Variant report

Variant	nsv912723
Chromosome Location	chr20:14743905-14992542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2432)
CpG islands
(count:61)
Chromatin interactive
region (count:58)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2432 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
7	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
15	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
16	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
18	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
19	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
20	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
21	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
22	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
23	ATF3	chr20:14859536-14860398	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	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
27	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
28	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
29	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
30	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
31	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
32	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
33	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
34	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
35	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
36	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
37	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
38	BATF	chr20:14810566-14810958	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	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
41	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
42	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
43	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
44	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
46	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
47	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
48	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
49	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
50	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	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	NHDF-neo	bronchial:	n/a
2	chr20:14904432-14904482	LNCaP	prostate:	n/a
3	chr20:14904432-14904482	MCF-7	breast:	n/a
4	chr20:14904432-14904482	HCM	heart:	n/a
5	chr20:14904432-14904482	SK-N-SH	brain:	n/a
6	chr20:14904432-14904482	BE2_C	brain:	n/a
7	chr20:14904432-14904482	NB4	blood:	n/a
8	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
9	chr20:14904432-14904482	AG04450	lung:	fetal
10	chr20:14904432-14904482	HRPEpiC	eye:	n/a
11	chr20:14904432-14904482	PFSK-1	brain:	n/a
12	chr20:14904432-14904482	SAEC	small airway:	n/a
13	chr20:14904432-14904482	AG09309	skin:	n/a
14	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
15	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
16	chr20:14904432-14904482	Caco-2	colon:	n/a
17	chr20:14904432-14904482	K562	blood:	n/a
18	chr20:14904432-14904482	GM06990	blood:	n/a
19	chr20:14904432-14904482	SKMC	muscle:	n/a
20	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
21	chr20:14904432-14904482	T-47D	breast:	n/a
22	chr20:14904432-14904482	HRE	kidney:	n/a
23	chr20:14904432-14904482	HMEC	breast:	n/a
24	chr20:14904432-14904482	Hepatocyte	liver:	n/a
25	chr20:14904432-14904482	SK-N-MC	brain:	n/a
26	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
27	chr20:14904432-14904482	HCF	heart:	n/a
28	chr20:14904432-14904482	A549	lung:	n/a
29	chr20:14904432-14904482	IMR90	lung:	fetal
30	chr20:14904432-14904482	NT2-D1	testis:	n/a
31	chr20:14904432-14904482	AG09319	gingival:	n/a
32	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
33	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
34	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
35	chr20:14904432-14904482	AG04449	skin:	fetal
36	chr20:14904432-14904482	HEK293	kidney:	embryo
37	chr20:14904432-14904482	PANC-1	pancreas:	n/a
38	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
39	chr20:14904432-14904482	GM12891	blood:	n/a
40	chr20:14904432-14904482	GM12892	blood:	n/a
41	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
42	chr20:14904432-14904482	NHBE	bronchial:	n/a
43	chr20:14904432-14904482	HL-60	blood:	n/a
44	chr20:14904432-14904482	CMK	blood:	n/a
45	chr20:14904432-14904482	BJ	skin:	n/a
46	chr20:14904432-14904482	HepG2	liver:	n/a
47	chr20:14904432-14904482	Hela-S3	cervix:	n/a
48	chr20:14904432-14904482	RPTEC	kidney:	n/a
49	chr20:14904432-14904482	GM12878	blood:	n/a
50	chr20:14904432-14904482	HCT-116	colon:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14983136..14983867-chr7:139874694..139875444,2	MCF-7	breast:
2	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
3	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
4	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
5	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
6	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
7	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
8	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
9	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
10	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
11	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
12	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
13	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
14	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
15	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
16	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
17	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
18	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
19	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
20	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
21	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
22	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
23	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
24	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
25	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
26	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
27	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
28	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
29	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
30	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
31	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
32	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
33	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
34	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
35	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
36	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
37	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
38	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
39	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
40	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
41	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
42	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
43	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
44	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
45	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
46	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
47	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
48	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
49	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
