Variant report

Variant	nsv1067404
Chromosome Location	chr20:14699839-14964658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2112)
CpG islands
(count:61)
Chromatin interactive
region (count:63)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2112 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
4	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
5	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
16	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
17	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
18	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
19	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
20	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
21	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
24	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
25	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
26	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
27	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
28	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
29	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
30	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
31	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
32	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
33	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
34	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
35	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
36	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
37	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
38	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
39	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
40	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
41	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
42	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
43	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
44	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
46	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
47	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
48	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
49	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
50	BCL11A	chr20:14813340-14813684	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	A549	lung:	n/a
2	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
3	chr20:14904432-14904482	Hela-S3	cervix:	n/a
4	chr20:14904432-14904482	SK-N-MC	brain:	n/a
5	chr20:14904432-14904482	HRE	kidney:	n/a
6	chr20:14904432-14904482	PrEC	prostate:	n/a
7	chr20:14904432-14904482	NB4	blood:	n/a
8	chr20:14904432-14904482	CMK	blood:	n/a
9	chr20:14904432-14904482	NHBE	bronchial:	n/a
10	chr20:14904432-14904482	HRPEpiC	eye:	n/a
11	chr20:14904432-14904482	BJ	skin:	n/a
12	chr20:14904432-14904482	NT2-D1	testis:	n/a
13	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
14	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
15	chr20:14904432-14904482	Hepatocyte	liver:	n/a
16	chr20:14904432-14904482	GM12878	blood:	n/a
17	chr20:14904432-14904482	RPTEC	kidney:	n/a
18	chr20:14904432-14904482	HCM	heart:	n/a
19	chr20:14904432-14904482	SAEC	small airway:	n/a
20	chr20:14904432-14904482	U87	brain:	n/a
21	chr20:14904432-14904482	IMR90	lung:	fetal
22	chr20:14904432-14904482	GM19239	blood:	n/a
23	chr20:14904432-14904482	ProgFib	skin:	n/a
24	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
25	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
26	chr20:14904432-14904482	HEK293	kidney:	embryo
27	chr20:14904432-14904482	NH-A	brain:	n/a
28	chr20:14904432-14904482	PANC-1	pancreas:	n/a
29	chr20:14904432-14904482	BE2_C	brain:	n/a
30	chr20:14904432-14904482	K562	blood:	n/a
31	chr20:14904432-14904482	HIPEpiC	eye:	n/a
32	chr20:14904432-14904482	HCT-116	colon:	n/a
33	chr20:14904432-14904482	Jurkat	blood:	n/a
34	chr20:14904432-14904482	GM06990	blood:	n/a
35	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
36	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
37	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
38	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
39	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
40	chr20:14904432-14904482	HepG2	liver:	n/a
41	chr20:14904432-14904482	PFSK-1	brain:	n/a
42	chr20:14904432-14904482	AG09309	skin:	n/a
43	chr20:14904432-14904482	HMEC	breast:	n/a
44	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
45	chr20:14904432-14904482	T-47D	breast:	n/a
46	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
47	chr20:14904432-14904482	LNCaP	prostate:	n/a
48	chr20:14904432-14904482	SK-N-SH	brain:	n/a
49	chr20:14904432-14904482	MCF-7	breast:	n/a
50	chr20:14904432-14904482	HUVEC	blood vessel:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
2	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
3	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
4	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
5	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
6	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
7	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
8	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
9	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
10	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
11	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
12	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
13	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
14	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
15	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
16	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
17	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
18	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
19	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
20	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
21	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
22	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
23	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
24	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
25	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
26	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
27	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
28	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
29	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
30	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
31	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
32	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
33	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
34	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
35	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
36	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
37	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
38	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
39	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
40	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
41	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
42	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
43	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
44	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
45	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
46	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
47	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
48	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
49	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
