Variant report

Variant	nsv872951
Chromosome Location	chr1:196027872-196166278
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:896)
CpG islands
(count:61)
Chromatin interactive
region (count:57)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:896 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:196116766-196116872	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:196117554-196117875	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:196117541-196117876	K562	blood:	n/a	chr1:196117542-196117558
4	ARID3A	chr1:196135561-196135602	K562	blood:	n/a	n/a
5	ARID3A	chr1:196047787-196048155	K562	blood:	n/a	n/a
6	ARID3A	chr1:196101898-196101993	K562	blood:	n/a	n/a
7	ATF1	chr1:196145565-196145830	K562	blood:	n/a	n/a
8	ATF1	chr1:196058516-196058524	K562	blood:	n/a	n/a
9	ATF1	chr1:196150338-196150600	K562	blood:	n/a	n/a
10	ATF3	chr1:196084865-196085028	K562	blood:	n/a	n/a
11	ATF3	chr1:196150155-196150653	A549	lung:	n/a	n/a
12	ATF3	chr1:196047912-196048181	K562	blood:	n/a	n/a
13	BACH1	chr1:196145870-196145898	K562	blood:	n/a	n/a
14	BACH1	chr1:196047833-196048241	H1-hESC	embryonic stem cell:	n/a	chr1:196048015-196048029
15	BACH1	chr1:196047726-196048424	K562	blood:	n/a	chr1:196048015-196048029
16	BATF	chr1:196122197-196122443	GM12878	blood:	n/a	n/a
17	BATF	chr1:196122193-196122432	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:196122194-196122473	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:196084884-196085034	K562	blood:	n/a	n/a
20	BHLHE40	chr1:196121277-196121492	K562	blood:	n/a	n/a
21	BHLHE40	chr1:196047988-196048167	K562	blood:	n/a	n/a
22	BHLHE40	chr1:196122209-196122408	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:196150445-196150467	K562	blood:	n/a	n/a
24	CBX3	chr1:196084822-196085224	K562	blood:	n/a	n/a
25	CBX3	chr1:196070301-196070636	K562	blood:	n/a	n/a
26	CBX3	chr1:196150161-196150675	K562	blood:	n/a	n/a
27	CBX3	chr1:196047874-196048274	HCT-116	colon:	n/a	n/a
28	CBX3	chr1:196150147-196151182	HCT-116	colon:	n/a	n/a
29	CBX3	chr1:196163279-196163637	K562	blood:	n/a	n/a
30	CCNT2	chr1:196047999-196048144	K562	blood:	n/a	n/a
31	CEBPB	chr1:196150105-196150820	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:196150294-196150693	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:196083463-196083660	A549	lung:	n/a	chr1:196083634-196083645
34	CEBPB	chr1:196129300-196130027	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:196150125-196150872	HCT-116	colon:	n/a	n/a
36	CEBPB	chr1:196150199-196150815	A549	lung:	n/a	n/a
37	CEBPB	chr1:196122071-196122446	IMR90	lung:	n/a	chr1:196122250-196122261
38	CEBPB	chr1:196150312-196150694	A549	lung:	n/a	n/a
39	CEBPB	chr1:196059415-196059560	K562	blood:	n/a	n/a
40	CEBPB	chr1:196155337-196155586	HepG2	liver:	n/a	chr1:196155506-196155517
41	CEBPB	chr1:196047732-196048187	HCT-116	colon:	n/a	chr1:196047933-196047944
42	CEBPB	chr1:196150157-196150782	HCT-116	colon:	n/a	n/a
43	CEBPB	chr1:196113170-196113272	K562	blood:	n/a	n/a
44	CEBPB	chr1:196113054-196113361	MCF-7	breast:	n/a	n/a
45	CEBPB	chr1:196150266-196150714	A549	lung:	n/a	n/a
46	CEBPB	chr1:196032486-196032826	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr1:196113112-196113331	HepG2	liver:	n/a	n/a
48	CEBPB	chr1:196083463-196083714	HepG2	liver:	n/a	chr1:196083634-196083645
49	CEBPB	chr1:196083359-196083715	IMR90	lung:	n/a	chr1:196083634-196083645
50	CEBPB	chr1:196150423-196150632	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:196112818-196112868	NT2-D1	testis:	n/a
2	chr1:196112818-196112868	PFSK-1	brain:	n/a
3	chr1:196112818-196112868	AG09309	skin:	n/a
4	chr1:196112818-196112868	A549	lung:	n/a
5	chr1:196112818-196112868	T-47D	breast:	n/a
6	chr1:196112818-196112868	GM12878	blood:	n/a
7	chr1:196112818-196112868	BE2_C	brain:	n/a
8	chr1:196112818-196112868	AG04449	skin:	fetal
9	chr1:196112818-196112868	ProgFib	skin:	n/a
10	chr1:196112818-196112868	NHBE	bronchial:	n/a
11	chr1:196112818-196112868	ovcar-3	ovarian:	n/a
12	chr1:196112818-196112868	H1-hESC	embryonic stem cell:	embryo
13	chr1:196112818-196112868	NH-A	brain:	n/a
14	chr1:196112818-196112868	NB4	blood:	n/a
15	chr1:196112818-196112868	SK-N-SH_RA	brain:	n/a
16	chr1:196112818-196112868	Caco-2	colon:	n/a
17	chr1:196112818-196112868	GM12892	blood:	n/a
18	chr1:196112818-196112868	LNCaP	prostate:	n/a
19	chr1:196112818-196112868	SKMC	muscle:	n/a
20	chr1:196112818-196112868	GM19239	blood:	n/a
21	chr1:196112818-196112868	HRE	kidney:	n/a
