Variant report

Variant	nsv566157
Chromosome Location	chr14:105607516-105634378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:637)
CpG islands
(count:2386)
Chromatin interactive
region (count:68)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr14:105633815-105634024	K562	blood:	n/a	n/a
2	BACH1	chr14:105634160-105634415	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:105633488-105634425	K562	blood:	n/a	chr14:105633626-105633642
4	BRCA1	chr14:105628806-105629067	HepG2	liver:	n/a	n/a
5	CBX3	chr14:105607430-105607762	K562	blood:	n/a	n/a
6	CCNT2	chr14:105633598-105634394	K562	blood:	n/a	n/a
7	CEBPB	chr14:105631426-105631943	ECC-1	luminal epithelium:	n/a	n/a
8	CHD2	chr14:105628806-105628928	HepG2	liver:	n/a	n/a
9	CHD2	chr14:105634239-105634449	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr14:105633690-105633737	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr14:105632638-105632642	K562	blood:	n/a	n/a
12	CREB1	chr14:105633974-105634413	A549	lung:	n/a	n/a
13	CTCF	chr14:105634117-105634323	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr14:105629380-105629530	SAEC	small airway:	n/a	n/a
15	CTCF	chr14:105634240-105634390	K562	blood:	n/a	n/a
16	CTCF	chr14:105611660-105611810	NB4	blood:	n/a	n/a
17	CTCF	chr14:105634120-105634270	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr14:105634173-105634297	GM10266	blood:	n/a	n/a
19	CTCF	chr14:105613201-105613342	HepG2	liver:	n/a	n/a
20	CTCF	chr14:105634160-105634310	HEK293	kidney:	n/a	n/a
21	CTCF	chr14:105633880-105634030	BE2_C	brain:	n/a	n/a
22	CTCF	chr14:105631433-105631725	MCF-7	breast:	n/a	chr14:105631554-105631562
23	CTCF	chr14:105633040-105633190	SAEC	small airway:	n/a	chr14:105633102-105633120 chr14:105633104-105633117
24	CTCF	chr14:105611580-105611730	HEEpiC	esophagus:	n/a	chr14:105611619-105611637 chr14:105611626-105611634
25	CTCF	chr14:105613140-105613290	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr14:105631443-105631720	MCF-7	breast:	n/a	chr14:105631554-105631562
27	CTCF	chr14:105633888-105633890	GM19239	blood:	n/a	n/a
28	CTCF	chr14:105634180-105634330	NHEK	skin:	n/a	n/a
29	CTCF	chr14:105633940-105634090	GM12874	blood:	n/a	n/a
30	CTCF	chr14:105633904-105634059	GM10248	blood:	n/a	n/a
31	CTCF	chr14:105634100-105634250	GM12874	blood:	n/a	n/a
32	CTCF	chr14:105633866-105634070	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr14:105633934-105634041	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr14:105633020-105633170	SAEC	small airway:	n/a	chr14:105633102-105633120 chr14:105633104-105633117
35	CTCF	chr14:105611560-105611710	GM12875	blood:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
36	CTCF	chr14:105634171-105634310	ProgFib	skin:	n/a	n/a
37	CTCF	chr14:105633860-105634010	GM12867	blood:	n/a	n/a
38	CTCF	chr14:105611604-105611661	MCF-7	breast:	n/a	chr14:105611619-105611637 chr14:105611626-105611634
39	CTCF	chr14:105633880-105634030	GM12868	blood:	n/a	n/a
40	CTCF	chr14:105633814-105634365	K562	blood:	n/a	n/a
41	CTCF	chr14:105634180-105634330	GM12875	blood:	n/a	n/a
42	CTCF	chr14:105633890-105634350	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:105611520-105611670	HepG2	liver:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
44	CTCF	chr14:105632320-105632470	HMEC	breast:	n/a	chr14:105632422-105632435
45	CTCF	chr14:105633900-105634050	GM12871	blood:	n/a	n/a
46	CTCF	chr14:105613209-105613302	GM19239	blood:	n/a	n/a
47	CTCF	chr14:105633784-105633790	NHEK	skin:	n/a	n/a
48	CTCF	chr14:105628840-105628990	AG04449	skin:	n/a	n/a
49	CTCF	chr14:105611420-105611570	GM12864	blood:	n/a	n/a
50	CTCF	chr14:105634180-105634330	GM12874	blood:	n/a	n/a

(count:2386 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105615401-105615451	PFSK-1	brain:	n/a
2	chr14:105612971-105613021	BJ	skin:	n/a
3	chr14:105615459-105615509	MCF-7	breast:	n/a
4	chr14:105625577-105625627	SK-N-SH_RA	brain:	n/a
5	chr14:105612753-105612803	CMK	blood:	n/a
6	chr14:105633697-105633747	ovcar-3	ovarian:	n/a
7	chr14:105619701-105619751	PANC-1	pancreas:	n/a
8	chr14:105615401-105615451	PFSK-1	brain:	n/a
9	chr14:105612971-105613021	BJ	skin:	n/a
10	chr14:105615459-105615509	MCF-7	breast:	n/a
11	chr14:105625577-105625627	SK-N-SH_RA	brain:	n/a
12	chr14:105612753-105612803	CMK	blood:	n/a
13	chr14:105633697-105633747	ovcar-3	ovarian:	n/a
14	chr14:105619701-105619751	PANC-1	pancreas:	n/a
15	chr14:105609831-105609881	Jurkat	blood:	n/a
16	chr14:105609516-105609566	K562	blood:	n/a
17	chr14:105617308-105617358	ProgFib	skin:	n/a
18	chr14:105613783-105613833	ProgFib	skin:	n/a
19	chr14:105614552-105614602	SK-N-MC	brain:	n/a
20	chr14:105617080-105617130	SK-N-SH	brain:	n/a
21	chr14:105620358-105620408	AG09319	gingival:	n/a
