Variant report

Variant	nsv1056310
Chromosome Location	chr20:14808051-15101602
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2623)
CpG islands
(count:61)
Chromatin interactive
region (count:45)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2623 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
9	ATF2	chr20:14813148-14813759	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	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
15	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
16	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
19	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
20	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
21	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
22	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
23	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
24	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
25	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
26	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
29	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
30	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
31	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
32	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
33	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
34	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
35	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
36	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
37	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
38	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
39	BATF	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
40	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
41	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
42	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
43	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
44	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
45	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
46	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
47	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
48	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
49	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
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	IMR90	lung:	fetal
2	chr20:14904432-14904482	SK-N-SH	brain:	n/a
3	chr20:14904432-14904482	BE2_C	brain:	n/a
4	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
5	chr20:14904432-14904482	AG10803	skin:	n/a
6	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
7	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
8	chr20:14904432-14904482	PANC-1	pancreas:	n/a
9	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
10	chr20:14904432-14904482	T-47D	breast:	n/a
11	chr20:14904432-14904482	Caco-2	colon:	n/a
12	chr20:14904432-14904482	GM19239	blood:	n/a
13	chr20:14904432-14904482	HCT-116	colon:	n/a
14	chr20:14904432-14904482	GM06990	blood:	n/a
15	chr20:14904432-14904482	SAEC	small airway:	n/a
16	chr20:14904432-14904482	LNCaP	prostate:	n/a
17	chr20:14904432-14904482	HepG2	liver:	n/a
18	chr20:14904432-14904482	NT2-D1	testis:	n/a
19	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
20	chr20:14904432-14904482	NHBE	bronchial:	n/a
21	chr20:14904432-14904482	NB4	blood:	n/a
22	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
23	chr20:14904432-14904482	SKMC	muscle:	n/a
24	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
25	chr20:14904432-14904482	ProgFib	skin:	n/a
26	chr20:14904432-14904482	BJ	skin:	n/a
27	chr20:14904432-14904482	AG04450	lung:	fetal
28	chr20:14904432-14904482	Jurkat	blood:	n/a
29	chr20:14904432-14904482	HRPEpiC	eye:	n/a
30	chr20:14904432-14904482	Hela-S3	cervix:	n/a
31	chr20:14904432-14904482	Hepatocyte	liver:	n/a
32	chr20:14904432-14904482	SK-N-MC	brain:	n/a
33	chr20:14904432-14904482	AG09319	gingival:	n/a
34	chr20:14904432-14904482	AG04449	skin:	fetal
35	chr20:14904432-14904482	HIPEpiC	eye:	n/a
36	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
37	chr20:14904432-14904482	PFSK-1	brain:	n/a
38	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
39	chr20:14904432-14904482	GM12891	blood:	n/a
40	chr20:14904432-14904482	CMK	blood:	n/a
41	chr20:14904432-14904482	NH-A	brain:	n/a
42	chr20:14904432-14904482	HEK293	kidney:	embryo
43	chr20:14904432-14904482	HMEC	breast:	n/a
44	chr20:14904432-14904482	HRE	kidney:	n/a
45	chr20:14904432-14904482	GM12878	blood:	n/a
46	chr20:14904432-14904482	RPTEC	kidney:	n/a
47	chr20:14904432-14904482	HCM	heart:	n/a
48	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
49	chr20:14904432-14904482	MCF-7	breast:	n/a
50	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
2	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
3	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
4	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
5	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
6	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
7	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
8	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
9	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
10	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
11	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
12	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
13	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
14	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
15	chr20:14983136..14983867-chr7:139874694..139875444,2	MCF-7	breast:
16	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
17	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
18	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
19	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
20	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
21	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
22	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
23	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
24	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
25	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
26	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
27	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
28	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
29	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
30	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
31	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
32	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
33	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
34	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
35	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
36	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
37	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
38	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
39	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
40	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
41	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
42	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
43	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
44	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
45	chr20:14837652..14840600-chr20:14844675..14847639,2	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_110318
2	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
3	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
4	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
5	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
6	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
7	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
8	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
9	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
10	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
11	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
12	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
13	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
14	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
15	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
16	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
17	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
18	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
19	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
20	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
21	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
22	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
23	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
24	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
25	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
26	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722

