Variant report

Variant	nsv1025171
Chromosome Location	chr6:164113981-164170027
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:818)
CpG islands
(count:122)
Chromatin interactive
region (count:53)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:818 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:164152559-164152980	K562	blood:	n/a	n/a
2	ATF1	chr6:164131638-164131906	K562	blood:	n/a	n/a
3	ATF1	chr6:164167040-164167415	K562	blood:	n/a	n/a
4	ATF1	chr6:164152416-164152769	K562	blood:	n/a	n/a
5	ATF2	chr6:164126940-164127432	GM12878	blood:	n/a	n/a
6	ATF2	chr6:164128942-164130110	GM12878	blood:	n/a	n/a
7	ATF2	chr6:164133080-164133669	GM12878	blood:	n/a	n/a
8	ATF2	chr6:164128839-164130052	GM12878	blood:	n/a	n/a
9	ATF2	chr6:164126818-164127557	GM12878	blood:	n/a	n/a
10	ATF3	chr6:164152470-164152727	K562	blood:	n/a	chr6:164152603-164152617
11	ATF3	chr6:164152439-164152799	K562	blood:	n/a	chr6:164152603-164152617
12	BACH1	chr6:164162901-164162987	K562	blood:	n/a	n/a
13	BACH1	chr6:164122730-164122736	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr6:164126985-164127397	GM12878	blood:	n/a	n/a
15	BATF	chr6:164129319-164129897	GM12878	blood:	n/a	chr6:164129594-164129604 chr6:164129593-164129604
16	BATF	chr6:164129433-164129777	GM12878	blood:	n/a	chr6:164129594-164129604 chr6:164129593-164129604
17	BCL11A	chr6:164126936-164127474	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:164129319-164129894	GM12878	blood:	n/a	chr6:164129596-164129605 chr6:164129597-164129606
19	BCLAF1	chr6:164133036-164133566	GM12878	blood:	n/a	n/a
20	BCLAF1	chr6:164126814-164127455	GM12878	blood:	n/a	n/a
21	BCLAF1	chr6:164126919-164127405	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:164128891-164129968	GM12878	blood:	n/a	chr6:164129596-164129605 chr6:164129597-164129606
23	BCLAF1	chr6:164128816-164130001	GM12878	blood:	n/a	chr6:164129596-164129605 chr6:164129597-164129606
24	BHLHE40	chr6:164116051-164116058	K562	blood:	n/a	n/a
25	BHLHE40	chr6:164129443-164129969	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:164162523-164163297	K562	blood:	n/a	chr6:164162717-164162733
27	BHLHE40	chr6:164151672-164151830	K562	blood:	n/a	n/a
28	BHLHE40	chr6:164152161-164152823	K562	blood:	n/a	chr6:164152687-164152703
29	BHLHE40	chr6:164115969-164116445	HepG2	liver:	n/a	chr6:164116116-164116125 chr6:164116115-164116128
30	BHLHE40	chr6:164150167-164150836	K562	blood:	n/a	n/a
31	BHLHE40	chr6:164166987-164167220	K562	blood:	n/a	n/a
32	BHLHE40	chr6:164126798-164127443	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:164132258-164132497	K562	blood:	n/a	chr6:164132372-164132381 chr6:164132372-164132381
34	BHLHE40	chr6:164147834-164148102	K562	blood:	n/a	n/a
35	BHLHE40	chr6:164141120-164141390	HepG2	liver:	n/a	n/a
36	BRCA1	chr6:164132846-164133001	H1-hESC	embryonic stem cell:	n/a	n/a
37	CBX3	chr6:164150484-164150848	K562	blood:	n/a	n/a
38	CBX3	chr6:164143338-164143748	K562	blood:	n/a	n/a
39	CBX3	chr6:164138096-164138711	K562	blood:	n/a	n/a
40	CBX3	chr6:164152132-164152774	K562	blood:	n/a	n/a
41	CBX3	chr6:164168009-164168540	K562	blood:	n/a	n/a
42	CCNT2	chr6:164152374-164152695	K562	blood:	n/a	n/a
43	CCNT2	chr6:164131695-164131912	K562	blood:	n/a	n/a
44	CEBPB	chr6:164152786-164153042	K562	blood:	n/a	chr6:164152931-164152942
45	CEBPB	chr6:164129418-164130042	GM12878	blood:	n/a	chr6:164129842-164129853
46	CEBPB	chr6:164152770-164153070	IMR90	lung:	n/a	chr6:164152931-164152942
47	CEBPB	chr6:164126995-164127360	GM12878	blood:	n/a	n/a
48	CEBPB	chr6:164152621-164153102	K562	blood:	n/a	chr6:164152931-164152942
49	CEBPB	chr6:164166980-164167512	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:164135444-164135490	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:164167085-164167135	HL-60	blood:	n/a
2	chr6:164137946-164137996	NHDF-neo	bronchial:	n/a
3	chr6:164137946-164137996	ovcar-3	ovarian:	n/a
4	chr6:164137946-164137996	GM19239	blood:	n/a
5	chr6:164137946-164137996	PrEC	prostate:	n/a
6	chr6:164137946-164137996	BJ	skin:	n/a
7	chr6:164137946-164137996	NB4	blood:	n/a
8	chr6:164137946-164137996	NT2-D1	testis:	n/a
9	chr6:164137946-164137996	IMR90	lung:	fetal
10	chr6:164137946-164137996	CMK	blood:	n/a
11	chr6:164167085-164167135	IMR90	lung:	fetal
12	chr6:164137946-164137996	MCF10A-Er-Src	breast:	n/a
13	chr6:164167085-164167135	HUVEC	blood vessel:	n/a
14	chr6:164167085-164167135	HEEpiC	esophagus:	n/a
15	chr6:164167085-164167135	HNPCEpiC	eye:	n/a
16	chr6:164167085-164167135	T-47D	breast:	n/a
17	chr6:164167085-164167135	PrEC	prostate:	n/a
18	chr6:164167085-164167135	RPTEC	kidney:	n/a
19	chr6:164167085-164167135	Hepatocyte	liver:	n/a
