Variant report

Variant	nsv872894
Chromosome Location	chr1:195053221-195745968
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2780)
CpG islands
(count:183)
Chromatin interactive
region (count:100)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2780 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:195198697-195198705	K562	blood:	n/a	n/a
2	ATF1	chr1:195181877-195181932	K562	blood:	n/a	n/a
3	ATF1	chr1:195543739-195543774	K562	blood:	n/a	n/a
4	ATF1	chr1:195481412-195481440	K562	blood:	n/a	n/a
5	ATF1	chr1:195609822-195609871	K562	blood:	n/a	n/a
6	ATF2	chr1:195666222-195666748	GM12878	blood:	n/a	n/a
7	ATF2	chr1:195164308-195165083	GM12878	blood:	n/a	n/a
8	ATF2	chr1:195666229-195666688	GM12878	blood:	n/a	n/a
9	ATF2	chr1:195164239-195165053	GM12878	blood:	n/a	n/a
10	ATF3	chr1:195735865-195736086	K562	blood:	n/a	n/a
11	BACH1	chr1:195683474-195683712	K562	blood:	n/a	n/a
12	BACH1	chr1:195735880-195736165	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:195122285-195122583	K562	blood:	n/a	n/a
14	BACH1	chr1:195737570-195737812	K562	blood:	n/a	n/a
15	BACH1	chr1:195250537-195250544	K562	blood:	n/a	n/a
16	BACH1	chr1:195122356-195122540	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:195735923-195736139	K562	blood:	n/a	n/a
18	BACH1	chr1:195731399-195731424	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr1:195301352-195301514	GM12878	blood:	n/a	n/a
20	BATF	chr1:195666322-195666574	GM12878	blood:	n/a	n/a
21	BATF	chr1:195164462-195165019	GM12878	blood:	n/a	n/a
22	BATF	chr1:195164439-195165066	GM12878	blood:	n/a	n/a
23	BATF	chr1:195666275-195666626	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:195164392-195165066	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:195666336-195666596	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:195164332-195165095	GM12878	blood:	n/a	n/a
27	BCL3	chr1:195164566-195164924	GM12878	blood:	n/a	n/a
28	BCL3	chr1:195164564-195164876	GM12878	blood:	n/a	n/a
29	BCLAF1	chr1:195164321-195165003	GM12878	blood:	n/a	n/a
30	BCLAF1	chr1:195164254-195165079	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:195666318-195666554	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:195164335-195165128	GM12878	blood:	n/a	n/a
33	BRCA1	chr1:195274225-195274324	H1-hESC	embryonic stem cell:	n/a	n/a
34	CBX3	chr1:195066119-195066969	HCT-116	colon:	n/a	n/a
35	CBX3	chr1:195554326-195554798	HCT-116	colon:	n/a	n/a
36	CBX3	chr1:195314296-195314811	HCT-116	colon:	n/a	n/a
37	CBX3	chr1:195066317-195066989	HCT-116	colon:	n/a	n/a
38	CBX3	chr1:195633005-195633371	K562	blood:	n/a	n/a
39	CCNT2	chr1:195082155-195082271	K562	blood:	n/a	n/a
40	CCNT2	chr1:195576812-195576978	K562	blood:	n/a	n/a
41	CEBPB	chr1:195730261-195730633	K562	blood:	n/a	chr1:195730461-195730472
42	CEBPB	chr1:195408383-195408670	HepG2	liver:	n/a	chr1:195408496-195408507
43	CEBPB	chr1:195725269-195725595	A549	lung:	n/a	chr1:195725431-195725442
44	CEBPB	chr1:195613085-195613372	H1-hESC	embryonic stem cell:	n/a	chr1:195613208-195613219
45	CEBPB	chr1:195716099-195716325	HepG2	liver:	n/a	chr1:195716243-195716254 chr1:195716243-195716254 chr1:195716241-195716252 chr1:195716241-195716254 chr1:195716241-195716254
46	CEBPB	chr1:195162289-195162607	K562	blood:	n/a	chr1:195162449-195162460
47	CEBPB	chr1:195725273-195725607	HepG2	liver:	n/a	chr1:195725431-195725442
48	CEBPB	chr1:195313227-195313513	A549	lung:	n/a	chr1:195313326-195313337
49	CEBPB	chr1:195546927-195547056	K562	blood:	n/a	n/a
50	CEBPB	chr1:195545028-195545268	A549	lung:	n/a	chr1:195545056-195545069

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:195692334-195692384	HCF	heart:	n/a
2	chr1:195691043-195691093	HMEC	breast:	n/a
3	chr1:195692334-195692384	HAEpiC	amniotic membrane:	n/a
4	chr1:195691043-195691093	NT2-D1	testis:	n/a
5	chr1:195692334-195692384	Hepatocyte	liver:	n/a
6	chr1:195691043-195691093	GM19239	blood:	n/a
7	chr1:195692334-195692384	LNCaP	prostate:	n/a
8	chr1:195692334-195692384	PANC-1	pancreas:	n/a
9	chr1:195691043-195691093	PANC-1	pancreas:	n/a
10	chr1:195684226-195684276	HCM	heart:	n/a
11	chr1:195684226-195684276	HAEpiC	amniotic membrane:	n/a
12	chr1:195692334-195692384	NH-A	brain:	n/a
13	chr1:195691043-195691093	Caco-2	colon:	n/a
14	chr1:195691043-195691093	MCF-7	breast:	n/a
15	chr1:195691043-195691093	HepG2	liver:	n/a
16	chr1:195691043-195691093	U87	brain:	n/a
17	chr1:195684226-195684276	NHBE	bronchial:	n/a
18	chr1:195691043-195691093	A549	lung:	n/a
19	chr1:195684226-195684276	K562	blood:	n/a
20	chr1:195684226-195684276	SK-N-SH	brain:	n/a
21	chr1:195691043-195691093	AG09319	gingival:	n/a
22	chr1:195692334-195692384	NB4	blood:	n/a
23	chr1:195691043-195691093	H1-hESC	embryonic stem cell:	embryo
24	chr1:195684226-195684276	A549	lung:	n/a
