Variant report

Variant	nsv1019790
Chromosome Location	chr5:96471680-96980633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3444)
CpG islands
(count:1772)
Chromatin interactive
region (count:104)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3444 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:96518910-96519735	K562	blood:	n/a	n/a
2	ARID3A	chr5:96559836-96560263	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:96517984-96519784	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:96632846-96633044	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:96869893-96870174	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:96517679-96517912	K562	blood:	n/a	n/a
7	ATF1	chr5:96566806-96567076	K562	blood:	n/a	n/a
8	ATF1	chr5:96518777-96519693	K562	blood:	n/a	n/a
9	ATF1	chr5:96925354-96925372	K562	blood:	n/a	n/a
10	ATF2	chr5:96883703-96884520	GM12878	blood:	n/a	n/a
11	ATF2	chr5:96518721-96519407	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:96736083-96736724	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr5:96503064-96503603	GM12878	blood:	n/a	n/a
14	ATF2	chr5:96503022-96503427	GM12878	blood:	n/a	n/a
15	ATF2	chr5:96736132-96736743	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr5:96518622-96519567	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr5:96518562-96519502	GM12878	blood:	n/a	n/a
18	ATF2	chr5:96883636-96884569	GM12878	blood:	n/a	n/a
19	ATF2	chr5:96518742-96519762	GM12878	blood:	n/a	n/a
20	ATF2	chr5:96691322-96691778	GM12878	blood:	n/a	n/a
21	ATF3	chr5:96518763-96519118	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr5:96518726-96519630	A549	lung:	n/a	n/a
23	ATF3	chr5:96518699-96519160	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr5:96518825-96519741	A549	lung:	n/a	n/a
25	ATF3	chr5:96485448-96485735	K562	blood:	n/a	n/a
26	ATF3	chr5:96518715-96519226	GM12878	blood:	n/a	n/a
27	ATF3	chr5:96518734-96519068	HepG2	liver:	n/a	n/a
28	ATF3	chr5:96518727-96519094	K562	blood:	n/a	n/a
29	BACH1	chr5:96518703-96519565	K562	blood:	n/a	n/a
30	BACH1	chr5:96600161-96600267	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr5:96885956-96886136	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr5:96514726-96514765	K562	blood:	n/a	n/a
33	BACH1	chr5:96861461-96861877	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr5:96883741-96884022	GM12878	blood:	n/a	n/a
35	BATF	chr5:96872429-96872695	GM12878	blood:	n/a	chr5:96872552-96872563
36	BATF	chr5:96528640-96528915	GM12878	blood:	n/a	n/a
37	BATF	chr5:96713332-96713631	GM12878	blood:	n/a	n/a
38	BATF	chr5:96884044-96884526	GM12878	blood:	n/a	chr5:96884341-96884350
39	BATF	chr5:96872418-96872668	GM12878	blood:	n/a	chr5:96872552-96872563
40	BATF	chr5:96503162-96503595	GM12878	blood:	n/a	chr5:96503383-96503394
41	BATF	chr5:96503177-96503536	GM12878	blood:	n/a	chr5:96503383-96503394
42	BATF	chr5:96883695-96884539	GM12878	blood:	n/a	chr5:96884341-96884350
43	BCL11A	chr5:96528575-96528962	GM12878	blood:	n/a	n/a
44	BCL11A	chr5:96883801-96884003	GM12878	blood:	n/a	chr5:96883828-96883837
45	BCL11A	chr5:96884033-96884506	GM12878	blood:	n/a	n/a
46	BCL11A	chr5:96736252-96736517	H1-hESC	embryonic stem cell:	n/a	n/a
47	BCL11A	chr5:96528568-96528924	GM12878	blood:	n/a	n/a
48	BCL11A	chr5:96736211-96736597	H1-hESC	embryonic stem cell:	n/a	n/a
49	BCL11A	chr5:96884015-96884504	GM12878	blood:	n/a	n/a
50	BCL11A	chr5:96713335-96713673	GM12878	blood:	n/a	n/a

