Variant report

Variant	nsv590232
Chromosome Location	chr3:47681881-47765547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:581)
CpG islands
(count:122)
Chromatin interactive
region (count:61)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:47706105-47706132	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:47764408-47764657	K562	blood:	n/a	n/a
3	ATF1	chr3:47764380-47764693	K562	blood:	n/a	n/a
4	BACH1	chr3:47706313-47706402	K562	blood:	n/a	n/a
5	BHLHE40	chr3:47764462-47764591	K562	blood:	n/a	n/a
6	BRCA1	chr3:47687856-47688084	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr3:47699869-47700311	K562	blood:	n/a	n/a
8	CCNT2	chr3:47753123-47753154	K562	blood:	n/a	n/a
9	CCNT2	chr3:47764367-47764687	K562	blood:	n/a	n/a
10	CEBPB	chr3:47687899-47688238	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:47738290-47738521	A549	lung:	n/a	chr3:47738406-47738417
12	CEBPB	chr3:47760411-47760504	K562	blood:	n/a	n/a
13	CEBPB	chr3:47738253-47738528	IMR90	lung:	n/a	chr3:47738406-47738417
14	CEBPB	chr3:47696005-47696318	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:47710493-47710880	MCF-7	breast:	n/a	chr3:47710691-47710702
16	CEBPB	chr3:47738303-47738554	K562	blood:	n/a	chr3:47738406-47738417
17	CEBPB	chr3:47738312-47738512	Hela-S3	cervix:	n/a	chr3:47738406-47738417
18	CEBPB	chr3:47710549-47710868	A549	lung:	n/a	chr3:47710691-47710702
19	CEBPB	chr3:47695987-47696271	A549	lung:	n/a	n/a
20	CEBPB	chr3:47710511-47710889	IMR90	lung:	n/a	chr3:47710691-47710702
21	CEBPB	chr3:47710557-47710816	A549	lung:	n/a	chr3:47710691-47710702
22	CEBPB	chr3:47710557-47710874	K562	blood:	n/a	chr3:47710691-47710702
23	CEBPB	chr3:47710580-47710805	MCF-7	breast:	n/a	chr3:47710691-47710702
24	CEBPB	chr3:47710537-47710888	Hela-S3	cervix:	n/a	chr3:47710691-47710702
25	CEBPB	chr3:47696041-47696321	K562	blood:	n/a	n/a
26	CEBPB	chr3:47710553-47710851	K562	blood:	n/a	chr3:47710691-47710702
27	CEBPB	chr3:47738246-47738556	HepG2	liver:	n/a	chr3:47738406-47738417
28	CEBPB	chr3:47695984-47696333	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:47759744-47760024	K562	blood:	n/a	n/a
30	CEBPB	chr3:47710469-47710928	A549	lung:	n/a	chr3:47710691-47710702
31	CEBPB	chr3:47710549-47710847	HepG2	liver:	n/a	chr3:47710691-47710702
32	CTCF	chr3:47706120-47706270	AG09319	gingival:	n/a	n/a
33	CTCF	chr3:47706120-47706270	NHLF	lung:	n/a	n/a
34	CTCF	chr3:47702720-47702870	SAEC	small airway:	n/a	n/a
35	CTCF	chr3:47706135-47706304	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:47702720-47702870	HAc	cerebellar:	n/a	n/a
37	CTCF	chr3:47706200-47706350	WI-38	lung:	n/a	n/a
38	CTCF	chr3:47706140-47706290	AG10803	skin:	n/a	n/a
39	CTCF	chr3:47706120-47706270	BE2_C	brain:	n/a	n/a
40	CTCF	chr3:47706140-47706290	GM12874	blood:	n/a	n/a
41	CTCF	chr3:47706124-47706304	ProgFib	skin:	n/a	n/a
42	CTCF	chr3:47749803-47749872	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr3:47706120-47706270	HVMF	connective:	n/a	n/a
44	CTCF	chr3:47706041-47706389	K562	blood:	n/a	n/a
45	CTCF	chr3:47706020-47706170	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr3:47706110-47706310	K562	blood:	n/a	n/a
47	CTCF	chr3:47706071-47706343	GM12878	blood:	n/a	n/a
48	CTCF	chr3:47706080-47706230	GM12870	blood:	n/a	n/a
49	CTCF	chr3:47706111-47706300	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr3:47706120-47706270	AG04449	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:47711947-47711997	CMK	blood:	n/a
2	chr3:47687980-47688030	SAEC	small airway:	n/a
3	chr3:47711947-47711997	ovcar-3	ovarian:	n/a
4	chr3:47711947-47711997	HL-60	blood:	n/a
5	chr3:47687980-47688030	HUVEC	blood vessel:	n/a
6	chr3:47711947-47711997	GM12892	blood:	n/a
7	chr3:47687980-47688030	BJ	skin:	n/a
8	chr3:47711947-47711997	LNCaP	prostate:	n/a
9	chr3:47711947-47711997	HNPCEpiC	eye:	n/a
10	chr3:47687980-47688030	AG10803	skin:	n/a
11	chr3:47711947-47711997	K562	blood:	n/a
12	chr3:47687980-47688030	AG04450	lung:	fetal
13	chr3:47711947-47711997	ProgFib	skin:	n/a
14	chr3:47711947-47711997	RPTEC	kidney:	n/a
15	chr3:47687980-47688030	GM12891	blood:	n/a
16	chr3:47711947-47711997	U87	brain:	n/a
17	chr3:47711947-47711997	NHBE	bronchial:	n/a
18	chr3:47687980-47688030	HNPCEpiC	eye:	n/a
19	chr3:47711947-47711997	HRE	kidney:	n/a
20	chr3:47687980-47688030	GM19239	blood:	n/a
21	chr3:47711947-47711997	BJ	skin:	n/a
