Variant report

Variant	nsv831904
Chromosome Location	chr1:172912110-173070429
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:172945212-172946158	HepG2	liver:	n/a	n/a
2	ATF1	chr1:172984967-172984996	K562	blood:	n/a	n/a
3	ATF1	chr1:173031317-173031600	K562	blood:	n/a	n/a
4	ATF1	chr1:172948792-172948824	K562	blood:	n/a	n/a
5	ATF1	chr1:172916321-172916552	K562	blood:	n/a	n/a
6	ATF2	chr1:172986900-172987399	GM12878	blood:	n/a	n/a
7	ATF2	chr1:172989419-172989968	GM12878	blood:	n/a	n/a
8	ATF3	chr1:172984772-172985237	HCT-116	colon:	n/a	n/a
9	ATF3	chr1:172945144-172946085	A549	lung:	n/a	chr1:172945623-172945631 chr1:172945620-172945633 chr1:172945619-172945634 chr1:172945620-172945633 chr1:172945619-172945632 chr1:172945623-172945630 chr1:172945620-172945630 chr1:172945620-172945631
10	BACH1	chr1:172949627-172950129	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:172949668-172949980	K562	blood:	n/a	n/a
12	BATF	chr1:172936318-172936656	GM12878	blood:	n/a	chr1:172936480-172936491
13	BATF	chr1:172936303-172936691	GM12878	blood:	n/a	chr1:172936480-172936491
14	BCL11A	chr1:172989589-172989823	GM12878	blood:	n/a	n/a
15	BCL3	chr1:172945223-172946190	A549	lung:	n/a	n/a
16	BCL3	chr1:172945403-172946003	A549	lung:	n/a	n/a
17	BCLAF1	chr1:172989462-172989938	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:172989499-172990037	GM12878	blood:	n/a	n/a
19	BRCA1	chr1:172946150-172946257	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr1:172945266-172945869	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:173021632-173022367	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr1:173031239-173031729	HCT-116	colon:	n/a	n/a
23	CBX3	chr1:173025441-173026014	HCT-116	colon:	n/a	n/a
24	CBX3	chr1:173021953-173022445	HCT-116	colon:	n/a	n/a
25	CBX3	chr1:173011863-173012825	HCT-116	colon:	n/a	n/a
26	CBX3	chr1:173031195-173031811	HCT-116	colon:	n/a	n/a
27	CEBPB	chr1:173024313-173024626	HepG2	liver:	n/a	chr1:173024443-173024452 chr1:173024443-173024452 chr1:173024443-173024452 chr1:173024441-173024454 chr1:173024442-173024453 chr1:173024441-173024454 chr1:173024443-173024452 chr1:173024531-173024544
28	CEBPB	chr1:172917596-172917971	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:172949640-172950211	A549	lung:	n/a	n/a
30	CEBPB	chr1:173069679-173069990	HepG2	liver:	n/a	chr1:173069826-173069837 chr1:173069809-173069820
31	CEBPB	chr1:172920910-172921402	MCF-7	breast:	n/a	chr1:172921190-172921201
32	CEBPB	chr1:172920977-172921358	K562	blood:	n/a	chr1:172921190-172921201
33	CEBPB	chr1:173024345-173024592	K562	blood:	n/a	chr1:173024443-173024452 chr1:173024443-173024452 chr1:173024443-173024452 chr1:173024441-173024454 chr1:173024442-173024453 chr1:173024441-173024454 chr1:173024443-173024452 chr1:173024531-173024544
34	CEBPB	chr1:172945333-172945556	K562	blood:	n/a	chr1:172945411-172945422
35	CEBPB	chr1:173024305-173024637	Hela-S3	cervix:	n/a	chr1:173024443-173024452 chr1:173024443-173024452 chr1:173024443-173024452 chr1:173024441-173024454 chr1:173024442-173024453 chr1:173024441-173024454 chr1:173024443-173024452 chr1:173024531-173024544
36	CEBPB	chr1:172972327-172972578	A549	lung:	n/a	chr1:172972470-172972481
37	CEBPB	chr1:173055760-173055961	IMR90	lung:	n/a	chr1:173055812-173055823 chr1:173055854-173055865
38	CEBPB	chr1:172949741-172950043	A549	lung:	n/a	n/a
39	CEBPB	chr1:172990806-172991006	K562	blood:	n/a	chr1:172990909-172990922 chr1:172990911-172990922
40	CEBPB	chr1:173017596-173018389	HCT-116	colon:	n/a	n/a
41	CEBPB	chr1:173024274-173024640	IMR90	lung:	n/a	chr1:173024443-173024452 chr1:173024443-173024452 chr1:173024443-173024452 chr1:173024441-173024454 chr1:173024442-173024453 chr1:173024441-173024454 chr1:173024443-173024452 chr1:173024531-173024544
42	CEBPB	chr1:173069740-173069921	K562	blood:	n/a	chr1:173069826-173069837 chr1:173069809-173069820
43	CEBPB	chr1:173069660-173069945	A549	lung:	n/a	chr1:173069826-173069837 chr1:173069809-173069820
44	CEBPB	chr1:173069694-173069899	Hela-S3	cervix:	n/a	chr1:173069826-173069837 chr1:173069809-173069820
45	CEBPB	chr1:172921009-172921303	H1-hESC	embryonic stem cell:	n/a	chr1:172921190-172921201
46	CEBPB	chr1:172945253-172945748	IMR90	lung:	n/a	chr1:172945411-172945422
47	CEBPB	chr1:173011650-173012622	HCT-116	colon:	n/a	n/a
48	CEBPB	chr1:172912395-172912522	A549	lung:	n/a	n/a
49	CEBPB	chr1:172945237-172945957	Hela-S3	cervix:	n/a	chr1:172945411-172945422
50	CEBPB	chr1:172920826-172921398	IMR90	lung:	n/a	chr1:172921190-172921201

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:172956177-172956227	HIPEpiC	eye:	n/a