20	chr6:164167085-164167135	Caco-2	colon:	n/a
21	chr6:164137946-164137996	HRPEpiC	eye:	n/a
22	chr6:164167085-164167135	HCPEpiC	choroid plexus:	n/a
23	chr6:164167085-164167135	ECC-1	luminal epithelium:	n/a
24	chr6:164167085-164167135	HAEpiC	amniotic membrane:	n/a
25	chr6:164137946-164137996	HL-60	blood:	n/a
26	chr6:164167085-164167135	HEK293	kidney:	embryo
27	chr6:164167085-164167135	HRE	kidney:	n/a
28	chr6:164137946-164137996	HMEC	breast:	n/a
29	chr6:164167085-164167135	SK-N-MC	brain:	n/a
30	chr6:164167085-164167135	GM19239	blood:	n/a
31	chr6:164137946-164137996	GM12891	blood:	n/a
32	chr6:164167085-164167135	AG09319	gingival:	n/a
33	chr6:164167085-164167135	HCF	heart:	n/a
34	chr6:164137946-164137996	Jurkat	blood:	n/a
35	chr6:164167085-164167135	SAEC	small airway:	n/a
36	chr6:164137946-164137996	HIPEpiC	eye:	n/a
37	chr6:164167085-164167135	NB4	blood:	n/a
38	chr6:164167085-164167135	AoSMC	blood vessel:	n/a
39	chr6:164137946-164137996	RPTEC	kidney:	n/a
40	chr6:164137946-164137996	ECC-1	luminal epithelium:	n/a
41	chr6:164137946-164137996	SK-N-SH_RA	brain:	n/a
42	chr6:164137946-164137996	T-47D	breast:	n/a
43	chr6:164137946-164137996	H1-hESC	embryonic stem cell:	embryo
44	chr6:164167085-164167135	SK-N-SH	brain:	n/a
45	chr6:164137946-164137996	NHBE	bronchial:	n/a
46	chr6:164137946-164137996	ProgFib	skin:	n/a
47	chr6:164167085-164167135	Jurkat	blood:	n/a
48	chr6:164167085-164167135	AG09309	skin:	n/a
49	chr6:164167085-164167135	GM12891	blood:	n/a
50	chr6:164137946-164137996	MCF-7	breast:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:164094751..164097351-chr6:164112738..164115220,2	K562	blood:
2	chr6:164126640..164128502-chr6:164313817..164315579,2	K562	blood:
3	chr6:164161305..164164067-chr6:164164278..164167269,3	K562	blood:
4	chr6:164149744..164152325-chr6:164152772..164156227,3	K562	blood:
5	chr6:164164066..164167011-chr6:164170527..164172238,3	K562	blood:
6	chr6:164130686..164133462-chr6:164319351..164322024,2	K562	blood:
7	chr6:164129205..164131317-chr6:164138569..164140374,2	MCF-7	breast:
8	chr6:164142799..164145043-chr6:164145124..164147466,3	MCF-7	breast:
9	chr6:164139141..164141274-chr6:164142590..164144971,2	K562	blood:
10	chr6:164104118..164105951-chr6:164112390..164114240,2	K562	blood:
11	chr6:164131958..164136902-chr6:164137750..164142946,6	K562	blood:
12	chr6:164147443..164149403-chr6:164151642..164153523,2	K562	blood:
13	chr6:164148787..164150602-chr6:164160193..164162376,2	K562	blood:
14	chr6:164123254..164126506-chr6:164128493..164130449,3	MCF-7	breast:
15	chr6:164142207..164144992-chr6:164152114..164154827,2	K562	blood:
16	chr6:164128182..164130278-chr6:164132166..164136192,3	K562	blood:
17	chr6:164148787..164150602-chr6:164160193..164162376,2	K562	blood:
18	chr6:164128425..164130009-chr6:164133926..164136192,2	K562	blood:
19	chr6:164131958..164135418-chr6:164137750..164141579,4	K562	blood:
20	chr6:164142799..164145043-chr6:164145124..164147466,3	MCF-7	breast:
21	chr6:27775500..27777130-chr6:164134294..164136651,2	MCF-7	breast:
22	chr6:164147443..164149403-chr6:164151642..164153523,2	K562	blood:
23	chr6:164150956..164153048-chr6:164160645..164162665,2	K562	blood:
24	chr6:164127592..164129611-chr6:164130012..164131653,2	K562	blood:
25	chr6:164149744..164152325-chr6:164152772..164156227,3	K562	blood:
26	chr6:164142207..164144992-chr6:164152114..164154827,2	K562	blood:
27	chr6:164139141..164141274-chr6:164142590..164144971,2	K562	blood:
28	chr6:164115301..164117140-chr6:164125243..164127219,2	K562	blood:
29	chr6:164158813..164160898-chr6:164198628..164201364,2	MCF-7	breast:
30	chr6:164161305..164164067-chr6:164164278..164167269,3	K562	blood:
31	chr6:164151367..164155187-chr6:164160904..164163779,4	MCF-7	breast:
32	chr6:164131958..164135418-chr6:164137750..164141579,4	K562	blood:
33	chr6:164108307..164110350-chr6:164112342..164114200,2	K562	blood:
34	chr6:164128425..164130009-chr6:164133926..164136192,2	K562	blood:
35	chr6:164143541..164145828-chr6:164241681..164243954,2	K562	blood:
36	chr6:164115301..164117140-chr6:164125243..164127219,2	K562	blood:
37	chr6:164150956..164153048-chr6:164160645..164162665,2	K562	blood:
38	chr6:164137255..164140112-chr6:164154106..164157033,2	K562	blood:
39	chr6:164151367..164155187-chr6:164160904..164163779,4	MCF-7	breast:
40	chr6:163989917..163992171-chr6:164159430..164162397,2	K562	blood:
41	chr6:164118210..164119752-chr6:164140006..164142481,2	K562	blood:
42	chr6:164117022..164118713-chr6:164126097..164128591,2	MCF-7	breast:
43	chr6:164129205..164131317-chr6:164138569..164140374,2	MCF-7	breast:
44	chr6:164128182..164130278-chr6:164132166..164136192,3	K562	blood:
45	chr6:164137255..164140112-chr6:164154106..164157033,2	K562	blood:
46	chr6:164118210..164119752-chr6:164140006..164142481,2	K562	blood:
47	chr6:164132884..164135744-chr6:164150540..164152159,2	K562	blood:
48	chr6:164154250..164155922-chr6:164197149..164199809,2	K562	blood:
49	chr6:164132884..164135744-chr6:164150540..164152159,2	K562	blood:
50	chr6:164117022..164118713-chr6:164126097..164128591,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL078585.1-19	chr6:164134590-164134640	NONHSAT115975
2	lnc-QKI-2	chr6:164124938-164125037	XLOC_005531
3	lnc-QKI-2	chr6:164124936-164125037	XLOC_005531
4	lnc-AL078585.1-19	chr6:164133908-164134374	NONHSAT115975
5	lnc-AL078585.1-19	chr6:164134769-164135824	NONHSAT115975
6	lnc-QKI-8	chr6:164114199-164114248	l_3315_chr6:164114198-164115583_testes
7	lnc-QKI-8	chr6:164114916-164115637	l_3315_chr6:164114198-164115583_testes
8	lnc-QKI-2	chr6:164124938-164125037	XLOC_005531

No data

Variant related genes	Relation type
ENSG00000235538	TF binding region
ENSG00000235538	CpG island
ENSG00000196747	chromatin interactions
ENSG00000235538	chromatin interactions
ENSG00000185130	chromatin interactions
CDKN1B	miRNA target sites
BCL2L11	miRNA target sites

Extended variants
information (count: 2348 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2348 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9283864	chr6:164113981-164113982	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150348166	chr6:164113989-164113990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376522948	chr6:164114028-164114029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539465848	chr6:164114037-164114038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150716415	chr6:164114083-164114084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534029539	chr6:164114110-164114111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs60425147	chr6:164114113-164114114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562609255	chr6:164114120-164114121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531657861	chr6:164114137-164114138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542603617	chr6:164114228-164114229	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs547707051	chr6:164114249-164114250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561701380	chr6:164114255-164114256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371217391	chr6:164114271-164114272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76544431	chr6:164114294-164114295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535578737	chr6:164114302-164114303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185126272	chr6:164114312-164114313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139118167	chr6:164114319-164114320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532556475	chr6:164114320-164114321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9347777	chr6:164114362-164114363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569419384	chr6:164114380-164114381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147155230	chr6:164114383-164114384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554525487	chr6:164114388-164114389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113561754	chr6:164114427-164114428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533937590	chr6:164114447-164114448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73241736	chr6:164114475-164114476	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9347778	chr6:164114521-164114522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs201331038	chr6:164114524-164114525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545655239	chr6:164114536-164114537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536711518	chr6:164114553-164114554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576242431	chr6:164114558-164114559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542187156	chr6:164114568-164114569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181198637	chr6:164114569-164114570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527237226	chr6:164114596-164114597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371111204	chr6:164114639-164114640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541035241	chr6:164114677-164114678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563991062	chr6:164114723-164114724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114190130	chr6:164114727-164114728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552470205	