Variant report

Variant	nsv1000357
Chromosome Location	chr3:98284283-98381473
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2258)
CpG islands
(count:1588)
Chromatin interactive
region (count:45)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:2258 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:98312425-98312859	K562	blood:	n/a	n/a
2	ARID3A	chr3:98315776-98316088	K562	blood:	n/a	n/a
3	ARID3A	chr3:98303816-98304523	K562	blood:	n/a	n/a
4	ARID3A	chr3:98315770-98316096	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:98293783-98294317	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:98302584-98303309	K562	blood:	n/a	n/a
7	ARID3A	chr3:98312443-98312835	HepG2	liver:	n/a	n/a
8	ATF1	chr3:98302561-98303000	K562	blood:	n/a	n/a
9	ATF1	chr3:98312428-98312843	K562	blood:	n/a	n/a
10	ATF2	chr3:98282120-98285186	GM12878	blood:	n/a	n/a
11	ATF2	chr3:98331491-98332456	GM12878	blood:	n/a	n/a
12	ATF2	chr3:98286226-98286856	GM12878	blood:	n/a	n/a
13	ATF2	chr3:98312342-98312911	GM12878	blood:	n/a	n/a
14	ATF2	chr3:98292032-98292547	GM12878	blood:	n/a	n/a
15	ATF2	chr3:98312225-98312860	GM12878	blood:	n/a	n/a
16	ATF2	chr3:98331729-98332499	GM12878	blood:	n/a	n/a
17	ATF2	chr3:98286327-98287069	GM12878	blood:	n/a	n/a
18	ATF2	chr3:98291848-98292665	GM12878	blood:	n/a	n/a
19	ATF2	chr3:98282143-98285138	GM12878	blood:	n/a	n/a
20	ATF3	chr3:98304182-98304503	K562	blood:	n/a	n/a
21	ATF3	chr3:98304192-98304405	K562	blood:	n/a	n/a
22	BACH1	chr3:98304373-98304490	K562	blood:	n/a	n/a
23	BACH1	chr3:98312399-98312894	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr3:98283984-98284324	GM12878	blood:	n/a	chr3:98284153-98284164 chr3:98284220-98284229
25	BATF	chr3:98284035-98284316	GM12878	blood:	n/a	chr3:98284153-98284164 chr3:98284220-98284229
26	BATF	chr3:98286504-98286803	GM12878	blood:	n/a	n/a
27	BATF	chr3:98284674-98284962	GM12878	blood:	n/a	n/a
28	BATF	chr3:98331781-98332375	GM12878	blood:	n/a	n/a
29	BATF	chr3:98286493-98286818	GM12878	blood:	n/a	n/a
30	BATF	chr3:98293055-98293341	GM12878	blood:	n/a	n/a
31	BATF	chr3:98361493-98361992	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:98286514-98286775	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:98286428-98286973	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:98331904-98332354	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:98331844-98332296	GM12878	blood:	n/a	n/a
36	BCL3	chr3:98282343-98285155	GM12878	blood:	n/a	chr3:98284058-98284067 chr3:98282606-98282615
37	BCL3	chr3:98331814-98332275	GM12878	blood:	n/a	n/a
38	BCL3	chr3:98331295-98332684	GM12878	blood:	n/a	n/a
39	BCL3	chr3:98363038-98363376	GM12878	blood:	n/a	n/a
40	BCL3	chr3:98286499-98286903	GM12878	blood:	n/a	n/a
41	BCLAF1	chr3:98320926-98321331	GM12878	blood:	n/a	n/a
42	BCLAF1	chr3:98291833-98292582	GM12878	blood:	n/a	chr3:98292275-98292284
43	BCLAF1	chr3:98331388-98332429	GM12878	blood:	n/a	n/a
44	BCLAF1	chr3:98331475-98332451	GM12878	blood:	n/a	n/a
45	BCLAF1	chr3:98286357-98287114	GM12878	blood:	n/a	n/a
46	BCLAF1	chr3:98376201-98376680	GM12878	blood:	n/a	chr3:98376421-98376434 chr3:98376499-98376512 chr3:98376513-98376526 chr3:98376506-98376519 chr3:98376426-98376435
47	BCLAF1	chr3:98312163-98312906	GM12878	blood:	n/a	chr3:98312521-98312529
48	BCLAF1	chr3:98312104-98313017	GM12878	blood:	n/a	chr3:98312521-98312529
49	BCLAF1	chr3:98282044-98284461	GM12878	blood:	n/a	chr3:98284058-98284067 chr3:98282606-98282615
50	BHLHE40	chr3:98312301-98312931	GM12878	blood:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:98376938-98376988	MCF10A-Er-Src	breast:	n/a
2	chr3:98376574-98376624	A549	lung:	n/a
3	chr3:98376938-98376988	MCF10A-Er-Src	breast:	n/a
4	chr3:98376574-98376624	A549	lung:	n/a
5	chr3:98312473-98312523	AG09319	gingival:	n/a
6	chr3:98299487-98299537	NH-A	brain:	n/a
7	chr3:98312473-98312523	Jurkat	blood:	n/a
8	chr3:98376478-98376528	HPAEpiC	pulmonary alveolar:	n/a
9	chr3:98312354-98312404	HRE	kidney:	n/a
10	chr3:98376029-98376079	NB4	blood:	n/a
11	chr3:98312547-98312597	ProgFib	skin:	n/a
12	chr3:98312354-98312404	LNCaP	prostate:	n/a
13	chr3:98312354-98312404	GM12891	blood:	n/a
14	chr3:98376029-98376079	AoSMC	blood vessel:	n/a
15	chr3:98312515-98312565	LNCaP	prostate:	n/a
16	chr3:98308022-98308072	HCM	heart:	n/a
17	chr3:98312534-98312584	NHDF-neo	bronchial:	n/a
18	chr3:98299487-98299537	GM12878	blood:	n/a
19	chr3:98312680-98312730	ProgFib	skin:	n/a
20	chr3:98311063-98311113	HCPEpiC	choroid plexus:	n/a
21	chr3:98313398-98313448	NT2-D1	testis:	n/a
22	chr3:98376938-98376988	NH-A	brain:	n/a
