Variant report

Variant	nsv456334
Chromosome Location	chr14:69793624-69831037
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:749)
CpG islands
(count:122)
Chromatin interactive
region (count:70)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:749 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:69813592-69813611	HepG2	liver:	n/a	n/a
2	ATF1	chr14:69821288-69821319	K562	blood:	n/a	n/a
3	ATF2	chr14:69821008-69822002	GM12878	blood:	n/a	n/a
4	ATF2	chr14:69820980-69821925	GM12878	blood:	n/a	n/a
5	BACH1	chr14:69813488-69813823	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:69821029-69821480	GM12878	blood:	n/a	n/a
7	BCL11A	chr14:69827363-69827553	GM12878	blood:	n/a	n/a
8	BCL11A	chr14:69821026-69821461	GM12878	blood:	n/a	chr14:69821252-69821261
9	BCLAF1	chr14:69820987-69821791	GM12878	blood:	n/a	chr14:69821252-69821261
10	BCLAF1	chr14:69820912-69822057	GM12878	blood:	n/a	chr14:69821252-69821261
11	BHLHE40	chr14:69808465-69808669	K562	blood:	n/a	chr14:69808614-69808623 chr14:69808613-69808622 chr14:69808611-69808624
12	BHLHE40	chr14:69818011-69818281	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:69827418-69827682	GM12878	blood:	n/a	chr14:69827626-69827642
14	BHLHE40	chr14:69821001-69822004	GM12878	blood:	n/a	n/a
15	BHLHE40	chr14:69808425-69808768	GM12878	blood:	n/a	chr14:69808614-69808623 chr14:69808613-69808622 chr14:69808611-69808624
16	BRCA1	chr14:69813567-69813627	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr14:69825478-69825678	GM12878	blood:	n/a	n/a
18	CEBPB	chr14:69793949-69794072	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:69820906-69822119	GM12878	blood:	n/a	n/a
20	CEBPB	chr14:69810978-69811076	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:69823529-69824637	MCF-7	breast:	n/a	n/a
22	CEBPB	chr14:69811427-69811498	HepG2	liver:	n/a	chr14:69811443-69811456 chr14:69811443-69811456 chr14:69811443-69811454
23	CHD1	chr14:69813483-69813537	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr14:69820923-69822194	GM12878	blood:	n/a	n/a
25	CHD2	chr14:69820994-69821999	GM12878	blood:	n/a	n/a
26	CHD2	chr14:69825064-69825586	GM12878	blood:	n/a	n/a
27	CHD2	chr14:69813528-69813766	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr14:69829897-69830046	Hela-S3	cervix:	n/a	chr14:69829912-69829930
29	CTCF	chr14:69829920-69830070	GM12870	blood:	n/a	n/a
30	CTCF	chr14:69829400-69829550	HCFaa	heart:	n/a	chr14:69829533-69829542
31	CTCF	chr14:69829860-69830010	HUVEC	blood vessel:	n/a	chr14:69829912-69829930
32	CTCF	chr14:69829820-69829970	MCF-7	breast:	n/a	chr14:69829912-69829930
33	CTCF	chr14:69813580-69813730	GM12865	blood:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
34	CTCF	chr14:69817760-69817910	AG04450	lung:	n/a	chr14:69817856-69817865 chr14:69817807-69817820 chr14:69817854-69817870
35	CTCF	chr14:69813497-69813755	MCF-7	breast:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
36	CTCF	chr14:69813540-69813690	HRPEpiC	eye:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
37	CTCF	chr14:69829880-69830030	AG09319	gingival:	n/a	chr14:69829912-69829930
38	CTCF	chr14:69813853-69813946	GM12891	blood:	n/a	n/a
39	CTCF	chr14:69829874-69830034	K562	blood:	n/a	chr14:69829912-69829930
40	CTCF	chr14:69813500-69813795	GM12892	blood:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
41	CTCF	chr14:69813540-69813690	RPTEC	kidney:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
42	CTCF	chr14:69821366-69821431	GM12878	blood:	n/a	chr14:69821387-69821408 chr14:69821385-69821403
43	CTCF	chr14:69813540-69813690	HA-sp	spinal cord:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
44	CTCF	chr14:69829860-69830010	RPTEC	kidney:	n/a	chr14:69829912-69829930
45	CTCF	chr14:69813114-69813969	A549	lung:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
46	CTCF	chr14:69813532-69813746	GM13977	blood:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
47	CTCF	chr14:69813560-69813710	GM12865	blood:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
48	CTCF	chr14:69829900-69830050	HRE	kidney:	n/a	chr14:69829912-69829930
49	CTCF	chr14:69813520-69813670	SAEC	small airway:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626
50	CTCF	chr14:69813600-69813750	GM12871	blood:	n/a	chr14:69813610-69813623 chr14:69813614-69813623 chr14:69813608-69813626

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69822950-69823000	CMK	blood:	n/a
2	chr14:69821049-69821099	AoSMC	blood vessel:	n/a
3	chr14:69821049-69821099	AG09319	gingival:	n/a
4	chr14:69822950-69823000	U87	brain:	n/a
5	chr14:69821049-69821099	HCT-116	colon:	n/a
6	chr14:69822950-69823000	HEK293	kidney:	embryo
7	chr14:69822950-69823000	PANC-1	pancreas:	n/a
8	chr14:69822950-69823000	MCF-7	breast:	n/a