2	chr1:173020492-173020542	NHDF-neo	bronchial:	n/a
3	chr1:172956177-172956227	HIPEpiC	eye:	n/a
4	chr1:173020492-173020542	NHDF-neo	bronchial:	n/a
5	chr1:173018989-173019039	MCF-7	breast:	n/a
6	chr1:172956177-172956227	PANC-1	pancreas:	n/a
7	chr1:173021195-173021245	SAEC	small airway:	n/a
8	chr1:173020492-173020542	NB4	blood:	n/a
9	chr1:173021195-173021245	HIPEpiC	eye:	n/a
10	chr1:172956177-172956227	SKMC	muscle:	n/a
11	chr1:173021195-173021245	HEEpiC	esophagus:	n/a
12	chr1:173021195-173021245	HNPCEpiC	eye:	n/a
13	chr1:172929351-172929401	AG09319	gingival:	n/a
14	chr1:172929351-172929401	NT2-D1	testis:	n/a
15	chr1:173018989-173019039	MCF10A-Er-Src	breast:	n/a
16	chr1:172929351-172929401	HRE	kidney:	n/a
17	chr1:172917851-172917901	MCF-7	breast:	n/a
18	chr1:173065092-173065142	NT2-D1	testis:	n/a
19	chr1:172956275-172956325	HUVEC	blood vessel:	n/a
20	chr1:173019720-173019770	CMK	blood:	n/a
21	chr1:172956177-172956227	HNPCEpiC	eye:	n/a
22	chr1:172929351-172929401	GM12892	blood:	n/a
23	chr1:172956275-172956325	GM12891	blood:	n/a
24	chr1:173012051-173012101	ProgFib	skin:	n/a
25	chr1:173020492-173020542	HEEpiC	esophagus:	n/a
26	chr1:173020492-173020542	HL-60	blood:	n/a
27	chr1:172956177-172956227	SK-N-MC	brain:	n/a
28	chr1:172917851-172917901	SKMC	muscle:	n/a
29	chr1:173018989-173019039	HIPEpiC	eye:	n/a
30	chr1:172917851-172917901	BE2_C	brain:	n/a
31	chr1:172956275-172956325	AG04450	lung:	fetal
32	chr1:172956275-172956325	K562	blood:	n/a
33	chr1:173020492-173020542	GM12878	blood:	n/a
34	chr1:172929351-172929401	H1-hESC	embryonic stem cell:	embryo
35	chr1:173019720-173019770	AoSMC	blood vessel:	n/a
36	chr1:172917851-172917901	HEK293	kidney:	embryo
37	chr1:173019720-173019770	HCF	heart:	n/a
38	chr1:172929351-172929401	HCPEpiC	choroid plexus:	n/a
39	chr1:173021195-173021245	MCF-7	breast:	n/a
40	chr1:173019720-173019770	GM06990	blood:	n/a
41	chr1:173065092-173065142	SK-N-MC	brain:	n/a
42	chr1:173018989-173019039	HL-60	blood:	n/a
43	chr1:173012051-173012101	GM12892	blood:	n/a
44	chr1:172956275-172956325	GM12892	blood:	n/a
45	chr1:173019720-173019770	PANC-1	pancreas:	n/a
46	chr1:172929351-172929401	AG10803	skin:	n/a
47	chr1:173019720-173019770	Jurkat	blood:	n/a
48	chr1:173019720-173019770	GM12892	blood:	n/a
49	chr1:173065092-173065142	HL-60	blood:	n/a
50	chr1:173020492-173020542	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:172977791..172981145-chr1:172982435..172984642,3	MCF-7	breast:
2	chr1:173047508..173049835-chr1:173069750..173072161,2	K562	blood:
3	chr1:173065791..173068355-chr1:173072416..173074777,2	K562	blood:
4	chr1:172855842..172858682-chr1:172958652..172961353,2	K562	blood:
5	chr1:173023243..173025518-chr1:173037424..173039678,2	K562	blood:
6	chr1:173065791..173068178-chr1:173072964..173074777,2	K562	blood:
7	chr1:172935873..172938818-chr1:172941293..172944064,2	MCF-7	breast:
8	chr1:172913673..172916975-chr1:172918949..172922757,3	K562	blood:
9	chr1:172923608..172926307-chr1:172941480..172943821,2	K562	blood:
10	chr1:172908894..172911352-chr1:172913551..172915186,2	MCF-7	breast:
11	chr1:172861260..172863626-chr1:172948311..172950341,2	K562	blood:
12	chr1:173011823..173014538-chr1:173018391..173020709,2	K562	blood:
13	chr1:172957647..172960074-chr1:172961636..172964536,3	K562	blood:
14	chr1:172909514..172913371-chr1:172916147..172919223,3	K562	blood:
15	chr1:172909766..172912196-chr1:172914192..172916042,2	K562	blood:
16	chr1:172990478..172992459-chr1:172994949..172996898,2	K562	blood:
17	chr1:172909766..172912196-chr1:172914192..172916042,2	K562	blood:
18	chr1:172977791..172981145-chr1:172982435..172984642,3	MCF-7	breast:
19	chr1:172957647..172960074-chr1:172961636..172964536,3	K562	blood:
20	chr1:173047508..173049835-chr1:173069750..173072161,2	K562	blood:
21	chr1:173055099..173057845-chr1:173067910..173069482,2	MCF-7	breast:
22	chr1:172935873..172938818-chr1:172941293..172944064,2	MCF-7	breast:
23	chr1:172909514..172913371-chr1:172916147..172919223,3	K562	blood:
24	chr1:172957647..172960074-chr1:172961636..172964536,2	K562	blood:
25	chr1:172957647..172960074-chr1:172961636..172964536,2	K562	blood:
26	chr1:173055099..173057845-chr1:173067910..173069482,2	MCF-7	breast:
27	chr1:172983131..172985017-chr10:82858351..82859851,2	MCF-7	breast:
28	chr1:172937098..172937996-chr20:22890442..22890942,2	MCF-7	breast:
29	chr1:173013039..173013740-chr3:135789899..135790668,2	MCF-7	breast:
30	chr1:172976210..172978094-chr1:172989483..172991773,2	K562	blood:
31	chr1:173023243..173025518-chr1:173037424..173039678,2	K562	blood:
32	chr1:172913673..172916975-chr1:172918949..172922757,3	K562	blood:
33	chr1:172976210..172978094-chr1:172989483..172991773,2	K562	blood:
34	chr1:172923608..172926307-chr1:172941480..172943821,2	K562	blood:
35	chr1:172990478..172992459-chr1:172994949..172996898,2	K562	blood:
36	chr1:172940580..172943092-chr1:173158852..173161378,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FASLG-2	chr1:172992638-172992713	ENSG00000224228.2
2	lnc-FASLG-2	chr1:172973422-172973575	ENSG00000224228.2
3	lnc-FASLG-2	chr1:172992638-172992713	ENSG00000224228.1
4	lnc-FASLG-2	chr1:172985453-172985664	ENSG00000224228.1
5	lnc-FASLG-2	chr1:172973431-172973575	ENSG00000224228.1
6	lnc-FASLG-2	chr1:172985453-172985664	ENSG00000224228.2
7	lnc-FASLG-2	chr1:173033013-173033155	ENSG00000224228.1
8	lnc-FASLG-2	chr1:173033013-173033155	ENSG00000224228.2

Variant related genes	Relation type
TNFSF18	TF binding region
TNFSF18	CpG island
ENSG00000120337	chromatin interactions

Extended variants
information (count: 4917 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4917 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190334415	chr1:172912149-172912150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545834805	chr1:172912164-172912165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372590439	chr1:172912172-172912173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557575892	chr1:172912200-172912201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572760113	chr1:172912291-172912292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540251792	chr1:172912304-172912305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139611112	chr1:172912331-172912332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569632637	chr1:172912349-172912350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530402053	chr1:172912360-172912361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542583899	chr1:172912382-172912383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114807305	chr1:172912396-172912397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531016231	chr1:172912414-172912415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535448431	chr1:172912439-172912440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552600678	chr1:172912482-172912483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555471735	chr1:172912487-172912488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560437363	chr1:172912503-172912504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182102786	chr1:172912571-172912572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528440074	chr1:172912578-172912579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375665353	chr1:172912629-172912630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565651693	chr1:172912639-172912640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186833704	chr1:172912671-172912672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568152914	chr1:172912731-172912732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149984242	chr1:172912750-172912751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556886504	chr1:172912760-172912761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534747869	chr1:172912799-172912800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568990804	chr1:172912842-172912843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554048342	chr1:172912925-172912926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190019173	chr1:172912961-172912962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538444627	chr1:172912962-172912963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183366784	chr1:172913009-172913010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528034390	chr1:172913045-172913046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115145581	chr1:172913107-172913108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555391940	chr1:172913141-172913142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573725607	chr1:172913230-172913231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577412322	chr1:172913233-172913234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374308427	chr1:172913240-172913241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542495550	chr1:172913294-172913295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563838345	chr1:172913321-172913322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531099299	chr1:172913435-172913436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188896274	chr1:172913441-172913442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113204127	chr1:172913457-172913458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528552702	