Variant report

Variant	nsv565043
Chromosome Location	chr14:71395604-71625112
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2507)
CpG islands
(count:734)
Chromatin interactive
region (count:70)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:71453850-71454159	K562	blood:	n/a	n/a
2	ARID3A	chr14:71584599-71585049	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:71583321-71583963	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:71439131-71439396	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:71610207-71610661	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:71596906-71597822	K562	blood:	n/a	n/a
7	ATF1	chr14:71610189-71610768	K562	blood:	n/a	n/a
8	ATF1	chr14:71609002-71609339	K562	blood:	n/a	n/a
9	ATF1	chr14:71597363-71597860	K562	blood:	n/a	n/a
10	ATF1	chr14:71455163-71455464	K562	blood:	n/a	n/a
11	ATF3	chr14:71488349-71488985	HCT-116	colon:	n/a	n/a
12	ATF3	chr14:71610318-71610639	K562	blood:	n/a	n/a
13	ATF3	chr14:71462500-71462644	K562	blood:	n/a	n/a
14	BATF	chr14:71609226-71609612	GM12878	blood:	n/a	n/a
15	BATF	chr14:71489604-71489981	GM12878	blood:	n/a	n/a
16	BCL11A	chr14:71597411-71597742	GM12878	blood:	n/a	n/a
17	BCLAF1	chr14:71609019-71609668	GM12878	blood:	n/a	chr14:71609253-71609262
18	BCLAF1	chr14:71422565-71423031	GM12878	blood:	n/a	n/a
19	BHLHE40	chr14:71597583-71597614	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:71609976-71610290	HepG2	liver:	n/a	n/a
21	BHLHE40	chr14:71597213-71597764	K562	blood:	n/a	n/a
22	BHLHE40	chr14:71610027-71610482	K562	blood:	n/a	n/a
23	BHLHE40	chr14:71462476-71462729	K562	blood:	n/a	n/a
24	BHLHE40	chr14:71455176-71455655	K562	blood:	n/a	n/a
25	BRCA1	chr14:71541284-71541304	GM12878	blood:	n/a	n/a
26	BRCA1	chr14:71488393-71489537	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr14:71501498-71501685	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr14:71438970-71438988	GM12878	blood:	n/a	n/a
29	BRCA1	chr14:71605864-71605925	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr14:71488110-71489423	HCT-116	colon:	n/a	n/a
31	CBX3	chr14:71545338-71545530	K562	blood:	n/a	n/a
32	CBX3	chr14:71410504-71410936	HCT-116	colon:	n/a	n/a
33	CBX3	chr14:71414498-71414801	K562	blood:	n/a	n/a
34	CCNT2	chr14:71453824-71454098	K562	blood:	n/a	n/a
35	CCNT2	chr14:71597368-71597644	K562	blood:	n/a	n/a
36	CEBPB	chr14:71612709-71613024	HepG2	liver:	n/a	chr14:71612862-71612875 chr14:71612862-71612873
37	CEBPB	chr14:71511098-71511378	IMR90	lung:	n/a	chr14:71511242-71511253
38	CEBPB	chr14:71516379-71516547	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr14:71610014-71611013	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr14:71527002-71527871	IMR90	lung:	n/a	chr14:71527177-71527188
41	CEBPB	chr14:71400833-71401045	HepG2	liver:	n/a	chr14:71400958-71400969
42	CEBPB	chr14:71488284-71489414	HCT-116	colon:	n/a	n/a
43	CEBPB	chr14:71542002-71542269	IMR90	lung:	n/a	chr14:71542124-71542137 chr14:71542124-71542135
44	CEBPB	chr14:71400783-71401145	H1-hESC	embryonic stem cell:	n/a	chr14:71400958-71400969
45	CEBPB	chr14:71488388-71489577	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr14:71400732-71401189	ECC-1	luminal epithelium:	n/a	chr14:71400958-71400969
47	CEBPB	chr14:71578097-71578293	A549	lung:	n/a	chr14:71578179-71578190
48	CEBPB	chr14:71584936-71586088	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr14:71400673-71401160	MCF-7	breast:	n/a	chr14:71400958-71400969
50	CEBPB	chr14:71585615-71585800	HepG2	liver:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:71605994-71606044	HPAEpiC	pulmonary alveolar:	n/a
2	chr14:71581031-71581081	BJ	skin:	n/a
3	chr14:71605994-71606044	HPAEpiC	pulmonary alveolar:	n/a
4	chr14:71581031-71581081	BJ	skin:	n/a
5	chr14:71577479-71577529	GM19239	blood:	n/a
6	chr14:71527576-71527626	AoSMC	blood vessel:	n/a
7	chr14:71527576-71527626	Jurkat	blood:	n/a
8	chr14:71472713-71472763	RPTEC	kidney:	n/a
9	chr14:71598219-71598269	RPTEC	kidney:	n/a
10	chr14:71605994-71606044	SAEC	small airway:	n/a
11	chr14:71585510-71585560	K562	blood:	n/a
12	chr14:71585510-71585560	AoSMC	blood vessel:	n/a
13	chr14:71527576-71527626	HRCEpiC	kidney:	n/a
14	chr14:71577479-71577529	HIPEpiC	eye:	n/a
15	chr14:71606506-71606556	GM12878	blood:	n/a
16	chr14:71605994-71606044	SK-N-SH_RA	brain:	n/a
17	chr14:71585510-71585560	MCF10A-Er-Src	breast:	n/a
18	chr14:71581031-71581081	AG09319	gingival:	n/a
19	chr14:71555837-71555887	HEEpiC	esophagus:	n/a
20	chr14:71606506-71606556	HNPCEpiC	eye:	n/a
21	chr14:71515513-71515563	AoSMC	blood vessel:	n/a
22	chr14:71605994-71606044	H1-hESC	embryonic stem cell:	embryo
23	chr14:71609158-71609208	SKMC	muscle:	n/a
24	chr14:71605994-71606044	SK-N-MC	brain:	n/a
