Variant report

Variant	nsv542128
Chromosome Location	chr14:71310954-71525720
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2972)
CpG islands
(count:1161)
Chromatin interactive
region (count:78)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2972 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:71351840-71352115	K562	blood:	n/a	n/a
2	ARID3A	chr14:71373929-71374421	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:71361461-71362018	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:71340419-71340591	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:71375376-71375583	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:71453850-71454159	K562	blood:	n/a	n/a
7	ARID3A	chr14:71439131-71439396	HepG2	liver:	n/a	n/a
8	ATF1	chr14:71455163-71455464	K562	blood:	n/a	n/a
9	ATF1	chr14:71351546-71352024	K562	blood:	n/a	n/a
10	ATF1	chr14:71349878-71350140	K562	blood:	n/a	n/a
11	ATF1	chr14:71353461-71353701	K562	blood:	n/a	n/a
12	ATF2	chr14:71349760-71350288	GM12878	blood:	n/a	n/a
13	ATF2	chr14:71348200-71349213	GM12878	blood:	n/a	n/a
14	ATF2	chr14:71349705-71350296	GM12878	blood:	n/a	n/a
15	ATF2	chr14:71353074-71354442	GM12878	blood:	n/a	n/a
16	ATF2	chr14:71348210-71348994	GM12878	blood:	n/a	n/a
17	ATF2	chr14:71360585-71361103	GM12878	blood:	n/a	n/a
18	ATF2	chr14:71353081-71354548	GM12878	blood:	n/a	n/a
19	ATF3	chr14:71315650-71315906	K562	blood:	n/a	n/a
20	ATF3	chr14:71488349-71488985	HCT-116	colon:	n/a	n/a
21	ATF3	chr14:71373936-71374105	K562	blood:	n/a	n/a
22	ATF3	chr14:71462500-71462644	K562	blood:	n/a	n/a
23	BACH1	chr14:71374691-71375583	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr14:71360476-71361068	GM12878	blood:	n/a	n/a
25	BATF	chr14:71351145-71351609	GM12878	blood:	n/a	chr14:71351366-71351377
26	BATF	chr14:71352121-71352407	GM12878	blood:	n/a	n/a
27	BATF	chr14:71348457-71348812	GM12878	blood:	n/a	n/a
28	BATF	chr14:71353839-71354389	GM12878	blood:	n/a	n/a
29	BATF	chr14:71352085-71352521	GM12878	blood:	n/a	n/a
30	BATF	chr14:71360734-71361016	GM12878	blood:	n/a	n/a
31	BATF	chr14:71489604-71489981	GM12878	blood:	n/a	n/a
32	BATF	chr14:71351186-71351547	GM12878	blood:	n/a	chr14:71351366-71351377
33	BATF	chr14:71348519-71349009	GM12878	blood:	n/a	n/a
34	BATF	chr14:71338863-71339242	GM12878	blood:	n/a	n/a
35	BATF	chr14:71353044-71354499	GM12878	blood:	n/a	n/a
36	BATF	chr14:71349828-71350124	GM12878	blood:	n/a	chr14:71349983-71349994
37	BATF	chr14:71349716-71350256	GM12878	blood:	n/a	chr14:71349983-71349994
38	BCL11A	chr14:71360680-71361030	GM12878	blood:	n/a	n/a
39	BCL11A	chr14:71348475-71348869	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:71351157-71351547	GM12878	blood:	n/a	n/a
41	BCL11A	chr14:71349784-71350255	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:71353433-71353755	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:71348485-71348838	GM12878	blood:	n/a	n/a
44	BCL11A	chr14:71353300-71354441	GM12878	blood:	n/a	chr14:71354221-71354230 chr14:71354222-71354231
45	BCL11A	chr14:71354108-71354356	GM12878	blood:	n/a	chr14:71354221-71354230 chr14:71354222-71354231
46	BCL11A	chr14:71349816-71350210	GM12878	blood:	n/a	n/a
47	BCL3	chr14:71360606-71361027	GM12878	blood:	n/a	n/a
48	BCL3	chr14:71315705-71316035	GM12878	blood:	n/a	n/a
49	BCL3	chr14:71315681-71316004	GM12878	blood:	n/a	n/a
50	BCL3	chr14:71373588-71374162	A549	lung:	n/a	chr14:71374105-71374114

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:71364830-71364880	AG09319	gingival:	n/a
2	chr14:71372869-71372919	H1-hESC	embryonic stem cell:	embryo
3	chr14:71364830-71364880	AG09319	gingival:	n/a
4	chr14:71372869-71372919	H1-hESC	embryonic stem cell:	embryo
5	chr14:71354913-71354963	AG10803	skin:	n/a
6	chr14:71373978-71374028	HNPCEpiC	eye:	n/a
7	chr14:71374612-71374662	NT2-D1	testis:	n/a
8	chr14:71354913-71354963	HIPEpiC	eye:	n/a
9	chr14:71373858-71373908	NB4	blood:	n/a
10	chr14:71373980-71374030	ECC-1	luminal epithelium:	n/a
11	chr14:71374784-71374834	Jurkat	blood:	n/a
12	chr14:71472713-71472763	GM12878	blood:	n/a
13	chr14:71515513-71515563	GM12892	blood:	n/a
14	chr14:71364830-71364880	PFSK-1	brain:	n/a
15	chr14:71372869-71372919	NHBE	bronchial:	n/a
16	chr14:71354913-71354963	LNCaP	prostate:	n/a
17	chr14:71323515-71323565	ECC-1	luminal epithelium:	n/a
18	chr14:71373980-71374030	SK-N-SH	brain:	n/a
19	chr14:71373980-71374030	HRCEpiC	kidney:	n/a
20	chr14:71373980-71374030	HRE	kidney:	n/a
21	chr14:71373858-71373908	GM19239	blood:	n/a
22	chr14:71354913-71354963	AG04450	lung:	fetal
23	chr14:71472713-71472763	T-47D	breast:	n/a
24	chr14:71373980-71374030	RPTEC	kidney:	n/a
25	chr14:71374612-71374662	AG04450	lung:	fetal