9	chr14:69821049-69821099	HL-60	blood:	n/a
10	chr14:69822950-69823000	ECC-1	luminal epithelium:	n/a
11	chr14:69821049-69821099	Jurkat	blood:	n/a
12	chr14:69821049-69821099	GM12878	blood:	n/a
13	chr14:69821049-69821099	AG04449	skin:	fetal
14	chr14:69821049-69821099	HNPCEpiC	eye:	n/a
15	chr14:69821049-69821099	HIPEpiC	eye:	n/a
16	chr14:69822950-69823000	SK-N-SH	brain:	n/a
17	chr14:69821049-69821099	IMR90	lung:	fetal
18	chr14:69822950-69823000	GM12891	blood:	n/a
19	chr14:69821049-69821099	GM12892	blood:	n/a
20	chr14:69821049-69821099	AG10803	skin:	n/a
21	chr14:69821049-69821099	Hela-S3	cervix:	n/a
22	chr14:69821049-69821099	PANC-1	pancreas:	n/a
23	chr14:69821049-69821099	LNCaP	prostate:	n/a
24	chr14:69821049-69821099	Caco-2	colon:	n/a
25	chr14:69821049-69821099	NT2-D1	testis:	n/a
26	chr14:69822950-69823000	IMR90	lung:	fetal
27	chr14:69822950-69823000	AG10803	skin:	n/a
28	chr14:69822950-69823000	T-47D	breast:	n/a
29	chr14:69821049-69821099	HCPEpiC	choroid plexus:	n/a
30	chr14:69821049-69821099	BJ	skin:	n/a
31	chr14:69822950-69823000	AoSMC	blood vessel:	n/a
32	chr14:69822950-69823000	HL-60	blood:	n/a
33	chr14:69822950-69823000	H1-hESC	embryonic stem cell:	embryo
34	chr14:69822950-69823000	AG09319	gingival:	n/a
35	chr14:69822950-69823000	ProgFib	skin:	n/a
36	chr14:69821049-69821099	HCF	heart:	n/a
37	chr14:69822950-69823000	HUVEC	blood vessel:	n/a
38	chr14:69821049-69821099	U87	brain:	n/a
39	chr14:69822950-69823000	NB4	blood:	n/a
40	chr14:69822950-69823000	HCM	heart:	n/a
41	chr14:69821049-69821099	NHBE	bronchial:	n/a
42	chr14:69821049-69821099	GM06990	blood:	n/a
43	chr14:69822950-69823000	GM06990	blood:	n/a
44	chr14:69821049-69821099	NH-A	brain:	n/a
45	chr14:69821049-69821099	MCF10A-Er-Src	breast:	n/a
46	chr14:69821049-69821099	A549	lung:	n/a
47	chr14:69822950-69823000	HNPCEpiC	eye:	n/a
48	chr14:69821049-69821099	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:69822950-69823000	NHDF-neo	bronchial:	n/a
50	chr14:69822950-69823000	SK-N-MC	brain:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:69813202..69813855-chr14:69926762..69927557,4	MCF-7	breast:
2	chr14:69799650..69801547-chr14:69801660..69803679,2	MCF-7	breast:
3	chr14:69830050..69832763-chr14:69863489..69865045,2	K562	blood:
4	chr14:69805502..69808106-chr14:69810708..69812563,2	MCF-7	breast:
5	chr14:69802180..69804922-chr14:69810829..69812465,2	K562	blood:
6	chr14:69800242..69802795-chr14:69820027..69823716,5	MCF-7	breast:
7	chr14:69709053..69710185-chr14:69829524..69830405,6	MCF-7	breast:
8	chr14:69823834..69826023-chr14:69826399..69829100,3	MCF-7	breast:
9	chr14:69823607..69825370-chr14:69868914..69871181,2	MCF-7	breast:
10	chr14:69808456..69811857-chr14:69822855..69826097,4	MCF-7	breast:
11	chr14:69805502..69808106-chr14:69810708..69812563,2	MCF-7	breast:
12	chr14:69781606..69784523-chr14:69813636..69815679,2	MCF-7	breast:
13	chr14:69825390..69827894-chr14:69869921..69871865,2	MCF-7	breast:
14	chr14:69826604..69828318-chr14:69864325..69866792,4	MCF-7	breast:
15	chr14:69821172..69826934-chr14:69835934..69842143,9	MCF-7	breast:
16	chr14:69800242..69802795-chr14:69820027..69823716,5	MCF-7	breast:
17	chr14:69726345..69728040-chr14:69823627..69825554,2	MCF-7	breast:
18	chr14:69791967..69794011-chr14:69799541..69801343,2	MCF-7	breast:
19	chr14:69791053..69792994-chr14:69824210..69827110,2	MCF-7	breast:
20	chr14:69618455..69620714-chr14:69822372..69824189,2	MCF-7	breast:
21	chr14:69714529..69715402-chr14:69829818..69830391,3	MCF-7	breast:
22	chr14:69714714..69715386-chr14:69829473..69830328,2	MCF-7	breast:
23	chr14:69808591..69811253-chr14:69813136..69815763,3	MCF-7	breast:
24	chr14:69725598..69728352-chr14:69809283..69810868,2	MCF-7	breast:
25	chr14:69810899..69813895-chr14:69838816..69841338,2	MCF-7	breast:
26	chr14:69810682..69812571-chr14:69823617..69825729,2	MCF-7	breast:
27	chr14:69790450..69793029-chr14:69793340..69796892,3	K562	blood:
28	chr14:69713333..69716497-chr14:69822464..69825610,4	MCF-7	breast:
29	chr14:69830172..69832846-chr14:69834096..69836793,3	K562	blood:
30	chr14:69823834..69826023-chr14:69826399..69829100,3	MCF-7	breast:
31	chr14:69810682..69812571-chr14:69823617..69825729,2	MCF-7	breast:
32	chr14:69811705..69814388-chr14:69822919..69825901,2	K562	blood:
33	chr14:69827353..69829184-chr14:69836864..69838973,2	MCF-7	breast:
34	chr14:69821722..69824231-chr14:69923203..69925103,2	MCF-7	breast:
35	chr14:69727618..69729790-chr14:69814011..69815808,2	MCF-7	breast:
36	chr14:69826955..69830951-chr14:69833365..69835395,4	MCF-7	breast:
37	chr14:69754386..69755016-chr14:69829801..69830400,2	MCF-7	breast:
38	chr14:69820575..69822363-chr14:69824777..69827563,2	MCF-7	breast:
39	chr14:69765777..69766916-chr14:69812899..69814107,5	MCF-7	breast:
