	HCM	heart:	n/a
39	chr20:23670089-23670139	AG04449	skin:	fetal
40	chr20:23669470-23669520	ovcar-3	ovarian:	n/a
41	chr20:23666505-23666555	ProgFib	skin:	n/a
42	chr20:23731367-23731417	Caco-2	colon:	n/a
43	chr20:23728432-23728482	SK-N-SH	brain:	n/a
44	chr20:23732595-23732645	Hepatocyte	liver:	n/a
45	chr20:23669470-23669520	U87	brain:	n/a
46	chr20:23669470-23669520	AG09309	skin:	n/a
47	chr20:23670047-23670097	AG10803	skin:	n/a
48	chr20:23731367-23731417	SAEC	small airway:	n/a
49	chr20:23728814-23728864	NT2-D1	testis:	n/a
50	chr20:23666505-23666555	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:
2	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:
3	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
4	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
5	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
6	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
7	chr20:23649611..23652412-chr20:23660454..23663208,2	MCF-7	breast:
8	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
9	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:
10	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
11	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-5	chr20:23732376-23732473	NONHSAT079083
2	lnc-CST8-5	chr20:23733871-23734300	NONHSAT079083
3	lnc-CST8-5	chr20:23733160-23733281	NONHSAT079083
4	lnc-CST8-5	chr20:23726778-23726924	NONHSAT079083

Variant related genes	Relation type
CST4	TF binding region
CST2P1	TF binding region
CST1	TF binding region
CST4	CpG island
CST2P1	CpG island
CST1	CpG island

Extended variants
information (count: 4373 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4373 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6048978	chr20:23654689-23654690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575153595	chr20:23654767-23654768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552767044	chr20:23654774-23654775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550144305	chr20:23654775-23654776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569902556	chr20:23654806-23654807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182097876	chr20:23654847-23654848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548151461	chr20:23654866-23654867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568386830	chr20:23654870-23654871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373685289	chr20:23654879-23654880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369221020	chr20:23654912-23654913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577005105	chr20:23654981-23654982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116512236	chr20:23654984-23654985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188815074	chr20:23655012-23655013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575909379	chr20:23655033-23655034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193207412	chr20:23655046-23655047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562020619	chr20:23655052-23655053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116168253	chr20:23655105-23655106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376917992	chr20:23655115-23655116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145817659	chr20:23655135-23655136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6048979	chr20:23655141-23655142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533574403	chr20:23655160-23655161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549964848	chr20:23655161-23655162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369569308	chr20:23655164-23655165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563820770	chr20:23655177-23655178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377469673	chr20:23655192-23655193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188817854	chr20:23655241-23655242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549386867	chr20:23655244-23655245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568346160	chr20:23655268-23655269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527627743	chr20:23655270-23655271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192091173	chr20:23655288-23655289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76853115	chr20:23655340-23655341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570615832	chr20:23655349-23655350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138665848	chr20:23655387-23655388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555953766	chr20:23655400-23655401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184271599	chr20:23655451-23655452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535085683	chr20:23655463-23655464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142731250	chr20:23655507-23655508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374261214	chr20:23655529-23655530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541279678	chr20:23655545-23655546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146962206	chr20:23655585-23655586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs578085155	chr20:23655626-23655627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544015744	chr20:23655670-23655671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376764621	chr20:23655752-23655753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138019646	chr20:23655758-23655759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529423883	chr20:23655792-23655793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543035519	chr20:23655811-23655812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559833589	chr20:23655837-23655838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528499714	chr20:23655843-23655844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149517745	chr20:23655867-23655868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144128157	chr20:23655874-23655875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23637200-23660000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:23659800-23660400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr20:23659800-23660600	Enhancers	HMEC	breast
4	chr20:23660000-23660600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr20:23660000-23661200	Enhancers	Right Atrium	heart
6	chr20:23660200-23660600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:23660400-23661000	Enhancers	Adipose Nuclei	Adipose
8	chr20:23660400-23661200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr20:23660400-23661200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr20:23660400-23661200	Enhancers	Left Ventricle	heart
11	chr20:23660400-23661200	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr20:23660600-23661200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr20:23660600-23661200	Enhancers	Lung	lung
14	chr20:23660600-23661200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr20:23660600-23668600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr20:23660800-23661200	Enhancers	Ovary	ovary
17	chr20:23660800-23662000	Enhancers	Brain Germinal Matrix	brain
18	chr20:23662400-23662800	Enhancers	NHLF	lung
19	chr20:23662800-23663200	Weak transcription	NHLF	lung
20	chr20:23662800-23664200	Enhancers	NHDF-Ad	bronchial
21	chr20:23662800-23665200	Enhancers	HUVEC	blood vessel
22	chr20:23663200-23663800	Enhancers	NHLF	lung
23	chr20:23663400-23664400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr20:23663600-23665000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr20:23663800-23672400	Weak transcription	NHLF	lung
26	chr20:23664800-23665000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr20:23665000-23666000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr20:23665200-23669000	Weak transcription	HUVEC	blood vessel
29	chr20:23665800-23666400	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr20:23666000-23666400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr20:23666000-23667000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr20:23667000-23672200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr20:23667200-23667400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr20:23667400-23668800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr20:23668600-23670000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr20:23668800-23669000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr20:23668800-23669000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr20:23668800-23669000	Enhancers	Spleen	Spleen
39	chr20:23669000-23669200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr20:23669000-23669800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr20:23669000-23671000	Enhancers	HUVEC	blood vessel
42	chr20:23669200-23670200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr20:23669800-23670000	Enhancers	Lung	lung
44	chr20:23669800-23670400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr20:23670000-23672000	Weak transcription	Lung	lung
46	chr20:23670200-23671200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr20:23670400-23671400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr20:23670800-23671000	Bivalent Enhancer	Placenta	Placenta
49	chr20:23670800-23673600	Weak transcription	Spleen	Spleen
50	chr20:23671000-23672000	Weak transcription	HUVEC	blood vessel

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