Variant report

Variant	nsv948821
Chromosome Location	chr1:72049987-72477221
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	chr1:72384415-72384667	HepG2	liver:	n/a	chr1:72384650-72384666
2	ATF1	chr1:72445759-72445819	K562	blood:	n/a	n/a
3	ATF2	chr1:72433360-72433766	GM12878	blood:	n/a	n/a
4	ATF2	chr1:72433342-72433674	GM12878	blood:	n/a	n/a
5	BATF	chr1:72082343-72082505	GM12878	blood:	n/a	chr1:72082460-72082471
6	BATF	chr1:72246451-72246721	GM12878	blood:	n/a	chr1:72246586-72246597 chr1:72246587-72246597
7	BATF	chr1:72051772-72051970	GM12878	blood:	n/a	n/a
8	BATF	chr1:72246439-72246725	GM12878	blood:	n/a	chr1:72246586-72246597 chr1:72246587-72246597
9	BATF	chr1:72049996-72050255	GM12878	blood:	n/a	n/a
10	BATF	chr1:72433420-72433717	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:72433421-72433695	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:72205203-72205242	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:72378156-72378200	GM12878	blood:	n/a	n/a
14	BRCA1	chr1:72391047-72391054	GM12878	blood:	n/a	n/a
15	CEBPB	chr1:72411635-72411888	IMR90	lung:	n/a	chr1:72411787-72411798
16	CEBPB	chr1:72290161-72290431	A549	lung:	n/a	chr1:72290286-72290297
17	CEBPB	chr1:72407709-72407906	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:72290112-72290442	HepG2	liver:	n/a	chr1:72290286-72290297
19	CEBPB	chr1:72240165-72240391	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:72474879-72475236	IMR90	lung:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073 chr1:72474884-72474897
21	CEBPB	chr1:72132835-72133315	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
22	CEBPB	chr1:72474893-72475164	A549	lung:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
23	CEBPB	chr1:72474908-72475232	HepG2	liver:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
24	CEBPB	chr1:72294559-72294726	HepG2	liver:	n/a	chr1:72294674-72294685
25	CEBPB	chr1:72122476-72122921	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:72290139-72290394	K562	blood:	n/a	chr1:72290286-72290297
27	CEBPB	chr1:72093008-72093050	K562	blood:	n/a	chr1:72093010-72093023 chr1:72093010-72093021 chr1:72093010-72093023
28	CEBPB	chr1:72396266-72396495	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:72138249-72138465	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:72132278-72133317	IMR90	lung:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
31	CEBPB	chr1:72322163-72322385	HepG2	liver:	n/a	chr1:72322284-72322295
32	CEBPB	chr1:72132850-72133320	Hela-S3	cervix:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
33	CEBPB	chr1:72353163-72353392	HepG2	liver:	n/a	chr1:72353242-72353253
34	CEBPB	chr1:72087468-72087896	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:72411685-72411897	HepG2	liver:	n/a	chr1:72411787-72411798
36	CEBPB	chr1:72132885-72133214	HepG2	liver:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
37	CEBPB	chr1:72230408-72230785	IMR90	lung:	n/a	chr1:72230589-72230600
38	CEBPB	chr1:72353101-72353423	IMR90	lung:	n/a	chr1:72353242-72353253
39	CEBPB	chr1:72230432-72230774	A549	lung:	n/a	chr1:72230589-72230600
40	CEBPB	chr1:72120017-72120305	HepG2	liver:	n/a	chr1:72120144-72120155
41	CEBPB	chr1:72132874-72133198	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
42	CEBPB	chr1:72103843-72104179	IMR90	lung:	n/a	n/a
43	CEBPB	chr1:72326678-72327071	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:72230419-72230782	HepG2	liver:	n/a	chr1:72230589-72230600
45	CEBPB	chr1:72161508-72161870	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:72128205-72128324	HepG2	liver:	n/a	chr1:72128261-72128272
47	CEBPB	chr1:72474965-72475177	K562	blood:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
48	CEBPB	chr1:72353187-72353408	A549	lung:	n/a	chr1:72353242-72353253
49	CEBPB	chr1:72396255-72396524	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr1:72230483-72230683	Hela-S3	cervix:	n/a	chr1:72230589-72230600

