Variant report

Variant	nsv433358
Chromosome Location	chr3:19547184-19996508
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2874)
CpG islands
(count:1893)
Chromatin interactive
region (count:104)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2874 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:19908154-19908565	K562	blood:	n/a	n/a
2	ARID3A	chr3:19988281-19988728	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:19974779-19974812	K562	blood:	n/a	n/a
4	ARID3A	chr3:19975714-19975914	K562	blood:	n/a	n/a
5	ARID3A	chr3:19838885-19838997	K562	blood:	n/a	n/a
6	ARID3A	chr3:19986723-19988668	K562	blood:	n/a	n/a
7	ARID3A	chr3:19971710-19971731	K562	blood:	n/a	n/a
8	ARID3A	chr3:19930083-19930989	K562	blood:	n/a	n/a
9	ARID3A	chr3:19940290-19940486	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:19970496-19970602	K562	blood:	n/a	n/a
11	ARID3A	chr3:19988883-19988922	K562	blood:	n/a	n/a
12	ARID3A	chr3:19972705-19973731	K562	blood:	n/a	n/a
13	ARID3A	chr3:19942947-19943100	K562	blood:	n/a	n/a
14	ARID3A	chr3:19926931-19927205	K562	blood:	n/a	n/a
15	ARID3A	chr3:19978769-19979488	K562	blood:	n/a	n/a
16	ARID3A	chr3:19989243-19989553	HepG2	liver:	n/a	n/a
17	ARID3A	chr3:19853257-19853541	K562	blood:	n/a	n/a
18	ARID3A	chr3:19979685-19979859	HepG2	liver:	n/a	n/a
19	ARID3A	chr3:19987115-19987639	HepG2	liver:	n/a	n/a
20	ATF1	chr3:19978931-19979563	K562	blood:	n/a	n/a
21	ATF1	chr3:19930581-19931040	K562	blood:	n/a	n/a
22	ATF1	chr3:19973259-19973741	K562	blood:	n/a	n/a
23	ATF1	chr3:19785640-19785860	K562	blood:	n/a	n/a
24	ATF1	chr3:19972653-19973054	K562	blood:	n/a	n/a
25	ATF1	chr3:19987645-19988784	K562	blood:	n/a	n/a
26	ATF2	chr3:19580877-19582458	GM12878	blood:	n/a	n/a
27	ATF2	chr3:19987825-19988939	GM12878	blood:	n/a	n/a
28	ATF2	chr3:19601146-19601590	GM12878	blood:	n/a	n/a
29	ATF2	chr3:19584169-19584688	GM12878	blood:	n/a	n/a
30	ATF2	chr3:19988400-19988707	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr3:19601108-19601992	GM12878	blood:	n/a	n/a
32	ATF2	chr3:19640324-19640769	GM12878	blood:	n/a	n/a
33	ATF2	chr3:19686507-19687102	GM12878	blood:	n/a	n/a
34	ATF2	chr3:19972720-19973301	GM12878	blood:	n/a	n/a
35	ATF2	chr3:19972636-19973243	GM12878	blood:	n/a	n/a
36	ATF2	chr3:19987979-19988412	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr3:19686532-19687019	GM12878	blood:	n/a	n/a
38	ATF2	chr3:19640384-19640732	GM12878	blood:	n/a	n/a
39	ATF2	chr3:19581327-19581963	GM12878	blood:	n/a	n/a
40	ATF3	chr3:19908260-19908576	K562	blood:	n/a	n/a
41	ATF3	chr3:19930543-19931223	A549	lung:	n/a	n/a
42	ATF3	chr3:19988110-19988819	A549	lung:	n/a	n/a
43	ATF3	chr3:19988313-19988710	K562	blood:	n/a	n/a
44	ATF3	chr3:19988976-19989324	K562	blood:	n/a	chr3:19989161-19989169
45	ATF3	chr3:19988385-19988823	A549	lung:	n/a	n/a
46	ATF3	chr3:19988213-19988679	GM12878	blood:	n/a	n/a
47	ATF3	chr3:19988926-19989373	K562	blood:	n/a	chr3:19989161-19989169
48	ATF3	chr3:19930414-19931207	A549	lung:	n/a	n/a
49	BACH1	chr3:19973368-19973877	K562	blood:	n/a	n/a
50	BACH1	chr3:19853360-19853374	K562	blood:	n/a	n/a

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:19988132-19988182	BE2_C	brain:	n/a
2	chr3:19791356-19791406	H1-hESC	embryonic stem cell:	embryo
3	chr3:19988132-19988182	BE2_C	brain:	n/a
4	chr3:19791356-19791406	H1-hESC	embryonic stem cell:	embryo
5	chr3:19791356-19791406	CMK	blood:	n/a
6	chr3:19744061-19744111	Caco-2	colon:	n/a
7	chr3:19989128-19989178	AG10803	skin:	n/a
8	chr3:19987665-19987715	HEEpiC	esophagus:	n/a
9	chr3:19987665-19987715	GM12878	blood:	n/a
10	chr3:19988680-19988730	HRE	kidney:	n/a
11	chr3:19791356-19791406	NHDF-neo	bronchial:	n/a
12	chr3:19818187-19818237	ovcar-3	ovarian:	n/a
13	chr3:19987528-19987578	HCM	heart:	n/a
14	chr3:19989218-19989268	NB4	blood:	n/a
15	chr3:19791304-19791354	HMEC	breast:	n/a
16	chr3:19988132-19988182	HUVEC	blood vessel:	n/a
17	chr3:19930780-19930830	PFSK-1	brain:	n/a
18	chr3:19989128-19989178	NH-A	brain:	n/a
19	chr3:19976136-19976186	HEK293	kidney:	embryo
20	chr3:19987665-19987715	BJ	skin:	n/a
21	chr3:19791304-19791354	Caco-2	colon:	n/a
22	chr3:19930780-19930830	Jurkat	blood:	n/a
23	chr3:19930780-19930830	ovcar-3	ovarian:	n/a
24	chr3:19990693-19990743	ovcar-3	ovarian:	n/a
25	chr3:19576826-19576876	SAEC	small airway:	n/a
26	chr3:19930780-19930830	HRE	kidney:	n/a
27	chr3:19740602-19740652	HEEpiC	esophagus:	n/a
28	chr3:19985031-19985081	HCPEpiC	choroid plexus:	n/a
29	chr3:19576826-19576876	MCF-7	breast:	n/a
30	chr3:19975514-19975564	NHBE	bronchial:	n/a
