Variant report

Variant	nsv544200
Chromosome Location	chr20:14782375-15019489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2311)
CpG islands
(count:61)
Chromatin interactive
region (count:45)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2311 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
7	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
16	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
18	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
19	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
20	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
21	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
22	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
23	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
24	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
27	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
28	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
29	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
30	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
31	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
32	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
33	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
34	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
35	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
36	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
37	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
38	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
39	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
40	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
41	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
42	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
44	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
46	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
47	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
48	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
49	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
50	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	RPTEC	kidney:	n/a
2	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
3	chr20:14904432-14904482	AG04450	lung:	fetal
4	chr20:14904432-14904482	AG04449	skin:	fetal
5	chr20:14904432-14904482	GM12878	blood:	n/a
6	chr20:14904432-14904482	HMEC	breast:	n/a
7	chr20:14904432-14904482	HCT-116	colon:	n/a
8	chr20:14904432-14904482	BJ	skin:	n/a
9	chr20:14904432-14904482	NHBE	bronchial:	n/a
10	chr20:14904432-14904482	A549	lung:	n/a
11	chr20:14904432-14904482	T-47D	breast:	n/a
12	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
13	chr20:14904432-14904482	NB4	blood:	n/a
14	chr20:14904432-14904482	HCF	heart:	n/a
15	chr20:14904432-14904482	GM12892	blood:	n/a
16	chr20:14904432-14904482	Jurkat	blood:	n/a
17	chr20:14904432-14904482	Caco-2	colon:	n/a
18	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
19	chr20:14904432-14904482	ProgFib	skin:	n/a
20	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
21	chr20:14904432-14904482	HRPEpiC	eye:	n/a
22	chr20:14904432-14904482	Hela-S3	cervix:	n/a
23	chr20:14904432-14904482	SK-N-SH	brain:	n/a
24	chr20:14904432-14904482	PFSK-1	brain:	n/a
25	chr20:14904432-14904482	GM19239	blood:	n/a
26	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
27	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
28	chr20:14904432-14904482	GM06990	blood:	n/a
29	chr20:14904432-14904482	CMK	blood:	n/a
30	chr20:14904432-14904482	AG09309	skin:	n/a
31	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
32	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
33	chr20:14904432-14904482	HCM	heart:	n/a
34	chr20:14904432-14904482	SK-N-MC	brain:	n/a
35	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
36	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
37	chr20:14904432-14904482	NH-A	brain:	n/a
38	chr20:14904432-14904482	PrEC	prostate:	n/a
39	chr20:14904432-14904482	SAEC	small airway:	n/a
40	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
41	chr20:14904432-14904482	IMR90	lung:	fetal
42	chr20:14904432-14904482	HepG2	liver:	n/a
43	chr20:14904432-14904482	HIPEpiC	eye:	n/a
44	chr20:14904432-14904482	NT2-D1	testis:	n/a
45	chr20:14904432-14904482	PANC-1	pancreas:	n/a
46	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
47	chr20:14904432-14904482	Hepatocyte	liver:	n/a
48	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
49	chr20:14904432-14904482	U87	brain:	n/a
50	chr20:14904432-14904482	HEK293	kidney:	embryo