No data

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

Extended variants
information (count: 9609 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:9609 , 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	rs565659176	chr20:14808075-14808076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533006894	chr20:14808079-14808080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188632218	chr20:14808080-14808081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181081445	chr20:14808095-14808096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185119117	chr20:14808102-14808103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150326533	chr20:14808118-14808119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189696737	chr20:14808144-14808145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534587847	chr20:14808156-14808157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562738130	chr20:14808164-14808165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6135272	chr20:14808253-14808254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552876074	chr20:14808267-14808268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577611713	chr20:14808278-14808279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs137960267	chr20:14808316-14808317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375827490	chr20:14808320-14808321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575600519	chr20:14808321-14808322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78586818	chr20:14808339-14808340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76057994	chr20:14808419-14808420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543126764	chr20:14808475-14808476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184204805	chr20:14808525-14808526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561289781	chr20:14808543-14808544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573507074	chr20:14808576-14808577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567592390	chr20:14808609-14808610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540926837	chr20:14808629-14808630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187130608	chr20:14808662-14808663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191989202	chr20:14808687-14808688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368960703	chr20:14808711-14808712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6110441	chr20:14808718-14808719	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs560180742	chr20:14808762-14808763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563318572	chr20:14808806-14808807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530488718	chr20:14808824-14808825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376439328	chr20:14808825-14808826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549096785	chr20:14808894-14808895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570602051	chr20:14808915-14808916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117517864	chr20:14808943-14808944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534552855	chr20:14808990-14808991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142171006	chr20:14809021-14809022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146352461	chr20:14809028-14809029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6105330	chr20:14809033-14809034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527805532	chr20:14809055-14809056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557041791	chr20:14809106-14809107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575607889	chr20:14809114-14809115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139677060	chr20:14809138-14809139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183519824	chr20:14809144-14809145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368884343	chr20:14809173-14809174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143092703	chr20:14809174-14809175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6110442	chr20:14809194-14809195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540791763	chr20:14809299-14809300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73266723	chr20:14809311-14809312	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs188511867	chr20:14809344-14809345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544905933	chr20:14809346-14809347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Williams Syndrome	20824207	CNVD
Melanoma	17363583	CNVD
Schizophrenia	20967226	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:1382 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14805000-14808200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr20:14805400-14808200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr20:14805800-14808200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr20:14806600-14808200	Enhancers	Fetal Brain Female	brain
5	chr20:14807200-14808200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr20:14807400-14808200	Enhancers	Fetal Brain Male	brain
7	chr20:14807800-14810600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr20:14808000-14808800	Enhancers	Brain Germinal Matrix	brain
9	chr20:14810000-14810800	Enhancers	GM12878-XiMat	blood
10	chr20:14810400-14811800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr20:14810600-14811000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr20:14810600-14812000	Enhancers	NHEK	skin
13	chr20:14810800-14811000	Enhancers	Brain Germinal Matrix	brain
14	chr20:14810800-14811800	Enhancers	Primary B cells from peripheral blood	blood
15	chr20:14810800-14812000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr20:14810800-14812000	Flanking Active TSS	GM12878-XiMat	blood
17	chr20:14811400-14811800	Enhancers	HMEC	breast
18	chr20:14811600-14812000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr20:14811800-14813200	Weak transcription	Primary B cells from peripheral blood	blood
20	chr20:14812000-14813000	Enhancers	GM12878-XiMat	blood
21	chr20:14813000-14814200	Flanking Active TSS	GM12878-XiMat	blood
22	chr20:14813200-14813800	Enhancers	Primary B cells from peripheral blood	blood
23	chr20:14814200-14815000	Enhancers	GM12878-XiMat	blood
24	chr20:14818000-14819400	Enhancers	GM12878-XiMat	blood
25	chr20:14818400-14820200	Enhancers	Hela-S3	cervix
26	chr20:14819200-14819600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr20:14819200-14820400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr20:14819400-14819800	Enhancers	NHDF-Ad	bronchial
29	chr20:14819400-14820000	Flanking Active TSS	GM12878-XiMat	blood
30	chr20:14819400-14820200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr20:14819400-14820200	Enhancers	Fetal Kidney	kidney
32	chr20:14819400-14820200	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr20:14819400-14820400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr20:14819600-14820000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr20:14819600-14820000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr20:14819600-14820200	Enhancers	Psoas Muscle	Psoas
37	chr20:14819600-14820200	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr20:14820000-14820200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr20:14820000-14820400	Enhancers	Muscle Satellite Cultured Cells	--
40	chr20:14820000-14820400	Enhancers	GM12878-XiMat	blood
41	chr20:14820200-14825600	Weak transcription	Fetal Kidney	kidney
42	chr20:14820200-14825600	Weak transcription	Hela-S3	cervix
43	chr20:14820800-14825400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr20:14821800-14822800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr20:14824400-14824800	Enhancers	Esophagus	oesophagus
46	chr20:14824600-14827000	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr20:14825400-14825800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr20:14825400-14826200	Enhancers	A549	lung
49	chr20:14825400-14826400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr20:14825400-14827000	Enhancers	HMEC	breast

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