50	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 7867 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7867 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536713797	chr20:14699876-14699877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78431914	chr20:14699886-14699887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114757865	chr20:14699923-14699924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532178140	chr20:14699947-14699948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368173172	chr20:14700020-14700021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545765563	chr20:14700084-14700085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201995395	chr20:14700117-14700118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11087105	chr20:14700120-14700121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200470794	chr20:14700121-14700122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557760946	chr20:14700130-14700131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78153673	chr20:14700131-14700132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397789761	chr20:14700133-14700134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572131892	chr20:14700161-14700162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184573825	chr20:14700194-14700195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs118113489	chr20:14700216-14700217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11906272	chr20:14700285-14700286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs188969057	chr20:14700340-14700341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540909261	chr20:14700363-14700364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192898815	chr20:14700425-14700426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11906293	chr20:14700445-14700446	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs565361136	chr20:14700480-14700481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368421688	chr20:14700484-14700485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374375677	chr20:14700488-14700489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551283128	chr20:14700507-14700508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372363268	chr20:14700513-14700514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530823107	chr20:14700542-14700543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549018068	chr20:14700570-14700571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567699272	chr20:14700576-14700577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145977140	chr20:14700610-14700611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553323919	chr20:14700612-14700613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571886396	chr20:14700636-14700637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530954494	chr20:14700638-14700639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138575709	chr20:14700673-14700674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539306809	chr20:14700683-14700684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4814320	chr20:14700718-14700719	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs576064327	chr20:14700758-14700759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142970279	chr20:14700778-14700779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555432254	chr20:14700849-14700850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573689682	chr20:14700887-14700888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75727176	chr20:14700951-14700952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567510453	chr20:14701008-14701009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78938122	chr20:14701013-14701014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs371316247	chr20:14701019-14701020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185052146	chr20:14701047-14701048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544863697	chr20:14701093-14701094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561464390	chr20:14701105-14701106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368291165	chr20:14701126-14701127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530432205	chr20:14701132-14701133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200760124	chr20:14701181-14701182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377294992	chr20:14701182-14701183	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:1127 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14694400-14700400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr20:14697600-14702200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr20:14697600-14703200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr20:14697600-14706200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:14698600-14707000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr20:14700400-14700600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr20:14700400-14701000	Enhancers	Primary hematopoietic stem cells	blood
8	chr20:14700400-14701600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr20:14700800-14701200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr20:14702200-14702800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr20:14702200-14703200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr20:14702200-14703200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr20:14702400-14702800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr20:14702400-14702800	Enhancers	Psoas Muscle	Psoas
15	chr20:14702600-14702800	Enhancers	GM12878-XiMat	blood
16	chr20:14702600-14703000	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr20:14702800-14703800	Weak transcription	GM12878-XiMat	blood
18	chr20:14703800-14705000	Enhancers	GM12878-XiMat	blood
19	chr20:14705000-14705200	Flanking Active TSS	GM12878-XiMat	blood
20	chr20:14705200-14705400	Enhancers	GM12878-XiMat	blood
21	chr20:14705400-14705600	Flanking Active TSS	GM12878-XiMat	blood
22	chr20:14705600-14705800	Enhancers	GM12878-XiMat	blood
23	chr20:14706200-14706400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr20:14706400-14707000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr20:14707000-14707200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr20:14707200-14709600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr20:14709400-14710200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr20:14710000-14710200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr20:14710000-14710400	Enhancers	Liver	Liver
30	chr20:14710000-14710400	Enhancers	HepG2	liver
31	chr20:14710000-14710600	Enhancers	Stomach Mucosa	stomach
32	chr20:14710200-14710400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr20:14710400-14713000	Weak transcription	Liver	Liver
34	chr20:14710600-14712000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr20:14710600-14713000	Weak transcription	Stomach Mucosa	stomach
36	chr20:14711600-14714600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr20:14712000-14713400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr20:14712800-14713600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr20:14713000-14713400	Enhancers	Fetal Kidney	kidney
40	chr20:14713000-14713600	Enhancers	Stomach Mucosa	stomach
41	chr20:14713000-14713800	Enhancers	Liver	Liver
42	chr20:14713200-14713600	Enhancers	Hela-S3	cervix
43	chr20:14713200-14713800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr20:14719000-14719200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr20:14719200-14721000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr20:14720600-14721800	Enhancers	Fetal Brain Male	brain
47	chr20:14721000-14721400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr20:14721000-14721400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr20:14721000-14721800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr20:14721200-14721600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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