40	chr14:69822116..69824651-chr14:69862569..69864900,2	MCF-7	breast:
41	chr14:69822349..69827857-chr14:69829114..69832930,7	MCF-7	breast:
42	chr14:69829365..69831341-chr14:69925811..69928602,2	MCF-7	breast:
43	chr14:69824235..69826782-chr14:69843380..69845607,3	MCF-7	breast:
44	chr14:69773449..69776033-chr14:69792393..69794108,2	MCF-7	breast:
45	chr14:69608802..69611757-chr14:69814393..69815974,2	K562	blood:
46	chr14:69785427..69787621-chr14:69822775..69825192,2	MCF-7	breast:
47	chr14:69826454..69828597-chr14:69865306..69867576,2	MCF-7	breast:
48	chr14:69811705..69814388-chr14:69822919..69825901,2	K562	blood:
49	chr14:69791967..69794011-chr14:69799541..69801343,2	MCF-7	breast:
50	chr14:69810681..69813205-chr14:69822055..69824419,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GALNTL1-1	chr14:69823727-69826025	NONHSAT037522

No data

Variant related genes	Relation type
GALNT16	TF binding region
GALNT16	CpG island
ENSG00000100626	chromatin interactions
ENSG00000100632	chromatin interactions
ENSG00000081177	chromatin interactions
ENSG00000258957	chromatin interactions
ENSG00000206768	chromatin interactions
ENSG00000139990	chromatin interactions
ENSG00000258520	chromatin interactions
ENSG00000029364	chromatin interactions

Extended variants
information (count: 1473 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1473 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1147465	chr14:69793624-69793625	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181860165	chr14:69793653-69793654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559137229	chr14:69793704-69793705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186543389	chr14:69793730-69793731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538402769	chr14:69793838-69793839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556602580	chr14:69793839-69793840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574750085	chr14:69793879-69793880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541859320	chr14:69793896-69793897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188256568	chr14:69793913-69793914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1147464	chr14:69793926-69793927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs55796152	chr14:69793972-69793973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181072586	chr14:69794031-69794032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543698417	chr14:69794032-69794033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186170933	chr14:69794059-69794060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562782466	chr14:69794061-69794062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146322124	chr14:69794079-69794080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548254080	chr14:69794087-69794088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562079996	chr14:69794167-69794168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529425186	chr14:69794205-69794206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566456782	chr14:69794206-69794207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527418761	chr14:69794223-69794224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs74059965	chr14:69794276-69794277	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs75029679	chr14:69794289-69794290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538062686	chr14:69794320-69794321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556705520	chr14:69794347-69794348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566281361	chr14:69794373-69794374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535723516	chr14:69794387-69794388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553783922	chr14:69794412-69794413	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139628933	chr14:69794417-69794418	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539791711	chr14:69794470-69794471	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557972111	chr14:69794472-69794473	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576442353	chr14:69794507-69794508	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144349712	chr14:69794530-69794531	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562669409	chr14:69794536-69794537	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151100914	chr14:69794539-69794540	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542132321	chr14:69794549-69794550	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12894211	chr14:69794551-69794552	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs527312932	