Variant report

Variant	nsv874858
Chromosome Location	chr2:112354445-112512202
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4000)
CpG islands
(count:795)
Chromatin interactive
region (count:128)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4000 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112382440-112382785	K562	blood:	n/a	n/a
2	ARID3A	chr2:112400566-112400827	K562	blood:	n/a	n/a
3	ARID3A	chr2:112376535-112377049	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:112456481-112457142	K562	blood:	n/a	n/a
5	ARID3A	chr2:112374864-112376031	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:112456187-112457145	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:112421055-112421554	K562	blood:	n/a	n/a
8	ARID3A	chr2:112377103-112377411	K562	blood:	n/a	n/a
9	ARID3A	chr2:112407331-112407538	K562	blood:	n/a	n/a
10	ARID3A	chr2:112383691-112384719	K562	blood:	n/a	n/a
11	ATF1	chr2:112391689-112391967	K562	blood:	n/a	n/a
12	ATF1	chr2:112400419-112400917	K562	blood:	n/a	n/a
13	ATF1	chr2:112409614-112409887	K562	blood:	n/a	n/a
14	ATF1	chr2:112456406-112457077	K562	blood:	n/a	n/a
15	ATF1	chr2:112383432-112384030	K562	blood:	n/a	n/a
16	ATF1	chr2:112382410-112382671	K562	blood:	n/a	n/a
17	ATF2	chr2:112463190-112463864	GM12878	blood:	n/a	n/a
18	ATF2	chr2:112390081-112390607	GM12878	blood:	n/a	n/a
19	ATF2	chr2:112390137-112390517	GM12878	blood:	n/a	n/a
20	ATF2	chr2:112463192-112463793	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr2:112463235-112463985	GM12878	blood:	n/a	n/a
22	ATF2	chr2:112463287-112463853	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr2:112456419-112457084	K562	blood:	n/a	n/a
24	ATF3	chr2:112456345-112457150	A549	lung:	n/a	n/a
25	ATF3	chr2:112456296-112457112	A549	lung:	n/a	n/a
26	ATF3	chr2:112383692-112384042	K562	blood:	n/a	n/a
27	BACH1	chr2:112455784-112457242	K562	blood:	n/a	n/a
28	BACH1	chr2:112459592-112460040	K562	blood:	n/a	n/a
29	BACH1	chr2:112436147-112436481	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr2:112409768-112409943	K562	blood:	n/a	n/a
31	BACH1	chr2:112425190-112425427	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr2:112456370-112457002	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr2:112459487-112460173	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr2:112400397-112400730	K562	blood:	n/a	n/a
35	BACH1	chr2:112434807-112435070	H1-hESC	embryonic stem cell:	n/a	n/a
36	BATF	chr2:112391706-112392054	GM12878	blood:	n/a	n/a
37	BATF	chr2:112463344-112463733	GM12878	blood:	n/a	chr2:112463539-112463550 chr2:112463544-112463554
38	BATF	chr2:112420627-112420977	GM12878	blood:	n/a	chr2:112420794-112420805
39	BATF	chr2:112493928-112494211	GM12878	blood:	n/a	n/a
40	BATF	chr2:112505291-112505565	GM12878	blood:	n/a	n/a
41	BATF	chr2:112471477-112471670	GM12878	blood:	n/a	n/a
42	BATF	chr2:112463258-112463790	GM12878	blood:	n/a	chr2:112463539-112463550 chr2:112463544-112463554
43	BATF	chr2:112456512-112456765	GM12878	blood:	n/a	chr2:112456597-112456608 chr2:112456598-112456608 chr2:112456648-112456659
44	BATF	chr2:112409684-112409970	GM12878	blood:	n/a	chr2:112409791-112409802
45	BATF	chr2:112420612-112421016	GM12878	blood:	n/a	chr2:112420794-112420805
46	BATF	chr2:112456533-112456724	GM12878	blood:	n/a	chr2:112456597-112456608 chr2:112456598-112456608 chr2:112456648-112456659
47	BATF	chr2:112505231-112505635	GM12878	blood:	n/a	n/a
48	BATF	chr2:112409676-112409939	GM12878	blood:	n/a	chr2:112409791-112409802
49	BCL11A	chr2:112463385-112463718	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:112463312-112463751	H1-hESC	embryonic stem cell:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112462079-112462129	HNPCEpiC	eye:	n/a
2	chr2:112439582-112439632	A549	lung:	n/a
3	chr2:112462079-112462129	HNPCEpiC	eye:	n/a
4	chr2:112439582-112439632	A549	lung:	n/a
5	chr2:112505362-112505412	GM19239	blood:	n/a
6	chr2:112417362-112417412	HEK293	kidney:	embryo
7	chr2:112439582-112439632	HRPEpiC	eye:	n/a
8	chr2:112435953-112436003	H1-hESC	embryonic stem cell:	embryo
9	chr2:112440678-112440728	NB4	blood:	n/a
10	chr2:112439582-112439632	ProgFib	skin:	n/a
11	chr2:112375854-112375904	LNCaP	prostate:	n/a
12	chr2:112505362-112505412	CMK	blood:	n/a
13	chr2:112430423-112430473	GM19239	blood:	n/a
14	chr2:112420098-112420148	HRCEpiC	kidney:	n/a
15	chr2:112383396-112383446	GM12891	blood:	n/a
16	chr2:112456811-112456861	HL-60	blood:	n/a
17	chr2:112430423-112430473	HMEC	breast:	n/a
18	chr2:112417362-112417412	NT2-D1	testis:	n/a
19	chr2:112456811-112456861	HMEC	breast:	n/a
20	chr2:112375854-112375904	GM12892	blood:	n/a
21	chr2:112439582-112439632	T-47D	breast:	n/a
