Variant report

Variant	nsv1056497
Chromosome Location	chr20:14628216-14910061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1857)
CpG islands
(count:61)
Chromatin interactive
region (count:60)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
2	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
3	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14810438-14811025	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	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
19	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
21	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
22	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
23	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
24	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
25	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
26	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
27	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
28	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
29	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
30	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
31	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
32	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
33	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
34	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
35	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
36	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
37	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
38	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
39	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
40	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
41	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
42	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
44	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
46	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
47	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
48	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
49	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
50	BCL11A	chr20:14811187-14811493	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	MCF-7	breast:	n/a
2	chr20:14904432-14904482	CMK	blood:	n/a
3	chr20:14904432-14904482	SK-N-MC	brain:	n/a
4	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
5	chr20:14904432-14904482	HL-60	blood:	n/a
6	chr20:14904432-14904482	PANC-1	pancreas:	n/a
7	chr20:14904432-14904482	Jurkat	blood:	n/a
8	chr20:14904432-14904482	GM06990	blood:	n/a
9	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
10	chr20:14904432-14904482	U87	brain:	n/a
11	chr20:14904432-14904482	AG09319	gingival:	n/a
12	chr20:14904432-14904482	SK-N-SH	brain:	n/a
13	chr20:14904432-14904482	A549	lung:	n/a
14	chr20:14904432-14904482	HCT-116	colon:	n/a
15	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
16	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
17	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
18	chr20:14904432-14904482	HRPEpiC	eye:	n/a
19	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
20	chr20:14904432-14904482	GM12878	blood:	n/a
21	chr20:14904432-14904482	PFSK-1	brain:	n/a
22	chr20:14904432-14904482	HepG2	liver:	n/a
23	chr20:14904432-14904482	GM19239	blood:	n/a
24	chr20:14904432-14904482	AG09309	skin:	n/a
25	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
26	chr20:14904432-14904482	HRE	kidney:	n/a
27	chr20:14904432-14904482	LNCaP	prostate:	n/a
28	chr20:14904432-14904482	NH-A	brain:	n/a
29	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
30	chr20:14904432-14904482	GM12891	blood:	n/a
31	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
32	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
33	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
34	chr20:14904432-14904482	ProgFib	skin:	n/a
35	chr20:14904432-14904482	SAEC	small airway:	n/a
36	chr20:14904432-14904482	RPTEC	kidney:	n/a
37	chr20:14904432-14904482	K562	blood:	n/a
38	chr20:14904432-14904482	AG04449	skin:	fetal
39	chr20:14904432-14904482	NHBE	bronchial:	n/a
40	chr20:14904432-14904482	SKMC	muscle:	n/a
41	chr20:14904432-14904482	AG10803	skin:	n/a
42	chr20:14904432-14904482	HIPEpiC	eye:	n/a
43	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
44	chr20:14904432-14904482	BE2_C	brain:	n/a
45	chr20:14904432-14904482	NT2-D1	testis:	n/a
46	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
47	chr20:14904432-14904482	BJ	skin:	n/a
48	chr20:14904432-14904482	Hela-S3	cervix:	n/a
49	chr20:14904432-14904482	AG04450	lung:	fetal
50	chr20:14904432-14904482	NB4	blood:	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	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
3	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
4	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
5	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
6	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
7	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
8	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
9	chr20:14657146..14658733-chr20:17661268..17663723,2	MCF-7	breast:
10	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
11	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
12	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
13	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
14	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
15	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
16	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
17	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
18	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
19	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
20	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
21	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
22	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
23	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
24	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
25	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
26	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
27	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
28	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
29	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
30	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
31	chr20:14606804..14608358-chr20:14690132..14692728,2	MCF-7	breast:
32	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
33	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
34	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
35	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
36	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
37	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
38	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
39	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
40	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
41	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
42	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
43	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
44	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
45	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
46	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
47	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
48	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
49	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
50	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
2	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
3	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
4	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
5	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
6	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
7	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
8	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078714
9	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
10	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
11	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
12	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078716
13	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
14	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
15	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
16	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
17	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
18	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
19	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
20	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
21	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
22	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
23	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
24	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
25	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841

No data

Variant related genes	Relation type
RPS10P2	TF binding region
RPS10P2	CpG island
ENSG00000125844	chromatin interactions
ENSG00000227927	chromatin interactions
ENSG00000237832	chromatin interactions

