Variant report

Variant	nsv901966
Chromosome Location	chr14:56160904-56436203
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2847)
CpG islands
(count:2014)
Chromatin interactive
region (count:73)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2847 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:56304237-56304385	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:56263450-56263638	K562	blood:	n/a	n/a
3	ARID3A	chr14:56269777-56270150	K562	blood:	n/a	n/a
4	ARID3A	chr14:56266440-56266575	K562	blood:	n/a	n/a
5	ARID3A	chr14:56298768-56299216	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:56269808-56270347	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:56392908-56392994	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:56331685-56331803	K562	blood:	n/a	n/a
9	ATF1	chr14:56273773-56274242	K562	blood:	n/a	n/a
10	ATF1	chr14:56247898-56248141	K562	blood:	n/a	n/a
11	ATF1	chr14:56281031-56281544	K562	blood:	n/a	n/a
12	ATF1	chr14:56435287-56435393	K562	blood:	n/a	n/a
13	ATF1	chr14:56269833-56270095	K562	blood:	n/a	n/a
14	ATF1	chr14:56430046-56430347	K562	blood:	n/a	n/a
15	ATF2	chr14:56331556-56331840	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr14:56424561-56424968	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr14:56286351-56286654	GM12878	blood:	n/a	n/a
18	ATF2	chr14:56286322-56286744	GM12878	blood:	n/a	n/a
19	ATF3	chr14:56269770-56270084	K562	blood:	n/a	n/a
20	ATF3	chr14:56269705-56270171	A549	lung:	n/a	n/a
21	ATF3	chr14:56165795-56166334	A549	lung:	n/a	n/a
22	ATF3	chr14:56312962-56313097	K562	blood:	n/a	n/a
23	BACH1	chr14:56280943-56281084	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr14:56348351-56348997	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr14:56174241-56174259	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr14:56269838-56270128	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr14:56280859-56281098	K562	blood:	n/a	n/a
28	BATF	chr14:56313832-56314092	GM12878	blood:	n/a	n/a
29	BATF	chr14:56286364-56286674	GM12878	blood:	n/a	n/a
30	BATF	chr14:56316171-56316445	GM12878	blood:	n/a	chr14:56316338-56316348 chr14:56316337-56316348
31	BATF	chr14:56430910-56431177	GM12878	blood:	n/a	n/a
32	BATF	chr14:56315776-56316012	GM12878	blood:	n/a	n/a
33	BATF	chr14:56286265-56286696	GM12878	blood:	n/a	n/a
34	BCL11A	chr14:56424621-56425049	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL11A	chr14:56424730-56425076	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL11A	chr14:56286277-56286757	GM12878	blood:	n/a	n/a
37	BCL11A	chr14:56286490-56286678	GM12878	blood:	n/a	n/a
38	BCL11A	chr14:56168405-56168683	GM12878	blood:	n/a	n/a
39	BCL11A	chr14:56168319-56168740	GM12878	blood:	n/a	n/a
40	BCL3	chr14:56298588-56299559	A549	lung:	n/a	n/a
41	BCL3	chr14:56269695-56270227	A549	lung:	n/a	n/a
42	BCL3	chr14:56219701-56220211	A549	lung:	n/a	n/a
43	BCL3	chr14:56165683-56166291	A549	lung:	n/a	n/a
44	BCL3	chr14:56355867-56356423	A549	lung:	n/a	n/a
45	BCL3	chr14:56219661-56220203	A549	lung:	n/a	n/a
46	BHLHE40	chr14:56263316-56263590	K562	blood:	n/a	n/a
47	BHLHE40	chr14:56348635-56348852	K562	blood:	n/a	n/a
48	BHLHE40	chr14:56286390-56286605	GM12878	blood:	n/a	n/a
49	BHLHE40	chr14:56266279-56266500	K562	blood:	n/a	n/a
50	BHLHE40	chr14:56229447-56229780	GM12878	blood:	n/a	n/a

(count:2014 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:56232921-56232971	HAEpiC	amniotic membrane:	n/a
2	chr14:56232921-56232971	HAEpiC	amniotic membrane:	n/a
3	chr14:56424872-56424922	HRCEpiC	kidney:	n/a
4	chr14:56304962-56305012	HUVEC	blood vessel:	n/a
5	chr14:56391960-56392010	HCPEpiC	choroid plexus:	n/a
6	chr14:56216951-56217001	U87	brain:	n/a
7	chr14:56233163-56233213	H1-hESC	embryonic stem cell:	embryo
8	chr14:56307253-56307303	H1-hESC	embryonic stem cell:	embryo
9	chr14:56216951-56217001	HCT-116	colon:	n/a
10	chr14:56229661-56229711	AoSMC	blood vessel:	n/a
11	chr14:56374714-56374764	AG09319	gingival:	n/a
12	chr14:56233163-56233213	A549	lung:	n/a
13	chr14:56299289-56299339	SK-N-MC	brain:	n/a
14	chr14:56229661-56229711	HRE	kidney:	n/a
15	chr14:56264572-56264622	HAEpiC	amniotic membrane:	n/a
