Variant report

Variant	nsv874901
Chromosome Location	chr2:114022569-114079565
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1176)
CpG islands
(count:1711)
Chromatin interactive
region (count:14)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1176 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:114045088-114045239	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:114040264-114041172	HepG2	liver:	n/a	n/a
3	ATF1	chr2:114075345-114075373	K562	blood:	n/a	n/a
4	ATF1	chr2:114055261-114055461	K562	blood:	n/a	n/a
5	ATF1	chr2:114024089-114024236	K562	blood:	n/a	n/a
6	ATF3	chr2:114040459-114040953	A549	lung:	n/a	n/a
7	ATF3	chr2:114041213-114041894	A549	lung:	n/a	n/a
8	ATF3	chr2:114041147-114041724	A549	lung:	n/a	n/a
9	BACH1	chr2:114035511-114035512	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:114040686-114040928	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr2:114055241-114055494	GM12878	blood:	n/a	n/a
12	BCL3	chr2:114041201-114041826	A549	lung:	n/a	n/a
13	BCL3	chr2:114040358-114041943	A549	lung:	n/a	n/a
14	BHLHE40	chr2:114046006-114046008	HepG2	liver:	n/a	n/a
15	BHLHE40	chr2:114040418-114041081	HepG2	liver:	n/a	n/a
16	BHLHE40	chr2:114046278-114046507	HepG2	liver:	n/a	n/a
17	BRCA1	chr2:114040643-114040957	HepG2	liver:	n/a	n/a
18	CBX3	chr2:114055345-114055649	HCT-116	colon:	n/a	n/a
19	CBX3	chr2:114055239-114055537	K562	blood:	n/a	n/a
20	CBX3	chr2:114040703-114040894	K562	blood:	n/a	n/a
21	CEBPB	chr2:114055822-114056129	HepG2	liver:	n/a	chr2:114055956-114055967
22	CEBPB	chr2:114040548-114041043	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr2:114040551-114040977	MCF-7	breast:	n/a	n/a
24	CEBPB	chr2:114039489-114039719	HepG2	liver:	n/a	chr2:114039653-114039664 chr2:114039625-114039636 chr2:114039627-114039638
25	CEBPB	chr2:114040619-114040920	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:114042176-114042465	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:114041258-114041910	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr2:114040237-114041052	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:114055816-114056060	K562	blood:	n/a	chr2:114055956-114055967
30	CEBPB	chr2:114040625-114040923	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:114055814-114056136	IMR90	lung:	n/a	chr2:114055956-114055967
32	CEBPB	chr2:114040619-114040924	K562	blood:	n/a	n/a
33	CEBPB	chr2:114067953-114068081	K562	blood:	n/a	n/a
34	CEBPB	chr2:114046495-114046655	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr2:114040670-114040864	MCF-7	breast:	n/a	n/a
36	CEBPB	chr2:114055798-114056148	A549	lung:	n/a	chr2:114055956-114055967
37	CEBPB	chr2:114067844-114068161	MCF-7	breast:	n/a	n/a
38	CEBPB	chr2:114040436-114041082	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr2:114055832-114056101	H1-hESC	embryonic stem cell:	n/a	chr2:114055956-114055967
40	CEBPB	chr2:114040146-114040965	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:114040682-114040865	K562	blood:	n/a	n/a
42	CEBPB	chr2:114040595-114040894	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:114040510-114041498	A549	lung:	n/a	n/a
44	CEBPB	chr2:114040515-114040992	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:114040466-114041006	A549	lung:	n/a	n/a
46	CEBPB	chr2:114044994-114045283	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:114023382-114023391	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:114039478-114039754	IMR90	lung:	n/a	chr2:114039653-114039664 chr2:114039625-114039636 chr2:114039627-114039638
49	CEBPB	chr2:114044511-114044514	A549	lung:	n/a	n/a
50	CEBPB	chr2:114036189-114037046	ECC-1	luminal epithelium:	n/a	chr2:114036613-114036626

