Variant report

Variant	nsv1065316
Chromosome Location	chr20:14720407-14974683
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2453)
CpG islands
(count:61)
Chromatin interactive
region (count:61)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2453 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14971646-14973208	HepG2	liver:	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	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
15	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
16	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
18	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
19	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
20	ATF3	chr20:14966529-14967363	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	chr20:14965454-14966225	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	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
27	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
28	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
29	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
30	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
31	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
32	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
33	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
34	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
35	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
36	BATF	chr20:14810566-14810958	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	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
40	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
41	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
42	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
43	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
44	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
46	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
47	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
48	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
49	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
50	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238

(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	AoSMC	blood vessel:	n/a
3	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
4	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
5	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
6	chr20:14904432-14904482	HMEC	breast:	n/a
7	chr20:14904432-14904482	HRE	kidney:	n/a
8	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
9	chr20:14904432-14904482	Hela-S3	cervix:	n/a
10	chr20:14904432-14904482	T-47D	breast:	n/a
11	chr20:14904432-14904482	BJ	skin:	n/a
12	chr20:14904432-14904482	BE2_C	brain:	n/a
13	chr20:14904432-14904482	K562	blood:	n/a
14	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
15	chr20:14904432-14904482	SK-N-MC	brain:	n/a
16	chr20:14904432-14904482	PFSK-1	brain:	n/a
17	chr20:14904432-14904482	NHBE	bronchial:	n/a
18	chr20:14904432-14904482	GM12892	blood:	n/a
19	chr20:14904432-14904482	HCT-116	colon:	n/a
20	chr20:14904432-14904482	ProgFib	skin:	n/a
21	chr20:14904432-14904482	A549	lung:	n/a
22	chr20:14904432-14904482	Caco-2	colon:	n/a
23	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
24	chr20:14904432-14904482	HIPEpiC	eye:	n/a
25	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
26	chr20:14904432-14904482	HEK293	kidney:	embryo
27	chr20:14904432-14904482	LNCaP	prostate:	n/a
28	chr20:14904432-14904482	NH-A	brain:	n/a
29	chr20:14904432-14904482	SK-N-SH	brain:	n/a
30	chr20:14904432-14904482	IMR90	lung:	fetal
31	chr20:14904432-14904482	HCF	heart:	n/a
32	chr20:14904432-14904482	RPTEC	kidney:	n/a
33	chr20:14904432-14904482	Jurkat	blood:	n/a
34	chr20:14904432-14904482	PrEC	prostate:	n/a
35	chr20:14904432-14904482	AG04450	lung:	fetal
36	chr20:14904432-14904482	NT2-D1	testis:	n/a
37	chr20:14904432-14904482	HCM	heart:	n/a
38	chr20:14904432-14904482	AG10803	skin:	n/a
39	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
40	chr20:14904432-14904482	AG04449	skin:	fetal
41	chr20:14904432-14904482	AG09309	skin:	n/a
42	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
43	chr20:14904432-14904482	GM12891	blood:	n/a
44	chr20:14904432-14904482	AG09319	gingival:	n/a
45	chr20:14904432-14904482	GM12878	blood:	n/a
46	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
47	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
48	chr20:14904432-14904482	HepG2	liver:	n/a
49	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
50	chr20:14904432-14904482	MCF-7	breast:	n/a

(count:61 , 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	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
3	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
4	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
5	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
6	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
7	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
8	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
9	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
10	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
11	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
12	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
13	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
14	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
15	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
16	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
17	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
18	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
19	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
20	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
21	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
22	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
23	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
24	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
25	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
26	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
27	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
28	chr20:14744879..14746579-chr20:14747938..14749575,2	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	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
32	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
33	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
34	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
35	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
36	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
37	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
38	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
39	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
40	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
41	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
42	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
43	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
44	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
45	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
46	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
47	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
48	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
49	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
50	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:

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

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

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: 7672 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7672 , 50 per page) page: 1 2 3 4 5 6 7 ... 154

