Variant report

Variant	nsv585464
Chromosome Location	chr20:14705888-15082546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3010)
CpG islands
(count:61)
Chromatin interactive
region (count:66)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3010 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

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	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
9	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
10	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
15	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
16	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
18	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
19	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
20	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
21	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
22	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
23	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
24	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
25	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
26	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
27	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
28	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
31	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
32	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
33	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
34	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
35	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
36	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
37	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
38	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
39	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
40	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
41	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
42	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
43	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
44	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
45	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
46	BATF	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
47	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
48	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
49	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
50	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	BE2_C	brain:	n/a
2	chr20:14904432-14904482	Jurkat	blood:	n/a
3	chr20:14904432-14904482	GM12892	blood:	n/a
4	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
5	chr20:14904432-14904482	AG04449	skin:	fetal
6	chr20:14904432-14904482	CMK	blood:	n/a
7	chr20:14904432-14904482	T-47D	breast:	n/a
8	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
9	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
10	chr20:14904432-14904482	HCT-116	colon:	n/a
11	chr20:14904432-14904482	Caco-2	colon:	n/a
12	chr20:14904432-14904482	Hepatocyte	liver:	n/a
13	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
14	chr20:14904432-14904482	SAEC	small airway:	n/a
15	chr20:14904432-14904482	SK-N-MC	brain:	n/a
16	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
17	chr20:14904432-14904482	HCF	heart:	n/a
18	chr20:14904432-14904482	IMR90	lung:	fetal
19	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
20	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
21	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
22	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
23	chr20:14904432-14904482	PFSK-1	brain:	n/a
24	chr20:14904432-14904482	NHBE	bronchial:	n/a
25	chr20:14904432-14904482	AG09319	gingival:	n/a
26	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
27	chr20:14904432-14904482	NH-A	brain:	n/a
28	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
29	chr20:14904432-14904482	LNCaP	prostate:	n/a
30	chr20:14904432-14904482	GM19239	blood:	n/a
31	chr20:14904432-14904482	AG09309	skin:	n/a
32	chr20:14904432-14904482	A549	lung:	n/a
33	chr20:14904432-14904482	GM12891	blood:	n/a
34	chr20:14904432-14904482	HL-60	blood:	n/a
35	chr20:14904432-14904482	HepG2	liver:	n/a
36	chr20:14904432-14904482	NT2-D1	testis:	n/a
37	chr20:14904432-14904482	PANC-1	pancreas:	n/a
38	chr20:14904432-14904482	BJ	skin:	n/a
39	chr20:14904432-14904482	HCM	heart:	n/a
40	chr20:14904432-14904482	ProgFib	skin:	n/a
41	chr20:14904432-14904482	RPTEC	kidney:	n/a
42	chr20:14904432-14904482	HRPEpiC	eye:	n/a
43	chr20:14904432-14904482	Hela-S3	cervix:	n/a
44	chr20:14904432-14904482	SK-N-SH	brain:	n/a
45	chr20:14904432-14904482	K562	blood:	n/a
46	chr20:14904432-14904482	AG04450	lung:	fetal
47	chr20:14904432-14904482	HRE	kidney:	n/a
48	chr20:14904432-14904482	MCF-7	breast:	n/a
49	chr20:14904432-14904482	GM12878	blood:	n/a
50	chr20:14904432-14904482	U87	brain:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
2	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
3	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
4	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
5	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
6	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
7	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
8	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
9	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
10	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
11	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
12	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
13	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
14	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
15	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
16	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
17	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
18	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
19	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
20	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
21	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
22	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
23	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
24	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
25	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
26	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
27	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
28	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
29	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
30	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
31	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
32	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
33	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
34	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
35	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
36	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
37	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
38	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
39	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
40	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
41	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
42	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
43	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
44	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
45	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
46	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
47	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
48	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
49	chr20:14901786..14904742-chr20:14908050..14909865,2	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	chr20:14830550-14830649	NONHSAT078714
2	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
3	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
4	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
5	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
6	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
7	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
8	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
9	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
10	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
11	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
12	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
13	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
14	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
15	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
16	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
17	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
18	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
19	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
20	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
21	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
22	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
23	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
24	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
25	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
26	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1

