Variant report

Variant	nsv463317
Chromosome Location	chr1:120107602-120162787
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1110)
CpG islands
(count:122)
Chromatin interactive
region (count:34)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1110 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:120156546-120156764	HepG2	liver:	n/a	n/a
2	ATF1	chr1:120125462-120125747	K562	blood:	n/a	n/a
3	ATF1	chr1:120151890-120151896	K562	blood:	n/a	n/a
4	ATF1	chr1:120157910-120157934	K562	blood:	n/a	n/a
5	ATF3	chr1:120154276-120154532	K562	blood:	n/a	n/a
6	ATF3	chr1:120154165-120154614	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr1:120156447-120156806	K562	blood:	n/a	n/a
8	BHLHE40	chr1:120156467-120156621	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:120154235-120154668	K562	blood:	n/a	n/a
10	BHLHE40	chr1:120156581-120156796	A549	lung:	n/a	n/a
11	BRCA1	chr1:120156426-120156738	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr1:120156588-120156779	HepG2	liver:	n/a	n/a
13	BRCA1	chr1:120125543-120125709	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:120154268-120154461	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:120144744-120145076	A549	lung:	n/a	chr1:120144889-120144900
16	CEBPB	chr1:120152140-120152301	H1-hESC	embryonic stem cell:	n/a	chr1:120152213-120152224
17	CEBPB	chr1:120144741-120145077	HepG2	liver:	n/a	chr1:120144889-120144900
18	CEBPB	chr1:120112719-120112961	K562	blood:	n/a	chr1:120112801-120112814
19	CEBPB	chr1:120144827-120145081	Hela-S3	cervix:	n/a	chr1:120144889-120144900
20	CEBPB	chr1:120152150-120152238	K562	blood:	n/a	chr1:120152213-120152224
21	CEBPB	chr1:120107540-120107630	K562	blood:	n/a	chr1:120107566-120107577 chr1:120107585-120107598
22	CEBPB	chr1:120112658-120112932	K562	blood:	n/a	chr1:120112801-120112814
23	CEBPB	chr1:120144888-120144965	H1-hESC	embryonic stem cell:	n/a	chr1:120144889-120144900
24	CEBPB	chr1:120107417-120107689	HepG2	liver:	n/a	chr1:120107566-120107577 chr1:120107585-120107598
25	CEBPB	chr1:120152171-120152183	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:120123093-120123321	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:120142586-120142702	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr1:120156604-120156671	GM12878	blood:	n/a	n/a
29	CHD2	chr1:120154302-120154481	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr1:120154059-120154552	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr1:120156617-120156737	K562	blood:	n/a	n/a
32	CHD2	chr1:120156558-120156728	GM12878	blood:	n/a	n/a
33	CTCF	chr1:120125840-120125990	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr1:120125560-120125710	HBMEC	blood vessel:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
35	CTCF	chr1:120156540-120156690	GM12866	blood:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
36	CTCF	chr1:120112900-120113050	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr1:120156540-120156690	HEK293	kidney:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578
38	CTCF	chr1:120154320-120154470	GM12869	blood:	n/a	chr1:120154411-120154432
39	CTCF	chr1:120112970-120113169	Pancreas_OC	pancreas:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
40	CTCF	chr1:120154300-120154450	AG04450	lung:	n/a	chr1:120154411-120154432
41	CTCF	chr1:120125525-120125733	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
42	CTCF	chr1:120150101-120150380	MCF-7	breast:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
43	CTCF	chr1:120125459-120125732	GM20000	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
44	CTCF	chr1:120125394-120125831	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
45	CTCF	chr1:120154217-120154549	HepG2	liver:	n/a	chr1:120154411-120154432
46	CTCF	chr1:120112900-120113050	AG04450	lung:	n/a	n/a
47	CTCF	chr1:120150110-120150383	GM12878	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
48	CTCF	chr1:120112964-120113194	ProgFib	skin:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
49	CTCF	chr1:120154320-120154470	WI-38	lung:	n/a	chr1:120154411-120154432
50	CTCF	chr1:120156443-120156683	ProgFib	skin:	n/a	chr1:120156563-120156584 chr1:120156564-120156577 chr1:120156562-120156578

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120156779-120156829	ProgFib	skin:	n/a
2	chr1:120156779-120156829	AG04450	lung:	fetal
3	chr1:120143242-120143292	AoSMC	blood vessel:	n/a
4	chr1:120156779-120156829	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:120143242-120143292	NHBE	bronchial:	n/a
6	chr1:120143242-120143292	HRE	kidney:	n/a
