Variant report

Variant	nsv1024423
Chromosome Location	chr7:100963863-101128424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2682)
CpG islands
(count:2321)
Chromatin interactive
region (count:83)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2682 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101034275-101034431	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:100995557-100996013	K562	blood:	n/a	n/a
3	ARID3A	chr7:101029701-101030402	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:100995510-100995986	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:101054542-101054748	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:101041212-101041406	HepG2	liver:	n/a	n/a
7	ATF1	chr7:100995667-100996035	K562	blood:	n/a	n/a
8	ATF2	chr7:101005691-101006042	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:100965008-100965341	GM12878	blood:	n/a	n/a
10	ATF2	chr7:101045113-101045819	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:101007153-101007579	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:101034154-101034562	GM12878	blood:	n/a	n/a
13	ATF2	chr7:101045260-101045884	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:101054507-101054909	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr7:100964776-100965119	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr7:101034206-101034498	GM12878	blood:	n/a	n/a
17	ATF3	chr7:101083791-101083930	K562	blood:	n/a	n/a
18	ATF3	chr7:100995608-100996147	K562	blood:	n/a	n/a
19	ATF3	chr7:100964964-100965260	K562	blood:	n/a	chr7:100965121-100965130
20	BACH1	chr7:101006064-101006399	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:101042008-101042270	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:100964807-100965060	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:101054392-101054843	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:100978932-100978958	K562	blood:	n/a	n/a
25	BACH1	chr7:101083766-101083964	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr7:101006969-101007517	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr7:101080560-101080609	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr7:101045151-101045712	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr7:101045447-101045692	H1-hESC	embryonic stem cell:	n/a	chr7:101045565-101045572 chr7:101045573-101045582
30	BCL11A	chr7:101034127-101034558	GM12878	blood:	n/a	n/a
31	BCL3	chr7:101006990-101007617	A549	lung:	n/a	chr7:101007240-101007249 chr7:101007424-101007437
32	BCL3	chr7:100995424-100996093	A549	lung:	n/a	chr7:100995867-100995874
33	BCL3	chr7:101045252-101045835	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
34	BCL3	chr7:101085899-101086361	GM12878	blood:	n/a	n/a
35	BCL3	chr7:101034235-101034520	GM12878	blood:	n/a	n/a
36	BCL3	chr7:101071768-101072139	GM12878	blood:	n/a	n/a
37	BCL3	chr7:100995430-100996053	A549	lung:	n/a	chr7:100995867-100995874
38	BCL3	chr7:101045065-101045790	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
39	BCL3	chr7:101085919-101086314	GM12878	blood:	n/a	n/a
40	BCL3	chr7:101071831-101072136	GM12878	blood:	n/a	n/a
41	BCLAF1	chr7:100964775-100965491	GM12878	blood:	n/a	chr7:100965115-100965124
42	BHLHE40	chr7:101007069-101007443	K562	blood:	n/a	n/a
43	BHLHE40	chr7:100995649-100996149	K562	blood:	n/a	n/a
44	BHLHE40	chr7:101085990-101086330	K562	blood:	n/a	n/a
45	BHLHE40	chr7:100995806-100995888	HepG2	liver:	n/a	n/a
46	BHLHE40	chr7:101054571-101054732	K562	blood:	n/a	n/a
47	BHLHE40	chr7:100965063-100965137	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:101034158-101034493	GM12878	blood:	n/a	n/a
49	BHLHE40	chr7:101006937-101007505	HepG2	liver:	n/a	n/a
50	BHLHE40	chr7:101083725-101083894	GM12878	blood:	n/a	n/a

(count:2321 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101005846-101005896	HCT-116	colon:	n/a
2	chr7:101006019-101006069	U87	brain:	n/a
3	chr7:100965709-100965759	HepG2	liver:	n/a
4	chr7:101005846-101005896	HCT-116	colon:	n/a
5	chr7:101006019-101006069	U87	brain:	n/a
6	chr7:100965709-100965759	HepG2	liver:	n/a
7	chr7:101005832-101005882	AoSMC	blood vessel:	n/a
8	chr7:101007190-101007240	NHDF-neo	bronchial:	n/a
9	chr7:101049372-101049422	HRPEpiC	eye:	n/a
10	chr7:101006363-101006413	H1-hESC	embryonic stem cell:	embryo
11	chr7:101079617-101079667	NB4	blood:	n/a
12	chr7:101006308-101006358	AG04450	lung:	fetal
13	chr7:101006052-101006102	HIPEpiC	eye:	n/a
14	chr7:101007603-101007653	MCF10A-Er-Src	breast:	n/a
15	chr7:100965200-100965250	GM06990	blood:	n/a
16	chr7:101007190-101007240	HRE	kidney:	n/a
17	chr7:100965198-100965248	Caco-2	colon:	n/a
18	chr7:100965709-100965759	AoSMC	blood vessel:	n/a
19	chr7:101007442-101007492	MCF10A-Er-Src	breast:	n/a