22	chr1:196112818-196112868	Hela-S3	cervix:	n/a
23	chr1:196112818-196112868	SK-N-MC	brain:	n/a
24	chr1:196112818-196112868	NHDF-neo	bronchial:	n/a
25	chr1:196112818-196112868	RPTEC	kidney:	n/a
26	chr1:196112818-196112868	HepG2	liver:	n/a
27	chr1:196112818-196112868	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:196112818-196112868	Jurkat	blood:	n/a
29	chr1:196112818-196112868	HCF	heart:	n/a
30	chr1:196112818-196112868	MCF-7	breast:	n/a
31	chr1:196112818-196112868	IMR90	lung:	fetal
32	chr1:196112818-196112868	HRPEpiC	eye:	n/a
33	chr1:196112818-196112868	HCT-116	colon:	n/a
34	chr1:196112818-196112868	HEEpiC	esophagus:	n/a
35	chr1:196112818-196112868	ECC-1	luminal epithelium:	n/a
36	chr1:196112818-196112868	HL-60	blood:	n/a
37	chr1:196112818-196112868	AG04450	lung:	fetal
38	chr1:196112818-196112868	GM12891	blood:	n/a
39	chr1:196112818-196112868	HCPEpiC	choroid plexus:	n/a
40	chr1:196112818-196112868	GM06990	blood:	n/a
41	chr1:196112818-196112868	Hepatocyte	liver:	n/a
42	chr1:196112818-196112868	HUVEC	blood vessel:	n/a
43	chr1:196112818-196112868	PrEC	prostate:	n/a
44	chr1:196112818-196112868	K562	blood:	n/a
45	chr1:196112818-196112868	HMEC	breast:	n/a
46	chr1:196112818-196112868	HRCEpiC	kidney:	n/a
47	chr1:196112818-196112868	HAEpiC	amniotic membrane:	n/a
48	chr1:196112818-196112868	U87	brain:	n/a
49	chr1:196112818-196112868	HEK293	kidney:	embryo
50	chr1:196112818-196112868	MCF10A-Er-Src	breast:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:196082312..196084819-chr1:196086856..196089362,2	K562	blood:
2	chr1:196084793..196086463-chr1:196093018..196095488,2	K562	blood:
3	chr1:196025180..196026882-chr1:196027419..196029109,2	K562	blood:
4	chr1:196024750..196028209-chr1:196030222..196033690,4	K562	blood:
5	chr1:196042086..196044811-chr1:196045371..196049542,3	K562	blood:
6	chr1:196052464..196053278-chr17:58633824..58634357,2	MCF-7	breast:
7	chr1:196036395..196038566-chr1:196046304..196047928,2	K562	blood:
8	chr1:196034151..196037732-chr1:196037758..196041366,3	K562	blood:
9	chr1:195868249..195869806-chr1:196117660..196119687,2	K562	blood:
10	chr1:196039321..196041899-chr1:196043061..196046155,3	K562	blood:
11	chr1:196053015..196055088-chr1:196056240..196058402,2	K562	blood:
12	chr1:196030521..196032166-chr1:196617172..196619617,2	K562	blood:
13	chr1:196078954..196080550-chr1:196080702..196082561,2	K562	blood:
14	chr1:196119772..196121474-chr1:196127458..196129985,2	MCF-7	breast:
15	chr1:196093766..196096415-chr1:196097794..196099859,3	K562	blood:
16	chr1:196094395..196096626-chr1:196097794..196100175,3	K562	blood:
17	chr1:196117223..196118153-chr1:196278402..196279435,4	MCF-7	breast:
18	chr1:196051756..196054719-chr1:196058554..196060673,2	MCF-7	breast:
19	chr1:196119772..196121474-chr1:196127458..196129985,2	MCF-7	breast:
20	chr1:196121049..196121874-chr1:196278478..196279171,2	MCF-7	breast:
21	chr1:196138443..196141334-chr1:196141782..196145397,4	K562	blood:
22	chr1:196023127..196024805-chr1:196041898..196043914,2	K562	blood:
23	chr1:196025146..196027992-chr1:196038512..196040205,2	K562	blood:
24	chr1:196082312..196084819-chr1:196086856..196089362,2	K562	blood:
25	chr1:196117077..196119162-chr1:196122659..196124600,2	K562	blood:
26	chr1:196084793..196086463-chr1:196093018..196095488,2	K562	blood:
27	chr1:196115298..196117734-chr1:196279190..196280706,2	MCF-7	breast:
28	chr1:196026031..196027668-chr1:196032772..196035089,2	K562	blood:
29	chr1:196034151..196037732-chr1:196037758..196041366,3	K562	blood:
30	chr1:195908986..195909573-chr1:196113721..196114467,3	MCF-7	breast:
31	chr1:196078954..196080550-chr1:196080702..196082561,2	K562	blood:
32	chr1:196025146..196027992-chr1:196038512..196040205,2	K562	blood:
33	chr1:196080775..196083436-chr1:196084849..196086558,2	K562	blood:
34	chr1:196149563..196151314-chr1:196152505..196155179,2	MCF-7	breast:
35	chr1:196042907..196044719-chr1:196047722..196049465,2	K562	blood:
36	chr1:196080775..196083436-chr1:196084849..196086558,2	K562	blood:
37	chr1:196144873..196146636-chr1:196151703..196153907,2	K562	blood:
38	chr1:196042086..196044811-chr1:196045371..196049542,3	K562	blood:
39	chr1:196138443..196141334-chr1:196141782..196145397,4	K562	blood:
40	chr1:196144873..196146636-chr1:196151703..196153907,2	K562	blood:
41	chr1:196094395..196096626-chr1:196097794..196100175,3	K562	blood:
42	chr1:196039321..196041899-chr1:196043061..196046155,3	K562	blood:
