Variant report

Variant	nsv901845
Chromosome Location	chr14:45619217-45772910
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2093)
CpG islands
(count:1098)
Chromatin interactive
region (count:61)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2093 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:45721346-45721411	K562	blood:	n/a	n/a
2	ARID3A	chr14:45719321-45719834	K562	blood:	n/a	n/a
3	ARID3A	chr14:45722356-45723128	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:45756958-45756994	K562	blood:	n/a	n/a
5	ARID3A	chr14:45722305-45722539	K562	blood:	n/a	n/a
6	ATF1	chr14:45719315-45719720	K562	blood:	n/a	n/a
7	ATF2	chr14:45654344-45654869	GM12878	blood:	n/a	n/a
8	ATF2	chr14:45654284-45654680	GM12878	blood:	n/a	n/a
9	ATF2	chr14:45722322-45723116	GM12878	blood:	n/a	n/a
10	ATF2	chr14:45721046-45721503	GM12878	blood:	n/a	n/a
11	ATF2	chr14:45722376-45723046	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr14:45722078-45723054	GM12878	blood:	n/a	n/a
13	ATF2	chr14:45720949-45721641	GM12878	blood:	n/a	n/a
14	ATF2	chr14:45722269-45723075	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr14:45722329-45723000	A549	lung:	n/a	n/a
16	ATF3	chr14:45722453-45723019	A549	lung:	n/a	n/a
17	ATF3	chr14:45722372-45722682	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr14:45741418-45741630	K562	blood:	n/a	n/a
19	BACH1	chr14:45722065-45723061	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr14:45721069-45721411	GM12878	blood:	n/a	n/a
21	BATF	chr14:45721023-45721508	GM12878	blood:	n/a	n/a
22	BATF	chr14:45654320-45654609	GM12878	blood:	n/a	chr14:45654495-45654506
23	BATF	chr14:45654382-45654581	GM12878	blood:	n/a	chr14:45654495-45654506
24	BATF	chr14:45625307-45625620	GM12878	blood:	n/a	n/a
25	BATF	chr14:45625249-45625630	GM12878	blood:	n/a	n/a
26	BCL11A	chr14:45721145-45721473	GM12878	blood:	n/a	n/a
27	BCL11A	chr14:45722473-45722840	GM12878	blood:	n/a	n/a
28	BCL3	chr14:45722180-45723071	A549	lung:	n/a	n/a
29	BCL3	chr14:45722203-45723416	A549	lung:	n/a	n/a
30	BCLAF1	chr14:45722060-45723125	GM12878	blood:	n/a	n/a
31	BCLAF1	chr14:45737709-45738137	GM12878	blood:	n/a	n/a
32	BCLAF1	chr14:45721060-45721557	GM12878	blood:	n/a	n/a
33	BCLAF1	chr14:45722194-45723134	GM12878	blood:	n/a	n/a
34	BHLHE40	chr14:45722164-45723101	GM12878	blood:	n/a	n/a
35	BHLHE40	chr14:45722265-45722799	K562	blood:	n/a	n/a
36	BHLHE40	chr14:45619850-45619857	K562	blood:	n/a	n/a
37	BHLHE40	chr14:45723324-45723381	GM12878	blood:	n/a	n/a
38	BHLHE40	chr14:45721077-45721534	GM12878	blood:	n/a	n/a
39	BHLHE40	chr14:45718701-45719749	GM12878	blood:	n/a	n/a
40	BHLHE40	chr14:45737784-45738081	GM12878	blood:	n/a	n/a
41	BHLHE40	chr14:45722198-45723003	HepG2	liver:	n/a	n/a
42	BHLHE40	chr14:45721733-45721803	K562	blood:	n/a	n/a
43	BRCA1	chr14:45722007-45723004	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr14:45722387-45723098	HepG2	liver:	n/a	n/a
45	BRCA1	chr14:45681497-45681782	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr14:45722287-45722946	GM12878	blood:	n/a	n/a
47	CBX3	chr14:45721964-45723196	HCT-116	colon:	n/a	n/a
48	CBX3	chr14:45727350-45727582	K562	blood:	n/a	n/a
49	CBX3	chr14:45751010-45751209	K562	blood:	n/a	n/a
50	CBX3	chr14:45727253-45727633	K562	blood:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:45759143-45759193	HIPEpiC	eye:	n/a
2	chr14:45722704-45722754	AG04450	lung:	fetal
3	chr14:45722532-45722582	MCF10A-Er-Src	breast:	n/a
4	chr14:45722532-45722582	HCPEpiC	choroid plexus:	n/a
5	chr14:45719962-45720012	BJ	skin:	n/a
6	chr14:45723353-45723403	NH-A	brain:	n/a
7	chr14:45722704-45722754	ECC-1	luminal epithelium:	n/a
8	chr14:45722711-45722761	T-47D	breast:	n/a
9	chr14:45722987-45723037	SK-N-MC	brain:	n/a
10	chr14:45722617-45722667	GM12891	blood:	n/a
11	chr14:45722711-45722761	H1-hESC	embryonic stem cell:	embryo
