Variant report

Variant	nsv1002498
Chromosome Location	chr1:190871238-191159750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:779)
CpG islands
(count:244)
Chromatin interactive
region (count:42)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:779 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:191035067-191035242	K562	blood:	n/a	n/a
2	ARID3A	chr1:190953437-190953466	K562	blood:	n/a	n/a
3	ATF1	chr1:190962269-190962469	K562	blood:	n/a	n/a
4	ATF1	chr1:191159156-191159163	K562	blood:	n/a	n/a
5	ATF1	chr1:191122236-191122374	K562	blood:	n/a	n/a
6	ATF1	chr1:190945893-190945964	K562	blood:	n/a	n/a
7	ATF1	chr1:191034981-191035158	K562	blood:	n/a	n/a
8	ATF2	chr1:191143328-191144013	GM12878	blood:	n/a	n/a
9	BATF	chr1:190919183-190919457	GM12878	blood:	n/a	chr1:190919328-190919339
10	BATF	chr1:191143451-191143751	GM12878	blood:	n/a	n/a
11	BATF	chr1:191143439-191143828	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:191143469-191143830	GM12878	blood:	n/a	n/a
13	BCLAF1	chr1:191143259-191143906	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:190919380-190919416	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:191143231-191143785	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:190872913-190872974	K562	blood:	n/a	n/a
17	BRCA1	chr1:190964984-190965019	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr1:191126404-191126763	K562	blood:	n/a	n/a
19	CBX3	chr1:191120966-191121245	K562	blood:	n/a	n/a
20	CBX3	chr1:190884962-190885312	K562	blood:	n/a	n/a
21	CCNT2	chr1:190874927-190875124	K562	blood:	n/a	n/a
22	CCNT2	chr1:190944493-190944593	K562	blood:	n/a	n/a
23	CEBPB	chr1:190973765-190974042	A549	lung:	n/a	chr1:190973884-190973895
24	CEBPB	chr1:191043395-191043822	HepG2	liver:	n/a	chr1:191043541-191043552 chr1:191043540-191043551
25	CEBPB	chr1:190966874-190967137	HepG2	liver:	n/a	chr1:190967033-190967046 chr1:190967033-190967046 chr1:190967033-190967044 chr1:190967033-190967046 chr1:190967034-190967045 chr1:190967023-190967036
26	CEBPB	chr1:190910098-190910471	K562	blood:	n/a	chr1:190910275-190910286
27	CEBPB	chr1:190966813-190967267	MCF-7	breast:	n/a	chr1:190967033-190967046 chr1:190967033-190967046 chr1:190967033-190967044 chr1:190967033-190967046 chr1:190967034-190967045 chr1:190967023-190967036
28	CEBPB	chr1:190966973-190967182	A549	lung:	n/a	chr1:190967033-190967046 chr1:190967033-190967046 chr1:190967033-190967044 chr1:190967033-190967046 chr1:190967034-190967045 chr1:190967023-190967036
29	CEBPB	chr1:191056092-191056364	K562	blood:	n/a	chr1:191056231-191056242
30	CEBPB	chr1:190966911-190967150	K562	blood:	n/a	chr1:190967033-190967046 chr1:190967033-190967046 chr1:190967033-190967044 chr1:190967033-190967046 chr1:190967034-190967045 chr1:190967023-190967036
31	CEBPB	chr1:191134053-191134241	MCF-7	breast:	n/a	n/a
32	CEBPB	chr1:191128034-191128422	IMR90	lung:	n/a	chr1:191128163-191128174
33	CEBPB	chr1:191006399-191006691	IMR90	lung:	n/a	chr1:191006579-191006592 chr1:191006581-191006592 chr1:191006579-191006592 chr1:191006579-191006590
34	CEBPB	chr1:191056077-191056367	A549	lung:	n/a	chr1:191056231-191056242
35	CEBPB	chr1:190904021-190904161	K562	blood:	n/a	n/a
36	CEBPB	chr1:191056058-191056415	IMR90	lung:	n/a	chr1:191056231-191056242
37	CEBPB	chr1:190910136-190910449	HepG2	liver:	n/a	chr1:190910275-190910286
38	CEBPB	chr1:191109191-191109512	IMR90	lung:	n/a	chr1:191109350-191109361
39	CEBPB	chr1:190910139-190910433	ECC-1	luminal epithelium:	n/a	chr1:190910275-190910286
40	CEBPB	chr1:190919006-190919346	HepG2	liver:	n/a	chr1:190919158-190919175
41	CEBPB	chr1:191044575-191044647	H1-hESC	embryonic stem cell:	n/a	chr1:191044606-191044617
42	CEBPB	chr1:191050206-191050422	HepG2	liver:	n/a	chr1:191050334-191050347
43	CEBPB	chr1:191043512-191043648	K562	blood:	n/a	chr1:191043541-191043552 chr1:191043540-191043551
44	CEBPB	chr1:190880740-190881052	IMR90	lung:	n/a	n/a
45	CEBPB	chr1:191109240-191109499	HepG2	liver:	n/a	chr1:191109350-191109361
46	CEBPB	chr1:190910122-190910421	A549	lung:	n/a	chr1:190910275-190910286
47	CEBPB	chr1:191134018-191134308	K562	blood:	n/a	n/a
48	CEBPB	chr1:191044439-191044785	K562	blood:	n/a	chr1:191044564-191044575 chr1:191044606-191044617
49	CEBPB	chr1:191044468-191044782	HepG2	liver:	n/a	chr1:191044564-191044575 chr1:191044606-191044617
50	CEBPB	chr1:191128031-191128288	K562	blood:	n/a	chr1:191128163-191128174

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:191120792-191120842	HepG2	liver:	n/a
2	chr1:191120830-191120880	HCPEpiC	choroid plexus:	n/a
3	chr1:190995429-190995479	NH-A	brain:	n/a
4	chr1:190995429-190995479	NHBE	bronchial:	n/a
5	chr1:191120792-191120842	SKMC	muscle:	n/a