22	chr2:112391213-112391263	MCF-7	breast:	n/a
23	chr2:112440678-112440728	HEK293	kidney:	embryo
24	chr2:112462079-112462129	IMR90	lung:	fetal
25	chr2:112430423-112430473	AG04449	skin:	fetal
26	chr2:112420098-112420148	HNPCEpiC	eye:	n/a
27	chr2:112439582-112439632	NB4	blood:	n/a
28	chr2:112420098-112420148	H1-hESC	embryonic stem cell:	embryo
29	chr2:112456811-112456861	GM12891	blood:	n/a
30	chr2:112375854-112375904	SAEC	small airway:	n/a
31	chr2:112468472-112468522	U87	brain:	n/a
32	chr2:112456811-112456861	HCPEpiC	choroid plexus:	n/a
33	chr2:112439582-112439632	MCF10A-Er-Src	breast:	n/a
34	chr2:112420098-112420148	U87	brain:	n/a
35	chr2:112383396-112383446	AG04450	lung:	fetal
36	chr2:112391213-112391263	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:112462079-112462129	HRCEpiC	kidney:	n/a
38	chr2:112391213-112391263	T-47D	breast:	n/a
39	chr2:112391213-112391263	HCPEpiC	choroid plexus:	n/a
40	chr2:112383396-112383446	BE2_C	brain:	n/a
41	chr2:112420098-112420148	Hepatocyte	liver:	n/a
42	chr2:112383396-112383446	AG04449	skin:	fetal
43	chr2:112417362-112417412	SKMC	muscle:	n/a
44	chr2:112375854-112375904	RPTEC	kidney:	n/a
45	chr2:112468472-112468522	NH-A	brain:	n/a
46	chr2:112456811-112456861	ECC-1	luminal epithelium:	n/a
47	chr2:112456811-112456861	BE2_C	brain:	n/a
48	chr2:112462079-112462129	Caco-2	colon:	n/a
49	chr2:112505362-112505412	HMEC	breast:	n/a
50	chr2:112420098-112420148	HAEpiC	amniotic membrane:	n/a

(count:128 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:112426158..112428552-chr2:112435022..112436930,2	MCF-7	breast:
2	chr2:112395688..112397342-chr2:112404915..112406866,2	K562	blood:
3	chr2:112395688..112397342-chr2:112404915..112406866,2	K562	blood:
4	chr2:111876801..111879359-chr2:112454758..112456829,3	K562	blood:
5	chr2:112415374..112417265-chr2:112463686..112465545,2	MCF-7	breast:
6	chr2:112377497..112380123-chr2:112459340..112461483,2	MCF-7	breast:
7	chr2:112424871..112427816-chr2:112455987..112457978,2	K562	blood:
8	chr2:112426158..112428552-chr2:112435022..112436930,2	MCF-7	breast:
9	chr2:111876869..111879041-chr2:112387692..112389774,2	MCF-7	breast:
10	chr2:112377428..112379190-chr2:112425946..112427813,2	MCF-7	breast:
11	chr2:112420650..112422209-chr2:112446178..112448541,2	MCF-7	breast:
12	chr2:112376832..112377622-chr2:112493675..112494396,3	MCF-7	breast:
13	chr2:112459900..112461419-chr2:112462104..112464419,2	K562	blood:
14	chr2:112407508..112410822-chr2:112413499..112416205,3	MCF-7	breast:
15	chr2:112397541..112399746-chr2:112416589..112418149,2	MCF-7	breast:
16	chr2:112397541..112399746-chr2:112416589..112418149,2	MCF-7	breast:
17	chr2:112412317..112414698-chr2:112415444..112417727,2	K562	blood:
18	chr2:112395623..112398484-chr2:112400861..112402821,2	K562	blood:
19	chr2:112395813..112398635-chr2:112411801..112413497,2	MCF-7	breast:
20	chr2:112412973..112414698-chr2:112415341..112416944,2	K562	blood:
21	chr2:112415609..112418598-chr2:112432941..112434486,2	MCF-7	breast:
22	chr2:112444088..112445707-chr2:112453009..112455817,2	K562	blood:
23	chr2:112392219..112395501-chr2:112398954..112401482,3	K562	blood:
24	chr2:112421208..112422895-chr2:112434298..112436276,2	MCF-7	breast:
25	chr2:112376861..112378670-chr2:112458387..112460460,2	K562	blood:
26	chr2:112415503..112417633-chr2:112463417..112464976,2	MCF-7	breast:
27	chr2:112382780..112385327-chr2:112409728..112411247,2	MCF-7	breast:
28	chr2:112390933..112393569-chr2:112395712..112398433,3	K562	blood:
29	chr2:112376815..112377394-chr2:112421087..112421873,3	MCF-7	breast:
30	chr2:112462219..112464486-chr2:112466010..112468775,3	K562	blood:
31	chr2:112418934..112421688-chr2:112422273..112424750,2	K562	blood:
32	chr2:112423717..112425251-chr2:112471117..112473005,2	MCF-7	breast:
33	chr2:112437626..112439337-chr2:112454101..112456706,2	MCF-7	breast:
34	chr2:112392219..112395501-chr2:112398954..112401482,3	K562	blood:
35	chr2:112443707..112446597-chr2:112448656..112451342,3	K562	blood:
36	chr2:112395623..112398484-chr2:112400861..112402821,2	K562	blood:
37	chr2:112420650..112422209-chr2:112446178..112448541,2	MCF-7	breast:
38	chr2:112445224..112447481-chr2:112456345..112458135,2	K562	blood:
39	chr2:112415609..112418598-chr2:112432941..112434486,2	MCF-7	breast:
40	chr2:112402419..112406237-chr2:112407904..112411161,4	MCF-7	breast:
41	chr2:112389816..112391811-chr2:112392544..112394680,2	MCF-7	breast:
42	chr2:112377428..112379190-chr2:112425946..112427813,2	MCF-7	breast:
43	chr2:112407508..112410822-chr2:112413499..112416205,3	MCF-7	breast:
44	chr2:111876801..111878957-chr2:112454944..112456829,2	K562	blood:
45	chr2:112374024..112376697-chr2:112377578..112380485,2	K562	blood:
46	chr2:112415314..112417347-chr2:112459623..112461902,2	MCF-7	breast:
47	chr2:112444088..112447481-chr2:112453009..112458135,6	K562	blood:
48	chr2:112409243..112412120-chr2:112414450..112416738,2	K562	blood:
49	chr2:112404706..112406626-chr2:112415850..112417469,2	MCF-7	breast:
50	chr2:112413487..112415634-chr2:112416547..112421397,4	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MERTK-1	chr2:112365277-112365592	NONHSAT073660
2	lnc-MERTK-4	chr2:112432603-112432920	NONHSAT073661
3	lnc-MERTK-1	chr2:112365418-112365592	XLOC_001626
4	lnc-MERTK-1	chr2:112369479-112369982	NONHSAT073660
5	lnc-MERTK-1	chr2:112369479-112370095	XLOC_001626

No data

Variant related genes	Relation type
ENSG00000237583	TF binding region
ENSG00000227842	TF binding region
ENSG00000228615	TF binding region
ENSG00000225744	TF binding region
ENSG00000237583	CpG island
ENSG00000227842	CpG island
ENSG00000228615	CpG island
ENSG00000225744	CpG island
ENSG00000135829	chromatin interactions
ENSG00000237583	chromatin interactions
ENSG00000227842	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000153094	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 5330 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:5330 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574674911	chr2:112354455-112354456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs71228255	chr2:112354468-112354469	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs536881540	chr2:112354515-112354516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs62164628	chr2:112354592-112354593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577032119	chr2:112354620-112354621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546097768	chr2:112354681-112354682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544860495	chr2:112354700-112354701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572510910	chr2:112354713-112354714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541522971	chr2:112354724-112354725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561488262	chr2:112354750-112354751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs62164629	chr2:112354909-112354910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114706598	chr2:112354941-112354942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564724923	chr2:112354969-112354970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533418190	chr2:112355026-112355027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547319498	chr2:112355096-112355097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566867274	chr2:112355260-112355261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535890785	chr2:112355274-112355275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2673264	chr2:112355291-112355292	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189578887	chr2:112355350-112355351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs180764596	chr2:112355362-112355363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62164630	chr2:112355363-112355364	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs556841272	chr2:112355372-112355373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563800541	chr2:112355376-112355377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113460654	chr2:112355379-112355380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576979335	chr2:112355389-112355390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112620675	chr2:112355391-112355392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs62164631	chr2:112355422-112355423	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs368654953	chr2:112355445-112355446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185379895	chr2:112355446-112355447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191025534	chr2:112355454-112355455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150595146	chr2:112355456-112355457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145134007	chr2:112355475-112355476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561425022	chr2:112355478-112355479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181389539	chr2:112355479-112355480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544304452	chr2:112355520-112355521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564475924	chr2:112355523-112355524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186534160	chr2:112355572-112355573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149674176	chr2:112355590-112355591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142810799	