Variant report

Variant	nsv1011551
Chromosome Location	chr4:78120872-78204224
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	ATF1	chr4:78153907-78154134	K562	blood:	n/a	n/a
2	ATF2	chr4:78124651-78125083	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:78124742-78125099	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:78140257-78140528	GM12878	blood:	n/a	chr4:78140400-78140410 chr4:78140399-78140410
5	BHLHE40	chr4:78169965-78170247	HepG2	liver:	n/a	n/a
6	BHLHE40	chr4:78161829-78161910	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:78124792-78125302	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:78161695-78162114	K562	blood:	n/a	n/a
9	BHLHE40	chr4:78124782-78125104	K562	blood:	n/a	n/a
10	BRCA1	chr4:78161727-78161966	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr4:78142599-78142677	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr4:78161761-78161808	GM12878	blood:	n/a	n/a
13	CEBPB	chr4:78142460-78142826	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:78136939-78137228	A549	lung:	n/a	chr4:78137093-78137104
15	CEBPB	chr4:78142464-78142815	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:78136969-78137231	HepG2	liver:	n/a	chr4:78137093-78137104
17	CEBPB	chr4:78171884-78171912	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:78169257-78169440	HepG2	liver:	n/a	n/a
19	CTCF	chr4:78161720-78161870	HFF-Myc	foreskin:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
20	CTCF	chr4:78124880-78125030	AoAF	blood vessel:	n/a	chr4:78124941-78124957 chr4:78124940-78124958 chr4:78124943-78124953
21	CTCF	chr4:78124860-78125010	NHLF	lung:	n/a	chr4:78124941-78124957 chr4:78124940-78124958 chr4:78124943-78124953
22	CTCF	chr4:78149327-78149409	K562	blood:	n/a	chr4:78149335-78149353
23	CTCF	chr4:78161760-78161910	BJ	skin:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
24	CTCF	chr4:78161740-78161890	HMF	breast:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
25	CTCF	chr4:78161740-78161890	HAc	cerebellar:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
26	CTCF	chr4:78124860-78125010	GM12870	blood:	n/a	chr4:78124941-78124957 chr4:78124940-78124958 chr4:78124943-78124953
27	CTCF	chr4:78161700-78161850	HCT-116	colon:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
28	CTCF	chr4:78124860-78125010	Hela-S3	cervix:	n/a	chr4:78124941-78124957 chr4:78124940-78124958 chr4:78124943-78124953
29	CTCF	chr4:78161668-78161976	GM19239	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
30	CTCF	chr4:78161632-78161966	H1-hESC	embryonic stem cell:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
31	CTCF	chr4:78161659-78161975	GM12891	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
32	CTCF	chr4:78161820-78161970	HAc	cerebellar:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
33	CTCF	chr4:78124880-78125030	SAEC	small airway:	n/a	chr4:78124941-78124957 chr4:78124940-78124958 chr4:78124943-78124953
34	CTCF	chr4:78161667-78161967	K562	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
35	CTCF	chr4:78161740-78161890	GM06990	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
36	CTCF	chr4:78161434-78162125	HCT-116	colon:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
37	CTCF	chr4:78124804-78125065	Medullo	brain:	n/a	chr4:78124941-78124957 chr4:78124940-78124958 chr4:78124943-78124953
38	CTCF	chr4:78161689-78161957	Pancreas_OC	pancreas:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
39	CTCF	chr4:78124840-78124990	HEK293	kidney:	n/a	chr4:78124941-78124957 chr4:78124940-78124958 chr4:78124943-78124953
40	CTCF	chr4:78161760-78161910	HCFaa	heart:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
41	CTCF	chr4:78124798-78125074	ECC-1	luminal epithelium:	n/a	chr4:78124941-78124957 chr4:78124940-78124958 chr4:78124943-78124953
42	CTCF	chr4:78124860-78125010	HCT-116	colon:	n/a	chr4:78124941-78124957 chr4:78124940-78124958 chr4:78124943-78124953
43	CTCF	chr4:78161760-78161910	GM12864	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
44	CTCF	chr4:78161645-78162148	K562	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
45	CTCF	chr4:78161740-78161890	HEEpiC	esophagus:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
46	CTCF	chr4:78170540-78170690	NHLF	lung:	n/a	chr4:78170664-78170685 chr4:78170669-78170687 chr4:78170675-78170684
47	CTCF	chr4:78161760-78161910	K562	blood:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
48	CTCF	chr4:78161435-78161572	GM10266	blood:	n/a	n/a
49	CTCF	chr4:78161667-78161988	NHEK	skin:	n/a	chr4:78161828-78161849 chr4:78161826-78161844 chr4:78161829-78161842
