Variant report

Variant	nsv879522
Chromosome Location	chr4:87473776-87644842
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1544)
CpG islands
(count:1038)
Chromatin interactive
region (count:63)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1544 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:87490265-87491109	GM12878	blood:	n/a	n/a
2	ATF2	chr4:87478593-87479112	GM12878	blood:	n/a	n/a
3	ATF2	chr4:87490269-87491004	GM12878	blood:	n/a	n/a
4	ATF2	chr4:87478684-87479066	GM12878	blood:	n/a	n/a
5	ATF3	chr4:87515061-87515440	A549	lung:	n/a	n/a
6	BACH1	chr4:87492139-87492150	K562	blood:	n/a	n/a
7	BACH1	chr4:87515824-87515971	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:87515055-87515599	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr4:87490313-87491053	GM12878	blood:	n/a	n/a
10	BATF	chr4:87478747-87479056	GM12878	blood:	n/a	chr4:87478875-87478886
11	BATF	chr4:87591451-87591713	GM12878	blood:	n/a	n/a
12	BATF	chr4:87490638-87490972	GM12878	blood:	n/a	n/a
13	BATF	chr4:87478757-87479050	GM12878	blood:	n/a	chr4:87478875-87478886
14	BATF	chr4:87566080-87566330	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:87536626-87536961	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:87490685-87491028	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:87478680-87479028	GM12878	blood:	n/a	chr4:87478874-87478883 chr4:87478969-87478978
18	BCL11A	chr4:87515119-87515322	GM12878	blood:	n/a	n/a
19	BCL3	chr4:87515036-87515682	GM12878	blood:	n/a	chr4:87515423-87515432 chr4:87515662-87515671
20	BCL3	chr4:87536670-87537064	GM12878	blood:	n/a	n/a
21	BCL3	chr4:87490312-87491115	GM12878	blood:	n/a	n/a
22	BCL3	chr4:87533699-87533997	GM12878	blood:	n/a	n/a
23	BCL3	chr4:87579173-87579425	GM12878	blood:	n/a	n/a
24	BCL3	chr4:87586206-87586457	GM12878	blood:	n/a	n/a
25	BCLAF1	chr4:87515089-87515656	GM12878	blood:	n/a	chr4:87515423-87515432
26	BHLHE40	chr4:87632109-87632314	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:87543755-87543930	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:87490769-87490771	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:87473967-87474078	K562	blood:	n/a	n/a
30	BHLHE40	chr4:87515048-87516419	GM12878	blood:	n/a	n/a
31	BRCA1	chr4:87514953-87515327	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr4:87489620-87489819	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:87534935-87535263	A549	lung:	n/a	chr4:87535092-87535103 chr4:87535093-87535104 chr4:87535094-87535103
34	CEBPB	chr4:87517997-87518376	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:87534961-87535239	H1-hESC	embryonic stem cell:	n/a	chr4:87535092-87535103 chr4:87535093-87535104 chr4:87535094-87535103
36	CEBPB	chr4:87591749-87592324	HCT-116	colon:	n/a	n/a
37	CEBPB	chr4:87591893-87592253	A549	lung:	n/a	n/a
38	CEBPB	chr4:87518005-87518358	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:87638311-87638443	A549	lung:	n/a	n/a
40	CEBPB	chr4:87534933-87535249	K562	blood:	n/a	chr4:87535092-87535103 chr4:87535093-87535104 chr4:87535094-87535103
41	CEBPB	chr4:87606586-87606895	HepG2	liver:	n/a	chr4:87606715-87606726
42	CEBPB	chr4:87598026-87598139	K562	blood:	n/a	chr4:87598087-87598098
43	CEBPB	chr4:87597918-87598257	HepG2	liver:	n/a	chr4:87598087-87598098
44	CEBPB	chr4:87606469-87606952	A549	lung:	n/a	chr4:87606715-87606726
45	CEBPB	chr4:87561774-87562073	HepG2	liver:	n/a	chr4:87561879-87561892 chr4:87561940-87561951 chr4:87561938-87561949 chr4:87561938-87561951
46	CEBPB	chr4:87534817-87535261	MCF-7	breast:	n/a	chr4:87535092-87535103 chr4:87535093-87535104 chr4:87535094-87535103
47	CEBPB	chr4:87606561-87606885	IMR90	lung:	n/a	chr4:87606715-87606726
48	CEBPB	chr4:87515997-87517076	Hela-S3	cervix:	n/a	chr4:87516467-87516484
49	CEBPB	chr4:87591918-87592286	HCT-116	colon:	n/a	n/a
50	CEBPB	chr4:87534912-87535284	IMR90	lung:	n/a	chr4:87535092-87535103 chr4:87535093-87535104 chr4:87535094-87535103

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:87514906-87514956	ECC-1	luminal epithelium:	n/a
2	chr4:87514906-87514956	ECC-1	luminal epithelium:	n/a
3	chr4:87515380-87515430	HEEpiC	esophagus:	n/a
4	chr4:87515700-87515750	ECC-1	luminal epithelium:	n/a
5	chr4:87514906-87514956	NB4	blood:	n/a
6	chr4:87515433-87515483	K562	blood:	n/a
7	chr4:87516011-87516061	NT2-D1	testis:	n/a
8	chr4:87515299-87515349	HCPEpiC	choroid plexus:	n/a
9	chr4:87516007-87516057	HEK293	kidney:	embryo
10	chr4:87515299-87515349	NB4	blood:	n/a
11	chr4:87515199-87515249	T-47D	breast:	n/a
12	chr4:87515395-87515445	IMR90	lung:	fetal
