Variant report

Variant	nsv998298
Chromosome Location	chr1:152288685-152319877
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	CEBPB	chr1:152309377-152309634	HepG2	liver:	n/a	chr1:152309480-152309491
2	CHD2	chr1:152312110-152312163	GM12878	blood:	n/a	n/a
3	CTCF	chr1:152319740-152319890	HA-sp	spinal cord:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
4	CTCF	chr1:152319760-152319910	GM12873	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
5	CTCF	chr1:152319540-152319969	T-47D	breast:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
6	CTCF	chr1:152319700-152319850	GM12864	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
7	CTCF	chr1:152319760-152319910	HFF-Myc	foreskin:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
8	CTCF	chr1:152319720-152319870	GM12871	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
9	CTCF	chr1:152319720-152319870	AoAF	blood vessel:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
10	CTCF	chr1:152319740-152319890	HEK293	kidney:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
11	CTCF	chr1:152319740-152319890	HCPEpiC	choroid plexus:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
12	CTCF	chr1:152319700-152319850	MCF-7	breast:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
13	CTCF	chr1:152319740-152319890	GM12865	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
14	CTCF	chr1:152319647-152319950	K562	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
15	CTCF	chr1:152319720-152319870	GM12868	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
16	CTCF	chr1:152319700-152319850	AG04449	skin:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
17	CTCF	chr1:152319701-152319932	ProgFib	skin:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
18	CTCF	chr1:152319720-152319870	HRPEpiC	eye:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
19	CTCF	chr1:152319700-152319850	WI-38	lung:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
20	CTCF	chr1:152319660-152319810	BE2_C	brain:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
21	CTCF	chr1:152319709-152319930	NHEK	skin:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
22	CTCF	chr1:152319720-152319870	GM12878	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
23	CTCF	chr1:152319720-152319870	BJ	skin:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
24	CTCF	chr1:152319720-152319870	HA-sp	spinal cord:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
25	CTCF	chr1:152319481-152320056	SK-N-SH	brain:	n/a	chr1:152319961-152319982 chr1:152319789-152319807 chr1:152319790-152319806
26	CTCF	chr1:152319631-152319968	HUVEC	blood vessel:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
27	CTCF	chr1:152319740-152319890	HMF	breast:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
28	CTCF	chr1:152319681-152319980	A549	lung:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
29	CTCF	chr1:152319583-152319922	A549	lung:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
30	CTCF	chr1:152319700-152319850	GM12866	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
31	CTCF	chr1:152319760-152319910	GM12801	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
32	CTCF	chr1:152319662-152319893	SK-N-SH_RA	brain:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
33	CTCF	chr1:152319740-152319890	HBMEC	blood vessel:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
34	CTCF	chr1:152319702-152319886	SK-N-SH_RA	brain:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
35	CTCF	chr1:152319760-152319910	HCT-116	colon:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
36	CTCF	chr1:152319768-152319863	MCF-7	breast:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
37	CTCF	chr1:152319691-152319920	GM10248	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
38	CTCF	chr1:152319720-152319870	HMF	breast:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
39	CTCF	chr1:152319721-152319926	Fibrobl	skin:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
40	CTCF	chr1:152319720-152319870	AG04450	lung:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
41	CTCF	chr1:152319597-152320001	IMR90	lung:	n/a	chr1:152319961-152319982 chr1:152319789-152319807 chr1:152319790-152319806
42	CTCF	chr1:152319671-152319928	LNCaP	prostate:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
43	CTCF	chr1:152319740-152319890	Caco-2	colon:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
44	CTCF	chr1:152319663-152319910	K562	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
45	CTCF	chr1:152319720-152319870	K562	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
46	CTCF	chr1:152319700-152319850	HCM	heart:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
47	CTCF	chr1:152319760-152319910	MCF-7	breast:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
48	CTCF	chr1:152319760-152319910	GM12871	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
49	CTCF	chr1:152319740-152319890	GM12874	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806
50	CTCF	chr1:152319700-152319850	GM12870	blood:	n/a	chr1:152319789-152319807 chr1:152319790-152319806

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152298884-152298934	NHBE	bronchial:	n/a
2	chr1:152290334-152290384	LNCaP	prostate:	n/a
3	chr1:152299041-152299091	HL-60	blood:	n/a
4	chr1:152297873-152297923	HUVEC	blood vessel:	n/a
5	chr1:152299078-152299128	SK-N-SH	brain:	n/a
6	chr1:152297873-152297923	MCF-7	breast:	n/a
7	chr1:152297873-152297923	PANC-1	pancreas:	n/a
8	chr1:152298884-152298934	SK-N-SH_RA	brain:	n/a
9	chr1:152299078-152299128	HNPCEpiC	eye:	n/a
10	chr1:152299041-152299091	NB4	blood:	n/a
11	chr1:152290334-152290384	HepG2	liver:	n/a
12	chr1:152297873-152297923	GM12891	blood:	n/a
13	chr1:152290334-152290384	AG10803	skin:	n/a
