Variant report

Variant	nsv886569
Chromosome Location	chr6:119055873-119132164
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:119121678-119121983	K562	blood:	n/a	n/a
2	ARID3A	chr6:119097718-119098102	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:119072412-119072526	HepG2	liver:	n/a	n/a
4	BACH1	chr6:119082922-119083174	K562	blood:	n/a	n/a
5	BACH1	chr6:119082954-119083132	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr6:119121635-119122077	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:119067355-119067632	K562	blood:	n/a	n/a
8	BHLHE40	chr6:119121706-119122049	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:119061284-119061889	K562	blood:	n/a	n/a
10	BHLHE40	chr6:119109918-119110067	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:119121689-119122052	K562	blood:	n/a	n/a
12	CBX3	chr6:119117561-119118070	K562	blood:	n/a	n/a
13	CBX3	chr6:119121660-119121974	K562	blood:	n/a	n/a
14	CBX3	chr6:119121610-119122025	K562	blood:	n/a	n/a
15	CCNT2	chr6:119083015-119083025	K562	blood:	n/a	n/a
16	CEBPB	chr6:119089107-119089436	HepG2	liver:	n/a	chr6:119089298-119089309
17	CEBPB	chr6:119098196-119098477	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:119090182-119090539	MCF-7	breast:	n/a	chr6:119090384-119090397 chr6:119090415-119090428
19	CEBPB	chr6:119095853-119095981	HepG2	liver:	n/a	chr6:119095921-119095932
20	CEBPB	chr6:119105174-119105414	IMR90	lung:	n/a	chr6:119105350-119105363
21	CEBPB	chr6:119092524-119092706	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:119090205-119090568	MCF-7	breast:	n/a	chr6:119090384-119090397 chr6:119090415-119090428
23	CEBPB	chr6:119098293-119098433	K562	blood:	n/a	n/a
24	CEBPB	chr6:119091768-119091929	HepG2	liver:	n/a	chr6:119091840-119091851
25	CEBPB	chr6:119089228-119089406	K562	blood:	n/a	chr6:119089298-119089309
26	CHD1	chr6:119097468-119098135	IMR90	lung:	n/a	n/a
27	CHD2	chr6:119056593-119056796	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr6:119097820-119097970	AoAF	blood vessel:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
29	CTCF	chr6:119121820-119121970	HCT-116	colon:	n/a	chr6:119121854-119121863 chr6:119121849-119121865 chr6:119121843-119121864 chr6:119121848-119121866 chr6:119121850-119121863
30	CTCF	chr6:119121800-119121950	HUVEC	blood vessel:	n/a	chr6:119121854-119121863 chr6:119121849-119121865 chr6:119121843-119121864 chr6:119121848-119121866 chr6:119121850-119121863
31	CTCF	chr6:119056518-119056881	H1-hESC	embryonic stem cell:	n/a	chr6:119056673-119056691 chr6:119056679-119056688 chr6:119056668-119056689 chr6:119056674-119056690
32	CTCF	chr6:119056680-119056830	RPTEC	kidney:	n/a	n/a
33	CTCF	chr6:119097780-119097930	GM12870	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
34	CTCF	chr6:119130100-119130250	GM12864	blood:	n/a	n/a
35	CTCF	chr6:119056640-119056790	Caco-2	colon:	n/a	chr6:119056673-119056691 chr6:119056679-119056688 chr6:119056668-119056689 chr6:119056674-119056690
36	CTCF	chr6:119056480-119056630	WI-38	lung:	n/a	n/a
37	CTCF	chr6:119097775-119098011	Kidney_OC	kidney:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
38	CTCF	chr6:119106931-119106990	MCF-7	breast:	n/a	chr6:119106970-119106979
39	CTCF	chr6:119121498-119122187	HCT-116	colon:	n/a	chr6:119121854-119121863 chr6:119121849-119121865 chr6:119121843-119121864 chr6:119121848-119121866 chr6:119121850-119121863
40	CTCF	chr6:119056600-119056750	GM06990	blood:	n/a	chr6:119056673-119056691 chr6:119056679-119056688 chr6:119056668-119056689 chr6:119056674-119056690
41	CTCF	chr6:119117940-119118090	GM06990	blood:	n/a	n/a
42	CTCF	chr6:119121649-119121960	H1-hESC	embryonic stem cell:	n/a	chr6:119121854-119121863 chr6:119121849-119121865 chr6:119121843-119121864 chr6:119121848-119121866 chr6:119121850-119121863
43	CTCF	chr6:119097820-119097970	GM12878	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
44	CTCF	chr6:119097840-119097990	GM12869	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
45	CTCF	chr6:119056620-119056770	AG09319	gingival:	n/a	chr6:119056673-119056691 chr6:119056679-119056688 chr6:119056668-119056689 chr6:119056674-119056690
46	CTCF	chr6:119097840-119097990	BE2_C	brain:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
47	CTCF	chr6:119121723-119121994	LNCaP	prostate:	n/a	chr6:119121854-119121863 chr6:119121849-119121865 chr6:119121843-119121864 chr6:119121848-119121866 chr6:119121850-119121863
48	CTCF	chr6:119097840-119097990	BJ	skin:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
49	CTCF	chr6:119121401-119122271	A549	lung:	n/a	chr6:119121854-119121863 chr6:119121849-119121865 chr6:119121843-119121864 chr6:119121848-119121866 chr6:119121850-119121863
50	CTCF	chr6:119121820-119121970	HFF	foreskin:	n/a	chr6:119121854-119121863 chr6:119121849-119121865 chr6:119121843-119121864 chr6:119121848-119121866 chr6:119121850-119121863

