Variant report

Variant	nsv877358
Chromosome Location	chr3:115396581-115551931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2917)
CpG islands
(count:1040)
Chromatin interactive
region (count:80)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2917 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:115411798-115412110	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:115541452-115542286	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:115538629-115538987	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:115533681-115533994	HepG2	liver:	n/a	chr3:115533806-115533814
5	ARID3A	chr3:115424968-115425829	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:115472045-115472115	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:115508235-115508262	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:115502881-115503082	K562	blood:	n/a	n/a
9	ARID3A	chr3:115503370-115503726	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:115503338-115503528	K562	blood:	n/a	n/a
11	ARID3A	chr3:115502797-115503114	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:115477124-115477545	HepG2	liver:	n/a	n/a
13	ARID3A	chr3:115511081-115511849	HepG2	liver:	n/a	n/a
14	ARID3A	chr3:115538682-115538941	K562	blood:	n/a	n/a
15	ARID3A	chr3:115532807-115533397	HepG2	liver:	n/a	n/a
16	ARID3A	chr3:115444417-115445014	HepG2	liver:	n/a	n/a
17	ATF1	chr3:115509736-115509959	K562	blood:	n/a	n/a
18	ATF2	chr3:115503293-115503657	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr3:115503241-115503732	GM12878	blood:	n/a	n/a
20	ATF3	chr3:115509557-115510013	A549	lung:	n/a	n/a
21	ATF3	chr3:115509549-115510003	K562	blood:	n/a	n/a
22	ATF3	chr3:115503346-115503599	K562	blood:	n/a	n/a
23	ATF3	chr3:115503230-115503649	A549	lung:	n/a	n/a
24	ATF3	chr3:115538600-115539053	HepG2	liver:	n/a	n/a
25	ATF3	chr3:115509599-115510030	A549	lung:	n/a	n/a
26	BACH1	chr3:115523710-115523773	K562	blood:	n/a	n/a
27	BACH1	chr3:115503270-115503382	K562	blood:	n/a	n/a
28	BACH1	chr3:115427609-115427636	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr3:115417917-115418215	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr3:115428861-115429130	K562	blood:	n/a	n/a
31	BACH1	chr3:115485442-115485798	H1-hESC	embryonic stem cell:	n/a	chr3:115485622-115485636
32	BACH1	chr3:115503284-115503650	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr3:115411729-115412051	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr3:115502839-115503034	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr3:115541989-115542202	GM12878	blood:	n/a	n/a
36	BATF	chr3:115403939-115404320	GM12878	blood:	n/a	n/a
37	BATF	chr3:115403964-115404281	GM12878	blood:	n/a	n/a
38	BCL3	chr3:115509429-115510074	A549	lung:	n/a	chr3:115509829-115509838 chr3:115509828-115509837 chr3:115509786-115509795 chr3:115509787-115509796
39	BCL3	chr3:115507717-115508219	A549	lung:	n/a	n/a
40	BCL3	chr3:115509535-115510102	A549	lung:	n/a	chr3:115509829-115509838 chr3:115509828-115509837 chr3:115509786-115509795 chr3:115509787-115509796
41	BCL3	chr3:115503205-115503770	A549	lung:	n/a	chr3:115503460-115503473
42	BCLAF1	chr3:115538579-115539032	GM12878	blood:	n/a	n/a
43	BCLAF1	chr3:115538654-115538957	GM12878	blood:	n/a	n/a
44	BCLAF1	chr3:115503229-115503695	GM12878	blood:	n/a	chr3:115503460-115503473
45	BHLHE40	chr3:115429931-115430242	K562	blood:	n/a	n/a
46	BHLHE40	chr3:115507955-115508344	A549	lung:	n/a	n/a
47	BHLHE40	chr3:115538667-115538895	K562	blood:	n/a	n/a
48	BHLHE40	chr3:115412811-115412935	K562	blood:	n/a	chr3:115412868-115412877 chr3:115412866-115412879 chr3:115412869-115412878 chr3:115412868-115412877
49	BHLHE40	chr3:115538643-115538994	GM12878	blood:	n/a	n/a
50	BHLHE40	chr3:115502731-115503925	K562	blood:	n/a	chr3:115503095-115503111 chr3:115503450-115503466 chr3:115503092-115503108

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:115510713-115510763	SK-N-SH_RA	brain:	n/a
2	chr3:115417878-115417928	HCPEpiC	choroid plexus:	n/a
3	chr3:115503964-115504014	GM06990	blood:	n/a
4	chr3:115510713-115510763	SK-N-SH_RA	brain:	n/a
5	chr3:115417878-115417928	HCPEpiC	choroid plexus:	n/a
6	chr3:115503964-115504014	GM06990	blood:	n/a
7	chr3:115503319-115503369	ProgFib	skin:	n/a
8	chr3:115510713-115510763	BE2_C	brain:	n/a
9	chr3:115417878-115417928	HEEpiC	esophagus:	n/a
10	chr3:115438561-115438611	HMEC	breast:	n/a
11	chr3:115500667-115500717	HCM	heart:	n/a
12	chr3:115500667-115500717	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:115502895-115502945	HUVEC	blood vessel:	n/a
14	chr3:115510713-115510763	PrEC	prostate:	n/a
15	chr3:115524031-115524081	CMK	blood:	n/a
16	chr3:115485166-115485216	HAEpiC	amniotic membrane:	n/a
17	chr3:115500771-115500821	SAEC	small airway:	n/a