7	chr1:120156779-120156829	HEK293	kidney:	embryo
8	chr1:120156779-120156829	Hepatocyte	liver:	n/a
9	chr1:120156779-120156829	HUVEC	blood vessel:	n/a
10	chr1:120156779-120156829	ovcar-3	ovarian:	n/a
11	chr1:120156779-120156829	Jurkat	blood:	n/a
12	chr1:120143242-120143292	HIPEpiC	eye:	n/a
13	chr1:120143242-120143292	HCPEpiC	choroid plexus:	n/a
14	chr1:120143242-120143292	PANC-1	pancreas:	n/a
15	chr1:120156779-120156829	GM19239	blood:	n/a
16	chr1:120156779-120156829	SK-N-SH	brain:	n/a
17	chr1:120143242-120143292	U87	brain:	n/a
18	chr1:120156779-120156829	HRCEpiC	kidney:	n/a
19	chr1:120156779-120156829	BE2_C	brain:	n/a
20	chr1:120143242-120143292	SK-N-SH_RA	brain:	n/a
21	chr1:120156779-120156829	HCF	heart:	n/a
22	chr1:120156779-120156829	PrEC	prostate:	n/a
23	chr1:120143242-120143292	SAEC	small airway:	n/a
24	chr1:120143242-120143292	SK-N-MC	brain:	n/a
25	chr1:120156779-120156829	SK-N-SH_RA	brain:	n/a
26	chr1:120143242-120143292	HepG2	liver:	n/a
27	chr1:120143242-120143292	LNCaP	prostate:	n/a
28	chr1:120156779-120156829	RPTEC	kidney:	n/a
29	chr1:120156779-120156829	AG04449	skin:	fetal
30	chr1:120143242-120143292	HMEC	breast:	n/a
31	chr1:120156779-120156829	HCPEpiC	choroid plexus:	n/a
32	chr1:120156779-120156829	HEEpiC	esophagus:	n/a
33	chr1:120143242-120143292	HL-60	blood:	n/a
34	chr1:120143242-120143292	GM19239	blood:	n/a
35	chr1:120156779-120156829	K562	blood:	n/a
36	chr1:120143242-120143292	HAEpiC	amniotic membrane:	n/a
37	chr1:120156779-120156829	MCF-7	breast:	n/a
38	chr1:120143242-120143292	HCF	heart:	n/a
39	chr1:120156779-120156829	NH-A	brain:	n/a
40	chr1:120143242-120143292	Hepatocyte	liver:	n/a
41	chr1:120156779-120156829	NHBE	bronchial:	n/a
42	chr1:120156779-120156829	T-47D	breast:	n/a
43	chr1:120156779-120156829	SKMC	muscle:	n/a
44	chr1:120156779-120156829	HCM	heart:	n/a
45	chr1:120143242-120143292	NHDF-neo	bronchial:	n/a
46	chr1:120143242-120143292	AG04450	lung:	fetal
47	chr1:120156779-120156829	BJ	skin:	n/a
48	chr1:120156779-120156829	GM12891	blood:	n/a
49	chr1:120156779-120156829	PFSK-1	brain:	n/a
50	chr1:120143242-120143292	HEK293	kidney:	embryo

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
2	chr1:119914912..119915700-chr1:120154301..120154847,3	MCF-7	breast:
3	chr1:120156154..120156980-chr1:120205229..120206054,4	MCF-7	breast:
4	chr1:120091982..120092950-chr1:120156090..120157044,3	MCF-7	breast:
5	chr1:120154024..120154620-chr1:120217678..120218364,2	MCF-7	breast:
6	chr1:120160558..120163551-chr1:120189552..120191710,2	MCF-7	breast:
7	chr1:120161786..120164966-chr1:120184691..120189749,4	K562	blood:
8	chr1:120162586..120166440-chr1:120167182..120171199,5	K562	blood:
9	chr1:120154003..120154965-chr1:120217033..120218809,10	K562	blood:
10	chr1:120153709..120155634-chr1:120202418..120204087,2	MCF-7	breast:
11	chr1:120091982..120092921-chr1:120150180..120150935,3	MCF-7	breast:
12	chr1:120156759..120158613-chr1:120204611..120207456,2	MCF-7	breast:
13	chr1:120154731..120156704-chr1:120158612..120160451,2	MCF-7	breast:
14	chr1:120151431..120154337-chr1:120190081..120192940,2	MCF-7	breast:
15	chr1:120156408..120157049-chr1:120218285..120218819,2	MCF-7	breast:
16	chr1:120161786..120164966-chr1:120187188..120189749,3	K562	blood:
17	chr1:120156097..120157073-chr1:120205512..120206469,8	MCF-7	breast:
18	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
19	chr1:120154067..120155007-chr1:120217498..120218673,7	MCF-7	breast:
20	chr1:120154731..120156704-chr1:120158612..120160451,2	MCF-7	breast:
21	chr1:120162086..120165079-chr1:120173514..120175556,2	MCF-7	breast:
22	chr1:120153476..120155640-chr1:120190161..120192811,2	K562	blood:
23	chr1:120125200..120126107-chr1:120217588..120218409,3	K562	blood:
24	chr1:120156150..120157072-chr1:120189041..120189869,2	MCF-7	breast:
25	chr1:120155133..120157085-chr1:120217009..120218744,10	K562	blood:
26	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
27	chr1:120154194..120154867-chr1:120205886..120206437,3	MCF-7	breast:
28	chr1:120156082..120157034-chr1:120205464..120206953,8	K562	blood:
29	chr1:120154324..120155309-chr1:120205532..120206464,6	MCF-7	breast:
30	chr1:120161780..120163387-chr1:120165272..120166902,2	MCF-7	breast:
31	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
32	chr1:120158069..120159004-chr1:120217770..120218396,2	K562	blood:
33	chr1:120156126..120157196-chr1:120217116..120218704,11	MCF-7	breast:
34	chr1:120159569..120162052-chr1:120189415..120191074,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF697-2	chr1:120162038-120164121	NONHSAT005572
