Variant report

Variant	nsv585456
Chromosome Location	chr20:14668243-14954943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2327)
CpG islands
(count:61)
Chromatin interactive
region (count:66)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2327 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
3	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
4	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
15	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
16	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
17	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
18	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
19	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
20	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
21	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
24	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
25	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
26	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
27	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
28	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
29	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
30	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
31	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
32	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
33	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
34	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
35	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
36	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
37	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
38	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
39	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
40	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
41	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
42	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
44	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
46	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
47	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
48	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
49	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
50	BCL11A	chr20:14883096-14883392	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	GM12878	blood:	n/a
2	chr20:14904432-14904482	AG10803	skin:	n/a
3	chr20:14904432-14904482	SK-N-SH	brain:	n/a
4	chr20:14904432-14904482	AG09309	skin:	n/a
5	chr20:14904432-14904482	LNCaP	prostate:	n/a
6	chr20:14904432-14904482	GM06990	blood:	n/a
7	chr20:14904432-14904482	SAEC	small airway:	n/a
8	chr20:14904432-14904482	BE2_C	brain:	n/a
9	chr20:14904432-14904482	CMK	blood:	n/a
10	chr20:14904432-14904482	SKMC	muscle:	n/a
11	chr20:14904432-14904482	NHBE	bronchial:	n/a
12	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
13	chr20:14904432-14904482	AG04449	skin:	fetal
14	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
15	chr20:14904432-14904482	NT2-D1	testis:	n/a
16	chr20:14904432-14904482	T-47D	breast:	n/a
17	chr20:14904432-14904482	GM12891	blood:	n/a
18	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
19	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
20	chr20:14904432-14904482	PANC-1	pancreas:	n/a
21	chr20:14904432-14904482	AG04450	lung:	fetal
22	chr20:14904432-14904482	U87	brain:	n/a
23	chr20:14904432-14904482	Jurkat	blood:	n/a
24	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
25	chr20:14904432-14904482	BJ	skin:	n/a
26	chr20:14904432-14904482	HCF	heart:	n/a
27	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
28	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
29	chr20:14904432-14904482	AG09319	gingival:	n/a
30	chr20:14904432-14904482	A549	lung:	n/a
31	chr20:14904432-14904482	HRPEpiC	eye:	n/a
32	chr20:14904432-14904482	HL-60	blood:	n/a
33	chr20:14904432-14904482	Caco-2	colon:	n/a
34	chr20:14904432-14904482	Hepatocyte	liver:	n/a
35	chr20:14904432-14904482	HIPEpiC	eye:	n/a
36	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
37	chr20:14904432-14904482	SK-N-MC	brain:	n/a
38	chr20:14904432-14904482	GM19239	blood:	n/a
39	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
40	chr20:14904432-14904482	HMEC	breast:	n/a
41	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
42	chr20:14904432-14904482	PFSK-1	brain:	n/a
43	chr20:14904432-14904482	K562	blood:	n/a
44	chr20:14904432-14904482	RPTEC	kidney:	n/a
45	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
46	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
47	chr20:14904432-14904482	IMR90	lung:	fetal
48	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
49	chr20:14904432-14904482	NH-A	brain:	n/a
50	chr20:14904432-14904482	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
2	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
3	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
4	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
5	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
6	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
7	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
8	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
9	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
10	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
11	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
12	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
13	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
14	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
15	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
16	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
17	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
18	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
19	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
20	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
21	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
22	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
23	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
24	chr20:14606804..14608358-chr20:14690132..14692728,2	MCF-7	breast:
25	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
26	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
27	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
28	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
29	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
30	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
31	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
32	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
33	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
34	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
35	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
36	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
37	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
38	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
39	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
40	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
41	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
42	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
43	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
44	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
45	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
46	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
47	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
48	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
49	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
50	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:

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

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

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
ENSG00000227927	chromatin interactions
ENSG00000237832	chromatin interactions

Extended variants
information (count: 8710 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:8710 , 50 per page) page: 1 2 3 4 5 6 7 ... 175

