Variant report

Variant	nsv998980
Chromosome Location	chr1:190812829-191509034
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1809)
CpG islands
(count:305)
Chromatin interactive
region (count:132)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1809 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:190953437-190953466	K562	blood:	n/a	n/a
2	ARID3A	chr1:191338195-191338459	K562	blood:	n/a	n/a
3	ARID3A	chr1:191467411-191467729	K562	blood:	n/a	n/a
4	ARID3A	chr1:191035067-191035242	K562	blood:	n/a	n/a
5	ATF1	chr1:191297314-191297326	K562	blood:	n/a	n/a
6	ATF1	chr1:191122236-191122374	K562	blood:	n/a	n/a
7	ATF1	chr1:191398326-191398421	K562	blood:	n/a	n/a
8	ATF1	chr1:191338119-191338421	K562	blood:	n/a	n/a
9	ATF1	chr1:191159156-191159163	K562	blood:	n/a	n/a
10	ATF1	chr1:190962269-190962469	K562	blood:	n/a	n/a
11	ATF1	chr1:191433147-191433178	K562	blood:	n/a	n/a
12	ATF1	chr1:191034981-191035158	K562	blood:	n/a	n/a
13	ATF1	chr1:190945893-190945964	K562	blood:	n/a	n/a
14	ATF2	chr1:191143328-191144013	GM12878	blood:	n/a	n/a
15	ATF3	chr1:191373403-191373752	K562	blood:	n/a	n/a
16	BACH1	chr1:191389471-191389476	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:191253401-191253595	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:191460518-191460521	K562	blood:	n/a	n/a
19	BACH1	chr1:191274761-191274805	K562	blood:	n/a	n/a
20	BATF	chr1:191143451-191143751	GM12878	blood:	n/a	n/a
21	BATF	chr1:191143439-191143828	GM12878	blood:	n/a	n/a
22	BATF	chr1:190919183-190919457	GM12878	blood:	n/a	chr1:190919328-190919339
23	BCL11A	chr1:191143469-191143830	GM12878	blood:	n/a	n/a
24	BCLAF1	chr1:191143259-191143906	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:190919380-190919416	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:190872913-190872974	K562	blood:	n/a	n/a
27	BHLHE40	chr1:191259569-191259784	K562	blood:	n/a	n/a
28	BHLHE40	chr1:191338189-191338354	K562	blood:	n/a	n/a
29	BHLHE40	chr1:191143231-191143785	GM12878	blood:	n/a	n/a
30	BRCA1	chr1:191370538-191370577	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr1:190964984-190965019	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr1:191253357-191253679	K562	blood:	n/a	n/a
33	CBX3	chr1:190884962-190885312	K562	blood:	n/a	n/a
34	CBX3	chr1:191357458-191357801	K562	blood:	n/a	n/a
35	CBX3	chr1:191126404-191126763	K562	blood:	n/a	n/a
36	CBX3	chr1:191506193-191506517	K562	blood:	n/a	n/a
37	CBX3	chr1:191120966-191121245	K562	blood:	n/a	n/a
38	CBX3	chr1:191186779-191187146	K562	blood:	n/a	n/a
39	CBX3	chr1:191253318-191253712	K562	blood:	n/a	n/a
40	CBX3	chr1:191458327-191458683	K562	blood:	n/a	n/a
41	CBX3	chr1:191441528-191441847	K562	blood:	n/a	n/a
42	CBX3	chr1:191482212-191482596	K562	blood:	n/a	n/a
43	CBX3	chr1:191297007-191297287	K562	blood:	n/a	n/a
44	CBX3	chr1:191373433-191373795	K562	blood:	n/a	n/a
45	CBX3	chr1:191367627-191368055	K562	blood:	n/a	n/a
46	CBX3	chr1:191506145-191506554	K562	blood:	n/a	n/a
47	CBX3	chr1:191365747-191366197	K562	blood:	n/a	n/a
48	CBX3	chr1:191275577-191275852	K562	blood:	n/a	n/a
49	CBX3	chr1:191357460-191357656	K562	blood:	n/a	n/a
50	CBX3	chr1:191365898-191366123	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:190873626-190873676	IMR90	lung:	fetal
2	chr1:191120830-191120880	GM06990	blood:	n/a
3	chr1:191503762-191503812	HEEpiC	esophagus:	n/a
4	chr1:190995429-190995479	BJ	skin:	n/a
5	chr1:191503762-191503812	AG09319	gingival:	n/a
6	chr1:191120792-191120842	SK-N-SH	brain:	n/a
7	chr1:191503762-191503812	HRPEpiC	eye:	n/a
8	chr1:191503762-191503812	Hela-S3	cervix:	n/a
9	chr1:190995429-190995479	PFSK-1	brain:	n/a
10	chr1:191120830-191120880	SK-N-MC	brain:	n/a
11	chr1:190873626-190873676	PFSK-1	brain:	n/a
12	chr1:191120830-191120880	NHBE	bronchial:	n/a
13	chr1:190995429-190995479	HRPEpiC	eye:	n/a
14	chr1:190873626-190873676	AG04450	lung:	fetal
15	chr1:190995429-190995479	PANC-1	pancreas:	n/a
16	chr1:190873626-190873676	PrEC	prostate:	n/a
17	chr1:191120830-191120880	Hepatocyte	liver:	n/a
18	chr1:190873626-190873676	HRPEpiC	eye:	n/a
19	chr1:190873626-190873676	BE2_C	brain:	n/a
20	chr1:191503762-191503812	HCF	heart:	n/a
21	chr1:191120830-191120880	Caco-2	colon:	n/a
22	chr1:191120792-191120842	HMEC	breast:	n/a
23	chr1:191120830-191120880	PrEC	prostate:	n/a
24	chr1:191120792-191120842	SAEC	small airway:	n/a
25	chr1:190873626-190873676	HUVEC	blood vessel:	n/a
26	chr1:191120792-191120842	K562	blood:	n/a
27	chr1:190995429-190995479	MCF-7	breast:	n/a
28	chr1:191503762-191503812	AoSMC	blood vessel:	n/a
29	chr1:191120830-191120880	SAEC	small airway:	n/a
30	chr1:191503762-191503812	HepG2	liver:	n/a
31	chr1:190873626-190873676	GM06990	blood:	n/a
32	chr1:191120792-191120842	GM19239	blood:	n/a
33	chr1:191503762-191503812	LNCaP	prostate:	n/a
