Variant report

Variant	nsv428752
Chromosome Location	chr1:57455083-57605082
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1047)
CpG islands
(count:549)
Chromatin interactive
region (count:22)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1047 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:57524288-57524625	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:57526249-57526690	HepG2	liver:	n/a	n/a
3	ATF1	chr1:57518319-57518517	K562	blood:	n/a	n/a
4	ATF2	chr1:57590546-57590837	GM12878	blood:	n/a	n/a
5	BACH1	chr1:57590909-57590984	K562	blood:	n/a	n/a
6	BACH1	chr1:57545173-57545722	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr1:57498970-57499318	GM12878	blood:	n/a	chr1:57499153-57499162 chr1:57499293-57499302
8	BATF	chr1:57590375-57590871	GM12878	blood:	n/a	n/a
9	BATF	chr1:57590567-57590878	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:57498996-57499244	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:57590457-57590870	GM12878	blood:	n/a	n/a
12	BCL3	chr1:57603696-57603969	GM12878	blood:	n/a	chr1:57603800-57603809
13	BCL3	chr1:57590472-57590757	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:57603726-57603996	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:57590541-57590767	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:57480489-57480587	K562	blood:	n/a	n/a
17	BRCA1	chr1:57532607-57532699	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:57502915-57502982	HepG2	liver:	n/a	chr1:57502927-57502938 chr1:57502926-57502937
19	CEBPB	chr1:57530982-57531317	IMR90	lung:	n/a	chr1:57531145-57531156
20	CEBPB	chr1:57598680-57599053	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:57598663-57599026	A549	lung:	n/a	n/a
22	CEBPB	chr1:57584647-57585111	MCF-7	breast:	n/a	chr1:57584936-57584953
23	CEBPB	chr1:57540739-57541044	HepG2	liver:	n/a	chr1:57540884-57540897 chr1:57540886-57540895 chr1:57540886-57540895 chr1:57540885-57540896 chr1:57540886-57540895 chr1:57540886-57540895 chr1:57540884-57540895
24	CEBPB	chr1:57576940-57577214	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:57550776-57550927	HepG2	liver:	n/a	chr1:57550854-57550865
26	CEBPB	chr1:57518930-57519106	K562	blood:	n/a	chr1:57518976-57518987
27	CEBPB	chr1:57598697-57599043	K562	blood:	n/a	n/a
28	CEBPB	chr1:57604186-57604403	H1-hESC	embryonic stem cell:	n/a	chr1:57604285-57604298
29	CEBPB	chr1:57469296-57469299	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:57598703-57599029	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:57531016-57531257	A549	lung:	n/a	chr1:57531145-57531156
32	CEBPB	chr1:57598673-57599032	A549	lung:	n/a	n/a
33	CEBPB	chr1:57530985-57531318	HepG2	liver:	n/a	chr1:57531145-57531156
34	CEBPB	chr1:57540719-57541063	IMR90	lung:	n/a	chr1:57540884-57540897 chr1:57540886-57540895 chr1:57540886-57540895 chr1:57540885-57540896 chr1:57540886-57540895 chr1:57540886-57540895 chr1:57540884-57540895
35	CEBPB	chr1:57490617-57490884	HepG2	liver:	n/a	chr1:57490744-57490757
36	CEBPB	chr1:57531014-57531329	K562	blood:	n/a	chr1:57531145-57531156
37	CEBPB	chr1:57518909-57519082	HepG2	liver:	n/a	chr1:57518976-57518987
38	CEBPB	chr1:57598679-57599042	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr1:57584787-57585002	Hela-S3	cervix:	n/a	chr1:57584936-57584953
40	CEBPB	chr1:57584622-57585174	MCF-7	breast:	n/a	chr1:57584936-57584953
41	CEBPB	chr1:57469112-57469414	IMR90	lung:	n/a	chr1:57469282-57469293
42	CEBPB	chr1:57499370-57499600	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:57518897-57519062	A549	lung:	n/a	chr1:57518976-57518987
44	CEBPB	chr1:57540801-57541062	A549	lung:	n/a	chr1:57540884-57540897 chr1:57540886-57540895 chr1:57540886-57540895 chr1:57540885-57540896 chr1:57540886-57540895 chr1:57540886-57540895 chr1:57540884-57540895
45	CEBPB	chr1:57469144-57469453	Hela-S3	cervix:	n/a	chr1:57469282-57469293
46	CEBPB	chr1:57598673-57599230	IMR90	lung:	n/a	n/a
47	CEBPB	chr1:57586129-57586253	A549	lung:	n/a	n/a
48	CEBPB	chr1:57598671-57599169	K562	blood:	n/a	n/a
49	CEBPB	chr1:57551457-57551587	IMR90	lung:	n/a	n/a
50	CEBPB	chr1:57469126-57469477	HepG2	liver:	n/a	chr1:57469282-57469293

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:57575654-57575704	PrEC	prostate:	n/a
2	chr1:57575654-57575704	HEK293	kidney:	embryo
3	chr1:57490967-57491017	HepG2	liver:	n/a