25	chr1:195692334-195692384	HCPEpiC	choroid plexus:	n/a
26	chr1:195692334-195692384	IMR90	lung:	fetal
27	chr1:195684226-195684276	H1-hESC	embryonic stem cell:	embryo
28	chr1:195684226-195684276	SK-N-MC	brain:	n/a
29	chr1:195684226-195684276	PANC-1	pancreas:	n/a
30	chr1:195691043-195691093	ECC-1	luminal epithelium:	n/a
31	chr1:195692334-195692384	HUVEC	blood vessel:	n/a
32	chr1:195684226-195684276	HNPCEpiC	eye:	n/a
33	chr1:195692334-195692384	GM06990	blood:	n/a
34	chr1:195691043-195691093	HIPEpiC	eye:	n/a
35	chr1:195691043-195691093	AG04449	skin:	fetal
36	chr1:195684226-195684276	SAEC	small airway:	n/a
37	chr1:195684226-195684276	HMEC	breast:	n/a
38	chr1:195691043-195691093	GM06990	blood:	n/a
39	chr1:195684226-195684276	AG10803	skin:	n/a
40	chr1:195684226-195684276	T-47D	breast:	n/a
41	chr1:195692334-195692384	AG09309	skin:	n/a
42	chr1:195692334-195692384	HCT-116	colon:	n/a
43	chr1:195684226-195684276	Hela-S3	cervix:	n/a
44	chr1:195684226-195684276	Caco-2	colon:	n/a
45	chr1:195692334-195692384	AG10803	skin:	n/a
46	chr1:195684226-195684276	AG04450	lung:	fetal
47	chr1:195684226-195684276	HUVEC	blood vessel:	n/a
48	chr1:195692334-195692384	HRPEpiC	eye:	n/a
49	chr1:195691043-195691093	SK-N-SH	brain:	n/a
50	chr1:195692334-195692384	RPTEC	kidney:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:195728301..195731398-chr1:195733712..195736941,3	MCF-7	breast:
2	chr1:195743372..195746056-chr1:195755378..195757167,2	K562	blood:
3	chr1:195518670..195520403-chr1:195533153..195535062,2	K562	blood:
4	chr1:195729478..195731927-chr1:195733670..195735429,2	K562	blood:
5	chr1:195510518..195512657-chr1:195516239..195517820,2	K562	blood:
6	chr1:195076488..195078314-chr16:29816661..29818822,2	MCF-7	breast:
7	chr1:195723006..195725382-chr1:195733358..195735246,2	K562	blood:
8	chr1:195467909..195469471-chr1:195476696..195479659,2	K562	blood:
9	chr1:195576625..195578238-chr1:195581661..195583174,2	K562	blood:
10	chr1:195270062..195272293-chr1:195296328..195299059,2	MCF-7	breast:
11	chr1:195605744..195607558-chr1:195610835..195613690,2	K562	blood:
12	chr1:195629416..195631503-chr1:195632294..195634517,2	K562	blood:
13	chr1:195681664..195684653-chr1:195687722..195689895,2	MCF-7	breast:
14	chr1:195340635..195342790-chr1:195343117..195345385,2	K562	blood:
15	chr1:195720981..195722711-chr1:195730556..195732740,2	K562	blood:
16	chr1:195314819..195316810-chr1:195319212..195320954,2	MCF-7	breast:
17	chr1:195728301..195731398-chr1:195733712..195736941,3	MCF-7	breast:
18	chr1:195514637..195515437-chr4:98218446..98219186,2	MCF-7	breast:
19	chr1:195676413..195678428-chr1:195679999..195681988,2	K562	blood:
20	chr1:195622545..195624939-chr1:195627607..195630301,2	K562	blood:
21	chr1:195622545..195624939-chr1:195627607..195630301,2	K562	blood:
22	chr1:195442462..195444603-chr1:195444759..195446417,2	MCF-7	breast:
23	chr1:195729478..195731927-chr1:195733670..195735429,2	K562	blood:
24	chr1:195576625..195578238-chr1:195581661..195583174,2	K562	blood:
25	chr1:195636006..195638492-chr1:195640156..195642682,2	K562	blood:
26	chr1:195385198..195387219-chr1:195683079..195685011,2	K562	blood:
27	chr1:195308037..195310638-chr1:195312070..195313866,2	MCF-7	breast:
28	chr1:195648419..195651037-chr1:195656672..195659397,2	K562	blood:
29	chr1:195553010..195555142-chr1:195558344..195561243,2	K562	blood:
30	chr1:195130839..195132878-chr1:195138252..195140071,2	K562	blood:
31	chr1:195474802..195477777-chr1:195478958..195481457,2	K562	blood:
32	chr1:195676413..195678428-chr1:195679999..195681988,2	K562	blood:
33	chr1:195398482..195401178-chr1:195401687..195404461,3	K562	blood:
34	chr1:195314819..195316810-chr1:195319212..195320954,2	MCF-7	breast:
35	chr1:195707846..195709349-chr1:195709392..195711387,2	K562	blood:
36	chr1:195180067..195181644-chr1:195189750..195192618,2	K562	blood:
37	chr1:195720981..195722711-chr1:195730556..195732740,2	K562	blood:
38	chr1:195385198..195387219-chr1:195683079..195685011,2	K562	blood:
39	chr1:195422390..195425246-chr1:195431885..195433646,2	K562	blood:
40	chr1:195707846..195709349-chr1:195709392..195711387,2	K562	blood:
41	chr1:195681664..195684653-chr1:195687722..195689895,2	MCF-7	breast:
42	chr1:195308037..195310638-chr1:195312070..195313866,2	MCF-7	breast:
43	chr1:195643603..195646404-chr1:195648016..195650352,3	K562	blood:
44	chr1:195502291..195505198-chr1:195514179..195516495,2	K562	blood:
45	chr1:195361839..195365274-chr1:195369633..195372261,3	K562	blood:
46	chr1:195211970..195213512-chr1:195217966..195220235,2	K562	blood:
47	chr1:195438395..195441122-chr1:195442393..195443903,2	K562	blood:
48	chr1:195648419..195651037-chr1:195656672..195659397,2	K562	blood:
49	chr1:195710497..195713809-chr1:195716668..195718919,3	K562	blood:
50	chr1:195361839..195365274-chr1:195369633..195372261,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNT2-2	chr1:195732379-195732530	NONHSAT008590
2	lnc-KCNT2-4	chr1:195436980-195437187	expReg_chr1_18917_-
3	lnc-KCNT2-2	chr1:195730397-195730538	NONHSAT008590
4	lnc-KCNT2-2	chr1:195727481-195728588	NONHSAT008590
5	lnc-CFH-1	chr1:195450556-195450708	XLOC_000511
6	lnc-CFH-1	chr1:195469301-195469368	XLOC_000511

No data

Variant related genes	Relation type
ENSG00000265108	TF binding region
ENSG00000265108	CpG island
ENSG00000103495	chromatin interactions
ENSG00000200997	chromatin interactions

Extended variants
information (count: 6017 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:6017 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7549038	chr1:195054266-195054267	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535352502	chr1:195054278-195054279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs698045	chr1:195054338-195054339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72730891	chr1:195054340-195054341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569011336	chr1:195054352-195054353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12125024	chr1:195054415-195054416	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557944740	chr1:195054424-195054425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542337078	chr1:195054426-195054427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563333841	chr1:195054486-195054487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2636337	chr1:195054491-195054492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530824988	chr1:195054520-195054521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534289712	chr1:195054532-195054533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1831473	chr1:195054533-195054534	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs574131911	chr1:195054534-195054535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374305102	chr1:195054553-195054554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189950197	chr1:195054599-195054600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148943454	chr1:195054639-195054640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182589619	chr1:195054662-195054663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12728887	chr1:195054699-195054700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12752869	chr1:195054700-195054701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560741371	chr1:195054750-195054751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528135418	chr1:195054755-195054756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78563526	chr1:195054777-195054778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12748853	chr1:195054779-195054780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572916940	chr1:195054783-195054784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561343162	chr1:195054793-195054794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368979065	chr1:195063086-195063087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35236785	chr1:195063088-195063089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs530419310	chr1:195063094-195063095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548629131	chr1:195063118-195063119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs67928178	chr1:195063122-195063123	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs183476643	chr1:195063125-195063126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552827979	chr1:195063126-195063127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10494722	chr1:195063150-195063151	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs35459023	chr1:195063188-195063189	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs547410502	chr1:195063189-195063190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7518089	chr1:195063243-195063244	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs373966497	chr1:195063246-195063247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7518103	chr1:195063274-195063275	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs554600441	chr1:195063275-195063276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576299975	chr1:195063306-195063307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571507682	chr1:195063311-195063312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536816254	chr1:195063315-195063316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34420016	chr1:195063326-195063327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558332383	chr1:195063359-195063360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188414766	chr1:195063363-195063364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142307953	chr1:195063387-195063388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7526195	chr1:195063390-195063391	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574775240	chr1:195063397-195063398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138629158	chr1:195063412-195063413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	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