31	chr3:19988460-19988510	CMK	blood:	n/a
32	chr3:19744061-19744111	AG04450	lung:	fetal
33	chr3:19992400-19992450	MCF-7	breast:	n/a
34	chr3:19818187-19818237	ProgFib	skin:	n/a
35	chr3:19818187-19818237	CMK	blood:	n/a
36	chr3:19988460-19988510	HRE	kidney:	n/a
37	chr3:19549017-19549067	SK-N-SH_RA	brain:	n/a
38	chr3:19988132-19988182	PrEC	prostate:	n/a
39	chr3:19988460-19988510	T-47D	breast:	n/a
40	chr3:19930780-19930830	Hela-S3	cervix:	n/a
41	chr3:19990693-19990743	HIPEpiC	eye:	n/a
42	chr3:19930780-19930830	HUVEC	blood vessel:	n/a
43	chr3:19791356-19791406	HRPEpiC	eye:	n/a
44	chr3:19791356-19791406	LNCaP	prostate:	n/a
45	chr3:19988132-19988182	PANC-1	pancreas:	n/a
46	chr3:19988460-19988510	NH-A	brain:	n/a
47	chr3:19985031-19985081	HUVEC	blood vessel:	n/a
48	chr3:19988460-19988510	ProgFib	skin:	n/a
49	chr3:19992400-19992450	CMK	blood:	n/a
50	chr3:19549017-19549067	HRE	kidney:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:200367178..200368137-chr3:19907997..19908546,2	MCF-7	breast:
2	chr3:19863239..19864953-chr3:20226349..20229139,2	K562	blood:
3	chr3:19986985..19992254-chr3:20079680..20083856,14	K562	blood:
4	chr3:19926681..19927540-chr3:20080667..20081886,4	MCF-7	breast:
5	chr3:19926567..19927530-chr3:21592329..21593167,2	MCF-7	breast:
6	chr3:19935726..19938656-chr3:19941159..19945067,3	K562	blood:
7	chr3:19390433..19391079-chr3:19907967..19908843,4	MCF-7	breast:
8	chr3:19960921..19963148-chr3:19974147..19975728,2	K562	blood:
9	chr3:19979101..19981901-chr3:20077826..20080437,2	K562	blood:
10	chr3:19525585..19527422-chr3:19576707..19579689,2	MCF-7	breast:
11	chr3:19923874..19927811-chr3:19988482..19992158,4	K562	blood:
12	chr3:19971502..19973500-chr3:19993301..19994870,2	K562	blood:
13	chr3:16317176..16319617-chr3:19576040..19578450,2	MCF-7	breast:
14	chr3:19973050..19975462-chr3:19977183..19979414,2	K562	blood:
15	chr3:19979250..19980946-chr3:19981520..19983771,2	K562	blood:
16	chr1:62901559..62902065-chr3:19594424..19594924,2	Hela-S3	cervix:
17	chr3:19679630..19681949-chr3:19683459..19685004,2	K562	blood:
18	chr3:19930434..19932349-chr3:19933276..19934867,2	K562	blood:
19	chr3:19968742..19970746-chr3:19973284..19975248,2	MCF-7	breast:
20	chr3:19950920..19952610-chr3:19955599..19957144,3	K562	blood:
21	chr3:19087867..19088435-chr3:19907906..19908471,2	MCF-7	breast:
22	chr1:155107729..155108614-chr3:19988180..19988972,2	Hela-S3	cervix:
23	chr3:19963049..19965826-chr3:19970318..19972819,2	MCF-7	breast:
24	chr3:19936727..19938285-chr3:19942132..19944334,2	K562	blood:
25	chr3:19188168..19190474-chr3:19988134..19989911,2	MCF-7	breast:
26	chr17:33895021..33895646-chr3:19988844..19989353,2	Hela-S3	cervix:
27	chr3:19987439..19992261-chr3:20226257..20229350,4	K562	blood:
28	chr3:19950920..19952610-chr3:19955599..19957144,3	K562	blood:
29	chr3:19389760..19391334-chr3:19907874..19909391,17	MCF-7	breast:
30	chr3:19980872..19982514-chr3:19987046..19988631,2	MCF-7	breast:
31	chr3:19390558..19391094-chr3:19584541..19585367,2	MCF-7	breast:
32	chr3:19930434..19932349-chr3:19933276..19934867,2	K562	blood:
33	chr3:19926646..19927515-chr3:20080662..20081812,4	K562	blood:
34	chr3:19979250..19980946-chr3:19981520..19983771,2	K562	blood:
35	chr3:19958393..19961139-chr3:19961701..19963581,2	K562	blood:
36	chr3:19679630..19681949-chr3:19683459..19685004,2	K562	blood:
37	chr3:19977189..19979348-chr3:20081334..20083177,2	K562	blood:
38	chr3:19963296..19965363-chr3:19967428..19970296,2	K562	blood:
39	chr3:19991110..19993492-chr3:20053410..20056377,2	K562	blood:
40	chr3:19988644..19989202-chr3:20081357..20082279,2	MCF-7	breast:
41	chr3:19961228..19962966-chr3:19967627..19969299,2	K562	blood:
42	chr3:19390113..19391205-chr3:19584358..19585952,11	MCF-7	breast:
43	chr3:19745768..19748356-chr3:19750935..19754447,3	K562	blood:
44	chr3:19976162..19983592-chr3:19985528..19991017,8	MCF-7	breast:
45	chr3:19928340..19930933-chr3:19988714..19991654,2	K562	blood:
46	chr3:19970366..19972921-chr3:19973495..19976654,3	K562	blood:
47	chr3:19908798..19910478-chr3:19922117..19924794,2	K562	blood:
48	chr3:19936510..19939152-chr3:19987860..19990168,2	MCF-7	breast:
49	chr3:19971930..19974485-chr3:19985453..19987123,2	MCF-7	breast:
50	chr3:19975611..19979082-chr3:19987774..19990681,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFHB-2	chr3:19987406-19987746	NONHSAT088605
2	lnc-EFHB-2	chr3:19988411-19988517	NONHSAT088605
3	lnc-EFHB-1	chr3:19717560-19717598	XLOC_003064
4	lnc-EFHB-1	chr3:19729726-19729972	XLOC_003064

