Variant report

Variant	esv3512354
Chromosome Location	chr20:14560087-15087661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3876)
CpG islands
(count:61)
Chromatin interactive
region (count:73)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3876 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:14590214-14590575	HepG2	liver:	n/a	n/a
9	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
10	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
11	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
18	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
19	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
20	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
21	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
22	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
23	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
24	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
25	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
26	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
27	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
28	ATF3	chr20:14603385-14603865	A549	lung:	n/a	n/a
29	ATF3	chr20:14613539-14613866	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr20:14613673-14613899	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
32	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
33	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
36	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
37	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
38	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
39	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
40	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
41	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
42	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
43	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
44	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
45	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
46	BATF	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
47	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
48	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
49	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
50	BATF	chr20:15041087-15041347	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	Jurkat	blood:	n/a
2	chr20:14904432-14904482	NB4	blood:	n/a
3	chr20:14904432-14904482	NHBE	bronchial:	n/a
4	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
5	chr20:14904432-14904482	Hela-S3	cervix:	n/a
6	chr20:14904432-14904482	AG10803	skin:	n/a
7	chr20:14904432-14904482	HCM	heart:	n/a
8	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
9	chr20:14904432-14904482	PFSK-1	brain:	n/a
10	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
11	chr20:14904432-14904482	BE2_C	brain:	n/a
12	chr20:14904432-14904482	BJ	skin:	n/a
13	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
14	chr20:14904432-14904482	T-47D	breast:	n/a
15	chr20:14904432-14904482	HMEC	breast:	n/a
16	chr20:14904432-14904482	HRE	kidney:	n/a
17	chr20:14904432-14904482	HL-60	blood:	n/a
18	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
19	chr20:14904432-14904482	AG04449	skin:	fetal
20	chr20:14904432-14904482	GM06990	blood:	n/a
21	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
22	chr20:14904432-14904482	GM12878	blood:	n/a
23	chr20:14904432-14904482	IMR90	lung:	fetal
24	chr20:14904432-14904482	LNCaP	prostate:	n/a
25	chr20:14904432-14904482	GM19239	blood:	n/a
26	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
27	chr20:14904432-14904482	NH-A	brain:	n/a
28	chr20:14904432-14904482	HCF	heart:	n/a
29	chr20:14904432-14904482	HepG2	liver:	n/a
30	chr20:14904432-14904482	Caco-2	colon:	n/a
31	chr20:14904432-14904482	RPTEC	kidney:	n/a
32	chr20:14904432-14904482	SK-N-MC	brain:	n/a
33	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
34	chr20:14904432-14904482	SK-N-SH	brain:	n/a
35	chr20:14904432-14904482	MCF-7	breast:	n/a
36	chr20:14904432-14904482	PrEC	prostate:	n/a
37	chr20:14904432-14904482	CMK	blood:	n/a
38	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
39	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
40	chr20:14904432-14904482	SKMC	muscle:	n/a
41	chr20:14904432-14904482	SAEC	small airway:	n/a
42	chr20:14904432-14904482	A549	lung:	n/a
43	chr20:14904432-14904482	GM12892	blood:	n/a
44	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
45	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
46	chr20:14904432-14904482	PANC-1	pancreas:	n/a
47	chr20:14904432-14904482	NT2-D1	testis:	n/a
48	chr20:14904432-14904482	AG09309	skin:	n/a
49	chr20:14904432-14904482	Hepatocyte	liver:	n/a
50	chr20:14904432-14904482	GM12891	blood:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
2	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
3	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
4	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
5	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
6	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
7	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
8	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
9	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
10	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
11	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
12	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
13	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
14	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
15	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
16	chr20:14983136..14983867-chr7:139874694..139875444,2	MCF-7	breast:
17	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
18	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
19	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
20	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
21	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
22	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
23	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
24	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
25	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
26	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
27	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
28	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
29	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
30	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
31	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
32	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
33	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
34	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
35	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
36	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
37	chr20:14601339..14605162-chr20:14611440..14614800,3	MCF-7	breast:
38	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
39	chr20:14606804..14608358-chr20:14690132..14692728,2	MCF-7	breast:
40	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
41	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
42	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
43	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
44	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
45	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
46	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
47	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
48	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
49	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
50	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
2	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
3	lnc-C20orf7-1	chr20:14602412-14602575	ENSG00000227927.1
4	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
5	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
6	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
7	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
8	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
9	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
10	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
11	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078716
12	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
13	lnc-C20orf7-4	chr20:14591719-14595690	NONHSAT078719
14	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
15	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
16	lnc-C20orf7-1	chr20:14609283-14609554	ENSG00000227927.1
17	lnc-C20orf7-1	chr20:14603520-14603660	ENSG00000227927.1
18	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
19	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
20	lnc-C20orf7-1	chr20:14612487-14612595	ENSG00000227927.2
21	lnc-C20orf7-1	chr20:14617092-14617170	ENSG00000227927.2
22	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
23	lnc-C20orf7-1	chr20:14607710-14607752	ENSG00000227927.1
24	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
25	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
26	lnc-C20orf7-1	chr20:14609283-14609475	ENSG00000227927.2
27	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
28	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
29	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
30	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
31	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
32	lnc-C20orf7-1	chr20:14607559-14607752	ENSG00000227927.2
33	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
34	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
35	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078714
36	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
37	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721

