Variant report

Variant	nsv1013820
Chromosome Location	chr3:82175705-82968181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2480)
CpG islands
(count:916)
Chromatin interactive
region (count:30)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:82378559-82378834	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:82213172-82213400	HepG2	liver:	n/a	chr3:82213382-82213398
3	ARID3A	chr3:82523895-82524148	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:82618076-82618425	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:82510345-82511417	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:82310265-82310567	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:82182138-82182400	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:82682321-82682798	HepG2	liver:	n/a	n/a
9	ATF1	chr3:82179198-82179569	K562	blood:	n/a	n/a
10	ATF2	chr3:82278485-82278877	GM12878	blood:	n/a	n/a
11	ATF2	chr3:82278469-82278954	GM12878	blood:	n/a	n/a
12	ATF2	chr3:82342876-82343525	GM12878	blood:	n/a	n/a
13	ATF2	chr3:82342943-82343353	GM12878	blood:	n/a	n/a
14	BACH1	chr3:82478194-82478294	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:82607265-82607633	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:82822413-82822675	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr3:82193203-82193459	GM12878	blood:	n/a	n/a
18	BATF	chr3:82435847-82436174	GM12878	blood:	n/a	n/a
19	BATF	chr3:82440092-82440346	GM12878	blood:	n/a	n/a
20	BATF	chr3:82278495-82278913	GM12878	blood:	n/a	n/a
21	BATF	chr3:82544166-82544400	GM12878	blood:	n/a	n/a
22	BATF	chr3:82544129-82544521	GM12878	blood:	n/a	n/a
23	BATF	chr3:82342967-82343442	GM12878	blood:	n/a	n/a
24	BATF	chr3:82543015-82543326	GM12878	blood:	n/a	n/a
25	BATF	chr3:82342976-82343425	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:82342979-82343429	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:82343054-82343277	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:82278530-82278839	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:82669980-82670148	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL3	chr3:82342980-82343386	GM12878	blood:	n/a	n/a
31	BCL3	chr3:82524504-82524869	GM12878	blood:	n/a	n/a
32	BCL3	chr3:82544257-82544621	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:82342970-82343372	GM12878	blood:	n/a	n/a
34	BHLHE40	chr3:82182080-82182456	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:82182000-82182459	K562	blood:	n/a	n/a
36	BHLHE40	chr3:82182126-82182462	HepG2	liver:	n/a	n/a
37	BHLHE40	chr3:82510081-82511066	HepG2	liver:	n/a	chr3:82510379-82510392
38	BHLHE40	chr3:82341550-82341750	GM12878	blood:	n/a	n/a
39	BHLHE40	chr3:82342993-82343586	GM12878	blood:	n/a	n/a
40	BRCA1	chr3:82786264-82786268	HepG2	liver:	n/a	n/a
41	BRCA1	chr3:82255949-82255989	GM12878	blood:	n/a	n/a
42	BRCA1	chr3:82915710-82915724	GM12878	blood:	n/a	n/a
43	CEBPB	chr3:82192911-82193039	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:82473848-82474106	HepG2	liver:	n/a	chr3:82473965-82473976
45	CEBPB	chr3:82352154-82352497	HepG2	liver:	n/a	chr3:82352326-82352337 chr3:82352328-82352339 chr3:82352326-82352339 chr3:82352328-82352337
46	CEBPB	chr3:82950972-82951173	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:82527016-82527265	HepG2	liver:	n/a	chr3:82527122-82527131 chr3:82527120-82527133 chr3:82527122-82527131 chr3:82527122-82527131 chr3:82527120-82527131 chr3:82527121-82527132 chr3:82527122-82527131
48	CEBPB	chr3:82560987-82561317	HepG2	liver:	n/a	chr3:82561151-82561160 chr3:82561151-82561160 chr3:82561151-82561160 chr3:82561149-82561160 chr3:82561151-82561160 chr3:82561150-82561161 chr3:82561149-82561162
49	CEBPB	chr3:82487420-82487603	HepG2	liver:	n/a	chr3:82487514-82487525 chr3:82487513-82487524 chr3:82487512-82487529
50	CEBPB	chr3:82732728-82732835	H1-hESC	embryonic stem cell:	n/a	chr3:82732781-82732792