34	chr1:191503762-191503812	H1-hESC	embryonic stem cell:	embryo
35	chr1:191120830-191120880	LNCaP	prostate:	n/a
36	chr1:190995429-190995479	GM12878	blood:	n/a
37	chr1:190995429-190995479	SAEC	small airway:	n/a
38	chr1:191503762-191503812	ProgFib	skin:	n/a
39	chr1:190873626-190873676	AG04449	skin:	fetal
40	chr1:191120792-191120842	BJ	skin:	n/a
41	chr1:191503762-191503812	RPTEC	kidney:	n/a
42	chr1:191120830-191120880	AG04450	lung:	fetal
43	chr1:191503762-191503812	PFSK-1	brain:	n/a
44	chr1:191120830-191120880	T-47D	breast:	n/a
45	chr1:191120792-191120842	IMR90	lung:	fetal
46	chr1:190995429-190995479	ovcar-3	ovarian:	n/a
47	chr1:191503762-191503812	MCF-7	breast:	n/a
48	chr1:191120792-191120842	GM12891	blood:	n/a
49	chr1:190873626-190873676	A549	lung:	n/a
50	chr1:190995429-190995479	HCPEpiC	choroid plexus:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:191502483..191504253-chr17:56707440..56709288,2	MCF-7	breast:
2	chr1:191476619..191478729-chr1:191489630..191491476,2	K562	blood:
3	chr1:191157793..191160088-chr1:191162179..191165102,2	K562	blood:
4	chr1:191450148..191453626-chr1:191453943..191457136,3	K562	blood:
5	chr1:191368248..191370695-chr1:191372787..191374561,2	K562	blood:
6	chr1:191160823..191162731-chr1:191477898..191480311,2	K562	blood:
7	chr1:191250975..191253394-chr1:191254576..191256855,3	K562	blood:
8	chr1:190889013..190890903-chr1:190897780..190899545,2	MCF-7	breast:
9	chr1:191391455..191393247-chr1:191395809..191398618,2	K562	blood:
10	chr1:191262328..191265076-chr1:191299134..191300928,2	K562	blood:
11	chr1:190846680..190849341-chr1:190853076..190854890,2	K562	blood:
12	chr1:191450148..191453626-chr1:191453943..191457136,3	K562	blood:
13	chr1:191420711..191422302-chr1:191475055..191477121,2	K562	blood:
14	chr1:191088572..191091264-chr1:191094632..191096483,2	MCF-7	breast:
15	chr1:191150998..191152501-chr1:191156325..191158082,2	K562	blood:
16	chr1:190907314..190910311-chr1:190988688..190990783,2	K562	blood:
17	chr1:191311585..191313743-chr1:191315163..191316847,2	K562	blood:
18	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
19	chr1:190949975..190952260-chr1:190953522..190955676,2	K562	blood:
20	chr1:191071401..191072988-chr1:191075213..191077807,2	MCF-7	breast:
21	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
22	chr1:191383700..191385993-chr1:191388618..191391301,2	MCF-7	breast:
23	chr1:191251451..191253394-chr1:191255335..191256855,2	K562	blood:
24	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
25	chr1:191455290..191457922-chr1:191460809..191463001,2	MCF-7	breast:
26	chr1:191446579..191448734-chr1:191448967..191451024,2	MCF-7	breast:
27	chr1:191006072..191007919-chr7:61967833..61970042,2	MCF-7	breast:
28	chr1:191078284..191080144-chr1:191088639..191091448,2	K562	blood:
29	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
30	chr1:190987156..190989063-chr1:190989667..190991830,2	K562	blood:
31	chr1:191476619..191478729-chr1:191489630..191491476,2	K562	blood:
32	chr1:190844875..190847195-chr1:190856499..190859471,2	MCF-7	breast:
33	chr1:191071401..191072988-chr1:191075213..191077807,2	MCF-7	breast:
34	chr1:191389236..191392425-chr1:191392487..191394511,3	K562	blood:
35	chr1:191015853..191018214-chr1:191018760..191021606,2	MCF-7	breast:
36	chr1:191433727..191435829-chr1:191471858..191473427,2	K562	blood:
37	chr1:191507022..191509468-chr1:191509511..191511062,2	K562	blood:
38	chr1:191251451..191253394-chr1:191255335..191256855,2	K562	blood:
39	chr1:191446749..191449835-chr1:191450213..191452486,3	K562	blood:
40	chr1:191088572..191091264-chr1:191094632..191096483,2	MCF-7	breast:
41	chr1:191466190..191469106-chr1:191473353..191475090,2	K562	blood:
42	chr1:191145894..191148873-chr1:191433449..191436245,2	K562	blood:
43	chr1:191357719..191359865-chr1:191368131..191370717,2	K562	blood:
44	chr1:191446579..191448734-chr1:191448967..191451024,2	MCF-7	breast:
45	chr1:191262328..191265076-chr1:191299134..191300928,2	K562	blood:
46	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
47	chr1:191250975..191253394-chr1:191254576..191256855,3	K562	blood:
48	chr1:191401913..191403539-chr1:191421067..191423069,2	K562	blood:
49	chr1:191191547..191193153-chr1:191196709..191199112,2	K562	blood:
50	chr1:191013676..191015855-chr1:191017030..191019137,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM5C-12	chr1:191190289-191190442	ENSG00000233882.2
2	lnc-FAM5C-11	chr1:191183856-191184010	NONHSAT008517
3	lnc-FAM5C-8	chr1:191001792-191001930	l_159_chr1:191000527-191001930_76bGuttman_hLF
4	lnc-FAM5C-8	chr1:191000528-191000708	l_159_chr1:191000527-191001930_76bGuttman_hLF
5	lnc-FAM5C-7	chr1:190851006-190851215	NONHSAT008513
6	lnc-FAM5C-9	chr1:191115155-191116091	NONHSAT008514