22	chr3:47711947-47711997	PrEC	prostate:	n/a
23	chr3:47687980-47688030	SKMC	muscle:	n/a
24	chr3:47687980-47688030	NHDF-neo	bronchial:	n/a
25	chr3:47711947-47711997	BE2_C	brain:	n/a
26	chr3:47687980-47688030	HCF	heart:	n/a
27	chr3:47687980-47688030	AoSMC	blood vessel:	n/a
28	chr3:47711947-47711997	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:47687980-47688030	HRPEpiC	eye:	n/a
30	chr3:47711947-47711997	HIPEpiC	eye:	n/a
31	chr3:47711947-47711997	HepG2	liver:	n/a
32	chr3:47711947-47711997	A549	lung:	n/a
33	chr3:47711947-47711997	HCF	heart:	n/a
34	chr3:47687980-47688030	GM12878	blood:	n/a
35	chr3:47687980-47688030	SK-N-MC	brain:	n/a
36	chr3:47687980-47688030	K562	blood:	n/a
37	chr3:47711947-47711997	HEEpiC	esophagus:	n/a
38	chr3:47687980-47688030	HCT-116	colon:	n/a
39	chr3:47711947-47711997	SK-N-SH	brain:	n/a
40	chr3:47687980-47688030	GM06990	blood:	n/a
41	chr3:47687980-47688030	ovcar-3	ovarian:	n/a
42	chr3:47711947-47711997	AG09309	skin:	n/a
43	chr3:47687980-47688030	ProgFib	skin:	n/a
44	chr3:47687980-47688030	HRCEpiC	kidney:	n/a
45	chr3:47687980-47688030	RPTEC	kidney:	n/a
46	chr3:47711947-47711997	HUVEC	blood vessel:	n/a
47	chr3:47687980-47688030	ECC-1	luminal epithelium:	n/a
48	chr3:47687980-47688030	NT2-D1	testis:	n/a
49	chr3:47711947-47711997	HEK293	kidney:	embryo
50	chr3:47711947-47711997	SK-N-MC	brain:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:47685721..47688792-chr3:47690541..47693401,3	K562	blood:
2	chr3:47705776..47708275-chr3:47720140..47722109,2	K562	blood:
3	chr3:47711241..47713073-chr3:47730336..47732605,2	K562	blood:
4	chr3:47762182..47765006-chr3:47770740..47772875,2	K562	blood:
5	chr3:47689489..47692026-chr3:47696833..47699675,2	K562	blood:
6	chr3:47689489..47692026-chr3:47696833..47699675,2	K562	blood:
7	chr3:47563405..47564597-chr3:47705742..47706701,3	K562	blood:
8	chr3:47734956..47737818-chr3:47752172..47754463,2	K562	blood:
9	chr3:47711154..47712847-chr3:47715505..47718289,2	K562	blood:
10	chr3:47695059..47697428-chr3:47699586..47701750,2	K562	blood:
11	chr3:47745986..47747604-chr3:47764734..47766437,2	MCF-7	breast:
12	chr3:47711154..47712847-chr3:47715505..47718289,2	K562	blood:
13	chr3:47720048..47725540-chr3:47728543..47732832,5	K562	blood:
14	chr3:47705662..47709431-chr3:47715334..47718501,4	K562	blood:
15	chr3:47563373..47563976-chr3:47705831..47706517,2	MCF-7	breast:
16	chr3:47720378..47723144-chr3:47726248..47728156,2	K562	blood:
17	chr3:47763076..47765102-chr3:47809881..47812587,2	K562	blood:
18	chr3:47747587..47750464-chr3:47750786..47752967,2	K562	blood:
19	chr3:47705662..47709431-chr3:47715334..47718501,4	K562	blood:
20	chr3:47695059..47697428-chr3:47699586..47701750,2	K562	blood:
21	chr3:47720048..47725540-chr3:47728543..47732832,5	K562	blood:
22	chr3:47738843..47740707-chr3:47820955..47824303,3	MCF-7	breast:
23	chr3:47605459..47608045-chr3:47691965..47694957,2	K562	blood:
24	chr3:47711241..47713073-chr3:47730336..47732605,2	K562	blood:
25	chr3:47634689..47636670-chr3:47707308..47709101,2	K562	blood:
26	chr3:47736501..47738373-chr3:47738805..47740740,2	K562	blood:
27	chr3:47713394..47715579-chr3:47725306..47727830,2	K562	blood:
28	chr3:47673593..47675835-chr3:47690323..47692402,2	K562	blood:
29	chr3:47736501..47738373-chr3:47738805..47740740,2	K562	blood:
30	chr3:47652393..47654345-chr3:47713182..47715815,2	K562	blood:
31	chr3:47765075..47767679-chr3:47818543..47820695,2	K562	blood:
32	chr3:47679931..47682770-chr3:47684521..47687009,2	K562	blood:
33	chr3:47673450..47676559-chr3:47679760..47683066,3	K562	blood:
34	chr3:47738086..47739801-chr3:47743562..47745766,3	K562	blood:
35	chr3:47745986..47747604-chr3:47764734..47766437,2	MCF-7	breast:
36	chr3:47693687..47696451-chr3:47703806..47705728,2	K562	blood:
37	chr3:47710605..47713015-chr3:47822972..47825720,2	MCF-7	breast:
38	chr3:47679307..47680868-chr3:47680979..47682600,2	K562	blood:
39	chr3:47685721..47688792-chr3:47690541..47693401,3	K562	blood:
40	chr3:47719420..47721462-chr3:47753783..47755825,2	K562	blood:
41	chr3:47715804..47717955-chr3:47720020..47722528,2	K562	blood:
42	chr3:47765531..47768373-chr3:47769962..47773520,5	K562	blood:
43	chr3:47738086..47739801-chr3:47743562..47745766,3	K562	blood:
44	chr3:47715804..47717955-chr3:47720020..47722528,2	K562	blood:
45	chr3:47680224..47682770-chr3:47683873..47686021,2	K562	blood:
46	chr3:47720378..47723144-chr3:47726248..47728156,2	K562	blood:
47	chr3:47689575..47691724-chr3:47691978..47693843,2	K562	blood:
48	chr3:47689575..47691724-chr3:47691978..47693843,2	K562	blood:
49	chr3:47734956..47737818-chr3:47752172..47754463,2	K562	blood:
50	chr3:47747587..47750464-chr3:47750786..47752967,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000235695	TF binding region
SMARCC1	TF binding region
ENSG00000235695	CpG island
SMARCC1	CpG island
ENSG00000173473	chromatin interactions
ENSG00000235695	chromatin interactions
ENSG00000163832	chromatin interactions
ENSG00000266457	chromatin interactions

Extended variants
information (count: 2685 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2685 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4858843	chr3:47681881-47681882	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541498494	chr3:47681945-47681946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555059938	chr3:47682059-47682060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190953419	chr3:47682134-47682135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7613934	chr3:47682171-47682172	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs138887570	chr3:47682203-47682204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564777444	chr3:47682267-47682268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540747899	chr3:47682271-47682272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528816909	chr3:47682331-47682332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540937190	chr3:47682351-47682352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183893028	chr3:47682388-47682389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188383843	chr3:47682401-47682402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551054406	chr3:47682415-47682416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563012608	chr3:47682453-47682454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192066347	chr3:47682474-47682475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141430198	chr3:47682476-47682477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369337138	chr3:47682485-47682486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570711957	chr3:47682514-47682515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534582274	chr3:47682530-47682531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546513102	chr3:47682552-47682553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372467586	chr3:47682575-47682576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567870098	chr3:47682579-47682580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535304584	chr3:47682602-47682603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556633236	chr3:47682614-47682615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183381146	chr3:47682672-47682673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539402107	chr3:47682703-47682704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188390582	chr3:47682752-47682753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115637138	chr3:47682771-47682772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146996156	chr3:47682772-47682773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562376113	chr3:47682841-47682842	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138092322	chr3:47682889-47682890	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544868799	chr3:47682893-47682894	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs578228485	chr3:47682895-47682896	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562949266	chr3:47682970-47682971	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533300048	chr3:47683058-47683059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551870848	chr3:47683158-47683159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114154316	chr3:47683179-47683180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115191576	chr3:47683199-47683200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374788767	chr3:47683224-47683225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546478192	chr3:47683256-47683257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568059140	chr3:47683324-47683325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141488189	