Variant report

Variant	nsv428741
Chromosome Location	chr1:63422898-63601892
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	chr1:63481440-63481604	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:63590486-63590731	HepG2	liver:	n/a	n/a
3	ATF1	chr1:63587751-63588059	K562	blood:	n/a	n/a
4	ATF1	chr1:63484955-63485026	K562	blood:	n/a	n/a
5	ATF2	chr1:63428776-63429288	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:63590467-63590998	GM12878	blood:	n/a	n/a
7	BACH1	chr1:63428271-63428287	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:63537254-63537322	K562	blood:	n/a	n/a
9	BACH1	chr1:63579632-63579680	K562	blood:	n/a	n/a
10	BACH1	chr1:63428891-63429167	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:63440161-63440368	H1-hESC	embryonic stem cell:	n/a	chr1:63440282-63440296
12	BACH1	chr1:63456994-63457178	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:63466234-63466493	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr1:63590597-63590889	GM12878	blood:	n/a	chr1:63590757-63590768
15	BATF	chr1:63577806-63578119	GM12878	blood:	n/a	chr1:63577996-63578007
16	BATF	chr1:63429884-63430168	GM12878	blood:	n/a	n/a
17	BATF	chr1:63590547-63590922	GM12878	blood:	n/a	chr1:63590757-63590768
18	BATF	chr1:63587637-63587852	GM12878	blood:	n/a	chr1:63587748-63587757
19	BCL11A	chr1:63429876-63430152	GM12878	blood:	n/a	n/a
20	BCL3	chr1:63577822-63578069	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:63429717-63429989	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:63429013-63429213	GM12878	blood:	n/a	n/a
23	CEBPB	chr1:63505250-63505503	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:63534263-63534632	MCF-7	breast:	n/a	chr1:63534436-63534447
25	CEBPB	chr1:63534250-63534639	K562	blood:	n/a	chr1:63534436-63534447
26	CEBPB	chr1:63534262-63534633	IMR90	lung:	n/a	chr1:63534436-63534447
27	CEBPB	chr1:63534243-63534633	H1-hESC	embryonic stem cell:	n/a	chr1:63534436-63534447
28	CEBPB	chr1:63464467-63464566	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:63581728-63582049	HepG2	liver:	n/a	chr1:63581895-63581906
30	CEBPB	chr1:63534316-63534620	K562	blood:	n/a	chr1:63534436-63534447
31	CEBPB	chr1:63453782-63454125	HepG2	liver:	n/a	chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453961-63453970 chr1:63453959-63453970 chr1:63453961-63453972 chr1:63453961-63453970 chr1:63453961-63453972 chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453959-63453972
32	CEBPB	chr1:63581742-63582046	IMR90	lung:	n/a	chr1:63581895-63581906
33	CEBPB	chr1:63534281-63534632	Hela-S3	cervix:	n/a	chr1:63534436-63534447
34	CEBPB	chr1:63453811-63454119	H1-hESC	embryonic stem cell:	n/a	chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453961-63453970 chr1:63453959-63453970 chr1:63453961-63453972 chr1:63453961-63453970 chr1:63453961-63453972 chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453959-63453972
35	CEBPB	chr1:63453797-63454140	K562	blood:	n/a	chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453961-63453970 chr1:63453959-63453970 chr1:63453961-63453972 chr1:63453961-63453970 chr1:63453961-63453972 chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453959-63453972
36	CEBPB	chr1:63453863-63454097	MCF-7	breast:	n/a	chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453961-63453970 chr1:63453959-63453970 chr1:63453961-63453972 chr1:63453961-63453970 chr1:63453961-63453972 chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453959-63453972
37	CEBPB	chr1:63581788-63582013	H1-hESC	embryonic stem cell:	n/a	chr1:63581895-63581906
38	CEBPB	chr1:63428949-63429210	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr1:63429489-63429689	HepG2	liver:	n/a	chr1:63429658-63429669 chr1:63429658-63429669 chr1:63429658-63429671
40	CEBPB	chr1:63561439-63561611	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:63477915-63478408	HepG2	liver:	n/a	chr1:63477920-63477933
42	CEBPB	chr1:63453824-63454136	A549	lung:	n/a	chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453961-63453970 chr1:63453959-63453970 chr1:63453961-63453972 chr1:63453961-63453970 chr1:63453961-63453972 chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453959-63453972
43	CEBPB	chr1:63429002-63429160	K562	blood:	n/a	n/a
44	CEBPB	chr1:63498933-63499138	K562	blood:	n/a	n/a
45	CEBPB	chr1:63534198-63534701	A549	lung:	n/a	chr1:63534436-63534447
46	CEBPB	chr1:63534329-63534632	MCF-7	breast:	n/a	chr1:63534436-63534447
47	CEBPB	chr1:63434166-63434366	HepG2	liver:	n/a	chr1:63434326-63434337
48	CEBPB	chr1:63534273-63534628	A549	lung:	n/a	chr1:63534436-63534447
