Variant report

Variant	esv1794421
Chromosome Location	chr14:105617042-105635756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:816)
CpG islands
(count:1528)
Chromatin interactive
region (count:63)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:816 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105635551-105635751	K562	blood:	n/a	n/a
2	ATF3	chr14:105633815-105634024	K562	blood:	n/a	n/a
3	BACH1	chr14:105634160-105634415	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:105635446-105635818	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr14:105633488-105634425	K562	blood:	n/a	chr14:105633626-105633642
6	BHLHE40	chr14:105635049-105635625	K562	blood:	n/a	n/a
7	BRCA1	chr14:105628806-105629067	HepG2	liver:	n/a	n/a
8	CBX3	chr14:105635458-105635833	K562	blood:	n/a	n/a
9	CCNT2	chr14:105634944-105635778	K562	blood:	n/a	chr14:105635426-105635435
10	CCNT2	chr14:105633598-105634394	K562	blood:	n/a	n/a
11	CEBPB	chr14:105631426-105631943	ECC-1	luminal epithelium:	n/a	n/a
12	CHD2	chr14:105635003-105635186	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr14:105634239-105634449	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr14:105633690-105633737	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr14:105635288-105635741	K562	blood:	n/a	n/a
16	CHD2	chr14:105635604-105635860	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr14:105628806-105628928	HepG2	liver:	n/a	n/a
18	CHD2	chr14:105632638-105632642	K562	blood:	n/a	n/a
19	CREB1	chr14:105633974-105634413	A549	lung:	n/a	n/a
20	CREB1	chr14:105634956-105635290	A549	lung:	n/a	n/a
21	CTCF	chr14:105633916-105634321	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:105633900-105634050	HCT-116	colon:	n/a	n/a
23	CTCF	chr14:105635560-105635710	GM12866	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
24	CTCF	chr14:105617724-105617869	MCF-7	breast:	n/a	n/a
25	CTCF	chr14:105633906-105634044	A549	lung:	n/a	n/a
26	CTCF	chr14:105634187-105634331	Fibrobl	skin:	n/a	n/a
27	CTCF	chr14:105635560-105635710	RPTEC	kidney:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
28	CTCF	chr14:105633774-105634152	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr14:105635600-105635750	GM12875	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
30	CTCF	chr14:105634081-105634084	GM19239	blood:	n/a	n/a
31	CTCF	chr14:105635528-105635804	GM19238	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
32	CTCF	chr14:105635620-105635770	SAEC	small airway:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
33	CTCF	chr14:105631470-105631685	MCF-7	breast:	n/a	chr14:105631554-105631562
34	CTCF	chr14:105629426-105629554	HepG2	liver:	n/a	n/a
35	CTCF	chr14:105634120-105634270	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr14:105635559-105635759	GM10248	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
37	CTCF	chr14:105632320-105632470	HMEC	breast:	n/a	chr14:105632422-105632435
38	CTCF	chr14:105635640-105635790	HPF	lung:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
39	CTCF	chr14:105633814-105634365	K562	blood:	n/a	n/a
40	CTCF	chr14:105633880-105634030	BE2_C	brain:	n/a	n/a
41	CTCF	chr14:105635580-105635730	HPAF	blood vessel:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
42	CTCF	chr14:105634377-105634416	GM10266	blood:	n/a	n/a
43	CTCF	chr14:105633934-105634041	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr14:105633840-105633990	HEK293	kidney:	n/a	n/a
45	CTCF	chr14:105633020-105633170	HMEC	breast:	n/a	chr14:105633102-105633120 chr14:105633104-105633117
46	CTCF	chr14:105634180-105634330	GM12874	blood:	n/a	n/a
47	CTCF	chr14:105633866-105634070	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr14:105635580-105635730	GM12866	blood:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
49	CTCF	chr14:105635600-105635750	AG09309	skin:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
50	CTCF	chr14:105635600-105635750	HCPEpiC	choroid plexus:	n/a	chr14:105635654-105635667 chr14:105635651-105635669

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105635081-105635131	CMK	blood:	n/a
2	chr14:105620358-105620408	IMR90	lung:	fetal
3	chr14:105635208-105635258	CMK	blood:	n/a
4	chr14:105635081-105635131	CMK	blood:	n/a
5	chr14:105620358-105620408	IMR90	lung:	fetal
6	chr14:105635208-105635258	CMK	blood:	n/a
7	chr14:105635239-105635289	HIPEpiC	eye:	n/a
8	chr14:105617308-105617358	GM06990	blood:	n/a
9	chr14:105617308-105617358	SK-N-SH_RA	brain:	n/a
10	chr14:105617839-105617889	Hepatocyte	liver:	n/a
11	chr14:105622312-105622362	AG04449	skin:	fetal
12	chr14:105617080-105617130	AG04450	lung:	fetal
13	chr14:105634387-105634437	PrEC	prostate:	n/a
14	chr14:105633697-105633747	Jurkat	blood:	n/a
