Variant report

Variant	nsv1055948
Chromosome Location	chr20:14719023-14938704
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1742)
CpG islands
(count:61)
Chromatin interactive
region (count:60)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1742 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

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	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
5	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
15	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
16	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
17	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
18	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
20	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
21	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
22	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
23	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
24	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
25	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
26	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
27	BATF	chr20:14725428-14725715	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	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
30	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
31	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
32	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
33	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
34	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
35	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
36	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
37	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
38	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
39	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
40	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
41	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
42	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
43	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
44	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
45	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
46	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
47	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
48	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
49	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
50	BCL11A	chr20:14833719-14834115	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	AG04449	skin:	fetal
2	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
3	chr20:14904432-14904482	GM12891	blood:	n/a
4	chr20:14904432-14904482	HIPEpiC	eye:	n/a
5	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
6	chr20:14904432-14904482	NHBE	bronchial:	n/a
7	chr20:14904432-14904482	GM19239	blood:	n/a
8	chr20:14904432-14904482	GM06990	blood:	n/a
9	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
10	chr20:14904432-14904482	BJ	skin:	n/a
11	chr20:14904432-14904482	HRPEpiC	eye:	n/a
12	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
13	chr20:14904432-14904482	HL-60	blood:	n/a
14	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
15	chr20:14904432-14904482	SKMC	muscle:	n/a
16	chr20:14904432-14904482	IMR90	lung:	fetal
17	chr20:14904432-14904482	Hela-S3	cervix:	n/a
18	chr20:14904432-14904482	MCF-7	breast:	n/a
19	chr20:14904432-14904482	PANC-1	pancreas:	n/a
20	chr20:14904432-14904482	NB4	blood:	n/a
21	chr20:14904432-14904482	K562	blood:	n/a
22	chr20:14904432-14904482	U87	brain:	n/a
23	chr20:14904432-14904482	A549	lung:	n/a
24	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
25	chr20:14904432-14904482	ProgFib	skin:	n/a
26	chr20:14904432-14904482	AG09309	skin:	n/a
27	chr20:14904432-14904482	Caco-2	colon:	n/a
28	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
29	chr20:14904432-14904482	SK-N-MC	brain:	n/a
30	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
31	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
32	chr20:14904432-14904482	HepG2	liver:	n/a
33	chr20:14904432-14904482	HMEC	breast:	n/a
34	chr20:14904432-14904482	HCF	heart:	n/a
35	chr20:14904432-14904482	GM12892	blood:	n/a
36	chr20:14904432-14904482	RPTEC	kidney:	n/a
37	chr20:14904432-14904482	SK-N-SH	brain:	n/a
38	chr20:14904432-14904482	HEK293	kidney:	embryo
39	chr20:14904432-14904482	NH-A	brain:	n/a
40	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
41	chr20:14904432-14904482	CMK	blood:	n/a
42	chr20:14904432-14904482	GM12878	blood:	n/a
43	chr20:14904432-14904482	Jurkat	blood:	n/a
44	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
45	chr20:14904432-14904482	T-47D	breast:	n/a
46	chr20:14904432-14904482	HCT-116	colon:	n/a
47	chr20:14904432-14904482	LNCaP	prostate:	n/a
48	chr20:14904432-14904482	AG09319	gingival:	n/a
49	chr20:14904432-14904482	AG10803	skin:	n/a
50	chr20:14904432-14904482	PFSK-1	brain:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
2	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
3	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
4	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
5	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
6	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
7	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
8	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
9	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
10	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
11	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
12	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
13	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
14	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
15	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
16	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
17	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
18	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
19	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
20	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
21	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
22	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
23	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
24	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
25	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
26	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
27	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
28	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
29	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
30	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
31	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
32	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
33	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
34	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
35	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
36	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
37	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
38	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
39	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
40	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
41	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
42	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
43	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
44	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
45	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
46	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
47	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
48	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
49	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
50	chr20:14835355..14837300-chr20:14840386..14842306,2	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	chr20:14910021-14910164	NR_110318
3	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
4	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
5	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
6	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
7	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
8	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
9	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
10	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
11	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
12	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
13	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
14	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
15	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
16	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
17	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
18	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
19	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
20	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
21	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
22	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
23	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
24	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
25	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
26	lnc-FLRT3-1	chr20:14885587-14886675	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
ENSG00000237832	chromatin interactions