6	chr1:190873626-190873676	SAEC	small airway:	n/a
7	chr1:191120792-191120842	LNCaP	prostate:	n/a
8	chr1:190995429-190995479	NHDF-neo	bronchial:	n/a
9	chr1:191120792-191120842	BJ	skin:	n/a
10	chr1:191120792-191120842	PrEC	prostate:	n/a
11	chr1:191120830-191120880	HAEpiC	amniotic membrane:	n/a
12	chr1:191120792-191120842	IMR90	lung:	fetal
13	chr1:191120830-191120880	GM12892	blood:	n/a
14	chr1:191120792-191120842	GM12878	blood:	n/a
15	chr1:191120830-191120880	NHBE	bronchial:	n/a
16	chr1:191120792-191120842	NH-A	brain:	n/a
17	chr1:190995429-190995479	Hepatocyte	liver:	n/a
18	chr1:191120830-191120880	CMK	blood:	n/a
19	chr1:190873626-190873676	AG04449	skin:	fetal
20	chr1:191120830-191120880	HEK293	kidney:	embryo
21	chr1:191120792-191120842	ECC-1	luminal epithelium:	n/a
22	chr1:191120792-191120842	HUVEC	blood vessel:	n/a
23	chr1:190995429-190995479	SAEC	small airway:	n/a
24	chr1:191120830-191120880	AG04449	skin:	fetal
25	chr1:191120830-191120880	ECC-1	luminal epithelium:	n/a
26	chr1:191120830-191120880	GM06990	blood:	n/a
27	chr1:190995429-190995479	GM19239	blood:	n/a
28	chr1:191120830-191120880	HL-60	blood:	n/a
29	chr1:190873626-190873676	GM19239	blood:	n/a
30	chr1:190873626-190873676	GM12891	blood:	n/a
31	chr1:191120830-191120880	NH-A	brain:	n/a
32	chr1:190873626-190873676	GM06990	blood:	n/a
33	chr1:190873626-190873676	IMR90	lung:	fetal
34	chr1:191120792-191120842	U87	brain:	n/a
35	chr1:190995429-190995479	RPTEC	kidney:	n/a
36	chr1:190995429-190995479	SK-N-SH	brain:	n/a
37	chr1:190995429-190995479	PANC-1	pancreas:	n/a
38	chr1:191120792-191120842	CMK	blood:	n/a
39	chr1:191120792-191120842	MCF-7	breast:	n/a
40	chr1:190995429-190995479	U87	brain:	n/a
41	chr1:190995429-190995479	NB4	blood:	n/a
42	chr1:190995429-190995479	LNCaP	prostate:	n/a
43	chr1:191120792-191120842	HEEpiC	esophagus:	n/a
44	chr1:190995429-190995479	HRPEpiC	eye:	n/a
45	chr1:191120830-191120880	AG10803	skin:	n/a
46	chr1:191120830-191120880	PrEC	prostate:	n/a
47	chr1:190873626-190873676	HNPCEpiC	eye:	n/a
48	chr1:191120792-191120842	PFSK-1	brain:	n/a
49	chr1:190873626-190873676	AoSMC	blood vessel:	n/a
50	chr1:190873626-190873676	AG10803	skin:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:191078284..191080144-chr1:191088639..191091448,2	K562	blood:
2	chr1:191102072..191104300-chr1:191107376..191108877,2	K562	blood:
3	chr1:190889013..190890903-chr1:190897780..190899545,2	MCF-7	breast:
4	chr1:190978633..190980595-chr1:190983607..190985514,2	K562	blood:
5	chr1:191102072..191104300-chr1:191107376..191108877,2	K562	blood:
6	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
7	chr1:191013676..191015855-chr1:191017030..191019137,2	K562	blood:
8	chr1:190926824..190927388-chr1:191800448..191800967,2	MCF-7	breast:
9	chr1:191013676..191015855-chr1:191017030..191019137,2	K562	blood:
10	chr1:191150998..191152501-chr1:191156325..191158082,2	K562	blood:
11	chr1:191117376..191119882-chr1:191120970..191122736,2	MCF-7	breast:
12	chr1:191015853..191018214-chr1:191018760..191021606,2	MCF-7	breast:
13	chr1:190889013..190890903-chr1:190897780..190899545,2	MCF-7	breast:
14	chr1:191056730..191058944-chr1:191065674..191068306,2	K562	blood:
15	chr1:191088572..191091264-chr1:191094632..191096483,2	MCF-7	breast:
16	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
17	chr1:191121690..191123350-chr1:191124411..191127560,3	K562	blood:
18	chr1:191157793..191160088-chr1:191162179..191165102,2	K562	blood:
19	chr1:190949975..190952260-chr1:190953522..190955676,2	K562	blood:
20	chr1:190987156..190989063-chr1:190989667..190991830,2	K562	blood:
21	chr1:190907314..190910311-chr1:190988688..190990783,2	K562	blood:
22	chr1:191006072..191007919-chr7:61967833..61970042,2	MCF-7	breast:
23	chr1:191056730..191058944-chr1:191065674..191068306,2	K562	blood:
24	chr1:191139593..191142388-chr1:191149120..191151841,2	MCF-7	breast:
25	chr1:191121690..191123350-chr1:191124411..191127560,3	K562	blood:
26	chr1:190907314..190910311-chr1:190988688..190990783,2	K562	blood:
27	chr1:190978633..190980595-chr1:190983607..190985514,2	K562	blood:
28	chr1:191117376..191119882-chr1:191120970..191122736,2	MCF-7	breast:
29	chr1:190949975..190952260-chr1:190953522..190955676,2	K562	blood:
30	chr1:191015853..191018214-chr1:191018760..191021606,2	MCF-7	breast:
31	chr1:190868639..190870374-chr1:190872516..190874922,2	K562	blood:
32	chr1:191071401..191072988-chr1:191075213..191077807,2	MCF-7	breast:
33	chr1:191078284..191080144-chr1:191088639..191091448,2	K562	blood:
34	chr1:191150998..191152501-chr1:191156325..191158082,2	K562	blood:
35	chr1:190987156..190989063-chr1:190989667..190991830,2	K562	blood:
36	chr1:191071401..191072988-chr1:191075213..191077807,2	MCF-7	breast:
37	chr1:191123228..191125504-chr1:191129557..191132140,2	K562	blood:
38	chr1:191010882..191013695-chr1:191014255..191017163,2	K562	blood:
39	chr1:191010882..191013695-chr1:191014255..191017163,2	K562	blood:
40	chr1:191088572..191091264-chr1:191094632..191096483,2	MCF-7	breast:
41	chr1:191123228..191125504-chr1:191129557..191132140,2	K562	blood:
42	chr1:191139593..191142388-chr1:191149120..191151841,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM5C-9	chr1:191115155-191116091	NONHSAT008514
2	lnc-FAM5C-7	chr1:190945550-190945655	NONHSAT008513
3	lnc-FAM5C-7	chr1:190946299-190946427	NONHSAT008513
4	lnc-FAM5C-8	chr1:191000528-191000708	l_159_chr1:191000527-191001930_76bGuttman_hLF
5	lnc-FAM5C-8	chr1:191001792-191001930	l_159_chr1:191000527-191001930_76bGuttman_hLF
6	lnc-FAM5C-10	chr1:191148651-191148869	NONHSAT008516

No data

Variant related genes	Relation type
ENSG00000261642	TF binding region
HNRNPA1P46	TF binding region
ENSG00000271187	TF binding region
ENSG00000261642	CpG island
HNRNPA1P46	CpG island
ENSG00000271187	CpG island

Extended variants
information (count: 2386 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2386 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79086224	chr1:190872222-190872223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538250672	chr1:190872283-190872284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2419931	chr1:190872337-190872338	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs543189530	chr1:190872350-190872351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564674428	chr1:190872382-190872383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571967674	chr1:190872428-190872429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138780914	chr1:190872481-190872482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571687158	chr1:190872484-190872485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532069204	chr1:190872493-190872494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553744860	chr1:190872496-190872497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs377670577	chr1:190872589-190872590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547038022	chr1:190872617-190872618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565624799	chr1:190872627-190872628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2419932	chr1:190872645-190872646	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs546262941	chr1:190872680-190872681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190859684	chr1:190872686-190872687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12040924	chr1:190872689-190872690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542010025	chr1:190872692-190872693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185827785	chr1:190872707-190872708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372573110	chr1:190872715-190872716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12401900	chr1:190872737-190872738	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs548155527	chr1:190872750-190872751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564049874	chr1:190872822-190872823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570179199	chr1:190872838-190872839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532994765	chr1:190872849-190872850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs58198108	chr1:190872861-190872862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190979888	chr1:190872868-190872869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535542026	chr1:190872883-190872884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548894058	chr1:190872898-190872899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141250008	chr1:190872899-190872900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534579687	chr1:190872917-190872918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557661603	chr1:190872922-190872923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10920834	chr1:190872933-190872934	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs377398461	chr1:190872953-190872954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556523305	chr1:190872980-190872981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183123965	chr1:190872984-190872985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370787618	chr1:190873014-190873015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375005147	chr1:190873034-190873035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150778834	