20	chr7:100965274-100965324	IMR90	lung:	fetal
21	chr7:100964799-100964849	GM12891	blood:	n/a
22	chr7:101006089-101006139	ECC-1	luminal epithelium:	n/a
23	chr7:100968383-100968433	HCPEpiC	choroid plexus:	n/a
24	chr7:100965200-100965250	AG09319	gingival:	n/a
25	chr7:101006963-101007013	HEEpiC	esophagus:	n/a
26	chr7:101079617-101079667	GM12878	blood:	n/a
27	chr7:100966078-100966128	PANC-1	pancreas:	n/a
28	chr7:100966076-100966126	T-47D	breast:	n/a
29	chr7:101006089-101006139	HCF	heart:	n/a
30	chr7:100965198-100965248	K562	blood:	n/a
31	chr7:101006052-101006102	GM19239	blood:	n/a
32	chr7:101006308-101006358	PFSK-1	brain:	n/a
33	chr7:100965200-100965250	HNPCEpiC	eye:	n/a
34	chr7:101049372-101049422	HMEC	breast:	n/a
35	chr7:100965680-100965730	A549	lung:	n/a
36	chr7:101055912-101055962	NHDF-neo	bronchial:	n/a
37	chr7:100964669-100964719	U87	brain:	n/a
38	chr7:101006035-101006085	HRE	kidney:	n/a
39	chr7:101007072-101007122	SK-N-MC	brain:	n/a
40	chr7:100966076-100966126	ovcar-3	ovarian:	n/a
41	chr7:101006963-101007013	AG09319	gingival:	n/a
42	chr7:101055912-101055962	K562	blood:	n/a
43	chr7:100964734-100964784	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:100965200-100965250	PANC-1	pancreas:	n/a
45	chr7:100965198-100965248	NH-A	brain:	n/a
46	chr7:100964734-100964784	NH-A	brain:	n/a
47	chr7:100993034-100993084	SK-N-MC	brain:	n/a
48	chr7:100966076-100966126	HCT-116	colon:	n/a
49	chr7:101006089-101006139	HRPEpiC	eye:	n/a
50	chr7:101007603-101007653	HUVEC	blood vessel:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:101012941..101015108-chr7:101017148..101018749,2	K562	blood:
2	chr7:101023195..101026718-chr7:101028403..101030293,3	K562	blood:
3	chr7:101006811..101007905-chr7:101150693..101151800,11	K562	blood:
4	chr7:101012360..101015108-chr7:101017249..101019175,2	K562	blood:
5	chr7:100967257..100969650-chr7:100972376..100975221,2	K562	blood:
6	chr7:101067571..101069515-chr7:101079650..101082212,2	MCF-7	breast:
7	chr7:101083724..101084446-chr7:101150709..101151315,2	MCF-7	breast:
8	chr7:101031371..101033701-chr7:101034998..101036873,2	K562	blood:
9	chr7:101068095..101068916-chr7:101150848..101151469,2	MCF-7	breast:
10	chr7:101006441..101008974-chr7:101023704..101025266,2	MCF-7	breast:
11	chr7:101110378..101112867-chr7:101115903..101117438,2	K562	blood:
12	chr7:101117670..101118572-chr7:101150768..101151530,2	MCF-7	breast:
13	chr7:101083863..101087245-chr7:101089520..101092470,3	K562	blood:
14	chr7:101006995..101008302-chr7:101082934..101084354,6	MCF-7	breast:
15	chr7:100964942..100967208-chr7:101081876..101083958,2	MCF-7	breast:
16	chr7:100950840..100954191-chr7:100963498..100966604,5	MCF-7	breast:
17	chr7:100965612..100969667-chr7:101005034..101007660,3	MCF-7	breast:
18	chr7:101012941..101015108-chr7:101017148..101018749,2	K562	blood:
19	chr7:101110378..101112867-chr7:101115903..101117438,2	K562	blood:
20	chr7:100964752..100967137-chr7:100978107..100980737,2	MCF-7	breast:
21	chr7:100989055..100991707-chr7:100994198..100995736,2	MCF-7	breast:
22	chr7:101015968..101018340-chr7:101024306..101026455,2	MCF-7	breast:
23	chr7:101037193..101039012-chr7:101045881..101047459,2	MCF-7	breast:
24	chr7:101054216..101055052-chr7:101150685..101151359,3	MCF-7	breast:
25	chr7:101043147..101045492-chr7:101051053..101052921,2	K562	blood:
26	chr7:100963124..100966014-chr7:101122778..101124584,2	MCF-7	breast:
27	chr15:65596698..65597638-chr7:100964826..100965617,2	HCT-116	colon:
28	chr7:101032377..101034733-chr7:101037402..101040388,2	MCF-7	breast:
29	chr7:101006966..101007850-chr7:101054283..101055103,3	MCF-7	breast:
30	chr7:100964710..100967141-chr7:101003077..101007417,4	MCF-7	breast:
31	chr7:101100607..101102049-chr7:101150824..101151606,9	MCF-7	breast:
32	chr7:101006530..101007875-chr7:101054200..101055148,9	MCF-7	breast:
33	chr7:101006510..101007838-chr7:101150604..101151700,15	MCF-7	breast:
34	chr7:101006441..101008974-chr7:101023704..101025266,2	MCF-7	breast:
35	chr7:101016391..101018815-chr7:101033017..101035506,2	K562	blood:
36	chr7:101016391..101018815-chr7:101033017..101035506,2	K562	blood:
37	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
38	chr7:101115888..101118705-chr7:101119430..101120969,2	MCF-7	breast:
39	chr7:101039985..101042024-chr7:101043789..101046579,2	MCF-7	breast:
40	chr7:101054544..101055233-chr7:101150595..101151343,2	K562	blood:
41	chr7:101023195..101025977-chr7:101028738..101030293,2	K562	blood:
42	chr7:100941519..100944089-chr7:100963395..100965508,2	K562	blood:
43	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
44	chr7:101006862..101007822-chr7:101083395..101084349,8	MCF-7	breast:
45	chr7:101037193..101039012-chr7:101045881..101047459,2	MCF-7	breast:
46	chr7:101041365..101043542-chr7:101048323..101050814,2	MCF-7	breast:
47	chr7:101039985..101042024-chr7:101043789..101046579,2	MCF-7	breast:
48	chr7:101006966..101007850-chr7:101054283..101055103,3	MCF-7	breast:
49	chr7:101012360..101015108-chr7:101017249..101019175,2	K562	blood:
50	chr7:101083863..101087245-chr7:101089520..101092470,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNHIT1-1	chr7:100964396-100964425	NR_110115
2	lnc-RABL5-1	chr7:100998850-100999006	ucscGeneNc_uc003uyp_2
3	lnc-RABL5-2	chr7:101032149-101032361	NONHSAT122467
4	lnc-RABL5-1	chr7:100995310-100996633	ucscGeneNc_uc003uyp_2

No data

Variant related genes	Relation type
RABL5	TF binding region
ENSG00000233683	TF binding region
COL26A1	TF binding region
RABL5	CpG island
ENSG00000233683	CpG island
COL26A1	CpG island
ENSG00000128581	chromatin interactions
ENSG00000233683	chromatin interactions
ENSG00000180447	chromatin interactions
ENSG00000160963	chromatin interactions
ENSG00000255992	chromatin interactions
ENSG00000177192	chromatin interactions
ENSG00000232301	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000232445	chromatin interactions

Extended variants
information (count: 7140 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:7140 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113614356	chr7:100963875-100963876	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
2	rs112700571	chr7:100963883-100963884	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552826534	chr7:100963954-100963955	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs572146935	chr7:100963960-100963961	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs183704769	chr7:100964035-100964036	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370402535	chr7:100964040-100964041	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs76804623	chr7:100964042-100964043	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554175798	chr7:100964046-100964047	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575707723	chr7:100964057-100964058	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs188855274	chr7:100964060-100964061	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs558319863	chr7:100964063-100964064	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576973533	chr7:100964137-100964138	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369842335	chr7:100964148-100964149	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs559409209	chr7:100964149-100964150	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs57916806	chr7:100964152-100964153	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs562938899	chr7:100964154-100964155	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs377278316	chr7:100964235-100964236	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs370175291	chr7:100964244-100964245	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs576098484	chr7:100964256-100964257	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs118149823	chr7:100964292-100964293	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191745168	chr7:100964368-100964369	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs2410817	chr7:100964409-100964410	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs563381084	chr7:100964426-100964427	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200691106	chr7:100964429-100964430	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs199629081	chr7:100964431-100964432	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs376312687	chr7:100964445-100964446	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs532619537	chr7:100964508-100964509	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs184561321	chr7:100964514-100964515	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs373216558	chr7:100964530-100964531	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs541753613	chr7:100964590-100964591	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs374730284	chr7:100964615-100964616	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs28719520	chr7:100964722-100964723	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs547776759	chr7:100964741-100964742	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs73410778	chr7:100964759-100964760	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs536706087	chr7:100964761-100964762	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs558232273	chr7:100964779-100964780	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs570595979	chr7:100964813-100964814	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs534533400	chr7:100964815-100964816	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs553161513	chr7:100964826-100964827	