Variant report

Variant	nsv536269
Chromosome Location	chr3:93948-337959
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:969)
CpG islands
(count:1403)
Chromatin interactive
region (count:19)
LncRNA
region (count:42)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:969 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:291259-291870	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:305517-307368	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:104725-105176	HepG2	liver:	n/a	n/a
4	ATF1	chr3:128118-128267	K562	blood:	n/a	n/a
5	ATF2	chr3:254098-254530	GM12878	blood:	n/a	n/a
6	ATF2	chr3:331761-332103	GM12878	blood:	n/a	n/a
7	ATF2	chr3:319829-320847	GM12878	blood:	n/a	n/a
8	ATF2	chr3:319964-320748	GM12878	blood:	n/a	n/a
9	ATF2	chr3:254017-254518	GM12878	blood:	n/a	n/a
10	ATF3	chr3:306304-306760	A549	lung:	n/a	n/a
11	BACH1	chr3:238302-238499	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:165624-165661	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:271174-271333	K562	blood:	n/a	n/a
14	BACH1	chr3:238826-240389	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr3:319906-320293	GM12878	blood:	n/a	n/a
16	BATF	chr3:166548-166773	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
17	BATF	chr3:259675-259847	GM12878	blood:	n/a	n/a
18	BATF	chr3:254085-254416	GM12878	blood:	n/a	n/a
19	BATF	chr3:319974-320310	GM12878	blood:	n/a	n/a
20	BATF	chr3:166561-166841	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
21	BATF	chr3:320384-320805	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:319927-320341	GM12878	blood:	n/a	chr3:320201-320210 chr3:320061-320069
23	BCL11A	chr3:319942-320280	GM12878	blood:	n/a	chr3:320201-320210 chr3:320061-320069
24	BCL3	chr3:320464-320727	GM12878	blood:	n/a	n/a
25	BCL3	chr3:306168-306863	A549	lung:	n/a	chr3:306285-306294 chr3:306282-306291
26	BCL3	chr3:306315-306750	A549	lung:	n/a	n/a
27	BCLAF1	chr3:320388-320763	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:152996-153196	A549	lung:	n/a	n/a
29	BHLHE40	chr3:260263-260618	GM12878	blood:	n/a	n/a
30	BHLHE40	chr3:150637-150664	A549	lung:	n/a	n/a
31	BHLHE40	chr3:260829-261058	GM12878	blood:	n/a	n/a
32	BHLHE40	chr3:306286-306823	HepG2	liver:	n/a	n/a
33	BHLHE40	chr3:319378-320826	GM12878	blood:	n/a	n/a
34	BRCA1	chr3:306367-306903	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr3:306406-306600	HepG2	liver:	n/a	n/a
36	CCNT2	chr3:238979-239034	K562	blood:	n/a	n/a
37	CCNT2	chr3:210502-210583	K562	blood:	n/a	n/a
38	CEBPB	chr3:110019-110065	A549	lung:	n/a	n/a
39	CEBPB	chr3:291542-291836	HepG2	liver:	n/a	chr3:291705-291716
40	CEBPB	chr3:306266-306559	MCF-7	breast:	n/a	chr3:306309-306322 chr3:306463-306480
41	CEBPB	chr3:157534-157826	IMR90	lung:	n/a	chr3:157561-157572 chr3:157692-157703
42	CEBPB	chr3:306331-306724	HepG2	liver:	n/a	chr3:306463-306480
43	CEBPB	chr3:242447-242817	IMR90	lung:	n/a	n/a
44	CEBPB	chr3:284758-286178	IMR90	lung:	n/a	chr3:284916-284933 chr3:285984-286001 chr3:284887-284900
45	CEBPB	chr3:306278-306814	A549	lung:	n/a	chr3:306309-306322 chr3:306463-306480
46	CEBPB	chr3:243974-244307	A549	lung:	n/a	chr3:244109-244120
47	CEBPB	chr3:216151-216444	HepG2	liver:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
48	CEBPB	chr3:215234-215549	HepG2	liver:	n/a	chr3:215398-215409 chr3:215397-215410
49	CEBPB	chr3:215306-215533	K562	blood:	n/a	chr3:215398-215409 chr3:215397-215410
50	CEBPB	chr3:104930-105426	HepG2	liver:	n/a	chr3:105311-105324