43	chr1:195908909..195909846-chr1:196117249..196118180,3	MCF-7	breast:
44	chr1:196117505..196118611-chr1:196278061..196278931,3	MCF-7	breast:
45	chr1:196093766..196096415-chr1:196097794..196099859,3	K562	blood:
46	chr1:196053015..196055088-chr1:196056240..196058402,2	K562	blood:
47	chr1:196051756..196054719-chr1:196058554..196060673,2	MCF-7	breast:
48	chr1:195891817..195893332-chr1:196109903..196112041,2	K562	blood:
49	chr1:196149563..196151314-chr1:196152505..196155179,2	MCF-7	breast:
50	chr1:196034889..196036641-chr1:196039866..196042568,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNT2-1	chr1:196129500-196129619	XLOC_001138
2	lnc-KCNT2-1	chr1:196030127-196030203	XLOC_001138

No data

Variant related genes	Relation type
ENSG00000227421	TF binding region
ENSG00000227421	CpG island
CFTR	miRNA target sites

Extended variants
information (count: 3236 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3236 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377671058	chr1:196030135-196030136	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs542086751	chr1:196030170-196030171	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs562968053	chr1:196030186-196030187	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs537047248	chr1:196030192-196030193	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs527976055	chr1:196032082-196032083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs138507336	chr1:196032101-196032102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs72746105	chr1:196032109-196032110	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs12732231	chr1:196032113-196032114	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs531716461	chr1:196032135-196032136	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs549833207	chr1:196032184-196032185	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs568724983	chr1:196032198-196032199	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs116207235	chr1:196032221-196032222	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs17637588	chr1:196032288-196032289	Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs143994558	chr1:196032319-196032320	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs189259175	chr1:196032436-196032437	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs566804164	chr1:196032467-196032468	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs533836381	chr1:196032581-196032582	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs555369252	chr1:196032599-196032600	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs17688769	chr1:196032605-196032606	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs537955814	chr1:196032617-196032618	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs147288130	chr1:196032667-196032668	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs556255153	chr1:196032712-196032713	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs534956244	chr1:196032730-196032731	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs181006658	chr1:196032734-196032735	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs552886669	chr1:196032753-196032754	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs560513031	chr1:196032768-196032769	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs111542837	chr1:196032788-196032789	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs542926836	chr1:196032823-196032824	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs185888542	chr1:196032866-196032867	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs372904350	chr1:196032874-196032875	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs531562140	chr1:196032916-196032917	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs541630188	chr1:196032973-196032974	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs561011748	chr1:196032988-196032989	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs377227918	chr1:196032997-196032998	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs12751292	chr1:196033008-196033009	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564989400	chr1:196033032-196033033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543389182	chr1:196033096-196033097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190792163	chr1:196033106-196033107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149369320	chr1:196033128-196033129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144697550	