No data

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

Extended variants
information (count: 11502 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:11502 , 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	rs6079540	chr20:14705888-14705889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557906529	chr20:14705934-14705935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185084682	chr20:14706005-14706006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556401708	chr20:14706069-14706070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562247749	chr20:14706097-14706098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111283871	chr20:14706121-14706122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541501304	chr20:14706132-14706133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76101471	chr20:14706188-14706189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188552872	chr20:14706248-14706249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74656442	chr20:14706293-14706294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575627175	chr20:14706326-14706327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78702133	chr20:14706327-14706328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143346592	chr20:14706337-14706338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78073960	chr20:14706394-14706395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531542498	chr20:14706398-14706399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544713808	chr20:14706417-14706418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62204771	chr20:14706424-14706425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs568306092	chr20:14706501-14706502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71331803	chr20:14706507-14706508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529274330	chr20:14706542-14706543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547504748	chr20:14706544-14706545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375978068	chr20:14706590-14706591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565762102	chr20:14706608-14706609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4813165	chr20:14706616-14706617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs191842750	chr20:14706620-14706621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569869237	chr20:14706648-14706649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184013541	chr20:14706662-14706663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556015289	chr20:14706726-14706727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574285227	chr20:14706733-14706734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574343092	chr20:14706790-14706791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560497345	chr20:14706863-14706864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6074780	chr20:14706879-14706880	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs6079542	chr20:14706916-14706917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371765919	chr20:14706935-14706936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553461400	chr20:14706937-14706938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572084200	chr20:14706995-14706996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6074781	chr20:14707003-14707004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545870812	chr20:14707005-14707006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs6074782	chr20:14707025-14707026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6074783	chr20:14707050-14707051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560573538	chr20:14707069-14707070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148361371	chr20:14707079-14707080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs16994837	chr20:14707127-14707128	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs6042882	chr20:14707144-14707145	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs367692358	chr20:14707281-14707282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562750248	chr20:14707317-14707318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141519240	chr20:14707331-14707332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73899274	chr20:14707334-14707335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs188304253	chr20:14707365-14707366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565699052	chr20:14707378-14707379	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
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:1500 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14697600-14706200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr20:14698600-14707000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr20:14706200-14706400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr20:14706400-14707000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:14707000-14707200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr20:14707200-14709600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr20:14709400-14710200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr20:14710000-14710200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr20:14710000-14710400	Enhancers	Liver	Liver
10	chr20:14710000-14710400	Enhancers	HepG2	liver
11	chr20:14710000-14710600	Enhancers	Stomach Mucosa	stomach
12	chr20:14710200-14710400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr20:14710400-14713000	Weak transcription	Liver	Liver
14	chr20:14710600-14712000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr20:14710600-14713000	Weak transcription	Stomach Mucosa	stomach
16	chr20:14711600-14714600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr20:14712000-14713400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr20:14712800-14713600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr20:14713000-14713400	Enhancers	Fetal Kidney	kidney
20	chr20:14713000-14713600	Enhancers	Stomach Mucosa	stomach
21	chr20:14713000-14713800	Enhancers	Liver	Liver
22	chr20:14713200-14713600	Enhancers	Hela-S3	cervix
23	chr20:14713200-14713800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr20:14719000-14719200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr20:14719200-14721000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr20:14720600-14721800	Enhancers	Fetal Brain Male	brain
27	chr20:14721000-14721400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr20:14721000-14721400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr20:14721000-14721800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr20:14721200-14721600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr20:14721200-14721800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr20:14721200-14721800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr20:14721200-14721800	Enhancers	Fetal Brain Female	brain
34	chr20:14721200-14722000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr20:14721200-14722000	Enhancers	Brain Germinal Matrix	brain
36	chr20:14721400-14721600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr20:14721600-14726800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr20:14724800-14726200	Enhancers	GM12878-XiMat	blood
39	chr20:14726000-14727600	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr20:14726200-14726600	Enhancers	Fetal Kidney	kidney
41	chr20:14726600-14727000	Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr20:14726800-14727000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr20:14727000-14727600	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr20:14738200-14738600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr20:14738400-14738600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr20:14740600-14740800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr20:14742800-14743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr20:14743000-14744000	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr20:14743400-14744200	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr20:14745200-14746200	Enhancers	Stomach Mucosa	stomach

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