Variant report

Variant	nsv1059579
Chromosome Location	chr20:14518849-14941319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2852)
CpG islands
(count:61)
Chromatin interactive
region (count:73)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2852 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14590214-14590575	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	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
5	ATF2	chr20:14519085-14519448	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
16	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
18	ATF3	chr20:14613539-14613866	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
20	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
21	ATF3	chr20:14613673-14613899	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
23	ATF3	chr20:14603385-14603865	A549	lung:	n/a	n/a
24	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
25	BACH1	chr20:14549483-14549672	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr20:14548845-14549180	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
29	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
30	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
31	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
32	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
33	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
34	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
35	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
36	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
37	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
38	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
39	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
40	BATF	chr20:14519115-14519423	GM12878	blood:	n/a	n/a
41	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
42	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
43	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
44	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
45	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
46	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
47	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
48	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
49	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
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	Caco-2	colon:	n/a
2	chr20:14904432-14904482	IMR90	lung:	fetal
3	chr20:14904432-14904482	AG04450	lung:	fetal
4	chr20:14904432-14904482	NHBE	bronchial:	n/a
5	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
6	chr20:14904432-14904482	AG09319	gingival:	n/a
7	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
8	chr20:14904432-14904482	HCM	heart:	n/a
9	chr20:14904432-14904482	SKMC	muscle:	n/a
10	chr20:14904432-14904482	AG04449	skin:	fetal
11	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
12	chr20:14904432-14904482	PANC-1	pancreas:	n/a
13	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
14	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
15	chr20:14904432-14904482	U87	brain:	n/a
16	chr20:14904432-14904482	HRE	kidney:	n/a
17	chr20:14904432-14904482	Hepatocyte	liver:	n/a
18	chr20:14904432-14904482	GM12878	blood:	n/a
19	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
20	chr20:14904432-14904482	NB4	blood:	n/a
21	chr20:14904432-14904482	SAEC	small airway:	n/a
22	chr20:14904432-14904482	BJ	skin:	n/a
23	chr20:14904432-14904482	Jurkat	blood:	n/a
24	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
25	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
26	chr20:14904432-14904482	GM06990	blood:	n/a
27	chr20:14904432-14904482	HEK293	kidney:	embryo
28	chr20:14904432-14904482	GM19239	blood:	n/a
29	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
30	chr20:14904432-14904482	GM12892	blood:	n/a
31	chr20:14904432-14904482	CMK	blood:	n/a
32	chr20:14904432-14904482	HMEC	breast:	n/a
33	chr20:14904432-14904482	PFSK-1	brain:	n/a
34	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
35	chr20:14904432-14904482	K562	blood:	n/a
36	chr20:14904432-14904482	RPTEC	kidney:	n/a
37	chr20:14904432-14904482	AG10803	skin:	n/a
38	chr20:14904432-14904482	MCF-7	breast:	n/a
39	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
40	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
41	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
42	chr20:14904432-14904482	T-47D	breast:	n/a
43	chr20:14904432-14904482	AG09309	skin:	n/a
44	chr20:14904432-14904482	HCF	heart:	n/a
45	chr20:14904432-14904482	LNCaP	prostate:	n/a
46	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
47	chr20:14904432-14904482	A549	lung:	n/a
48	chr20:14904432-14904482	SK-N-MC	brain:	n/a
49	chr20:14904432-14904482	ProgFib	skin:	n/a
50	chr20:14904432-14904482	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:14606804..14608358-chr20:14690132..14692728,2	MCF-7	breast:
2	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
3	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
4	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
5	chr19:30441690..30442493-chr20:14547650..14548282,2	MCF-7	breast:
6	chr20:14601339..14605162-chr20:14611440..14614800,3	MCF-7	breast:
7	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
8	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
9	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
10	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
11	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
12	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
13	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
14	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
15	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
16	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
17	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
18	chr20:14601339..14605162-chr20:14611440..14614800,3	MCF-7	breast:
19	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
20	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
21	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
22	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
23	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
24	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
25	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
26	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
27	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
28	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
29	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
30	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
31	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
32	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
33	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
34	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
35	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
36	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
37	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
38	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
39	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
40	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
41	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
42	chr20:14657146..14658733-chr20:17661268..17663723,2	MCF-7	breast:
43	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
44	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
45	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
46	chr20:14527106..14529484-chr20:14530662..14532376,3	MCF-7	breast:
47	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
48	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
49	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
50	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
2	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
3	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
4	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
5	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
6	lnc-C20orf7-1	chr20:14607710-14607752	ENSG00000227927.1
7	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
8	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
9	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
10	lnc-C20orf7-1	chr20:14602412-14602575	ENSG00000227927.1
11	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
12	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
13	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
14	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
15	lnc-C20orf7-1	chr20:14603520-14603660	ENSG00000227927.1
16	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
17	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078714
18	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
19	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078716
20	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
21	lnc-C20orf7-1	chr20:14612487-14612595	ENSG00000227927.2
22	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
23	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
24	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
25	lnc-C20orf7-1	chr20:14617092-14617170	ENSG00000227927.2
26	lnc-C20orf7-1	chr20:14535030-14535074	ENSG00000227927.1
27	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
28	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
29	lnc-FLRT3-3	chr20:14527830-14528269	NONHSAT078717
30	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
31	lnc-C20orf7-4	chr20:14591719-14595690	NONHSAT078719
32	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
33	lnc-C20orf7-1	chr20:14609283-14609554	ENSG00000227927.1
34	lnc-C20orf7-1	chr20:14609283-14609475	ENSG00000227927.2
35	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
36	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
37	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
38	lnc-C20orf7-1	chr20:14607559-14607752	ENSG00000227927.2
39	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1

