Variant report

Variant	nsv1055499
Chromosome Location	chr20:14224873-14848061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3684)
CpG islands
(count:550)
Chromatin interactive
region (count:71)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3684 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14318093-14318568	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14590214-14590575	HepG2	liver:	n/a	n/a
3	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
4	ATF2	chr20:14519085-14519448	GM12878	blood:	n/a	n/a
5	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14318056-14318625	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr20:14318135-14318567	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr20:14318117-14318567	GM12878	blood:	n/a	n/a
15	ATF2	chr20:14318094-14318593	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
17	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
18	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
20	ATF3	chr20:14613673-14613899	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr20:14603385-14603865	A549	lung:	n/a	n/a
22	ATF3	chr20:14386976-14387666	A549	lung:	n/a	n/a
23	ATF3	chr20:14613539-14613866	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
25	ATF3	chr20:14317954-14318560	A549	lung:	n/a	chr20:14318315-14318328 chr20:14318314-14318329
26	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
27	ATF3	chr20:14386986-14387654	A549	lung:	n/a	n/a
28	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
29	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr20:14549483-14549672	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr20:14433593-14433608	K562	blood:	n/a	n/a
32	BACH1	chr20:14548845-14549180	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr20:14324408-14324687	GM12878	blood:	n/a	n/a
34	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
35	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
36	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
37	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
38	BATF	chr20:14470918-14471200	GM12878	blood:	n/a	chr20:14471085-14471095 chr20:14471084-14471095
39	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
40	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
41	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
42	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
43	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
44	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
45	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
46	BATF	chr20:14519115-14519423	GM12878	blood:	n/a	n/a
47	BATF	chr20:14382155-14382397	GM12878	blood:	n/a	chr20:14382255-14382266
48	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
49	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
50	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14318398-14318448	IMR90	lung:	fetal
2	chr20:14318398-14318448	IMR90	lung:	fetal
3	chr20:14319035-14319085	BJ	skin:	n/a
4	chr20:14318174-14318224	SK-N-SH_RA	brain:	n/a
5	chr20:14307665-14307715	ProgFib	skin:	n/a
6	chr20:14318152-14318202	AoSMC	blood vessel:	n/a
7	chr20:14318152-14318202	AG09309	skin:	n/a
8	chr20:14318174-14318224	H1-hESC	embryonic stem cell:	embryo
9	chr20:14319035-14319085	HCF	heart:	n/a
10	chr20:14318174-14318224	AG09319	gingival:	n/a
11	chr20:14319035-14319085	HL-60	blood:	n/a
12	chr20:14318297-14318347	NHDF-neo	bronchial:	n/a
13	chr20:14318152-14318202	HCM	heart:	n/a
14	chr20:14318174-14318224	SAEC	small airway:	n/a
15	chr20:14318297-14318347	NH-A	brain:	n/a
16	chr20:14318410-14318460	GM06990	blood:	n/a
17	chr20:14318398-14318448	HCPEpiC	choroid plexus:	n/a
18	chr20:14318152-14318202	PFSK-1	brain:	n/a
19	chr20:14318398-14318448	SK-N-SH	brain:	n/a
20	chr20:14318398-14318448	LNCaP	prostate:	n/a
21	chr20:14318231-14318281	NB4	blood:	n/a
22	chr20:14318231-14318281	AG10803	skin:	n/a
23	chr20:14318174-14318224	HCT-116	colon:	n/a
24	chr20:14318231-14318281	U87	brain:	n/a
25	chr20:14318297-14318347	GM12892	blood:	n/a
26	chr20:14318410-14318460	HEK293	kidney:	embryo
27	chr20:14318174-14318224	NB4	blood:	n/a
28	chr20:14319035-14319085	GM12878	blood:	n/a
29	chr20:14318410-14318460	SAEC	small airway:	n/a
30	chr20:14318174-14318224	ProgFib	skin:	n/a
31	chr20:14307665-14307715	H1-hESC	embryonic stem cell:	embryo
32	chr20:14318174-14318224	SK-N-MC	brain:	n/a
33	chr20:14319035-14319085	SK-N-SH	brain:	n/a
34	chr20:14318398-14318448	HL-60	blood:	n/a
35	chr20:14319125-14319175	GM19239	blood:	n/a
36	chr20:14318231-14318281	AoSMC	blood vessel:	n/a
37	chr20:14319125-14319175	ovcar-3	ovarian:	n/a
38	chr20:14318398-14318448	AG04450	lung:	fetal
39	chr20:14318297-14318347	GM12878	blood:	n/a
40	chr20:14318174-14318224	CMK	blood:	n/a