50	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 7943 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7943 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs204104	chr20:14743905-14743906	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540700834	chr20:14743924-14743925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553002059	chr20:14743942-14743943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201545590	chr20:14743963-14743964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147614313	chr20:14743964-14743965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369430286	chr20:14743999-14744000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150179450	chr20:14744038-14744039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564884092	chr20:14744055-14744056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541256161	chr20:14744104-14744105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563340631	chr20:14744144-14744145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189389223	chr20:14744150-14744151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs80058350	chr20:14744154-14744155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35394480	chr20:14744165-14744166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6079556	chr20:14745223-14745224	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187863620	chr20:14745232-14745233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548327271	chr20:14745237-14745238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370338986	chr20:14745271-14745272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527976394	chr20:14745328-14745329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552628948	chr20:14745330-14745331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571201241	chr20:14745340-14745341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538229390	chr20:14745343-14745344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550566782	chr20:14745368-14745369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374202896	chr20:14745397-14745398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568932273	chr20:14745419-14745420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79282690	chr20:14745487-14745488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6079557	chr20:14745525-14745526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs80016821	chr20:14745526-14745527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550189843	chr20:14745531-14745532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534081306	chr20:14745537-14745538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558609482	chr20:14745543-14745544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs367686211	chr20:14745551-14745552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556751249	chr20:14745560-14745561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73897208	chr20:14745572-14745573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570293167	chr20:14745614-14745615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78019035	chr20:14745615-14745616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6034033	chr20:14745660-14745661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574586985	chr20:14745675-14745676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6034034	chr20:14745680-14745681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541959323	chr20:14745799-14745800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560297532	chr20:14745800-14745801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548635277	chr20:14745807-14745808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192032916	chr20:14745901-14745902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75973	chr20:14745902-14745903	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs527732257	chr20:14745904-14745905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535837137	chr20:14745925-14745926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532041507	chr20:14745988-14745989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550549738	chr20:14745992-14745993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs735796	chr20:14745993-14745994	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs6110424	chr20:14746004-14746005	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs5840632	chr20:14746025-14746026	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:1237 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14743000-14744000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr20:14743400-14744200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr20:14745200-14746200	Enhancers	Stomach Mucosa	stomach
4	chr20:14746000-14746200	Enhancers	Sigmoid Colon	Sigmoid Colon
5	chr20:14750600-14756200	Weak transcription	Psoas Muscle	Psoas
6	chr20:14755800-14757200	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr20:14756000-14756400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr20:14756000-14756400	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr20:14756000-14756800	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr20:14756000-14756800	Enhancers	Hela-S3	cervix
11	chr20:14756000-14757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr20:14756000-14757200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr20:14756000-14757200	Enhancers	A549	lung
14	chr20:14756000-14759200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr20:14756200-14756800	Enhancers	Psoas Muscle	Psoas
16	chr20:14756200-14757000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr20:14756200-14757000	Enhancers	HepG2	liver
18	chr20:14756200-14757000	Enhancers	HMEC	breast
19	chr20:14756200-14757200	Enhancers	NHEK	skin
20	chr20:14756600-14757000	Enhancers	Fetal Intestine Small	intestine
21	chr20:14756600-14757200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr20:14756800-14757000	Enhancers	NHDF-Ad	bronchial
23	chr20:14757000-14758000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr20:14757000-14758000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr20:14757000-14758200	Weak transcription	HMEC	breast
26	chr20:14757200-14757600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr20:14757200-14757600	Weak transcription	NHEK	skin
28	chr20:14757200-14758000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr20:14757600-14759000	Enhancers	NHEK	skin
30	chr20:14757600-14759600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr20:14758000-14758600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr20:14758000-14758800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr20:14758000-14759200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr20:14758200-14758800	Enhancers	HMEC	breast
35	chr20:14758600-14758800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr20:14758600-14759400	Enhancers	NHDF-Ad	bronchial
37	chr20:14758600-14761200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr20:14759200-14760800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr20:14759200-14760800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr20:14760600-14761600	Enhancers	HUVEC	blood vessel
41	chr20:14760800-14761800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr20:14760800-14762200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr20:14761200-14761800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr20:14763200-14763800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr20:14763200-14764000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr20:14763400-14763800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr20:14763400-14764200	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr20:14764200-14764800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr20:14764800-14765000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr20:14764800-14765200	Enhancers	Fetal Lung	lung

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