Extended variants
information (count: 6273 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6273 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76358177	chr20:14719030-14719031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs16994866	chr20:14719049-14719050	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs556275386	chr20:14719074-14719075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373992377	chr20:14719080-14719081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34333338	chr20:14719119-14719120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574560456	chr20:14719132-14719133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138173316	chr20:14719139-14719140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560345856	chr20:14719192-14719193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs367903451	chr20:14719211-14719212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572207006	chr20:14719238-14719239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545774144	chr20:14719247-14719248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561765781	chr20:14719260-14719261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564444486	chr20:14719267-14719268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142760593	chr20:14719290-14719291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6034023	chr20:14719384-14719385	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs112417638	chr20:14719429-14719430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561768002	chr20:14719434-14719435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184944567	chr20:14719436-14719437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6042890	chr20:14719467-14719468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9941743	chr20:14719481-14719482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113940179	chr20:14719566-14719567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567971317	chr20:14719587-14719588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180973721	chr20:14719631-14719632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530652554	chr20:14719691-14719692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4814323	chr20:14719720-14719721	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs140182341	chr20:14719747-14719748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551773245	chr20:14719753-14719754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185393296	chr20:14719770-14719771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537766465	chr20:14719857-14719858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138857968	chr20:14719913-14719914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78051021	chr20:14719988-14719989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs36053997	chr20:14719993-14719994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535499184	chr20:14720057-14720058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553880705	chr20:14720089-14720090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188139292	chr20:14720094-14720095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148482651	chr20:14720098-14720099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6034024	chr20:14720114-14720115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs181943457	chr20:14720132-14720133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs13044671	chr20:14720134-14720135	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186290330	chr20:14720162-14720163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10581089	chr20:14720186-14720187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75056167	chr20:14720189-14720190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546336895	chr20:14720191-14720192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199580842	chr20:14720192-14720193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561700242	chr20:14720199-14720200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529293477	chr20:14720223-14720224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541116233	chr20:14720263-14720264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559830148	chr20:14720384-14720385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533340675	chr20:14720411-14720412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191773859	chr20:14720445-14720446	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:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14719000-14719200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr20:14719200-14721000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr20:14720600-14721800	Enhancers	Fetal Brain Male	brain
4	chr20:14721000-14721400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:14721000-14721400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr20:14721000-14721800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr20:14721200-14721600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr20:14721200-14721800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr20:14721200-14721800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr20:14721200-14721800	Enhancers	Fetal Brain Female	brain
11	chr20:14721200-14722000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr20:14721200-14722000	Enhancers	Brain Germinal Matrix	brain
13	chr20:14721400-14721600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr20:14721600-14726800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr20:14724800-14726200	Enhancers	GM12878-XiMat	blood
16	chr20:14726000-14727600	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr20:14726200-14726600	Enhancers	Fetal Kidney	kidney
18	chr20:14726600-14727000	Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr20:14726800-14727000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr20:14727000-14727600	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr20:14738200-14738600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr20:14738400-14738600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr20:14740600-14740800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr20:14742800-14743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr20:14743000-14744000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr20:14743400-14744200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr20:14745200-14746200	Enhancers	Stomach Mucosa	stomach
28	chr20:14746000-14746200	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr20:14750600-14756200	Weak transcription	Psoas Muscle	Psoas
30	chr20:14755800-14757200	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr20:14756000-14756400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr20:14756000-14756400	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr20:14756000-14756800	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr20:14756000-14756800	Enhancers	Hela-S3	cervix
35	chr20:14756000-14757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr20:14756000-14757200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr20:14756000-14757200	Enhancers	A549	lung
38	chr20:14756000-14759200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr20:14756200-14756800	Enhancers	Psoas Muscle	Psoas
40	chr20:14756200-14757000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr20:14756200-14757000	Enhancers	HepG2	liver
42	chr20:14756200-14757000	Enhancers	HMEC	breast
43	chr20:14756200-14757200	Enhancers	NHEK	skin
44	chr20:14756600-14757000	Enhancers	Fetal Intestine Small	intestine
45	chr20:14756600-14757200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr20:14756800-14757000	Enhancers	NHDF-Ad	bronchial
47	chr20:14757000-14758000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr20:14757000-14758000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr20:14757000-14758200	Weak transcription	HMEC	breast
50	chr20:14757200-14757600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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