Variant report

Variant	nsv585476
Chromosome Location	chr20:14737843-14954943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1910)
CpG islands
(count:61)
Chromatin interactive
region (count:58)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1910 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

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	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
5	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
14	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
15	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
16	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
17	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
20	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
21	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
22	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
23	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
24	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
25	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
26	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
27	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
28	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
29	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
30	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
31	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
32	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
33	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
34	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
35	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
36	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
37	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
38	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
39	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
40	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
41	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
42	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
44	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
45	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
46	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
47	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
48	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
49	BCL3	chr20:14826038-14826561	A549	lung:	n/a	chr20:14826452-14826461
50	BCL3	chr20:14859331-14860569	A549	lung:	n/a	chr20:14860151-14860160 chr20:14859419-14859428 chr20:14860265-14860274

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	PANC-1	pancreas:	n/a
2	chr20:14904432-14904482	HL-60	blood:	n/a
3	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
4	chr20:14904432-14904482	IMR90	lung:	fetal
5	chr20:14904432-14904482	Hepatocyte	liver:	n/a
6	chr20:14904432-14904482	GM12892	blood:	n/a
7	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
8	chr20:14904432-14904482	PrEC	prostate:	n/a
9	chr20:14904432-14904482	AG10803	skin:	n/a
10	chr20:14904432-14904482	AG09309	skin:	n/a
11	chr20:14904432-14904482	A549	lung:	n/a
12	chr20:14904432-14904482	HMEC	breast:	n/a
13	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
14	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
15	chr20:14904432-14904482	GM19239	blood:	n/a
16	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
17	chr20:14904432-14904482	BJ	skin:	n/a
18	chr20:14904432-14904482	RPTEC	kidney:	n/a
19	chr20:14904432-14904482	AG04450	lung:	fetal
20	chr20:14904432-14904482	SK-N-MC	brain:	n/a
21	chr20:14904432-14904482	HRE	kidney:	n/a
22	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
23	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
24	chr20:14904432-14904482	CMK	blood:	n/a
25	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
26	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
27	chr20:14904432-14904482	GM06990	blood:	n/a
28	chr20:14904432-14904482	HCF	heart:	n/a
29	chr20:14904432-14904482	AG04449	skin:	fetal
30	chr20:14904432-14904482	HepG2	liver:	n/a
31	chr20:14904432-14904482	PFSK-1	brain:	n/a
32	chr20:14904432-14904482	HIPEpiC	eye:	n/a
33	chr20:14904432-14904482	T-47D	breast:	n/a
34	chr20:14904432-14904482	Jurkat	blood:	n/a
35	chr20:14904432-14904482	Hela-S3	cervix:	n/a
36	chr20:14904432-14904482	SKMC	muscle:	n/a
37	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
38	chr20:14904432-14904482	MCF-7	breast:	n/a
39	chr20:14904432-14904482	HCT-116	colon:	n/a
40	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
41	chr20:14904432-14904482	GM12878	blood:	n/a
42	chr20:14904432-14904482	K562	blood:	n/a
43	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
44	chr20:14904432-14904482	HEK293	kidney:	embryo
45	chr20:14904432-14904482	NT2-D1	testis:	n/a
46	chr20:14904432-14904482	NB4	blood:	n/a
47	chr20:14904432-14904482	HRPEpiC	eye:	n/a
48	chr20:14904432-14904482	NH-A	brain:	n/a
49	chr20:14904432-14904482	AG09319	gingival:	n/a
50	chr20:14904432-14904482	SK-N-SH	brain:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
2	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
3	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
4	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
5	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
6	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
7	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
8	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
9	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
10	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
11	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
12	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
13	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
14	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
15	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
16	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
17	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
18	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
19	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
20	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
21	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
22	chr20:14819830..14820468-chr4:11534089..11534643,2	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	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
26	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
27	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
28	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
29	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
30	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
31	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
32	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
33	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
34	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
35	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
36	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
37	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
38	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
39	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
40	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
41	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
42	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
43	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
44	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
45	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
46	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
47	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
48	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
49	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