49	CEBPB	chr1:63534241-63534606	ECC-1	luminal epithelium:	n/a	chr1:63534436-63534447
50	CEBPB	chr1:63464426-63464723	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:63539873-63539923	T-47D	breast:	n/a
2	chr1:63539873-63539923	T-47D	breast:	n/a
3	chr1:63540205-63540255	AoSMC	blood vessel:	n/a
4	chr1:63540205-63540255	HAEpiC	amniotic membrane:	n/a
5	chr1:63540217-63540267	MCF-7	breast:	n/a
6	chr1:63539873-63539923	NT2-D1	testis:	n/a
7	chr1:63540205-63540255	HCPEpiC	choroid plexus:	n/a
8	chr1:63539613-63539663	T-47D	breast:	n/a
9	chr1:63539613-63539663	GM12878	blood:	n/a
10	chr1:63539729-63539779	ovcar-3	ovarian:	n/a
11	chr1:63539613-63539663	LNCaP	prostate:	n/a
12	chr1:63539729-63539779	Hela-S3	cervix:	n/a
13	chr1:63540217-63540267	SAEC	small airway:	n/a
14	chr1:63466707-63466757	H1-hESC	embryonic stem cell:	embryo
15	chr1:63571356-63571406	SAEC	small airway:	n/a
16	chr1:63466707-63466757	GM12891	blood:	n/a
17	chr1:63429038-63429088	HepG2	liver:	n/a
18	chr1:63539613-63539663	BE2_C	brain:	n/a
19	chr1:63571356-63571406	HAEpiC	amniotic membrane:	n/a
20	chr1:63429038-63429088	AG09319	gingival:	n/a
21	chr1:63457296-63457346	ProgFib	skin:	n/a
22	chr1:63457296-63457346	H1-hESC	embryonic stem cell:	embryo
23	chr1:63540205-63540255	HCM	heart:	n/a
24	chr1:63466707-63466757	HRCEpiC	kidney:	n/a
25	chr1:63466707-63466757	ProgFib	skin:	n/a
26	chr1:63540205-63540255	PANC-1	pancreas:	n/a
27	chr1:63457296-63457346	PANC-1	pancreas:	n/a
28	chr1:63464679-63464729	PANC-1	pancreas:	n/a
29	chr1:63540217-63540267	GM12892	blood:	n/a
30	chr1:63540205-63540255	MCF10A-Er-Src	breast:	n/a
31	chr1:63539729-63539779	NHDF-neo	bronchial:	n/a
32	chr1:63571356-63571406	U87	brain:	n/a
33	chr1:63540205-63540255	HIPEpiC	eye:	n/a
34	chr1:63464679-63464729	SAEC	small airway:	n/a
35	chr1:63540205-63540255	Hepatocyte	liver:	n/a
36	chr1:63540217-63540267	HAEpiC	amniotic membrane:	n/a
37	chr1:63539729-63539779	AG09309	skin:	n/a
38	chr1:63540217-63540267	PrEC	prostate:	n/a
39	chr1:63571356-63571406	MCF-7	breast:	n/a
40	chr1:63464679-63464729	HMEC	breast:	n/a
41	chr1:63429038-63429088	Hepatocyte	liver:	n/a
42	chr1:63539873-63539923	ovcar-3	ovarian:	n/a
43	chr1:63571356-63571406	SK-N-SH_RA	brain:	n/a
44	chr1:63540217-63540267	Jurkat	blood:	n/a
45	chr1:63464679-63464729	NHDF-neo	bronchial:	n/a
46	chr1:63539729-63539779	HepG2	liver:	n/a
47	chr1:63540217-63540267	ovcar-3	ovarian:	n/a
48	chr1:63539613-63539663	HCPEpiC	choroid plexus:	n/a
49	chr1:63571356-63571406	HNPCEpiC	eye:	n/a
50	chr1:63540217-63540267	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:63306962..63307948-chr1:63455117..63455729,2	MCF-7	breast:
2	chr1:63460944..63463320-chr1:63464866..63467278,2	MCF-7	breast:
3	chr1:63459871..63461877-chr1:63466416..63469144,2	K562	blood:
4	chr1:63465009..63465619-chr4:18102338..18103085,2	MCF-7	breast:
5	chr1:63449158..63452125-chr1:63453992..63456042,2	K562	blood:
6	chr1:63459764..63462718-chr1:63464961..63468406,4	K562	blood:
7	chr1:63470306..63471213-chr1:63614433..63615672,4	MCF-7	breast:
8	chr1:63563848..63566657-chr1:63583740..63586220,2	K562	blood:
9	chr1:63577832..63580180-chr1:63617272..63619794,2	MCF-7	breast:
10	chr1:63425794..63427328-chr1:63429160..63430808,2	K562	blood:
11	chr1:63459764..63462718-chr1:63464961..63468406,4	K562	blood:
12	chr1:63449158..63452125-chr1:63453992..63456042,2	K562	blood:
13	chr1:63514661..63516542-chr1:63519183..63521519,2	K562	blood:
14	chr1:63460944..63463320-chr1:63464866..63467278,2	MCF-7	breast:
15	chr1:63459871..63461877-chr1:63466416..63469144,2	K562	blood:
16	chr1:63514661..63516542-chr1:63519183..63521519,2	K562	blood:
17	chr1:63425794..63427328-chr1:63429160..63430808,2	K562	blood:
18	chr1:63410664..63413172-chr1:63421317..63423276,2	K562	blood:
19	chr1:63563848..63566657-chr1:63583740..63586220,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK7-5	chr1:63436975-63437279	ucscGeneNc_uc001daw_1
2	lnc-DOCK7-5	chr1:63428699-63428783	ucscGeneNc_uc001daw_1
3	lnc-DOCK7-5	chr1:63496244-63496309	ucscGeneNc_uc001daw_1
4	lnc-DOCK7-1	chr1:63466168-63466474	XLOC_000857
5	lnc-DOCK7-5	chr1:63554208-63554346	ucscGeneNc_uc001daw_1
6	lnc-ITGB3BP-9	chr1:63559559-63559722	l_68_chr1:63559140-63560715_76bGuttman_hES
7	lnc-ITGB3BP-9	chr1:63559884-63560203	l_68_chr1:63559140-63560715_76bGuttman_hES
8	lnc-DOCK7-1	chr1:63466168-63466474	XLOC_000857
9	lnc-DOCK7-5	chr1:63542954-63543005	ucscGeneNc_uc001daw_1
10	lnc-DOCK7-1	chr1:63476757-63476939	XLOC_000857
11	lnc-DOCK7-5	chr1:63555317-63555489	ucscGeneNc_uc001daw_1
