Variant report

Variant	nsv1058593
Chromosome Location	chr20:14848001-15084545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2075)
CpG islands
(count:61)
Chromatin interactive
region (count:30)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
9	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
10	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
11	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
12	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
13	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
14	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
15	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
17	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
18	BATF	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
19	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
20	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
21	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
22	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
23	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
24	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
25	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
26	BCL3	chr20:14859514-14860394	A549	lung:	n/a	chr20:14860151-14860160 chr20:14860265-14860274
27	BCL3	chr20:14966411-14967352	A549	lung:	n/a	n/a
28	BCL3	chr20:14965529-14966338	A549	lung:	n/a	chr20:14966177-14966184
29	BCL3	chr20:14966427-14967324	A549	lung:	n/a	n/a
30	BCL3	chr20:14859331-14860569	A549	lung:	n/a	chr20:14860151-14860160 chr20:14859419-14859428 chr20:14860265-14860274
31	BHLHE40	chr20:14860191-14860193	HepG2	liver:	n/a	n/a
32	BHLHE40	chr20:14960125-14960599	HepG2	liver:	n/a	n/a
33	BHLHE40	chr20:14965455-14966238	HepG2	liver:	n/a	n/a
34	BHLHE40	chr20:15042548-15042950	HepG2	liver:	n/a	n/a
35	BHLHE40	chr20:15041038-15041678	HepG2	liver:	n/a	n/a
36	BHLHE40	chr20:14977538-14977786	HepG2	liver:	n/a	n/a
37	BRCA1	chr20:14965501-14966238	HepG2	liver:	n/a	n/a
38	BRCA1	chr20:15043714-15043822	HepG2	liver:	n/a	n/a
39	BRCA1	chr20:14966739-14967191	HepG2	liver:	n/a	n/a
40	BRCA1	chr20:15042587-15042806	HepG2	liver:	n/a	n/a
41	BRCA1	chr20:15041931-15042029	HepG2	liver:	n/a	n/a
42	BRCA1	chr20:14960587-14960671	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr20:15054620-15054671	HepG2	liver:	n/a	n/a
44	BRCA1	chr20:14943807-14944695	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr20:14936483-14937509	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr20:14859909-14860533	HCT-116	colon:	n/a	n/a
47	CEBPB	chr20:14940183-14940581	A549	lung:	n/a	n/a
48	CEBPB	chr20:14932458-14932731	A549	lung:	n/a	n/a
49	CEBPB	chr20:14943912-14944387	A549	lung:	n/a	n/a
50	CEBPB	chr20:14900166-14900714	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	HEK293	kidney:	embryo
2	chr20:14904432-14904482	ProgFib	skin:	n/a
3	chr20:14904432-14904482	MCF-7	breast:	n/a
4	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
5	chr20:14904432-14904482	AG04450	lung:	fetal
6	chr20:14904432-14904482	HepG2	liver:	n/a
7	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
8	chr20:14904432-14904482	GM06990	blood:	n/a
9	chr20:14904432-14904482	SAEC	small airway:	n/a
10	chr20:14904432-14904482	HIPEpiC	eye:	n/a
11	chr20:14904432-14904482	AG04449	skin:	fetal
12	chr20:14904432-14904482	PANC-1	pancreas:	n/a
13	chr20:14904432-14904482	HMEC	breast:	n/a
14	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
15	chr20:14904432-14904482	PFSK-1	brain:	n/a
16	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
17	chr20:14904432-14904482	HRPEpiC	eye:	n/a
18	chr20:14904432-14904482	CMK	blood:	n/a
19	chr20:14904432-14904482	BE2_C	brain:	n/a
20	chr20:14904432-14904482	SK-N-MC	brain:	n/a
21	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
22	chr20:14904432-14904482	SK-N-SH	brain:	n/a
23	chr20:14904432-14904482	RPTEC	kidney:	n/a
24	chr20:14904432-14904482	Jurkat	blood:	n/a
25	chr20:14904432-14904482	SKMC	muscle:	n/a
26	chr20:14904432-14904482	U87	brain:	n/a
27	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
28	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
29	chr20:14904432-14904482	A549	lung:	n/a
30	chr20:14904432-14904482	HL-60	blood:	n/a
31	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
32	chr20:14904432-14904482	GM12892	blood:	n/a
33	chr20:14904432-14904482	NT2-D1	testis:	n/a
34	chr20:14904432-14904482	T-47D	breast:	n/a
35	chr20:14904432-14904482	NH-A	brain:	n/a
36	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
37	chr20:14904432-14904482	K562	blood:	n/a
38	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
39	chr20:14904432-14904482	AG09319	gingival:	n/a
40	chr20:14904432-14904482	HCM	heart:	n/a
41	chr20:14904432-14904482	AG10803	skin:	n/a
42	chr20:14904432-14904482	GM12891	blood:	n/a
43	chr20:14904432-14904482	LNCaP	prostate:	n/a
44	chr20:14904432-14904482	HRE	kidney:	n/a
45	chr20:14904432-14904482	GM12878	blood:	n/a
46	chr20:14904432-14904482	Hela-S3	cervix:	n/a
47	chr20:14904432-14904482	Caco-2	colon:	n/a
48	chr20:14904432-14904482	BJ	skin:	n/a
49	chr20:14904432-14904482	NB4	blood:	n/a
50	chr20:14904432-14904482	HRCEpiC	kidney:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
2	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
3	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
4	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
5	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
6	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
7	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
8	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
9	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
10	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
11	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
12	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
13	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
14	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
15	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
16	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
17	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
18	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
19	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
20	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
21	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
22	chr20:14983136..14983867-chr7:139874694..139875444,2	MCF-7	breast:
23	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
24	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
25	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
26	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
27	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
28	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
29	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
30	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
2	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
3	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
4	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
5	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
6	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
7	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
8	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
9	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
10	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
11	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
12	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
13	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
14	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
15	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
16	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
17	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
18	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
19	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
20	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
21	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
22	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318