chr1:196033159-196033160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148505734	chr1:196033171-196033172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72746107	chr1:196033201-196033202	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs548973696	chr1:196033300-196033301	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs532687211	chr1:196033305-196033306	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs567281792	chr1:196033308-196033309	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs373141712	chr1:196033310-196033311	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs115788411	chr1:196033319-196033320	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs79188278	chr1:196033320-196033321	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs143532785	chr1:196033348-196033349	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs181777219	chr1:196033360-196033361	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196032200-196032600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:196032400-196033200	Enhancers	A549	lung
3	chr1:196032600-196033400	Enhancers	Hela-S3	cervix
4	chr1:196032600-196033400	Enhancers	NH-A	brain
5	chr1:196032800-196033600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:196033000-196033400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:196033000-196033800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:196033200-196033600	Enhancers	HMEC	breast
9	chr1:196047800-196048000	Enhancers	A549	lung
10	chr1:196047800-196048400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr1:196048000-196048400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:196048000-196048400	Flanking Active TSS	A549	lung
13	chr1:196048000-196048400	Enhancers	HMEC	breast
14	chr1:196048000-196048400	Enhancers	NHEK	skin
15	chr1:196055200-196055400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr1:196057600-196058200	Enhancers	NHDF-Ad	bronchial
17	chr1:196058800-196059600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:196059200-196059400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:196059600-196060800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:196059600-196061000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:196060800-196061600	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr1:196060800-196061600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:196060800-196061800	Enhancers	Fetal Brain Male	brain
24	chr1:196061000-196061400	Enhancers	Primary hematopoietic stem cells	blood
25	chr1:196061000-196061800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:196064000-196064200	Enhancers	Fetal Stomach	stomach
27	chr1:196064200-196065600	Weak transcription	Fetal Stomach	stomach
28	chr1:196065600-196065800	Enhancers	Fetal Stomach	stomach
29	chr1:196065600-196067600	Enhancers	Fetal Lung	lung
30	chr1:196065800-196066600	Weak transcription	Fetal Stomach	stomach
31	chr1:196066000-196067400	Enhancers	Brain Hippocampus Middle	brain
32	chr1:196066000-196067600	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr1:196066200-196068200	Enhancers	Brain Cingulate Gyrus	brain
34	chr1:196066400-196067000	Enhancers	Brain Germinal Matrix	brain
35	chr1:196066400-196067200	Enhancers	Brain Angular Gyrus	brain
36	chr1:196066400-196067600	Enhancers	Brain Substantia Nigra	brain
37	chr1:196066400-196067800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr1:196066600-196067000	Enhancers	Fetal Stomach	stomach
39	chr1:196066600-196067600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:196066600-196067600	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr1:196066600-196067800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr1:196066800-196067800	Enhancers	Brain Anterior Caudate	brain
43	chr1:196067000-196067600	Weak transcription	Brain Germinal Matrix	brain
44	chr1:196067000-196067800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr1:196067200-196067400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:196067400-196069200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:196067600-196067800	Enhancers	Brain Germinal Matrix	brain
48	chr1:196069200-196070400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:196073800-196074200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr1:196074200-196078000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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