7	lnc-FAM5C-7	chr1:190844364-190848977	NONHSAT008513
8	lnc-FAM5C-13	chr1:191487184-191487423	predAs_chen_BG220711_1
9	lnc-FAM5C-7	chr1:190945550-190945655	NONHSAT008513
10	lnc-FAM5C-7	chr1:190946299-190946427	NONHSAT008513
11	lnc-FAM5C-10	chr1:191148651-191148869	NONHSAT008516
12	lnc-FAM5C-11	chr1:191173053-191173173	NONHSAT008517
13	lnc-FAM5C-12	chr1:191197453-191197597	ENSG00000233882.2
14	lnc-RGS18-10	chr1:191494155-191494355	expReg_chr1_21196_+
15	lnc-RGS18-2	chr1:191190289-191190442	XLOC_000506
16	lnc-RGS18-2	chr1:191197453-191197597	XLOC_000506

No data

Variant related genes	Relation type
ENSG00000261642	TF binding region
HNRNPA1P46	TF binding region
ENSG00000233882	TF binding region
ENSG00000271187	TF binding region
ENSG00000261642	CpG island
HNRNPA1P46	CpG island
ENSG00000233882	CpG island
ENSG00000271187	CpG island
ENSG00000212195	chromatin interactions
ENSG00000233882	chromatin interactions
ENSG00000057468	chromatin interactions
ENSG00000271187	chromatin interactions
GSK3B	miRNA target sites
BCOR	miRNA target sites

Extended variants
information (count: 5602 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:5602 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11313830	chr1:190818800-190818801	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs398053637	chr1:190818810-190818811	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs397863776	chr1:190818811-190818812	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs536011204	chr1:190818830-190818831	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs546818078	chr1:190818841-190818842	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs181092881	chr1:190818850-190818851	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs35266801	chr1:190818865-190818866	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs397863076	chr1:190818867-190818868	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs201744051	chr1:190818868-190818869	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs538960740	chr1:190818917-190818918	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs557710699	chr1:190818970-190818971	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs577589119	chr1:190818973-190818974	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs34996937	chr1:190818999-190819000	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556995208	chr1:190819015-190819016	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs369898236	chr1:190819151-190819152	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs140776629	chr1:190819153-190819154	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs2419925	chr1:190819195-190819196	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs566972897	chr1:190826873-190826874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189256194	chr1:190826923-190826924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552535805	chr1:190826965-190826966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180891286	chr1:190826968-190826969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184964614	chr1:190826971-190826972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554805613	chr1:190826978-190826979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539004803	chr1:190826987-190826988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190115521	chr1:190827012-190827013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567684793	chr1:190827036-190827037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112331675	chr1:190827065-190827066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2226228	chr1:190827087-190827088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543635939	chr1:190827094-190827095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368247522	chr1:190827170-190827171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553407122	chr1:190827173-190827174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576579619	chr1:190827177-190827178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545576118	chr1:190827178-190827179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556110893	chr1:190827179-190827180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576206471	chr1:190827180-190827181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541721915	chr1:190827214-190827215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562023964	chr1:190827224-190827225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372843371	chr1:190827226-190827227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530068365	chr1:190827256-190827257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181120642	chr1:190827266-190827267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186316814	