chr6:164114801-164114802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186706566	chr6:164114813-164114814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114968739	chr6:164114872-164114873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs57308664	chr6:164114901-164114902	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs188003159	chr6:164114902-164114903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117353576	chr6:164114910-164114911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs57770616	chr6:164114912-164114913	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs376156416	chr6:164114921-164114922	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs554161997	chr6:164114960-164114961	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs570839334	chr6:164114970-164114971	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs112496534	chr6:164115025-164115026	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs556076241	chr6:164115050-164115051	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs576234736	chr6:164115064-164115065	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164109000-164116600	Weak transcription	Pancreas	Pancrea
2	chr6:164111400-164116800	Weak transcription	Ovary	ovary
3	chr6:164114600-164116400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr6:164115800-164116000	Bivalent Enhancer	K562	blood
5	chr6:164116000-164117000	Enhancers	Liver	Liver
6	chr6:164116000-164119800	Enhancers	GM12878-XiMat	blood
7	chr6:164116200-164116400	Bivalent Enhancer	A549	lung
8	chr6:164116200-164116600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
9	chr6:164116200-164116800	Bivalent Enhancer	HepG2	liver
10	chr6:164116400-164117800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:164116400-164119000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr6:164116600-164117000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:164116600-164117200	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:164116600-164117400	Enhancers	Gastric	stomach
15	chr6:164116600-164117600	Enhancers	Pancreas	Pancrea
16	chr6:164116600-164120000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr6:164116800-164117000	Enhancers	Ovary	ovary
18	chr6:164116800-164117000	Flanking Bivalent TSS/Enh	HepG2	liver
19	chr6:164116800-164117200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr6:164116800-164118400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr6:164117000-164117400	Bivalent Enhancer	HepG2	liver
22	chr6:164117200-164117400	Enhancers	Lung	lung
23	chr6:164117200-164117400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr6:164117200-164117600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:164117400-164117600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:164117400-164117800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr6:164117400-164120800	Weak transcription	Lung	lung
28	chr6:164117800-164118200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr6:164118200-164119000	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr6:164118400-164118800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr6:164118800-164119800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr6:164119000-164119600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr6:164119000-164119600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr6:164119000-164120000	Enhancers	Primary B cells from peripheral blood	blood
35	chr6:164119200-164119800	Enhancers	Primary B cells from cord blood	blood
36	chr6:164119400-164119600	Enhancers	Primary hematopoietic stem cells	blood
37	chr6:164119600-164120000	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr6:164119600-164122000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:164119800-164121800	Weak transcription	Primary B cells from cord blood	blood
40	chr6:164119800-164122200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr6:164119800-164122400	Weak transcription	GM12878-XiMat	blood
42	chr6:164120000-164122000	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr6:164120800-164122800	Enhancers	Lung	lung
44	chr6:164121000-164121800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:164121200-164121800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr6:164121200-164135200	Enhancers	Primary B cells from peripheral blood	blood
47	chr6:164121400-164122600	Enhancers	Placenta	Placenta
48	chr6:164121400-164122800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:164121800-164122600	Enhancers	Primary hematopoietic stem cells	blood
50	chr6:164121800-164123600	Enhancers	Monocytes-CD14+_RO01746	blood

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