12	chr14:45722711-45722761	BE2_C	brain:	n/a
13	chr14:45722289-45722339	HCF	heart:	n/a
14	chr14:45722532-45722582	GM12891	blood:	n/a
15	chr14:45723353-45723403	AG04450	lung:	fetal
16	chr14:45722532-45722582	Caco-2	colon:	n/a
17	chr14:45722711-45722761	NB4	blood:	n/a
18	chr14:45722438-45722488	GM12878	blood:	n/a
19	chr14:45722987-45723037	AG09309	skin:	n/a
20	chr14:45722721-45722771	GM06990	blood:	n/a
21	chr14:45722704-45722754	GM12892	blood:	n/a
22	chr14:45722043-45722093	T-47D	breast:	n/a
23	chr14:45722721-45722771	HNPCEpiC	eye:	n/a
24	chr14:45619710-45619760	HUVEC	blood vessel:	n/a
25	chr14:45719962-45720012	CMK	blood:	n/a
26	chr14:45722438-45722488	HNPCEpiC	eye:	n/a
27	chr14:45725455-45725505	NH-A	brain:	n/a
28	chr14:45723353-45723403	HCT-116	colon:	n/a
29	chr14:45722987-45723037	Caco-2	colon:	n/a
30	chr14:45722438-45722488	ECC-1	luminal epithelium:	n/a
31	chr14:45722289-45722339	GM12878	blood:	n/a
32	chr14:45759143-45759193	HepG2	liver:	n/a
33	chr14:45725455-45725505	CMK	blood:	n/a
34	chr14:45722617-45722667	AG04449	skin:	fetal
35	chr14:45722622-45722672	NHDF-neo	bronchial:	n/a
36	chr14:45719962-45720012	Caco-2	colon:	n/a
37	chr14:45722745-45722795	GM12892	blood:	n/a
38	chr14:45719962-45720012	GM19239	blood:	n/a
39	chr14:45722745-45722795	SKMC	muscle:	n/a
40	chr14:45693776-45693826	NHBE	bronchial:	n/a
41	chr14:45725455-45725505	AG09319	gingival:	n/a
42	chr14:45693776-45693826	AG04449	skin:	fetal
43	chr14:45722622-45722672	HRPEpiC	eye:	n/a
44	chr14:45723353-45723403	A549	lung:	n/a
45	chr14:45693776-45693826	GM06990	blood:	n/a
46	chr14:45722721-45722771	SK-N-SH	brain:	n/a
47	chr14:45722289-45722339	LNCaP	prostate:	n/a
48	chr14:45693776-45693826	ProgFib	skin:	n/a
49	chr14:45619710-45619760	SAEC	small airway:	n/a
50	chr14:45722043-45722093	SK-N-SH	brain:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:45679707..45681443-chr14:45682954..45685431,2	MCF-7	breast:
2	chr14:45710936..45712506-chr14:45717032..45718785,2	K562	blood:
3	chr14:45642220..45642925-chr3:15744255..15744957,2	MCF-7	breast:
4	chr14:45656403..45658516-chr14:45660944..45662467,2	K562	blood:
5	chr14:45646929..45649462-chr14:45654558..45656763,2	MCF-7	breast:
6	chr14:45705828..45707853-chr14:45712067..45713833,2	MCF-7	breast:
7	chr14:45625132..45625884-chr14:45737446..45738063,2	MCF-7	breast:
8	chr14:45728008..45730307-chr14:45736451..45738128,2	MCF-7	breast:
9	chr14:45601339..45606570-chr14:45722040..45724234,5	MCF-7	breast:
10	chr14:45633384..45635477-chr14:45696963..45699903,2	K562	blood:
11	chr14:45691934..45693449-chr14:45696943..45699176,2	K562	blood:
12	chr14:45602127..45604753-chr14:45663280..45664995,2	K562	blood:
13	chr14:45678908..45681403-chr14:45684566..45687731,3	K562	blood:
14	chr14:45588121..45589844-chr14:45722977..45725072,2	MCF-7	breast:
15	chr14:45701019..45703145-chr14:45705910..45707479,2	MCF-7	breast:
16	chr14:45429725..45432587-chr14:45720437..45723992,3	MCF-7	breast:
17	chr14:45728008..45730307-chr14:45736451..45738128,2	MCF-7	breast:
18	chr14:45656819..45659506-chr14:45660040..45662429,2	MCF-7	breast:
19	chr14:45687729..45690041-chr14:45727283..45730126,2	MCF-7	breast:
20	chr14:45679707..45681443-chr14:45682954..45685431,2	MCF-7	breast:
21	chr14:45710340..45712436-chr14:45717199..45718785,2	K562	blood:
22	chr14:45686107..45687762-chr14:45690823..45693059,2	MCF-7	breast:
23	chr14:45727473..45730434-chr14:45734970..45737678,2	MCF-7	breast:
24	chr14:45720720..45725312-chr14:45736349..45740437,5	MCF-7	breast:
25	chr14:45721734..45722708-chr16:28565152..28565667,2	Hela-S3	cervix:
26	chr14:45705828..45707853-chr14:45712067..45713833,2	MCF-7	breast:
27	chr14:45553320..45554876-chr14:45714486..45717051,2	MCF-7	breast:
28	chr14:45717265..45719179-chr14:45721039..45722598,2	K562	blood:
29	chr14:45727473..45730434-chr14:45734970..45737678,2	MCF-7	breast:
30	chr14:45427536..45430475-chr14:45702216..45704003,2	MCF-7	breast:
31	chr12:57039223..57039923-chr14:45722606..45723303,3	Hela-S3	cervix:
32	chr14:45694223..45697049-chr14:45698740..45700285,2	MCF-7	breast:
33	chr14:45701847..45703730-chr14:45720111..45722706,2	MCF-7	breast:
34	chr14:45382584..45383476-chr14:45670758..45671337,2	MCF-7	breast:
35	chr14:45721810..45725859-chr14:45742099..45745950,4	MCF-7	breast:
36	chr14:45364937..45368444-chr14:45721075..45725396,9	MCF-7	breast:
37	chr14:45625132..45625884-chr14:45737446..45738063,2	MCF-7	breast:
38	chr14:45644589..45646805-chr14:45647065..45649190,2	MCF-7	breast:
39	chr14:45382903..45383965-chr14:45737675..45738717,4	MCF-7	breast:
40	chr14:45686107..45687762-chr14:45690823..45693059,2	MCF-7	breast:
41	chr14:45383078..45384611-chr14:45736865..45739302,2	MCF-7	breast:
42	chr14:45669652..45672262-chr14:45722530..45724163,2	MCF-7	breast:
43	chr14:45721810..45725859-chr14:45742099..45745950,4	MCF-7	breast:
44	chr14:45722471..45723281-chr15:75743983..75744975,2	Hela-S3	cervix:
45	chr14:45722872..45725627-chr6:151936857..151939807,2	MCF-7	breast:
46	chr14:45656819..45659506-chr14:45660040..45662429,2	MCF-7	breast:
47	chr14:45646929..45649462-chr14:45654558..45656763,2	MCF-7	breast:
48	chr14:45678908..45681403-chr14:45684566..45687731,3	K562	blood:
49	chr14:45701019..45703145-chr14:45705910..45707479,2	MCF-7	breast:
50	chr14:45602054..45606945-chr14:45719959..45724414,9	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FKBP3-6	chr14:45710671-45711073	NONHSAT036649
2	lnc-FKBP3-4	chr14:45673040-45673415	NONHSAT036646
3	lnc-FANCM-8	chr14:45759239-45759589	NONHSAT036654
4	lnc-FKBP3-5	chr14:45696890-45697017	NONHSAT036648
5	lnc-FKBP3-5	chr14:45700344-45700644	NONHSAT036648
6	lnc-FANCM-8	chr14:45759448-45759479	NONHSAT036652
7	lnc-FKBP3-6	chr14:45711237-45711589	NONHSAT036649
8	lnc-FANCM-8	chr14:45759144-45759367	NONHSAT036652
9	lnc-FKBP3-4	chr14:45673583-45673656	NONHSAT036647
10	lnc-FANCM-8	chr14:45759209-45759392	NONHSAT036653
11	lnc-FKBP3-4	chr14:45673602-45673656	NONHSAT036646
12	lnc-FKBP3-4	chr14:45675286-45675647	NONHSAT036646
13	lnc-FKBP3-4	chr14:45675286-45675477	NONHSAT036647
14	lnc-FANCM-8	chr14:45759448-45759483	NONHSAT036653

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C14orf106	hsa-miR-421	chr14:45672809-45672831

Variant related genes	Relation type
DNAJC19P9	TF binding region
RNU6-552P	TF binding region
FANCM	TF binding region
MIS18BP1	TF binding region
DNAJC19P9	CpG island
RNU6-552P	CpG island
FANCM	CpG island
MIS18BP1	CpG island
ENSG00000179476	chromatin interactions
ENSG00000179454	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000207422	chromatin interactions
ENSG00000199739	chromatin interactions
ENSG00000185246	chromatin interactions
ENSG00000176476	chromatin interactions
ENSG00000198718	chromatin interactions
ENSG00000258633	chromatin interactions
ENSG00000129534	chromatin interactions
ENSG00000110955	chromatin interactions
ENSG00000100442	chromatin interactions
ENSG00000266401	chromatin interactions
ENSG00000187790	chromatin interactions

Extended variants
information (count: 4914 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4914 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11157432	chr14:45619217-45619218	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77025737	chr14:45619239-45619240	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558490257	chr14:45619241-45619242	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181826473	chr14:45619255-45619256	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187074599	chr14:45619280-45619281	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556028956	