chr3:47683326-47683327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550393009	chr3:47683340-47683341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569048083	chr3:47683342-47683343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150842788	chr3:47683373-47683374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539131189	chr3:47683379-47683380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1403577	chr3:47683382-47683383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574555344	chr3:47683407-47683408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557837642	chr3:47683490-47683491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114417598	chr3:47683501-47683502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:2408 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47626200-47698600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr3:47626600-47688600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr3:47626600-47699800	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr3:47635000-47686800	Strong transcription	Dnd41	blood
5	chr3:47643600-47684800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr3:47654400-47707600	Weak transcription	Stomach Mucosa	stomach
7	chr3:47655600-47684600	Strong transcription	Liver	Liver
8	chr3:47655800-47686800	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr3:47655800-47698800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:47655800-47765600	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr3:47656200-47699800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr3:47656400-47693800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr3:47656400-47698200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:47656600-47790800	Strong transcription	Fetal Thymus	thymus
15	chr3:47657000-47690600	Weak transcription	Fetal Heart	heart
16	chr3:47657000-47700000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr3:47658000-47699800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:47661400-47711400	Weak transcription	Colonic Mucosa	Colon
19	chr3:47661600-47682600	Weak transcription	Aorta	Aorta
20	chr3:47661600-47688000	Weak transcription	Rectal Smooth Muscle	rectum
21	chr3:47664400-47689400	Weak transcription	Psoas Muscle	Psoas
22	chr3:47667400-47689800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr3:47668200-47685000	Strong transcription	Placenta	Placenta
24	chr3:47672000-47718600	Weak transcription	Right Ventricle	heart
25	chr3:47672400-47683200	Weak transcription	Spleen	Spleen
26	chr3:47672800-47684200	Weak transcription	Pancreas	Pancrea
27	chr3:47673200-47682600	Weak transcription	Esophagus	oesophagus
28	chr3:47673200-47700200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr3:47673600-47719200	Weak transcription	Small Intestine	intestine
30	chr3:47674000-47682600	Weak transcription	NHLF	lung
31	chr3:47674200-47684000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr3:47674200-47705000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr3:47674400-47682800	Weak transcription	Gastric	stomach
34	chr3:47674600-47685000	Strong transcription	Fetal Lung	lung
35	chr3:47674800-47688400	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr3:47675000-47682800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:47675000-47703800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr3:47676400-47684000	Weak transcription	Fetal Kidney	kidney
39	chr3:47676800-47694800	Weak transcription	Fetal Brain Male	brain
40	chr3:47677000-47682800	Weak transcription	NHEK	skin
41	chr3:47677200-47682600	Weak transcription	HSMMtube	muscle
42	chr3:47677200-47683400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr3:47677200-47707400	Weak transcription	HMEC	breast
44	chr3:47677200-47715400	Weak transcription	Brain Hippocampus Middle	brain
45	chr3:47677200-47720000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr3:47677400-47686600	Weak transcription	Brain Anterior Caudate	brain
47	chr3:47677400-47687800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr3:47677400-47711600	Weak transcription	Brain Substantia Nigra	brain
49	chr3:47677600-47684600	Weak transcription	Brain Germinal Matrix	brain
50	chr3:47677600-47690200	Weak transcription	A549	lung

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