Variant report

Variant	nsv1064871
Chromosome Location	chr20:14756392-15134217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2921)
CpG islands
(count:61)
Chromatin interactive
region (count:54)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2921 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

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	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
9	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
15	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
18	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
19	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
21	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
22	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
23	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
24	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
25	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
26	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
29	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
30	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
31	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
32	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
33	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
34	BATF	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
35	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
36	BATF	chr20:14813339-14813704	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	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
39	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
40	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
41	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
42	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
43	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
44	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
45	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
46	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
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	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	HL-60	blood:	n/a
2	chr20:14904432-14904482	SK-N-MC	brain:	n/a
3	chr20:14904432-14904482	AG09319	gingival:	n/a
4	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
5	chr20:14904432-14904482	BE2_C	brain:	n/a
6	chr20:14904432-14904482	Jurkat	blood:	n/a
7	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
8	chr20:14904432-14904482	HMEC	breast:	n/a
9	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
10	chr20:14904432-14904482	T-47D	breast:	n/a
11	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
12	chr20:14904432-14904482	HCM	heart:	n/a
13	chr20:14904432-14904482	HEK293	kidney:	embryo
14	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
15	chr20:14904432-14904482	IMR90	lung:	fetal
16	chr20:14904432-14904482	Caco-2	colon:	n/a
17	chr20:14904432-14904482	SKMC	muscle:	n/a
18	chr20:14904432-14904482	AG04450	lung:	fetal
19	chr20:14904432-14904482	PFSK-1	brain:	n/a
20	chr20:14904432-14904482	HCF	heart:	n/a
21	chr20:14904432-14904482	GM06990	blood:	n/a
22	chr20:14904432-14904482	SAEC	small airway:	n/a
23	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
24	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
25	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
26	chr20:14904432-14904482	NT2-D1	testis:	n/a
27	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
28	chr20:14904432-14904482	AG09309	skin:	n/a
29	chr20:14904432-14904482	HIPEpiC	eye:	n/a
30	chr20:14904432-14904482	PANC-1	pancreas:	n/a
31	chr20:14904432-14904482	PrEC	prostate:	n/a
32	chr20:14904432-14904482	HRE	kidney:	n/a
33	chr20:14904432-14904482	SK-N-SH	brain:	n/a
34	chr20:14904432-14904482	AG10803	skin:	n/a
35	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
36	chr20:14904432-14904482	Hepatocyte	liver:	n/a
37	chr20:14904432-14904482	BJ	skin:	n/a
38	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
39	chr20:14904432-14904482	NB4	blood:	n/a
40	chr20:14904432-14904482	MCF-7	breast:	n/a
41	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
42	chr20:14904432-14904482	LNCaP	prostate:	n/a
43	chr20:14904432-14904482	Hela-S3	cervix:	n/a
44	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
45	chr20:14904432-14904482	HepG2	liver:	n/a
46	chr20:14904432-14904482	RPTEC	kidney:	n/a
47	chr20:14904432-14904482	ProgFib	skin:	n/a
48	chr20:14904432-14904482	HCT-116	colon:	n/a
49	chr20:14904432-14904482	GM19239	blood:	n/a
50	chr20:14904432-14904482	NH-A	brain:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
2	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
3	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
4	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
5	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
6	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
7	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
8	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
9	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
10	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
11	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
12	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
13	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
14	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
15	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
16	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
17	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
18	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
19	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
20	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
21	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
22	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
23	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
24	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
25	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
26	chr20:14983136..14983867-chr7:139874694..139875444,2	MCF-7	breast:
27	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
28	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
29	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
30	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
31	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
32	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
33	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
34	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
35	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
36	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
37	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
38	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
39	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
40	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
41	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
42	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
43	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
44	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
45	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
46	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
47	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
48	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
49	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
50	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 11529 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:11529 , 50 per page) page: 1 2 3 4 5 6 7 ... 231