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6034010	chr20:14668243-14668244	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557750685	chr20:14668261-14668262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561028004	chr20:14668273-14668274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529374186	chr20:14668286-14668287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146765756	chr20:14668310-14668311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540425635	chr20:14668412-14668413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140375599	chr20:14668444-14668445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145264782	chr20:14668450-14668451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182112573	chr20:14668493-14668494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563267618	chr20:14668561-14668562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186863342	chr20:14668592-14668593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529872886	chr20:14668644-14668645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549033694	chr20:14668652-14668653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374340730	chr20:14668666-14668667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567365465	chr20:14668742-14668743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150919366	chr20:14668744-14668745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546732645	chr20:14668745-14668746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140782557	chr20:14668792-14668793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538896270	chr20:14668806-14668807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556951711	chr20:14668929-14668930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575188863	chr20:14668985-14668986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536233280	chr20:14668986-14668987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554592915	chr20:14668996-14668997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572957111	chr20:14669113-14669114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190372142	chr20:14669144-14669145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565444000	chr20:14669181-14669182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577390012	chr20:14669200-14669201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544819377	chr20:14669209-14669210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142260846	chr20:14669226-14669227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563160614	chr20:14669245-14669246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375807125	chr20:14669372-14669373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114196589	chr20:14669392-14669393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548951942	chr20:14669403-14669404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560875211	chr20:14669424-14669425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138451602	chr20:14669428-14669429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181240400	chr20:14669445-14669446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534801751	chr20:14669533-14669534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6079529	chr20:14669539-14669540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537125730	chr20:14669582-14669583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551813650	chr20:14669593-14669594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538437894	chr20:14669612-14669613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141508442	chr20:14669695-14669696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117884014	chr20:14669714-14669715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568810966	chr20:14669723-14669724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149622650	chr20:14669762-14669763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554504941	chr20:14669764-14669765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185293325	chr20:14669807-14669808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368349381	chr20:14669838-14669839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534272127	chr20:14669942-14669943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558761995	chr20:14670036-14670037	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:1436 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14667400-14668800	Enhancers	HMEC	breast
2	chr20:14667600-14668600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr20:14667600-14668800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr20:14667600-14668800	Enhancers	NHEK	skin
5	chr20:14667600-14669000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr20:14667800-14668400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:14668000-14668400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr20:14668400-14680800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr20:14668800-14678000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr20:14671000-14671200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr20:14671600-14672800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr20:14672800-14673400	Enhancers	GM12878-XiMat	blood
13	chr20:14672800-14673600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr20:14673400-14675800	Weak transcription	GM12878-XiMat	blood
15	chr20:14674600-14674800	Enhancers	Pancreas	Pancrea
16	chr20:14674800-14681400	Weak transcription	Pancreas	Pancrea
17	chr20:14675400-14677800	Enhancers	Fetal Heart	heart
18	chr20:14675800-14676400	Enhancers	GM12878-XiMat	blood
19	chr20:14676000-14676400	Enhancers	Fetal Lung	lung
20	chr20:14676200-14676600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr20:14676400-14677800	Weak transcription	Fetal Lung	lung
22	chr20:14676400-14681200	Weak transcription	GM12878-XiMat	blood
23	chr20:14677000-14677800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr20:14677000-14677800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr20:14677000-14678000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr20:14677200-14678600	Enhancers	Adipose Nuclei	Adipose
27	chr20:14677200-14678800	Enhancers	Colon Smooth Muscle	Colon
28	chr20:14677600-14677800	Enhancers	Fetal Kidney	kidney
29	chr20:14677600-14677800	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr20:14677600-14678000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr20:14677600-14678200	Enhancers	Rectal Smooth Muscle	rectum
32	chr20:14677600-14678800	Enhancers	Liver	Liver
33	chr20:14677800-14678000	Enhancers	Fetal Lung	lung
34	chr20:14677800-14678000	Enhancers	NHEK	skin
35	chr20:14677800-14678200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr20:14677800-14679600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr20:14677800-14681000	Weak transcription	Fetal Kidney	kidney
38	chr20:14677800-14681200	Weak transcription	Fetal Heart	heart
39	chr20:14677800-14681600	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr20:14678000-14678200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr20:14678000-14679600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr20:14678000-14679800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr20:14678000-14679800	Weak transcription	NHEK	skin
44	chr20:14678000-14682000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr20:14678200-14678400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr20:14678200-14680000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr20:14678200-14681400	Weak transcription	Rectal Smooth Muscle	rectum
48	chr20:14678400-14680800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr20:14678600-14678800	Enhancers	Fetal Intestine Large	intestine
50	chr20:14678600-14679000	Enhancers	Skeletal Muscle Female	skeletal muscle

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