22	chr14:105620358-105620408	IMR90	lung:	fetal
23	chr14:105608567-105608617	NT2-D1	testis:	n/a
24	chr14:105617308-105617358	HMEC	breast:	n/a
25	chr14:105616988-105617038	HRPEpiC	eye:	n/a
26	chr14:105625577-105625627	AG09319	gingival:	n/a
27	chr14:105613102-105613152	AG10803	skin:	n/a
28	chr14:105615401-105615451	CMK	blood:	n/a
29	chr14:105615459-105615509	BJ	skin:	n/a
30	chr14:105608474-105608524	HUVEC	blood vessel:	n/a
31	chr14:105612787-105612837	HRPEpiC	eye:	n/a
32	chr14:105609472-105609522	Hela-S3	cervix:	n/a
33	chr14:105614564-105614614	HepG2	liver:	n/a
34	chr14:105614818-105614868	AG09309	skin:	n/a
35	chr14:105618576-105618626	CMK	blood:	n/a
36	chr14:105618576-105618626	HEEpiC	esophagus:	n/a
37	chr14:105615459-105615509	HCPEpiC	choroid plexus:	n/a
38	chr14:105633697-105633747	AG04450	lung:	fetal
39	chr14:105613783-105613833	HCPEpiC	choroid plexus:	n/a
40	chr14:105614564-105614614	GM06990	blood:	n/a
41	chr14:105609411-105609461	HCF	heart:	n/a
42	chr14:105609516-105609566	GM12892	blood:	n/a
43	chr14:105622312-105622362	HNPCEpiC	eye:	n/a
44	chr14:105612787-105612837	AoSMC	blood vessel:	n/a
45	chr14:105617839-105617889	HCT-116	colon:	n/a
46	chr14:105622312-105622362	H1-hESC	embryonic stem cell:	embryo
47	chr14:105609472-105609522	AoSMC	blood vessel:	n/a
48	chr14:105617080-105617130	PANC-1	pancreas:	n/a
49	chr14:105608973-105609023	GM19239	blood:	n/a
50	chr14:105617080-105617130	SK-N-MC	brain:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:105618086..105620322-chr14:105622917..105625684,2	MCF-7	breast:
2	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
3	chr14:105555328..105560254-chr14:105631379..105635555,5	MCF-7	breast:
4	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
5	chr14:105632764..105636922-chr14:105637769..105642057,5	MCF-7	breast:
6	chr14:105633713..105635633-chr7:75987137..75988852,2	K562	blood:
7	chr14:105620616..105622856-chr14:105624629..105627730,3	MCF-7	breast:
8	chr14:105602588..105606045-chr14:105617930..105622124,4	MCF-7	breast:
9	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
10	chr14:105556904..105557457-chr14:105630667..105631594,2	MCF-7	breast:
11	chr14:105557317..105562216-chr14:105628986..105634761,7	MCF-7	breast:
12	chr14:105633273..105637288-chr14:105642227..105645314,5	MCF-7	breast:
13	chr14:105620927..105623497-chr14:105711846..105714187,2	MCF-7	breast:
14	chr14:105620302..105622152-chr14:105646136..105647731,2	MCF-7	breast:
15	chr14:105610604..105613096-chr14:105619107..105620769,2	K562	blood:
16	chr14:105606160..105607990-chr14:105612669..105614397,2	MCF-7	breast:
17	chr14:105556907..105557905-chr14:105631981..105632717,2	MCF-7	breast:
18	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
19	chr14:105611401..105614212-chr14:105625101..105627298,2	MCF-7	breast:
20	chr14:105613499..105615482-chr14:105618517..105620945,3	MCF-7	breast:
21	chr14:105191017..105193582-chr14:105615897..105618849,2	MCF-7	breast:
22	chr14:105617835..105619717-chr14:105620167..105621698,2	MCF-7	breast:
23	chr14:105445649..105448428-chr14:105631488..105633523,2	MCF-7	breast:
24	chr14:105620616..105622856-chr14:105624629..105627730,3	MCF-7	breast:
25	chr14:105603827..105606395-chr14:105610368..105612251,2	MCF-7	breast:
26	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
27	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
28	chr14:105605939..105608674-chr14:105628049..105630309,2	K562	blood:
29	chr14:105632765..105635152-chr14:105864248..105866641,2	K562	blood:
30	chr14:105632643..105634203-chr14:105776322..105778030,2	K562	blood:
31	chr14:105603768..105606019-chr14:105630363..105631971,2	K562	blood:
32	chr14:105559890..105560867-chr14:105633779..105634301,2	MCF-7	breast:
33	chr14:105556047..105558699-chr14:105620485..105622825,2	K562	blood:
34	chr14:105618156..105621334-chr14:105628329..105630360,3	K562	blood:
35	chr14:105441844..105444735-chr14:105632724..105634694,2	MCF-7	breast:
36	chr14:105631465..105635896-chr14:105645452..105649219,9	MCF-7	breast:
37	chr14:105556509..105557265-chr14:105631240..105632200,2	MCF-7	breast:
38	chr14:105552235..105554666-chr14:105628025..105629965,2	MCF-7	breast:
39	chr14:105605892..105608252-chr14:105621955..105625449,3	K562	blood:
40	chr14:105584234..105586859-chr14:105605626..105608481,2	MCF-7	breast:
41	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
42	chr14:105631482..105635033-chr14:105765939..105767661,3	K562	blood:
43	chr14:105633069..105635536-chr14:105714407..105716304,2	MCF-7	breast:
44	chr14:105502174..105504922-chr14:105632204..105633983,2	MCF-7	breast:
45	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
