Variant report

Variant	nsv1030250
Chromosome Location	chr5:37478163-37734859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2255)
CpG islands
(count:366)
Chromatin interactive
region (count:100)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2255 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37561556-37561928	K562	blood:	n/a	n/a
2	ARID3A	chr5:37717456-37718839	HepG2	liver:	n/a	chr5:37718035-37718051
3	ARID3A	chr5:37725466-37725597	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:37566412-37566482	K562	blood:	n/a	n/a
5	ARID3A	chr5:37552742-37553918	K562	blood:	n/a	n/a
6	ARID3A	chr5:37668578-37669026	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:37555087-37555396	K562	blood:	n/a	n/a
8	ARID3A	chr5:37576244-37577007	K562	blood:	n/a	chr5:37576689-37576705 chr5:37576688-37576704
9	ARID3A	chr5:37554224-37554305	K562	blood:	n/a	n/a
10	ARID3A	chr5:37723608-37723756	K562	blood:	n/a	n/a
11	ARID3A	chr5:37723622-37723741	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:37723042-37723269	HepG2	liver:	n/a	n/a
13	ATF1	chr5:37723031-37723344	K562	blood:	n/a	n/a
14	ATF1	chr5:37672268-37672700	K562	blood:	n/a	n/a
15	ATF1	chr5:37668620-37669142	K562	blood:	n/a	n/a
16	ATF1	chr5:37552974-37553744	K562	blood:	n/a	n/a
17	ATF1	chr5:37576224-37576625	K562	blood:	n/a	n/a
18	ATF1	chr5:37614336-37614416	K562	blood:	n/a	n/a
19	ATF2	chr5:37721531-37722125	GM12878	blood:	n/a	n/a
20	ATF2	chr5:37672199-37672626	GM12878	blood:	n/a	n/a
21	ATF2	chr5:37722812-37723380	GM12878	blood:	n/a	n/a
22	ATF2	chr5:37722807-37723371	GM12878	blood:	n/a	n/a
23	ATF3	chr5:37668523-37668997	K562	blood:	n/a	n/a
24	ATF3	chr5:37722947-37723383	K562	blood:	n/a	n/a
25	ATF3	chr5:37668562-37669111	HCT-116	colon:	n/a	n/a
26	ATF3	chr5:37668528-37669122	HCT-116	colon:	n/a	n/a
27	ATF3	chr5:37668466-37669039	A549	lung:	n/a	n/a
28	ATF3	chr5:37668695-37668903	K562	blood:	n/a	n/a
29	BACH1	chr5:37637658-37637891	H1-hESC	embryonic stem cell:	n/a	chr5:37637759-37637773
30	BACH1	chr5:37553100-37553687	K562	blood:	n/a	n/a
31	BACH1	chr5:37512136-37512171	K562	blood:	n/a	n/a
32	BATF	chr5:37723059-37723351	GM12878	blood:	n/a	chr5:37723209-37723220
33	BATF	chr5:37672269-37672626	GM12878	blood:	n/a	n/a
34	BATF	chr5:37672308-37672700	GM12878	blood:	n/a	n/a
35	BATF	chr5:37721677-37722017	GM12878	blood:	n/a	chr5:37721867-37721878
36	BATF	chr5:37711144-37711407	GM12878	blood:	n/a	chr5:37711278-37711289
37	BATF	chr5:37721687-37721984	GM12878	blood:	n/a	chr5:37721867-37721878
38	BATF	chr5:37722967-37723392	GM12878	blood:	n/a	chr5:37723209-37723220
39	BCL11A	chr5:37722940-37723281	GM12878	blood:	n/a	n/a
40	BCL11A	chr5:37722872-37723247	GM12878	blood:	n/a	n/a
41	BCL11A	chr5:37672314-37672635	GM12878	blood:	n/a	n/a
42	BCL3	chr5:37668388-37669097	A549	lung:	n/a	n/a
43	BCLAF1	chr5:37672256-37672703	GM12878	blood:	n/a	n/a
44	BCLAF1	chr5:37672321-37672667	GM12878	blood:	n/a	n/a
45	BHLHE40	chr5:37723675-37723901	K562	blood:	n/a	n/a
46	BHLHE40	chr5:37672282-37672647	K562	blood:	n/a	n/a
47	BHLHE40	chr5:37722945-37723364	GM12878	blood:	n/a	n/a
48	BHLHE40	chr5:37668678-37668956	HepG2	liver:	n/a	n/a
49	BHLHE40	chr5:37555099-37555292	K562	blood:	n/a	n/a
50	BHLHE40	chr5:37717589-37717921	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37721782-37721832	AG04450	lung:	fetal
2	chr5:37723683-37723733	SKMC	muscle:	n/a
3	chr5:37666865-37666915	HCF	heart:	n/a
4	chr5:37717768-37717818	AoSMC	blood vessel:	n/a
5	chr5:37721782-37721832	GM19239	blood:	n/a
6	chr5:37638144-37638194	SK-N-SH_RA	brain:	n/a
7	chr5:37638144-37638194	PANC-1	pancreas:	n/a
8	chr5:37484025-37484075	HRCEpiC	kidney:	n/a
9	chr5:37638144-37638194	HNPCEpiC	eye:	n/a
10	chr5:37638144-37638194	Caco-2	colon:	n/a
11	chr5:37484025-37484075	PFSK-1	brain:	n/a
12	chr5:37638144-37638194	NHBE	bronchial:	n/a
13	chr5:37638144-37638194	CMK	blood:	n/a
14	chr5:37721782-37721832	T-47D	breast:	n/a
15	chr5:37717768-37717818	HNPCEpiC	eye:	n/a
16	chr5:37723683-37723733	CMK	blood:	n/a
17	chr5:37721782-37721832	HCPEpiC	choroid plexus:	n/a
18	chr5:37484025-37484075	SK-N-SH	brain:	n/a
19	chr5:37717768-37717818	K562	blood:	n/a
20	chr5:37638144-37638194	GM12891	blood:	n/a
21	chr5:37638144-37638194	AG10803	skin:	n/a
22	chr5:37666865-37666915	BE2_C	brain:	n/a
23	chr5:37723683-37723733	GM12878	blood:	n/a
24	chr5:37666865-37666915	SAEC	small airway:	n/a