23	chr3:98379208-98379258	HCPEpiC	choroid plexus:	n/a
24	chr3:98312651-98312701	NB4	blood:	n/a
25	chr3:98342807-98342857	HepG2	liver:	n/a
26	chr3:98299487-98299537	BE2_C	brain:	n/a
27	chr3:98313516-98313566	Jurkat	blood:	n/a
28	chr3:98312534-98312584	NB4	blood:	n/a
29	chr3:98312544-98312594	K562	blood:	n/a
30	chr3:98376478-98376528	PFSK-1	brain:	n/a
31	chr3:98312473-98312523	GM12878	blood:	n/a
32	chr3:98312651-98312701	U87	brain:	n/a
33	chr3:98311063-98311113	ProgFib	skin:	n/a
34	chr3:98311910-98311960	HCT-116	colon:	n/a
35	chr3:98376390-98376440	Hepatocyte	liver:	n/a
36	chr3:98379208-98379258	PFSK-1	brain:	n/a
37	chr3:98299487-98299537	HCT-116	colon:	n/a
38	chr3:98312547-98312597	HIPEpiC	eye:	n/a
39	chr3:98342807-98342857	BJ	skin:	n/a
40	chr3:98312547-98312597	NH-A	brain:	n/a
41	chr3:98308022-98308072	GM12892	blood:	n/a
42	chr3:98313398-98313448	ECC-1	luminal epithelium:	n/a
43	chr3:98312680-98312730	GM19239	blood:	n/a
44	chr3:98312473-98312523	HCT-116	colon:	n/a
45	chr3:98312547-98312597	HUVEC	blood vessel:	n/a
46	chr3:98312534-98312584	PFSK-1	brain:	n/a
47	chr3:98308022-98308072	AG09309	skin:	n/a
48	chr3:98312971-98313021	NT2-D1	testis:	n/a
49	chr3:98376390-98376440	GM12891	blood:	n/a
50	chr3:98313398-98313448	GM12892	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:98236014..98237762-chr3:98314366..98316058,2	K562	blood:
2	chr3:98289153..98292045-chr3:98293949..98295528,2	K562	blood:
3	chr3:98316857..98318853-chr3:98318886..98321058,2	K562	blood:
4	chr3:98307277..98308985-chr3:98312690..98314425,2	K562	blood:
5	chr3:98282871..98285029-chr3:98286675..98289199,2	K562	blood:
6	chr3:98241309..98243234-chr3:98301701..98304609,2	K562	blood:
7	chr20:46129382..46132079-chr3:98291150..98293500,2	MCF-7	breast:
8	chr3:98303079..98306972-chr3:98311108..98314146,5	K562	blood:
9	chr3:98303079..98306972-chr3:98311108..98314146,5	K562	blood:
10	chr3:98293731..98295757-chr3:98296962..98298884,2	MCF-7	breast:
11	chr16:68344315..68345025-chr3:98311977..98312615,2	HCT-116	colon:
12	chr3:98311227..98312951-chr3:98314970..98316859,2	K562	blood:
13	chr3:98287743..98290049-chr3:98291155..98295348,3	K562	blood:
14	chr3:98282871..98285029-chr3:98286675..98289199,2	K562	blood:
15	chr3:98293731..98295757-chr3:98296962..98298884,2	MCF-7	breast:
16	chr3:98307277..98308985-chr3:98312690..98314425,2	K562	blood:
17	chr3:98315462..98316376-chr3:98520278..98520831,2	MCF-7	breast:
18	chr3:97757965..97758653-chr3:98306720..98307286,2	MCF-7	breast:
19	chr3:98315529..98316439-chr3:98531389..98532230,2	MCF-7	breast:
20	chr3:98289153..98292045-chr3:98293949..98295528,2	K562	blood:
21	chr3:98257605..98258242-chr3:98291111..98291831,2	K562	blood:
22	chr3:98078662..98079479-chr3:98306722..98307655,3	MCF-7	breast:
23	chr3:98175989..98176774-chr3:98306461..98307236,2	MCF-7	breast:
24	chr3:98314191..98315885-chr3:98317245..98319751,3	K562	blood:
25	chr20:52332749..52333464-chr3:98352060..98352684,2	MCF-7	breast:
26	chr3:98300331..98302518-chr3:98312399..98314281,2	K562	blood:
27	chr3:98292600..98294311-chr3:98296464..98299165,2	K562	blood:
28	chr3:98311356..98313726-chr3:98530079..98532585,2	MCF-7	breast:
29	chr3:98306181..98309113-chr3:98310458..98312557,3	K562	blood:
30	chr3:98306990..98308896-chr3:98311622..98313547,2	MCF-7	breast:
31	chr3:98320433..98321618-chr3:98424245..98425562,4	MCF-7	breast:
32	chr3:97689639..97691921-chr3:98303800..98305616,2	K562	blood:
33	chr3:98292600..98294311-chr3:98296464..98299165,2	K562	blood:
34	chr3:98303079..98305719-chr3:98311231..98314146,3	K562	blood:
35	chr3:98302949..98305459-chr3:98308547..98310946,2	K562	blood:
36	chr3:98316857..98318853-chr3:98318886..98321058,2	K562	blood:
37	chr3:98240168..98242320-chr3:98310651..98312763,2	K562	blood:
38	chr3:98315543..98316397-chr3:98531264..98532318,3	MCF-7	breast:
39	chr3:98320682..98321287-chr3:98531748..98532391,2	MCF-7	breast:
40	chr3:98303079..98305719-chr3:98311231..98314146,3	K562	blood:
41	chr3:98310880..98314109-chr3:98314173..98316859,5	K562	blood:
42	chr3:98321530..98322415-chr3:98531181..98531955,2	MCF-7	breast:
43	chr3:98314191..98315885-chr3:98317245..98319751,3	K562	blood:
44	chr3:98287743..98290049-chr3:98291155..98295348,3	K562	blood:
45	chr3:98320901..98321587-chr3:98530671..98531252,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR15-2	chr3:98338909-98339462	NONHSAT090806
2	lnc-ST3GAL6-5	chr3:98376584-98377010	NONHSAT090808

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CPOX	hsa-miR-124-3p	chr3:98299425-98299443
2	CPOX	hsa-miR-361-5p	chr3:98298773-98298792
