Variant report

Variant	nsv585488
Chromosome Location	chr20:14764611-15150730
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2943)
CpG islands
(count:61)
Chromatin interactive
region (count:51)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2943 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:15139111-15139485	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:15144336-15144711	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
9	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
11	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
15	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
16	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
18	ATF2	chr20:15142645-15143351	GM12878	blood:	n/a	n/a
19	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
20	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
22	ATF2	chr20:15142556-15143423	GM12878	blood:	n/a	n/a
23	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
25	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
26	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
27	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
28	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
29	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
30	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr20:15144468-15144534	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
34	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
35	BATF	chr20:15142631-15143004	GM12878	blood:	n/a	n/a
36	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
37	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
38	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
39	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
40	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
41	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
42	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
43	BATF	chr20:15143005-15143338	GM12878	blood:	n/a	n/a
44	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
45	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
46	BATF	chr20:15142669-15143382	GM12878	blood:	n/a	n/a
47	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
48	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
49	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
50	BATF	chr20:14810508-14810959	GM12878	blood:	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	NH-A	brain:	n/a
2	chr20:14904432-14904482	HIPEpiC	eye:	n/a
3	chr20:14904432-14904482	HEK293	kidney:	embryo
4	chr20:14904432-14904482	AG04450	lung:	fetal
5	chr20:14904432-14904482	GM12892	blood:	n/a
6	chr20:14904432-14904482	AG09309	skin:	n/a
7	chr20:14904432-14904482	HMEC	breast:	n/a
8	chr20:14904432-14904482	T-47D	breast:	n/a
9	chr20:14904432-14904482	HCT-116	colon:	n/a
10	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
11	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
12	chr20:14904432-14904482	IMR90	lung:	fetal
13	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
14	chr20:14904432-14904482	Hepatocyte	liver:	n/a
15	chr20:14904432-14904482	Jurkat	blood:	n/a
16	chr20:14904432-14904482	ProgFib	skin:	n/a
17	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
18	chr20:14904432-14904482	BE2_C	brain:	n/a
19	chr20:14904432-14904482	LNCaP	prostate:	n/a
20	chr20:14904432-14904482	NT2-D1	testis:	n/a
21	chr20:14904432-14904482	PFSK-1	brain:	n/a
22	chr20:14904432-14904482	A549	lung:	n/a
23	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
24	chr20:14904432-14904482	CMK	blood:	n/a
25	chr20:14904432-14904482	SK-N-SH	brain:	n/a
26	chr20:14904432-14904482	BJ	skin:	n/a
27	chr20:14904432-14904482	Caco-2	colon:	n/a
28	chr20:14904432-14904482	HepG2	liver:	n/a
29	chr20:14904432-14904482	HCF	heart:	n/a
30	chr20:14904432-14904482	MCF-7	breast:	n/a
31	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
32	chr20:14904432-14904482	HRE	kidney:	n/a
33	chr20:14904432-14904482	GM06990	blood:	n/a
34	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
35	chr20:14904432-14904482	Hela-S3	cervix:	n/a
36	chr20:14904432-14904482	NHBE	bronchial:	n/a
37	chr20:14904432-14904482	SK-N-MC	brain:	n/a
38	chr20:14904432-14904482	SAEC	small airway:	n/a
39	chr20:14904432-14904482	AG04449	skin:	fetal
40	chr20:14904432-14904482	K562	blood:	n/a
41	chr20:14904432-14904482	SKMC	muscle:	n/a
42	chr20:14904432-14904482	U87	brain:	n/a
43	chr20:14904432-14904482	HL-60	blood:	n/a
44	chr20:14904432-14904482	PrEC	prostate:	n/a
45	chr20:14904432-14904482	AG09319	gingival:	n/a
46	chr20:14904432-14904482	GM12878	blood:	n/a
47	chr20:14904432-14904482	HRPEpiC	eye:	n/a
48	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
49	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
50	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
2	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
3	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
4	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
5	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
6	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
7	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
8	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
9	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
10	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
11	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
12	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
13	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
14	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
15	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
16	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
17	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
18	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
19	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
20	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
21	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
22	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
23	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
24	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
25	chr20:14983136..14983867-chr7:139874694..139875444,2	MCF-7	breast:
26	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
27	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
28	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
29	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
30	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
31	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
32	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
33	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
34	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
35	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
36	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
37	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
38	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
39	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
40	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
41	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
42	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
43	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
44	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
45	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
46	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
47	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
48	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
49	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
50	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
2	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
3	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
4	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
5	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
6	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
7	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
8	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
9	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
10	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
11	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
12	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
13	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
14	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
15	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
16	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
17	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
18	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
19	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
20	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
21	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
22	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
23	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
24	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
25	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
26	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1

No data

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

Extended variants
information (count: 11912 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:11912 , 50 per page) page: 1 2 3 4 5 6 7 ... 239