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KCNH8	hsa-miR-143-3p	chr3:19576050-19576073
2	KCNH8	hsa-miR-143-3p	chr3:19576066-19576072

Variant related genes	Relation type
EFHB	TF binding region
RAB5A	TF binding region
HSPA8P18	TF binding region
EFHB	CpG island
RAB5A	CpG island
HSPA8P18	CpG island
ENSG00000129810	chromatin interactions
ENSG00000229468	chromatin interactions
ENSG00000183960	chromatin interactions
ENSG00000162607	chromatin interactions
ENSG00000270739	chromatin interactions
ENSG00000183977	chromatin interactions
ENSG00000114166	chromatin interactions
ENSG00000267321	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000100441	chromatin interactions
ENSG00000144566	chromatin interactions
ENSG00000163576	chromatin interactions
ESYT1	miRNA target sites

Extended variants
information (count: 8200 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:8200 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4858318	chr3:19547184-19547185	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565066819	chr3:19547234-19547235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548832835	chr3:19547254-19547255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183486286	chr3:19547292-19547293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568817861	chr3:19547293-19547294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142818281	chr3:19547296-19547297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs151026616	chr3:19547317-19547318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548711468	chr3:19547352-19547353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570205104	chr3:19547396-19547397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547145874	chr3:19547406-19547407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112954417	chr3:19547424-19547425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552525403	chr3:19547434-19547435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560607600	chr3:19547442-19547443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563767665	chr3:19547445-19547446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571010230	chr3:19547446-19547447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188377982	chr3:19547447-19547448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547225175	chr3:19547463-19547464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533810573	chr3:19547470-19547471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535883208	chr3:19547480-19547481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140887572	chr3:19547485-19547486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575757485	chr3:19547509-19547510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537131799	chr3:19547518-19547519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs80112588	chr3:19547550-19547551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193225150	chr3:19547560-19547561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79665909	chr3:19547575-19547576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559648026	chr3:19547587-19547588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575706398	chr3:19547613-19547614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183946312	chr3:19547631-19547632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534091921	chr3:19547656-19547657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35952096	chr3:19547663-19547664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188022715	chr3:19547729-19547730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553976988	chr3:19547737-19547738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191335633	chr3:19547750-19547751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149732930	chr3:19547810-19547811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183946647	chr3:19547853-19547854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552610890	chr3:19547871-19547872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564527542	chr3:19547877-19547878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs367551759	chr3:19547919-19547920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117917336	chr3:19547931-19547932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546780068	chr3:19547968-19547969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375824985	chr3:19547978-19547979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568460633	chr3:19547988-19547989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188523139	