13	chr4:87515380-87515430	HMEC	breast:	n/a
14	chr4:87515480-87515530	BE2_C	brain:	n/a
15	chr4:87515419-87515469	U87	brain:	n/a
16	chr4:87515184-87515234	GM12878	blood:	n/a
17	chr4:87515419-87515469	NH-A	brain:	n/a
18	chr4:87516011-87516061	NHBE	bronchial:	n/a
19	chr4:87515674-87515724	IMR90	lung:	fetal
20	chr4:87515380-87515430	HNPCEpiC	eye:	n/a
21	chr4:87515480-87515530	Caco-2	colon:	n/a
22	chr4:87515480-87515530	AG09319	gingival:	n/a
23	chr4:87515395-87515445	GM12892	blood:	n/a
24	chr4:87515279-87515329	Caco-2	colon:	n/a
25	chr4:87515279-87515329	NB4	blood:	n/a
26	chr4:87515419-87515469	AG09319	gingival:	n/a
27	chr4:87515433-87515483	SAEC	small airway:	n/a
28	chr4:87516007-87516057	MCF10A-Er-Src	breast:	n/a
29	chr4:87515700-87515750	HNPCEpiC	eye:	n/a
30	chr4:87511439-87511489	SK-N-MC	brain:	n/a
31	chr4:87517859-87517909	HRPEpiC	eye:	n/a
32	chr4:87514906-87514956	SAEC	small airway:	n/a
33	chr4:87515199-87515249	GM06990	blood:	n/a
34	chr4:87515395-87515445	GM12891	blood:	n/a
35	chr4:87515184-87515234	AoSMC	blood vessel:	n/a
36	chr4:87514906-87514956	PrEC	prostate:	n/a
37	chr4:87515395-87515445	CMK	blood:	n/a
38	chr4:87515279-87515329	NHDF-neo	bronchial:	n/a
39	chr4:87515467-87515517	NT2-D1	testis:	n/a
40	chr4:87514906-87514956	HCM	heart:	n/a
41	chr4:87514906-87514956	U87	brain:	n/a
42	chr4:87515467-87515517	NB4	blood:	n/a
43	chr4:87511439-87511489	PANC-1	pancreas:	n/a
44	chr4:87515700-87515750	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:87514906-87514956	GM12891	blood:	n/a
46	chr4:87516007-87516057	ovcar-3	ovarian:	n/a
47	chr4:87515467-87515517	AoSMC	blood vessel:	n/a
48	chr4:87515674-87515724	PFSK-1	brain:	n/a
49	chr4:87515380-87515430	BJ	skin:	n/a
50	chr4:87511439-87511489	HCPEpiC	choroid plexus:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:87495934..87497626-chr4:87503744..87506364,2	K562	blood:
2	chr4:87507143..87508934-chr4:87512831..87514813,2	MCF-7	breast:
3	chr4:87514091..87516787-chr4:87546977..87549306,2	MCF-7	breast:
4	chr4:87592727..87594779-chr4:87641743..87643865,2	MCF-7	breast:
5	chr4:87493805..87495855-chr4:87500562..87503508,2	MCF-7	breast:
6	chr4:87591850..87593506-chr4:87595973..87598861,2	MCF-7	breast:
7	chr4:87519701..87522542-chr4:87523831..87525544,2	MCF-7	breast:
8	chr4:87512086..87513946-chr4:87514218..87517249,3	MCF-7	breast:
9	chr4:87513620..87519829-chr4:87520022..87526083,14	MCF-7	breast:
10	chr4:87514131..87516860-chr4:87590483..87592754,2	MCF-7	breast:
11	chr4:87507716..87510350-chr4:87515376..87516928,2	MCF-7	breast:
12	chr4:87485932..87486733-chr4:87816558..87817197,3	MCF-7	breast:
13	chr4:87491871..87493629-chr4:87496523..87499181,2	K562	blood:
14	chr4:87507433..87508945-chr4:87512741..87515141,2	MCF-7	breast:
15	chr4:87442312..87445005-chr4:87478694..87481365,2	MCF-7	breast:
16	chr4:87513830..87516265-chr4:87582019..87584958,2	MCF-7	breast:
17	chr4:87514311..87516955-chr4:87516961..87519676,2	MCF-7	breast:
18	chr4:87598063..87600452-chr4:87602693..87604467,2	MCF-7	breast:
19	chr4:87515788..87518508-chr4:87520031..87521572,2	K562	blood:
20	chr4:87495934..87497626-chr4:87503744..87506364,2	K562	blood:
21	chr4:87522636..87524731-chr4:87524767..87527790,3	K562	blood:
22	chr4:87592727..87594779-chr4:87641743..87643865,2	MCF-7	breast:
23	chr4:87516507..87518409-chr4:87595594..87597208,2	MCF-7	breast:
24	chr4:87526249..87528781-chr4:87528891..87530850,2	MCF-7	breast:
25	chr4:87491871..87493629-chr4:87496523..87499181,2	K562	blood:
26	chr4:87514663..87516668-chr4:87519694..87521369,2	MCF-7	breast:
27	chr4:87626677..87627413-chr9:20510998..20511530,2	MCF-7	breast:
28	chr4:30768208..30768709-chr4:87513954..87514454,2	HCT-116	colon:
29	chr4:87595555..87598937-chr4:87600350..87602837,3	K562	blood:
30	chr4:87515391..87517685-chr4:87812251..87815383,4	MCF-7	breast:
31	chr4:87493805..87495855-chr4:87500562..87503508,2	MCF-7	breast:
32	chr4:87526249..87528781-chr4:87528891..87530850,2	MCF-7	breast:
33	chr17:56756591..56757518-chr4:87515320..87516003,2	Hela-S3	cervix:
34	chr4:87574443..87576554-chr4:87578304..87580063,2	MCF-7	breast:
35	chr4:87598063..87600452-chr4:87602693..87604467,2	MCF-7	breast:
36	chr4:87617245..87619402-chr4:87619927..87623760,3	K562	blood:
37	chr4:87481451..87483202-chr4:87532633..87534262,2	MCF-7	breast:
38	chr4:87483039..87485486-chr4:87514855..87517675,2	MCF-7	breast:
39	chr4:87600177..87602980-chr4:87604745..87606408,2	K562	blood:
40	chr4:87592344..87595158-chr4:87604628..87606755,2	K562	blood:
41	chr4:87481451..87483202-chr4:87532633..87534262,2	MCF-7	breast:
42	chr4:87507453..87509396-chr4:87819000..87821913,2	K562	blood:
43	chr4:87530294..87531963-chr4:87533296..87535743,2	K562	blood:
44	chr4:87534871..87536613-chr4:87547091..87549143,2	K562	blood:
45	chr4:87534871..87536613-chr4:87547091..87549143,2	K562	blood:
46	chr4:87595555..87598937-chr4:87600350..87602837,3	K562	blood:
47	chr4:87514897..87517003-chr4:87606417..87607965,2	MCF-7	breast:
48	chr4:87530490..87533389-chr4:87533491..87536660,3	MCF-7	breast:
49	chr4:87507143..87508934-chr4:87512831..87514813,2	MCF-7	breast:
50	chr4:87510138..87512928-chr4:87514603..87517692,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC10A6-4	chr4:87514886-87515272	NONHSAT097281

No data

Variant related genes	Relation type
PTPN13	TF binding region
MAPK10	TF binding region
PTPN13	CpG island
MAPK10	CpG island
ENSG00000200997	chromatin interactions
ENSG00000163629	chromatin interactions
ENSG00000243312	chromatin interactions
ENSG00000109339	chromatin interactions
ENSG00000163633	chromatin interactions

Extended variants
information (count: 5601 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5601 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4478147	chr4:87473776-87473777	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs114597769	chr4:87473804-87473805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192613718	chr4:87473912-87473913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547244641	chr4:87473926-87473927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568756219	chr4:87473930-87473931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536172187	chr4:87473940-87473941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556969430	chr4:87473946-87473947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376738491	chr4:87473958-87473959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568872379	chr4:87474077-87474078	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs539120776	chr4:87474098-87474099	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs184546314	chr4:87474116-87474117	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs111721938	chr4:87474149-87474150	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs112072272	chr4:87474155-87474156	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs571196267	chr4:87474174-87474175	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs188236298	chr4:87474194-87474195	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs35585991	chr4:87474226-87474227	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs72665748	chr4:87474239-87474240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs563305388	chr4:87474348-87474349	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs530926489	chr4:87474426-87474427	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs545927145	chr4:87474492-87474493	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182015757	chr4:87474623-87474624	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs528613718	chr4:87474637-87474638	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs547181380	chr4:87474650-87474651	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs562290151	chr4:87474723-87474724	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs77524663	chr4:87474729-87474730	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs551305915	chr4:87474760-87474761	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs184910994	chr4:87474762-87474763	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs539414318	chr4:87474836-87474837	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs551116392	chr4:87474858-87474859	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs566545454	chr4:87474941-87474942	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs533663350	chr4:87474951-87474952	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs555112582	chr4:87474986-87474987	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs146576549	chr4:87475043-87475044	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531930991	chr4:87475045-87475046	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs397745362	chr4:87475057-87475058	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573513115	chr4:87475133-87475134	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537692493	chr4:87475162-87475163	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113180302	chr4:87475188-87475189	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35331797	chr4:87475231-87475232	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145811958	