15	chr14:105619511-105619561	PFSK-1	brain:	n/a
16	chr14:105617173-105617223	HCT-116	colon:	n/a
17	chr14:105618816-105618866	MCF10A-Er-Src	breast:	n/a
18	chr14:105617173-105617223	HAEpiC	amniotic membrane:	n/a
19	chr14:105620358-105620408	HUVEC	blood vessel:	n/a
20	chr14:105635708-105635758	GM12878	blood:	n/a
21	chr14:105635236-105635286	HCF	heart:	n/a
22	chr14:105633697-105633747	AoSMC	blood vessel:	n/a
23	chr14:105635081-105635131	HEEpiC	esophagus:	n/a
24	chr14:105622312-105622362	NH-A	brain:	n/a
25	chr14:105633697-105633747	AG09319	gingival:	n/a
26	chr14:105622992-105623042	HCF	heart:	n/a
27	chr14:105618576-105618626	NH-A	brain:	n/a
28	chr14:105618482-105618532	BE2_C	brain:	n/a
29	chr14:105635236-105635286	HCM	heart:	n/a
30	chr14:105635208-105635258	Caco-2	colon:	n/a
31	chr14:105617080-105617130	MCF-7	breast:	n/a
32	chr14:105620358-105620408	AG04449	skin:	fetal
33	chr14:105624483-105624533	RPTEC	kidney:	n/a
34	chr14:105618482-105618532	GM12891	blood:	n/a
35	chr14:105622992-105623042	SK-N-SH	brain:	n/a
36	chr14:105625577-105625627	HCT-116	colon:	n/a
37	chr14:105635208-105635258	HCF	heart:	n/a
38	chr14:105619701-105619751	ovcar-3	ovarian:	n/a
39	chr14:105635081-105635131	NHDF-neo	bronchial:	n/a
40	chr14:105619701-105619751	Hela-S3	cervix:	n/a
41	chr14:105618576-105618626	AG04449	skin:	fetal
42	chr14:105618576-105618626	NT2-D1	testis:	n/a
43	chr14:105635706-105635756	AG09309	skin:	n/a
44	chr14:105622992-105623042	NH-A	brain:	n/a
45	chr14:105635236-105635286	GM12891	blood:	n/a
46	chr14:105622312-105622362	GM19239	blood:	n/a
47	chr14:105635236-105635286	NHBE	bronchial:	n/a
48	chr14:105620358-105620408	ProgFib	skin:	n/a
49	chr14:105633697-105633747	HRE	kidney:	n/a
50	chr14:105633697-105633747	LNCaP	prostate:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:105611401..105614212-chr14:105625101..105627298,2	MCF-7	breast:
2	chr14:105632765..105635152-chr14:105864248..105866641,2	K562	blood:
3	chr14:105620616..105622856-chr14:105624629..105627730,3	MCF-7	breast:
4	chr14:105502174..105504922-chr14:105632204..105633983,2	MCF-7	breast:
5	chr14:105635510..105639334-chr14:105658974..105662269,3	K562	blood:
6	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
7	chr14:105556907..105557905-chr14:105631981..105632717,2	MCF-7	breast:
8	chr14:105618156..105621334-chr14:105628329..105630360,3	K562	blood:
9	chr14:105633510..105636132-chr14:105956968..105959602,2	K562	blood:
10	chr14:105635244..105636129-chr14:105665708..105667054,3	K562	blood:
11	chr14:105618326..105620016-chr14:105627831..105630426,2	MCF-7	breast:
12	chr14:105605939..105608674-chr14:105628049..105630309,2	K562	blood:
13	chr14:105445649..105448428-chr14:105631488..105633523,2	MCF-7	breast:
14	chr14:105559890..105560867-chr14:105633779..105634301,2	MCF-7	breast:
15	chr14:105620302..105622152-chr14:105646136..105647731,2	MCF-7	breast:
16	chr14:105615698..105618053-chr14:105622347..105625638,3	MCF-7	breast:
17	chr14:105552235..105554666-chr14:105628025..105629965,2	MCF-7	breast:
18	chr14:105631465..105635896-chr14:105645452..105649219,9	MCF-7	breast:
19	chr14:105617835..105619717-chr14:105620167..105621698,2	MCF-7	breast:
20	chr14:105557317..105562216-chr14:105628986..105634761,7	MCF-7	breast:
21	chr14:105555328..105560254-chr14:105631379..105635555,5	MCF-7	breast:
22	chr14:105441844..105444735-chr14:105632724..105634694,2	MCF-7	breast:
23	chr14:105633273..105637288-chr14:105642227..105645314,5	MCF-7	breast:
24	chr14:105631482..105635033-chr14:105765939..105767661,3	K562	blood:
25	chr14:105511711..105512332-chr14:105633666..105634346,2	MCF-7	breast:
26	chr14:105268465..105270651-chr14:105635461..105637238,2	K562	blood:
27	chr14:105629335..105630135-chr14:105669031..105669954,2	K562	blood:
28	chr14:105611629..105615687-chr14:105625576..105630230,4	K562	blood:
29	chr14:105556861..105558363-chr14:105628903..105631842,2	K562	blood:
30	chr14:105610604..105613096-chr14:105619107..105620769,2	K562	blood:
31	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
32	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
33	chr14:105633713..105635633-chr7:75987137..75988852,2	K562	blood:
34	chr14:105539437..105542411-chr14:105625371..105627547,2	K562	blood:
35	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
36	chr14:105620616..105622856-chr14:105624629..105627730,3	MCF-7	breast:
37	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
38	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
39	chr14:105632764..105636922-chr14:105637769..105642057,5	MCF-7	breast:
40	chr14:105556904..105557457-chr14:105630667..105631594,2	MCF-7	breast:
41	chr14:105614456..105616179-chr14:105620874..105623619,2	MCF-7	breast:
42	chr14:105617835..105619717-chr14:105620167..105621698,2	MCF-7	breast:
43	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
44	chr14:105450462..105452951-chr14:105633617..105637647,3	MCF-7	breast:
45	chr14:105618326..105620016-chr14:105627831..105630426,2	MCF-7	breast:
46	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
47	chr14:105635593..105636402-chr14:105818301..105819224,3	K562	blood:
48	chr14:105620927..105623497-chr14:105711846..105714187,2	MCF-7	breast:
49	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
50	chr14:105602588..105606045-chr14:105617930..105622124,4	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

No data

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

Extended variants
information (count: 821 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1057744	chr14:105617042-105617043	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs587675104	chr14:105617058-105617059	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587707453	chr14:105617073-105617074	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs140376952	chr14:105617081-105617082	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs374092502	chr14:105617121-105617122	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region miRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs111330665	chr14:105617143-105617144	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs371620673	chr14:105617156-105617157	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs186020705	chr14:105617166-105617167	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs587679646	chr14:105617173-105617174	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs587718189	chr14:105617174-105617175	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs368185909	chr14:105617195-105617196	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region miRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs372928725	chr14:105617264-105617265	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs200795940	chr14:105617277-105617278	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs377202261	chr14:105617290-105617291	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs368948370	chr14:105617293-105617294	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs587629778	chr14:105617294-105617295	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373113193	chr14:105617305-105617306	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs587657435	chr14:105617306-105617307	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs374843608	chr14:105617309-105617310	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs587763712	chr14:105617313-105617314	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs374331901	chr14:105617314-105617315	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs367891113	chr14:105617379-105617380	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs369448615	chr14:105617407-105617408	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs1135540	chr14:105617434-105617435	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs1135539	chr14:105617438-105617439	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs144248956	chr14:105617440-105617441	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs372743058	chr14:105617452-105617453	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs369352271	chr14:105617466-105617467	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs116916276	chr14:105617467-105617468	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs199970757	chr14:105617472-105617473	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201910428	chr14:105617475-105617476	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs587765173	chr14:105617478-105617479	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs587646477	chr14:105617511-105617512	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113561600	chr14:105617512-105617513	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs587760039	chr14:105617515-105617516	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs181335951	chr14:105617532-105617533	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs79441490	chr14:105617541-105617542	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs76260431	chr14:105617550-105617551	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs201854766	chr14:105617560-105617561	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs185514534	chr14:105617563-105617564	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs11283160	chr14:105617567-105617568	