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114048829-114048879	Caco-2	colon:	n/a
2	chr2:114062344-114062394	RPTEC	kidney:	n/a
3	chr2:114037060-114037110	HAEpiC	amniotic membrane:	n/a
4	chr2:114048829-114048879	Caco-2	colon:	n/a
5	chr2:114062344-114062394	RPTEC	kidney:	n/a
6	chr2:114037060-114037110	HAEpiC	amniotic membrane:	n/a
7	chr2:114039512-114039562	HEEpiC	esophagus:	n/a
8	chr2:114036953-114037003	Caco-2	colon:	n/a
9	chr2:114050884-114050934	GM06990	blood:	n/a
10	chr2:114030824-114030874	LNCaP	prostate:	n/a
11	chr2:114036571-114036621	SAEC	small airway:	n/a
12	chr2:114033830-114033880	PrEC	prostate:	n/a
13	chr2:114049041-114049091	GM12891	blood:	n/a
14	chr2:114036571-114036621	AG09309	skin:	n/a
15	chr2:114039512-114039562	NT2-D1	testis:	n/a
16	chr2:114048973-114049023	PFSK-1	brain:	n/a
17	chr2:114047065-114047115	A549	lung:	n/a
18	chr2:114036444-114036494	GM12891	blood:	n/a
19	chr2:114033360-114033410	HL-60	blood:	n/a
20	chr2:114033360-114033410	H1-hESC	embryonic stem cell:	embryo
21	chr2:114037060-114037110	HUVEC	blood vessel:	n/a
22	chr2:114033490-114033540	HAEpiC	amniotic membrane:	n/a
23	chr2:114049041-114049091	AG09319	gingival:	n/a
24	chr2:114036953-114037003	RPTEC	kidney:	n/a
25	chr2:114030824-114030874	HEK293	kidney:	embryo
26	chr2:114031854-114031904	SAEC	small airway:	n/a
27	chr2:114033360-114033410	HIPEpiC	eye:	n/a
28	chr2:114035619-114035669	AG10803	skin:	n/a
29	chr2:114033360-114033410	MCF-7	breast:	n/a
30	chr2:114036953-114037003	HCF	heart:	n/a
31	chr2:114047065-114047115	SKMC	muscle:	n/a
32	chr2:114034595-114034645	HEEpiC	esophagus:	n/a
33	chr2:114033581-114033631	K562	blood:	n/a
34	chr2:114034534-114034584	Caco-2	colon:	n/a
35	chr2:114033581-114033631	HEEpiC	esophagus:	n/a
36	chr2:114045972-114046022	HUVEC	blood vessel:	n/a
37	chr2:114033490-114033540	SK-N-SH_RA	brain:	n/a
38	chr2:114035619-114035669	ECC-1	luminal epithelium:	n/a
39	chr2:114048868-114048918	GM12892	blood:	n/a
40	chr2:114050884-114050934	MCF10A-Er-Src	breast:	n/a
41	chr2:114033830-114033880	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:114034595-114034645	Hela-S3	cervix:	n/a
43	chr2:114048264-114048314	PANC-1	pancreas:	n/a
44	chr2:114033830-114033880	NHDF-neo	bronchial:	n/a
45	chr2:114037060-114037110	AG09309	skin:	n/a
46	chr2:114035983-114036033	GM12892	blood:	n/a
47	chr2:114048829-114048879	MCF10A-Er-Src	breast:	n/a
48	chr2:114035619-114035669	NHDF-neo	bronchial:	n/a
49	chr2:114037060-114037110	Hepatocyte	liver:	n/a
50	chr2:114048932-114048982	BJ	skin:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:114026056..114028346-chr2:114029301..114030897,2	MCF-7	breast:
2	chr2:114034404..114036046-chr2:114042741..114044743,2	K562	blood:
3	chr2:114041343..114041852-chr8:123235626..123236502,2	MCF-7	breast:
4	chr2:114031113..114032698-chr2:114037168..114039837,2	MCF-7	breast:
5	chr2:113996531..113999009-chr2:114030396..114033362,2	K562	blood:
6	chr2:114026056..114028346-chr2:114029301..114030897,2	MCF-7	breast:
7	chr2:114033208..114035776-chr2:114039656..114042402,2	K562	blood:
8	chr2:114023172..114025279-chr2:114025318..114027200,2	MCF-7	breast:
9	chr2:114040686..114041186-chr2:114127813..114128575,2	MCF-7	breast:
10	chr2:114035943..114037997-chr2:114049469..114051321,2	K562	blood:
11	chr2:114067489..114069342-chr2:114085282..114087156,2	MCF-7	breast:
12	chr2:114033208..114035776-chr2:114039656..114042402,2	K562	blood:
13	chr2:114023172..114025279-chr2:114025318..114027200,2	MCF-7	breast:
14	chr2:114031113..114032698-chr2:114037168..114039837,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC016745.1-7	chr2:114031713-114033283	NONHSAT073774
2	lnc-PSD4-6	chr2:114052336-114052898	l_1929_NR_026821
3	lnc-PSD4-1	chr2:114027778-114027808	NONHSAT073773
4	lnc-PSD4-1	chr2:114030634-114030847	ENSG00000189223.9
5	lnc-PSD4-6	chr2:114052628-114052956	NONHSAT073775
6	lnc-PSD4-6	chr2:114051429-114051789	NONHSAT073775
7	lnc-PSD4-1	chr2:114023053-114024550	ENSG00000189223
8	lnc-PSD4-6	chr2:114051662-114051789	NONHSAT073776
9	lnc-PSD4-1	chr2:114023053-114023157	NONHSAT073773
10	lnc-PSD4-1	chr2:114023053-114023157	ENSG00000189223.9
11	lnc-PSD4-1	chr2:114027778-114027884	ENSG00000189223.9
12	lnc-PSD4-6	chr2:114052336-114052823	NONHSAT073776
13	lnc-PSD4-6	chr2:114052029-114052233	NONHSAT073776
14	lnc-PSD4-1	chr2:114023053-114023747	ENSG00000189223
15	lnc-PSD4-1	chr2:114029413-114029548	ENSG00000189223.9
16	lnc-PSD4-6	chr2:114052029-114052431	NONHSAT073775
17	lnc-PSD4-6	chr2:114051429-114051789	l_1929_NR_026821
18	lnc-PSD4-1	chr2:114023053-114024587	ENSG00000189223
19	lnc-PSD4-1	chr2:114023053-114034158	ENSG00000189223.9
20	lnc-PSD4-1	chr2:114023053-114023294	ENSG00000189223
21	lnc-PSD4-6	chr2:114052029-114052233	l_1929_NR_026821