18	chr3:115507015-115507065	ovcar-3	ovarian:	n/a
19	chr3:115503520-115503570	HEEpiC	esophagus:	n/a
20	chr3:115440301-115440351	IMR90	lung:	fetal
21	chr3:115500667-115500717	HRPEpiC	eye:	n/a
22	chr3:115510713-115510763	HepG2	liver:	n/a
23	chr3:115524190-115524240	Hepatocyte	liver:	n/a
24	chr3:115503319-115503369	ECC-1	luminal epithelium:	n/a
25	chr3:115417878-115417928	SK-N-SH	brain:	n/a
26	chr3:115500667-115500717	IMR90	lung:	fetal
27	chr3:115485166-115485216	H1-hESC	embryonic stem cell:	embryo
28	chr3:115507015-115507065	SK-N-SH	brain:	n/a
29	chr3:115503964-115504014	AG04450	lung:	fetal
30	chr3:115500771-115500821	HAEpiC	amniotic membrane:	n/a
31	chr3:115438561-115438611	NB4	blood:	n/a
32	chr3:115510713-115510763	HNPCEpiC	eye:	n/a
33	chr3:115503319-115503369	Hela-S3	cervix:	n/a
34	chr3:115503520-115503570	AG04450	lung:	fetal
35	chr3:115524190-115524240	RPTEC	kidney:	n/a
36	chr3:115503319-115503369	AoSMC	blood vessel:	n/a
37	chr3:115510713-115510763	AG10803	skin:	n/a
38	chr3:115500667-115500717	ProgFib	skin:	n/a
39	chr3:115509674-115509724	HMEC	breast:	n/a
40	chr3:115524190-115524240	AG09319	gingival:	n/a
41	chr3:115502895-115502945	T-47D	breast:	n/a
42	chr3:115524190-115524240	NB4	blood:	n/a
43	chr3:115500771-115500821	HRE	kidney:	n/a
44	chr3:115440301-115440351	A549	lung:	n/a
45	chr3:115524031-115524081	HUVEC	blood vessel:	n/a
46	chr3:115524031-115524081	HEEpiC	esophagus:	n/a
47	chr3:115507015-115507065	GM12878	blood:	n/a
48	chr3:115500771-115500821	PANC-1	pancreas:	n/a
49	chr3:115502895-115502945	HCT-116	colon:	n/a
50	chr3:115417878-115417928	PANC-1	pancreas:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:115518137..115520040-chr3:115528623..115530348,2	K562	blood:
2	chr3:115501869..115503461-chr3:115508798..115511509,2	MCF-7	breast:
3	chr3:114936525..114937105-chr3:115502871..115503769,3	MCF-7	breast:
4	chr3:115532714..115535646-chr3:115536109..115538866,3	MCF-7	breast:
5	chr3:114102625..114103252-chr3:115503068..115503621,2	MCF-7	breast:
6	chr3:114936144..114937050-chr3:115533340..115534259,4	MCF-7	breast:
7	chr3:114810729..114811584-chr3:115533285..115533888,2	MCF-7	breast:
8	chr3:115411426..115412183-chr3:115503115..115504011,2	K562	blood:
9	chr3:115501869..115503461-chr3:115508798..115511509,2	MCF-7	breast:
10	chr3:115477319..115479189-chr3:115481176..115482912,2	MCF-7	breast:
11	chr3:114936055..114936988-chr3:115504261..115505159,2	MCF-7	breast:
12	chr3:115498634..115499220-chrX:151838935..151839816,2	MCF-7	breast:
13	chr3:114811119..114811642-chr3:115533522..115534412,2	K562	blood:
14	chr3:115477319..115479189-chr3:115481176..115482912,2	MCF-7	breast:
15	chr3:115411475..115412251-chr3:115533417..115534281,5	MCF-7	breast:
16	chr3:115411441..115412281-chr3:115533704..115534273,2	MCF-7	breast:
17	chr3:115492435..115494382-chr3:115502269..115504038,2	MCF-7	breast:
18	chr3:115409272..115410853-chr3:115416247..115418221,2	K562	blood:
19	chr3:115477468..115479081-chr3:115503033..115504547,2	K562	blood:
20	chr3:115538349..115538909-chr3:115641300..115642205,2	MCF-7	breast:
21	chr3:115496345..115501641-chr3:115501691..115504560,6	MCF-7	breast:
22	chr3:115518137..115520040-chr3:115528623..115530348,2	K562	blood:
23	chr3:115411441..115412281-chr3:115533704..115534273,2	MCF-7	breast:
24	chr3:114810564..114811142-chr3:115502456..115503407,2	MCF-7	breast:
25	chr3:115551783..115554624-chr3:115559636..115561873,2	K562	blood:
26	chr3:114102415..114103103-chr3:115533735..115534288,2	MCF-7	breast:
27	chr3:115411475..115412251-chr3:115533417..115534281,5	MCF-7	breast:
28	chr3:114102398..114103175-chr3:115538575..115539288,2	MCF-7	breast:
29	chr3:114935748..114937032-chr3:115503319..115503977,3	MCF-7	breast:
30	chr3:115477468..115479081-chr3:115503033..115504547,2	K562	blood:
31	chr3:114935787..114937252-chr3:115411439..115412510,14	MCF-7	breast:
32	chr3:114936206..114937103-chr3:115411442..115412145,4	K562	blood:
33	chr3:115487531..115489865-chr3:115496763..115498704,2	K562	blood:
34	chr3:115411598..115412539-chr3:115502911..115503945,4	MCF-7	breast:
35	chr3:115502780..115503568-chr8:146017569..146018126,2	Hela-S3	cervix:
36	chr3:115409272..115410853-chr3:115416247..115418221,2	K562	blood:
37	chr3:115375306..115377693-chr3:115501955..115504872,2	K562	blood:
38	chr3:115521930..115524892-chr3:115524896..115526525,2	K562	blood:
39	chr3:115503109..115503905-chr3:115538714..115539251,2	MCF-7	breast:
40	chr3:114810826..114811584-chr3:115538342..115539212,2	MCF-7	breast:
41	chr3:115502263..115504489-chr3:115506354..115508281,2	MCF-7	breast:
42	chr3:115501914..115505039-chr3:115538992..115541569,3	K562	blood:
43	chr3:115500349..115503826-chr3:115506654..115511474,7	MCF-7	breast:
44	chr3:115532714..115535646-chr3:115536109..115538866,3	MCF-7	breast:
45	chr3:114081376..114081975-chr3:115538427..115539222,2	MCF-7	breast:
46	chr3:114936124..114936973-chr3:115411350..115412285,4	MCF-7	breast:
47	chr3:115487531..115489865-chr3:115496763..115498704,2	K562	blood:
48	chr3:114936072..114937081-chr3:115538338..115539235,5	MCF-7	breast:
49	chr3:115411462..115412193-chr3:115538778..115539306,2	K562	blood:
50	chr3:114546104..114546664-chr3:115503246..115503983,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LSAMP-4	chr3:115507500-115507710	NONHSAT091305
2	lnc-LSAMP-2	chr3:115521222-115524018	NONHSAT091306
3	lnc-LSAMP-4	chr3:115511147-115511378	NONHSAT091305
4	lnc-LSAMP-3	chr3:115516372-115518165	ucscGeneNc_uc003ebh_1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LSAMP	hsa-miR-335-5p	chr3:115521620-115521614

Variant related genes	Relation type
RN7SL815P	TF binding region
RN7SL815P	CpG island
ENSG00000161016	chromatin interactions
ENSG00000181722	chromatin interactions
ENSG00000120733	chromatin interactions
ENSG00000185565	chromatin interactions
ENSG00000241596	chromatin interactions

Extended variants
information (count: 4649 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4649 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1370807	chr3:115396581-115396582	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75173136	chr3:115396582-115396583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147438525	chr3:115396594-115396595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77554196	chr3:115396628-115396629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554977207	chr3:115396665-115396666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545389265	chr3:115396676-115396677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563864528	chr3:115396696-115396697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531299372	chr3:115396713-115396714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35598551	chr3:115396942-115396943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569858090	chr3:115396943-115396944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550619357	chr3:115397025-115397026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs80121802	chr3:115397200-115397201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184495647	chr3:115397262-115397263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs3772920	chr3:115397299-115397300	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs566360733	chr3:115397316-115397317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533391615	chr3:115397320-115397321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139751861	chr3:115397321-115397322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141829177	chr3:115397423-115397424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189427332	chr3:115397435-115397436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537156157	chr3:115397453-115397454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193146783	chr3:115397555-115397556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145277756	chr3:115397614-115397615	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535235584	chr3:115397640-115397641	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553681642	chr3:115397644-115397645	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572008643	chr3:115397698-115397699	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147145641	chr3:115397719-115397720	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557342476	chr3:115397781-115397782	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1370808	chr3:115397785-115397786	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs184919290	chr3:115397846-115397847	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371652482	chr3:115397865-115397866	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574166208	chr3:115397894-115397895	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374811432	chr3:115397906-115397907	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189294998	chr3:115397929-115397930	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529496847	chr3:115397939-115397940	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181639179	chr3:115397946-115397947	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140246290	chr3:115397955-115397956	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62269625	chr3:115398031-115398032	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552060561	chr3:115398042-115398043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569951584	chr3:115398054-115398055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530904018	