4	chr1:57567746-57567796	LNCaP	prostate:	n/a
5	chr1:57490967-57491017	HEEpiC	esophagus:	n/a
6	chr1:57567746-57567796	HRCEpiC	kidney:	n/a
7	chr1:57480925-57480975	HUVEC	blood vessel:	n/a
8	chr1:57458781-57458831	Hepatocyte	liver:	n/a
9	chr1:57570305-57570355	NHDF-neo	bronchial:	n/a
10	chr1:57458781-57458831	AG09319	gingival:	n/a
11	chr1:57480925-57480975	T-47D	breast:	n/a
12	chr1:57567746-57567796	CMK	blood:	n/a
13	chr1:57575654-57575704	GM12892	blood:	n/a
14	chr1:57490967-57491017	HMEC	breast:	n/a
15	chr1:57567746-57567796	HCPEpiC	choroid plexus:	n/a
16	chr1:57458781-57458831	HRPEpiC	eye:	n/a
17	chr1:57514244-57514294	HCT-116	colon:	n/a
18	chr1:57567746-57567796	H1-hESC	embryonic stem cell:	embryo
19	chr1:57514244-57514294	GM19239	blood:	n/a
20	chr1:57470853-57470903	AG09319	gingival:	n/a
21	chr1:57575654-57575704	HCT-116	colon:	n/a
22	chr1:57575654-57575704	NHBE	bronchial:	n/a
23	chr1:57535755-57535805	ECC-1	luminal epithelium:	n/a
24	chr1:57575654-57575704	ProgFib	skin:	n/a
25	chr1:57570305-57570355	BJ	skin:	n/a
26	chr1:57575654-57575704	HMEC	breast:	n/a
27	chr1:57480925-57480975	A549	lung:	n/a
28	chr1:57567746-57567796	Caco-2	colon:	n/a
29	chr1:57570305-57570355	GM12892	blood:	n/a
30	chr1:57490967-57491017	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:57458781-57458831	HepG2	liver:	n/a
32	chr1:57570305-57570355	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:57570305-57570355	HRCEpiC	kidney:	n/a
34	chr1:57490967-57491017	SK-N-SH	brain:	n/a
35	chr1:57480925-57480975	HNPCEpiC	eye:	n/a
36	chr1:57490967-57491017	NHBE	bronchial:	n/a
37	chr1:57567746-57567796	AoSMC	blood vessel:	n/a
38	chr1:57567746-57567796	AG04449	skin:	fetal
39	chr1:57514244-57514294	ovcar-3	ovarian:	n/a
40	chr1:57470853-57470903	NH-A	brain:	n/a
41	chr1:57535755-57535805	H1-hESC	embryonic stem cell:	embryo
42	chr1:57480925-57480975	HRCEpiC	kidney:	n/a
43	chr1:57480925-57480975	K562	blood:	n/a
44	chr1:57570305-57570355	MCF10A-Er-Src	breast:	n/a
45	chr1:57535755-57535805	SAEC	small airway:	n/a
46	chr1:57570305-57570355	Hepatocyte	liver:	n/a
47	chr1:57535755-57535805	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:57514244-57514294	A549	lung:	n/a
49	chr1:57458781-57458831	K562	blood:	n/a
50	chr1:57570305-57570355	IMR90	lung:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:57479613..57481966-chr1:57490580..57493279,2	K562	blood:
2	chr1:57531940..57535705-chr1:57536134..57539998,5	K562	blood:
3	chr1:57571162..57573727-chr1:57574083..57575763,2	MCF-7	breast:
4	chr1:57531940..57535705-chr1:57536134..57539998,5	K562	blood:
5	chr1:57561067..57563455-chr1:57563927..57566507,2	K562	blood:
6	chr1:57537146..57539862-chr1:57547524..57549494,2	K562	blood:
7	chr1:57537146..57539862-chr1:57547524..57549494,2	K562	blood:
8	chr1:57561067..57563455-chr1:57563927..57566507,2	K562	blood:
9	chr1:57510764..57512729-chr1:57516872..57518806,2	MCF-7	breast:
10	chr1:57571162..57573727-chr1:57574083..57575763,2	MCF-7	breast:
11	chr1:57571164..57573212-chr1:57625317..57627807,2	MCF-7	breast:
12	chr1:57474408..57475958-chr1:57482944..57485883,2	K562	blood:
13	chr1:57479454..57482343-chr1:57482459..57484417,2	MCF-7	breast:
14	chr1:57501264..57504904-chr1:57505961..57509544,3	K562	blood:
15	chr1:57297206..57298203-chr1:57526862..57527650,4	MCF-7	breast:
16	chr1:57479613..57481966-chr1:57490580..57493279,2	K562	blood:
17	chr1:57501264..57504904-chr1:57505961..57509544,3	K562	blood:
18	chr1:57474408..57475958-chr1:57482944..57485883,2	K562	blood:
19	chr1:57424333..57426873-chr1:57465525..57467884,2	K562	blood:
20	chr1:57544234..57547035-chr1:57693675..57695976,2	K562	blood:
21	chr1:57479454..57482343-chr1:57482459..57484417,2	MCF-7	breast:
22	chr1:57510764..57512729-chr1:57516872..57518806,2	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8A-1	chr1:57470035-57470242	NONHSAT003466
2	lnc-C8A-1	chr1:57467511-57467711	NONHSAT003466
3	lnc-C8A-1	chr1:57458012-57458138	NONHSAT003469
4	lnc-C8A-1	chr1:57466994-57467051	NONHSAT003472
5	lnc-C8A-1	chr1:57470035-57470621	NONHSAT003473
6	lnc-C8A-2	chr1:57479407-57480373	ENSG00000231229.1
7	lnc-C8A-1	chr1:57467202-57467319	NONHSAT003472
8	lnc-C8A-1	chr1:57479407-57480189	NONHSAT003466
9	lnc-C8A-1	chr1:57463593-57463820	NONHSAT003471
10	lnc-C8A-2	chr1:57470035-57470242	ENSG00000231229.1