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96477502-96477552	NHBE	bronchial:	n/a
2	chr5:96845117-96845167	AG10803	skin:	n/a
3	chr5:96479253-96479303	SKMC	muscle:	n/a
4	chr5:96477502-96477552	NHBE	bronchial:	n/a
5	chr5:96845117-96845167	AG10803	skin:	n/a
6	chr5:96479253-96479303	SKMC	muscle:	n/a
7	chr5:96518721-96518771	H1-hESC	embryonic stem cell:	embryo
8	chr5:96518721-96518771	A549	lung:	n/a
9	chr5:96519005-96519055	HCT-116	colon:	n/a
10	chr5:96519644-96519694	AG09319	gingival:	n/a
11	chr5:96519010-96519060	NB4	blood:	n/a
12	chr5:96519005-96519055	ProgFib	skin:	n/a
13	chr5:96519401-96519451	SAEC	small airway:	n/a
14	chr5:96522767-96522817	GM12891	blood:	n/a
15	chr5:96478573-96478623	BE2_C	brain:	n/a
16	chr5:96478495-96478545	NT2-D1	testis:	n/a
17	chr5:96519566-96519616	HCF	heart:	n/a
18	chr5:96477502-96477552	HRE	kidney:	n/a
19	chr5:96742935-96742985	AG09319	gingival:	n/a
20	chr5:96855476-96855526	HCF	heart:	n/a
21	chr5:96747223-96747273	HEK293	kidney:	embryo
22	chr5:96519548-96519598	GM06990	blood:	n/a
23	chr5:96915770-96915820	AG04449	skin:	fetal
24	chr5:96519465-96519515	SAEC	small airway:	n/a
25	chr5:96479253-96479303	AG09319	gingival:	n/a
26	chr5:96876834-96876884	SK-N-SH	brain:	n/a
27	chr5:96845117-96845167	ProgFib	skin:	n/a
28	chr5:96519401-96519451	HMEC	breast:	n/a
29	chr5:96855476-96855526	AG04450	lung:	fetal
30	chr5:96497888-96497938	HRPEpiC	eye:	n/a
31	chr5:96497888-96497938	CMK	blood:	n/a
32	chr5:96890257-96890307	A549	lung:	n/a
33	chr5:96478573-96478623	HRE	kidney:	n/a
34	chr5:96519644-96519694	HRE	kidney:	n/a
35	chr5:96522767-96522817	MCF10A-Er-Src	breast:	n/a
36	chr5:96855476-96855526	HepG2	liver:	n/a
37	chr5:96519465-96519515	HNPCEpiC	eye:	n/a
38	chr5:96519401-96519451	GM12878	blood:	n/a
39	chr5:96519644-96519694	NH-A	brain:	n/a
40	chr5:96789385-96789435	NH-A	brain:	n/a
41	chr5:96497888-96497938	HUVEC	blood vessel:	n/a
42	chr5:96519566-96519616	PrEC	prostate:	n/a
43	chr5:96855476-96855526	SK-N-SH_RA	brain:	n/a
44	chr5:96519644-96519694	PANC-1	pancreas:	n/a
45	chr5:96519566-96519616	H1-hESC	embryonic stem cell:	embryo
46	chr5:96845117-96845167	PANC-1	pancreas:	n/a
47	chr5:96881859-96881909	HCM	heart:	n/a
48	chr5:96478495-96478545	NHDF-neo	bronchial:	n/a
49	chr5:96519465-96519515	PrEC	prostate:	n/a
50	chr5:96789385-96789435	AoSMC	blood vessel:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:96695823..96698804-chr6:142366314..142367822,2	K562	blood:
2	chr5:96869180..96869850-chr5:98103055..98104021,2	MCF-7	breast:
3	chr5:96087837..96088851-chr5:96497370..96499403,9	K562	blood:
4	chr5:96379467..96380324-chr5:96497473..96498285,2	MCF-7	breast:
5	chr5:96505549..96507976-chr5:96519747..96521338,2	MCF-7	breast:
6	chr5:96517839..96519465-chr5:96545763..96548016,2	K562	blood:
7	chr5:96533022..96535910-chr5:96537589..96540065,2	K562	blood:
8	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
9	chr5:96381723..96383480-chr5:96500362..96502420,2	K562	blood:
10	chr17:41464548..41466257-chr5:96697324..96698824,2	MCF-7	breast:
11	chr5:96687334..96689961-chr5:96691050..96693898,2	MCF-7	breast:
12	chr5:96496426..96497975-chr5:96509660..96511880,2	K562	blood:
13	chr5:96078120..96080024-chr5:96498248..96500707,2	K562	blood:
14	chr5:96521057..96523981-chr5:96536109..96539029,2	K562	blood:
15	chr11:62608625..62609592-chr5:96518540..96519360,2	Hela-S3	cervix:
16	chr1:21112901..21113842-chr5:96518449..96519338,2	Hela-S3	cervix:
17	chr5:96517922..96519748-chr5:96562831..96564407,2	MCF-7	breast:
18	chr5:96706066..96707837-chr5:96722435..96724433,2	K562	blood:
19	chr5:96519642..96521582-chr5:96527509..96529068,2	MCF-7	breast:
20	chr5:96566532..96567370-chr5:96632847..96633430,3	MCF-7	breast:
21	chr5:96517922..96519748-chr5:96562831..96564407,2	MCF-7	breast:
22	chr5:96518600..96520567-chr5:96529112..96530644,2	MCF-7	breast:
23	chr5:96142348..96145031-chr5:96516210..96518138,3	K562	blood:
24	chr5:96656999..96658653-chr5:96658674..96662108,3	K562	blood:
25	chr17:41398650..41400853-chr5:96695801..96698804,5	K562	blood:
26	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
27	chr5:96087839..96088456-chr5:96497483..96498165,2	MCF-7	breast:
28	chr5:95680165..95680955-chr5:96498665..96499236,2	K562	blood:
29	chr5:96513502..96516317-chr5:96517939..96521183,3	K562	blood:
30	chr17:41380182..41383606-chr5:96695801..96698822,3	K562	blood:
31	chr5:96517799..96519630-chr9:91924359..91927202,2	MCF-7	breast:
32	chr5:96503041..96507630-chr5:96507953..96511468,4	K562	blood:
33	chr5:95949882..95950863-chr5:96497777..96498341,2	K562	blood:
34	chr5:96720114..96721922-chr5:96728191..96729748,2	MCF-7	breast:
35	chr5:96549287..96551402-chr5:96556377..96559080,2	K562	blood:
36	chr5:96711348..96714233-chr5:96714673..96716999,2	MCF-7	breast:
37	chr5:96484050..96486367-chr5:96488023..96491599,3	K562	blood:
38	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
39	chr17:41380182..41383629-chr5:96695802..96698822,5	K562	blood:
40	chr5:96505549..96507976-chr5:96519747..96521338,2	MCF-7	breast:
41	chr5:96269896..96271438-chr5:96517931..96519494,2	MCF-7	breast:
42	chr5:96566460..96567205-chr5:96869494..96870442,2	MCF-7	breast:
43	chr5:96534501..96536985-chr5:96538534..96540888,2	MCF-7	breast:
44	chr17:41462273..41467084-chr5:96695804..96698803,5	K562	blood:
45	chr5:96518678..96521273-chr5:96521348..96524678,3	MCF-7	breast:
46	chr5:96521334..96524159-chr5:96530024..96533344,3	K562	blood:
47	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
48	chr5:96268592..96270496-chr5:96515475..96517242,2	MCF-7	breast:
49	chr5:96203527..96205559-chr5:96508441..96510333,2	K562	blood:
50	chr5:96142588..96144739-chr5:96517628..96519299,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-1	chr5:96772257-96772921	ENSG00000251513.1
2	lnc-CTD-2215E18.1.1-1	chr5:96519303-96519373	ENSG00000251513.1
3	lnc-CTD-2215E18.1.1-1	chr5:96767448-96767604	ENSG00000251513.1
4	lnc-LIX1-2	chr5:96514534-96514897	NONHSAT102923
5	lnc-RIOK2-1	chr5:96523794-96523947	ENSG00000248758.1
6	lnc-RIOK2-1	chr5:96537546-96537584	ENSG00000248758.1
7	lnc-RIOK2-2	chr5:96563572-96563661	XLOC_004934
8	lnc-CTD-2215E18.1.1-5	chr5:96704480-96706125	NONHSAT102928
9	lnc-CTD-2215E18.1.1-2	chr5:96840399-96840496	NONHSAT102931
10	lnc-RIOK2-2	chr5:96559075-96559398	XLOC_004934
11	lnc-LIX1-2	chr5:96518830-96518864	NONHSAT102923
12	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	XLOC_004483
13	lnc-CTD-2215E18.1.1-2	chr5:96856932-96856994	NONHSAT102931
14	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	NR_105028
15	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	XLOC_004483
16	lnc-RIOK2-3	chr5:96785062-96785445	NONHSAT102929
17	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	NR_105028
18	lnc-RIOK2-4	chr5:96786031-96786319	NONHSAT102930