14	chr1:152299078-152299128	NHDF-neo	bronchial:	n/a
15	chr1:152299041-152299091	GM12892	blood:	n/a
16	chr1:152297873-152297923	Hepatocyte	liver:	n/a
17	chr1:152299041-152299091	HIPEpiC	eye:	n/a
18	chr1:152297873-152297923	A549	lung:	n/a
19	chr1:152297873-152297923	NHBE	bronchial:	n/a
20	chr1:152299078-152299128	IMR90	lung:	fetal
21	chr1:152299041-152299091	H1-hESC	embryonic stem cell:	embryo
22	chr1:152299041-152299091	AG04449	skin:	fetal
23	chr1:152290334-152290384	PrEC	prostate:	n/a
24	chr1:152290334-152290384	SK-N-MC	brain:	n/a
25	chr1:152299078-152299128	ovcar-3	ovarian:	n/a
26	chr1:152297873-152297923	SK-N-MC	brain:	n/a
27	chr1:152290334-152290384	IMR90	lung:	fetal
28	chr1:152297873-152297923	Caco-2	colon:	n/a
29	chr1:152290334-152290384	T-47D	breast:	n/a
30	chr1:152290334-152290384	ProgFib	skin:	n/a
31	chr1:152299078-152299128	HCT-116	colon:	n/a
32	chr1:152299078-152299128	HEEpiC	esophagus:	n/a
33	chr1:152299041-152299091	GM19239	blood:	n/a
34	chr1:152297873-152297923	K562	blood:	n/a
35	chr1:152298884-152298934	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:152299078-152299128	AG09319	gingival:	n/a
37	chr1:152298884-152298934	AG09309	skin:	n/a
38	chr1:152290334-152290384	GM12878	blood:	n/a
39	chr1:152299041-152299091	HCM	heart:	n/a
40	chr1:152290334-152290384	HAEpiC	amniotic membrane:	n/a
41	chr1:152290334-152290384	Caco-2	colon:	n/a
42	chr1:152298884-152298934	PANC-1	pancreas:	n/a
43	chr1:152299078-152299128	BE2_C	brain:	n/a
44	chr1:152298884-152298934	AG04449	skin:	fetal
45	chr1:152298884-152298934	GM12878	blood:	n/a
46	chr1:152298884-152298934	AG09319	gingival:	n/a
47	chr1:152299041-152299091	AoSMC	blood vessel:	n/a
48	chr1:152290334-152290384	AG04450	lung:	fetal
49	chr1:152298884-152298934	IMR90	lung:	fetal
50	chr1:152298884-152298934	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:152297727..152299355-chr1:152302860..152305582,2	MCF-7	breast:
2	chr1:152297812..152299892-chr1:152301033..152302777,2	MCF-7	breast:
3	chr1:152319648..152320224-chr1:152423526..152424376,2	MCF-7	breast:
4	chr1:152162116..152162772-chr1:152319294..152319814,2	MCF-7	breast:
5	chr1:152162006..152163447-chr1:152318869..152320295,9	MCF-7	breast:
6	chr1:152024825..152025690-chr1:152319322..152320214,4	K562	blood:
7	chr1:152319612..152320487-chr1:152371083..152372082,2	MCF-7	breast:
8	chr1:152163614..152164697-chr1:152319285..152320275,3	MCF-7	breast:
9	chr1:152297727..152299355-chr1:152302860..152305582,2	MCF-7	breast:
10	chr1:152161155..152163543-chr1:152319469..152321157,2	MCF-7	breast:
11	chr1:152297812..152299892-chr1:152301033..152302777,2	MCF-7	breast:
12	chr1:152319630..152320287-chr1:152413308..152413947,2	MCF-7	breast:
13	chr1:152307475..152309601-chr1:152314750..152316743,2	MCF-7	breast:
14	chr1:152319690..152320209-chr1:152430662..152431472,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LCE5A-2	chr1:152305059-152305224	ENSG00000237975
2	lnc-LCE5A-2	chr1:152313563-152313686	ENSG00000237975
3	lnc-LCE5A-2	chr1:152305059-152305162	ENSG00000237975.2
4	lnc-LCE5A-2	chr1:152313563-152313686	ENSG00000237975
5	lnc-LCE5A-2	chr1:152307815-152307915	ENSG00000237975
6	lnc-LCE5A-2	chr1:152309544-152309570	ENSG00000237975
7	lnc-LCE5A-2	chr1:152310465-152310565	NONHSAT006480
8	lnc-LCE5A-2	chr1:152310465-152310565	ENSG00000237975
9	lnc-LCE5A-2	chr1:152310465-152310565	ENSG00000237975
10	lnc-LCE5A-2	chr1:152313563-152313686	NONHSAT006483
11	lnc-LCE5A-2	chr1:152307815-152307915	ENSG00000237975
12	lnc-LCE5A-2	chr1:152305059-152305224	ENSG00000237975
13	lnc-LCE5A-2	chr1:152313563-152313686	NONHSAT006480
14	lnc-LCE5A-2	chr1:152305059-152305224	NONHSAT006480
15	lnc-LCE5A-2	chr1:152313563-152313586	ENSG00000237975
16	lnc-LCE5A-2	chr1:152309544-152309570	NONHSAT006483
17	lnc-LCE5A-2	chr1:152307815-152307915	NONHSAT006480

Variant related genes	Relation type
FLG-AS1	TF binding region
FLG	TF binding region
FLG-AS1	CpG island
FLG	CpG island
ENSG00000183586	chromatin interactions
ENSG00000237975	chromatin interactions
C20orf29	miRNA target sites
DUSP6	miRNA target sites
PDSS1	miRNA target sites
SLC7A11	miRNA target sites
KIAA1530	miRNA target sites
MRPS14	miRNA target sites
SCD	miRNA target sites
SYNJ1	miRNA target sites
ABT1	miRNA target sites

Extended variants
information (count: 1004 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574108395	chr1:152288750-152288751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542983087	chr1:152288791-152288792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113217277	chr1:152288833-152288834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556649807	chr1:152288927-152288928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs3134868	chr1:152288944-152288945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569238288	chr1:152288968-152288969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530077838	chr1:152288973-152288974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368917963	chr1:152288987-152288988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150987306	chr1:152289000-152289001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75143354	chr1:152289043-152289044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75552667	chr1:152289045-152289046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565367949	chr1:152289055-152289056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538145283	chr1:152289064-152289065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542201251	chr1:152289076-152289077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560027810	chr1:152289081-152289082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140807124	chr1:152289122-152289123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527549400	