chr14:69794638-69794639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75167451	chr14:69794662-69794663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191469658	chr14:69794694-69794695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531429835	chr14:69794745-69794746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549988537	chr14:69794760-69794761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183307309	chr14:69794804-69794805	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535618126	chr14:69794821-69794822	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35040986	chr14:69794824-69794825	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547705549	chr14:69794882-69794883	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370284604	chr14:69794948-69794949	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186868490	chr14:69794953-69794954	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77946430	chr14:69795025-69795026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558124889	chr14:69795053-69795054	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69781600-69794800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr14:69784200-69800200	Weak transcription	Brain Hippocampus Middle	brain
3	chr14:69784400-69801600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr14:69784800-69794000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr14:69788800-69810400	Weak transcription	NHDF-Ad	bronchial
6	chr14:69789000-69797800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:69790800-69793800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr14:69791000-69795600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr14:69791000-69817400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:69791200-69795400	Strong transcription	Fetal Intestine Small	intestine
11	chr14:69791400-69795000	Strong transcription	Right Ventricle	heart
12	chr14:69791400-69802000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr14:69791600-69794400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:69791600-69798200	Strong transcription	Fetal Muscle Trunk	muscle
15	chr14:69792000-69795600	Strong transcription	Fetal Brain Female	brain
16	chr14:69792200-69812000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr14:69792400-69801400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:69792600-69805800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr14:69793000-69795000	Weak transcription	Brain Germinal Matrix	brain
20	chr14:69793200-69800200	Weak transcription	Fetal Muscle Leg	muscle
21	chr14:69793400-69798200	Weak transcription	Fetal Stomach	stomach
22	chr14:69793400-69800200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr14:69793400-69818800	Weak transcription	Spleen	Spleen
24	chr14:69793400-69821200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr14:69793400-69822600	Weak transcription	Brain Angular Gyrus	brain
26	chr14:69793600-69798200	Weak transcription	Left Ventricle	heart
27	chr14:69793600-69800000	Weak transcription	Brain Anterior Caudate	brain
28	chr14:69793600-69805800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr14:69793600-69806200	Weak transcription	Fetal Intestine Large	intestine
30	chr14:69794400-69794600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr14:69794600-69800800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:69794800-69795400	Enhancers	Brain Cingulate Gyrus	brain
33	chr14:69795000-69796200	Enhancers	Brain Germinal Matrix	brain
34	chr14:69795000-69796200	Weak transcription	Right Ventricle	heart
35	chr14:69795400-69805400	Weak transcription	Fetal Intestine Small	intestine
36	chr14:69795400-69805600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr14:69795600-69796000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr14:69795600-69805200	Weak transcription	Fetal Brain Female	brain
39	chr14:69796200-69800200	Weak transcription	Brain Germinal Matrix	brain
40	chr14:69796200-69801400	Strong transcription	Right Ventricle	heart
41	chr14:69797600-69798000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr14:69797800-69798000	Enhancers	HSMMtube	muscle
43	chr14:69797800-69798200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr14:69798000-69798200	Enhancers	Pancreas	Pancrea
45	chr14:69798200-69798600	Strong transcription	Fetal Stomach	stomach
46	chr14:69798200-69798800	Strong transcription	Left Ventricle	heart
47	chr14:69798200-69799800	Weak transcription	Fetal Muscle Trunk	muscle
48	chr14:69798200-69802800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr14:69798200-69809400	Weak transcription	Pancreas	Pancrea
50	chr14:69798600-69798800	Enhancers	HSMMtube	muscle

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