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RIOK2	hsa-miR-155-5p	chr5:96498413-96498438
2	RIOK2	hsa-miR-101-3p	chr5:96498716-96498737

Variant related genes	Relation type
ENSG00000251054	TF binding region
ENSG00000249761	TF binding region
ENSG00000250331	TF binding region
ENSG00000251513	TF binding region
YTHDF1P1	TF binding region
ENSG00000248758	TF binding region
LIX1	TF binding region
RNU1-73P	TF binding region
RIOK2	TF binding region
ENSG00000249977	TF binding region
ENSG00000251054	CpG island
ENSG00000249761	CpG island
ENSG00000250331	CpG island
ENSG00000251513	CpG island
YTHDF1P1	CpG island
ENSG00000248758	CpG island
LIX1	CpG island
RNU1-73P	CpG island
RIOK2	CpG island
ENSG00000249977	CpG island
ENSG00000247121	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000251513	chromatin interactions
ENSG00000206698	chromatin interactions
ENSG00000249180	chromatin interactions
ENSG00000123975	chromatin interactions
ENSG00000265112	chromatin interactions
ENSG00000246763	chromatin interactions
ENSG00000251054	chromatin interactions
ENSG00000174136	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000113441	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000127483	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000248758	chromatin interactions
ENSG00000153113	chromatin interactions
ENSG00000058729	chromatin interactions
ENSG00000164307	chromatin interactions