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs143758628	chr14:105617568-105617569	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs147914644	chr14:105617575-105617576	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs373530904	chr14:105617580-105617581	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs200745390	chr14:105617583-105617584	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs376410237	chr14:105617584-105617585	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs370937583	chr14:105617598-105617599	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs374425230	chr14:105617600-105617601	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs367554058	chr14:105617605-105617606	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs112817342	chr14:105617608-105617609	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	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
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:800 , 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	chr14:105606400-105617800	Strong transcription	Skeletal Muscle Female	skeletal muscle
3	chr14:105606800-105618000	Weak transcription	Psoas Muscle	Psoas
4	chr14:105606800-105619600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr14:105606800-105631600	Weak transcription	Hela-S3	cervix
6	chr14:105607000-105618200	Strong transcription	Gastric	stomach
7	chr14:105607000-105621600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr14:105607200-105619600	Weak transcription	Colonic Mucosa	Colon
9	chr14:105607400-105619200	Strong transcription	Pancreas	Pancrea
10	chr14:105607600-105617600	Strong transcription	Skeletal Muscle Male	skeletal muscle
11	chr14:105607600-105625400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr14:105607600-105632000	Weak transcription	Brain Angular Gyrus	brain
13	chr14:105608000-105618000	Strong transcription	Adipose Nuclei	Adipose
14	chr14:105608800-105618400	Strong transcription	Lung	lung
15	chr14:105609400-105631400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr14:105609600-105618800	Weak transcription	Placenta	Placenta
17	chr14:105609600-105622000	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr14:105610000-105631400	Weak transcription	HUVEC	blood vessel
19	chr14:105610200-105625200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:105612800-105621000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr14:105613400-105623000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr14:105613400-105631400	Weak transcription	Brain Anterior Caudate	brain
23	chr14:105613600-105618400	Weak transcription	HSMMtube	muscle
24	chr14:105613600-105619200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr14:105613600-105631400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr14:105613800-105631400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr14:105614000-105620200	Weak transcription	Fetal Brain Female	brain
28	chr14:105614000-105621600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr14:105614000-105622000	Weak transcription	Brain Hippocampus Middle	brain
30	chr14:105614600-105619000	Strong transcription	Fetal Stomach	stomach
31	chr14:105615200-105621600	Weak transcription	Esophagus	oesophagus
32	chr14:105615200-105625600	Weak transcription	A549	lung
33	chr14:105615800-105618400	Weak transcription	Left Ventricle	heart
34	chr14:105615800-105633200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr14:105616000-105618000	Weak transcription	Fetal Intestine Small	intestine
36	chr14:105616000-105619000	Weak transcription	Spleen	Spleen
37	chr14:105616000-105621800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr14:105616000-105623600	Weak transcription	NHEK	skin
39	chr14:105616000-105623800	Weak transcription	HMEC	breast
40	chr14:105616200-105619000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr14:105616200-105619600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:105616600-105617200	Strong transcription	Brain Germinal Matrix	brain
43	chr14:105616600-105617600	Strong transcription	Fetal Muscle Leg	muscle
44	chr14:105616600-105617800	Strong transcription	Right Ventricle	heart
45	chr14:105617000-105618400	Genic enhancers	Fetal Muscle Trunk	muscle
46	chr14:105617000-105619600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:105617200-105617600	Weak transcription	Brain Germinal Matrix	brain
48	chr14:105617600-105618200	Strong transcription	Brain Germinal Matrix	brain
49	chr14:105617600-105618200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
50	chr14:105617600-105618400	Genic enhancers	Fetal Muscle Leg	muscle

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