Variant report

Variant	nsv829773
Chromosome Location	chr3:161150422-161315189
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1090)
CpG islands
(count:427)
Chromatin interactive
region (count:73)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:161277231-161277618	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:161218298-161218514	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:161226693-161226986	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:161161749-161162203	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:161193695-161193972	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:161277333-161277383	K562	blood:	n/a	n/a
7	ATF2	chr3:161207143-161207600	GM12878	blood:	n/a	n/a
8	ATF2	chr3:161207135-161207665	GM12878	blood:	n/a	n/a
9	BATF	chr3:161206101-161206441	GM12878	blood:	n/a	chr3:161206249-161206260
10	BATF	chr3:161267143-161267316	GM12878	blood:	n/a	chr3:161267240-161267251 chr3:161267241-161267251
11	BATF	chr3:161208702-161209025	GM12878	blood:	n/a	chr3:161208861-161208872
12	BATF	chr3:161258392-161258655	GM12878	blood:	n/a	n/a
13	BATF	chr3:161208701-161208987	GM12878	blood:	n/a	chr3:161208861-161208872
14	BATF	chr3:161206062-161206350	GM12878	blood:	n/a	chr3:161206249-161206260
15	BCL11A	chr3:161208700-161208983	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:161208665-161209032	GM12878	blood:	n/a	n/a
17	BCL11A	chr3:161206093-161206417	GM12878	blood:	n/a	n/a
18	BCL11A	chr3:161206114-161206392	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:161207246-161207577	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:161277229-161277550	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:161226756-161226773	GM12878	blood:	n/a	n/a
22	BHLHE40	chr3:161283713-161283865	GM12878	blood:	n/a	n/a
23	BRCA1	chr3:161278123-161278365	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr3:161193633-161194039	HCT-116	colon:	n/a	n/a
25	CEBPB	chr3:161161846-161162103	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr3:161256826-161257096	IMR90	lung:	n/a	chr3:161256941-161256952
27	CEBPB	chr3:161161801-161162199	HepG2	liver:	n/a	n/a
28	CEBPB	chr3:161256795-161257058	HepG2	liver:	n/a	chr3:161256941-161256952
29	CEBPB	chr3:161256854-161257154	MCF-7	breast:	n/a	chr3:161256941-161256952
30	CEBPB	chr3:161206186-161206446	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:161256843-161257084	A549	lung:	n/a	chr3:161256941-161256952
32	CEBPB	chr3:161215414-161215626	HepG2	liver:	n/a	chr3:161215545-161215556
33	CEBPB	chr3:161302532-161302900	A549	lung:	n/a	chr3:161302621-161302634
34	CEBPB	chr3:161256725-161257124	MCF-7	breast:	n/a	chr3:161256941-161256952
35	CEBPB	chr3:161267011-161267211	HepG2	liver:	n/a	chr3:161267055-161267066 chr3:161267057-161267066
36	CEBPB	chr3:161161871-161162056	HepG2	liver:	n/a	n/a
37	CEBPB	chr3:161161805-161162238	MCF-7	breast:	n/a	n/a
38	CHD1	chr3:161185194-161185205	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr3:161283702-161283879	HepG2	liver:	n/a	n/a
40	CHD2	chr3:161283728-161283927	GM12878	blood:	n/a	n/a
41	CTCF	chr3:161235037-161235106	Lung_OC	lung:	n/a	n/a
42	CTCF	chr3:161226572-161227136	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:161277218-161277539	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr3:161277300-161277450	HCM	heart:	n/a	n/a
45	CTCF	chr3:161278118-161278336	Pancreas_OC	pancreas:	n/a	chr3:161278226-161278247 chr3:161278224-161278242
46	CTCF	chr3:161277360-161277510	GM12864	blood:	n/a	n/a
47	CTCF	chr3:161277280-161277430	WI-38	lung:	n/a	n/a
48	CTCF	chr3:161277300-161277450	GM06990	blood:	n/a	n/a
49	CTCF	chr3:161277242-161277536	GM13977	blood:	n/a	n/a
50	CTCF	chr3:161277240-161277535	ECC-1	luminal epithelium:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:161277848-161277898	SK-N-SH_RA	brain:	n/a
2	chr3:161294050-161294100	HUVEC	blood vessel:	n/a
3	chr3:161213521-161213571	HL-60	blood:	n/a
4	chr3:161214813-161214863	HNPCEpiC	eye:	n/a
5	chr3:161235909-161235959	SKMC	muscle:	n/a
6	chr3:161163295-161163345	BE2_C	brain:	n/a
7	chr3:161213521-161213571	HIPEpiC	eye:	n/a
8	chr3:161235909-161235959	AoSMC	blood vessel:	n/a
9	chr3:161213521-161213571	GM06990	blood:	n/a
10	chr3:161163295-161163345	AG09319	gingival:	n/a
11	chr3:161214813-161214863	RPTEC	kidney:	n/a
12	chr3:161163295-161163345	HIPEpiC	eye:	n/a
13	chr3:161235909-161235959	HepG2	liver:	n/a
14	chr3:161163295-161163345	HCF	heart:	n/a
15	chr3:161277848-161277898	HCM	heart:	n/a
16	chr3:161277848-161277898	A549	lung:	n/a
17	chr3:161214813-161214863	Hela-S3	cervix:	n/a
18	chr3:161294050-161294100	ProgFib	skin:	n/a
19	chr3:161213521-161213571	ovcar-3	ovarian:	n/a
