Variant report

Variant	nsv585453
Chromosome Location	chr20:14609957-14936935
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2264)
CpG islands
(count:61)
Chromatin interactive
region (count:67)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2264 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

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	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
4	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
5	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
15	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
17	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
18	ATF3	chr20:14613673-14613899	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
20	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
21	ATF3	chr20:14613539-14613866	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
23	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
25	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
26	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
27	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
28	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
29	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
30	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
31	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
32	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
33	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
34	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
35	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
36	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
37	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
38	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
39	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
40	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
41	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
42	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
43	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
44	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
45	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
46	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
47	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
48	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
49	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
50	BCL11A	chr20:14813268-14813779	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	BJ	skin:	n/a
2	chr20:14904432-14904482	BE2_C	brain:	n/a
3	chr20:14904432-14904482	T-47D	breast:	n/a
4	chr20:14904432-14904482	SK-N-SH	brain:	n/a
5	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
6	chr20:14904432-14904482	AG04449	skin:	fetal
7	chr20:14904432-14904482	Hepatocyte	liver:	n/a
8	chr20:14904432-14904482	GM06990	blood:	n/a
9	chr20:14904432-14904482	AG10803	skin:	n/a
10	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
11	chr20:14904432-14904482	GM12892	blood:	n/a
12	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
13	chr20:14904432-14904482	AG09309	skin:	n/a
14	chr20:14904432-14904482	A549	lung:	n/a
15	chr20:14904432-14904482	Hela-S3	cervix:	n/a
16	chr20:14904432-14904482	LNCaP	prostate:	n/a
17	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
18	chr20:14904432-14904482	PrEC	prostate:	n/a
19	chr20:14904432-14904482	K562	blood:	n/a
20	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
21	chr20:14904432-14904482	ProgFib	skin:	n/a
22	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
23	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
24	chr20:14904432-14904482	HCF	heart:	n/a
25	chr20:14904432-14904482	CMK	blood:	n/a
26	chr20:14904432-14904482	HCT-116	colon:	n/a
27	chr20:14904432-14904482	HCM	heart:	n/a
28	chr20:14904432-14904482	Jurkat	blood:	n/a
29	chr20:14904432-14904482	HepG2	liver:	n/a
30	chr20:14904432-14904482	HIPEpiC	eye:	n/a
31	chr20:14904432-14904482	SAEC	small airway:	n/a
32	chr20:14904432-14904482	PFSK-1	brain:	n/a
33	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
34	chr20:14904432-14904482	HMEC	breast:	n/a
35	chr20:14904432-14904482	SKMC	muscle:	n/a
36	chr20:14904432-14904482	AG09319	gingival:	n/a
37	chr20:14904432-14904482	PANC-1	pancreas:	n/a
38	chr20:14904432-14904482	NH-A	brain:	n/a
39	chr20:14904432-14904482	Caco-2	colon:	n/a
40	chr20:14904432-14904482	GM19239	blood:	n/a
41	chr20:14904432-14904482	GM12878	blood:	n/a
42	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
43	chr20:14904432-14904482	NHBE	bronchial:	n/a
44	chr20:14904432-14904482	HEK293	kidney:	embryo
45	chr20:14904432-14904482	NT2-D1	testis:	n/a
46	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
47	chr20:14904432-14904482	RPTEC	kidney:	n/a
48	chr20:14904432-14904482	GM12891	blood:	n/a
49	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
50	chr20:14904432-14904482	SK-N-MC	brain:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
2	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
3	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
4	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
5	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
6	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
7	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
8	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
9	chr20:14601339..14605162-chr20:14611440..14614800,3	MCF-7	breast:
10	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
11	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
12	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
13	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
14	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
15	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
16	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
17	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
18	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
19	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
20	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
21	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
22	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
23	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
24	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
25	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
26	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
27	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
28	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
29	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
30	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
31	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
32	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
33	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
34	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
35	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
36	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
37	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
38	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
39	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
40	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
41	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
42	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
43	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
44	chr20:14657146..14658733-chr20:17661268..17663723,2	MCF-7	breast:
45	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
46	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
47	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
48	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
49	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
50	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
2	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
3	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
4	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
5	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
6	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
7	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
8	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
9	lnc-C20orf7-1	chr20:14612487-14612595	ENSG00000227927.2
10	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
11	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
12	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
13	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078714
14	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
15	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
16	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
17	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
18	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
19	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
20	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078716
21	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
22	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
23	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
24	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
25	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
26	lnc-C20orf7-1	chr20:14617092-14617170	ENSG00000227927.2
27	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
28	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
29	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
30	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988