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:82857026-82857076	BJ	skin:	n/a
2	chr3:82857026-82857076	BJ	skin:	n/a
3	chr3:82178370-82178420	HEK293	kidney:	embryo
4	chr3:82764684-82764734	HMEC	breast:	n/a
5	chr3:82860625-82860675	HIPEpiC	eye:	n/a
6	chr3:82857215-82857265	AG09309	skin:	n/a
7	chr3:82857215-82857265	NB4	blood:	n/a
8	chr3:82547324-82547374	T-47D	breast:	n/a
9	chr3:82547324-82547374	IMR90	lung:	fetal
10	chr3:82854345-82854395	SK-N-SH_RA	brain:	n/a
11	chr3:82764684-82764734	Jurkat	blood:	n/a
12	chr3:82314701-82314751	AG04450	lung:	fetal
13	chr3:82854345-82854395	AG10803	skin:	n/a
14	chr3:82764684-82764734	NB4	blood:	n/a
15	chr3:82178370-82178420	ECC-1	luminal epithelium:	n/a
16	chr3:82293457-82293507	HEK293	kidney:	embryo
17	chr3:82857285-82857335	SK-N-SH_RA	brain:	n/a
18	chr3:82547324-82547374	Jurkat	blood:	n/a
19	chr3:82547324-82547374	SK-N-MC	brain:	n/a
20	chr3:82764684-82764734	HepG2	liver:	n/a
21	chr3:82857285-82857335	HepG2	liver:	n/a
22	chr3:82314701-82314751	AG10803	skin:	n/a
23	chr3:82860625-82860675	HAEpiC	amniotic membrane:	n/a
24	chr3:82857215-82857265	HepG2	liver:	n/a
25	chr3:82854345-82854395	RPTEC	kidney:	n/a
26	chr3:82547556-82547606	GM12891	blood:	n/a
27	chr3:82857144-82857194	RPTEC	kidney:	n/a
28	chr3:82314701-82314751	HepG2	liver:	n/a
29	chr3:82860625-82860675	AG10803	skin:	n/a
30	chr3:82857215-82857265	HPAEpiC	pulmonary alveolar:	n/a
31	chr3:82633652-82633702	NB4	blood:	n/a
32	chr3:82857285-82857335	NH-A	brain:	n/a
33	chr3:82764684-82764734	NHBE	bronchial:	n/a
34	chr3:82293457-82293507	HepG2	liver:	n/a
35	chr3:82857144-82857194	ProgFib	skin:	n/a
36	chr3:82860625-82860675	MCF10A-Er-Src	breast:	n/a
37	chr3:82857215-82857265	ProgFib	skin:	n/a
38	chr3:82857215-82857265	AG10803	skin:	n/a
39	chr3:82314701-82314751	HCPEpiC	choroid plexus:	n/a
40	chr3:82860625-82860675	Hela-S3	cervix:	n/a
41	chr3:82855983-82856033	HCM	heart:	n/a
42	chr3:82547556-82547606	AG10803	skin:	n/a
43	chr3:82764684-82764734	GM12892	blood:	n/a
44	chr3:82178370-82178420	GM12878	blood:	n/a
45	chr3:82857285-82857335	Hela-S3	cervix:	n/a
46	chr3:82293457-82293507	HCPEpiC	choroid plexus:	n/a
47	chr3:82293457-82293507	AG09319	gingival:	n/a
48	chr3:82854345-82854395	K562	blood:	n/a
49	chr3:82855983-82856033	HCF	heart:	n/a
50	chr3:82857285-82857335	LNCaP	prostate:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:82182859..82185317-chr3:82190117..82192068,2	MCF-7	breast:
2	chr3:82182859..82185317-chr3:82190117..82192068,2	MCF-7	breast:
3	chr3:82636523..82638043-chr3:82639849..82642054,2	MCF-7	breast:
4	chr3:82338513..82340160-chr3:82342810..82345015,2	MCF-7	breast:
5	chr12:6500232..6500748-chr3:82698547..82699324,2	MCF-7	breast:
6	chr3:82597360..82600131-chr3:82600295..82602284,2	MCF-7	breast:
7	chr3:82454694..82457422-chr3:82457978..82460293,2	K562	blood:
8	chr3:82783149..82783905-chr5:6821092..6821880,2	MCF-7	breast:
9	chr14:34024754..34025254-chr3:82638711..82639233,2	MCF-7	breast:
10	chr3:82813887..82816029-chr3:82820671..82822909,2	K562	blood:
11	chr3:82831963..82834033-chr3:82835758..82837856,2	K562	blood:
12	chr3:82825031..82826876-chr3:82842800..82845056,2	K562	blood:
13	chr3:82454694..82457422-chr3:82457978..82460293,2	K562	blood:
14	chr3:82551622..82554530-chr3:82556949..82558842,2	K562	blood:
15	chr3:82134680..82135474-chr3:82182067..82182736,2	MCF-7	breast:
16	chr3:82376131..82377766-chr3:82390133..82393109,2	MCF-7	breast:
17	chr3:82813887..82816029-chr3:82820671..82822909,2	K562	blood:
18	chr3:82831963..82834033-chr3:82835758..82837856,2	K562	blood:
19	chr3:82831608..82833347-chr3:82961368..82963419,2	MCF-7	breast:
20	chr3:82851223..82851782-chr7:20236254..20237120,2	MCF-7	breast:
21	chr3:82597360..82600131-chr3:82600295..82602284,2	MCF-7	breast:
22	chr3:82044423..82045130-chr3:82182277..82182777,2	MCF-7	breast:
23	chr3:82636523..82638043-chr3:82639849..82642054,2	MCF-7	breast:
24	chr3:82831608..82833347-chr3:82961368..82963419,2	MCF-7	breast:
25	chr3:82825031..82826876-chr3:82842800..82845056,2	K562	blood:
26	chr3:81630866..81631772-chr3:82182178..82183039,2	MCF-7	breast:
27	chr3:82551622..82554530-chr3:82556949..82558842,2	K562	blood:
28	chr3:82376131..82377766-chr3:82390133..82393109,2	MCF-7	breast:
29	chr3:82170424..82171997-chr3:82175422..82177557,2	MCF-7	breast:
30	chr3:82338513..82340160-chr3:82342810..82345015,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CADM2-13	chr3:82317193-82317294	ucscGeneNc_uc003dqh_1
2	lnc-GBE1-8	chr3:82369268-82369430	NONHSAT090629
3	lnc-CADM2-13	chr3:82587513-82587656	ucscGeneNc_uc003dqh_1
4	lnc-CADM2-13	chr3:82586227-82586351	ucscGeneNc_uc003dqh_1
5	lnc-GBE1-8	chr3:82368323-82368935	NONHSAT090629
6	lnc-CADM2-13	chr3:82585323-82585393	ucscGeneNc_uc003dqh_1
7	lnc-CADM2-6	chr3:82234526-82234604	NONHSAT090628
8	lnc-CADM2-13	chr3:82334170-82334295	ucscGeneNc_uc003dqh_1
9	lnc-CADM2-6	chr3:82251480-82251605	ENSG00000239440
10	lnc-CADM2-6	chr3:82251480-82251605	ENSG00000239440
11	lnc-CADM2-6	chr3:82234503-82234604	ENSG00000239440
12	lnc-CADM2-6	chr3:82502633-82502703	ENSG00000239440
13	lnc-CADM2-6	chr3:82503537-82503661	ENSG00000239440
14	lnc-CADM2-13	chr3:82594757-82595516	ucscGeneNc_uc003dqh_1
15	lnc-CADM2-6	chr3:82504823-82504966	ENSG00000239440
16	lnc-CADM2-6	chr3:82234503-82234604	ENSG00000239440
17	lnc-CADM2-13	chr3:82547961-82548142	ucscGeneNc_uc003dqh_1
18	lnc-CADM2-6	chr3:82251480-82251605	NONHSAT090628
19	lnc-CADM2-6	chr3:82507102-82507298	ENSG00000239440
20	lnc-CADM2-6	chr3:82465271-82465452	ENSG00000239440
21	lnc-CADM2-6	chr3:82465271-82466416	NONHSAT090628
22	lnc-CADM2-13	chr3:82589792-82589988	ucscGeneNc_uc003dqh_1
23	lnc-CADM2-6	chr3:82512067-82512826	ENSG00000239440

