Variant report

Variant	nsv871929
Chromosome Location	chr1:103393457-103466917
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	chr1:103424463-103424755	HepG2	liver:	n/a	n/a
2	BRCA1	chr1:103436155-103436294	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr1:103420192-103420500	IMR90	lung:	n/a	chr1:103420350-103420361
4	CEBPB	chr1:103420192-103420551	H1-hESC	embryonic stem cell:	n/a	chr1:103420350-103420361
5	CEBPB	chr1:103424437-103424754	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:103457286-103457644	H1-hESC	embryonic stem cell:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
7	CEBPB	chr1:103420205-103420542	A549	lung:	n/a	chr1:103420350-103420361
8	CEBPB	chr1:103420187-103420500	HepG2	liver:	n/a	chr1:103420350-103420361
9	CEBPB	chr1:103457305-103457616	HepG2	liver:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
10	CEBPB	chr1:103463557-103463788	A549	lung:	n/a	chr1:103463691-103463704 chr1:103463691-103463702 chr1:103463691-103463702 chr1:103463712-103463725 chr1:103463691-103463704
11	CEBPB	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
12	CTCF	chr1:103436160-103436310	AG09319	gingival:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
13	CTCF	chr1:103436140-103436290	AG09319	gingival:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
14	CTCF	chr1:103436142-103436410	Gliobla	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
15	CTCF	chr1:103436437-103436466	GM20000	blood:	n/a	n/a
16	CTCF	chr1:103436188-103436416	GM12892	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
17	CTCF	chr1:103420312-103420383	GM13976	blood:	n/a	n/a
18	CTCF	chr1:103436191-103436388	GM19240	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
19	CTCF	chr1:103436140-103436290	HMF	breast:	n/a	chr1:103436238-103436256 chr1:103436233-103436254 chr1:103436240-103436253 chr1:103436239-103436255 chr1:103436243-103436251
20	CTCF	chr1:103436140-103436290	GM12878	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
21	CTCF	chr1:103436277-103436287	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:103436140-103436290	GM12864	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
23	CTCF	chr1:103436115-103436389	GM12878	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
24	CTCF	chr1:103436140-103436290	NHLF	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
25	CTCF	chr1:103436112-103436424	Medullo	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
26	CTCF	chr1:103436200-103436350	SK-N-SH_RA	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
27	CTCF	chr1:103436180-103436330	HAc	cerebellar:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
28	CTCF	chr1:103436047-103436361	A549	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
29	CTCF	chr1:103436080-103436230	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:103436112-103436368	HUVEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
31	CTCF	chr1:103436180-103436330	GM12873	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
32	CTCF	chr1:103436140-103436290	HEK293	kidney:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
33	CTCF	chr1:103436140-103436290	HPF	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
34	CTCF	chr1:103436200-103436350	HepG2	liver:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
35	CTCF	chr1:103436160-103436310	HFF-Myc	foreskin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
36	CTCF	chr1:103436220-103436370	AoAF	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
37	CTCF	chr1:103436180-103436330	GM12872	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
38	CTCF	chr1:103436500-103436650	HCM	heart:	n/a	n/a
39	CTCF	chr1:103436190-103436341	MCF-7	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
40	CTCF	chr1:103436140-103436290	AG09309	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
41	CTCF	chr1:103436140-103436290	SAEC	small airway:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
42	CTCF	chr1:103436180-103436330	WERI-Rb-1	eye:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
43	CTCF	chr1:103436146-103436396	H1-hESC	embryonic stem cell:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
44	CTCF	chr1:103436180-103436330	GM12864	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
45	CTCF	chr1:103436160-103436310	HUVEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
46	CTCF	chr1:103436112-103436394	GM10248	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
47	CTCF	chr1:103436160-103436310	AoAF	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
48	CTCF	chr1:103436140-103436290	HUVEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
49	CTCF	chr1:103436131-103436400	SK-N-SH_RA	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
50	CTCF	chr1:103436140-103436290	NHDF-neo	bronchial:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:103399388-103399438	BE2_C	brain:	n/a
2	chr1:103399388-103399438	BE2_C	brain:	n/a
3	chr1:103399388-103399438	HCM	heart:	n/a
4	chr1:103399388-103399438	MCF-7	breast:	n/a
5	chr1:103399388-103399438	IMR90	lung:	fetal
6	chr1:103399388-103399438	AG09319	gingival:	n/a
7	chr1:103399388-103399438	Jurkat	blood:	n/a
8	chr1:103399388-103399438	U87	brain:	n/a
9	chr1:103399388-103399438	Hela-S3	cervix:	n/a
10	chr1:103399388-103399438	NHBE	bronchial:	n/a
11	chr1:103399388-103399438	SK-N-SH_RA	brain:	n/a
12	chr1:103399388-103399438	AG09309	skin:	n/a
13	chr1:103399388-103399438	HIPEpiC	eye:	n/a
14	chr1:103399388-103399438	HMEC	breast:	n/a
15	chr1:103399388-103399438	ProgFib	skin:	n/a
16	chr1:103399388-103399438	HepG2	liver:	n/a
17	chr1:103399388-103399438	H1-hESC	embryonic stem cell:	embryo
18	chr1:103399388-103399438	HEK293	kidney:	embryo
19	chr1:103399388-103399438	HUVEC	blood vessel:	n/a
20	chr1:103399388-103399438	Caco-2	colon:	n/a
21	chr1:103399388-103399438	GM12878	blood:	n/a
22	chr1:103399388-103399438	SAEC	small airway:	n/a
23	chr1:103399388-103399438	SK-N-SH	brain:	n/a
24	chr1:103399388-103399438	NB4	blood:	n/a
25	chr1:103399388-103399438	HCF	heart:	n/a
26	chr1:103399388-103399438	HAEpiC	amniotic membrane:	n/a
27	chr1:103399388-103399438	BJ	skin:	n/a
28	chr1:103399388-103399438	ovcar-3	ovarian:	n/a
29	chr1:103399388-103399438	NT2-D1	testis:	n/a
30	chr1:103399388-103399438	RPTEC	kidney:	n/a
31	chr1:103399388-103399438	SKMC	muscle:	n/a
32	chr1:103399388-103399438	NHDF-neo	bronchial:	n/a
33	chr1:103399388-103399438	AG04450	lung:	fetal
34	chr1:103399388-103399438	K562	blood:	n/a
35	chr1:103399388-103399438	HNPCEpiC	eye:	n/a
36	chr1:103399388-103399438	AoSMC	blood vessel:	n/a
37	chr1:103399388-103399438	MCF10A-Er-Src	breast:	n/a
38	chr1:103399388-103399438	T-47D	breast:	n/a
39	chr1:103399388-103399438	AG04449	skin:	fetal
40	chr1:103399388-103399438	PrEC	prostate:	n/a
41	chr1:103399388-103399438	GM19239	blood:	n/a
42	chr1:103399388-103399438	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:103399388-103399438	HCT-116	colon:	n/a
44	chr1:103399388-103399438	PFSK-1	brain:	n/a
45	chr1:103399388-103399438	HL-60	blood:	n/a
46	chr1:103399388-103399438	GM12891	blood:	n/a
47	chr1:103399388-103399438	SK-N-MC	brain:	n/a
48	chr1:103399388-103399438	LNCaP	prostate:	n/a
49	chr1:103399388-103399438	ECC-1	luminal epithelium:	n/a
50	chr1:103399388-103399438	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:103259174..103259873-chr1:103435676..103436665,2	MCF-7	breast:
2	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
3	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
4	chr1:103303886..103305574-chr1:103404633..103406434,2	MCF-7	breast:
5	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:
6	chr1:103016225..103017019-chr1:103436153..103436688,2	MCF-7	breast:
7	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:

Variant related genes	Relation type
COL11A1	TF binding region
COL11A1	CpG island

Extended variants
information (count: 3047 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3047 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12138977	chr1:103393457-103393458	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542436646	chr1:103393509-103393510	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs149306338	chr1:103393525-103393526	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs191553164	chr1:103393538-103393539	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs370798351	chr1:103393554-103393555	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs546557211	chr1:103393556-103393557	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs568394367	chr1:103393629-103393630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532140507	chr1:103393637-103393638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183742591	chr1:103393639-103393640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568993806	chr1:103393653-103393654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199552225	chr1:103393659-103393660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534926019	chr1:103393673-103393674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536805198	chr1:103393692-103393693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528080738	chr1:103393702-103393703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527661485	chr1:103393703-103393704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548833806	chr1:103393728-103393729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567146284	chr1:103393735-103393736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143545111	chr1:103393753-103393754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558902629	chr1:103393762-103393763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190024903	chr1:103393763-103393764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35876926	chr1:103393802-103393803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148072148	chr1:103393813-103393814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574611150	chr1:103393858-103393859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542399825	chr1:103393911-103393912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560779190	chr1:103393947-103393948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs61813929	chr1:103394014-103394015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572800037	chr1:103394026-103394027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs61812677	chr1:103394039-103394040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12729158	chr1:103394058-103394059	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs7418985	chr1:103394078-103394079	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs531982244	chr1:103394080-103394081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550564524	chr1:103394090-103394091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529617596	chr1:103394098-103394099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562554635	chr1:103394107-103394108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541344271	chr1:103394115-103394116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138515643	chr1:103394119-103394120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548797159	chr1:103394127-103394128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567109543	chr1:103394145-103394146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192711047	chr1:103394179-103394180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560132351	chr1:103394191-103394192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552547890	chr1:103394203-103394204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71483859	chr1:103394234-103394235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9433948	chr1:103394235-103394236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12125205	chr1:103394253-103394254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12043753	chr1:103394264-103394265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568195274	chr1:103394281-103394282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9434371	chr1:103394360-103394361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554337127	chr1:103394371-103394372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368314403	chr1:103394441-103394442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199728852	chr1:103394477-103394478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103352600-103403200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr1:103369600-103498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:103378800-103400000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:103380000-103399000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:103381200-103399400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:103385800-103401000	Weak transcription	HSMM	muscle
7	chr1:103386000-103407000	Weak transcription	NH-A	brain
8	chr1:103386200-103399600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:103386200-103482000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:103387000-103394400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:103392800-103394200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:103392800-103394200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:103393000-103393600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:103393000-103394200	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr1:103393400-103393600	Flanking Active TSS	Osteobl	bone
16	chr1:103393600-103399200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:103394200-103399000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:103394200-103399000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr1:103394200-103399000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:103394400-103395000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:103395000-103395200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:103395200-103397800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:103397800-103399400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:103397800-103414200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:103398600-103407200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr1:103399000-103400200	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr1:103399000-103400400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:103399000-103401400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:103399000-103404000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:103399200-103399400	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr1:103399200-103400000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr1:103399200-103400800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:103399400-103399600	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr1:103399400-103399600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr1:103399400-103400200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr1:103399400-103400800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr1:103399400-103406800	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr1:103399600-103400200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr1:103399600-103400200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:103399600-103406800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr1:103400000-103400200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:103400000-103400200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr1:103400000-103400200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
44	chr1:103400000-103402800	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr1:103400200-103402800	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr1:103400200-103403000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr1:103400200-103403000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr1:103400200-103424400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:103400200-103444200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:103400200-103462000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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