Variant report

Variant	nsv1030797
Chromosome Location	chr5:37335832-37445040
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1916)
CpG islands
(count:1591)
Chromatin interactive
region (count:79)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1916 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37349046-37349675	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:37412949-37413405	K562	blood:	n/a	n/a
3	ARID3A	chr5:37424736-37424788	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:37371166-37371527	K562	blood:	n/a	chr5:37371175-37371187
5	ARID3A	chr5:37435813-37436000	K562	blood:	n/a	chr5:37435891-37435907
6	ARID3A	chr5:37371072-37371329	HepG2	liver:	n/a	chr5:37371175-37371187
7	ARID3A	chr5:37413045-37413386	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:37379206-37379473	K562	blood:	n/a	n/a
9	ARID3A	chr5:37435399-37435833	HepG2	liver:	n/a	n/a
10	ATF1	chr5:37379197-37379483	K562	blood:	n/a	n/a
11	ATF1	chr5:37370938-37371803	K562	blood:	n/a	n/a
12	ATF1	chr5:37413139-37413402	K562	blood:	n/a	n/a
13	ATF2	chr5:37379198-37379480	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr5:37370951-37371687	GM12878	blood:	n/a	n/a
15	ATF2	chr5:37370963-37371677	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr5:37370974-37371643	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr5:37370933-37371743	GM12878	blood:	n/a	n/a
18	ATF2	chr5:37379058-37379502	GM12878	blood:	n/a	n/a
19	ATF3	chr5:37370943-37371319	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
20	ATF3	chr5:37371001-37371307	HepG2	liver:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
21	ATF3	chr5:37370782-37371385	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
22	ATF3	chr5:37371073-37371320	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
23	ATF3	chr5:37379108-37379491	K562	blood:	n/a	n/a
24	ATF3	chr5:37379100-37379507	A549	lung:	n/a	n/a
25	ATF3	chr5:37370920-37371369	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
26	ATF3	chr5:37379172-37379508	A549	lung:	n/a	n/a
27	ATF3	chr5:37413096-37413476	K562	blood:	n/a	n/a
28	ATF3	chr5:37370910-37371420	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
29	ATF3	chr5:37371024-37371385	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
30	ATF3	chr5:37370993-37371683	A549	lung:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
31	BACH1	chr5:37371532-37371839	K562	blood:	n/a	n/a
32	BATF	chr5:37379223-37379461	GM12878	blood:	n/a	n/a
33	BATF	chr5:37413135-37413360	GM12878	blood:	n/a	n/a
34	BCL11A	chr5:37436356-37436593	GM12878	blood:	n/a	n/a
35	BCL3	chr5:37370886-37371778	A549	lung:	n/a	chr5:37371215-37371224
36	BCL3	chr5:37379056-37379575	A549	lung:	n/a	n/a
37	BCL3	chr5:37379009-37379598	A549	lung:	n/a	n/a
38	BCL3	chr5:37370732-37371729	A549	lung:	n/a	chr5:37371215-37371224
39	BCLAF1	chr5:37379021-37379585	GM12878	blood:	n/a	n/a
40	BCLAF1	chr5:37370930-37371950	GM12878	blood:	n/a	chr5:37371215-37371224
41	BCLAF1	chr5:37370979-37371786	GM12878	blood:	n/a	chr5:37371215-37371224
42	BCLAF1	chr5:37379017-37379502	K562	blood:	n/a	n/a
43	BCLAF1	chr5:37379066-37379572	K562	blood:	n/a	n/a
44	BCLAF1	chr5:37379111-37379567	GM12878	blood:	n/a	n/a
45	BHLHE40	chr5:37370906-37372116	GM12878	blood:	n/a	n/a
46	BHLHE40	chr5:37379191-37379467	K562	blood:	n/a	n/a
47	BHLHE40	chr5:37379174-37379470	GM12878	blood:	n/a	n/a
48	BHLHE40	chr5:37370765-37371943	K562	blood:	n/a	n/a
49	BRCA1	chr5:37371002-37371503	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr5:37413063-37413459	Hela-S3	cervix:	n/a	n/a