20	chr3:161163295-161163345	PrEC	prostate:	n/a
21	chr3:161235909-161235959	ovcar-3	ovarian:	n/a
22	chr3:161214813-161214863	PrEC	prostate:	n/a
23	chr3:161214813-161214863	T-47D	breast:	n/a
24	chr3:161213521-161213571	RPTEC	kidney:	n/a
25	chr3:161214813-161214863	ovcar-3	ovarian:	n/a
26	chr3:161277848-161277898	AG09319	gingival:	n/a
27	chr3:161294050-161294100	HRE	kidney:	n/a
28	chr3:161213521-161213571	NHBE	bronchial:	n/a
29	chr3:161214690-161214740	SK-N-MC	brain:	n/a
30	chr3:161235909-161235959	K562	blood:	n/a
31	chr3:161277848-161277898	AG04450	lung:	fetal
32	chr3:161235909-161235959	ECC-1	luminal epithelium:	n/a
33	chr3:161277848-161277898	NHBE	bronchial:	n/a
34	chr3:161294050-161294100	ECC-1	luminal epithelium:	n/a
35	chr3:161213521-161213571	HRE	kidney:	n/a
36	chr3:161163295-161163345	GM12878	blood:	n/a
37	chr3:161213521-161213571	SK-N-SH	brain:	n/a
38	chr3:161213521-161213571	HCT-116	colon:	n/a
39	chr3:161214690-161214740	HRPEpiC	eye:	n/a
40	chr3:161294050-161294100	AG04450	lung:	fetal
41	chr3:161163295-161163345	SK-N-SH_RA	brain:	n/a
42	chr3:161163295-161163345	SAEC	small airway:	n/a
43	chr3:161163295-161163345	LNCaP	prostate:	n/a
44	chr3:161235909-161235959	HEK293	kidney:	embryo
45	chr3:161214690-161214740	AoSMC	blood vessel:	n/a
46	chr3:161277848-161277898	HL-60	blood:	n/a
47	chr3:161294050-161294100	MCF10A-Er-Src	breast:	n/a
48	chr3:161277848-161277898	GM06990	blood:	n/a
49	chr3:161214690-161214740	HepG2	liver:	n/a
50	chr3:161214813-161214863	HCF	heart:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:160889184..160889706-chr3:161286958..161287780,2	MCF-7	breast:
2	chr3:161141625..161142575-chr3:161277741..161278641,2	MCF-7	breast:
3	chr3:161258952..161261503-chr3:161267723..161269425,2	MCF-7	breast:
4	chr3:161149348..161152131-chr3:161159932..161161916,2	MCF-7	breast:
5	chr16:13221858..13222514-chr3:161192650..161193500,2	MCF-7	breast:
6	chr3:161149987..161152257-chr3:161152281..161153980,2	MCF-7	breast:
7	chr3:161288935..161292971-chr3:161293220..161296787,4	K562	blood:
8	chr3:161085159..161090097-chr3:161151244..161155377,5	MCF-7	breast:
9	chr3:161260574..161262753-chr3:161263348..161265146,2	MCF-7	breast:
10	chr3:161153934..161156092-chr3:161162530..161165225,2	MCF-7	breast:
11	chr3:161156686..161159483-chr3:161160092..161163012,3	MCF-7	breast:
12	chr3:161137315..161139728-chr3:161159914..161161772,2	MCF-7	breast:
13	chr3:161163174..161165677-chr3:161166380..161168356,2	MCF-7	breast:
14	chr3:161192914..161194705-chr3:161200640..161203069,2	MCF-7	breast:
15	chr3:161149987..161152257-chr3:161152281..161153980,2	MCF-7	breast:
16	chr3:161186330..161188713-chr3:161191015..161194014,3	MCF-7	breast:
17	chr3:161310251..161314365-chr3:161314679..161319678,4	MCF-7	breast:
18	chr3:161277610..161278375-chr3:161317637..161318163,2	MCF-7	breast:
19	chr3:161139196..161140956-chr3:161159538..161162067,2	MCF-7	breast:
20	chr3:161149348..161152131-chr3:161159932..161161916,2	MCF-7	breast:
21	chr3:161159586..161162271-chr3:161162430..161165084,3	MCF-7	breast:
22	chr3:161156686..161159483-chr3:161160092..161163012,3	MCF-7	breast:
23	chr3:161129149..161131196-chr3:161149547..161152393,3	MCF-7	breast:
24	chr3:161161864..161163648-chr3:161163998..161165965,2	MCF-7	breast:
25	chr3:161288935..161292971-chr3:161293220..161296787,4	K562	blood:
26	chr3:161186330..161188713-chr3:161191015..161194014,3	MCF-7	breast:
27	chr3:161167642..161168268-chr3:161276756..161277746,3	MCF-7	breast:
28	chr3:161310251..161314365-chr3:161314679..161319678,4	MCF-7	breast:
29	chr3:161089138..161091531-chr3:161277246..161278957,3	MCF-7	breast:
30	chr3:161226423..161227058-chr3:161276669..161277342,2	MCF-7	breast:
31	chr3:161147373..161149064-chr3:161153544..161155803,2	MCF-7	breast:
32	chr3:161145758..161147913-chr3:161160739..161163339,2	MCF-7	breast:
33	chr3:161161602..161163726-chr3:161192340..161193989,2	MCF-7	breast:
34	chr3:161167642..161168268-chr3:161276756..161277746,3	MCF-7	breast:
35	chr3:161153934..161156092-chr3:161162530..161165225,2	MCF-7	breast:
36	chr3:161172276..161174982-chr3:161177335..161179468,2	MCF-7	breast:
37	chr3:161161864..161163648-chr3:161163998..161165965,2	MCF-7	breast:
38	chr3:161157860..161160581-chr3:161168208..161171597,3	MCF-7	breast:
39	chr3:161258952..161261503-chr3:161267723..161269425,2	MCF-7	breast:
40	chr3:161139368..161142098-chr3:161277561..161279557,2	MCF-7	breast:
41	chr3:161211149..161213795-chr3:161215661..161218407,2	MCF-7	breast:
42	chr3:161260574..161262753-chr3:161263348..161265146,2	MCF-7	breast:
43	chr3:160962395..160964121-chr3:161225961..161227918,2	MCF-7	breast:
44	chr3:161163174..161165677-chr3:161166380..161168356,2	MCF-7	breast:
45	chr3:161192914..161194705-chr3:161200640..161203069,2	MCF-7	breast:
46	chr3:161144496..161147090-chr3:161151361..161154232,2	MCF-7	breast:
47	chr3:161087867..161091778-chr3:161159434..161163634,9	MCF-7	breast:
48	chr3:161157860..161160581-chr3:161168208..161171597,3	MCF-7	breast:
49	chr3:161160203..161162184-chr3:161166453..161168231,2	MCF-7	breast:
50	chr3:161137896..161142184-chr3:161162436..161166379,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTSSB-4	chr3:161216177-161216342	ucscGeneNc_uc003fcy_1
2	lnc-SPTSSB-4	chr3:161211947-161212032	ucscGeneNc_uc003fcy_1
3	lnc-SPTSSB-4	chr3:161198655-161198798	ucscGeneNc_uc003fcy_1
4	lnc-SPTSSB-4	chr3:161212146-161212591	ucscGeneNc_uc003fcy_1
5	lnc-SPTSSB-4	chr3:161209593-161209738	ucscGeneNc_uc003fcy_1

No data

Variant related genes	Relation type
OTOL1	TF binding region
ENSG00000234851	TF binding region
OTOL1	CpG island
ENSG00000234851	CpG island
ENSG00000234851	chromatin interactions
ENSG00000269888	chromatin interactions
ENSG00000240567	chromatin interactions
ENSG00000196542	chromatin interactions

Extended variants
information (count: 3133 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3133 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73878332	chr3:161150431-161150432	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115165415	chr3:161150445-161150446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73878333	chr3:161150455-161150456	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs569465380	chr3:161150467-161150468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555733334	chr3:161150481-161150482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574184210	chr3:161150547-161150548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140242451	chr3:161150559-161150560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs180828683	chr3:161150587-161150588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577036770	chr3:161150604-161150605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12163613	chr3:161150665-161150666	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs373747343	chr3:161150672-161150673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533021714	chr3:161150675-161150676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545056087	chr3:161150683-161150684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546178555	chr3:161150694-161150695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150289116	chr3:161150724-161150725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201150778	chr3:161150739-161150740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372486441	chr3:161150770-161150771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12163614	chr3:161150771-161150772	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs555257802	chr3:161150804-161150805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6787829	chr3:161150807-161150808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs185462661	chr3:161150827-161150828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190221503	chr3:161150828-161150829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7633191	chr3:161150878-161150879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs540757578	chr3:161150948-161150949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554184961	chr3:161150956-161150957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145421279	chr3:161150985-161150986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549249809	chr3:161150986-161150987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563181476	chr3:161151023-161151024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531885603	chr3:161151069-161151070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114886631	chr3:161151081-161151082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149213487	chr3:161151118-161151119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532869846	chr3:161151145-161151146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532068650	chr3:161151206-161151207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566096631	chr3:161151217-161151218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182682860	chr3:161151272-161151273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7645213	chr3:161151274-161151275	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs548820996	chr3:161151311-161151312	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569057023	chr3:161151381-161151382	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs185925941	chr3:161151415-161151416	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs1450525	