(count:45 , 50 per page) page: 1

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

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

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

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: 7702 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:7702 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547300583	chr20:14782375-14782376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565961957	chr20:14782432-14782433	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539707631	chr20:14782510-14782511	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115770900	chr20:14782531-14782532	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368857636	chr20:14782540-14782541	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570020854	chr20:14782541-14782542	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537062246	chr20:14782559-14782560	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2876390	chr20:14782587-14782588	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574100696	chr20:14782634-14782635	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144429814	chr20:14782658-14782659	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117533064	chr20:14782671-14782672	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577833952	chr20:14782688-14782689	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116433214	chr20:14782702-14782703	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556467667	chr20:14782720-14782721	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544471597	chr20:14782734-14782735	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1028542	chr20:14782742-14782743	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184701379	chr20:14782759-14782760	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539985902	chr20:14782760-14782761	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561799931	chr20:14782769-14782770	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116227009	chr20:14782771-14782772	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147833513	chr20:14782872-14782873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565850000	chr20:14782874-14782875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554002051	chr20:14782974-14782975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533162540	chr20:14782977-14782978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs80227301	chr20:14783001-14783002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113041123	chr20:14783006-14783007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs79025740	chr20:14783040-14783041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555506912	chr20:14783098-14783099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532054275	chr20:14783129-14783130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141313418	chr20:14783130-14783131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139158213	chr20:14783136-14783137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs13043371	chr20:14783143-14783144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577774281	chr20:14783166-14783167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150388854	chr20:14783187-14783188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145083631	chr20:14783193-14783194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575875605	chr20:14783203-14783204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369722597	chr20:14783238-14783239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199965208	chr20:14783251-14783252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543388082	chr20:14783256-14783257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561489190	chr20:14783257-14783258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375532564	chr20:14783293-14783294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573600756	chr20:14783329-14783330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs60079618	chr20:14783334-14783335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541078110	chr20:14783379-14783380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200767507	chr20:14783418-14783419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs74326784	chr20:14783423-14783424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139541677	chr20:14783424-14783425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200866209	chr20:14783427-14783428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559501697	chr20:14783436-14783437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs71190147	chr20:14783449-14783450	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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:1227 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14782200-14782400	Enhancers	Liver	Liver
2	chr20:14782200-14783800	Enhancers	Fetal Brain Female	brain
3	chr20:14782400-14782800	Flanking Active TSS	Liver	Liver
4	chr20:14782600-14783400	Enhancers	GM12878-XiMat	blood
5	chr20:14782800-14783000	Enhancers	Liver	Liver
6	chr20:14787600-14788000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr20:14798200-14798400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr20:14798200-14798600	Enhancers	Fetal Kidney	kidney
9	chr20:14798400-14800400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr20:14800400-14800800	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr20:14800800-14801400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr20:14801200-14801800	Enhancers	Fetal Brain Male	brain
13	chr20:14801200-14801800	Enhancers	Fetal Brain Female	brain
14	chr20:14801400-14801800	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr20:14801800-14806000	Weak transcription	Fetal Brain Female	brain
16	chr20:14801800-14807400	Weak transcription	Fetal Brain Male	brain
17	chr20:14805000-14805800	Enhancers	Colon Smooth Muscle	Colon
18	chr20:14805000-14808200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr20:14805200-14805400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr20:14805200-14806400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr20:14805400-14808200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr20:14805600-14806000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr20:14805600-14807600	Enhancers	Brain Germinal Matrix	brain
24	chr20:14805600-14807800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr20:14805800-14806200	Enhancers	Fetal Kidney	kidney
26	chr20:14805800-14808200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr20:14806000-14806200	Enhancers	Fetal Brain Female	brain
28	chr20:14806000-14806800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr20:14806000-14807200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr20:14806200-14806600	Weak transcription	Fetal Brain Female	brain
31	chr20:14806600-14808200	Enhancers	Fetal Brain Female	brain
32	chr20:14807200-14808000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr20:14807200-14808200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr20:14807400-14808200	Enhancers	Fetal Brain Male	brain
35	chr20:14807600-14808000	Flanking Active TSS	Brain Germinal Matrix	brain
36	chr20:14807800-14810600	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr20:14808000-14808800	Enhancers	Brain Germinal Matrix	brain
38	chr20:14810000-14810800	Enhancers	GM12878-XiMat	blood
39	chr20:14810400-14811800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr20:14810600-14811000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr20:14810600-14812000	Enhancers	NHEK	skin
42	chr20:14810800-14811000	Enhancers	Brain Germinal Matrix	brain
43	chr20:14810800-14811800	Enhancers	Primary B cells from peripheral blood	blood
44	chr20:14810800-14812000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr20:14810800-14812000	Flanking Active TSS	GM12878-XiMat	blood
46	chr20:14811400-14811800	Enhancers	HMEC	breast
47	chr20:14811600-14812000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr20:14811800-14813200	Weak transcription	Primary B cells from peripheral blood	blood
49	chr20:14812000-14813000	Enhancers	GM12878-XiMat	blood
50	chr20:14813000-14814200	Flanking Active TSS	GM12878-XiMat	blood

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