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76301632	chr20:14756396-14756397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563723211	chr20:14756458-14756459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531005448	chr20:14756463-14756464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs202180256	chr20:14756514-14756515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79282015	chr20:14756515-14756516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561450894	chr20:14756560-14756561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182737046	chr20:14756626-14756627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs377552653	chr20:14756634-14756635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6135257	chr20:14756647-14756648	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs571566309	chr20:14756685-14756686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370332054	chr20:14756694-14756695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187505822	chr20:14756695-14756696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569336165	chr20:14756710-14756711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200573108	chr20:14756761-14756762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs454775	chr20:14756762-14756763	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs538778583	chr20:14756772-14756773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371268370	chr20:14756818-14756819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139948175	chr20:14756820-14756821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192560810	chr20:14756821-14756822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566434936	chr20:14756846-14756847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553246768	chr20:14756879-14756880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577998374	chr20:14756897-14756898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545352101	chr20:14756901-14756902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149672703	chr20:14756911-14756912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575515369	chr20:14757058-14757059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543030653	chr20:14757100-14757101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184550080	chr20:14757125-14757126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116816564	chr20:14757196-14757197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535190316	chr20:14757199-14757200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145443272	chr20:14757214-14757215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187372706	chr20:14757316-14757317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550894099	chr20:14757357-14757358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569221800	chr20:14757387-14757388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537246756	chr20:14757392-14757393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530395036	chr20:14757394-14757395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192058107	chr20:14757425-14757426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567242110	chr20:14757467-14757468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77609952	chr20:14757483-14757484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371722244	chr20:14757512-14757513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184915740	chr20:14757535-14757536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189763148	chr20:14757558-14757559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565639503	chr20:14757613-14757614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113145654	chr20:14757620-14757621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148398856	chr20:14757638-14757639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142578419	chr20:14757640-14757641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575498987	chr20:14757663-14757664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181183851	chr20:14757692-14757693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554988663	chr20:14757701-14757702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573253901	chr20:14757715-14757716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540355864	chr20:14757716-14757717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Schizophrenia	19805367	CNVD

Chromatin state (count:1546 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14755800-14757200	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr20:14756000-14756400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr20:14756000-14756400	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr20:14756000-14756800	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr20:14756000-14756800	Enhancers	Hela-S3	cervix
6	chr20:14756000-14757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr20:14756000-14757200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr20:14756000-14757200	Enhancers	A549	lung
9	chr20:14756000-14759200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr20:14756200-14756800	Enhancers	Psoas Muscle	Psoas
11	chr20:14756200-14757000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr20:14756200-14757000	Enhancers	HepG2	liver
13	chr20:14756200-14757000	Enhancers	HMEC	breast
14	chr20:14756200-14757200	Enhancers	NHEK	skin
15	chr20:14756600-14757000	Enhancers	Fetal Intestine Small	intestine
16	chr20:14756600-14757200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr20:14756800-14757000	Enhancers	NHDF-Ad	bronchial
18	chr20:14757000-14758000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr20:14757000-14758000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr20:14757000-14758200	Weak transcription	HMEC	breast
21	chr20:14757200-14757600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr20:14757200-14757600	Weak transcription	NHEK	skin
23	chr20:14757200-14758000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr20:14757600-14759000	Enhancers	NHEK	skin
25	chr20:14757600-14759600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr20:14758000-14758600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr20:14758000-14758800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr20:14758000-14759200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr20:14758200-14758800	Enhancers	HMEC	breast
30	chr20:14758600-14758800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr20:14758600-14759400	Enhancers	NHDF-Ad	bronchial
32	chr20:14758600-14761200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr20:14759200-14760800	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr20:14759200-14760800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr20:14760600-14761600	Enhancers	HUVEC	blood vessel
36	chr20:14760800-14761800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr20:14760800-14762200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr20:14761200-14761800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr20:14763200-14763800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr20:14763200-14764000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr20:14763400-14763800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr20:14763400-14764200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr20:14764200-14764800	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr20:14764800-14765000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr20:14764800-14765200	Enhancers	Fetal Lung	lung
46	chr20:14765200-14765600	Weak transcription	Fetal Lung	lung
47	chr20:14765600-14766000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr20:14765600-14766200	Enhancers	Fetal Lung	lung
49	chr20:14765600-14766400	Enhancers	Stomach Mucosa	stomach
50	chr20:14765800-14766000	Enhancers	Fetal Intestine Small	intestine

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