chr1:172913533-172913534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546731596	chr1:172913539-172913540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193038959	chr1:172913563-172913564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11799419	chr1:172913564-172913565	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550815103	chr1:172913565-172913566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7517726	chr1:172913577-172913578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs183521435	chr1:172913587-172913588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188067880	chr1:172913645-172913646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575982126	chr1:172913677-172913678	Weak transcription Enhancers	n/a	n/a	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
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	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
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Parkinson disease	21829596	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172903600-172914200	Weak transcription	Aorta	Aorta
2	chr1:172905600-172916000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:172910800-172914200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:172910800-172916200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:172911000-172914400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr1:172911200-172914200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:172911200-172914400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:172911200-172915800	Weak transcription	NHDF-Ad	bronchial
9	chr1:172911200-172916000	Weak transcription	HSMMtube	muscle
10	chr1:172911200-172916200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:172911200-172917000	Weak transcription	Fetal Stomach	stomach
12	chr1:172911200-172917600	Weak transcription	Fetal Lung	lung
13	chr1:172911400-172912600	Weak transcription	Fetal Brain Female	brain
14	chr1:172911400-172916000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr1:172911400-172916000	Weak transcription	NH-A	brain
16	chr1:172912800-172913000	Enhancers	Fetal Brain Female	brain
17	chr1:172913600-172919200	Enhancers	HUVEC	blood vessel
18	chr1:172914200-172914400	Enhancers	Aorta	Aorta
19	chr1:172914200-172914800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:172914200-172915000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:172914400-172914600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr1:172914400-172914600	Enhancers	Placenta Amnion	Placenta Amnion
23	chr1:172914400-172914800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr1:172914600-172914800	Enhancers	Dnd41	blood
25	chr1:172914600-172915000	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr1:172914600-172917800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr1:172914800-172915000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:172914800-172915400	Weak transcription	Dnd41	blood
29	chr1:172914800-172916000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:172915000-172915200	Enhancers	Placenta Amnion	Placenta Amnion
31	chr1:172915000-172917000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:172915000-172918000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:172915200-172924600	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr1:172915400-172918600	Enhancers	Dnd41	blood
35	chr1:172915600-172917200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:172915800-172917000	Enhancers	Primary hematopoietic stem cells	blood
37	chr1:172915800-172917000	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr1:172915800-172917000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:172915800-172918800	Enhancers	NHDF-Ad	bronchial
40	chr1:172916000-172916200	Enhancers	HSMMtube	muscle
41	chr1:172916000-172916600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:172916000-172916600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr1:172916000-172916600	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr1:172916000-172916600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr1:172916000-172916800	Enhancers	NHEK	skin
46	chr1:172916000-172917000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:172916000-172917000	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr1:172916000-172918600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr1:172916000-172918600	Enhancers	NH-A	brain
50	chr1:172916000-172918800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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