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Breast cancer	21364760	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Maculopathy	22355348	CNVD
Schizophrenia	21346763	CNVD
early-passage human iPS cells	21368824	CNVD
Recurrent pregnancy loss	19789632	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Ollier disease	21235737	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Maculopathy	21850184	CNVD
Schizophrenia	20967226	CNVD
Oral cancer	21386901	CNVD
Maculopathy	22022419	CNVD
Breast cancer	22522925	CNVD
Asthma	20841430	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD
Intellectual disability	21811512	CNVD
Neuroblastoma	20406844	CNVD

Chromatin state (count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:195054200-195054800	Enhancers	Fetal Lung	lung
2	chr1:195063000-195065400	Weak transcription	Right Atrium	heart
3	chr1:195063600-195064000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr1:195064000-195066200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:195065200-195065600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:195065200-195065600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:195065400-195065600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr1:195065400-195065600	ZNF genes & repeats	Right Atrium	heart
9	chr1:195066200-195067200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:195066200-195067200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:195066200-195067600	Enhancers	HMEC	breast
12	chr1:195066400-195066800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:195066400-195067000	Enhancers	NHEK	skin
14	chr1:195066400-195067200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:195128600-195129200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr1:195128800-195130200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr1:195128800-195130400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr1:195129200-195129600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:195129200-195130200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr1:195129600-195130400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr1:195130000-195130400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr1:195130000-195130400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr1:195130200-195130600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr1:195135800-195136200	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr1:195154600-195155800	Enhancers	Fetal Brain Female	brain
26	chr1:195157200-195157800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:195157200-195157800	Enhancers	Colon Smooth Muscle	Colon
28	chr1:195157600-195158000	Enhancers	Rectal Smooth Muscle	rectum
29	chr1:195157800-195159000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:195159000-195160000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:195163800-195164000	Enhancers	GM12878-XiMat	blood
32	chr1:195164000-195164600	Weak transcription	GM12878-XiMat	blood
33	chr1:195164400-195165000	Active TSS	Primary T cells from cord blood	blood
34	chr1:195164400-195165000	Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr1:195164400-195165000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr1:195164400-195165000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:195164400-195165000	Active TSS	NHDF-Ad	bronchial
38	chr1:195164400-195165200	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr1:195164400-195165200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr1:195164600-195164800	Enhancers	GM12878-XiMat	blood
41	chr1:195164600-195165000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr1:195164600-195165000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr1:195164600-195165000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr1:195164800-195165000	Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr1:195164800-195165200	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr1:195164800-195165200	Enhancers	Placenta	Placenta
47	chr1:195164800-195165200	Flanking Active TSS	GM12878-XiMat	blood
48	chr1:195164800-195165400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr1:195165000-195165200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr1:195165000-195165200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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