Variant report

Variant	nsv1027574
Chromosome Location	chr7:101654060-101718950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:911)
CpG islands
(count:978)
Chromatin interactive
region (count:46)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:911 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101685684-101685947	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:101656159-101656653	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:101667927-101668675	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:101663659-101663683	K562	blood:	n/a	n/a
5	ARID3A	chr7:101663221-101663249	K562	blood:	n/a	n/a
6	ATF2	chr7:101705008-101705884	GM12878	blood:	n/a	n/a
7	ATF2	chr7:101705065-101705763	GM12878	blood:	n/a	n/a
8	ATF2	chr7:101689235-101689601	GM12878	blood:	n/a	n/a
9	ATF2	chr7:101673858-101674327	GM12878	blood:	n/a	n/a
10	ATF2	chr7:101698816-101699190	GM12878	blood:	n/a	n/a
11	BACH1	chr7:101707125-101707347	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr7:101715275-101715515	GM12878	blood:	n/a	n/a
13	BATF	chr7:101698772-101699268	GM12878	blood:	n/a	n/a
14	BATF	chr7:101705126-101705709	GM12878	blood:	n/a	chr7:101705696-101705704
15	BATF	chr7:101689231-101689611	GM12878	blood:	n/a	chr7:101689378-101689389
16	BATF	chr7:101698849-101699202	GM12878	blood:	n/a	n/a
17	BATF	chr7:101689187-101689511	GM12878	blood:	n/a	chr7:101689378-101689389
18	BCL11A	chr7:101673950-101674296	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:101705243-101705706	GM12878	blood:	n/a	chr7:101705578-101705591
20	BCL11A	chr7:101673906-101674298	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:101705249-101705669	GM12878	blood:	n/a	chr7:101705578-101705591
22	BCL11A	chr7:101689283-101689435	GM12878	blood:	n/a	n/a
23	BCL3	chr7:101683991-101684228	GM12878	blood:	n/a	n/a
24	BCL3	chr7:101689217-101689578	GM12878	blood:	n/a	chr7:101689491-101689500 chr7:101689513-101689522
25	BCL3	chr7:101691164-101691591	GM12878	blood:	n/a	n/a
26	BCL3	chr7:101656036-101656645	A549	lung:	n/a	chr7:101656111-101656120
27	BCL3	chr7:101705133-101705731	GM12878	blood:	n/a	chr7:101705578-101705591
28	BCLAF1	chr7:101673836-101674435	GM12878	blood:	n/a	n/a
29	BCLAF1	chr7:101705157-101705795	GM12878	blood:	n/a	chr7:101705578-101705591
30	BCLAF1	chr7:101698783-101699172	GM12878	blood:	n/a	n/a
31	BCLAF1	chr7:101683749-101684275	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:101698953-101699166	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:101667963-101668509	HepG2	liver:	n/a	n/a
34	BHLHE40	chr7:101705269-101705746	GM12878	blood:	n/a	chr7:101705517-101705530
35	BHLHE40	chr7:101688413-101688423	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:101673824-101674323	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:101707985-101708122	K562	blood:	n/a	n/a
38	BRCA1	chr7:101706993-101708260	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr7:101699654-101699925	K562	blood:	n/a	n/a
40	CBX3	chr7:101697410-101697840	K562	blood:	n/a	n/a
41	CBX3	chr7:101697498-101697772	K562	blood:	n/a	n/a
42	CEBPB	chr7:101694163-101694355	K562	blood:	n/a	n/a
43	CEBPB	chr7:101656140-101656501	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:101668038-101668282	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:101667924-101668579	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:101656060-101656491	A549	lung:	n/a	n/a
47	CEBPB	chr7:101656107-101656547	MCF-7	breast:	n/a	n/a
48	CEBPB	chr7:101705027-101705824	GM12878	blood:	n/a	n/a
49	CEBPB	chr7:101668014-101668234	A549	lung:	n/a	n/a
50	CEBPB	chr7:101667962-101668361	HepG2	liver:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101688648-101688698	RPTEC	kidney:	n/a
2	chr7:101707668-101707718	AG04450	lung:	fetal
3	chr7:101688648-101688698	RPTEC	kidney:	n/a
4	chr7:101707668-101707718	AG04450	lung:	fetal
5	chr7:101667129-101667179	HCF	heart:	n/a
6	chr7:101707668-101707718	NHDF-neo	bronchial:	n/a
7	chr7:101656975-101657025	Caco-2	colon:	n/a
8	chr7:101707668-101707718	HEEpiC	esophagus:	n/a
9	chr7:101688730-101688780	LNCaP	prostate:	n/a
10	chr7:101667129-101667179	NB4	blood:	n/a
11	chr7:101712363-101712413	SK-N-SH_RA	brain:	n/a
12	chr7:101712308-101712358	ProgFib	skin:	n/a
13	chr7:101688675-101688725	SAEC	small airway:	n/a
14	chr7:101688675-101688725	HRE	kidney:	n/a
15	chr7:101688675-101688725	HEEpiC	esophagus:	n/a
16	chr7:101712363-101712413	HRE	kidney:	n/a
17	chr7:101680429-101680479	HL-60	blood:	n/a
18	chr7:101712363-101712413	ECC-1	luminal epithelium:	n/a
19	chr7:101662182-101662232	SK-N-SH_RA	brain:	n/a