chr1:190827267-190827268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376059620	chr1:190827292-190827293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565320778	chr1:190827297-190827298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141791740	chr1:190827298-190827299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531949875	chr1:190827302-190827303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532680034	chr1:190827318-190827319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145451175	chr1:190827325-190827326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568419862	chr1:190827380-190827381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533544152	chr1:190827454-190827455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553394944	chr1:190827474-190827475	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	17086460	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Lung adenocarcinoma	21935476	CNVD
Glioblastoma multiforme	21510904	CNVD
Intellectual disability	21811512	CNVD
Parathyroid adenoma	20824076	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:190818800-190819200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr1:190826800-190828000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:190829200-190829800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:190832800-190834000	Enhancers	HMEC	breast
5	chr1:190832800-190834200	Enhancers	NHEK	skin
6	chr1:190833000-190834000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:190833000-190834000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:190833000-190834400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:190833200-190833600	Enhancers	Gastric	stomach
10	chr1:190833400-190833800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:190833400-190833800	Enhancers	Esophagus	oesophagus
12	chr1:190858200-190858400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:190860600-190860800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:190872200-190873400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr1:190872600-190873800	Enhancers	NH-A	brain
16	chr1:190872800-190873600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:190873000-190873800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:190873400-190873800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr1:190873400-190873800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:190873400-190873800	Enhancers	HMEC	breast
21	chr1:190873800-190874000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:190873800-190874800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:190874000-190877600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:190875000-190875200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr1:190875600-190875800	Enhancers	Colon Smooth Muscle	Colon
26	chr1:190876000-190878400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr1:190876400-190876600	Enhancers	Colon Smooth Muscle	Colon
28	chr1:190877600-190878400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:190881000-190881400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:190881200-190881400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr1:190884800-190885400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:190885000-190886000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr1:190885400-190898800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:190898800-190899000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr1:190898800-190899200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr1:190899000-190899200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:190903000-190903200	Enhancers	Fetal Brain Male	brain
38	chr1:190903400-190904400	Weak transcription	Fetal Brain Male	brain
39	chr1:190904400-190905200	Enhancers	Fetal Brain Male	brain
40	chr1:190904400-190905800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr1:190904400-190906000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr1:190904400-190906200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:190904400-190906200	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr1:190904600-190904800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr1:190904800-190905400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:190904800-190905600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr1:190904800-190905600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:190904800-190905800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr1:190904800-190906600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:190905000-190905600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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