50	CTCF	chr4:78162430-78162487	Fibrobl	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78156196-78156246	NH-A	brain:	n/a
2	chr4:78156196-78156246	H1-hESC	embryonic stem cell:	embryo
3	chr4:78156196-78156246	GM12878	blood:	n/a
4	chr4:78156196-78156246	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:78156196-78156246	RPTEC	kidney:	n/a
6	chr4:78156196-78156246	HCPEpiC	choroid plexus:	n/a
7	chr4:78156196-78156246	GM12892	blood:	n/a
8	chr4:78156196-78156246	HCF	heart:	n/a
9	chr4:78156196-78156246	U87	brain:	n/a
10	chr4:78156196-78156246	Caco-2	colon:	n/a
11	chr4:78156196-78156246	HCM	heart:	n/a
12	chr4:78156196-78156246	BE2_C	brain:	n/a
13	chr4:78156196-78156246	PANC-1	pancreas:	n/a
14	chr4:78156196-78156246	CMK	blood:	n/a
15	chr4:78156196-78156246	SK-N-MC	brain:	n/a
16	chr4:78156196-78156246	GM12891	blood:	n/a
17	chr4:78156196-78156246	HRE	kidney:	n/a
18	chr4:78156196-78156246	HUVEC	blood vessel:	n/a
19	chr4:78156196-78156246	HAEpiC	amniotic membrane:	n/a
20	chr4:78156196-78156246	HMEC	breast:	n/a
21	chr4:78156196-78156246	SKMC	muscle:	n/a
22	chr4:78156196-78156246	LNCaP	prostate:	n/a
23	chr4:78156196-78156246	Jurkat	blood:	n/a
24	chr4:78156196-78156246	HNPCEpiC	eye:	n/a
25	chr4:78156196-78156246	AG10803	skin:	n/a
26	chr4:78156196-78156246	SK-N-SH_RA	brain:	n/a
27	chr4:78156196-78156246	HRCEpiC	kidney:	n/a
28	chr4:78156196-78156246	SK-N-SH	brain:	n/a
29	chr4:78156196-78156246	HEK293	kidney:	embryo
30	chr4:78156196-78156246	NB4	blood:	n/a
31	chr4:78156196-78156246	Hepatocyte	liver:	n/a
32	chr4:78156196-78156246	A549	lung:	n/a
33	chr4:78156196-78156246	HEEpiC	esophagus:	n/a
34	chr4:78156196-78156246	MCF10A-Er-Src	breast:	n/a
35	chr4:78156196-78156246	AoSMC	blood vessel:	n/a
36	chr4:78156196-78156246	AG04450	lung:	fetal
37	chr4:78156196-78156246	AG09309	skin:	n/a
38	chr4:78156196-78156246	SAEC	small airway:	n/a
39	chr4:78156196-78156246	ProgFib	skin:	n/a
40	chr4:78156196-78156246	PFSK-1	brain:	n/a
41	chr4:78156196-78156246	GM06990	blood:	n/a
42	chr4:78156196-78156246	BJ	skin:	n/a
43	chr4:78156196-78156246	MCF-7	breast:	n/a
44	chr4:78156196-78156246	K562	blood:	n/a
45	chr4:78156196-78156246	NHBE	bronchial:	n/a
46	chr4:78156196-78156246	IMR90	lung:	fetal
47	chr4:78156196-78156246	GM19239	blood:	n/a
48	chr4:78156196-78156246	T-47D	breast:	n/a
49	chr4:78156196-78156246	HIPEpiC	eye:	n/a
50	chr4:78156196-78156246	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:78161398..78162211-chr4:78229720..78230660,3	MCF-7	breast:
2	chr4:77993291..77996240-chr4:78123279..78125310,2	K562	blood:
3	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
4	chr4:77996630..77998488-chr4:78129645..78132473,2	MCF-7	breast:
5	chr4:77966536..77967346-chr4:78124518..78125381,3	MCF-7	breast:
6	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
7	chr4:78132153..78134677-chr4:78134780..78136645,2	MCF-7	breast:
8	chr4:78130169..78132632-chr4:78133437..78136630,3	K562	blood:
9	chr4:78161284..78162458-chr4:78229777..78230742,7	K562	blood:
10	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:
11	chr4:78149304..78151645-chr4:78154973..78157716,3	K562	blood:
12	chr4:78162165..78163774-chr4:78227168..78228953,2	MCF-7	breast:
13	chr4:78016448..78019261-chr4:78148834..78151500,2	MCF-7	breast:
14	chr4:78130169..78132632-chr4:78133437..78136630,3	K562	blood:
15	chr4:78161311..78162711-chr4:78226629..78227614,14	MCF-7	breast:
16	chr4:78161416..78162110-chr4:78226527..78227315,3	MCF-7	breast:
17	chr4:78111226..78111821-chr4:78124414..78125004,2	MCF-7	breast:
18	chr4:77991930..77994376-chr4:78120322..78122333,2	K562	blood:
19	chr4:77995909..77997574-chr4:78122547..78125037,2	MCF-7	breast:
20	chr4:78119460..78121220-chr4:78122778..78124442,2	MCF-7	breast:
21	chr4:78122483..78124874-chr4:78125132..78127042,2	MCF-7	breast:
22	chr4:77972517..77973832-chr4:78124536..78125312,3	MCF-7	breast:
23	chr4:78132153..78134677-chr4:78134780..78136645,2	MCF-7	breast:
24	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:
25	chr4:78084268..78085795-chr4:78119137..78120989,2	K562	blood:
26	chr4:78161721..78162270-chr4:78279119..78279681,2	MCF-7	breast:
27	chr4:78161473..78162127-chr4:78394685..78395318,2	K562	blood:
28	chr4:78161188..78162532-chr4:78229476..78230856,15	MCF-7	breast:
29	chr4:78114444..78117366-chr4:78117947..78121379,3	K562	blood:
30	chr4:78177354..78179710-chr4:78180664..78183643,2	MCF-7	breast:
31	chr4:78122483..78124874-chr4:78125132..78127042,2	MCF-7	breast:
32	chr4:78155252..78157365-chr4:78224145..78227144,3	MCF-7	breast:
33	chr4:77973136..77974149-chr4:78124472..78125396,4	K562	blood:
34	chr4:78161324..78162321-chr4:78279149..78280134,4	MCF-7	breast:
35	chr4:78182930..78185790-chr4:78187841..78189605,2	K562	blood:
36	chr4:78119460..78121220-chr4:78122778..78124442,2	MCF-7	breast:
37	chr4:78116886..78120148-chr4:78122009..78124874,3	K562	blood:
38	chr4:78041474..78042648-chr4:78124907..78125575,3	MCF-7	breast:
39	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:
40	chr4:78158067..78160012-chr4:78227264..78228770,2	MCF-7	breast:
41	chr4:78161365..78162334-chr4:78279195..78280134,7	K562	blood:
42	chr4:77997759..78000070-chr4:78123881..78125820,2	MCF-7	breast:
43	chr4:78077855..78079830-chr4:78121652..78124230,4	MCF-7	breast:
44	chr4:77968037..77968611-chr4:78124042..78125032,2	MCF-7	breast:
45	chr4:78160754..78162321-chr4:78226906..78228617,2	MCF-7	breast:
46	chr4:78016602..78017111-chr4:78134180..78134764,2	MCF-7	breast:
47	chr4:78155142..78157870-chr4:78168469..78170209,2	MCF-7	breast:
48	chr4:77994973..77997901-chr4:78150275..78153619,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNI-4	chr4:78137569-78138031	NONHSAT097051

Variant related genes	Relation type
ENSG00000270669	TF binding region
ENSG00000270669	CpG island
ENSG00000138764	chromatin interactions
ENSG00000118816	chromatin interactions

Extended variants
information (count: 3529 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3529 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200098655	chr4:78120873-78120874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180932317	chr4:78120889-78120890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375137314	chr4:78120912-78120913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145645545	chr4:78120932-78120933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538549061	chr4:78120942-78120943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563920477	chr4:78121025-78121026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185599250	chr4:78121052-78121053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548766105	chr4:78121089-78121090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568695231	chr4:78121100-78121101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534434017	chr4:78121106-78121107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369425237	chr4:78121136-78121137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190263720	chr4:78121150-78121151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115990843	chr4:78121206-78121207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538689461	chr4:78121254-78121255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183287517	chr4:78121257-78121258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531079911	chr4:78121267-78121268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536503262	chr4:78121302-78121303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139634141	chr4:78121317-78121318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs72863245	chr4:78121346-78121347	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs544113283	chr4:78121354-78121355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560720237	chr4:78121371-78121372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574269490	chr4:78121422-78121423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149191157	chr4:78121425-78121426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10030957	chr4:78121442-78121443	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs532642442	chr4:78121443-78121444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75519656	chr4:78121458-78121459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4582179	chr4:78121478-78121479	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs558720050	chr4:78121508-78121509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532015578	chr4:78121515-78121516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548880797	chr4:78121533-78121534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568807196	chr4:78121536-78121537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143344016	chr4:78121537-78121538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369658135	chr4:78121575-78121576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186939527	chr4:78121584-78121585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566395089	chr4:78121622-78121623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34757592	chr4:78121632-78121633	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191785944	chr4:78121659-78121660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376202699	chr4:78121671-78121672	