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72382645-72382695	NHDF-neo	bronchial:	n/a
2	chr1:72382645-72382695	NHDF-neo	bronchial:	n/a
3	chr1:72190606-72190656	BJ	skin:	n/a
4	chr1:72190606-72190656	NHDF-neo	bronchial:	n/a
5	chr1:72190606-72190656	SK-N-SH	brain:	n/a
6	chr1:72382835-72382885	HCF	heart:	n/a
7	chr1:72302970-72303020	PrEC	prostate:	n/a
8	chr1:72302970-72303020	GM12891	blood:	n/a
9	chr1:72302970-72303020	HL-60	blood:	n/a
10	chr1:72058414-72058464	HRCEpiC	kidney:	n/a
11	chr1:72058414-72058464	HNPCEpiC	eye:	n/a
12	chr1:72382645-72382695	HEEpiC	esophagus:	n/a
13	chr1:72382835-72382885	HEK293	kidney:	embryo
14	chr1:72382835-72382885	MCF-7	breast:	n/a
15	chr1:72302970-72303020	CMK	blood:	n/a
16	chr1:72354156-72354206	NB4	blood:	n/a
17	chr1:72058414-72058464	AG10803	skin:	n/a
18	chr1:72382645-72382695	AG04449	skin:	fetal
19	chr1:72058414-72058464	AG09309	skin:	n/a
20	chr1:72354156-72354206	PANC-1	pancreas:	n/a
21	chr1:72302970-72303020	HMEC	breast:	n/a
22	chr1:72382835-72382885	HCPEpiC	choroid plexus:	n/a
23	chr1:72058414-72058464	Caco-2	colon:	n/a
24	chr1:72190606-72190656	MCF10A-Er-Src	breast:	n/a
25	chr1:72190606-72190656	AG04450	lung:	fetal
26	chr1:72190606-72190656	NT2-D1	testis:	n/a
27	chr1:72058414-72058464	Hela-S3	cervix:	n/a
28	chr1:72190606-72190656	AoSMC	blood vessel:	n/a
29	chr1:72382645-72382695	Jurkat	blood:	n/a
30	chr1:72302970-72303020	PANC-1	pancreas:	n/a
31	chr1:72302970-72303020	HNPCEpiC	eye:	n/a
32	chr1:72382835-72382885	HRE	kidney:	n/a
33	chr1:72190606-72190656	PANC-1	pancreas:	n/a
34	chr1:72058414-72058464	NHDF-neo	bronchial:	n/a
35	chr1:72382835-72382885	PFSK-1	brain:	n/a
36	chr1:72302970-72303020	HEEpiC	esophagus:	n/a
37	chr1:72354156-72354206	HepG2	liver:	n/a
38	chr1:72302970-72303020	T-47D	breast:	n/a
39	chr1:72382645-72382695	H1-hESC	embryonic stem cell:	embryo
40	chr1:72354156-72354206	MCF10A-Er-Src	breast:	n/a
41	chr1:72382645-72382695	AG10803	skin:	n/a
42	chr1:72190606-72190656	HCF	heart:	n/a
43	chr1:72190606-72190656	HUVEC	blood vessel:	n/a
44	chr1:72354156-72354206	HIPEpiC	eye:	n/a
45	chr1:72190606-72190656	NHBE	bronchial:	n/a
46	chr1:72058414-72058464	AG04449	skin:	fetal
47	chr1:72302970-72303020	HCPEpiC	choroid plexus:	n/a
48	chr1:72302970-72303020	RPTEC	kidney:	n/a
49	chr1:72190606-72190656	HNPCEpiC	eye:	n/a
50	chr1:72382645-72382695	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:72381957..72383996-chr1:72389950..72392631,2	K562	blood:
2	chr1:72129396..72131726-chr1:72132350..72134861,2	K562	blood:
3	chr1:72187008..72189556-chr1:72189903..72192438,2	MCF-7	breast:
4	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:
5	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:
6	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
7	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
8	chr1:71662113..71662902-chr1:72053492..72054309,2	MCF-7	breast:
9	chr1:72053665..72054637-chr1:72503102..72503767,2	MCF-7	breast:
10	chr1:72472788..72474801-chr1:72492789..72495541,2	K562	blood:
11	chr1:72463115..72465700-chr1:72466215..72468715,2	K562	blood:
12	chr1:72467998..72470410-chr1:72472067..72474561,2	K562	blood:
13	chr1:72187008..72189556-chr1:72189903..72192438,2	MCF-7	breast:
14	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
15	chr1:72381957..72383996-chr1:72389950..72392631,2	K562	blood:
16	chr1:72463115..72465700-chr1:72466215..72468715,2	K562	blood:
17	chr1:71915989..71918426-chr1:72103464..72106010,2	K562	blood:
18	chr1:72142368..72144115-chr1:72151008..72153823,2	K562	blood:
19	chr1:72129396..72131726-chr1:72132350..72134861,2	K562	blood:
20	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
21	chr1:72399874..72402263-chr1:72409207..72411359,2	K562	blood:
22	chr1:72142368..72144115-chr1:72151008..72153823,2	K562	blood:
23	chr1:72399874..72402263-chr1:72409207..72411359,2	K562	blood:
24	chr1:72467998..72470410-chr1:72472067..72474561,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZRANB2-1	chr1:72259915-72260219	ENSG00000228853.1
2	lnc-ZRANB2-1	chr1:72263758-72263953	ENSG00000228853.1
3	lnc-ZRANB2-1	chr1:72302663-72302695	ENSG00000228853.1