16	chr14:56264322-56264372	HRE	kidney:	n/a
17	chr14:56359470-56359520	GM19239	blood:	n/a
18	chr14:56232813-56232863	Hepatocyte	liver:	n/a
19	chr14:56232985-56233035	GM06990	blood:	n/a
20	chr14:56207327-56207377	SKMC	muscle:	n/a
21	chr14:56231604-56231654	HNPCEpiC	eye:	n/a
22	chr14:56264322-56264372	AG04450	lung:	fetal
23	chr14:56391960-56392010	NB4	blood:	n/a
24	chr14:56348939-56348989	H1-hESC	embryonic stem cell:	embryo
25	chr14:56233068-56233118	SAEC	small airway:	n/a
26	chr14:56225464-56225514	AG04449	skin:	fetal
27	chr14:56232985-56233035	SAEC	small airway:	n/a
28	chr14:56232921-56232971	HRE	kidney:	n/a
29	chr14:56233676-56233726	GM12878	blood:	n/a
30	chr14:56299289-56299339	K562	blood:	n/a
31	chr14:56232650-56232700	PFSK-1	brain:	n/a
32	chr14:56304962-56305012	K562	blood:	n/a
33	chr14:56281968-56282018	ovcar-3	ovarian:	n/a
34	chr14:56231604-56231654	MCF-7	breast:	n/a
35	chr14:56299289-56299339	Hela-S3	cervix:	n/a
36	chr14:56233163-56233213	HAEpiC	amniotic membrane:	n/a
37	chr14:56307253-56307303	PrEC	prostate:	n/a
38	chr14:56424872-56424922	PrEC	prostate:	n/a
39	chr14:56304962-56305012	GM12891	blood:	n/a
40	chr14:56264651-56264701	Caco-2	colon:	n/a
41	chr14:56264651-56264701	HPAEpiC	pulmonary alveolar:	n/a
42	chr14:56247892-56247942	NH-A	brain:	n/a
43	chr14:56225464-56225514	NH-A	brain:	n/a
44	chr14:56233163-56233213	HepG2	liver:	n/a
45	chr14:56289611-56289661	H1-hESC	embryonic stem cell:	embryo
46	chr14:56348939-56348989	CMK	blood:	n/a
47	chr14:56225464-56225514	HCT-116	colon:	n/a
48	chr14:56257750-56257800	NB4	blood:	n/a
49	chr14:56207327-56207377	AG09309	skin:	n/a
50	chr14:56391960-56392010	LNCaP	prostate:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:56224023..56226441-chr14:56261049..56262918,2	MCF-7	breast:
2	chr14:56172874..56174577-chr14:56174772..56176710,2	MCF-7	breast:
3	chr14:55737454..55740283-chr14:56178729..56181502,2	MCF-7	breast:
4	chr14:56304789..56307595-chr14:56316105..56318121,2	K562	blood:
5	chr14:56269404..56272163-chr14:56272459..56274714,3	MCF-7	breast:
6	chr14:56263621..56267640-chr14:56269558..56273646,4	K562	blood:
7	chr14:56219849..56221518-chr14:56225046..56227362,2	MCF-7	breast:
8	chr14:56300351..56302227-chr14:56304134..56305783,2	MCF-7	breast:
9	chr14:56361180..56363338-chr14:56369643..56372390,2	MCF-7	breast:
10	chr14:56264314..56267640-chr14:56270614..56273646,3	K562	blood:
11	chr14:56269404..56272163-chr14:56272459..56274714,3	MCF-7	breast:
12	chr14:56331802..56332310-chr14:56747361..56748275,2	MCF-7	breast:
13	chr14:56226675..56229343-chr14:56231799..56234788,2	K562	blood:
14	chr14:56207089..56208058-chr14:56265155..56265723,2	MCF-7	breast:
15	chr14:56304789..56307595-chr14:56316105..56318121,2	K562	blood:
16	chr14:56357306..56359037-chr14:56360348..56362523,2	K562	blood:
17	chr14:56399761..56402429-chr14:56440899..56442886,2	K562	blood:
18	chr14:56300351..56302227-chr14:56304134..56305783,2	MCF-7	breast:
19	chr14:56172874..56174577-chr14:56174772..56176710,2	MCF-7	breast:
20	chr14:56264314..56267640-chr14:56270614..56273646,3	K562	blood:
21	chr14:56256977..56259600-chr14:56273193..56275837,3	K562	blood:
22	chr14:56266308..56267973-chr14:56270310..56271812,2	MCF-7	breast:
23	chr14:55890007..55892259-chr14:56172820..56174391,2	K562	blood:
24	chr14:56197898..56198585-chr14:56888977..56889535,2	MCF-7	breast:
25	chr14:56260506..56263007-chr14:56264941..56267935,2	K562	blood:
26	chr14:56220561..56223458-chr14:56223829..56226647,2	K562	blood:
27	chr14:56302735..56305640-chr14:56310752..56313567,2	MCF-7	breast:
28	chr14:56264106..56265769-chr14:56291458..56293554,2	MCF-7	breast:
29	chr14:56256977..56259600-chr14:56273193..56275837,3	K562	blood:
30	chr14:56396115..56397620-chr14:56399759..56401612,2	K562	blood:
31	chr14:56198307..56199262-chr14:56551982..56552868,6	MCF-7	breast:
32	chr14:56238761..56241278-chr14:56243560..56245184,2	MCF-7	breast:
33	chr14:56390153..56391038-chr18:24814712..24815423,2	MCF-7	breast:
34	chr14:56279834..56282515-chr14:56285363..56287657,2	K562	blood:
35	chr14:56273918..56276327-chr14:56286651..56288892,2	MCF-7	breast:
36	chr14:56259914..56261848-chr14:56268841..56271820,2	K562	blood:
37	chr14:56207915..56209917-chr14:56216169..56218035,2	MCF-7	breast:
38	chr14:56207915..56209917-chr14:56216169..56218035,2	MCF-7	breast:
39	chr14:56266308..56267973-chr14:56270310..56271812,2	MCF-7	breast:
40	chr14:56198273..56199200-chr14:56551636..56552463,2	MCF-7	breast:
41	chr14:55904850..55905413-chr14:56172276..56173086,2	MCF-7	breast:
42	chr14:56361180..56363338-chr14:56369643..56372390,2	MCF-7	breast:
43	chr14:56215726..56218304-chr14:56218749..56222273,3	K562	blood:
44	chr14:56209789..56211421-chr14:56215723..56218469,2	MCF-7	breast:
45	chr14:56215726..56218304-chr14:56218749..56222273,3	K562	blood:
46	chr14:56357306..56359037-chr14:56360348..56362523,2	K562	blood:
47	chr14:56220561..56223458-chr14:56223829..56226647,2	K562	blood:
48	chr14:56209789..56211421-chr14:56215723..56218469,2	MCF-7	breast:
49	chr14:56248252..56249940-chr14:56263162..56264665,2	MCF-7	breast:
50	chr14:56173843..56174384-chr14:56948949..56949696,2	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KTN1-1	chr14:56239474-56239567	ENSG00000258784.1
2	lnc-KTN1-AS1-1	chr14:56247432-56247714	NONHSAT037025
3	lnc-KTN1-AS1-1	chr14:56260086-56260174	NONHSAT037026
4	lnc-KTN1-2	chr14:56221453-56222019	NONHSAT037023
5	lnc-KTN1-AS1-1	chr14:56263323-56263406	ENSG00000258791.2
6	lnc-KTN1-AS1-1	chr14:56263321-56263392	NONHSAT037026
7	lnc-KTN1-AS1-1	chr14:56263321-56263406	ENSG00000258791.2
8	lnc-KTN1-AS1-1	chr14:56248785-56249492	ENSG00000258791.3
9	lnc-KTN1-AS1-1	chr14:56247853-56249698	NONHSAT037027
10	lnc-KTN1-AS1-1	chr14:56248785-56249492	ENSG00000258791.2
11	lnc-PELI2-5	chr14:56382445-56383044	ENSG00000259868.1
12	lnc-KTN1-AS1-1	chr14:56263321-56263374	ENSG00000258791.2
13	lnc-KTN1-AS1-1	chr14:56263321-56263392	XLOC_011037
14	lnc-KTN1-AS1-1	chr14:56263265-56263417	NONHSAT037025
15	lnc-KTN1-AS1-1	chr14:56260086-56260174	XLOC_011037
16	lnc-KTN1-AS1-1	chr14:56260086-56260174	ENSG00000258791.2
17	lnc-KTN1-AS1-1	chr14:56249127-56249299	ENSG00000258791.2
18	lnc-KTN1-AS1-1	chr14:56260086-56260174	ENSG00000258791.2
19	lnc-KTN1-AS1-1	chr14:56260015-56260078	ENSG00000258791.2
20	lnc-KTN1-AS1-1	chr14:56247853-56249698	NONHSAT037026
21	lnc-KTN1-AS1-1	chr14:56247854-56249698	XLOC_011037
22	lnc-KTN1-1	chr14:56214926-56215000	ENSG00000258784.1
23	lnc-KTN1-AS1-1	chr14:56260086-56260174	ENSG00000258791.2
24	lnc-KTN1-AS1-1	chr14:56263321-56263392	ENSG00000258791.2
25	lnc-KTN1-AS1-1	chr14:56260086-56260178	NONHSAT037025
26	lnc-PELI2-5	chr14:56382445-56383047	NONHSAT037033
27	lnc-KTN1-AS1-1	chr14:56261002-56261063	ENSG00000258791.2
28	lnc-KTN1-AS1-1	chr14:56263321-56263392	NONHSAT037027
29	lnc-KTN1-AS1-1	chr14:56247864-56248070	ENSG00000258791.2
30	lnc-KTN1-AS1-1	chr14:56260086-56260174	NONHSAT037027
31	lnc-KTN1-AS1-1	chr14:56261002-56261063	ENSG00000258791.2
32	lnc-KTN1-AS1-1	chr14:56247800-56248072	NONHSAT037025
33	lnc-KTN1-AS1-1	chr14:56261002-56261063	ENSG00000258791.2
34	lnc-KTN1-AS1-1	chr14:56263321-56263357	ENSG00000258791.2
35	lnc-KTN1-AS1-1	chr14:56254645-56255094	ENSG00000258791.2
36	lnc-KTN1-AS1-1	chr14:56249144-56249698	ENSG00000258791.2
37	lnc-KTN1-AS1-1	chr14:56263321-56263406	ENSG00000258791.3
38	lnc-KTN1-AS1-1	chr14:56261002-56261063	NONHSAT037026
39	lnc-KTN1-1	chr14:56238349-56238423	ENSG00000258784.1
40	lnc-KTN1-AS1-1	chr14:56259443-56260174	ENSG00000258791.2
41	lnc-KTN1-1	chr14:56239707-56239921	ENSG00000258784.1
42	lnc-KTN1-AS1-1	chr14:56260086-56260174	ENSG00000258791.3
43	lnc-KTN1-AS1-1	chr14:56259764-56259828	NONHSAT037025

No data

Variant related genes	Relation type
ENSG00000259868	TF binding region
LINC00520	TF binding region
ENSG00000258784	TF binding region
RPL13AP3	TF binding region
ENSG00000259868	CpG island
LINC00520	CpG island
ENSG00000258784	CpG island
RPL13AP3	CpG island
ENSG00000258413	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000258791	chromatin interactions
ENSG00000177350	chromatin interactions

Extended variants
information (count: 10924 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:10924 , 50 per page) page: 1 2 3 4 5 6 7 ... 219