chr3:115398056-115398057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549222717	chr3:115398086-115398087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73858059	chr3:115398119-115398120	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs535314507	chr3:115398124-115398125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553544147	chr3:115398186-115398187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185980334	chr3:115398255-115398256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539352397	chr3:115398296-115398297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115492670	chr3:115398312-115398313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188785599	chr3:115398316-115398317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149694466	chr3:115398330-115398331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555198870	chr3:115398341-115398342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Ovarian cancer	22174824	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115378800-115412000	Weak transcription	Fetal Brain Male	brain
2	chr3:115380400-115397600	Weak transcription	Brain Germinal Matrix	brain
3	chr3:115385800-115397800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr3:115386800-115400400	Weak transcription	Aorta	Aorta
5	chr3:115391200-115411400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr3:115395000-115397400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr3:115395400-115400800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr3:115395600-115408600	Weak transcription	Fetal Brain Female	brain
9	chr3:115396000-115410400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr3:115396200-115396600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:115396600-115410200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr3:115397400-115397600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:115397600-115398000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr3:115397600-115398400	Strong transcription	Brain Germinal Matrix	brain
15	chr3:115398000-115399400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr3:115398400-115411200	Weak transcription	Brain Germinal Matrix	brain
17	chr3:115399400-115407400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:115399600-115399800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:115399800-115400000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr3:115399800-115400200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr3:115399800-115400200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr3:115400000-115400800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:115400200-115401200	Enhancers	Fetal Heart	heart
24	chr3:115400400-115400800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:115400400-115400800	Enhancers	Aorta	Aorta
26	chr3:115400400-115400800	Enhancers	Colon Smooth Muscle	Colon
27	chr3:115400800-115401000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr3:115403800-115404200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr3:115403800-115404200	Enhancers	GM12878-XiMat	blood
30	chr3:115406200-115407200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr3:115407200-115411600	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr3:115407400-115407600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:115407400-115407800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr3:115407400-115408000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:115407400-115408200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:115407600-115417800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr3:115408200-115411400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr3:115408600-115409200	Genic enhancers	Fetal Brain Female	brain
39	chr3:115409200-115410400	Weak transcription	Fetal Brain Female	brain
40	chr3:115410200-115410400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr3:115410400-115410600	Enhancers	Fetal Brain Female	brain
42	chr3:115410400-115410800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr3:115410400-115412200	Enhancers	Fetal Heart	heart
44	chr3:115410400-115413800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr3:115410600-115410800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr3:115410600-115411200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr3:115410600-115411200	Weak transcription	Fetal Brain Female	brain
48	chr3:115410600-115412200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:115410600-115414800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr3:115410800-115411000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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