chr1:190873035-190873036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572706429	chr1:190873041-190873042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114189789	chr1:190873069-190873070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11808887	chr1:190873081-190873082	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs10800991	chr1:190873103-190873104	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs187013548	chr1:190873105-190873106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192263617	chr1:190873246-190873247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34806043	chr1:190873247-190873248	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs553099157	chr1:190873259-190873260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182746245	chr1:190873330-190873331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187769133	chr1:190873391-190873392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528237299	chr1:190873582-190873583	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:190872200-190873400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:190872600-190873800	Enhancers	NH-A	brain
3	chr1:190872800-190873600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:190873000-190873800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:190873400-190873800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:190873400-190873800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:190873400-190873800	Enhancers	HMEC	breast
8	chr1:190873800-190874000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:190873800-190874800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:190874000-190877600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:190875000-190875200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:190875600-190875800	Enhancers	Colon Smooth Muscle	Colon
13	chr1:190876000-190878400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr1:190876400-190876600	Enhancers	Colon Smooth Muscle	Colon
15	chr1:190877600-190878400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:190881000-190881400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:190881200-190881400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr1:190884800-190885400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:190885000-190886000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:190885400-190898800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:190898800-190899000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:190898800-190899200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr1:190899000-190899200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr1:190903000-190903200	Enhancers	Fetal Brain Male	brain
25	chr1:190903400-190904400	Weak transcription	Fetal Brain Male	brain
26	chr1:190904400-190905200	Enhancers	Fetal Brain Male	brain
27	chr1:190904400-190905800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr1:190904400-190906000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr1:190904400-190906200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:190904400-190906200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr1:190904600-190904800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr1:190904800-190905400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:190904800-190905600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr1:190904800-190905600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:190904800-190905800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr1:190904800-190906600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:190905000-190905600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr1:190905000-190906000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr1:190905600-190906400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:190919000-190919200	Enhancers	Ovary	ovary
41	chr1:190919000-190919400	Active TSS	Colon Smooth Muscle	Colon
42	chr1:190919000-190919400	Active TSS	Stomach Smooth Muscle	stomach
43	chr1:190919000-190919800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:190919000-190919800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr1:190919000-190920200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:190919200-190919600	Active TSS	Ovary	ovary
47	chr1:190921200-190921600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr1:190921400-190921800	Enhancers	H9 Cell Line	embryonic stem cell
49	chr1:190921400-190921800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr1:190930200-190931200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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