No data

Variant related genes	Relation type
ENSG00000237832	TF binding region
ENSG00000227563	TF binding region
MACROD2-AS1	TF binding region
RPS10P2	TF binding region
MACROD2-IT1	TF binding region
ENSG00000237832	CpG island
ENSG00000227563	CpG island
MACROD2-AS1	CpG island
RPS10P2	CpG island
MACROD2-IT1	CpG island
ENSG00000227927	chromatin interactions
ENSG00000237832	chromatin interactions
ENSG00000125844	chromatin interactions
ENSG00000227563	chromatin interactions

Extended variants
information (count: 12721 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:12721 , 50 per page) page: 1 2 3 4 5 6 7 ... 255

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544246078	chr20:14518908-14518909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73901272	chr20:14518966-14518967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs78865862	chr20:14519052-14519053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142898749	chr20:14519118-14519119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150787987	chr20:14519171-14519172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139195635	chr20:14519178-14519179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577306530	chr20:14519236-14519237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552037546	chr20:14519254-14519255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78473077	chr20:14519265-14519266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149891326	chr20:14519269-14519270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556154683	chr20:14519285-14519286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188268231	chr20:14519321-14519322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535583017	chr20:14519340-14519341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143859846	chr20:14519380-14519381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191505311	chr20:14519436-14519437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79068693	chr20:14519490-14519491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558459655	chr20:14519497-14519498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1015581	chr20:14519512-14519513	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs143230058	chr20:14519518-14519519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116023856	chr20:14519540-14519541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574421470	chr20:14519575-14519576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543523536	chr20:14519578-14519579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541550573	chr20:14519661-14519662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112877248	chr20:14519662-14519663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114381754	chr20:14519689-14519690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73612367	chr20:14519777-14519778	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs564006413	chr20:14519790-14519791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369346447	chr20:14519823-14519824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531513528	chr20:14519862-14519863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374097422	chr20:14519877-14519878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549720282	chr20:14519895-14519896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116865069	chr20:14519989-14519990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535886246	chr20:14519996-14519997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527417705	chr20:14520002-14520003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547067129	chr20:14520020-14520021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183659767	chr20:14520057-14520058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540003591	chr20:14520179-14520180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199508285	chr20:14520232-14520233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376807376	chr20:14520269-14520270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2327861	chr20:14520303-14520304	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs576762206	chr20:14520327-14520328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537736080	chr20:14520373-14520374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556065210	chr20:14520399-14520400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574335050	chr20:14520407-14520408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2423807	chr20:14520442-14520443	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs139124275	chr20:14520464-14520465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56246076	chr20:14520570-14520571	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370124289	chr20:14520589-14520590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146612756	chr20:14520627-14520628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563944679	chr20:14520628-14520629	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
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

Chromatin state (count:1741 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14517200-14519200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr20:14517400-14519000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr20:14517800-14519000	Enhancers	HMEC	breast
4	chr20:14518600-14519000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr20:14518600-14519800	Enhancers	GM12878-XiMat	blood
6	chr20:14518600-14520200	Enhancers	Primary hematopoietic stem cells	blood
7	chr20:14518800-14519800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr20:14519000-14519200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr20:14519200-14523800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr20:14519600-14520200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr20:14519800-14520000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr20:14519800-14520200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr20:14520200-14521200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr20:14521200-14521400	Enhancers	Primary hematopoietic stem cells	blood
15	chr20:14522800-14523000	Enhancers	Gastric	stomach
16	chr20:14523000-14529600	Weak transcription	Gastric	stomach
17	chr20:14523800-14524000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr20:14524400-14526400	Enhancers	Fetal Heart	heart
19	chr20:14529600-14529800	ZNF genes & repeats	Gastric	stomach
20	chr20:14533200-14533400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr20:14533400-14534800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr20:14534200-14535400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr20:14534200-14535400	Enhancers	HSMM	muscle
24	chr20:14534200-14535400	Enhancers	HSMMtube	muscle
25	chr20:14534200-14535600	Enhancers	Hela-S3	cervix
26	chr20:14534400-14537600	Enhancers	NHEK	skin
27	chr20:14534600-14534800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr20:14534600-14535200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr20:14534600-14535400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr20:14534600-14535400	Enhancers	Placenta Amnion	Placenta Amnion
31	chr20:14534600-14537400	Enhancers	HMEC	breast
32	chr20:14534800-14535200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr20:14534800-14535200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr20:14534800-14537400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr20:14535000-14537400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr20:14535200-14535400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr20:14535200-14536200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr20:14535400-14540400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr20:14535400-14540400	Weak transcription	HSMM	muscle
40	chr20:14535400-14542000	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr20:14535400-14548800	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr20:14535600-14536000	Weak transcription	Hela-S3	cervix
43	chr20:14535800-14537200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr20:14536000-14536400	Enhancers	Hela-S3	cervix
45	chr20:14536200-14536400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr20:14536200-14537000	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr20:14536400-14536800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr20:14536800-14537400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr20:14537400-14540000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr20:14537400-14540400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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