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533340675	chr20:14720411-14720412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191773859	chr20:14720445-14720446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150586762	chr20:14720498-14720499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531192966	chr20:14720533-14720534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2151395	chr20:14720538-14720539	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs139489102	chr20:14720572-14720573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6074785	chr20:14720630-14720631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535485172	chr20:14720641-14720642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553571974	chr20:14720676-14720677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530406312	chr20:14720720-14720721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6074786	chr20:14720734-14720735	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs557899729	chr20:14720744-14720745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575835481	chr20:14720756-14720757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543309365	chr20:14720758-14720759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555282048	chr20:14720804-14720805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573681586	chr20:14720885-14720886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183626995	chr20:14720937-14720938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76633844	chr20:14720974-14720975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533429038	chr20:14720998-14720999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545184245	chr20:14721072-14721073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563861349	chr20:14721092-14721093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6042892	chr20:14721127-14721128	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs186494002	chr20:14721199-14721200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567995762	chr20:14721206-14721207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372354471	chr20:14721292-14721293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3925915	chr20:14721349-14721350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528874205	chr20:14721389-14721390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547343088	chr20:14721470-14721471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139527437	chr20:14721479-14721480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539472076	chr20:14721534-14721535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551233267	chr20:14721619-14721620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191510801	chr20:14721714-14721715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182837279	chr20:14721741-14721742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375860716	chr20:14721784-14721785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368284810	chr20:14721822-14721823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117934870	chr20:14721834-14721835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144823587	chr20:14721847-14721848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186691023	chr20:14721860-14721861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189541976	chr20:14721921-14721922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115113436	chr20:14722020-14722021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376762786	chr20:14722021-14722022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553632205	chr20:14722042-14722043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567720348	chr20:14722055-14722056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75702245	chr20:14722157-14722158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367608944	chr20:14722233-14722234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536363955	chr20:14722247-14722248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543273603	chr20:14722265-14722266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111870278	chr20:14722298-14722299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183451060	chr20:14722317-14722318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528761354	chr20:14722319-14722320	Weak transcription	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:1171 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14719200-14721000	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr20:14720600-14721800	Enhancers	Fetal Brain Male	brain
3	chr20:14721000-14721400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr20:14721000-14721400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr20:14721000-14721800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr20:14721200-14721600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr20:14721200-14721800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr20:14721200-14721800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr20:14721200-14721800	Enhancers	Fetal Brain Female	brain
10	chr20:14721200-14722000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr20:14721200-14722000	Enhancers	Brain Germinal Matrix	brain
12	chr20:14721400-14721600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr20:14721600-14726800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr20:14724800-14726200	Enhancers	GM12878-XiMat	blood
15	chr20:14726000-14727600	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr20:14726200-14726600	Enhancers	Fetal Kidney	kidney
17	chr20:14726600-14727000	Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr20:14726800-14727000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr20:14727000-14727600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr20:14738200-14738600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr20:14738400-14738600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr20:14740600-14740800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr20:14742800-14743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr20:14743000-14744000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr20:14743400-14744200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr20:14745200-14746200	Enhancers	Stomach Mucosa	stomach
27	chr20:14746000-14746200	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr20:14750600-14756200	Weak transcription	Psoas Muscle	Psoas
29	chr20:14755800-14757200	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr20:14756000-14756400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr20:14756000-14756400	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr20:14756000-14756800	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr20:14756000-14756800	Enhancers	Hela-S3	cervix
34	chr20:14756000-14757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr20:14756000-14757200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr20:14756000-14757200	Enhancers	A549	lung
37	chr20:14756000-14759200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr20:14756200-14756800	Enhancers	Psoas Muscle	Psoas
39	chr20:14756200-14757000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr20:14756200-14757000	Enhancers	HepG2	liver
41	chr20:14756200-14757000	Enhancers	HMEC	breast
42	chr20:14756200-14757200	Enhancers	NHEK	skin
43	chr20:14756600-14757000	Enhancers	Fetal Intestine Small	intestine
44	chr20:14756600-14757200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr20:14756800-14757000	Enhancers	NHDF-Ad	bronchial
46	chr20:14757000-14758000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr20:14757000-14758000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr20:14757000-14758200	Weak transcription	HMEC	breast
49	chr20:14757200-14757600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr20:14757200-14757600	Weak transcription	NHEK	skin

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