20	chr7:101712212-101712262	GM12891	blood:	n/a
21	chr7:101671556-101671606	CMK	blood:	n/a
22	chr7:101712363-101712413	RPTEC	kidney:	n/a
23	chr7:101680927-101680977	MCF-7	breast:	n/a
24	chr7:101688648-101688698	U87	brain:	n/a
25	chr7:101671556-101671606	SK-N-SH_RA	brain:	n/a
26	chr7:101712087-101712137	Jurkat	blood:	n/a
27	chr7:101671556-101671606	HUVEC	blood vessel:	n/a
28	chr7:101712212-101712262	HAEpiC	amniotic membrane:	n/a
29	chr7:101688730-101688780	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:101680429-101680479	MCF10A-Er-Src	breast:	n/a
31	chr7:101680927-101680977	SK-N-SH_RA	brain:	n/a
32	chr7:101667129-101667179	GM19239	blood:	n/a
33	chr7:101667129-101667179	NH-A	brain:	n/a
34	chr7:101688730-101688780	ProgFib	skin:	n/a
35	chr7:101671556-101671606	T-47D	breast:	n/a
36	chr7:101656975-101657025	CMK	blood:	n/a
37	chr7:101680927-101680977	HIPEpiC	eye:	n/a
38	chr7:101680429-101680479	HAEpiC	amniotic membrane:	n/a
39	chr7:101680429-101680479	AoSMC	blood vessel:	n/a
40	chr7:101667129-101667179	Hela-S3	cervix:	n/a
41	chr7:101712087-101712137	HIPEpiC	eye:	n/a
42	chr7:101662182-101662232	GM19239	blood:	n/a
43	chr7:101667129-101667179	SAEC	small airway:	n/a
44	chr7:101688675-101688725	HCF	heart:	n/a
45	chr7:101662116-101662166	U87	brain:	n/a
46	chr7:101712087-101712137	Caco-2	colon:	n/a
47	chr7:101688730-101688780	HNPCEpiC	eye:	n/a
48	chr7:101680927-101680977	HNPCEpiC	eye:	n/a
49	chr7:101667129-101667179	AG09319	gingival:	n/a
50	chr7:101688675-101688725	SK-N-SH_RA	brain:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:101698449..101701130-chr7:101703905..101706013,2	MCF-7	breast:
2	chr7:101698449..101701130-chr7:101703905..101706013,2	MCF-7	breast:
3	chr7:101647281..101648020-chr7:101707540..101708409,2	MCF-7	breast:
4	chr7:101654464..101657712-chr7:101662423..101666684,4	MCF-7	breast:
5	chr20:60641089..60641822-chr7:101688169..101689168,2	MCF-7	breast:
6	chr7:101714618..101716538-chr7:101724031..101725533,2	K562	blood:
7	chr7:101657254..101660021-chr7:101660679..101662867,2	MCF-7	breast:
8	chr7:101673753..101675283-chr7:101675530..101677556,2	MCF-7	breast:
9	chr7:101688104..101690930-chr7:101693641..101697108,3	MCF-7	breast:
10	chr7:101584833..101587634-chr7:101667426..101668972,2	MCF-7	breast:
11	chr7:101706528..101709517-chr7:101721356..101724154,2	K562	blood:
12	chr7:101460537..101463033-chr7:101654903..101656505,2	MCF-7	breast:
13	chr7:101459264..101462006-chr7:101705742..101707719,3	MCF-7	breast:
14	chr7:101705153..101708097-chr7:101711212..101713863,3	K562	blood:
15	chr7:101656842..101659859-chr7:101660301..101664311,4	K562	blood:
16	chr7:101458855..101462085-chr7:101664015..101667033,4	MCF-7	breast:
17	chr7:101462493..101465700-chr7:101703860..101705566,3	MCF-7	breast:
18	chr20:60639525..60641886-chr7:101687189..101690169,2	MCF-7	breast:
19	chr7:101715723..101719126-chr7:101720326..101723914,4	K562	blood:
20	chr7:101627966..101630739-chr7:101669621..101671157,2	MCF-7	breast:
21	chr7:101459310..101462268-chr7:101682411..101685217,4	MCF-7	breast:
22	chr20:60640319..60642125-chr7:101687169..101688689,2	K562	blood:
23	chr7:101705153..101708097-chr7:101711212..101713863,3	K562	blood:
24	chr7:101663065..101665225-chr7:101668023..101670728,2	K562	blood:
25	chr7:101663065..101665225-chr7:101668023..101670728,2	K562	blood:
26	chr7:101645872..101649176-chr7:101651087..101654410,4	MCF-7	breast:
27	chr20:60640086..60642079-chr7:101687169..101688689,3	MCF-7	breast:
28	chr7:101647260..101647782-chr7:101656357..101656872,2	MCF-7	breast:
29	chr7:101654464..101657712-chr7:101662423..101666684,4	MCF-7	breast:
30	chr7:101652466..101655257-chr7:101700349..101702104,2	MCF-7	breast:
31	chr7:101652466..101655257-chr7:101700349..101702104,2	MCF-7	breast:
32	chr7:101717039..101718587-chr7:101722028..101724096,2	K562	blood:
33	chr7:101458593..101460129-chr7:101669075..101671130,2	MCF-7	breast:
34	chr7:101457163..101465176-chr7:101645974..101654631,24	MCF-7	breast:
35	chr7:101677836..101679461-chr7:101681645..101683380,2	K562	blood:
36	chr7:101619172..101621456-chr7:101707365..101710139,2	MCF-7	breast:
37	chr7:101657254..101660021-chr7:101660679..101662867,2	MCF-7	breast:
38	chr7:101714618..101716441-chr7:101723476..101725531,2	K562	blood:
39	chr7:101677836..101679461-chr7:101681645..101683380,2	K562	blood:
40	chr7:101525260..101527111-chr7:101652933..101654478,2	MCF-7	breast:
41	chr7:101711827..101713959-chr7:101721934..101723640,2	MCF-7	breast:
42	chr7:101458190..101460276-chr7:101714926..101717278,2	MCF-7	breast:
43	chr7:101688104..101690930-chr7:101693641..101697108,3	MCF-7	breast:
44	chr7:101647454..101647990-chr7:101665487..101666095,2	MCF-7	breast:
45	chr7:101704873..101706493-chr7:101731658..101734496,2	K562	blood:
46	chr7:101656842..101659859-chr7:101660301..101664311,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH2B2-6	chr7:101676303-101677447	ENSG00000272544.1
2	lnc-SH2B2-5	chr7:101685040-101688225	ucscGeneNc_uc003uyy_2

No data

Variant related genes	Relation type
ENSG00000272544	TF binding region
ENSG00000272544	CpG island
ENSG00000265306	chromatin interactions
ENSG00000272544	chromatin interactions
ENSG00000130699	chromatin interactions
ENSG00000257923	chromatin interactions

Extended variants
information (count: 2668 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2668 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542090985	chr7:101654061-101654062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs541259990	chr7:101654110-101654111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563475365	chr7:101654116-101654117	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144836781	chr7:101654117-101654118	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs6973714	chr7:101654120-101654121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535294095	chr7:101654127-101654128	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532569787	chr7:101654140-101654141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs111241639	chr7:101654217-101654218	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547459317	chr7:101654221-101654222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559461643	chr7:101654261-101654262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200460478	chr7:101654278-101654279	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs552706850	chr7:101654322-101654323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs35114699	chr7:101654366-101654367	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530131448	chr7:101654377-101654378	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200007540	chr7:101654400-101654401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577697046	chr7:101654401-101654402	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375854589	chr7:101654402-101654403	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542102833	chr7:101654427-101654428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375820759	chr7:101654428-101654429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569930287	chr7:101654429-101654430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140337237	chr7:101654447-101654448	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552861717	chr7:101654475-101654476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571041313	chr7:101654482-101654483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534651567	chr7:101654496-101654497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552999407	chr7:101654510-101654511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557089433	chr7:101654516-101654517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77108197	chr7:101654555-101654556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535551993	chr7:101654556-101654557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs145492665	chr7:101654557-101654558	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575420167	chr7:101654568-101654569	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545661377	chr7:101654569-101654570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564442478	chr7:101654638-101654639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573045124	chr7:101654688-101654689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541462402	chr7:101654708-101654709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572579528	chr7:101654718-101654719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71286263	chr7:101654735-101654736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs58598138	chr7:101654777-101654778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs529997971	chr7:101654782-101654783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548297195	chr7:101654811-101654812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563419668	chr7:101654812-101654813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531168182	chr7:101654850-101654851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552482653	