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs531893637	chr7:100964865-100964866	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs368833663	chr7:100964869-100964870	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs190049687	chr7:100964872-100964873	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs554963337	chr7:100964876-100964877	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs576510163	chr7:100964897-100964898	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs370416834	chr7:100964910-100964911	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs374119786	chr7:100964940-100964941	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs543908510	chr7:100964978-100964979	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs151026923	chr7:100965006-100965007	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs532676178	chr7:100965007-100965008	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs200233985	chr7:100965012-100965013	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2354 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100951800-100964000	Weak transcription	Fetal Heart	heart
2	chr7:100952200-100964000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr7:100952400-100964000	Weak transcription	Liver	Liver
4	chr7:100952400-100964000	Weak transcription	Right Ventricle	heart
5	chr7:100952400-100964200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr7:100952400-100964200	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr7:100952400-100964400	Weak transcription	Psoas Muscle	Psoas
8	chr7:100952400-100964400	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr7:100952400-100964400	Weak transcription	NHLF	lung
10	chr7:100952600-100964000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:100952600-100964000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr7:100952600-100964000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr7:100952600-100964000	Weak transcription	Colonic Mucosa	Colon
14	chr7:100952600-100964000	Weak transcription	Duodenum Mucosa	Duodenum
15	chr7:100952600-100964000	Weak transcription	Esophagus	oesophagus
16	chr7:100952600-100964000	Weak transcription	HUVEC	blood vessel
17	chr7:100952600-100964400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:100952600-100964400	Weak transcription	Gastric	stomach
19	chr7:100953200-100964200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:100953800-100964000	Weak transcription	Colon Smooth Muscle	Colon
21	chr7:100953800-100964200	Weak transcription	Left Ventricle	heart
22	chr7:100954200-100964000	Weak transcription	HepG2	liver
23	chr7:100954600-100964400	Weak transcription	NHEK	skin
24	chr7:100955000-100964000	Weak transcription	HMEC	breast
25	chr7:100955000-100964400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr7:100955000-100964400	Weak transcription	K562	blood
27	chr7:100955200-100964200	Weak transcription	Primary B cells from cord blood	blood
28	chr7:100955200-100964200	Weak transcription	Primary T cells from cord blood	blood
29	chr7:100955400-100964000	Weak transcription	Brain Angular Gyrus	brain
30	chr7:100955400-100964000	Weak transcription	Stomach Mucosa	stomach
31	chr7:100955400-100964000	Weak transcription	Hela-S3	cervix
32	chr7:100955600-100964200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr7:100955600-100964400	Weak transcription	HSMMtube	muscle
34	chr7:100955800-100964000	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr7:100956000-100964000	Weak transcription	Fetal Brain Male	brain
36	chr7:100956400-100964000	Weak transcription	Spleen	Spleen
37	chr7:100956800-100964000	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr7:100957000-100964600	Weak transcription	Primary hematopoietic stem cells	blood
39	chr7:100957400-100964000	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr7:100957800-100964000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr7:100958400-100964000	Weak transcription	Osteobl	bone
42	chr7:100958600-100964000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr7:100958600-100964000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr7:100958600-100964200	Weak transcription	HSMM	muscle
45	chr7:100958800-100964200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr7:100959400-100964000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr7:100959400-100964000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr7:100959400-100964600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr7:100959800-100964000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr7:100959800-100964000	Weak transcription	Duodenum Smooth Muscle	Duodenum

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