11	lnc-C8A-1	chr1:57463593-57463856	NONHSAT003469
12	lnc-C8A-2	chr1:57467510-57467711	ENSG00000231229.1
13	lnc-C8A-1	chr1:57467244-57467711	NONHSAT003473
14	lnc-C8A-1	chr1:57462018-57462508	NONHSAT003471
15	lnc-C8B-1	chr1:57460452-57462521	NONHSAT003470
16	lnc-C8A-1	chr1:57462308-57462595	NONHSAT003468
17	lnc-C8A-2	chr1:57457023-57457582	ENSG00000231229.1
18	lnc-C8A-1	chr1:57457023-57457583	NONHSAT003466
19	lnc-C8A-1	chr1:57462308-57462508	NONHSAT003469
20	lnc-C8A-1	chr1:57462308-57462430	ENSG00000236341.1
21	lnc-C8A-1	chr1:57463462-57463820	NONHSAT003472
22	lnc-C8A-1	chr1:57466994-57467051	NONHSAT003471
23	lnc-C8A-1	chr1:57467202-57467319	NONHSAT003471
24	lnc-C8A-1	chr1:57457936-57458138	NONHSAT003468

No data

Variant related genes	Relation type
DAB1	TF binding region
DAB1	CpG island

Extended variants
information (count: 5712 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5712 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371303738	chr1:57455101-57455102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541733999	chr1:57455113-57455114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77579173	chr1:57455128-57455129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1329452	chr1:57455181-57455182	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs112343414	chr1:57455224-57455225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560166150	chr1:57455248-57455249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532479958	chr1:57455251-57455252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376520050	chr1:57455261-57455262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545934428	chr1:57455324-57455325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182735590	chr1:57455332-57455333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576656359	chr1:57455423-57455424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562540387	chr1:57455446-57455447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531762839	chr1:57455483-57455484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548587596	chr1:57455568-57455569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114810650	chr1:57455614-57455615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536674794	chr1:57455649-57455650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185838662	chr1:57455650-57455651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149027590	chr1:57455689-57455690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561235547	chr1:57455741-57455742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571094476	chr1:57455755-57455756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542462673	chr1:57455790-57455791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539534575	chr1:57455824-57455825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143012220	chr1:57455854-57455855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555338576	chr1:57455869-57455870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569653873	chr1:57455887-57455888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191758151	chr1:57455935-57455936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542909191	chr1:57455945-57455946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572306340	chr1:57455950-57455951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75182945	chr1:57455971-57455972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111617148	chr1:57455974-57455975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183639265	chr1:57455988-57455989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557521052	chr1:57455996-57455997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577463456	chr1:57456033-57456034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545871125	chr1:57456067-57456068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs953753	chr1:57456081-57456082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs375026745	chr1:57456119-57456120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77120216	chr1:57456142-57456143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113981507	chr1:57456157-57456158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189028092	chr1:57456163-57456164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191986398	