(count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37371213-37371263	HCT-116	colon:	n/a
2	chr5:37379272-37379322	AoSMC	blood vessel:	n/a
3	chr5:37379269-37379319	HRPEpiC	eye:	n/a
4	chr5:37379396-37379446	SK-N-SH_RA	brain:	n/a
5	chr5:37370967-37371017	HIPEpiC	eye:	n/a
6	chr5:37371213-37371263	HCT-116	colon:	n/a
7	chr5:37379272-37379322	AoSMC	blood vessel:	n/a
8	chr5:37379269-37379319	HRPEpiC	eye:	n/a
9	chr5:37379396-37379446	SK-N-SH_RA	brain:	n/a
10	chr5:37370967-37371017	HIPEpiC	eye:	n/a
11	chr5:37378229-37378279	GM12892	blood:	n/a
12	chr5:37371082-37371132	HCPEpiC	choroid plexus:	n/a
13	chr5:37371555-37371605	Hela-S3	cervix:	n/a
14	chr5:37382801-37382851	ovcar-3	ovarian:	n/a
15	chr5:37370947-37370997	HL-60	blood:	n/a
16	chr5:37379267-37379317	Hela-S3	cervix:	n/a
17	chr5:37378272-37378322	AG09319	gingival:	n/a
18	chr5:37371628-37371678	AG09309	skin:	n/a
19	chr5:37379272-37379322	HRE	kidney:	n/a
20	chr5:37378229-37378279	RPTEC	kidney:	n/a
21	chr5:37370947-37370997	SAEC	small airway:	n/a
22	chr5:37379267-37379317	PFSK-1	brain:	n/a
23	chr5:37379267-37379317	GM12892	blood:	n/a
24	chr5:37379374-37379424	GM19239	blood:	n/a
25	chr5:37371213-37371263	H1-hESC	embryonic stem cell:	embryo
26	chr5:37378050-37378100	GM12878	blood:	n/a
27	chr5:37379269-37379319	AG09309	skin:	n/a
28	chr5:37379358-37379408	A549	lung:	n/a
29	chr5:37378360-37378410	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:37371555-37371605	HCM	heart:	n/a
31	chr5:37382801-37382851	SKMC	muscle:	n/a
32	chr5:37371555-37371605	HIPEpiC	eye:	n/a
33	chr5:37379461-37379511	HUVEC	blood vessel:	n/a
34	chr5:37371082-37371132	NHDF-neo	bronchial:	n/a
35	chr5:37371555-37371605	NH-A	brain:	n/a
36	chr5:37370967-37371017	PrEC	prostate:	n/a
37	chr5:37379269-37379319	HRCEpiC	kidney:	n/a
38	chr5:37371192-37371242	A549	lung:	n/a
39	chr5:37379272-37379322	GM12878	blood:	n/a
40	chr5:37371192-37371242	NH-A	brain:	n/a
41	chr5:37371628-37371678	AG10803	skin:	n/a
42	chr5:37370967-37371017	RPTEC	kidney:	n/a
43	chr5:37379267-37379317	AG10803	skin:	n/a
44	chr5:37379396-37379446	ECC-1	luminal epithelium:	n/a
45	chr5:37379358-37379408	HRE	kidney:	n/a
46	chr5:37370967-37371017	HNPCEpiC	eye:	n/a
47	chr5:37371179-37371229	GM06990	blood:	n/a
48	chr5:37379358-37379408	HRPEpiC	eye:	n/a
49	chr5:37379269-37379319	SK-N-SH_RA	brain:	n/a
50	chr5:37379822-37379872	MCF-7	breast:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:37412800..37413850-chr5:37837177..37838175,5	MCF-7	breast:
2	chr19:10443916..10444436-chr5:37370772..37371335,2	NB4	blood:
3	chr17:61358570..61359089-chr5:37412803..37413392,2	MCF-7	breast:
4	chr5:37369538..37373129-chr5:37377393..37380859,4	MCF-7	breast:
5	chr5:37412738..37413377-chr5:38194610..38195311,2	MCF-7	breast:
6	chr1:11967776..11968487-chr5:37370635..37371332,2	Hela-S3	cervix:
7	chr5:37348597..37351209-chr5:37351351..37353763,2	K562	blood:
8	chr5:37341337..37344195-chr5:37360002..37362809,2	K562	blood:
9	chr5:37379216..37379885-chr6:58287233..58287739,2	Hela-S3	cervix:
10	chr5:37398413..37401041-chr5:37401249..37404698,3	K562	blood:
11	chr5:37423699..37426165-chr5:37428640..37431370,2	MCF-7	breast:
12	chr5:37412783..37413436-chr5:37723453..37724202,2	K562	blood:
13	chr1:117601635..117602147-chr5:37379314..37380058,2	Hela-S3	cervix:
14	chr5:37402668..37405027-chr5:37408741..37410429,2	K562	blood:
15	chr5:37343556..37345615-chr5:37366480..37369895,3	K562	blood:
16	chr5:37392088..37394720-chr5:37398631..37400477,2	K562	blood:
17	chr5:37326722..37329430-chr5:37348015..37351389,3	K562	blood:
18	chr5:37413098..37413750-chr5:37837537..37838115,2	MCF-7	breast:
19	chr5:37412852..37413708-chr5:37554717..37555628,3	MCF-7	breast:
20	chr5:37438128..37441611-chr5:37451601..37454118,3	K562	blood:
21	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:
22	chr5:37343556..37345615-chr5:37366480..37369895,3	K562	blood:
23	chr5:37370138..37373249-chr5:37374935..37377740,7	K562	blood:
24	chr1:52831372..52832067-chr5:37371102..37371661,2	HCT-116	colon:
25	chr5:37402028..37404137-chr5:37405155..37406834,2	K562	blood:
26	chr5:37329127..37329843-chr5:37340391..37341109,2	Hela-S3	cervix:
27	chr5:37318176..37320415-chr5:37333622..37336534,2	K562	blood:
28	chr2:61404229..61405117-chr5:37371163..37371819,2	Hela-S3	cervix:
29	chr5:37389025..37391631-chr5:37392336..37394905,2	K562	blood:
30	chr5:37370692..37371320-chr5:72794239..72794798,2	Hela-S3	cervix:
31	chr5:37351031..37353005-chr5:37354563..37356913,2	K562	blood:
32	chr5:37296733..37298868-chr5:37344772..37346341,2	K562	blood:
33	chr12:7052910..7053902-chr5:37371084..37371594,2	Hela-S3	cervix:
34	chr5:37395673..37397370-chr5:37410862..37413241,2	MCF-7	breast:
35	chr5:37370037..37373489-chr5:37377973..37381470,5	K562	blood:
36	chr5:37365691..37367751-chr5:37369538..37372240,3	K562	blood:
37	chr5:37358150..37361413-chr5:37362395..37366227,3	K562	blood:
38	chr5:37412768..37413768-chr5:38192655..38193859,13	MCF-7	breast:
39	chr5:37402028..37404137-chr5:37405155..37406834,2	K562	blood:
40	chr5:21459174..21459727-chr5:37379374..37379881,2	Hela-S3	cervix:
41	chr5:37370064..37373071-chr5:37393227..37395634,3	K562	blood:
42	chr5:37363225..37366000-chr5:37368563..37371283,3	K562	blood:
43	chr15:94515130..94515844-chr5:37350902..37351467,2	MCF-7	breast:
44	chr5:37412788..37413557-chr5:38023669..38024455,2	MCF-7	breast:
45	chr5:37413185..37413702-chr5:37723532..37724165,2	MCF-7	breast:
46	chr5:37358150..37361413-chr5:37362395..37366227,3	K562	blood:
47	chr5:37353747..37356748-chr5:37369994..37371965,3	K562	blood:
48	chr5:37349723..37351295-chr5:37369578..37371440,2	K562	blood:
49	chr5:37412794..37413863-chr5:38192922..38193865,5	K562	blood:
50	chr5:37397085..37398718-chr5:37402352..37404618,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR70-4	chr5:37377151-37377385	NONHSAT101062
2	lnc-NIPBL-7	chr5:37379591-37379656	NONHSAT101065
3	lnc-NIPBL-7	chr5:37379404-37379494	NONHSAT101065
4	lnc-NIPBL-7	chr5:37381704-37381911	NONHSAT101065
5	lnc-WDR70-4	chr5:37377986-37378073	NONHSAT101062