41	chr20:14318297-14318347	HRCEpiC	kidney:	n/a
42	chr20:14318297-14318347	PANC-1	pancreas:	n/a
43	chr20:14307665-14307715	Hepatocyte	liver:	n/a
44	chr20:14318152-14318202	AG09319	gingival:	n/a
45	chr20:14307665-14307715	AG10803	skin:	n/a
46	chr20:14318152-14318202	GM12892	blood:	n/a
47	chr20:14307665-14307715	U87	brain:	n/a
48	chr20:14318297-14318347	T-47D	breast:	n/a
49	chr20:14319035-14319085	AG09319	gingival:	n/a
50	chr20:14318152-14318202	HCT-116	colon:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
2	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
3	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
4	chr20:14606804..14608358-chr20:14690132..14692728,2	MCF-7	breast:
5	chr20:14601339..14605162-chr20:14611440..14614800,3	MCF-7	breast:
6	chr20:14349761..14351392-chr20:14353398..14355373,2	K562	blood:
7	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
8	chr20:14314454..14317198-chr20:14325361..14327046,2	K562	blood:
9	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
10	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
11	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
12	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
13	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
14	chr20:14246857..14249567-chr20:14268278..14270770,2	K562	blood:
15	chr20:14469605..14471318-chr20:14479870..14481906,2	MCF-7	breast:
16	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
17	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
18	chr20:14246857..14249567-chr20:14268278..14270770,2	K562	blood:
19	chr20:14487196..14489290-chr20:14493950..14495618,2	MCF-7	breast:
20	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
21	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
22	chr20:14527106..14529484-chr20:14530662..14532376,3	MCF-7	breast:
23	chr20:14349761..14351392-chr20:14353398..14355373,2	K562	blood:
24	chr20:14392722..14394222-chr20:14395947..14398400,2	MCF-7	breast:
25	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
26	chr20:14314454..14317198-chr20:14325361..14327046,2	K562	blood:
27	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
28	chr20:14657146..14658733-chr20:17661268..17663723,2	MCF-7	breast:
29	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
30	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
31	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
32	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
33	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
34	chr20:14601339..14605162-chr20:14611440..14614800,3	MCF-7	breast:
35	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
36	chr20:14512165..14513979-chr20:14521499..14523425,2	MCF-7	breast:
37	chr20:14392722..14394222-chr20:14395947..14398400,2	MCF-7	breast:
38	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
39	chr20:14170212..14170967-chr20:14245501..14246136,3	MCF-7	breast:
40	chr20:14305353..14307056-chr20:14308528..14310326,2	MCF-7	breast:
41	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
42	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
43	chr20:14305353..14307056-chr20:14308528..14310326,2	MCF-7	breast:
44	chr17:41399300..41401884-chr20:14313065..14316065,3	K562	blood:
45	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
46	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
47	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
48	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
49	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
50	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
2	lnc-C20orf7-1	chr20:14607710-14607752	ENSG00000227927.1
3	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078716
4	lnc-C20orf7-1	chr20:14602412-14602575	ENSG00000227927.1
5	lnc-C20orf7-1	chr20:14607559-14607752	ENSG00000227927.2
6	lnc-C20orf7-1	chr20:14603520-14603660	ENSG00000227927.1
7	lnc-C20orf7-4	chr20:14591719-14595690	NONHSAT078719
8	lnc-C20orf7-1	chr20:14609283-14609475	ENSG00000227927.2
9	lnc-SEL1L2-3	chr20:14309568-14309973	NONHSAT078712
10	lnc-C20orf7-3	chr20:14504044-14504100	NONHSAT078716
11	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
12	lnc-FLRT3-3	chr20:14527830-14528269	NONHSAT078717
13	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
14	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078714
15	lnc-SEL1L2-3	chr20:14318050-14318260	NONHSAT078712
16	lnc-C20orf7-3	chr20:14474125-14474154	NONHSAT078714
17	lnc-C20orf7-1	chr20:14535030-14535074	ENSG00000227927.1
18	lnc-C20orf7-1	chr20:14617092-14617170	ENSG00000227927.2
19	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
20	lnc-C20orf7-1	chr20:14609283-14609554	ENSG00000227927.1
21	lnc-C20orf7-1	chr20:14612487-14612595	ENSG00000227927.2

