Variant report

Variant	nsv881492
Chromosome Location	chr5:37239240-37543121
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3216)
CpG islands
(count:2198)
Chromatin interactive
region (count:145)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3216 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37412949-37413405	K562	blood:	n/a	n/a
2	ARID3A	chr5:37435813-37436000	K562	blood:	n/a	chr5:37435891-37435907
3	ARID3A	chr5:37413045-37413386	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:37249328-37249415	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:37379206-37379473	K562	blood:	n/a	n/a
6	ARID3A	chr5:37371166-37371527	K562	blood:	n/a	chr5:37371175-37371187
7	ARID3A	chr5:37371072-37371329	HepG2	liver:	n/a	chr5:37371175-37371187
8	ARID3A	chr5:37349046-37349675	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:37435399-37435833	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:37424736-37424788	HepG2	liver:	n/a	n/a
11	ATF1	chr5:37379197-37379483	K562	blood:	n/a	n/a
12	ATF1	chr5:37370938-37371803	K562	blood:	n/a	n/a
13	ATF1	chr5:37413139-37413402	K562	blood:	n/a	n/a
14	ATF2	chr5:37370951-37371687	GM12878	blood:	n/a	n/a
15	ATF2	chr5:37249330-37249721	GM12878	blood:	n/a	n/a
16	ATF2	chr5:37370933-37371743	GM12878	blood:	n/a	n/a
17	ATF2	chr5:37370963-37371677	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:37379198-37379480	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr5:37370974-37371643	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:37379058-37379502	GM12878	blood:	n/a	n/a
21	ATF3	chr5:37370943-37371319	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
22	ATF3	chr5:37379100-37379507	A549	lung:	n/a	n/a
23	ATF3	chr5:37370782-37371385	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
24	ATF3	chr5:37379172-37379508	A549	lung:	n/a	n/a
25	ATF3	chr5:37371024-37371385	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
26	ATF3	chr5:37371001-37371307	HepG2	liver:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
27	ATF3	chr5:37379108-37379491	K562	blood:	n/a	n/a
28	ATF3	chr5:37370993-37371683	A549	lung:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
29	ATF3	chr5:37413096-37413476	K562	blood:	n/a	n/a
30	ATF3	chr5:37371073-37371320	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
31	ATF3	chr5:37370910-37371420	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
32	ATF3	chr5:37370920-37371369	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
33	ATF3	chr5:37272710-37273010	A549	lung:	n/a	n/a
34	BACH1	chr5:37512136-37512171	K562	blood:	n/a	n/a
35	BACH1	chr5:37371532-37371839	K562	blood:	n/a	n/a
36	BACH1	chr5:37305059-37305259	K562	blood:	n/a	n/a
37	BACH1	chr5:37249622-37249625	H1-hESC	embryonic stem cell:	n/a	n/a
38	BATF	chr5:37379223-37379461	GM12878	blood:	n/a	n/a
39	BATF	chr5:37413135-37413360	GM12878	blood:	n/a	n/a
40	BCL11A	chr5:37436356-37436593	GM12878	blood:	n/a	n/a
41	BCL3	chr5:37379009-37379598	A549	lung:	n/a	n/a
42	BCL3	chr5:37249087-37249607	A549	lung:	n/a	chr5:37249490-37249503 chr5:37249563-37249572
43	BCL3	chr5:37379056-37379575	A549	lung:	n/a	n/a
44	BCL3	chr5:37370886-37371778	A549	lung:	n/a	chr5:37371215-37371224
45	BCL3	chr5:37370732-37371729	A549	lung:	n/a	chr5:37371215-37371224
46	BCLAF1	chr5:37379021-37379585	GM12878	blood:	n/a	n/a
47	BCLAF1	chr5:37379017-37379502	K562	blood:	n/a	n/a
48	BCLAF1	chr5:37370930-37371950	GM12878	blood:	n/a	chr5:37371215-37371224
49	BCLAF1	chr5:37370979-37371786	GM12878	blood:	n/a	chr5:37371215-37371224
50	BCLAF1	chr5:37248901-37249584	GM12878	blood:	n/a	chr5:37249490-37249503 chr5:37249563-37249572

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37249567-37249617	HCF	heart:	n/a
2	chr5:37382801-37382851	GM12878	blood:	n/a
3	chr5:37249567-37249617	HCF	heart:	n/a
4	chr5:37382801-37382851	GM12878	blood:	n/a
5	chr5:37248894-37248944	HPAEpiC	pulmonary alveolar:	n/a
6	chr5:37378050-37378100	HCT-116	colon:	n/a
7	chr5:37379269-37379319	HRE	kidney:	n/a
8	chr5:37371047-37371097	HCM	heart:	n/a