46	chr14:105556861..105558363-chr14:105628903..105631842,2	K562	blood:
47	chr14:105556528..105557420-chr14:105633531..105634669,3	MCF-7	breast:
48	chr14:105618156..105621334-chr14:105628329..105630360,3	K562	blood:
49	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
50	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6765-5p	chr14:105617177-105617201	MIMAT0027430
hsa-miR-6765-3p	chr14:105617115-105617135	MIMAT0027431

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	JAG2	hsa-miR-124-3p	chr14:105608227-105608246
2	JAG2	hsa-miR-124-3p	chr14:105608233-105608227

Variant related genes	Relation type
JAG2	TF binding region
JAG2	CpG island
ENSG00000185347	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000226174	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000140104	chromatin interactions
ENSG00000257556	chromatin interactions
ENSG00000170027	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000179364	chromatin interactions

Extended variants
information (count: 1382 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1382 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12147336	chr14:105607516-105607517	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs181226135	chr14:105607534-105607535	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587652902	chr14:105607551-105607552	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587708015	chr14:105607558-105607559	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587765964	chr14:105607570-105607571	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1056310	chr14:105607615-105607616	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587638467	chr14:105607638-105607639	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs587716896	chr14:105607736-105607737	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72707610	chr14:105607743-105607744	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187164593	chr14:105607747-105607748	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587707903	chr14:105607750-105607751	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs587631770	chr14:105607765-105607766	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs587686948	chr14:105607784-105607785	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587768276	chr14:105607806-105607807	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs147432624	chr14:105607808-105607809	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113613721	chr14:105607829-105607830	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587731435	chr14:105607887-105607888	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587611606	chr14:105607892-105607893	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs376370969	chr14:105607898-105607899	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587696565	chr14:105607929-105607930	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs587753758	chr14:105607935-105607936	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs741859	chr14:105607979-105607980	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs587683645	chr14:105608006-105608007	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs181635212	chr14:105608008-105608009	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs370031751	chr14:105608009-105608010	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587709992	chr14:105608065-105608066	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187270215	chr14:105608121-105608122	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587651349	chr14:105608149-105608150	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372998097	chr14:105608169-105608170	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587631360	chr14:105608194-105608195	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190793754	chr14:105608199-105608200	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377333807	chr14:105608201-105608202	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs113348026	chr14:105608202-105608203	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138171813	chr14:105608241-105608242	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
35	rs370622006	chr14:105608242-105608243	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