25	chr14:71581031-71581081	RPTEC	kidney:	n/a
26	chr14:71606506-71606556	Hepatocyte	liver:	n/a
27	chr14:71555837-71555887	PrEC	prostate:	n/a
28	chr14:71606506-71606556	K562	blood:	n/a
29	chr14:71515513-71515563	HL-60	blood:	n/a
30	chr14:71606506-71606556	HAEpiC	amniotic membrane:	n/a
31	chr14:71606506-71606556	HEEpiC	esophagus:	n/a
32	chr14:71577479-71577529	NB4	blood:	n/a
33	chr14:71605994-71606044	GM12892	blood:	n/a
34	chr14:71581031-71581081	GM12891	blood:	n/a
35	chr14:71606274-71606324	HRE	kidney:	n/a
36	chr14:71606274-71606324	GM19239	blood:	n/a
37	chr14:71581031-71581081	NHBE	bronchial:	n/a
38	chr14:71585510-71585560	AG10803	skin:	n/a
39	chr14:71472713-71472763	GM12891	blood:	n/a
40	chr14:71581031-71581081	AG04449	skin:	fetal
41	chr14:71598219-71598269	HMEC	breast:	n/a
42	chr14:71527576-71527626	HPAEpiC	pulmonary alveolar:	n/a
43	chr14:71585510-71585560	ovcar-3	ovarian:	n/a
44	chr14:71605994-71606044	ovcar-3	ovarian:	n/a
45	chr14:71605994-71606044	GM19239	blood:	n/a
46	chr14:71515513-71515563	ECC-1	luminal epithelium:	n/a
47	chr14:71581031-71581081	HEK293	kidney:	embryo
48	chr14:71609158-71609208	SK-N-MC	brain:	n/a
49	chr14:71598219-71598269	HEEpiC	esophagus:	n/a
50	chr14:71585510-71585560	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:71511687..71514106-chr14:71519945..71521504,2	MCF-7	breast:
2	chr14:71373895..71374580-chr14:71438774..71439742,5	MCF-7	breast:
3	chr14:71608562..71610263-chr14:71786915..71789760,2	MCF-7	breast:
4	chr14:71372532..71376222-chr14:71415679..71419226,4	MCF-7	breast:
5	chr14:71605416..71606618-chr14:72219460..72220340,5	MCF-7	breast:
6	chr14:71179105..71181314-chr14:71570757..71573577,2	K562	blood:
7	chr14:71438802..71440447-chr14:71441088..71442805,2	MCF-7	breast:
8	chr14:71605350..71606109-chr14:71870362..71870894,2	MCF-7	breast:
9	chr14:71570724..71571280-chr14:72321914..72322593,2	K562	blood:
10	chr14:71423548..71425055-chr14:71436128..71438876,2	MCF-7	breast:
11	chr14:71294085..71294861-chr14:71422503..71423266,2	MCF-7	breast:
12	chr14:71521439..71523990-chr14:71537038..71539301,2	MCF-7	breast:
13	chr14:71570663..71571191-chr14:72219553..72220390,2	MCF-7	breast:
14	chr14:71441488..71443872-chr14:71448426..71449969,2	MCF-7	breast:
15	chr14:71605592..71606386-chr14:71869586..71870379,2	MCF-7	breast:
16	chr14:71540159..71540880-chr9:91932962..91933924,2	NB4	blood:
17	chr14:71570510..71571060-chr14:71673984..71674688,2	K562	blood:
18	chr14:71511687..71514106-chr14:71519945..71521504,2	MCF-7	breast:
19	chr14:71273334..71275325-chr14:71487514..71489742,2	MCF-7	breast:
20	chr14:71487547..71489766-chr14:72170994..72172928,2	MCF-7	breast:
21	chr14:71472106..71474140-chr14:71476821..71478999,2	K562	blood:
22	chr14:71287734..71288653-chr14:71422559..71423263,2	MCF-7	breast:
23	chr14:71576318..71579821-chr14:71580472..71584172,4	MCF-7	breast:
24	chr14:71284164..71285160-chr14:71438670..71439594,2	MCF-7	breast:
25	chr14:71276294..71278299-chr14:71400053..71402975,2	MCF-7	breast:
26	chr14:71284167..71284899-chr14:71438728..71439703,4	K562	blood:
27	chr14:71568448..71570902-chr14:71575240..71577944,2	MCF-7	breast:
28	chr14:71373776..71374491-chr14:71438799..71439724,2	K562	blood:
29	chr14:71580577..71583944-chr14:71584359..71586589,3	K562	blood:
30	chr14:71605408..71606120-chr14:72322432..72323318,2	K562	blood:
31	chr14:71605537..71606405-chr14:72219506..72220423,5	K562	blood:
32	chr14:71580577..71583944-chr14:71584359..71586589,3	K562	blood:
33	chr14:71373536..71374504-chr14:71422306..71423404,6	MCF-7	breast:
34	chr14:71370886..71377633-chr14:71420060..71424849,9	MCF-7	breast:
35	chr14:71275608..71277948-chr14:71417626..71419303,2	MCF-7	breast:
36	chr14:71576010..71578175-chr14:71578987..71581734,2	K562	blood:
37	chr14:71428566..71431049-chr14:71438511..71440761,2	MCF-7	breast:
38	chr14:71438802..71440447-chr14:71441088..71442805,2	MCF-7	breast:
39	chr14:71607200..71607876-chr14:72219653..72220319,2	MCF-7	breast:
40	chr14:71428566..71431049-chr14:71438511..71440761,2	MCF-7	breast:
41	chr14:71570776..71571452-chr14:72219467..72220345,2	MCF-7	breast:
42	chr14:71521439..71523990-chr14:71537038..71539301,2	MCF-7	breast:
43	chr14:71371849..71374730-chr14:71399686..71402743,4	MCF-7	breast:
44	chr14:71373548..71375387-chr14:71412068..71413840,2	MCF-7	breast:
45	chr14:71604707..71606600-chr14:72213499..72215384,2	MCF-7	breast:
46	chr14:71624159..71626402-chr14:71786636..71788555,2	MCF-7	breast:
47	chr14:71582880..71584385-chr14:71586431..71588999,2	MCF-7	breast:
48	chr14:71604769..71607668-chr14:71786929..71789620,2	MCF-7	breast:
49	chr14:71340301..71340951-chr14:71422324..71423179,2	MCF-7	breast:
50	chr14:71414782..71415566-chr17:56717102..56717602,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAP3K9-6	chr14:71425183-71425396	NONHSAT037599
2	lnc-MAP3K9-6	chr14:71416315-71416475	NONHSAT037599
3	lnc-SIPA1L1-5	chr14:71581486-71582098	NONHSAT037606
4	lnc-MAP3K9-9	chr14:71552199-71552550	NONHSAT037605
5	lnc-MAP3K9-10	chr14:71607842-71609970	ENSG00000269927.1
6	lnc-MAP3K9-8	chr14:71511092-71511357	NONHSAT037604
7	lnc-MAP3K9-7	chr14:71498403-71498687	NONHSAT037603

No data

Variant related genes	Relation type
PCNX	TF binding region
ENSG00000258930	TF binding region
ENSG00000269927	TF binding region
PTTG4P	TF binding region
ENSG00000258966	TF binding region
PCNX	CpG island
ENSG00000258930	CpG island
ENSG00000269927	CpG island
PTTG4P	CpG island
ENSG00000258966	CpG island
ENSG00000258930	chromatin interactions
ENSG00000197555	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000258951	chromatin interactions
ENSG00000259153	chromatin interactions
ENSG00000080815	chromatin interactions
ENSG00000259146	chromatin interactions
ENSG00000100731	chromatin interactions
ENSG00000006432	chromatin interactions

Extended variants
information (count: 8787 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:8787 , 50 per page) page: 1 2 3 4 5 6 7 ... 176

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2810114	chr14:71395604-71395605	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs546346696	chr14:71395632-71395633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79385311	chr14:71395645-71395646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77597263	chr14:71395654-71395655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561527075	chr14:71395673-71395674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112272720	chr14:71395694-71395695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561659031	chr14:71395711-71395712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188332790	chr14:71395726-71395727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2810113	chr14:71395770-71395771	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs544258696	chr14:71395807-71395808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374050574	chr14:71395808-71395809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535828277	chr14:71395928-71395929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551113008	chr14:71395955-71395956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77791278	chr14:71395956-71395957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs56857664	chr14:71395966-71395967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs61988720	chr14:71395970-71395971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114524001	chr14:71396062-71396063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201511909	chr14:71396104-71396105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35557661	chr14:71396105-71396106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs67986258	chr14:71396106-71396107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545346279	chr14:71396171-71396172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549794762	chr14:71396180-71396181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs36123215	chr14:71396354-71396355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568338362	chr14:71396452-71396453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183698789	chr14:71396479-71396480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147025225	chr14:71396532-71396533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76764514	chr14:71396611-71396612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534027511	chr14:71396652-71396653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138285958	chr14:71396705-71396706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368879116	chr14:71396756-71396757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566127437	chr14:71396763-71396764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540042786	chr14:71396806-71396807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2526866	chr14:71396807-71396808	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs576851210	chr14:71396814-71396815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141014472	chr14:71396832-71396833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7149960	chr14:71396842-71396843	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs10220406	chr14:71396845-71396846	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs188563893	chr14:71396847-71396848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559185705	chr14:71396944-71396945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs117881160	