9	chr5:37484025-37484075	PrEC	prostate:	n/a
10	chr5:37379461-37379511	HCM	heart:	n/a
11	chr5:37371074-37371124	CMK	blood:	n/a
12	chr5:37371074-37371124	HepG2	liver:	n/a
13	chr5:37378360-37378410	ProgFib	skin:	n/a
14	chr5:37379358-37379408	Caco-2	colon:	n/a
15	chr5:37370880-37370930	AG09309	skin:	n/a
16	chr5:37249567-37249617	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:37379272-37379322	AG09309	skin:	n/a
18	chr5:37249567-37249617	HRPEpiC	eye:	n/a
19	chr5:37382801-37382851	AoSMC	blood vessel:	n/a
20	chr5:37379272-37379322	HepG2	liver:	n/a
21	chr5:37371074-37371124	GM06990	blood:	n/a
22	chr5:37370880-37370930	HMEC	breast:	n/a
23	chr5:37379822-37379872	IMR90	lung:	fetal
24	chr5:37379461-37379511	PANC-1	pancreas:	n/a
25	chr5:37370947-37370997	NHBE	bronchial:	n/a
26	chr5:37371082-37371132	AG09309	skin:	n/a
27	chr5:37371179-37371229	GM12891	blood:	n/a
28	chr5:37382801-37382851	HEK293	kidney:	embryo
29	chr5:37371628-37371678	GM19239	blood:	n/a
30	chr5:37379269-37379319	H1-hESC	embryonic stem cell:	embryo
31	chr5:37371213-37371263	PANC-1	pancreas:	n/a
32	chr5:37379358-37379408	RPTEC	kidney:	n/a
33	chr5:37371082-37371132	HCPEpiC	choroid plexus:	n/a
34	chr5:37371555-37371605	PANC-1	pancreas:	n/a
35	chr5:37378050-37378100	IMR90	lung:	fetal
36	chr5:37248984-37249034	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:37249223-37249273	GM19239	blood:	n/a
38	chr5:37248984-37249034	HRE	kidney:	n/a
39	chr5:37484025-37484075	HEEpiC	esophagus:	n/a
40	chr5:37371047-37371097	AG10803	skin:	n/a
41	chr5:37382801-37382851	Hepatocyte	liver:	n/a
42	chr5:37379272-37379322	IMR90	lung:	fetal
43	chr5:37484025-37484075	T-47D	breast:	n/a
44	chr5:37371074-37371124	HCF	heart:	n/a
45	chr5:37484025-37484075	SK-N-SH_RA	brain:	n/a
46	chr5:37371555-37371605	HIPEpiC	eye:	n/a
47	chr5:37371179-37371229	AoSMC	blood vessel:	n/a
48	chr5:37484025-37484075	BJ	skin:	n/a
49	chr5:37370947-37370997	GM19239	blood:	n/a
50	chr5:37379269-37379319	HAEpiC	amniotic membrane:	n/a

(count:145 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr19:11450158..11450732-chr5:37248969..37249920,2	Hela-S3	cervix:
2	chr5:37290610..37293343-chr5:37317784..37320761,2	K562	blood:
3	chr5:37358150..37361413-chr5:37362395..37366227,3	K562	blood:
4	chr5:36733395..36735929-chr5:37371507..37374356,2	MCF-7	breast:
5	chr5:37296733..37298868-chr5:37344772..37346341,2	K562	blood:
6	chr5:37353747..37356748-chr5:37369994..37371965,3	K562	blood:
7	chr5:37370037..37373489-chr5:37377973..37381470,5	K562	blood:
8	chr5:37395673..37397370-chr5:37410862..37413241,2	MCF-7	breast:
9	chr5:37225065..37226567-chr5:37275200..37277689,2	K562	blood:
10	chr12:95867838..95868385-chr5:37249139..37249647,2	Hela-S3	cervix:
11	chr5:37370064..37373071-chr5:37393227..37395634,3	K562	blood:
12	chr5:37230434..37232617-chr5:37243518..37246467,2	K562	blood:
13	chr5:37402668..37405027-chr5:37408741..37410429,2	K562	blood:
14	chr5:37412766..37413683-chr5:37757982..37759001,7	MCF-7	breast:
15	chr19:10222166..10222747-chr5:37249630..37250278,2	NB4	blood:
16	chr5:37509914..37511896-chr5:37518755..37521412,2	K562	blood:
17	chr5:36875375..36878248-chr5:37375352..37377665,2	K562	blood:
18	chr5:37370774..37371595-chr8:126009906..126010854,2	Hela-S3	cervix:
19	chr5:37349723..37351295-chr5:37369578..37371440,2	K562	blood:
20	chr5:37392088..37394720-chr5:37398631..37400477,2	K562	blood:
21	chr5:37313041..37316016-chr5:37316235..37319015,2	K562	blood:
22	chr11:75110443..75111008-chr5:37248561..37249187,2	Hela-S3	cervix:
23	chr5:37370037..37373489-chr5:37377973..37381470,5	K562	blood:
24	chr5:37363225..37366000-chr5:37368563..37371283,3	K562	blood:
25	chr5:37397085..37398718-chr5:37402352..37404618,2	MCF-7	breast:
26	chr5:37369760..37372730-chr5:37375256..37380889,7	MCF-7	breast:
27	chr5:37349723..37351295-chr5:37369578..37371440,2	K562	blood:
28	chr5:37412768..37413768-chr5:38192655..38193859,13	MCF-7	breast:
29	chr5:37313041..37316016-chr5:37316235..37320190,3	K562	blood:
30	chr5:37326722..37329430-chr5:37348015..37351389,3	K562	blood:
31	chr5:37369538..37373129-chr5:37377393..37380859,4	MCF-7	breast:
32	chr5:37365691..37367751-chr5:37369538..37372240,3	K562	blood:
33	chr17:41465731..41466245-chr5:37249205..37250047,2	Hela-S3	cervix:
34	chr19:10612852..10613551-chr5:37248973..37249815,2	NB4	blood:
35	chr5:37242850..37244799-chr5:37268818..37270992,2	MCF-7	breast:
36	chr5:37299270..37301087-chr5:37332798..37335148,2	K562	blood:
37	chr5:37247385..37249387-chr5:37291319..37293555,2	MCF-7	breast:
38	chr2:61404229..61405117-chr5:37371163..37371819,2	Hela-S3	cervix:
39	chr5:37423699..37426165-chr5:37428640..37431370,2	MCF-7	breast:
40	chr1:117601635..117602147-chr5:37379314..37380058,2	Hela-S3	cervix:
41	chr5:37438128..37441611-chr5:37451601..37454118,3	K562	blood:
42	chr5:37308340..37310527-chr5:37313095..37315302,2	K562	blood:
43	chr5:37495049..37495731-chr5:37758036..37758591,2	MCF-7	breast:
44	chr5:37270941..37273083-chr5:37281934..37283634,2	MCF-7	breast:
45	chr5:37326836..37328413-chr5:37330631..37332181,2	K562	blood:
46	chr5:37412788..37413557-chr5:38023669..38024455,2	MCF-7	breast:
47	chr5:37370692..37371320-chr5:72794239..72794798,2	Hela-S3	cervix:
48	chr5:37367445..37369110-chr5:37369671..37371335,2	MCF-7	breast:
49	chr5:37341224..37342807-chr5:37371137..37373027,2	K562	blood:
50	chr5:37329127..37329843-chr5:37340391..37341109,2	Hela-S3	cervix:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR70-5	chr5:37248948-37249323	NONHSAT101057
2	lnc-WDR70-5	chr5:37249174-37249323	NONHSAT101058
3	lnc-NIPBL-7	chr5:37379591-37379656	NONHSAT101065
4	lnc-WDR70-5	chr5:37250499-37250654	NONHSAT101058
5	lnc-WDR70-4	chr5:37377986-37378073	NONHSAT101062
6	lnc-NUP155-5	chr5:37505790-37506959	NONHSAT101066
7	lnc-C5orf42-5	chr5:37324306-37324596	expReg_chr5_1217_-
8	lnc-WDR70-5	chr5:37254685-37254730	NONHSAT101057
9	lnc-NUP155-1	chr5:37286551-37287079	NONHSAT101059
10	lnc-WDR70-4	chr5:37377151-37377385	NONHSAT101062
11	lnc-NUP155-2	chr5:37246277-37246581	NONHSAT101056
12	lnc-NIPBL-7	chr5:37381704-37381911	NONHSAT101065
13	lnc-NIPBL-7	chr5:37379404-37379494	NONHSAT101065

No data

Variant related genes	Relation type
ENSG00000250455	TF binding region
ENSG00000270558	TF binding region
C5orf42	TF binding region
WDR70	TF binding region
ENSG00000248216	TF binding region
RN7SL37P	TF binding region
RNU7-75P	TF binding region
NUP155	TF binding region
ENSG00000250455	CpG island
ENSG00000270558	CpG island
C5orf42	CpG island
WDR70	CpG island
ENSG00000248216	CpG island
RN7SL37P	CpG island
RNU7-75P	CpG island
NUP155	CpG island
ENSG00000105514	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000110721	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000197603	chromatin interactions
ENSG00000111142	chromatin interactions
ENSG00000243989	chromatin interactions
ENSG00000173209	chromatin interactions
ENSG00000214770	chromatin interactions
ENSG00000079999	chromatin interactions
ENSG00000248587	chromatin interactions
ENSG00000250133	chromatin interactions
ENSG00000236137	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000253513	chromatin interactions
ENSG00000183666	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000154222	chromatin interactions
ENSG00000113569	chromatin interactions
ENSG00000145741	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000259895	chromatin interactions
ENSG00000211455	chromatin interactions
ENSG00000250455	chromatin interactions
ENSG00000180806	chromatin interactions
ENSG00000251880	chromatin interactions
ENSG00000082068	chromatin interactions
ENSG00000104549	chromatin interactions
ENSG00000244165	chromatin interactions
ENSG00000242493	chromatin interactions
ENSG00000149273	chromatin interactions
ENSG00000215190	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000272173	chromatin interactions

Extended variants
information (count: 11728 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:11728 , 50 per page) page: 1 2 3 4 5 6 7 ... 235