No data

Variant related genes	Relation type
MACROD2-AS1	TF binding region
ENSG00000237832	TF binding region
RPS10P2	TF binding region
MACROD2-AS1	CpG island
ENSG00000237832	CpG island
RPS10P2	CpG island
ENSG00000125844	chromatin interactions
ENSG00000237832	chromatin interactions
ENSG00000227927	chromatin interactions

Extended variants
information (count: 9625 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:9625 , 50 per page) page: 1 2 3 4 5 6 7 ... 193

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2038909	chr20:14609957-14609958	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372470081	chr20:14609983-14609984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577763501	chr20:14610083-14610084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544917543	chr20:14610169-14610170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549154317	chr20:14610184-14610185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370100573	chr20:14610185-14610186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184190273	chr20:14610259-14610260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112237947	chr20:14610268-14610269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372621254	chr20:14610286-14610287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6110364	chr20:14610289-14610290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs561283250	chr20:14610365-14610366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528523244	chr20:14610370-14610371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532232808	chr20:14610386-14610387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565418315	chr20:14610398-14610399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532696709	chr20:14610424-14610425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200023701	chr20:14610471-14610472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150192917	chr20:14610564-14610565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201078091	chr20:14610598-14610599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs72250866	chr20:14610599-14610600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374482825	chr20:14610609-14610610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141635400	chr20:14610613-14610614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72030809	chr20:14610614-14610615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76468337	chr20:14610616-14610617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11696614	chr20:14610617-14610618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138086683	chr20:14610619-14610620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548501930	chr20:14610645-14610646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374335035	chr20:14610646-14610647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566904661	chr20:14610665-14610666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534365065	chr20:14610723-14610724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181030742	chr20:14610770-14610771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370198691	chr20:14610814-14610815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185251383	chr20:14610843-14610844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538781289	chr20:14610866-14610867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556900352	chr20:14610873-14610874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1932937	chr20:14610967-14610968	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs6079508	chr20:14610984-14610985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568484456	chr20:14611004-14611005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554949149	chr20:14611068-14611069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs6079509	chr20:14611073-14611074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6079510	chr20:14611087-14611088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192412949	chr20:14611095-14611096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375974938	chr20:14611169-14611170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs6079511	chr20:14611174-14611175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79707382	chr20:14611188-14611189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540639527	chr20:14611240-14611241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565330433	chr20:14611272-14611273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547292785	chr20:14611293-14611294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532518642	chr20:14611301-14611302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77974283	chr20:14611320-14611321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369330423	chr20:14611338-14611339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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

Chromatin state (count:1450 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14604000-14614600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:14610600-14611000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr20:14610800-14611400	Enhancers	Brain Germinal Matrix	brain
4	chr20:14611800-14612400	Enhancers	Fetal Intestine Large	intestine
5	chr20:14611800-14612600	Enhancers	Fetal Intestine Small	intestine
6	chr20:14612600-14615400	Weak transcription	Fetal Intestine Small	intestine
7	chr20:14613600-14615800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr20:14614200-14616200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr20:14614200-14616200	Enhancers	HMEC	breast
10	chr20:14614400-14615800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr20:14614400-14616200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr20:14614400-14616200	Enhancers	NHEK	skin
13	chr20:14614600-14615800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr20:14614600-14616000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr20:14614600-14616000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr20:14615000-14616200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr20:14615400-14616000	Enhancers	Fetal Intestine Small	intestine
18	chr20:14616000-14621800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr20:14621800-14623400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr20:14623400-14625000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr20:14625200-14625600	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr20:14625200-14625600	Enhancers	Fetal Lung	lung
23	chr20:14629800-14632200	Enhancers	Stomach Mucosa	stomach
24	chr20:14630000-14631000	Enhancers	Gastric	stomach
25	chr20:14631200-14631800	Enhancers	Fetal Lung	lung
26	chr20:14631800-14632200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr20:14632200-14635400	Weak transcription	Stomach Mucosa	stomach
28	chr20:14633600-14636000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr20:14635400-14636000	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr20:14635400-14636000	Enhancers	Stomach Mucosa	stomach
31	chr20:14635600-14636800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr20:14636000-14636600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr20:14636000-14636800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr20:14636000-14636800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr20:14636200-14636800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr20:14636400-14637000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr20:14636600-14636800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr20:14636800-14637600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr20:14636800-14638200	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr20:14637200-14639000	Enhancers	Fetal Lung	lung
41	chr20:14637600-14638200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr20:14637600-14638600	Enhancers	Fetal Stomach	stomach
43	chr20:14637600-14638800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr20:14637800-14638200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr20:14638000-14638200	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr20:14638000-14638600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr20:14638200-14638400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr20:14638400-14638800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr20:14638600-14640000	Weak transcription	Fetal Stomach	stomach
50	chr20:14639000-14640600	Weak transcription	Fetal Lung	lung

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