36	rs587743989	chr14:105608256-105608257	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13358	chr14:105608268-105608269	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1057753	chr14:105608278-105608279	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1057752	chr14:105608280-105608281	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587615382	chr14:105608281-105608282	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587675919	chr14:105608282-105608283	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587738122	chr14:105608292-105608293	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587598967	chr14:105608358-105608359	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182298946	chr14:105608368-105608369	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143673839	chr14:105608387-105608388	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs760269	chr14:105608403-105608404	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs185026649	chr14:105608430-105608431	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587738980	chr14:105608464-105608465	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587608719	chr14:105608469-105608470	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587702507	chr14:105608505-105608506	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105602800-105629800	Weak transcription	K562	blood
2	chr14:105604600-105608400	Weak transcription	Primary T cells from cord blood	blood
3	chr14:105605800-105607600	ZNF genes & repeats	Brain Hippocampus Middle	brain
4	chr14:105605800-105607600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
5	chr14:105605800-105608600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
6	chr14:105606000-105607600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:105606200-105607600	ZNF genes & repeats	Brain Angular Gyrus	brain
8	chr14:105606200-105607600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
9	chr14:105606200-105607600	ZNF genes & repeats	Fetal Stomach	stomach
10	chr14:105606400-105607600	ZNF genes & repeats	Adipose Nuclei	Adipose
11	chr14:105606400-105608000	ZNF genes & repeats	NHEK	skin
12	chr14:105606400-105608800	ZNF genes & repeats	Lung	lung
13	chr14:105606400-105617800	Strong transcription	Skeletal Muscle Female	skeletal muscle
14	chr14:105606600-105607600	ZNF genes & repeats	Fetal Intestine Small	intestine
15	chr14:105606800-105618000	Weak transcription	Psoas Muscle	Psoas
16	chr14:105606800-105619600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr14:105606800-105631600	Weak transcription	Hela-S3	cervix
18	chr14:105607000-105608000	Weak transcription	HSMMtube	muscle
19	chr14:105607000-105609800	Strong transcription	Left Ventricle	heart
20	chr14:105607000-105610000	Strong transcription	HUVEC	blood vessel
21	chr14:105607000-105615200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr14:105607000-105615400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr14:105607000-105618200	Strong transcription	Gastric	stomach
24	chr14:105607000-105621600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr14:105607200-105608200	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr14:105607200-105608200	Weak transcription	Right Ventricle	heart
27	chr14:105607200-105608400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr14:105607200-105608400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr14:105607200-105608800	Strong transcription	A549	lung
30	chr14:105607200-105610400	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr14:105607200-105611200	Strong transcription	Esophagus	oesophagus
32	chr14:105607200-105613000	Strong transcription	Fetal Muscle Leg	muscle
33	chr14:105607200-105614000	Strong transcription	Fetal Brain Female	brain
34	chr14:105607200-105616000	Strong transcription	HMEC	breast
35	chr14:105607200-105619600	Weak transcription	Colonic Mucosa	Colon
36	chr14:105607400-105608600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:105607400-105609200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
38	chr14:105607400-105609400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr14:105607400-105610000	Strong transcription	Brain Germinal Matrix	brain
40	chr14:105607400-105611000	Weak transcription	Fetal Muscle Trunk	muscle
41	chr14:105607400-105611200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr14:105607400-105612000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:105607400-105612400	Weak transcription	Brain Anterior Caudate	brain
44	chr14:105607400-105619200	Strong transcription	Pancreas	Pancrea
45	chr14:105607600-105608000	Weak transcription	Adipose Nuclei	Adipose
46	chr14:105607600-105608400	Weak transcription	Spleen	Spleen
47	chr14:105607600-105608800	Strong transcription	Fetal Stomach	stomach
48	chr14:105607600-105611800	Weak transcription	Brain Hippocampus Middle	brain
49	chr14:105607600-105612000	Weak transcription	Brain Cingulate Gyrus	brain
50	chr14:105607600-105616000	Strong transcription	Fetal Intestine Small	intestine

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