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:239506-239556	ECC-1	luminal epithelium:	n/a
2	chr3:239188-239238	T-47D	breast:	n/a
3	chr3:240139-240189	SK-N-SH	brain:	n/a
4	chr3:239733-239783	HCM	heart:	n/a
5	chr3:285234-285284	MCF-7	breast:	n/a
6	chr3:239188-239238	ovcar-3	ovarian:	n/a
7	chr3:239506-239556	NHBE	bronchial:	n/a
8	chr3:239733-239783	NHBE	bronchial:	n/a
9	chr3:285234-285284	PFSK-1	brain:	n/a
10	chr3:114243-114293	U87	brain:	n/a
11	chr3:238392-238442	Caco-2	colon:	n/a
12	chr3:238161-238211	HL-60	blood:	n/a
13	chr3:153242-153292	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:241182-241232	AG09319	gingival:	n/a
15	chr3:238615-238665	AoSMC	blood vessel:	n/a
16	chr3:238615-238665	AG04450	lung:	fetal
17	chr3:243996-244046	HNPCEpiC	eye:	n/a
18	chr3:243996-244046	H1-hESC	embryonic stem cell:	embryo
19	chr3:239506-239556	PANC-1	pancreas:	n/a
20	chr3:240139-240189	Hela-S3	cervix:	n/a
21	chr3:238161-238211	PFSK-1	brain:	n/a
22	chr3:239506-239556	NT2-D1	testis:	n/a
23	chr3:238048-238098	CMK	blood:	n/a
24	chr3:153242-153292	AG09309	skin:	n/a
25	chr3:238318-238368	Caco-2	colon:	n/a
26	chr3:238048-238098	AG10803	skin:	n/a
27	chr3:238161-238211	BJ	skin:	n/a
28	chr3:238048-238098	A549	lung:	n/a
29	chr3:239188-239238	AG10803	skin:	n/a
30	chr3:238048-238098	AG09319	gingival:	n/a
31	chr3:238161-238211	AG09309	skin:	n/a
32	chr3:239665-239715	MCF10A-Er-Src	breast:	n/a
33	chr3:243996-244046	AG10803	skin:	n/a
34	chr3:238611-238661	RPTEC	kidney:	n/a
35	chr3:238496-238546	HNPCEpiC	eye:	n/a
36	chr3:239733-239783	AG09319	gingival:	n/a
37	chr3:239733-239783	LNCaP	prostate:	n/a
38	chr3:239207-239257	BJ	skin:	n/a
39	chr3:239207-239257	LNCaP	prostate:	n/a
40	chr3:236078-236128	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:238392-238442	HCF	heart:	n/a
42	chr3:236078-236128	ProgFib	skin:	n/a
43	chr3:239229-239279	AG09319	gingival:	n/a
44	chr3:243996-244046	T-47D	breast:	n/a
45	chr3:238496-238546	Caco-2	colon:	n/a
46	chr3:271185-271235	H1-hESC	embryonic stem cell:	embryo
47	chr3:239665-239715	AG04450	lung:	fetal
48	chr3:238615-238665	HRPEpiC	eye:	n/a
49	chr3:238611-238661	MCF10A-Er-Src	breast:	n/a
50	chr3:239733-239783	HUVEC	blood vessel:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:169328..170327-chr3:184848..185564,2	MCF-7	breast:
2	chr3:333238..334968-chr3:337821..339342,2	MCF-7	breast:
3	chr3:297411..299702-chr3:300779..302869,2	K562	blood:
4	chr3:163984..165661-chr3:172610..174560,2	K562	blood:
5	chr3:321596..323780-chr3:337949..340526,2	MCF-7	breast:
6	chr11:73160067..73160822-chr3:118894..119482,2	MCF-7	breast:
7	chr3:291331..293955-chr3:294697..297452,2	MCF-7	breast:
8	chr3:217250..219144-chr3:222760..225297,2	MCF-7	breast:
9	chr3:291331..293955-chr3:294697..297452,2	MCF-7	breast:
10	chr3:321596..323780-chr3:337949..340526,2	MCF-7	breast:
11	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:
12	chr3:188824..190368-chr3:386265..388997,2	MCF-7	breast:
13	chr14:56081549..56082133-chr3:97763..98653,2	MCF-7	breast:
14	chr3:163984..165661-chr3:172610..174560,2	K562	blood:
15	chr3:297411..299702-chr3:300779..302869,2	K562	blood:
16	chr3:169328..170327-chr3:184848..185564,2	MCF-7	breast:
17	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:
18	chr3:217250..219144-chr3:222760..225297,2	MCF-7	breast:
19	chr3:333238..334968-chr3:337821..339342,2	MCF-7	breast:

(count:42 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL5RA-16	chr3:153782-154143	NONHSAT087554
2	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
3	lnc-IL5RA-6	chr3:238290-238385	ENSG00000224318.1
4	lnc-IL5RA-6	chr3:237540-237597	NONHSAT087559
5	lnc-IL5RA-7	chr3:95031-95375	XLOC_003014
6	lnc-IL5RA-6	chr3:238650-238882	ENSG00000224318.1
7	lnc-CNTN6-7	chr3:254887-255362	NONHSAT087562
8	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
9	lnc-CHL1-1	chr3:95888-96275	XLOC_002563
10	lnc-CNTN6-7	chr3:288251-290282	NONHSAT087561
11	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
12	lnc-IL5RA-16	chr3:157540-157624	NONHSAT087555
13	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
14	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
15	lnc-IL5RA-6	chr3:237679-237723	NONHSAT087559
16	lnc-CNTN6-7	chr3:238454-238746	NONHSAT087560
17	lnc-CHL1-1	chr3:95888-96275	XLOC_002563
18	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
19	lnc-IL5RA-7	chr3:95976-96029	XLOC_003014
20	lnc-CNTN6-7	chr3:288251-288539	NONHSAT087560
21	lnc-CHL1-1	chr3:109310-109435	XLOC_002563
22	lnc-IL5RA-16	chr3:153927-154143	NONHSAT087555
23	lnc-CHL1-1	chr3:109310-109695	XLOC_002563
24	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
25	lnc-CHL1-1	chr3:109401-109695	XLOC_002563
26	lnc-CHL1-1	chr3:109008-109196	XLOC_002563
27	lnc-IL5RA-17	chr3:147879-148034	l_2301_chr3:147013-148034_heart
28	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
29	lnc-CNTN6-7	chr3:286296-286375	NONHSAT087560
30	lnc-CNTN6-7	chr3:286296-286375	NONHSAT087561
31	lnc-CNTN6-7	chr3:239326-239775	NONHSAT087561
32	lnc-CHL1-1	chr3:111531-111663	XLOC_002563
33	lnc-IL5RA-6	chr3:238290-238542	ENSG00000224318.1
34	lnc-CHL1-1	chr3:111531-111980	XLOC_002563
35	lnc-IL5RA-17	chr3:147014-147245	l_2301_chr3:147013-148034_heart
36	lnc-IL5RA-6	chr3:238650-239024	ENSG00000224318.1
37	lnc-IL5RA-6	chr3:238139-238386	NONHSAT087559
38	lnc-CHL1-1	chr3:109008-109196	XLOC_002563
39	lnc-IL5RA-16	chr3:157540-157620	NONHSAT087554
40	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
41	lnc-IL5RA-16	chr3:172879-173007	NONHSAT087554
42	lnc-CNTN6-7	chr3:239697-239775	NONHSAT087562

No data

Variant related genes	Relation type
RNU6-1194P	TF binding region
ENSG00000224918	TF binding region
CHL1-AS2	TF binding region
CHL1	TF binding region
RNU6-1194P	CpG island
ENSG00000224918	CpG island
CHL1-AS2	CpG island
CHL1	CpG island

Extended variants
information (count: 9869 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:9869 , 50 per page) page: 1 2 3 4 5 6 7 ... 198