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554490035	chr4:78121673-78121674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs373432225	chr4:78121674-78121675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs74960616	chr4:78121701-78121702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs4582180	chr4:78121779-78121780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs368169063	chr4:78121803-78121804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs6840204	chr4:78121828-78121829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs540006601	chr4:78121856-78121857	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs115200752	chr4:78121857-78121858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs377424342	chr4:78121876-78121877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560006252	chr4:78121945-78121946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs183953044	chr4:78121966-78121967	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs187881909	chr4:78121980-78121981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Glioblastoma multiforme	21922591	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78116400-78124600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr4:78118400-78123000	Weak transcription	Primary T cells from cord blood	blood
3	chr4:78118800-78124600	Weak transcription	Fetal Thymus	thymus
4	chr4:78119200-78124400	Weak transcription	Primary B cells from cord blood	blood
5	chr4:78119200-78124600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:78120000-78121600	Enhancers	Placenta	Placenta
7	chr4:78120200-78121600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr4:78120400-78121200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:78120400-78123000	Enhancers	HMEC	breast
10	chr4:78120400-78124800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:78120600-78121000	Enhancers	Placenta Amnion	Placenta Amnion
12	chr4:78120600-78121400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:78120600-78121600	Enhancers	Fetal Muscle Leg	muscle
14	chr4:78120600-78121600	Enhancers	Right Atrium	heart
15	chr4:78120600-78122800	Enhancers	NHEK	skin
16	chr4:78120600-78125200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:78120800-78121000	Enhancers	Esophagus	oesophagus
18	chr4:78121000-78123600	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr4:78121200-78123800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:78121400-78122400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:78121600-78123600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:78121600-78124600	Weak transcription	Fetal Muscle Leg	muscle
23	chr4:78122400-78125000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:78122600-78124800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr4:78122600-78125200	Enhancers	Stomach Mucosa	stomach
26	chr4:78122800-78123200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr4:78122800-78124000	Flanking Active TSS	NHEK	skin
28	chr4:78122800-78124800	Enhancers	Fetal Intestine Large	intestine
29	chr4:78122800-78125400	Enhancers	HSMM	muscle
30	chr4:78123000-78123200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:78123000-78123400	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr4:78123000-78123400	Enhancers	Primary T cells from cord blood	blood
33	chr4:78123000-78123600	Flanking Active TSS	HMEC	breast
34	chr4:78123000-78123800	Enhancers	Hela-S3	cervix
35	chr4:78123000-78124800	Enhancers	Fetal Intestine Small	intestine
36	chr4:78123200-78124600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr4:78123200-78124600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:78123400-78124600	Weak transcription	Primary T cells from cord blood	blood
39	chr4:78123400-78124800	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr4:78123600-78123800	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr4:78123600-78124000	Enhancers	Colonic Mucosa	Colon
42	chr4:78123600-78124800	Enhancers	Duodenum Mucosa	Duodenum
43	chr4:78123600-78124800	Enhancers	Placenta Amnion	Placenta Amnion
44	chr4:78123600-78125200	Enhancers	HMEC	breast
45	chr4:78123800-78124000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr4:78123800-78124200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr4:78124000-78124400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr4:78124000-78124800	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr4:78124000-78125200	Enhancers	NHEK	skin
50	chr4:78124200-78125200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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