Extended variants
information (count: 11403 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:11403 , 50 per page) page: 1 2 3 4 5 6 7 ... 229

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530639239	chr5:96471683-96471684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186598016	chr5:96471768-96471769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140149995	chr5:96471792-96471793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548860012	chr5:96471818-96471819	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368474148	chr5:96471841-96471842	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567589271	chr5:96471865-96471866	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541393503	chr5:96471881-96471882	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149884840	chr5:96471899-96471900	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553159517	chr5:96471935-96471936	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191503935	chr5:96471936-96471937	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144876447	chr5:96471941-96471942	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184021213	chr5:96471959-96471960	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557351423	chr5:96471966-96471967	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371254285	chr5:96471968-96471969	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564335205	chr5:96471990-96471991	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543092586	chr5:96472001-96472002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200222279	chr5:96472046-96472047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555293896	chr5:96472051-96472052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116943601	chr5:96472064-96472065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543401091	chr5:96472087-96472088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1544779	chr5:96472133-96472134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188382571	chr5:96472180-96472181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532856482	chr5:96472188-96472189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs316178	chr5:96472197-96472198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs149029161	chr5:96472218-96472219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530413949	chr5:96472290-96472291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146217854	chr5:96472310-96472311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs80128405	chr5:96472341-96472342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138927195	chr5:96472342-96472343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192900795	chr5:96472374-96472375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185459875	chr5:96472375-96472376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539089120	chr5:96472403-96472404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190036514	chr5:96472429-96472430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141378814	chr5:96472441-96472442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566255142	chr5:96472447-96472448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530373990	chr5:96472459-96472460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6885162	chr5:96472460-96472461	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs569416802	chr5:96472478-96472479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536633428	chr5:96472481-96472482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565388937	chr5:96472561-96472562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554978528	chr5:96472596-96472597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146972708	chr5:96472608-96472609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540939538	chr5:96472616-96472617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558835036	chr5:96472622-96472623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577362597	chr5:96472645-96472646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148114188	chr5:96472700-96472701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563026990	chr5:96472756-96472757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181730701	chr5:96472772-96472773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528181934	chr5:96472774-96472775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569879339	chr5:96472830-96472831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:2715 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96455400-96491800	Weak transcription	Primary B cells from peripheral blood	blood
2	chr5:96456400-96478000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr5:96459800-96491800	Weak transcription	Primary B cells from cord blood	blood
4	chr5:96467200-96474000	Weak transcription	Brain Anterior Caudate	brain
5	chr5:96468600-96471800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:96470000-96472400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:96470000-96475600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:96470200-96471800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:96470200-96472000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr5:96470200-96472000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:96470200-96472000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr5:96470200-96472600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:96470200-96473000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr5:96470400-96472000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr5:96470400-96474200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:96470800-96471800	Weak transcription	Fetal Muscle Leg	muscle
17	chr5:96471000-96473000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:96471200-96475800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr5:96471200-96476200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr5:96471600-96471800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:96471600-96471800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr5:96471600-96472000	Enhancers	Fetal Brain Female	brain
23	chr5:96471800-96472000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr5:96471800-96472000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:96471800-96472400	Enhancers	Brain Germinal Matrix	brain
26	chr5:96471800-96472400	Enhancers	Fetal Muscle Leg	muscle
27	chr5:96471800-96475000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:96472000-96472400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:96472000-96473800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr5:96472000-96474200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr5:96472000-96475200	Weak transcription	Fetal Brain Female	brain
32	chr5:96472000-96476200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr5:96472000-96476200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr5:96472000-96476800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr5:96472400-96473600	Weak transcription	Brain Germinal Matrix	brain
36	chr5:96472400-96474000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:96472400-96474800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr5:96472400-96475200	Weak transcription	Fetal Muscle Leg	muscle
39	chr5:96472600-96474800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:96473000-96476000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr5:96473000-96476400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr5:96473600-96474000	Enhancers	Brain Germinal Matrix	brain
43	chr5:96473800-96474200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr5:96474000-96474200	Enhancers	Brain Anterior Caudate	brain
45	chr5:96474000-96474400	Enhancers	Brain Substantia Nigra	brain
46	chr5:96474000-96475400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:96474000-96476400	Weak transcription	Brain Germinal Matrix	brain
48	chr5:96474200-96474400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr5:96474200-96475800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr5:96474200-96476000	Weak transcription	Brain Anterior Caudate	brain

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