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7735138	chr5:37239240-37239241	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552781691	chr5:37239354-37239355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs13181187	chr5:37239377-37239378	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs559175491	chr5:37239385-37239386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375521840	chr5:37239388-37239389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532039438	chr5:37239544-37239545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12054924	chr5:37239567-37239568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528039970	chr5:37239617-37239618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550012760	chr5:37239640-37239641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs578057289	chr5:37239642-37239643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75671301	chr5:37239645-37239646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568533052	chr5:37239648-37239649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540658614	chr5:37239662-37239663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535809677	chr5:37239678-37239679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10591482	chr5:37239683-37239684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs397997397	chr5:37239702-37239703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150622775	chr5:37239710-37239711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs66769463	chr5:37239717-37239718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4869496	chr5:37239721-37239722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78378437	chr5:37239732-37239733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542756856	chr5:37239762-37239763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562299747	chr5:37239768-37239769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373984590	chr5:37239800-37239801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566588740	chr5:37239816-37239817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4869497	chr5:37239850-37239851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117995360	chr5:37239884-37239885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370977871	chr5:37239891-37239892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576923188	chr5:37239944-37239945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367627463	chr5:37239946-37239947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113907029	chr5:37240047-37240048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186278746	chr5:37240115-37240116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372198756	chr5:37240153-37240154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531416262	chr5:37240225-37240226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551230209	chr5:37240228-37240229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542280757	chr5:37240303-37240304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113171567	chr5:37240323-37240324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191805177	chr5:37240345-37240346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143917473	chr5:37240409-37240410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181951757	chr5:37240469-37240470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144166243	chr5:37240476-37240477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549696789	chr5:37240540-37240541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185961851	chr5:37240548-37240549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550076098	chr5:37240575-37240576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190721130	chr5:37240576-37240577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183134646	chr5:37240621-37240622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368790688	chr5:37240629-37240630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187913073	chr5:37240667-37240668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527276886	chr5:37240689-37240690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191581584	chr5:37240725-37240726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76919163	chr5:37240825-37240826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Breast cancer	22522925	CNVD