No data

Variant related genes	Relation type
MACROD2-AS1	TF binding region
ENSG00000237832	TF binding region
RPS10P2	TF binding region
RNU6-1159P	TF binding region
MACROD2-IT1	TF binding region
RNU6-115P	TF binding region
MACROD2-AS1	CpG island
ENSG00000237832	CpG island
RPS10P2	CpG island
RNU6-1159P	CpG island
MACROD2-IT1	CpG island
RNU6-115P	CpG island
ENSG00000227927	chromatin interactions
ENSG00000237832	chromatin interactions
ENSG00000125844	chromatin interactions

Extended variants
information (count: 16123 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:16123 , 50 per page) page: 1 2 3 4 5 6 7 ... 323

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552973266	chr20:14560100-14560101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558494341	chr20:14560108-14560109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77772386	chr20:14560149-14560150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183504717	chr20:14560159-14560160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570492941	chr20:14560207-14560208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556859616	chr20:14560225-14560226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575110801	chr20:14560242-14560243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542487837	chr20:14560247-14560248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554449633	chr20:14560270-14560271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539276357	chr20:14560332-14560333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187833910	chr20:14560400-14560401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147229683	chr20:14560450-14560451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139620555	chr20:14560506-14560507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554392713	chr20:14560529-14560530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149674169	chr20:14560562-14560563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562907193	chr20:14560576-14560577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35942273	chr20:14560582-14560583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530320222	chr20:14560607-14560608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548858369	chr20:14560649-14560650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567161469	chr20:14560654-14560655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528038596	chr20:14560689-14560690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144434634	chr20:14560718-14560719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571252532	chr20:14560847-14560848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148433722	chr20:14560914-14560915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553085719	chr20:14560933-14560934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs118040135	chr20:14561019-14561020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11468142	chr20:14561088-14561089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546929297	chr20:14561089-14561090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs397704005	chr20:14561098-14561099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11467360	chr20:14561099-14561100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs193196300	chr20:14561147-14561148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144028432	chr20:14561148-14561149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146849350	chr20:14561170-14561171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572800011	chr20:14561181-14561182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575612902	chr20:14561216-14561217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534122772	chr20:14561232-14561233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566661903	chr20:14561238-14561239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34216189	chr20:14561256-14561257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574285872	chr20:14561345-14561346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543325446	chr20:14561350-14561351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540521222	chr20:14561409-14561410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183428251	chr20:14561427-14561428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542610596	chr20:14561521-14561522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577184777	chr20:14561555-14561556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140643933	chr20:14561617-14561618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188282333	chr20:14561618-14561619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575028023	chr20:14561627-14561628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73901893	chr20:14561628-14561629	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs553197129	chr20:14561633-14561634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560692840	chr20:14561639-14561640	Enhancers Weak transcription	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
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	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:2096 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14557200-14563600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr20:14557400-14561200	Weak transcription	Fetal Intestine Large	intestine
3	chr20:14557800-14561200	Weak transcription	Liver	Liver
4	chr20:14560600-14561000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr20:14560600-14561600	Enhancers	Fetal Brain Female	brain
6	chr20:14560800-14562000	Enhancers	A549	lung
7	chr20:14561000-14561800	Enhancers	Stomach Mucosa	stomach
8	chr20:14561200-14561400	Enhancers	Pancreas	Pancrea
9	chr20:14561200-14561600	Enhancers	Fetal Intestine Large	intestine
10	chr20:14561200-14561800	Enhancers	Liver	Liver
11	chr20:14561200-14561800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr20:14561400-14561800	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr20:14561400-14569200	Weak transcription	Pancreas	Pancrea
14	chr20:14561800-14563200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr20:14562000-14563800	Weak transcription	A549	lung
16	chr20:14562400-14564800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr20:14562400-14564800	Enhancers	HMEC	breast
18	chr20:14563000-14564000	Enhancers	Dnd41	blood
19	chr20:14563400-14564000	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr20:14563400-14564200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr20:14563400-14564600	Enhancers	HSMM	muscle
22	chr20:14563600-14564200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr20:14563600-14564200	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr20:14563600-14564400	Enhancers	HSMMtube	muscle
25	chr20:14563600-14564800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr20:14563600-14564800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr20:14563600-14564800	Enhancers	NHEK	skin
28	chr20:14563600-14565000	Enhancers	Hela-S3	cervix
29	chr20:14563800-14564200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr20:14563800-14564800	Enhancers	A549	lung
31	chr20:14564800-14569800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr20:14569200-14569400	ZNF genes & repeats	Pancreas	Pancrea
33	chr20:14569800-14570600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr20:14570600-14577400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr20:14572600-14573000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr20:14572600-14573000	Enhancers	HMEC	breast
37	chr20:14574000-14574600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr20:14574200-14574600	Enhancers	Fetal Kidney	kidney
39	chr20:14574200-14575200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr20:14574600-14575000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr20:14575200-14580000	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr20:14575600-14575800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr20:14575800-14576200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr20:14575800-14576400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr20:14577800-14578200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr20:14578200-14578400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr20:14578200-14578800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr20:14578200-14579800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr20:14578800-14579800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr20:14579800-14580800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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