chr1:152289133-152289134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75481929	chr1:152289159-152289160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373161101	chr1:152289169-152289170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77114446	chr1:152289221-152289222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150115494	chr1:152289273-152289274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554855999	chr1:152289335-152289336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552617780	chr1:152289371-152289372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565769416	chr1:152289395-152289396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534779469	chr1:152289462-152289463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77891119	chr1:152289482-152289483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201817504	chr1:152289494-152289495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs3120656	chr1:152289542-152289543	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs76385639	chr1:152289573-152289574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs3120657	chr1:152289628-152289629	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs570343734	chr1:152289635-152289636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531518604	chr1:152289656-152289657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545616518	chr1:152289697-152289698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115807046	chr1:152289730-152289731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549651421	chr1:152289731-152289732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572574910	chr1:152289758-152289759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541592027	chr1:152289793-152289794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78360904	chr1:152289812-152289813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530458226	chr1:152289852-152289853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs193022849	chr1:152289854-152289855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563559924	chr1:152289873-152289874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532521088	chr1:152289952-152289953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552404291	chr1:152290029-152290030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370976072	chr1:152290061-152290062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138451301	chr1:152290098-152290099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375129159	chr1:152290123-152290124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528271177	chr1:152290129-152290130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184980386	chr1:152290131-152290132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187421711	chr1:152290135-152290136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536978415	chr1:152290184-152290185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Atopic	22158606	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152285200-152297200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:152286200-152289200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:152286600-152322200	Weak transcription	Ovary	ovary
4	chr1:152287000-152291400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:152291400-152291600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:152291600-152291800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:152291800-152297800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:152296800-152297200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:152297200-152297600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:152297200-152297800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:152297600-152298000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:152297600-152298200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:152297600-152298200	Enhancers	HMEC	breast
14	chr1:152297800-152298200	Enhancers	NHEK	skin
15	chr1:152297800-152300000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:152298000-152301600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr1:152298200-152301000	Weak transcription	HMEC	breast
18	chr1:152298200-152301200	Weak transcription	NHEK	skin
19	chr1:152298200-152301600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:152299200-152300200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr1:152300000-152303800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:152300400-152302000	Enhancers	HSMM	muscle
23	chr1:152301000-152301800	Enhancers	HSMMtube	muscle
24	chr1:152301000-152302200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr1:152301000-152302200	Enhancers	HMEC	breast
26	chr1:152301200-152302000	Enhancers	NHEK	skin
27	chr1:152301200-152302400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:152301400-152301800	Enhancers	Placenta Amnion	Placenta Amnion
29	chr1:152301600-152301800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:152301600-152302000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:152302000-152309600	Weak transcription	Aorta	Aorta
32	chr1:152312400-152323800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr1:152314400-152317400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:152315600-152315800	Enhancers	Fetal Lung	lung
35	chr1:152316600-152317400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:152317000-152317400	Enhancers	NHEK	skin
37	chr1:152317000-152318200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr1:152317400-152331200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:152319000-152319400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr1:152319600-152320000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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