Autism	22549408	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:6245 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37171600-37249000	Weak transcription	Spleen	Spleen
2	chr5:37209600-37239800	Weak transcription	Small Intestine	intestine
3	chr5:37209600-37240200	Weak transcription	Colonic Mucosa	Colon
4	chr5:37209600-37248000	Weak transcription	Gastric	stomach
5	chr5:37209600-37248400	Weak transcription	NHEK	skin
6	chr5:37215000-37248400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr5:37215200-37248200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr5:37216600-37248000	Weak transcription	Pancreas	Pancrea
9	chr5:37224200-37247200	Weak transcription	HUVEC	blood vessel
10	chr5:37225600-37248600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:37226800-37248000	Weak transcription	HepG2	liver
12	chr5:37227200-37248400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr5:37227400-37239800	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr5:37227400-37248400	Weak transcription	HMEC	breast
15	chr5:37227400-37248400	Weak transcription	NHLF	lung
16	chr5:37227400-37248600	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr5:37227800-37246200	Weak transcription	NH-A	brain
18	chr5:37227800-37248600	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr5:37228000-37240400	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr5:37231000-37241800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:37232600-37240800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr5:37232800-37245000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:37233200-37241400	Strong transcription	Fetal Thymus	thymus
24	chr5:37233400-37248600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:37233600-37240800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr5:37233800-37242400	Strong transcription	Fetal Lung	lung
27	chr5:37234000-37248600	Weak transcription	Esophagus	oesophagus
28	chr5:37234400-37248200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr5:37234400-37248400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr5:37235000-37247200	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr5:37235200-37244800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:37235400-37245000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:37235600-37241400	Strong transcription	Fetal Brain Female	brain
34	chr5:37235600-37243400	Strong transcription	Dnd41	blood
35	chr5:37235600-37245000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:37235600-37248200	Weak transcription	Primary B cells from peripheral blood	blood
37	chr5:37235800-37240800	Strong transcription	Brain Hippocampus Middle	brain
38	chr5:37235800-37241000	Strong transcription	Left Ventricle	heart
39	chr5:37235800-37242600	Strong transcription	Fetal Muscle Trunk	muscle
40	chr5:37236000-37240800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr5:37236000-37243200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr5:37236000-37243200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr5:37236000-37244600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:37236200-37240800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr5:37236200-37240800	Strong transcription	Stomach Smooth Muscle	stomach
46	chr5:37236200-37240800	Strong transcription	HSMMtube	muscle
47	chr5:37236200-37241000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:37236200-37241400	Strong transcription	Muscle Satellite Cultured Cells	--
49	chr5:37236200-37243600	Strong transcription	Placenta	Placenta
50	chr5:37236400-37240800	Strong transcription	Placenta Amnion	Placenta Amnion

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