No data

Variant related genes	Relation type
ENSG00000237832	TF binding region
RNU6-1159P	TF binding region
RNU6-115P	TF binding region
MACROD2-AS1	TF binding region
ENSG00000237832	CpG island
RNU6-1159P	CpG island
RNU6-115P	CpG island
MACROD2-AS1	CpG island
ENSG00000237832	chromatin interactions

Extended variants
information (count: 7781 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:7781 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191190802	chr20:14848075-14848076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558231133	chr20:14848094-14848095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531491754	chr20:14848107-14848108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543273283	chr20:14848132-14848133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562874800	chr20:14848194-14848195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs407223	chr20:14848196-14848197	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs529223646	chr20:14848214-14848215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547787222	chr20:14848232-14848233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566028362	chr20:14848266-14848267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138984774	chr20:14848270-14848271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544406394	chr20:14848282-14848283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182668325	chr20:14848293-14848294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142101764	chr20:14848357-14848358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537641628	chr20:14848373-14848374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562799235	chr20:14848421-14848422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186938156	chr20:14848522-14848523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367895453	chr20:14848538-14848539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146395323	chr20:14848571-14848572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569875454	chr20:14848630-14848631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs449849	chr20:14848659-14848660	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs191353930	chr20:14848723-14848724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185020066	chr20:14848769-14848770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539560373	chr20:14848815-14848816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557441144	chr20:14848819-14848820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202237692	chr20:14848834-14848835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200762657	chr20:14848838-14848839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377525277	chr20:14848839-14848840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs193221030	chr20:14848848-14848849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs454821	chr20:14848860-14848861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs573915637	chr20:14848869-14848870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35937173	chr20:14848958-14848959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541046496	chr20:14848961-14848962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185212499	chr20:14848977-14848978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190059316	chr20:14849047-14849048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79697202	chr20:14849159-14849160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs408182	chr20:14849165-14849166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs138313727	chr20:14849201-14849202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181354367	chr20:14849225-14849226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567936668	chr20:14849233-14849234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542098357	chr20:14849243-14849244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79563633	chr20:14849246-14849247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372320543	chr20:14849247-14849248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570463524	chr20:14849249-14849250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149567237	chr20:14849314-14849315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539490463	chr20:14849345-14849346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549539129	chr20:14849375-14849376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371365	chr20:14849388-14849389	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs144253182	chr20:14849398-14849399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575749130	chr20:14849424-14849425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535423533	chr20:14849426-14849427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
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
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
Multiple sclerosis	20663923	CNVD
Schizophrenia	20663923	CNVD
brain infarct	20663923	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	17363583	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	20967226	CNVD
Cancer	21272361	CNVD
Schizophrenia	19805367	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:1166 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14846600-14848600	Enhancers	HepG2	liver
2	chr20:14847400-14858400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr20:14857200-14857400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr20:14857400-14859600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr20:14857400-14861000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr20:14858000-14859600	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr20:14858200-14858600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr20:14858400-14858600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr20:14858400-14858800	Enhancers	NH-A	brain
10	chr20:14858400-14859000	Enhancers	NHDF-Ad	bronchial
11	chr20:14858400-14859600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr20:14858400-14861400	Enhancers	HMEC	breast
13	chr20:14858600-14859000	Enhancers	Brain Germinal Matrix	brain
14	chr20:14858600-14859400	Enhancers	A549	lung
15	chr20:14858600-14859600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr20:14858600-14860000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr20:14858600-14861200	Enhancers	NHEK	skin
18	chr20:14858600-14861600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr20:14858800-14859600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr20:14858800-14859800	Weak transcription	NH-A	brain
21	chr20:14859000-14860600	Weak transcription	NHDF-Ad	bronchial
22	chr20:14859200-14860000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr20:14859400-14859600	Enhancers	Fetal Intestine Small	intestine
24	chr20:14859400-14860400	Enhancers	Liver	Liver
25	chr20:14859400-14861000	Flanking Active TSS	A549	lung
26	chr20:14859400-14861200	Enhancers	Hela-S3	cervix
27	chr20:14859400-14861800	Enhancers	HepG2	liver
28	chr20:14859400-14862600	Enhancers	Duodenum Mucosa	Duodenum
29	chr20:14859600-14860200	Enhancers	Stomach Mucosa	stomach
30	chr20:14859600-14860400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr20:14859600-14860400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr20:14859600-14860600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr20:14859600-14860600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr20:14859600-14860600	Weak transcription	Fetal Intestine Small	intestine
35	chr20:14859600-14861000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr20:14859800-14860800	Enhancers	NH-A	brain
37	chr20:14859800-14861000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr20:14859800-14861000	Enhancers	HUVEC	blood vessel
39	chr20:14860000-14860400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr20:14860000-14860600	Enhancers	Brain Hippocampus Middle	brain
41	chr20:14860000-14860800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr20:14860000-14860800	Enhancers	Dnd41	blood
43	chr20:14860000-14861400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr20:14860200-14860600	Enhancers	Brain Substantia Nigra	brain
45	chr20:14860200-14862400	Enhancers	Fetal Intestine Large	intestine
46	chr20:14860200-14865600	Weak transcription	Stomach Mucosa	stomach
47	chr20:14860400-14860600	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr20:14860400-14860800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr20:14860400-14861000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr20:14860600-14860800	Active TSS	Brain Angular Gyrus	brain

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