chr3:19547996-19547997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75750212	chr3:19548006-19548007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4417890	chr3:19548027-19548028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569597010	chr3:19548081-19548082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113385609	chr3:19548090-19548091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553811405	chr3:19548104-19548105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536770891	chr3:19548105-19548106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76570061	chr3:19548106-19548107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495311	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1847 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19540200-19557200	Weak transcription	Primary B cells from cord blood	blood
2	chr3:19542200-19552800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:19547600-19548600	Enhancers	Primary B cells from peripheral blood	blood
4	chr3:19547600-19548600	Enhancers	GM12878-XiMat	blood
5	chr3:19548000-19549200	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr3:19548200-19549200	Enhancers	Brain Hippocampus Middle	brain
7	chr3:19548200-19549400	Enhancers	Brain Substantia Nigra	brain
8	chr3:19548400-19549200	Enhancers	Brain Cingulate Gyrus	brain
9	chr3:19548600-19550800	Weak transcription	Fetal Brain Male	brain
10	chr3:19548600-19551200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr3:19549200-19555800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr3:19549400-19552000	Weak transcription	Brain Substantia Nigra	brain
13	chr3:19550000-19557600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr3:19550200-19550400	Enhancers	Brain Germinal Matrix	brain
15	chr3:19550400-19566200	Weak transcription	Brain Germinal Matrix	brain
16	chr3:19551000-19551200	Enhancers	Fetal Brain Male	brain
17	chr3:19551200-19551800	Enhancers	Primary B cells from peripheral blood	blood
18	chr3:19551600-19551800	Enhancers	Gastric	stomach
19	chr3:19551800-19559200	Weak transcription	Primary B cells from peripheral blood	blood
20	chr3:19552000-19552600	Enhancers	Brain Substantia Nigra	brain
21	chr3:19552800-19564200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:19553200-19565200	Weak transcription	Pancreas	Pancrea
23	chr3:19553600-19567400	Weak transcription	Fetal Brain Female	brain
24	chr3:19554400-19555200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:19555200-19557600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:19557200-19557600	Strong transcription	Primary B cells from cord blood	blood
27	chr3:19557600-19558800	Weak transcription	Primary B cells from cord blood	blood
28	chr3:19557600-19561200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr3:19557600-19561200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr3:19558800-19559000	Enhancers	Primary B cells from cord blood	blood
31	chr3:19559000-19559400	Weak transcription	Primary B cells from cord blood	blood
32	chr3:19559200-19561200	Enhancers	Primary B cells from peripheral blood	blood
33	chr3:19559400-19561400	Enhancers	Primary B cells from cord blood	blood
34	chr3:19560400-19560800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr3:19560400-19560800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:19561200-19561800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr3:19561200-19564000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr3:19561200-19572600	Weak transcription	Primary B cells from peripheral blood	blood
39	chr3:19561400-19571000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr3:19561400-19572800	Weak transcription	Primary B cells from cord blood	blood
41	chr3:19561800-19562800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr3:19562800-19563800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr3:19563800-19564000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:19564000-19564200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
45	chr3:19564000-19566200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr3:19564200-19567400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:19564200-19569200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:19566200-19566600	Enhancers	Brain Germinal Matrix	brain
49	chr3:19566200-19566800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr3:19566600-19577000	Weak transcription	Brain Germinal Matrix	brain

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