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6034040	chr20:14764611-14764612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147132373	chr20:14764631-14764632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577331906	chr20:14764659-14764660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140416310	chr20:14764674-14764675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556776811	chr20:14764690-14764691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377275817	chr20:14764691-14764692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377006148	chr20:14764698-14764699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs117327325	chr20:14764700-14764701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548307635	chr20:14764738-14764739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144340107	chr20:14764778-14764779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369982744	chr20:14764779-14764780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6042918	chr20:14764801-14764802	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs528182594	chr20:14764852-14764853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200450829	chr20:14764899-14764900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79355811	chr20:14764930-14764931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564853345	chr20:14764964-14764965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114119187	chr20:14765038-14765039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147372133	chr20:14765049-14765050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186558890	chr20:14765065-14765066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543567393	chr20:14765091-14765092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6034041	chr20:14765094-14765095	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs529981317	chr20:14765102-14765103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190947448	chr20:14765110-14765111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6034042	chr20:14765140-14765141	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs80006848	chr20:14765164-14765165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558597928	chr20:14765235-14765236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs8183481	chr20:14765297-14765298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570866399	chr20:14765299-14765300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538425496	chr20:14765303-14765304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556527000	chr20:14765304-14765305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575055877	chr20:14765315-14765316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371815074	chr20:14765319-14765320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201640811	chr20:14765320-14765321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs5840633	chr20:14765321-14765322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370161267	chr20:14765323-14765324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572850245	chr20:14765324-14765325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564951348	chr20:14765325-14765326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79417075	chr20:14765327-14765328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532147465	chr20:14765332-14765333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs59950276	chr20:14765333-14765334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377111072	chr20:14765360-14765361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558916069	chr20:14765362-14765363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76406630	chr20:14765410-14765411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543967730	chr20:14765438-14765439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562567460	chr20:14765439-14765440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544608327	chr20:14765481-14765482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139928250	chr20:14765489-14765490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548046072	chr20:14765522-14765523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566449753	chr20:14765529-14765530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563004853	chr20:14765593-14765594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	21272361	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:1604 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14764200-14764800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr20:14764800-14765000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr20:14764800-14765200	Enhancers	Fetal Lung	lung
4	chr20:14765200-14765600	Weak transcription	Fetal Lung	lung
5	chr20:14765600-14766000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr20:14765600-14766200	Enhancers	Fetal Lung	lung
7	chr20:14765600-14766400	Enhancers	Stomach Mucosa	stomach
8	chr20:14765800-14766000	Enhancers	Fetal Intestine Small	intestine
9	chr20:14765800-14766400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr20:14766000-14767400	Weak transcription	Fetal Intestine Small	intestine
11	chr20:14767400-14768200	Enhancers	Fetal Intestine Small	intestine
12	chr20:14767400-14768600	Enhancers	Fetal Intestine Large	intestine
13	chr20:14768200-14768800	Weak transcription	Fetal Intestine Small	intestine
14	chr20:14768600-14770400	Weak transcription	Fetal Intestine Large	intestine
15	chr20:14768800-14769000	Enhancers	Fetal Intestine Small	intestine
16	chr20:14769000-14771000	Weak transcription	Fetal Intestine Small	intestine
17	chr20:14770400-14772400	Enhancers	Fetal Intestine Large	intestine
18	chr20:14770600-14773000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr20:14771000-14771800	Enhancers	Small Intestine	intestine
20	chr20:14771000-14772400	Enhancers	Fetal Intestine Small	intestine
21	chr20:14771400-14772200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr20:14771400-14772200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr20:14771800-14773000	Weak transcription	Small Intestine	intestine
24	chr20:14772400-14772800	Weak transcription	Fetal Intestine Large	intestine
25	chr20:14772400-14772800	Weak transcription	Fetal Intestine Small	intestine
26	chr20:14772800-14774200	Enhancers	Fetal Intestine Small	intestine
27	chr20:14772800-14774400	Enhancers	Fetal Intestine Large	intestine
28	chr20:14773000-14773400	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr20:14773200-14773400	Enhancers	Small Intestine	intestine
30	chr20:14774600-14774800	Enhancers	Gastric	stomach
31	chr20:14780000-14780400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr20:14780000-14780600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr20:14780200-14780600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr20:14780400-14780600	Enhancers	Fetal Brain Female	brain
35	chr20:14780600-14782200	Weak transcription	Fetal Brain Female	brain
36	chr20:14782200-14782400	Enhancers	Liver	Liver
37	chr20:14782200-14783800	Enhancers	Fetal Brain Female	brain
38	chr20:14782400-14782800	Flanking Active TSS	Liver	Liver
39	chr20:14782600-14783400	Enhancers	GM12878-XiMat	blood
40	chr20:14782800-14783000	Enhancers	Liver	Liver
41	chr20:14787600-14788000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr20:14798200-14798400	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr20:14798200-14798600	Enhancers	Fetal Kidney	kidney
44	chr20:14798400-14800400	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr20:14800400-14800800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr20:14800800-14801400	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr20:14801200-14801800	Enhancers	Fetal Brain Male	brain
48	chr20:14801200-14801800	Enhancers	Fetal Brain Female	brain
49	chr20:14801400-14801800	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr20:14801800-14806000	Weak transcription	Fetal Brain Female	brain

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