3	CPOX	hsa-miR-361-5p	chr3:98298779-98298773
4	CPOX	hsa-miR-30c-5p	chr3:98299277-98299299
5	CPOX	hsa-miR-30a-5p	chr3:98299277-98299298

Variant related genes	Relation type
ENSG00000266233	TF binding region
CPOX	TF binding region
WWP1P1	TF binding region
ENSG00000240827	TF binding region
ENSG00000266233	CpG island
CPOX	CpG island
WWP1P1	CpG island
ENSG00000240827	CpG island
ENSG00000124151	chromatin interactions
ENSG00000170854	chromatin interactions
ENSG00000057019	chromatin interactions
ENSG00000248839	chromatin interactions
ENSG00000080819	chromatin interactions
ENSG00000103061	chromatin interactions
ENSG00000080822	chromatin interactions
ENSG00000132600	chromatin interactions

Extended variants
information (count: 2983 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2983 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1461161	chr3:98284283-98284284	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554531569	chr3:98284294-98284295	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs61691130	chr3:98284306-98284307	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs1729976	chr3:98284330-98284331	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs144461730	chr3:98284350-98284351	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs147821481	chr3:98284351-98284352	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs1569234	chr3:98284443-98284444	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs141263091	chr3:98284444-98284445	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs531629292	chr3:98284458-98284459	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs548464972	chr3:98284481-98284482	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs561531352	chr3:98284496-98284497	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs146951124	chr3:98284511-98284512	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs144903664	chr3:98284541-98284542	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs538337937	chr3:98284614-98284615	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs538872565	chr3:98284644-98284645	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs570511447	chr3:98284665-98284666	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs368390362	chr3:98284674-98284675	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs538874612	chr3:98284675-98284676	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs55995650	chr3:98284706-98284707	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569248025	chr3:98284724-98284725	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs185425058	chr3:98284743-98284744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs114241690	chr3:98284755-98284756	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs574758822	chr3:98284779-98284780	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs549580450	chr3:98284780-98284781	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs554005205	chr3:98284846-98284847	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs149023496	chr3:98284857-98284858	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs546062538	chr3:98284863-98284864	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs562683418	chr3:98284872-98284873	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs576259724	chr3:98284922-98284923	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs377125375	chr3:98284935-98284936	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs369141611	chr3:98284991-98284992	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs527323123	chr3:98285012-98285013	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs569559827	chr3:98285019-98285020	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs143822438	chr3:98285032-98285033	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs1675505	chr3:98285043-98285044	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs549422267	chr3:98285093-98285094	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs569110207	chr3:98285149-98285150	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs538016981	chr3:98285182-98285183	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs548637277	chr3:98285192-98285193	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs148155188	chr3:98285205-98285206	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs75839074	chr3:98285214-98285215	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs554127314	chr3:98285215-98285216	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs577269603	chr3:98285218-98285219	