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187046988	chr3:95006-95007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542506363	chr3:95026-95027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539230420	chr3:95035-95036	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs559045695	chr3:95049-95050	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs554859245	chr3:95059-95060	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs577261913	chr3:95091-95092	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs541417200	chr3:95130-95131	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs538864381	chr3:95141-95142	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs575223468	chr3:95154-95155	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs17323863	chr3:95172-95173	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs141385216	chr3:95198-95199	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs191902830	chr3:95207-95208	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs5019322	chr3:95214-95215	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs114940036	chr3:95241-95242	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs184330632	chr3:95257-95258	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs546585797	chr3:95314-95315	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs567684597	chr3:95315-95316	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs529175223	chr3:95332-95333	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs550491742	chr3:95347-95348	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs568798490	chr3:95356-95357	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs17075510	chr3:95357-95358	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs551239145	chr3:95361-95362	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs564760430	chr3:95404-95405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534772012	chr3:95409-95410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190158673	chr3:95414-95415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541171975	chr3:95506-95507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146952269	chr3:95532-95533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74777740	chr3:95545-95546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369287552	chr3:95559-95560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138050890	chr3:95572-95573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142083116	chr3:95579-95580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17040271	chr3:95597-95598	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564482320	chr3:95602-95603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530327564	chr3:95613-95614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78386762	chr3:95727-95728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577046845	chr3:95728-95729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs398061995	chr3:95737-95738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11293547	chr3:95738-95739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572910963	chr3:95779-95780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143012311	chr3:95802-95803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs193239735	chr3:95824-95825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548551720	chr3:95837-95838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9866377	chr3:95854-95855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528893980	chr3:95859-95860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550153610	chr3:95863-95864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148194766	chr3:95868-95869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376233037	chr3:95933-95934	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs73816907	chr3:95935-95936	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs566518364	chr3:95967-95968	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs1400176	chr3:95973-95974	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Ependymoma	20639864	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495311	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:1119 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:95000-95600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:95000-96600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr3:95600-104600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:97400-97600	Enhancers	Brain Hippocampus Middle	brain
5	chr3:97600-98000	Enhancers	Fetal Brain Male	brain
6	chr3:97800-98200	Active TSS	Fetal Brain Female	brain
7	chr3:98000-98600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:98000-104800	Weak transcription	Fetal Brain Male	brain
9	chr3:98200-98600	Enhancers	Fetal Brain Female	brain
10	chr3:103600-104400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:103800-104200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:104200-104400	Enhancers	Gastric	stomach
13	chr3:104400-104800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr3:104400-105000	Weak transcription	Gastric	stomach
15	chr3:104400-105400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:104400-105400	Enhancers	HepG2	liver
17	chr3:104400-105600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:104600-104800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr3:104600-104800	Enhancers	Adipose Nuclei	Adipose
20	chr3:104600-104800	Enhancers	Brain Substantia Nigra	brain
21	chr3:104600-105600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr3:104600-105600	Enhancers	Fetal Lung	lung
23	chr3:104800-105000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:104800-105000	Active TSS	Brain Germinal Matrix	brain
25	chr3:104800-105000	Enhancers	Stomach Mucosa	stomach
26	chr3:104800-105200	Enhancers	Fetal Brain Male	brain
27	chr3:104800-105400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:104800-105400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:104800-105400	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr3:104800-105400	Enhancers	Brain Angular Gyrus	brain
31	chr3:104800-105400	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr3:104800-105600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr3:104800-105600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr3:104800-105600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr3:104800-105600	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr3:104800-105600	Enhancers	Brain Hippocampus Middle	brain
37	chr3:104800-105600	Flanking Active TSS	Brain Substantia Nigra	brain
38	chr3:104800-105600	Enhancers	Fetal Brain Female	brain
39	chr3:104800-105600	Enhancers	Psoas Muscle	Psoas
40	chr3:104800-105800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr3:105000-105200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr3:105000-105200	Enhancers	Liver	Liver
43	chr3:105000-105400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr3:105000-105400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr3:105000-105400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr3:105000-105400	Enhancers	Pancreas	Pancrea
47	chr3:105000-105600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr3:105000-105600	Flanking Active TSS	Brain Anterior Caudate	brain
49	chr3:105000-105600	Enhancers	Brain Cingulate Gyrus	brain
50	chr3:105000-105600	Flanking Active TSS	Brain Germinal Matrix	brain

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