26	chr14:71354913-71354963	RPTEC	kidney:	n/a
27	chr14:71370423-71370473	PrEC	prostate:	n/a
28	chr14:71323515-71323565	Caco-2	colon:	n/a
29	chr14:71364830-71364880	HIPEpiC	eye:	n/a
30	chr14:71372869-71372919	A549	lung:	n/a
31	chr14:71377000-71377050	GM06990	blood:	n/a
32	chr14:71364830-71364880	T-47D	breast:	n/a
33	chr14:71374784-71374834	GM06990	blood:	n/a
34	chr14:71472713-71472763	BE2_C	brain:	n/a
35	chr14:71374784-71374834	HepG2	liver:	n/a
36	chr14:71373858-71373908	AoSMC	blood vessel:	n/a
37	chr14:71353208-71353258	GM06990	blood:	n/a
38	chr14:71375349-71375399	HCPEpiC	choroid plexus:	n/a
39	chr14:71374612-71374662	PrEC	prostate:	n/a
40	chr14:71373980-71374030	SKMC	muscle:	n/a
41	chr14:71364830-71364880	AoSMC	blood vessel:	n/a
42	chr14:71374299-71374349	SK-N-MC	brain:	n/a
43	chr14:71373888-71373938	BE2_C	brain:	n/a
44	chr14:71373858-71373908	SAEC	small airway:	n/a
45	chr14:71374299-71374349	SK-N-SH	brain:	n/a
46	chr14:71373888-71373938	GM12892	blood:	n/a
47	chr14:71373858-71373908	ovcar-3	ovarian:	n/a
48	chr14:71372869-71372919	NHDF-neo	bronchial:	n/a
49	chr14:71374299-71374349	Hepatocyte	liver:	n/a
50	chr14:71364830-71364880	AG04449	skin:	fetal

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:71372741..71377071-chr14:71387271..71391625,6	MCF-7	breast:
2	chr14:71372585..71374647-chr14:71376260..71377778,2	K562	blood:
3	chr14:71392610..71393238-chr8:101964260..101964764,2	NB4	blood:
4	chr14:71371849..71374730-chr14:71399686..71402743,4	MCF-7	breast:
5	chr14:71441488..71443872-chr14:71448426..71449969,2	MCF-7	breast:
6	chr14:71386633..71388150-chr14:71388348..71391134,2	MCF-7	breast:
7	chr14:71284167..71284899-chr14:71438728..71439703,4	K562	blood:
8	chr14:71373112..71375503-chr14:71384629..71386969,3	MCF-7	breast:
9	chr14:71355468..71357237-chr14:71359840..71362416,2	MCF-7	breast:
10	chr14:71472106..71474140-chr14:71476821..71478999,2	K562	blood:
11	chr14:71315330..71318187-chr14:71353000..71355911,2	K562	blood:
12	chr14:71373840..71374362-chr8:136469426..136469930,2	MCF-7	breast:
13	chr14:71370886..71377633-chr14:71420060..71424849,9	MCF-7	breast:
14	chr14:71381579..71383875-chr14:71386950..71389719,2	MCF-7	breast:
15	chr14:71372925..71376620-chr14:71377787..71383660,12	MCF-7	breast:
16	chr14:71441488..71443872-chr14:71448426..71449969,2	MCF-7	breast:
17	chr14:71315330..71318187-chr14:71353000..71355911,2	K562	blood:
18	chr14:71359505..71362289-chr14:71363900..71365887,4	MCF-7	breast:
19	chr14:71367722..71371068-chr14:71372863..71375706,4	MCF-7	breast:
20	chr14:71284164..71285160-chr14:71438670..71439594,2	MCF-7	breast:
21	chr14:71376408..71378571-chr14:71380621..71383425,3	MCF-7	breast:
22	chr14:71379419..71381346-chr14:71385671..71388258,2	MCF-7	breast:
23	chr14:71487547..71489766-chr14:72170994..72172928,2	MCF-7	breast:
24	chr14:71304429..71307285-chr14:71311780..71314188,2	K562	blood:
25	chr14:71060100..71062359-chr14:71423521..71425831,2	K562	blood:
26	chr14:71373774..71374385-chr17:61045448..61046114,2	Hela-S3	cervix:
27	chr14:71423548..71425055-chr14:71436128..71438876,2	MCF-7	breast:
28	chr14:71273334..71275325-chr14:71487514..71489742,2	MCF-7	breast:
29	chr14:71372532..71376222-chr14:71415679..71419226,4	MCF-7	breast:
30	chr14:71362952..71365427-chr14:71368027..71370762,2	MCF-7	breast:
31	chr14:71438802..71440447-chr14:71441088..71442805,2	MCF-7	breast:
32	chr14:71438802..71440447-chr14:71441088..71442805,2	MCF-7	breast:
33	chr14:71428566..71431049-chr14:71438511..71440761,2	MCF-7	breast:
34	chr14:71378921..71381459-chr14:71390825..71392481,2	MCF-7	breast:
35	chr14:71355596..71357238-chr14:71373559..71375113,2	MCF-7	breast:
36	chr14:71386633..71388150-chr14:71388348..71391134,2	MCF-7	breast:
37	chr14:71362952..71365427-chr14:71368027..71370762,2	MCF-7	breast:
38	chr14:71340301..71340951-chr14:71422324..71423179,2	MCF-7	breast:
39	chr14:71359184..71361695-chr14:71373251..71375700,2	MCF-7	breast:
40	chr14:71373975..71375521-chr14:71375860..71378276,2	MCF-7	breast:
41	chr14:71374157..71374728-chr2:38603975..38604567,2	Hela-S3	cervix:
42	chr14:71283754..71285089-chr14:71421790..71423652,9	MCF-7	breast:
43	chr14:71275608..71277948-chr14:71417626..71419303,2	MCF-7	breast:
44	chr14:71414782..71415566-chr17:56717102..56717602,2	MCF-7	breast:
45	chr14:71373895..71374580-chr14:71438774..71439742,5	MCF-7	breast:
46	chr14:71521439..71523990-chr14:71537038..71539301,2	MCF-7	breast:
47	chr14:71373776..71374491-chr14:71438799..71439724,2	K562	blood:
48	chr14:71373548..71375387-chr14:71412068..71413840,2	MCF-7	breast:
49	chr14:71373548..71375387-chr14:71412068..71413840,2	MCF-7	breast:
50	chr14:71373536..71374504-chr14:71422306..71423404,6	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAP3K9-5	chr14:71337844-71338071	FPKM1_group_9264_transcript_1
2	lnc-MAP3K9-6	chr14:71416315-71416475	NONHSAT037599
3	lnc-MAP3K9-4	chr14:71325561-71326146	NONHSAT037595
4	lnc-MAP3K9-6	chr14:71425183-71425396	NONHSAT037599
5	lnc-MAP3K9-5	chr14:71337707-71338125	FPKM1_group_9264_transcript_1
6	lnc-MAP3K9-8	chr14:71511092-71511357	NONHSAT037604
7	lnc-MAP3K9-5	chr14:71339077-71339304	NONHSAT037596
8	lnc-MAP3K9-5	chr14:71337707-71338125	NONHSAT037596
9	lnc-MAP3K9-7	chr14:71498403-71498687	NONHSAT037603

No data

Variant related genes	Relation type
ENSG00000258431	TF binding region
PCNX	TF binding region
ENSG00000258930	TF binding region
ENSG00000258966	TF binding region
ENSG00000258431	CpG island
PCNX	CpG island
ENSG00000258930	CpG island
ENSG00000258966	CpG island
ENSG00000259153	chromatin interactions
ENSG00000100731	chromatin interactions
ENSG00000006432	chromatin interactions
ENSG00000258930	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000266411	chromatin interactions
ENSG00000131773	chromatin interactions
ENSG00000119787	chromatin interactions
ENSG00000258951	chromatin interactions

Extended variants
information (count: 8293 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:8293 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189393043	chr14:71310954-71310955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542686456	chr14:71310977-71310978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561025982	chr14:71310993-71310994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528696765	chr14:71311055-71311056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35174039	chr14:71311086-71311087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75850431	chr14:71311092-71311093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145334385	chr14:71311101-71311102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138073749	chr14:71311110-71311111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550314182	chr14:71311136-71311137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568799665	chr14:71311157-71311158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116147018	chr14:71311184-71311185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548331844	chr14:71311199-71311200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200729008	chr14:71311230-71311231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371989894	chr14:71311250-71311251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398057213	chr14:71311262-71311263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs56376636	chr14:71311265-71311266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566554799	chr14:71311276-71311277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373170783	chr14:71311277-71311278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534016398	chr14:71311284-71311285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10137965	chr14:71311369-71311370	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs371018308	chr14:71311370-71311371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577074470	chr14:71311391-71311392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs180954036	chr14:71311392-71311393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185184595	chr14:71311422-71311423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370008849	chr14:71311424-71311425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190272232	chr14:71311451-71311452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112726728	chr14:71311482-71311483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557258626	chr14:71311584-71311585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114670755	chr14:71311589-71311590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs116456337	chr14:71311595-71311596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17108623	chr14:71311602-71311603	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs146040389	chr14:71311625-71311626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532707983	chr14:71311652-71311653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs117017300	chr14:71311686-71311687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563150814	chr14:71311732-71311733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545281367	chr14:71311746-71311747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529747545	chr14:71311758-71311759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548195307	