Extended variants
information (count: 8034 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:8034 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574528398	chr20:14629813-14629814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541679307	chr20:14629884-14629885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6042838	chr20:14629913-14629914	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs535534032	chr20:14629924-14629925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527566776	chr20:14629939-14629940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545721256	chr20:14629964-14629965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555109141	chr20:14629972-14629973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564137360	chr20:14629988-14629989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531638492	chr20:14630000-14630001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550211451	chr20:14630001-14630002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568467352	chr20:14630023-14630024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529464827	chr20:14630069-14630070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12626056	chr20:14630071-14630072	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs566289594	chr20:14630074-14630075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540131848	chr20:14630147-14630148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140201221	chr20:14630151-14630152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192189978	chr20:14630157-14630158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150312978	chr20:14630172-14630173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556195641	chr20:14630178-14630179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574463453	chr20:14630279-14630280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184090275	chr20:14630418-14630419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534571046	chr20:14630432-14630433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113450804	chr20:14630433-14630434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545684389	chr20:14630442-14630443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs8119230	chr20:14630445-14630446	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs531554101	chr20:14630493-14630494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549058875	chr20:14630522-14630523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543475892	chr20:14630527-14630528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562180027	chr20:14630534-14630535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529344969	chr20:14630577-14630578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs193200089	chr20:14630607-14630608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543280156	chr20:14630638-14630639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528957744	chr20:14630648-14630649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566264642	chr20:14630687-14630688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533572917	chr20:14630691-14630692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6074769	chr20:14630824-14630825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6042839	chr20:14630871-14630872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552056195	chr20:14630887-14630888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138008784	chr20:14630888-14630889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143240923	chr20:14630892-14630893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111650626	chr20:14630917-14630918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555869772	chr20:14630961-14630962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147084181	chr20:14630962-14630963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74624743	chr20:14630963-14630964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553874137	chr20:14630966-14630967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542886411	chr20:14631009-14631010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73260863	chr20:14631026-14631027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557604323	chr20:14631027-14631028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184489553	chr20:14631058-14631059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188803890	chr20:14631127-14631128	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:1242 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14629800-14632200	Enhancers	Stomach Mucosa	stomach
2	chr20:14630000-14631000	Enhancers	Gastric	stomach
3	chr20:14631200-14631800	Enhancers	Fetal Lung	lung
4	chr20:14631800-14632200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr20:14632200-14635400	Weak transcription	Stomach Mucosa	stomach
6	chr20:14633600-14636000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr20:14635400-14636000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr20:14635400-14636000	Enhancers	Stomach Mucosa	stomach
9	chr20:14635600-14636800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr20:14636000-14636600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr20:14636000-14636800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr20:14636000-14636800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr20:14636200-14636800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr20:14636400-14637000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr20:14636600-14636800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr20:14636800-14637600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr20:14636800-14638200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr20:14637200-14639000	Enhancers	Fetal Lung	lung
19	chr20:14637600-14638200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr20:14637600-14638600	Enhancers	Fetal Stomach	stomach
21	chr20:14637600-14638800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr20:14637800-14638200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr20:14638000-14638200	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr20:14638000-14638600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr20:14638200-14638400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr20:14638400-14638800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr20:14638600-14640000	Weak transcription	Fetal Stomach	stomach
28	chr20:14639000-14640600	Weak transcription	Fetal Lung	lung
29	chr20:14640000-14640400	Enhancers	Fetal Stomach	stomach
30	chr20:14640400-14647400	Weak transcription	Fetal Stomach	stomach
31	chr20:14640600-14640800	Enhancers	Fetal Lung	lung
32	chr20:14644000-14645600	Enhancers	Fetal Brain Male	brain
33	chr20:14644800-14645200	Enhancers	Rectal Smooth Muscle	rectum
34	chr20:14644800-14645400	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr20:14645200-14645400	Weak transcription	Rectal Smooth Muscle	rectum
36	chr20:14645400-14645800	Enhancers	Rectal Smooth Muscle	rectum
37	chr20:14645600-14647400	Weak transcription	Fetal Brain Male	brain
38	chr20:14645800-14647600	Weak transcription	Rectal Smooth Muscle	rectum
39	chr20:14647000-14648600	Enhancers	Fetal Kidney	kidney
40	chr20:14647400-14647800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr20:14647400-14647800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr20:14647400-14647800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr20:14647400-14647800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr20:14647400-14647800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr20:14647400-14648600	Enhancers	Colon Smooth Muscle	Colon
46	chr20:14647400-14648600	Enhancers	Fetal Brain Female	brain
47	chr20:14647400-14648600	Enhancers	Fetal Stomach	stomach
48	chr20:14647400-14648800	Enhancers	Fetal Brain Male	brain
49	chr20:14647600-14647800	Enhancers	Rectal Smooth Muscle	rectum
50	chr20:14647600-14647800	Enhancers	Small Intestine	intestine

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