Variant related genes	Relation type
NEGR1-IT1	TF binding region
NEGR1	TF binding region
ENSG00000271618	TF binding region
NEGR1-IT1	CpG island
NEGR1	CpG island
ENSG00000271618	CpG island

Extended variants
information (count: 12361 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:12361 , 50 per page) page: 1 2 3 4 5 6 7 ... 248

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1213524	chr1:72049987-72049988	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12073053	chr1:72050001-72050002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71651480	chr1:72050010-72050011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111770288	chr1:72050080-72050081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541243824	chr1:72050088-72050089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78439813	chr1:72050121-72050122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570743195	chr1:72050135-72050136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539378343	chr1:72050152-72050153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377073818	chr1:72050153-72050154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552904121	chr1:72050173-72050174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187218794	chr1:72050220-72050221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535490852	chr1:72050224-72050225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117925638	chr1:72050236-72050237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575039999	chr1:72050257-72050258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146669784	chr1:72050297-72050298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557164482	chr1:72050356-72050357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192594794	chr1:72050357-72050358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546197642	chr1:72050376-72050377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185429650	chr1:72050382-72050383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189604113	chr1:72050415-72050416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542291188	chr1:72050469-72050470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79998153	chr1:72050543-72050544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531060604	chr1:72050544-72050545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572646471	chr1:72050555-72050556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141558345	chr1:72050579-72050580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12073347	chr1:72050611-72050612	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370896686	chr1:72050644-72050645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533218048	chr1:72050698-72050699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546585280	chr1:72050728-72050729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566414405	chr1:72050882-72050883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375680562	chr1:72050983-72050984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558363032	chr1:72051008-72051009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180791498	chr1:72051114-72051115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150515988	chr1:72051147-72051148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568591728	chr1:72051159-72051160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1334992	chr1:72051206-72051207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs185079648	chr1:72051224-72051225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542355482	chr1:72051238-72051239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577375484	chr1:72051294-72051295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374928833	chr1:72051299-72051300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540078509	chr1:72051328-72051329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563536438	chr1:72051372-72051373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553388169	chr1:72051412-72051413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563523291	chr1:72051413-72051414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530943146	chr1:72051417-72051418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544450137	chr1:72051418-72051419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546072389	chr1:72051502-72051503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139450288	chr1:72051520-72051521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542227698	chr1:72051647-72051648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562091322	chr1:72051657-72051658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
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
Papillary thyroid carcinoma	21436994	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
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Epilepsy	20502679	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1172 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72040800-72062000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:72048400-72050800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr1:72049200-72050800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:72049400-72050000	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr1:72050600-72054400	Weak transcription	Adipose Nuclei	Adipose
6	chr1:72050800-72054000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:72054000-72054800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:72054000-72055000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:72054000-72055000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:72054000-72055000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:72054200-72054400	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr1:72054400-72055000	Enhancers	Adipose Nuclei	Adipose
13	chr1:72054400-72055000	Enhancers	Fetal Heart	heart
14	chr1:72054400-72055000	Enhancers	Fetal Stomach	stomach
15	chr1:72054400-72056800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr1:72054600-72054800	Enhancers	Colon Smooth Muscle	Colon
17	chr1:72054600-72055000	Enhancers	Rectal Smooth Muscle	rectum
18	chr1:72054800-72055000	Enhancers	Stomach Smooth Muscle	stomach
19	chr1:72054800-72071800	Weak transcription	Colon Smooth Muscle	Colon
20	chr1:72055000-72056800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:72055000-72058400	Weak transcription	Fetal Stomach	stomach
22	chr1:72055000-72058800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:72055000-72062200	Weak transcription	Rectal Smooth Muscle	rectum
24	chr1:72055000-72075800	Weak transcription	Stomach Smooth Muscle	stomach
25	chr1:72055400-72058600	Weak transcription	Osteobl	bone
26	chr1:72056400-72058800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr1:72056800-72058200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr1:72058200-72058400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr1:72058200-72058400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr1:72058200-72058600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr1:72058200-72059400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr1:72058200-72059400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr1:72058200-72059400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr1:72058400-72058600	Enhancers	Fetal Stomach	stomach
35	chr1:72058400-72059000	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr1:72058400-72059200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr1:72058400-72059400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr1:72058600-72058800	Weak transcription	Fetal Stomach	stomach
39	chr1:72058600-72059000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr1:72058600-72059200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:72058800-72059600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:72059000-72059200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr1:72059000-72059200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr1:72059200-72065000	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr1:72059600-72067000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:72062200-72062400	Enhancers	Rectal Smooth Muscle	rectum
47	chr1:72065000-72066600	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr1:72066200-72066400	Enhancers	Primary B cells from peripheral blood	blood
49	chr1:72066400-72067200	Weak transcription	Primary B cells from peripheral blood	blood
50	chr1:72067000-72067200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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