2	lnc-PHGDH-1	chr1:120144910-120145118	ENSG00000242959.1
3	lnc-ZNF697-3	chr1:120111655-120111668	NONHSAT005569
4	lnc-ZNF697-1	chr1:120140325-120141914	NONHSAT005570
5	lnc-ZNF697-3	chr1:120148999-120149695	NONHSAT005569
6	lnc-ZNF697-1	chr1:120140325-120141894	ENSG00000260941.1
7	lnc-PHGDH-1	chr1:120143780-120144107	ENSG00000242959.1

No data

Variant related genes	Relation type
HSD3BP4	TF binding region
LINC00622	TF binding region
GAPDHP33	TF binding region
HSD3BP5	TF binding region
HSD3BP4	CpG island
LINC00622	CpG island
GAPDHP33	CpG island
HSD3BP5	CpG island
ENSG00000143067	chromatin interactions
ENSG00000092621	chromatin interactions

Extended variants
information (count: 2494 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2494 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10494226	chr1:120107602-120107603	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587631269	chr1:120107667-120107668	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375340837	chr1:120107704-120107705	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74729199	chr1:120107705-120107706	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150555468	chr1:120107713-120107714	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587647124	chr1:120107725-120107726	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188821699	chr1:120107750-120107751	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190857278	chr1:120107811-120107812	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs12754284	chr1:120107828-120107829	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs182279796	chr1:120107833-120107834	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs186870388	chr1:120107843-120107844	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs587610660	chr1:120107844-120107845	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs118134378	chr1:120107900-120107901	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs139794491	chr1:120107952-120107953	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs191604872	chr1:120107963-120107964	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs74506250	chr1:120107982-120107983	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs587752042	chr1:120108104-120108105	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs587647927	chr1:120108120-120108121	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs149788445	chr1:120108133-120108134	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs34178115	chr1:120108145-120108146	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs35485231	chr1:120108156-120108157	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs587756987	chr1:120108270-120108271	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs184085258	chr1:120108320-120108321	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs587687465	chr1:120108326-120108327	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs587751552	chr1:120108357-120108358	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs587646990	chr1:120108367-120108368	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs587726572	chr1:120108371-120108372	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs587760041	chr1:120108390-120108391	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs10923862	chr1:120108452-120108453	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs145710900	chr1:120108477-120108478	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs12563561	chr1:120108501-120108502	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs112366213	chr1:120108549-120108550	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs587722975	chr1:120108565-120108566	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs587642390	chr1:120108572-120108573	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs587715922	chr1:120108587-120108588	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs587615311	chr1:120108613-120108614	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs587694949	chr1:120108745-120108746	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs587598485	chr1:120108810-120108811	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs587752025	chr1:120108839-120108840	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs139869168	chr1:120108850-120108851	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs145706184	chr1:120108854-120108855	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs147741650	chr1:120108870-120108871	