12	lnc-DOCK7-4	chr1:63520365-63520399	NONHSAT003652
13	lnc-ATG4C-3	chr1:63491075-63491329	XLOC_000230
14	lnc-ITGB3BP-3	chr1:63544571-63544702	ENSG00000229225
15	lnc-ITGB3BP-9	chr1:63560575-63560715	l_68_chr1:63559140-63560715_76bGuttman_hES
16	lnc-ITGB3BP-9	chr1:63559141-63559449	l_68_chr1:63559140-63560715_76bGuttman_hES
17	lnc-ITGB3BP-3	chr1:63543752-63543776	ENSG00000229225
18	lnc-ATG4C-3	chr1:63489878-63489981	XLOC_000230
19	lnc-ATG4C-3	chr1:63488282-63488719	NONHSAT003650
20	lnc-DOCK7-1	chr1:63466168-63466474	XLOC_000857
21	lnc-DOCK7-4	chr1:63519904-63520265	NONHSAT003652
22	lnc-ATG4C-3	chr1:63489715-63490030	NONHSAT003650
23	lnc-DOCK7-1	chr1:63476549-63476596	XLOC_000857
24	lnc-DOCK7-1	chr1:63478005-63478142	XLOC_000857

Variant related genes	Relation type
ENSG00000203605	TF binding region
ENSG00000227485	TF binding region
ENSG00000229225	TF binding region
ENSG00000229537	TF binding region
ENSG00000203605	CpG island
ENSG00000227485	CpG island
ENSG00000229225	CpG island
ENSG00000229537	CpG island
CHSY1	miRNA target sites

Extended variants
information (count: 5044 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:5044 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1191758	chr1:63422910-63422911	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537635419	chr1:63422915-63422916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141934593	chr1:63422944-63422945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571082013	chr1:63422962-63422963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535009076	chr1:63422994-63422995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201747533	chr1:63423029-63423030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552907901	chr1:63423059-63423060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191438961	chr1:63423100-63423101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539338634	chr1:63423155-63423156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs665958	chr1:63423172-63423173	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs61150003	chr1:63423181-63423182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549578765	chr1:63423184-63423185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560163917	chr1:63423206-63423207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369192435	chr1:63423262-63423263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150679315	chr1:63423264-63423265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12039553	chr1:63423307-63423308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545584610	chr1:63423391-63423392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs60582562	chr1:63423411-63423412	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183357763	chr1:63423440-63423441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188041759	chr1:63423471-63423472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528694348	chr1:63423502-63423503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192867556	chr1:63423643-63423644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530021708	chr1:63423679-63423680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571932099	chr1:63423723-63423724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs60107830	chr1:63423742-63423743	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs570152685	chr1:63423744-63423745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185388439	chr1:63423825-63423826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552756145	chr1:63423856-63423857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144681786	chr1:63423863-63423864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535292107	chr1:63423926-63423927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569883304	chr1:63423984-63423985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147904752	chr1:63423986-63423987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535079799	chr1:63424003-63424004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547009971	chr1:63424040-63424041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74079339	chr1:63424091-63424092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574954657	chr1:63424099-63424100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542722060	chr1:63424289-63424290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138186652	chr1:63424290-63424291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545498581	chr1:63424387-63424388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557494338	