No data

Variant related genes	Relation type
PAX8	TF binding region
PAX8	CpG island
ENSG00000125618	chromatin interactions
ENSG00000258395	chromatin interactions
C12orf35	miRNA target sites
SLC39A6	miRNA target sites
RPSA	miRNA target sites

Extended variants
information (count: 2097 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2097 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6542126	chr2:114022569-114022570	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149928758	chr2:114022573-114022574	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75832520	chr2:114022625-114022626	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6542127	chr2:114022658-114022659	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs185197445	chr2:114022679-114022680	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531423269	chr2:114022706-114022707	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551510095	chr2:114022719-114022720	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571307939	chr2:114022771-114022772	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189767424	chr2:114022772-114022773	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11691437	chr2:114022856-114022857	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs567534457	chr2:114022891-114022892	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565593562	chr2:114022919-114022920	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182424359	chr2:114022922-114022923	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568922657	chr2:114022924-114022925	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs80314227	chr2:114022947-114022948	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34065581	chr2:114023046-114023047	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs895416	chr2:114023079-114023080	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs578085299	chr2:114023085-114023086	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs143984194	chr2:114023208-114023209	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
20	rs895415	chr2:114023217-114023218	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs895414	chr2:114023243-114023244	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs543381606	chr2:114023282-114023283	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
23	rs562427120	chr2:114023311-114023312	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
24	rs148633064	chr2:114023334-114023335	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
25	rs34084732	chr2:114023350-114023351	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
26	rs377753887	chr2:114023359-114023360	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
27	rs371157204	chr2:114023435-114023436	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs545094023	chr2:114023516-114023517	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs374929878	chr2:114023609-114023610	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs142080649	chr2:114023638-114023639	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs547545962	chr2:114023640-114023641	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs567391046	chr2:114023673-114023674	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs151147844	chr2:114023705-114023706	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs188266131	chr2:114023726-114023727	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs568886479	chr2:114023780-114023781	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs537864852	chr2:114023810-114023811	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs557901027	chr2:114023832-114023833	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs571693641	chr2:114023849-114023850	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs534080491	chr2:114023883-114023884	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs554333688	chr2:114023903-114023904	Genic enhancers Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs574292884	chr2:114024108-114024109	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs536899934	chr2:114024114-114024115	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs556918222	chr2:114024226-114024227	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs576070702	chr2:114024249-114024250	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs568173192	chr2:114024257-114024258	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs532679002	chr2:114024308-114024309	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs114934707	chr2:114024337-114024338	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs78987244	chr2:114024420-114024421	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs560070999	chr2:114024447-114024448	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs576837359	chr2:114024487-114024488	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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	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
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
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD

Chromatin state (count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113999600-114028400	Weak transcription	Ovary	ovary
2	chr2:114010200-114030400	Weak transcription	GM12878-XiMat	blood
3	chr2:114015200-114022800	Weak transcription	Colon Smooth Muscle	Colon
4	chr2:114015800-114023600	Weak transcription	HSMM	muscle
5	chr2:114016200-114023600	Weak transcription	HSMMtube	muscle
6	chr2:114016200-114028000	Weak transcription	Fetal Brain Female	brain
7	chr2:114016400-114026000	Weak transcription	Fetal Heart	heart
8	chr2:114018800-114023800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr2:114019000-114022600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr2:114019200-114024000	Weak transcription	Fetal Muscle Trunk	muscle
11	chr2:114019200-114026800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr2:114019400-114028200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr2:114019600-114026000	Weak transcription	Spleen	Spleen
14	chr2:114020000-114027800	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr2:114020400-114023800	Enhancers	Liver	Liver
16	chr2:114020600-114023000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
17	chr2:114021000-114024200	Strong transcription	Placenta	Placenta
18	chr2:114021200-114024000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr2:114021200-114024000	Strong transcription	Lung	lung
20	chr2:114021200-114028200	Strong transcription	Duodenum Mucosa	Duodenum
21	chr2:114021400-114022800	Weak transcription	Fetal Muscle Leg	muscle
22	chr2:114021400-114023600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr2:114021400-114024800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr2:114021600-114026200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr2:114021600-114028200	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr2:114021800-114024000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr2:114022000-114024600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr2:114022200-114023000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr2:114022200-114023400	Enhancers	Pancreas	Pancrea
30	chr2:114022200-114026400	Strong transcription	Primary T cells from cord blood	blood
31	chr2:114022200-114027600	Genic enhancers	Fetal Kidney	kidney
32	chr2:114022400-114023400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:114022400-114023800	Strong transcription	Adipose Nuclei	Adipose
34	chr2:114022400-114025000	Strong transcription	Fetal Thymus	thymus
35	chr2:114022800-114023200	Enhancers	Colon Smooth Muscle	Colon
36	chr2:114022800-114023200	Enhancers	Fetal Intestine Large	intestine
37	chr2:114022800-114024200	Genic enhancers	Fetal Muscle Leg	muscle
38	chr2:114023000-114023200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr2:114023000-114023200	Enhancers	Gastric	stomach
40	chr2:114023000-114023800	Enhancers	Fetal Intestine Small	intestine
41	chr2:114023000-114026800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr2:114023000-114027200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:114023200-114023400	Bivalent Enhancer	HepG2	liver
44	chr2:114023200-114026800	Weak transcription	Colon Smooth Muscle	Colon
45	chr2:114023200-114039800	Weak transcription	Gastric	stomach
46	chr2:114023400-114025000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:114023400-114025000	Weak transcription	Pancreas	Pancrea
48	chr2:114023400-114027000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr2:114023600-114023800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr2:114023600-114024600	Enhancers	HSMMtube	muscle

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