chr4:87475252-87475253	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577889036	chr4:87475262-87475263	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148596294	chr4:87475363-87475364	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145673296	chr4:87475384-87475385	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573260593	chr4:87475398-87475399	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540734498	chr4:87475473-87475474	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs4693777	chr4:87475509-87475510	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs529501503	chr4:87475554-87475555	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs4235081	chr4:87475556-87475557	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs116042374	chr4:87475619-87475620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76981575	chr4:87475654-87475655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2355 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:87462600-87474000	Weak transcription	Ovary	ovary
2	chr4:87462600-87478000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:87465400-87473800	Weak transcription	HMEC	breast
4	chr4:87466200-87478200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr4:87466600-87479400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:87471000-87473800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:87471000-87475800	Weak transcription	Osteobl	bone
8	chr4:87471200-87473800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr4:87471200-87474000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:87471200-87478000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:87472400-87473800	Weak transcription	NHEK	skin
12	chr4:87473800-87474200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:87473800-87474600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:87473800-87474800	Enhancers	HMEC	breast
15	chr4:87473800-87475000	Enhancers	NHEK	skin
16	chr4:87473800-87475800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr4:87474000-87474200	Active TSS	Primary T helper naive cells from peripheral blood	blood
18	chr4:87474000-87474200	Enhancers	Ovary	ovary
19	chr4:87474000-87474600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:87474000-87475000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:87474000-87476600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr4:87474000-87477800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:87474200-87474600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:87474400-87479200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr4:87474600-87475000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:87474600-87475400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
27	chr4:87474600-87475400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:87474600-87476600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr4:87474600-87476800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:87474600-87479000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:87474800-87478000	Weak transcription	HMEC	breast
32	chr4:87475000-87476600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:87475000-87477200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:87475000-87478000	Weak transcription	NHEK	skin
35	chr4:87475400-87475600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
36	chr4:87475400-87476400	Enhancers	Primary hematopoietic stem cells	blood
37	chr4:87475400-87478000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:87475400-87478200	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr4:87475600-87475800	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr4:87475600-87476200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:87475600-87476200	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr4:87475600-87476600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr4:87475800-87476000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:87475800-87476000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
45	chr4:87475800-87476200	Enhancers	Osteobl	bone
46	chr4:87475800-87476400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr4:87476000-87476200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr4:87476000-87477600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:87476200-87476400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr4:87476200-87476400	Enhancers	GM12878-XiMat	blood

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