chr7:101654855-101654856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571167174	chr7:101654908-101654909	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs573071474	chr7:101654941-101654942	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs535007415	chr7:101654950-101654951	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547273131	chr7:101654962-101654963	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185875323	chr7:101654994-101654995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs568080577	chr7:101655037-101655038	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535415527	chr7:101655050-101655051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190201036	chr7:101655064-101655065	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1762 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101578200-101671200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:101627000-101671200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:101630000-101668000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr7:101639800-101655800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:101641600-101672000	Weak transcription	K562	blood
6	chr7:101642000-101661600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr7:101642200-101666600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr7:101642200-101671400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:101642200-101671600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:101642200-101674600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr7:101642400-101661800	Weak transcription	Spleen	Spleen
12	chr7:101642400-101668000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr7:101642400-101671200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:101642400-101671400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:101642400-101675400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr7:101642800-101668000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr7:101642800-101697600	Weak transcription	Primary B cells from cord blood	blood
18	chr7:101643000-101655600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr7:101643000-101657400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:101643000-101665200	Weak transcription	Primary B cells from peripheral blood	blood
21	chr7:101643000-101672800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr7:101643000-101675600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr7:101643200-101666400	Weak transcription	Primary hematopoietic stem cells	blood
24	chr7:101644200-101661800	Weak transcription	Right Atrium	heart
25	chr7:101644400-101657400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr7:101646800-101671600	Weak transcription	GM12878-XiMat	blood
27	chr7:101647200-101662000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:101647600-101655800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:101648200-101656200	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr7:101648200-101656200	Weak transcription	Fetal Lung	lung
31	chr7:101648200-101671200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr7:101648200-101681400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:101648200-101688000	Weak transcription	Ovary	ovary
34	chr7:101648400-101656000	Weak transcription	Colon Smooth Muscle	Colon
35	chr7:101649000-101666800	Weak transcription	Fetal Muscle Leg	muscle
36	chr7:101649000-101671400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr7:101649200-101667000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr7:101649400-101666600	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr7:101649400-101672800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr7:101649600-101665000	Weak transcription	Lung	lung
41	chr7:101649800-101666800	Weak transcription	Fetal Muscle Trunk	muscle
42	chr7:101649800-101671600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:101650600-101657400	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr7:101650800-101657600	Weak transcription	Brain Germinal Matrix	brain
45	chr7:101650800-101664600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr7:101651000-101657200	Weak transcription	NHLF	lung
47	chr7:101652000-101659000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr7:101652400-101671600	Weak transcription	Pancreas	Pancrea
49	chr7:101652400-101683200	Weak transcription	Right Ventricle	heart
50	chr7:101652600-101656800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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