25	chr5:37721782-37721832	LNCaP	prostate:	n/a
26	chr5:37638144-37638194	H1-hESC	embryonic stem cell:	embryo
27	chr5:37638144-37638194	HMEC	breast:	n/a
28	chr5:37638144-37638194	NHDF-neo	bronchial:	n/a
29	chr5:37484025-37484075	MCF-7	breast:	n/a
30	chr5:37723683-37723733	ovcar-3	ovarian:	n/a
31	chr5:37723683-37723733	MCF-7	breast:	n/a
32	chr5:37721782-37721832	NHBE	bronchial:	n/a
33	chr5:37721782-37721832	BJ	skin:	n/a
34	chr5:37721782-37721832	SK-N-SH_RA	brain:	n/a
35	chr5:37484025-37484075	HRPEpiC	eye:	n/a
36	chr5:37484025-37484075	NT2-D1	testis:	n/a
37	chr5:37638144-37638194	Hepatocyte	liver:	n/a
38	chr5:37638144-37638194	A549	lung:	n/a
39	chr5:37638144-37638194	LNCaP	prostate:	n/a
40	chr5:37717768-37717818	NHDF-neo	bronchial:	n/a
41	chr5:37484025-37484075	RPTEC	kidney:	n/a
42	chr5:37723683-37723733	HCT-116	colon:	n/a
43	chr5:37638144-37638194	HRE	kidney:	n/a
44	chr5:37721782-37721832	SKMC	muscle:	n/a
45	chr5:37484025-37484075	GM19239	blood:	n/a
46	chr5:37717768-37717818	GM06990	blood:	n/a
47	chr5:37717768-37717818	LNCaP	prostate:	n/a
48	chr5:37717768-37717818	HCT-116	colon:	n/a
49	chr5:37721782-37721832	U87	brain:	n/a
50	chr5:37484025-37484075	ProgFib	skin:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:37595713..37598522-chr5:37598796..37602630,3	MCF-7	breast:
2	chr5:37713205..37715908-chr5:37718081..37720863,2	K562	blood:
3	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
4	chr5:37565296..37570234-chr5:37571928..37578079,8	K562	blood:
5	chr5:37550616..37553710-chr5:37559318..37562633,4	K562	blood:
6	chr10:132633168..132634098-chr5:37613234..37613734,2	NB4	blood:
7	chr5:37536707..37538331-chr5:37538401..37541156,2	K562	blood:
8	chr5:37702513..37704538-chr5:37716164..37718117,2	MCF-7	breast:
9	chr5:37619614..37621754-chr5:37668153..37669761,2	MCF-7	breast:
10	chr5:37539872..37542556-chr5:37548847..37552617,3	K562	blood:
11	chr5:37413185..37413702-chr5:37723532..37724165,2	MCF-7	breast:
12	chr5:37702838..37705165-chr5:37705788..37708573,2	MCF-7	breast:
13	chr5:37550784..37553523-chr5:37560304..37561961,2	MCF-7	breast:
14	chr5:37658934..37661849-chr5:37667178..37669216,3	MCF-7	breast:
15	chr5:37583782..37585545-chr5:37586859..37589248,2	K562	blood:
16	chr5:37583782..37585545-chr5:37586859..37589248,2	K562	blood:
17	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
18	chr5:37559780..37563110-chr5:37563759..37567373,3	K562	blood:
19	chr5:37495049..37495731-chr5:37758036..37758591,2	MCF-7	breast:
20	chr5:37728379..37730456-chr5:37761987..37763560,2	K562	blood:
21	chr5:37659630..37663695-chr5:37665450..37669812,5	K562	blood:
22	chr5:37628723..37630359-chr5:37632589..37634816,2	K562	blood:
23	chr5:37713779..37717092-chr5:37718712..37720863,3	K562	blood:
24	chr5:37553408..37554969-chr5:37565315..37567049,2	K562	blood:
25	chr5:37664491..37667181-chr5:37703176..37705396,2	MCF-7	breast:
26	chr5:37559780..37563110-chr5:37563759..37567373,3	K562	blood:
27	chr5:37551824..37554603-chr5:37555317..37558093,4	K562	blood:
28	chr5:37723298..37724139-chr5:38192927..38193812,2	K562	blood:
29	chr5:37541266..37543534-chr5:37545440..37547559,2	K562	blood:
30	chr5:37661443..37663164-chr5:37664838..37666948,2	MCF-7	breast:
31	chr5:37539872..37542556-chr5:37548847..37552617,3	K562	blood:
32	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:
33	chr5:37708278..37710296-chr5:37714841..37716793,2	K562	blood:
34	chr5:37576360..37578315-chr5:37581420..37583139,2	K562	blood:
35	chr5:37578232..37579991-chr5:37581584..37583169,2	MCF-7	breast:
36	chr5:37713779..37717092-chr5:37718712..37720863,3	K562	blood:
37	chr5:37711811..37713434-chr5:37718883..37721366,2	MCF-7	breast:
38	chr5:37700803..37702469-chr5:37717736..37720672,2	MCF-7	breast:
39	chr5:37574620..37576476-chr5:37584938..37587005,2	K562	blood:
40	chr5:37662824..37665076-chr5:37668148..37670201,3	MCF-7	breast:
41	chr5:37541266..37543534-chr5:37545440..37547559,2	K562	blood:
42	chr5:37551824..37554603-chr5:37555317..37558093,4	K562	blood:
43	chr5:37572624..37576201-chr5:37577602..37583153,5	K562	blood:
44	chr5:37667989..37670619-chr5:37702239..37705026,2	MCF-7	breast:
45	chr5:37595713..37598522-chr5:37598796..37602630,3	MCF-7	breast:
46	chr5:37378807..37379355-chr5:37554382..37555285,2	K562	blood:
47	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
48	chr5:37536707..37538331-chr5:37538401..37541156,2	K562	blood:
49	chr5:37702513..37704538-chr5:37716164..37718117,2	MCF-7	breast:
50	chr5:37553408..37554969-chr5:37565315..37567049,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP155-5	chr5:37505790-37506959	NONHSAT101066

No data

Variant related genes	Relation type
RNU6-1190P	TF binding region
WDR70	TF binding region
ENSG00000248216	TF binding region
RNU6-484P	TF binding region
RNU6-1190P	CpG island
WDR70	CpG island
ENSG00000248216	CpG island
RNU6-484P	CpG island
ENSG00000082068	chromatin interactions
ENSG00000222743	chromatin interactions

Extended variants
information (count: 9384 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:9384 , 50 per page) page: 1 2 3 4 5 6 7 ... 188

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76215364	chr5:37478198-37478199	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs4370304	chr5:37478238-37478239	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs4334908	chr5:37478269-37478270	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs545933524	chr5:37478293-37478294	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs374282864	chr5:37478301-37478302	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs563527288	chr5:37478324-37478325	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs146645785	chr5:37478330-37478331	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs543733239	chr5:37478341-37478342	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs562027081	chr5:37478368-37478369	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs141337820	chr5:37478378-37478379	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs75224133	chr5:37478385-37478386	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs566304391	chr5:37478386-37478387	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs527400387	chr5:37478391-37478392	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs552276912	chr5:37478396-37478397	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs115474804	chr5:37478400-37478401	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs538024730	chr5:37478405-37478406	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555348011	chr5:37478472-37478473	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76139680	chr5:37478500-37478501	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568339148	chr5:37478508-37478509	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535340006	chr5:37478523-37478524	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537838926	chr5:37478538-37478539	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73072281	chr5:37478556-37478557	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572315760	chr5:37478566-37478567	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375154110	chr5:37478572-37478573	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558263827	chr5:37478588-37478589	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539567166	chr5:37478644-37478645	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557806726	chr5:37478711-37478712	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527601819	chr5:37478730-37478731	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs578016155	chr5:37478756-37478757	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79179699	chr5:37478773-37478774	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543607825	chr5:37478777-37478778	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570664484	chr5:37478799-37478800	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562095788	chr5:37478807-37478808	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150257443	chr5:37478809-37478810	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4074950	chr5:37478954-37478955	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs113291614	chr5:37478978-37478979	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527272910	chr5:37478982-37478983	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552337813	chr5:37479006-37479007	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564162470	chr5:37479013-37479014	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531581197	chr5:37479060-37479061	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76583804	chr5:37479073-37479074	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553929424	chr5:37479165-37479166	