chr2:112355635-112355636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550812872	chr2:112355678-112355679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567355872	chr2:112355730-112355731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529281351	chr2:112355737-112355738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549367015	chr2:112355757-112355758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139663790	chr2:112355772-112355773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536038759	chr2:112355779-112355780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371506634	chr2:112355822-112355823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531674134	chr2:112355843-112355844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551858921	chr2:112355872-112355873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570552649	chr2:112355946-112355947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553092445	chr2:112355973-112355974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1973 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112354400-112354600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr2:112354400-112355600	Enhancers	Fetal Thymus	thymus
3	chr2:112354400-112356800	Enhancers	HUVEC	blood vessel
4	chr2:112354800-112355400	Enhancers	Dnd41	blood
5	chr2:112355200-112355400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr2:112355200-112355600	Enhancers	HepG2	liver
7	chr2:112355400-112356400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr2:112355600-112356000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:112356200-112356800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:112356400-112356800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr2:112356400-112356800	Enhancers	K562	blood
12	chr2:112363400-112363800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr2:112364000-112364200	Enhancers	Primary hematopoietic stem cells	blood
14	chr2:112364400-112365000	Weak transcription	Primary hematopoietic stem cells	blood
15	chr2:112365000-112365200	Enhancers	Primary hematopoietic stem cells	blood
16	chr2:112365200-112368000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr2:112367600-112369200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr2:112367600-112369600	Enhancers	Dnd41	blood
19	chr2:112367600-112369800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr2:112367600-112369800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr2:112368000-112369800	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr2:112368000-112369800	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr2:112368000-112369800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr2:112368200-112369600	Enhancers	Fetal Thymus	thymus
25	chr2:112369800-112374200	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr2:112369800-112374200	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr2:112369800-112374400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr2:112372800-112374600	Enhancers	HepG2	liver
29	chr2:112373000-112373200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:112373000-112373200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr2:112373000-112373200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr2:112373200-112375200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:112373400-112374600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr2:112373600-112375200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:112373800-112374400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:112373800-112376800	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr2:112374000-112376400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr2:112374000-112376400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:112374200-112374400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr2:112374200-112374800	Enhancers	Left Ventricle	heart
41	chr2:112374200-112375400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr2:112374200-112375400	Enhancers	Hela-S3	cervix
43	chr2:112374200-112375400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr2:112374200-112375800	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr2:112374200-112376400	Enhancers	Ovary	ovary
46	chr2:112374200-112376600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:112374200-112377000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr2:112374400-112374600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:112374400-112374600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr2:112374400-112374600	Enhancers	Lung	lung

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