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs188639596	chr1:120108909-120108910	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs142608063	chr1:120108928-120108929	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs587749034	chr1:120108934-120108935	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs587622447	chr1:120108957-120108958	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs392532	chr1:120108969-120108970	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs587702006	chr1:120108981-120108982	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs74114703	chr1:120108992-120108993	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs587654777	chr1:120109023-120109024	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	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
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	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Cancer	21272361	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120092800-120116600	Weak transcription	Spleen	Spleen
2	chr1:120105000-120108000	Enhancers	Fetal Lung	lung
3	chr1:120105000-120108800	Enhancers	Fetal Intestine Large	intestine
4	chr1:120105200-120108600	Enhancers	Fetal Intestine Small	intestine
5	chr1:120106800-120108600	Weak transcription	Ovary	ovary
6	chr1:120106800-120111600	Weak transcription	Lung	lung
7	chr1:120106800-120112400	Enhancers	Placenta	Placenta
8	chr1:120107000-120109200	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr1:120107000-120109200	Enhancers	Primary B cells from peripheral blood	blood
10	chr1:120107200-120108600	Enhancers	Primary B cells from cord blood	blood
11	chr1:120107200-120108600	Enhancers	Brain Substantia Nigra	brain
12	chr1:120107200-120110000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr1:120107200-120110600	Enhancers	HMEC	breast
14	chr1:120107400-120107800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
15	chr1:120107400-120107800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr1:120107400-120108000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:120107400-120108200	Flanking Active TSS	GM12878-XiMat	blood
18	chr1:120107400-120108600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:120107400-120108600	Enhancers	Brain Cingulate Gyrus	brain
20	chr1:120107400-120108800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:120107400-120108800	Enhancers	Brain Hippocampus Middle	brain
22	chr1:120107400-120109400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:120107400-120109600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:120107400-120110600	Enhancers	NHEK	skin
25	chr1:120107600-120108000	Enhancers	Right Atrium	heart
26	chr1:120107600-120108600	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr1:120107600-120109200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:120107600-120111400	Weak transcription	Primary hematopoietic stem cells	blood
29	chr1:120107800-120108800	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr1:120107800-120111200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr1:120107800-120111600	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr1:120108000-120109200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:120108000-120110400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:120108000-120111200	Weak transcription	Fetal Lung	lung
35	chr1:120108000-120111600	Weak transcription	Right Atrium	heart
36	chr1:120108200-120108400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr1:120108200-120109200	Enhancers	GM12878-XiMat	blood
38	chr1:120108600-120108800	Enhancers	Ovary	ovary
39	chr1:120108600-120111200	Weak transcription	Primary B cells from cord blood	blood
40	chr1:120108800-120111000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr1:120108800-120111800	Weak transcription	Ovary	ovary
42	chr1:120109000-120109200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:120109200-120110400	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr1:120109200-120111400	Weak transcription	Primary B cells from peripheral blood	blood
45	chr1:120109200-120111400	Weak transcription	GM12878-XiMat	blood
46	chr1:120109400-120110400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:120109600-120117200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:120110000-120110400	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr1:120110400-120110600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:120110400-120110600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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