chr3:161151441-161151442	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs571445580	chr3:161151443-161151444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs143361869	chr3:161151447-161151448	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs554321949	chr3:161151463-161151464	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs574040528	chr3:161151472-161151473	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs76250268	chr3:161151480-161151481	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs543045787	chr3:161151483-161151484	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs34436128	chr3:161151533-161151534	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs1450524	chr3:161151534-161151535	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs191976298	chr3:161151535-161151536	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs183561514	chr3:161151547-161151548	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161149000-161152000	Weak transcription	HepG2	liver
2	chr3:161150400-161150800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:161152000-161152400	Enhancers	HepG2	liver
4	chr3:161161200-161163200	Enhancers	HepG2	liver
5	chr3:161161400-161162600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:161161600-161162200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr3:161162200-161162400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr3:161162400-161162600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:161162600-161162800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:161162600-161163600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr3:161163400-161163600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr3:161169400-161170400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:161170200-161170400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr3:161170200-161170600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr3:161170200-161170600	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
16	chr3:161170400-161171800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:161170400-161171800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr3:161170600-161172000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:161171800-161172000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr3:161171800-161173200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:161171800-161173400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr3:161172000-161172200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr3:161172200-161172800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr3:161172400-161172800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr3:161172800-161173000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr3:161182000-161182600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:161182200-161182600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:161182600-161185400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:161188200-161188600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr3:161188200-161189200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:161188600-161189000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr3:161189000-161189200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr3:161189200-161191200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr3:161189200-161191200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr3:161191200-161191600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr3:161191200-161191800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr3:161191400-161191600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr3:161192400-161194600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr3:161193400-161194000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr3:161193400-161194400	Enhancers	Liver	Liver
41	chr3:161193600-161194400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:161193800-161194400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr3:161193800-161194400	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr3:161193800-161194400	Enhancers	Brain Substantia Nigra	brain
45	chr3:161193800-161194400	Enhancers	Hela-S3	cervix
46	chr3:161197000-161199200	Weak transcription	Right Atrium	heart
47	chr3:161199800-161200400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr3:161200200-161200600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr3:161202000-161202400	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr3:161202000-161202800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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