chr14:71311855-71311856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563935184	chr14:71311863-71311864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34051728	chr14:71311925-71311926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537765823	chr14:71311938-71311939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148681481	chr14:71311960-71311961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10140837	chr14:71311976-71311977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577223442	chr14:71312029-71312030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531034792	chr14:71312031-71312032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs118169396	chr14:71312036-71312037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141425593	chr14:71312060-71312061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2332468	chr14:71312108-71312109	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs573881753	chr14:71312110-71312111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556456150	chr14:71312117-71312118	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
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:6458 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71309200-71311400	Enhancers	Right Atrium	heart
2	chr14:71310200-71323000	Weak transcription	HSMMtube	muscle
3	chr14:71310600-71315800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr14:71310800-71311600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr14:71310800-71312200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr14:71311600-71312000	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr14:71312000-71312400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr14:71313200-71313400	Enhancers	Fetal Brain Female	brain
9	chr14:71313400-71314400	Weak transcription	Fetal Brain Female	brain
10	chr14:71313600-71313800	Enhancers	Fetal Brain Male	brain
11	chr14:71313800-71314800	Weak transcription	Fetal Brain Male	brain
12	chr14:71314400-71314800	Enhancers	Fetal Brain Female	brain
13	chr14:71314800-71315200	Enhancers	Fetal Brain Male	brain
14	chr14:71315800-71316200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr14:71322600-71324600	Enhancers	HMEC	breast
16	chr14:71322800-71324600	Enhancers	HSMM	muscle
17	chr14:71322800-71324800	Enhancers	Muscle Satellite Cultured Cells	--
18	chr14:71323000-71324600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr14:71323000-71324600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:71323000-71324600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr14:71323000-71324600	Enhancers	HSMMtube	muscle
22	chr14:71323000-71324600	Enhancers	NH-A	brain
23	chr14:71323000-71324800	Enhancers	NHEK	skin
24	chr14:71323200-71324200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr14:71323200-71324400	Enhancers	NHDF-Ad	bronchial
26	chr14:71323200-71324600	Enhancers	Osteobl	bone
27	chr14:71323400-71324400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr14:71323400-71324400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr14:71323600-71324600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr14:71323600-71324800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr14:71323800-71324200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr14:71323800-71324600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr14:71324600-71331800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr14:71324800-71331600	Weak transcription	NHEK	skin
35	chr14:71324800-71331800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr14:71325400-71325800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr14:71326200-71326400	Enhancers	HSMMtube	muscle
38	chr14:71331000-71334400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr14:71331600-71332200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr14:71331600-71332200	Enhancers	HMEC	breast
41	chr14:71331600-71332200	Enhancers	NHEK	skin
42	chr14:71331800-71332200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:71331800-71332200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr14:71331800-71332600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr14:71331800-71332800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:71332200-71337000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:71337000-71338000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr14:71337000-71338600	ZNF genes & repeats	GM12878-XiMat	blood
49	chr14:71337800-71338600	ZNF genes & repeats	HepG2	liver
50	chr14:71337800-71338800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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