chr14:71396976-71396977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368801850	chr14:71396988-71396989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563125283	chr14:71397022-71397023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138909184	chr14:71397087-71397088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10148594	chr14:71397106-71397107	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs556354122	chr14:71397124-71397125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9323552	chr14:71397161-71397162	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs78316910	chr14:71397177-71397178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs917066	chr14:71397183-71397184	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs192122729	chr14:71397241-71397242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185021772	chr14:71397244-71397245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	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	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:6767 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71375600-71398400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:71376000-71396800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr14:71376000-71401000	Weak transcription	Lung	lung
4	chr14:71376600-71398400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr14:71377400-71396800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr14:71378000-71400600	Weak transcription	Fetal Kidney	kidney
7	chr14:71379600-71408200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:71379600-71410400	Weak transcription	Aorta	Aorta
9	chr14:71380000-71398200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr14:71380400-71400800	Weak transcription	Fetal Intestine Large	intestine
11	chr14:71384000-71401200	Weak transcription	Fetal Muscle Leg	muscle
12	chr14:71384200-71408400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr14:71384600-71402000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:71386800-71396800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr14:71386800-71400600	Weak transcription	Fetal Stomach	stomach
16	chr14:71387000-71396600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr14:71387000-71398000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr14:71387200-71408400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr14:71388200-71402000	Weak transcription	HSMM	muscle
20	chr14:71388200-71410400	Weak transcription	Thymus	Thymus
21	chr14:71388400-71400800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr14:71388800-71396800	Weak transcription	HMEC	breast
23	chr14:71388800-71397600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr14:71388800-71400200	Weak transcription	Fetal Intestine Small	intestine
25	chr14:71388800-71400400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr14:71388800-71400600	Weak transcription	NHLF	lung
27	chr14:71388800-71408000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:71389000-71396200	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr14:71389000-71396600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr14:71389000-71396800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr14:71389000-71396800	Weak transcription	NHEK	skin
32	chr14:71389000-71400400	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr14:71389200-71398600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr14:71389800-71396800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr14:71389800-71396800	Weak transcription	NHDF-Ad	bronchial
36	chr14:71389800-71400600	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr14:71392800-71401600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr14:71393200-71396800	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr14:71393200-71400800	Weak transcription	Brain Hippocampus Middle	brain
40	chr14:71393400-71396400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr14:71393400-71396800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr14:71393400-71396800	Weak transcription	Psoas Muscle	Psoas
43	chr14:71393400-71396800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr14:71393400-71396800	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr14:71393400-71396800	Weak transcription	Small Intestine	intestine
46	chr14:71393400-71397000	Weak transcription	Brain Substantia Nigra	brain
47	chr14:71393400-71397800	Weak transcription	Fetal Lung	lung
48	chr14:71393400-71397800	Weak transcription	Stomach Smooth Muscle	stomach
49	chr14:71393400-71400200	Weak transcription	GM12878-XiMat	blood
50	chr14:71393400-71408800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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