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8015588	chr14:56160904-56160905	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534259597	chr14:56160922-56160923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540847070	chr14:56160985-56160986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146962710	chr14:56160994-56160995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182298479	chr14:56161009-56161010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542111092	chr14:56161062-56161063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375891080	chr14:56161110-56161111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527851533	chr14:56161146-56161147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575228795	chr14:56161147-56161148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545459577	chr14:56161150-56161151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34218733	chr14:56161268-56161269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34218796	chr14:56161295-56161296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563709502	chr14:56161300-56161301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186767042	chr14:56161311-56161312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs137961973	chr14:56161419-56161420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539898585	chr14:56161425-56161426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567478141	chr14:56161429-56161430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375305343	chr14:56161442-56161443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35775942	chr14:56161527-56161528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367777690	chr14:56161529-56161530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561945757	chr14:56161533-56161534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533048635	chr14:56161625-56161626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187916253	chr14:56161636-56161637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529458892	chr14:56161637-56161638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551300967	chr14:56161689-56161690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549763114	chr14:56161690-56161691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533393149	chr14:56161723-56161724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149459486	chr14:56161763-56161764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143147309	chr14:56161784-56161785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566840251	chr14:56161785-56161786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117194869	chr14:56161804-56161805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562336492	chr14:56161897-56161898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555851096	chr14:56161930-56161931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568308666	chr14:56161949-56161950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs17253744	chr14:56161950-56161951	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs7142205	chr14:56161967-56161968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114557708	chr14:56161973-56161974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76271445	chr14:56161975-56161976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539683832	chr14:56161983-56161984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192086491	chr14:56161986-56161987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532410010	chr14:56162022-56162023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs59412666	chr14:56162041-56162042	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs183976483	chr14:56162043-56162044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7142744	chr14:56162186-56162187	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs17832371	chr14:56162302-56162303	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs372051957	chr14:56162315-56162316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574213026	chr14:56162332-56162333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544459691	chr14:56162334-56162335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143048309	chr14:56162371-56162372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148192034	chr14:56162447-56162448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	21163964	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