chr14:45619282-45619283	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574128452	chr14:45619321-45619322	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148790369	chr14:45619331-45619332	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565256827	chr14:45619383-45619384	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143906343	chr14:45619415-45619416	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532952294	chr14:45619460-45619461	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs367554274	chr14:45619501-45619502	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572653584	chr14:45619535-45619536	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544557453	chr14:45619567-45619568	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372179493	chr14:45619693-45619694	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373879052	chr14:45619762-45619763	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191555804	chr14:45619764-45619765	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs76518554	chr14:45619777-45619778	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs77142566	chr14:45619789-45619790	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs567482956	chr14:45619824-45619825	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs146835441	chr14:45619840-45619841	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs140687897	chr14:45619851-45619852	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561564792	chr14:45619916-45619917	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1431050	chr14:45619930-45619931	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs539860763	chr14:45619955-45619956	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535434920	chr14:45619997-45619998	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144268096	chr14:45620017-45620018	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183419231	chr14:45620077-45620078	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555782282	chr14:45620084-45620085	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35321318	chr14:45620090-45620091	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574215335	chr14:45620111-45620112	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114246290	chr14:45620129-45620130	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553036671	chr14:45620136-45620137	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4374080	chr14:45620138-45620139	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577291602	chr14:45620243-45620244	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375165246	chr14:45620258-45620259	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562980561	chr14:45620286-45620287	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76768362	chr14:45620307-45620308	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77415294	chr14:45620319-45620320	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549366477	chr14:45620357-45620358	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561018972	chr14:45620360-45620361	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187820010	chr14:45620364-45620365	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562458999	chr14:45620384-45620385	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546446591	chr14:45620479-45620480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559811102	chr14:45620509-45620510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533497727	chr14:45620543-45620544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112948377	chr14:45620548-45620549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371481234	chr14:45620581-45620582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143006771	chr14:45620607-45620608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189856413	chr14:45620615-45620616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2354 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45606000-45622200	Weak transcription	Pancreas	Pancrea