No data

Variant related genes	Relation type
MACROD2	TF binding region
RPS10P2	TF binding region
ENSG00000227563	TF binding region
FLRT3	TF binding region
MACROD2-IT1	TF binding region
RNU6-228P	TF binding region
MACROD2	CpG island
RPS10P2	CpG island
ENSG00000227563	CpG island
FLRT3	CpG island
MACROD2-IT1	CpG island
RNU6-228P	CpG island
ENSG00000227563	chromatin interactions
ENSG00000227927	chromatin interactions
ENSG00000125844	chromatin interactions

Extended variants
information (count: 18607 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:18607 , 50 per page) page: 1 2 3 4 5 6 7 ... 373

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548341801	chr20:14224900-14224901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189741997	chr20:14224904-14224905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537583779	chr20:14224907-14224908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6079371	chr20:14224943-14224944	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs544576731	chr20:14225032-14225033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191501808	chr20:14225040-14225041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539796861	chr20:14225044-14225045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62209006	chr20:14225046-14225047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553312426	chr20:14225099-14225100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541366722	chr20:14225102-14225103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535667860	chr20:14225127-14225128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551159066	chr20:14225148-14225149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6042614	chr20:14225155-14225156	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs575330929	chr20:14225160-14225161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544334728	chr20:14225205-14225206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74501010	chr20:14225270-14225271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6042615	chr20:14225294-14225295	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs145375274	chr20:14225314-14225315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183885335	chr20:14225336-14225337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528733734	chr20:14225345-14225346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548583454	chr20:14225354-14225355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6042616	chr20:14225402-14225403	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538269536	chr20:14225432-14225433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77170225	chr20:14225439-14225440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114990572	chr20:14225465-14225466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570816888	chr20:14225475-14225476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201795080	chr20:14225514-14225515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116618555	chr20:14225534-14225535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556634348	chr20:14225563-14225564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111781123	chr20:14225589-14225590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568814844	chr20:14225703-14225704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188262709	chr20:14225704-14225705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537744888	chr20:14225713-14225714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554787502	chr20:14225732-14225733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112572582	chr20:14225798-14225799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7270429	chr20:14225834-14225835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113281258	chr20:14225851-14225852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7270435	chr20:14225865-14225866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577287250	chr20:14225878-14225879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6042617	chr20:14225901-14225902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559749764	chr20:14225948-14225949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11477339	chr20:14226009-14226010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570534614	chr20:14226025-14226026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573290759	chr20:14226029-14226030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542553884	chr20:14226075-14226076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189995106	chr20:14226099-14226100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77143974	chr20:14226103-14226104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544443619	chr20:14226109-14226110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144383565	chr20:14226111-14226112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140751603	chr20:14226119-14226120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Esophageal adenocarcinoma	18519675	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

Chromatin state (count:2592 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14222000-14235200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr20:14224400-14227400	Enhancers	Fetal Heart	heart
3	chr20:14224800-14225400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr20:14225000-14225400	Enhancers	Rectal Smooth Muscle	rectum
5	chr20:14225400-14226400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr20:14225400-14226600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr20:14225600-14226800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr20:14226200-14226600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr20:14226200-14226600	Enhancers	Adipose Nuclei	Adipose
10	chr20:14226200-14227200	Enhancers	Colon Smooth Muscle	Colon
11	chr20:14226400-14227000	Enhancers	Rectal Smooth Muscle	rectum
12	chr20:14226800-14227000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr20:14227400-14228000	Weak transcription	Fetal Heart	heart
14	chr20:14228000-14228600	Enhancers	Fetal Heart	heart
15	chr20:14228600-14229800	Weak transcription	Fetal Heart	heart
16	chr20:14229800-14231000	Enhancers	Fetal Heart	heart
17	chr20:14230000-14230400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr20:14236600-14240200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr20:14237200-14237600	Enhancers	Colon Smooth Muscle	Colon
20	chr20:14240000-14241000	Enhancers	NHDF-Ad	bronchial
21	chr20:14240000-14241200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr20:14240000-14241200	Enhancers	HMEC	breast
23	chr20:14240000-14241400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr20:14240000-14241400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr20:14240000-14241800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr20:14240200-14240600	Enhancers	NHLF	lung
27	chr20:14240200-14240800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr20:14240200-14240800	Enhancers	Fetal Heart	heart
29	chr20:14240200-14241000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr20:14240200-14241000	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr20:14240200-14241000	Enhancers	NHEK	skin
32	chr20:14240200-14241400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr20:14240200-14241400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr20:14240200-14241400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr20:14240400-14241000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr20:14240400-14241200	Enhancers	Adipose Nuclei	Adipose
37	chr20:14248200-14248400	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr20:14248600-14249600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr20:14249600-14250000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr20:14258400-14259000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr20:14258400-14259200	Enhancers	NHEK	skin
42	chr20:14258400-14260000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr20:14258600-14259200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr20:14258600-14261600	Enhancers	HMEC	breast
45	chr20:14259000-14263400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr20:14259200-14261000	Weak transcription	NHEK	skin
47	chr20:14260000-14263200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr20:14260800-14261400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr20:14261000-14261400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr20:14261000-14261600	Enhancers	NHEK	skin

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