ocular or pituitary abnormalities	19965921	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2326 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56101800-56162800	Weak transcription	Brain Germinal Matrix	brain
2	chr14:56102400-56185400	Weak transcription	Right Ventricle	heart
3	chr14:56109200-56164000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr14:56122400-56164800	Weak transcription	Small Intestine	intestine
5	chr14:56142800-56168400	Weak transcription	Fetal Kidney	kidney
6	chr14:56147400-56170400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr14:56147800-56164200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr14:56148000-56161800	Weak transcription	Pancreas	Pancrea
9	chr14:56148000-56174000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr14:56148400-56165600	Weak transcription	NHDF-Ad	bronchial
11	chr14:56151200-56165800	Weak transcription	Hela-S3	cervix
12	chr14:56152200-56162200	Weak transcription	Fetal Intestine Small	intestine
13	chr14:56152800-56164400	Weak transcription	HMEC	breast
14	chr14:56153000-56167800	Weak transcription	Primary hematopoietic stem cells	blood
15	chr14:56153400-56174000	Weak transcription	Brain Cingulate Gyrus	brain
16	chr14:56153600-56162400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr14:56153600-56163200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr14:56153600-56164200	Weak transcription	HSMMtube	muscle
19	chr14:56153600-56164400	Weak transcription	Brain Angular Gyrus	brain
20	chr14:56153600-56165200	Weak transcription	NH-A	brain
21	chr14:56153600-56165600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr14:56153600-56165600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr14:56153600-56165800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:56153800-56161400	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr14:56153800-56162200	Weak transcription	Fetal Intestine Large	intestine
26	chr14:56153800-56163200	Weak transcription	Colonic Mucosa	Colon
27	chr14:56153800-56164000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:56153800-56164000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr14:56153800-56164200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:56153800-56165000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr14:56153800-56165600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:56153800-56170600	Weak transcription	Fetal Stomach	stomach
33	chr14:56153800-56172000	Weak transcription	Esophagus	oesophagus
34	chr14:56153800-56172400	Weak transcription	Dnd41	blood
35	chr14:56153800-56173800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr14:56153800-56174000	Weak transcription	Brain Anterior Caudate	brain
37	chr14:56154000-56162200	Weak transcription	Ovary	ovary
38	chr14:56154000-56167800	Weak transcription	Stomach Smooth Muscle	stomach
39	chr14:56154000-56172400	Weak transcription	Lung	lung
40	chr14:56154000-56173800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr14:56154000-56177800	Weak transcription	Left Ventricle	heart
42	chr14:56154000-56191000	Weak transcription	Aorta	Aorta
43	chr14:56154200-56162000	Weak transcription	Liver	Liver
44	chr14:56154200-56162200	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr14:56154200-56163400	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr14:56154400-56163800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr14:56154400-56177800	Weak transcription	Fetal Muscle Leg	muscle
48	chr14:56154800-56164400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr14:56154800-56165600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr14:56154800-56174000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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