2	chr14:45606000-45634600	Weak transcription	Esophagus	oesophagus
3	chr14:45606000-45679600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr14:45606200-45622400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr14:45606400-45620600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr14:45606400-45641200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr14:45606600-45630600	Weak transcription	Fetal Muscle Leg	muscle
8	chr14:45606600-45634400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr14:45606600-45636400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr14:45607000-45636400	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr14:45607000-45660000	Weak transcription	Ovary	ovary
12	chr14:45607200-45619600	Weak transcription	Colon Smooth Muscle	Colon
13	chr14:45607200-45633200	Weak transcription	Fetal Thymus	thymus
14	chr14:45607200-45634800	Weak transcription	HSMM	muscle
15	chr14:45607200-45638800	Weak transcription	Fetal Brain Female	brain
16	chr14:45607200-45639000	Weak transcription	Liver	Liver
17	chr14:45607400-45633200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr14:45607400-45633200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr14:45607400-45633600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr14:45607400-45633600	Weak transcription	Adipose Nuclei	Adipose
21	chr14:45607400-45633600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr14:45607400-45634400	Weak transcription	Fetal Intestine Small	intestine
23	chr14:45607400-45635600	Weak transcription	Fetal Lung	lung
24	chr14:45607400-45636600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr14:45607400-45650200	Weak transcription	NH-A	brain
26	chr14:45607400-45656000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr14:45607400-45678400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr14:45607600-45624600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr14:45607600-45633400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:45607600-45633400	Weak transcription	Primary hematopoietic stem cells	blood
31	chr14:45608000-45683000	Weak transcription	K562	blood
32	chr14:45608200-45633400	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr14:45608200-45635000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr14:45608200-45635600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr14:45608200-45636200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr14:45608200-45639400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr14:45608400-45620400	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr14:45608400-45622200	Weak transcription	Fetal Heart	heart
39	chr14:45608400-45633600	Weak transcription	HUVEC	blood vessel
40	chr14:45608400-45635000	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr14:45608400-45668400	Weak transcription	NHDF-Ad	bronchial
42	chr14:45608800-45633000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr14:45609800-45623800	Weak transcription	Hela-S3	cervix
44	chr14:45610200-45636800	Weak transcription	NHEK	skin
45	chr14:45610200-45667400	Weak transcription	HMEC	breast
46	chr14:45610400-45633000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:45614000-45638000	Weak transcription	Lung	lung
48	chr14:45614200-45632400	Weak transcription	Primary B cells from peripheral blood	blood
49	chr14:45614200-45633400	Weak transcription	A549	lung
50	chr14:45614400-45629400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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