No data

Variant related genes	Relation type
CYP51A1P1	TF binding region
RPL7AP23	TF binding region
CYP51A1P1	CpG island
RPL7AP23	CpG island
KREMEN2	miRNA target sites
MYCN	miRNA target sites
YWHAH	miRNA target sites
SPARC	miRNA target sites
TNFAIP3	miRNA target sites
ZFP91	miRNA target sites
RET	miRNA target sites
NAV3	miRNA target sites
ERO1LB	miRNA target sites

Extended variants
information (count: 8775 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:8775 , 50 per page) page: 1 2 3 4 5 6 7 ... 176

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559908335	chr3:82176688-82176689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528721147	chr3:82176696-82176697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542508851	chr3:82176702-82176703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537204488	chr3:82176747-82176748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562074138	chr3:82176770-82176771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373327712	chr3:82176821-82176822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146548321	chr3:82176844-82176845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141175882	chr3:82176849-82176850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143311070	chr3:82176870-82176871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs76981031	chr3:82176883-82176884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148324927	chr3:82176902-82176903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78887689	chr3:82176949-82176950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75831823	chr3:82176974-82176975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535336423	chr3:82176985-82176986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189405851	chr3:82176996-82176997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114801104	chr3:82176997-82176998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537805247	chr3:82177020-82177021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141538794	chr3:82177062-82177063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192916890	chr3:82177072-82177073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150452445	chr3:82177079-82177080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377158175	chr3:82177099-82177100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552916220	chr3:82177102-82177103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369864180	chr3:82177106-82177107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138451118	chr3:82177134-82177135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144096641	chr3:82177189-82177190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542095690	chr3:82177195-82177196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184962154	chr3:82177206-82177207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372835907	chr3:82177210-82177211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74447617	chr3:82177258-82177259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371936342	chr3:82177284-82177285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146842161	chr3:82177294-82177295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575554307	chr3:82177321-82177322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147314461	chr3:82177345-82177346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538931013	chr3:82177402-82177403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79705555	chr3:82177463-82177464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533210890	chr3:82177483-82177484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553195724	chr3:82177494-82177495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78002909	chr3:82177533-82177534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138689143	chr3:82177584-82177585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116083302	chr3:82177695-82177696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569143498	chr3:82177718-82177719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188900842	chr3:82177722-82177723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181641843	chr3:82177800-82177801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544360306	chr3:82177814-82177815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186159129	chr3:82177824-82177825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563653133	chr3:82177950-82177951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35601265	chr3:82178107-82178108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533583124	chr3:82178130-82178131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73133748	chr3:82178177-82178178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573670845	chr3:82178248-82178249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Oral squamous cell carcinoma	17134496	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
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	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
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Autism	20808228	CNVD
Urothelial carcinoma	21177765	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD

Chromatin state (count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:82176600-82177400	Enhancers	Colon Smooth Muscle	Colon
2	chr3:82177200-82177800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:82177400-82177800	Enhancers	Fetal Muscle Leg	muscle
4	chr3:82177400-82178600	Enhancers	Primary hematopoietic stem cells	blood
5	chr3:82177400-82179000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:82177400-82179400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr3:82177400-82181800	Weak transcription	Colon Smooth Muscle	Colon
8	chr3:82177600-82178400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr3:82177600-82179000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:82177600-82179600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr3:82177800-82178400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr3:82177800-82178600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:82177800-82178800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr3:82178000-82179800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr3:82178200-82178600	Enhancers	Primary B cells from cord blood	blood
16	chr3:82178200-82178800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr3:82178400-82179600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr3:82178600-82179200	Enhancers	Primary B cells from peripheral blood	blood
19	chr3:82178600-82179400	Flanking Active TSS	Primary B cells from cord blood	blood
20	chr3:82178600-82179400	Flanking Active TSS	Primary hematopoietic stem cells	blood
21	chr3:82178800-82179400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
22	chr3:82178800-82179600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr3:82179000-82179400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr3:82179400-82179600	Enhancers	Primary B cells from cord blood	blood
25	chr3:82179400-82179800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr3:82179600-82180200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr3:82179600-82180200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr3:82181400-82181600	Enhancers	Liver	Liver
29	chr3:82181400-82182400	Enhancers	HepG2	liver
30	chr3:82181600-82182000	Flanking Active TSS	Liver	Liver
31	chr3:82181600-82182200	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr3:82181800-82182200	Enhancers	Colon Smooth Muscle	Colon
33	chr3:82182000-82182400	Enhancers	Liver	Liver
34	chr3:82187400-82188200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:82188200-82188800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr3:82188200-82189000	ZNF genes & repeats	Aorta	Aorta
37	chr3:82188400-82188600	Enhancers	Gastric	stomach
38	chr3:82189000-82189400	Weak transcription	Aorta	Aorta
39	chr3:82190600-82191400	Enhancers	Fetal Brain Male	brain
40	chr3:82191400-82192000	Weak transcription	Fetal Brain Male	brain
41	chr3:82192000-82192200	Enhancers	Fetal Brain Male	brain
42	chr3:82192200-82193400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr3:82192400-82193400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr3:82192600-82193600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:82193400-82194600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr3:82194800-82195000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr3:82200600-82202000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr3:82203400-82204200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr3:82203400-82204800	Enhancers	HepG2	liver
50	chr3:82204200-82205000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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