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs558121172	chr3:98285242-98285243	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs539943224	chr3:98285312-98285313	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs376452878	chr3:98285373-98285374	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs113781807	chr3:98285376-98285377	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs76906538	chr3:98285393-98285394	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs541990762	chr3:98285446-98285447	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs189788395	chr3:98285461-98285462	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	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
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
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1644 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98273600-98292600	Weak transcription	K562	blood
2	chr3:98279600-98286000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr3:98280400-98285800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr3:98280400-98287000	Enhancers	Primary T cells fromperipheralblood	blood
5	chr3:98280600-98285000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr3:98280600-98286800	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr3:98280600-98287000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr3:98280600-98288000	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr3:98280800-98284400	Enhancers	HSMM	muscle
10	chr3:98280800-98285000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr3:98280800-98287200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr3:98280800-98288200	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr3:98280800-98288200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr3:98281200-98285800	Enhancers	Primary T cells from cord blood	blood
15	chr3:98281200-98286600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr3:98281200-98296200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr3:98281400-98295800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:98282000-98285800	Enhancers	Dnd41	blood
19	chr3:98282600-98288200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr3:98283000-98284600	Enhancers	Muscle Satellite Cultured Cells	--
21	chr3:98283000-98292200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr3:98283000-98295200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr3:98283200-98285200	Enhancers	Fetal Thymus	thymus
24	chr3:98283200-98285800	Flanking Active TSS	GM12878-XiMat	blood
25	chr3:98283400-98284400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr3:98283400-98284400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr3:98283400-98284400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr3:98283400-98288200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr3:98283600-98295800	Weak transcription	Primary B cells from cord blood	blood
30	chr3:98283800-98284800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr3:98283800-98286600	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr3:98283800-98298400	Weak transcription	Primary B cells from peripheral blood	blood
33	chr3:98284200-98284400	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr3:98284200-98284600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:98284200-98285000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr3:98284400-98284600	Enhancers	Thymus	Thymus
37	chr3:98284400-98285000	Enhancers	Primary hematopoietic stem cells	blood
38	chr3:98284400-98285000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr3:98284400-98285000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr3:98284400-98285200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:98284600-98292200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr3:98284600-98292200	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr3:98284600-98295800	Weak transcription	Thymus	Thymus
44	chr3:98284800-98285200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:98284800-98285800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
46	chr3:98285000-98286600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr3:98285000-98295800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr3:98285000-98296200	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr3:98285000-98296200	Weak transcription	Primary hematopoietic stem cells	blood
50	chr3:98285000-98296200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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