50	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 6578 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6578 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528347975	chr20:14738222-14738223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542402363	chr20:14738228-14738229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184541428	chr20:14738301-14738302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532575923	chr20:14738346-14738347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550777137	chr20:14738375-14738376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569308671	chr20:14738424-14738425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188942781	chr20:14738443-14738444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572505335	chr20:14738459-14738460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192074095	chr20:14738462-14738463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371963368	chr20:14738469-14738470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566768269	chr20:14738478-14738479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534212431	chr20:14738491-14738492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558856370	chr20:14738497-14738498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561814578	chr20:14738544-14738545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538600426	chr20:14738571-14738572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556700047	chr20:14738572-14738573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185041476	chr20:14738592-14738593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189502052	chr20:14738597-14738598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116963724	chr20:14740618-14740619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527747547	chr20:14740637-14740638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556006297	chr20:14740652-14740653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190802302	chr20:14740671-14740672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566518089	chr20:14740684-14740685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145377319	chr20:14740686-14740687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532837574	chr20:14740723-14740724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181683408	chr20:14740780-14740781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4814324	chr20:14742830-14742831	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs545730465	chr20:14742840-14742841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563917473	chr20:14742846-14742847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576023016	chr20:14742847-14742848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543131449	chr20:14742885-14742886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs16994918	chr20:14742886-14742887	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528972437	chr20:14742909-14742910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547151104	chr20:14742917-14742918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559128112	chr20:14742945-14742946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs204101	chr20:14742951-14742952	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs370273126	chr20:14742962-14742963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557925766	chr20:14742971-14742972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551686228	chr20:14742972-14742973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184695057	chr20:14743003-14743004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537421966	chr20:14743157-14743158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188470076	chr20:14743175-14743176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567720788	chr20:14743236-14743237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs204102	chr20:14743248-14743249	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553601812	chr20:14743249-14743250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs578154395	chr20:14743259-14743260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs204103	chr20:14743269-14743270	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs557664569	chr20:14743303-14743304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575871359	chr20:14743330-14743331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147907159	chr20:14743339-14743340	Enhancers	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:1026 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14738200-14738600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr20:14738400-14738600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr20:14740600-14740800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr20:14742800-14743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr20:14743000-14744000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr20:14743400-14744200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr20:14745200-14746200	Enhancers	Stomach Mucosa	stomach
8	chr20:14746000-14746200	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr20:14750600-14756200	Weak transcription	Psoas Muscle	Psoas
10	chr20:14755800-14757200	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr20:14756000-14756400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr20:14756000-14756400	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr20:14756000-14756800	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr20:14756000-14756800	Enhancers	Hela-S3	cervix
15	chr20:14756000-14757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr20:14756000-14757200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr20:14756000-14757200	Enhancers	A549	lung
18	chr20:14756000-14759200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr20:14756200-14756800	Enhancers	Psoas Muscle	Psoas
20	chr20:14756200-14757000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr20:14756200-14757000	Enhancers	HepG2	liver
22	chr20:14756200-14757000	Enhancers	HMEC	breast
23	chr20:14756200-14757200	Enhancers	NHEK	skin
24	chr20:14756600-14757000	Enhancers	Fetal Intestine Small	intestine
25	chr20:14756600-14757200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr20:14756800-14757000	Enhancers	NHDF-Ad	bronchial
27	chr20:14757000-14758000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr20:14757000-14758000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr20:14757000-14758200	Weak transcription	HMEC	breast
30	chr20:14757200-14757600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr20:14757200-14757600	Weak transcription	NHEK	skin
32	chr20:14757200-14758000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr20:14757600-14759000	Enhancers	NHEK	skin
34	chr20:14757600-14759600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr20:14758000-14758600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr20:14758000-14758800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr20:14758000-14759200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr20:14758200-14758800	Enhancers	HMEC	breast
39	chr20:14758600-14758800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr20:14758600-14759400	Enhancers	NHDF-Ad	bronchial
41	chr20:14758600-14761200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr20:14759200-14760800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr20:14759200-14760800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr20:14760600-14761600	Enhancers	HUVEC	blood vessel
45	chr20:14760800-14761800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr20:14760800-14762200	Enhancers	Muscle Satellite Cultured Cells	--
47	chr20:14761200-14761800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr20:14763200-14763800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr20:14763200-14764000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr20:14763400-14763800	Enhancers	HUES6 Cell Line	embryonic stem cell

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