chr1:57456186-57456187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141187715	chr1:57456189-57456190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548153466	chr1:57456219-57456220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182040963	chr1:57456229-57456230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186722346	chr1:57456251-57456252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549867517	chr1:57456274-57456275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565253356	chr1:57456279-57456280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569753423	chr1:57456285-57456286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544771130	chr1:57456290-57456291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535058908	chr1:57456347-57456348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191530654	chr1:57456369-57456370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57454400-57459200	Weak transcription	Liver	Liver
2	chr1:57456600-57457800	Enhancers	Fetal Intestine Small	intestine
3	chr1:57456800-57457400	Enhancers	Fetal Intestine Large	intestine
4	chr1:57457400-57462400	Weak transcription	Fetal Intestine Large	intestine
5	chr1:57457800-57480400	Weak transcription	Fetal Intestine Small	intestine
6	chr1:57458000-57458400	Enhancers	Psoas Muscle	Psoas
7	chr1:57458200-57458400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr1:57458200-57458600	Enhancers	Fetal Kidney	kidney
9	chr1:57458200-57458800	Active TSS	Skeletal Muscle Female	skeletal muscle
10	chr1:57458200-57458800	Active TSS	Stomach Smooth Muscle	stomach
11	chr1:57458400-57458800	Active TSS	Skeletal Muscle Male	skeletal muscle
12	chr1:57458400-57459000	Enhancers	Fetal Brain Female	brain
13	chr1:57458400-57460400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr1:57458400-57466600	Weak transcription	Psoas Muscle	Psoas
15	chr1:57458600-57459600	Weak transcription	Fetal Kidney	kidney
16	chr1:57458800-57459400	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr1:57458800-57459600	Enhancers	Brain Germinal Matrix	brain
18	chr1:57458800-57459600	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr1:57459000-57459200	Enhancers	Aorta	Aorta
20	chr1:57459000-57459400	Enhancers	Ovary	ovary
21	chr1:57459000-57474600	Weak transcription	Fetal Brain Female	brain
22	chr1:57459200-57459800	Enhancers	Liver	Liver
23	chr1:57459200-57459800	Enhancers	HepG2	liver
24	chr1:57459200-57460200	Weak transcription	Aorta	Aorta
25	chr1:57459200-57460400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr1:57459200-57460400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr1:57459400-57460000	Enhancers	Fetal Brain Male	brain
28	chr1:57459400-57460200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr1:57459400-57460400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr1:57459400-57464000	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr1:57459600-57460000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr1:57459600-57460400	Enhancers	Fetal Kidney	kidney
33	chr1:57459600-57460400	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr1:57459600-57460600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr1:57459600-57466200	Weak transcription	Brain Germinal Matrix	brain
36	chr1:57459800-57460800	Weak transcription	Liver	Liver
37	chr1:57459800-57461200	Weak transcription	HepG2	liver
38	chr1:57459800-57463200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr1:57460200-57460400	Enhancers	Aorta	Aorta
40	chr1:57460400-57462200	Weak transcription	Fetal Kidney	kidney
41	chr1:57460400-57463800	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr1:57460400-57464400	Weak transcription	Aorta	Aorta
43	chr1:57460400-57483000	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr1:57460800-57461800	Enhancers	Liver	Liver
45	chr1:57461000-57464200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:57461200-57461400	Enhancers	HepG2	liver
47	chr1:57461800-57468000	Weak transcription	Liver	Liver
48	chr1:57462200-57462400	Enhancers	Fetal Kidney	kidney
49	chr1:57462400-57463600	Strong transcription	Fetal Intestine Large	intestine
50	chr1:57463200-57463800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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