No data

Variant related genes	Relation type
WDR70	TF binding region
ENSG00000250455	TF binding region
NUP155	TF binding region
WDR70	CpG island
ENSG00000250455	CpG island
NUP155	CpG island
ENSG00000164190	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000250455	chromatin interactions
ENSG00000113569	chromatin interactions
ENSG00000173209	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000154222	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000251880	chromatin interactions
ENSG00000183666	chromatin interactions
ENSG00000104549	chromatin interactions
ENSG00000082068	chromatin interactions
ENSG00000236137	chromatin interactions
ENSG00000253513	chromatin interactions
ENSG00000145741	chromatin interactions
ENSG00000215190	chromatin interactions
ENSG00000248587	chromatin interactions

Extended variants
information (count: 4211 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:4211 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564930481	chr5:37335833-37335834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189407917	chr5:37335869-37335870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550779256	chr5:37335879-37335880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34632034	chr5:37335890-37335891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550260226	chr5:37335905-37335906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569465326	chr5:37335915-37335916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181446738	chr5:37335956-37335957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548768087	chr5:37335976-37335977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116898248	chr5:37336003-37336004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534447819	chr5:37336058-37336059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553050817	chr5:37336087-37336088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577558213	chr5:37336142-37336143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538761163	chr5:37336154-37336155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148867704	chr5:37336199-37336200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554978842	chr5:37336202-37336203	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185583841	chr5:37336225-37336226	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112839465	chr5:37336228-37336229	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147699590	chr5:37336230-37336231	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570167777	chr5:37336253-37336254	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560701979	chr5:37336285-37336286	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181004407	chr5:37336330-37336331	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540123535	chr5:37336355-37336356	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539158753	chr5:37336362-37336363	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532378261	chr5:37336363-37336364	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558693054	chr5:37336393-37336394	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11744730	chr5:37336487-37336488	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs372846953	chr5:37336488-37336489	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112235683	chr5:37336524-37336525	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374531961	chr5:37336526-37336527	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192313438	chr5:37336563-37336564	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146992994	chr5:37336601-37336602	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183289342	chr5:37336618-37336619	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574771778	chr5:37336661-37336662	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543403016	chr5:37336677-37336678	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs137991149	chr5:37336680-37336681	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs216377	chr5:37336711-37336712	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs571096195	chr5:37336720-37336721	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538269990	chr5:37336723-37336724	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556875030	chr5:37336773-37336774	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568861655	chr5:37336777-37336778	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535936775	chr5:37336861-37336862	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577373901	chr5:37336951-37336952	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188731926	chr5:37336980-37336981	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546341606	chr5:37337012-37337013	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572685087	chr5:37337069-37337070	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540162447	chr5:37337077-37337078	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558602936	chr5:37337145-37337146	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs125682	chr5:37337147-37337148	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs542264030	chr5:37337150-37337151	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544291804	chr5:37337165-37337166	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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

Chromatin state (count:2975 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37289000-37369200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr5:37296400-37365400	Strong transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:37296400-37369000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr5:37296800-37353200	Strong transcription	Fetal Thymus	thymus
5	chr5:37296800-37358400	Strong transcription	Placenta	Placenta
6	chr5:37296800-37358600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:37296800-37358600	Strong transcription	Liver	Liver
8	chr5:37296800-37359000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:37296800-37359800	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:37296800-37359800	Strong transcription	Fetal Intestine Large	intestine
11	chr5:37296800-37360000	Strong transcription	Adipose Nuclei	Adipose
12	chr5:37296800-37364600	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr5:37296800-37364600	Strong transcription	Dnd41	blood
14	chr5:37296800-37365600	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr5:37297000-37364200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:37297000-37365400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:37297200-37358800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr5:37297400-37364600	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr5:37297800-37359800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:37298600-37337800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:37307800-37368600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:37308800-37337800	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr5:37308800-37353200	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr5:37308800-37365400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr5:37311600-37351400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr5:37311600-37365400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:37311600-37365400	Strong transcription	Fetal Muscle Leg	muscle
28	chr5:37312000-37337600	Strong transcription	Stomach Smooth Muscle	stomach
29	chr5:37317600-37339800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr5:37318400-37359000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr5:37319000-37358400	Strong transcription	Duodenum Mucosa	Duodenum
32	chr5:37319200-37337400	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr5:37319200-37364600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr5:37319400-37365400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr5:37319600-37347800	Strong transcription	Rectal Mucosa Donor 29	rectum
36	chr5:37319800-37349200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr5:37321200-37337400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:37321600-37359600	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr5:37322200-37360000	Strong transcription	Hela-S3	cervix
40	chr5:37322800-37347600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr5:37323200-37358800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr5:37323400-37363600	Weak transcription	Stomach Mucosa	stomach
43	chr5:37324400-37365400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:37324600-37342400	Strong transcription	Brain Germinal Matrix	brain
45	chr5:37325400-37336800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:37325400-37342600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:37325800-37336400	Weak transcription	Aorta	Aorta
48	chr5:37326000-37336800	Weak transcription	Colonic Mucosa	Colon
49	chr5:37326000-37338200	Strong transcription	Osteobl	bone
50	chr5:37327000-37336400	Weak transcription	Pancreas	Pancrea

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