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:119131733-119131783	BJ	skin:	n/a
2	chr6:119069624-119069674	U87	brain:	n/a
3	chr6:119069624-119069674	GM12892	blood:	n/a
4	chr6:119105122-119105172	ECC-1	luminal epithelium:	n/a
5	chr6:119069624-119069674	HMEC	breast:	n/a
6	chr6:119105122-119105172	HCF	heart:	n/a
7	chr6:119105122-119105172	LNCaP	prostate:	n/a
8	chr6:119105122-119105172	PFSK-1	brain:	n/a
9	chr6:119105122-119105172	HMEC	breast:	n/a
10	chr6:119105122-119105172	HUVEC	blood vessel:	n/a
11	chr6:119105122-119105172	A549	lung:	n/a
12	chr6:119131733-119131783	ProgFib	skin:	n/a
13	chr6:119131733-119131783	GM06990	blood:	n/a
14	chr6:119105122-119105172	AoSMC	blood vessel:	n/a
15	chr6:119105122-119105172	Caco-2	colon:	n/a
16	chr6:119105122-119105172	HepG2	liver:	n/a
17	chr6:119105122-119105172	HCT-116	colon:	n/a
18	chr6:119131733-119131783	HUVEC	blood vessel:	n/a
19	chr6:119131733-119131783	HRPEpiC	eye:	n/a
20	chr6:119131733-119131783	AG09319	gingival:	n/a
21	chr6:119131733-119131783	HEEpiC	esophagus:	n/a
22	chr6:119105122-119105172	BJ	skin:	n/a
23	chr6:119131733-119131783	HEK293	kidney:	embryo
24	chr6:119069624-119069674	HL-60	blood:	n/a
25	chr6:119131733-119131783	HNPCEpiC	eye:	n/a
26	chr6:119069624-119069674	PrEC	prostate:	n/a
27	chr6:119131733-119131783	K562	blood:	n/a
28	chr6:119069624-119069674	HAEpiC	amniotic membrane:	n/a
29	chr6:119131733-119131783	A549	lung:	n/a
30	chr6:119069624-119069674	ECC-1	luminal epithelium:	n/a
31	chr6:119131733-119131783	HIPEpiC	eye:	n/a
32	chr6:119069624-119069674	SK-N-MC	brain:	n/a
33	chr6:119069624-119069674	GM12891	blood:	n/a
34	chr6:119131733-119131783	T-47D	breast:	n/a
35	chr6:119105122-119105172	SKMC	muscle:	n/a
36	chr6:119131733-119131783	PrEC	prostate:	n/a
37	chr6:119131733-119131783	NT2-D1	testis:	n/a
38	chr6:119131733-119131783	AG10803	skin:	n/a
39	chr6:119105122-119105172	SK-N-MC	brain:	n/a
40	chr6:119131733-119131783	AoSMC	blood vessel:	n/a
41	chr6:119105122-119105172	HCM	heart:	n/a
42	chr6:119105122-119105172	IMR90	lung:	fetal
43	chr6:119131733-119131783	BE2_C	brain:	n/a
44	chr6:119131733-119131783	HCPEpiC	choroid plexus:	n/a
45	chr6:119105122-119105172	NH-A	brain:	n/a
46	chr6:119131733-119131783	SK-N-SH_RA	brain:	n/a
47	chr6:119131733-119131783	Caco-2	colon:	n/a
48	chr6:119131733-119131783	GM12892	blood:	n/a
49	chr6:119069624-119069674	PFSK-1	brain:	n/a
50	chr6:119105122-119105172	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:119098916..119101415-chr6:119102887..119105983,3	K562	blood:
2	chr6:119109578..119112343-chr6:119334552..119337073,2	K562	blood:
3	chr6:119120439..119121965-chr6:119219112..119221592,2	K562	blood:
4	chr6:119084540..119086156-chr6:119087548..119090160,2	K562	blood:
5	chr6:119066428..119069279-chr6:119071576..119073945,2	K562	blood:
6	chr6:119057902..119060681-chr6:119068005..119070664,2	K562	blood:
7	chr6:119018340..119019295-chr6:119097391..119098460,8	MCF-7	breast:
8	chr6:119128908..119130462-chr6:119213970..119215913,2	MCF-7	breast:
9	chr6:119091223..119093581-chr6:119115948..119118630,2	MCF-7	breast:
10	chr6:119090089..119093226-chr6:119095000..119099014,4	K562	blood:
11	chr6:118970885..118973094-chr6:119064943..119066835,2	MCF-7	breast:
12	chr6:119086471..119089736-chr6:119091626..119095598,3	K562	blood:
13	chr6:119030431..119032047-chr6:119056887..119059760,2	K562	blood:
14	chr6:119125219..119127915-chr6:119131589..119133462,2	MCF-7	breast:
15	chr6:119060047..119062597-chr6:119065156..119068895,3	K562	blood:
16	chr3:10690679..10691531-chr6:119085240..119086216,2	MCF-7	breast:
17	chr6:119095345..119097623-chr6:119099653..119102563,2	K562	blood:
18	chr6:119018713..119019314-chr6:119121262..119121860,2	MCF-7	breast:
19	chr6:119050506..119052588-chr6:119054244..119056935,2	K562	blood:
20	chr6:119104519..119106736-chr6:119106969..119109771,2	K562	blood:
21	chr6:119086471..119089736-chr6:119091626..119095598,3	K562	blood:
22	chr6:118886433..118887071-chr6:119121474..119122076,2	MCF-7	breast:
23	chr6:119129761..119131785-chr6:119132717..119134280,2	MCF-7	breast:
24	chr6:119050585..119052961-chr6:119056269..119058945,2	MCF-7	breast:
25	chr6:119066428..119069279-chr6:119071576..119073945,2	K562	blood:
26	chr6:119075050..119077178-chr6:119080430..119083071,2	K562	blood:
27	chr6:119028583..119031260-chr6:119072061..119073893,2	K562	blood:
28	chr6:119095345..119097623-chr6:119099653..119102563,2	K562	blood:
29	chr6:119060949..119064802-chr6:119066880..119068506,4	K562	blood:
30	chr6:119090089..119093226-chr6:119095000..119099014,4	K562	blood:
31	chr6:119099349..119102563-chr6:119103399..119106439,3	K562	blood:
32	chr6:118971950..118973530-chr6:119120433..119122628,2	K562	blood:
33	chr6:119018692..119019285-chr6:119121454..119122042,2	MCF-7	breast:
34	chr6:119026092..119028989-chr6:119074948..119078427,3	K562	blood:
35	chr6:118604989..118605598-chr6:119097517..119098373,3	K562	blood:
36	chr6:119075050..119077178-chr6:119080430..119083071,2	K562	blood:
37	chr6:118977602..118979632-chr6:119069204..119070765,2	K562	blood:
38	chr6:119029559..119031931-chr6:119056887..119058919,2	K562	blood:
39	chr6:119091223..119093581-chr6:119115948..119118630,2	MCF-7	breast:
40	chr6:118939806..118940379-chr6:119121824..119122493,2	MCF-7	breast:
41	chr6:119029112..119030655-chr6:119123182..119125902,2	K562	blood:
42	chr6:119125219..119127915-chr6:119131589..119133462,2	MCF-7	breast:
43	chr6:119104519..119106736-chr6:119106969..119109771,2	K562	blood:
44	chr6:119128642..119130899-chr6:119172400..119174088,2	K562	blood:
45	chr6:119060949..119064802-chr6:119066880..119068506,4	K562	blood:
46	chr6:118604722..118606041-chr6:119121374..119122599,5	K562	blood:
47	chr6:119084540..119086156-chr6:119087548..119090160,2	K562	blood:
48	chr6:119071895..119074006-chr6:119076150..119078886,2	K562	blood:
49	chr6:119060047..119062597-chr6:119065156..119068895,3	K562	blood:
50	chr6:119057902..119060681-chr6:119068005..119070664,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASF1A-5	chr6:119104011-119104294	NONHSAT114700
2	lnc-ASF1A-5	chr6:119103871-119104581	NONHSAT114699
3	lnc-ASF1A-5	chr6:119100386-119100768	NONHSAT114698
4	lnc-ASF1A-5	chr6:119103875-119104583	NONHSAT114698
5	lnc-ASF1A-5	chr6:119078681-119078767	NONHSAT114698

Variant related genes	Relation type
ENSG00000225549	TF binding region
ENSG00000225549	CpG island
ENSG00000225549	chromatin interactions
ENSG00000111860	chromatin interactions
ENSG00000111875	chromatin interactions
ENSG00000111877	chromatin interactions

Extended variants
information (count: 2817 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2817 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs794880	chr6:119055873-119055874	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556052110	chr6:119055880-119055881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9481854	chr6:119055892-119055893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs73768544	chr6:119055897-119055898	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs558955981	chr6:119055912-119055913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143056687	chr6:119055932-119055933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148194990	chr6:119055943-119055944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35487093	chr6:119055947-119055948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533854892	chr6:119055999-119056000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141136457	chr6:119056056-119056057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112695636	chr6:119056096-119056097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs794881	chr6:119056116-119056117	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs563974516	chr6:119056119-119056120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543893994	chr6:119056121-119056122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532890438	chr6:119056159-119056160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552588704	chr6:119056173-119056174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556270004	chr6:119056192-119056193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564931392	chr6:119056204-119056205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181500793	chr6:119056205-119056206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565885689	chr6:119056313-119056314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372001769	chr6:119056314-119056315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545542681	chr6:119056358-119056359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555928432	chr6:119056373-119056374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566986230	chr6:119056375-119056376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536044706	chr6:119056376-119056377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549518032	chr6:119056394-119056395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572663522	chr6:119056439-119056440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569747505	chr6:119056456-119056457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186279280	chr6:119056504-119056505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371705646	chr6:119056558-119056559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150802981	chr6:119056582-119056583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534677070	chr6:119056594-119056595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555110060	chr6:119056600-119056601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574940674	chr6:119056609-119056610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375016192	chr6:119056730-119056731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs386705172	