chr1:63424392-63424393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115667127	chr1:63424393-63424394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540448814	chr1:63424434-63424435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576188262	chr1:63424443-63424444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561832059	chr1:63424481-63424482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192848687	chr1:63424500-63424501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539115493	chr1:63424504-63424505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542201790	chr1:63424557-63424558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139844412	chr1:63424574-63424575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184822247	chr1:63424604-63424605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543173039	chr1:63424633-63424634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:63419200-63429200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:63421600-63427400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr1:63425600-63427200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:63426800-63429000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr1:63426800-63429800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:63427200-63427400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:63427400-63428800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:63427400-63429800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr1:63427600-63429400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr1:63427600-63434200	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr1:63427800-63428000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:63427800-63429000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr1:63427800-63429000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr1:63427800-63429400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr1:63427800-63429600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:63427800-63429600	Enhancers	Duodenum Mucosa	Duodenum
17	chr1:63427800-63430600	Enhancers	Fetal Muscle Leg	muscle
18	chr1:63428000-63428800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:63428000-63430600	Weak transcription	Right Atrium	heart
20	chr1:63428200-63429000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:63428200-63429200	Enhancers	Fetal Intestine Small	intestine
22	chr1:63428200-63429400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr1:63428200-63429400	Enhancers	Fetal Intestine Large	intestine
24	chr1:63428200-63429800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr1:63428600-63429000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:63428600-63429400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:63428600-63429400	Enhancers	Stomach Mucosa	stomach
28	chr1:63428600-63429800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:63428800-63429000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:63428800-63429000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:63428800-63429000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr1:63428800-63429400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:63428800-63430400	Enhancers	Fetal Muscle Trunk	muscle
34	chr1:63429000-63429200	Enhancers	HepG2	liver
35	chr1:63429000-63430200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:63429000-63431000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr1:63429000-63432400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr1:63429200-63429400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:63429400-63430400	Enhancers	GM12878-XiMat	blood
40	chr1:63429400-63432200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr1:63429400-63432400	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr1:63429800-63432400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr1:63430200-63430400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:63430400-63432400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:63431400-63431600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr1:63432200-63432600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr1:63432400-63432600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr1:63432400-63432600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr1:63432400-63433200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr1:63432600-63433200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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