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4298274	chr5:37479198-37479199	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs74707037	chr5:37479243-37479244	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547346777	chr5:37479245-37479246	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566092908	chr5:37479295-37479296	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539431896	chr5:37479343-37479344	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs367624131	chr5:37479375-37479376	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148735913	chr5:37479457-37479458	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs375410231	chr5:37479464-37479465	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	19197363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3031 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37420800-37480200	Weak transcription	Brain Hippocampus Middle	brain
2	chr5:37421600-37478400	Weak transcription	Aorta	Aorta
3	chr5:37425400-37480200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:37426000-37479800	Weak transcription	HSMM	muscle
5	chr5:37435600-37480000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr5:37445200-37479800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr5:37445200-37480200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr5:37445200-37480200	Weak transcription	Ovary	ovary
9	chr5:37445200-37480200	Weak transcription	Thymus	Thymus
10	chr5:37445400-37480200	Weak transcription	Hela-S3	cervix
11	chr5:37445600-37480000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr5:37458000-37480200	Weak transcription	Right Ventricle	heart
13	chr5:37463800-37489600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr5:37466000-37494400	Weak transcription	Osteobl	bone
15	chr5:37469200-37480200	Weak transcription	Placenta	Placenta
16	chr5:37469600-37480200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr5:37469600-37481200	Weak transcription	Gastric	stomach
18	chr5:37470200-37480200	Weak transcription	Pancreas	Pancrea
19	chr5:37471400-37479600	Weak transcription	Fetal Intestine Small	intestine
20	chr5:37471400-37479600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr5:37471400-37479800	Weak transcription	Fetal Thymus	thymus
22	chr5:37471400-37480000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr5:37471400-37480000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:37471400-37480000	Weak transcription	A549	lung
25	chr5:37471400-37480200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr5:37471400-37480200	Weak transcription	Left Ventricle	heart
27	chr5:37471600-37480000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr5:37471600-37480200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr5:37471600-37480200	Weak transcription	Brain Angular Gyrus	brain
30	chr5:37471600-37492400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr5:37471800-37479200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr5:37472200-37479200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:37472200-37479400	Weak transcription	Fetal Muscle Trunk	muscle
34	chr5:37472200-37479800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr5:37472200-37479800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr5:37472200-37479800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:37472200-37479800	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr5:37472200-37479800	Weak transcription	Dnd41	blood
39	chr5:37472200-37481600	Weak transcription	Colon Smooth Muscle	Colon
40	chr5:37472400-37479600	Weak transcription	Liver	Liver
41	chr5:37472400-37480000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr5:37472400-37480000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr5:37472400-37480000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr5:37472800-37479400	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr5:37472800-37483800	Weak transcription	Fetal Heart	heart
46	chr5:37473000-37479600	Weak transcription	Fetal Intestine Large	intestine
47	chr5:37473000-37479600	Weak transcription	Fetal Stomach	stomach
48	chr5:37473000-37479800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:37473000-37480200	Weak transcription	Esophagus	oesophagus
50	chr5:37473000-37481000	Weak transcription	Small Intestine	intestine

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