chr6:119056731-119056732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9401084	chr6:119056733-119056734	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs546506329	chr6:119056826-119056827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534481643	chr6:119056891-119056892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559765682	chr6:119056913-119056914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190290971	chr6:119056945-119056946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181530594	chr6:119056954-119056955	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187438049	chr6:119056983-119056984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138116693	chr6:119057019-119057020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543373238	chr6:119057020-119057021	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376038878	chr6:119057075-119057076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529785801	chr6:119057083-119057084	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549456581	chr6:119057090-119057091	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs191204055	chr6:119057102-119057103	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79921202	chr6:119057112-119057113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119046000-119056200	Weak transcription	K562	blood
2	chr6:119048200-119056200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr6:119054400-119056200	Weak transcription	Psoas Muscle	Psoas
4	chr6:119056000-119056400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr6:119056000-119056400	Enhancers	Fetal Heart	heart
6	chr6:119056000-119056800	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr6:119056200-119056400	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr6:119056200-119056600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:119056200-119056600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr6:119056200-119056600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr6:119056200-119056600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr6:119056200-119056800	Enhancers	Primary B cells from peripheral blood	blood
13	chr6:119056200-119056800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr6:119056200-119056800	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr6:119056200-119056800	Enhancers	Fetal Muscle Leg	muscle
16	chr6:119056200-119056800	Enhancers	Psoas Muscle	Psoas
17	chr6:119056200-119056800	Enhancers	K562	blood
18	chr6:119056200-119058200	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr6:119056400-119056600	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr6:119056400-119056600	Enhancers	Brain Cingulate Gyrus	brain
21	chr6:119056400-119056800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:119056400-119056800	Enhancers	Fetal Thymus	thymus
23	chr6:119056400-119058000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr6:119056400-119061400	Weak transcription	Fetal Heart	heart
25	chr6:119056600-119056800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr6:119056600-119056800	Enhancers	Pancreas	Pancrea
27	chr6:119056600-119056800	Enhancers	Spleen	Spleen
28	chr6:119056600-119060000	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr6:119056600-119067400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr6:119056600-119069000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr6:119056800-119057400	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr6:119056800-119057400	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr6:119056800-119057800	Weak transcription	Spleen	Spleen
34	chr6:119056800-119057800	Weak transcription	K562	blood
35	chr6:119056800-119060200	Weak transcription	Fetal Muscle Leg	muscle
36	chr6:119056800-119060400	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr6:119056800-119061200	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr6:119056800-119065400	Weak transcription	Fetal Thymus	thymus
39	chr6:119056800-119069800	Weak transcription	Pancreas	Pancrea
40	chr6:119057200-119059200	Weak transcription	Aorta	Aorta
41	chr6:119057400-119058000	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr6:119057400-119059200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr6:119057600-119059400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr6:119057800-119058000	Enhancers	Spleen	Spleen
45	chr6:119057800-119058600	Enhancers	K562	blood
46	chr6:119058000-119061200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr6:119058200-119058400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr6:119058200-119068800	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr6:119058600-119060400	Weak transcription	K562	blood
50	chr6:119058600-119060600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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