Variant report

Variant	nsv1008876
Chromosome Location	chr3:105554580-105645373
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1379)
CpG islands
(count:978)
Chromatin interactive
region (count:32)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1379 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:105585509-105586380	HepG2	liver:	n/a	chr3:105586167-105586183 chr3:105586166-105586182
2	ARID3A	chr3:105587863-105588737	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:105585818-105586201	K562	blood:	n/a	chr3:105586167-105586183 chr3:105586166-105586182
4	ARID3A	chr3:105589162-105589763	K562	blood:	n/a	n/a
5	ARID3A	chr3:105587675-105587689	K562	blood:	n/a	n/a
6	ATF1	chr3:105585767-105586053	K562	blood:	n/a	n/a
7	ATF2	chr3:105595572-105596190	GM12878	blood:	n/a	n/a
8	ATF2	chr3:105555006-105556555	GM12878	blood:	n/a	n/a
9	ATF2	chr3:105580947-105581508	GM12878	blood:	n/a	n/a
10	ATF2	chr3:105580861-105581573	GM12878	blood:	n/a	n/a
11	ATF2	chr3:105585388-105586146	GM12878	blood:	n/a	n/a
12	ATF2	chr3:105555089-105556855	GM12878	blood:	n/a	n/a
13	ATF2	chr3:105585205-105586067	GM12878	blood:	n/a	n/a
14	ATF2	chr3:105587598-105588488	GM12878	blood:	n/a	n/a
15	ATF2	chr3:105595539-105596366	GM12878	blood:	n/a	n/a
16	ATF2	chr3:105572870-105573413	GM12878	blood:	n/a	n/a
17	BACH1	chr3:105587072-105587843	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr3:105587604-105587758	K562	blood:	n/a	n/a
19	BACH1	chr3:105618506-105618522	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr3:105555902-105556461	GM12878	blood:	n/a	n/a
21	BATF	chr3:105555258-105555816	GM12878	blood:	n/a	n/a
22	BATF	chr3:105555372-105555798	GM12878	blood:	n/a	n/a
23	BATF	chr3:105581067-105581390	GM12878	blood:	n/a	n/a
24	BATF	chr3:105555829-105556416	GM12878	blood:	n/a	n/a
25	BATF	chr3:105572994-105573215	GM12878	blood:	n/a	chr3:105573099-105573110
26	BCL11A	chr3:105581047-105581407	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:105555899-105556412	GM12878	blood:	n/a	chr3:105556290-105556299
28	BCL11A	chr3:105556021-105556272	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:105555291-105555805	GM12878	blood:	n/a	n/a
30	BCL11A	chr3:105580964-105581420	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:105572988-105573229	GM12878	blood:	n/a	chr3:105573156-105573165
32	BCL11A	chr3:105595692-105595945	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:105555391-105555731	GM12878	blood:	n/a	n/a
34	BCL3	chr3:105555902-105556520	GM12878	blood:	n/a	chr3:105556290-105556299
35	BCL3	chr3:105555156-105555852	GM12878	blood:	n/a	n/a
36	BCL3	chr3:105572845-105573261	GM12878	blood:	n/a	chr3:105573156-105573165
37	BCL3	chr3:105595498-105596045	GM12878	blood:	n/a	n/a
38	BCL3	chr3:105580978-105581434	GM12878	blood:	n/a	n/a
39	BCL3	chr3:105585379-105586100	GM12878	blood:	n/a	chr3:105586015-105586024
40	BCL3	chr3:105554538-105554977	A549	lung:	n/a	n/a
41	BCL3	chr3:105555301-105555807	GM12878	blood:	n/a	n/a
42	BCLAF1	chr3:105587933-105588389	GM12878	blood:	n/a	chr3:105587996-105588009
43	BCLAF1	chr3:105572725-105573396	GM12878	blood:	n/a	chr3:105573156-105573165
44	BCLAF1	chr3:105587474-105587835	GM12878	blood:	n/a	n/a
45	BCLAF1	chr3:105555077-105555848	GM12878	blood:	n/a	n/a
46	BCLAF1	chr3:105587100-105587858	GM12878	blood:	n/a	chr3:105587411-105587424
47	BCLAF1	chr3:105585321-105586110	GM12878	blood:	n/a	chr3:105586015-105586024
48	BCLAF1	chr3:105580940-105581537	GM12878	blood:	n/a	n/a
49	BCLAF1	chr3:105555856-105556553	GM12878	blood:	n/a	chr3:105556290-105556299
50	BCLAF1	chr3:105580891-105581495	GM12878	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:105587981-105588031	IMR90	lung:	fetal
2	chr3:105583527-105583577	LNCaP	prostate:	n/a
3	chr3:105587981-105588031	IMR90	lung:	fetal
4	chr3:105583527-105583577	LNCaP	prostate:	n/a
5	chr3:105588208-105588258	GM12892	blood:	n/a
6	chr3:105588211-105588261	HCPEpiC	choroid plexus:	n/a
7	chr3:105601834-105601884	ECC-1	luminal epithelium:	n/a
8	chr3:105588247-105588297	AG04449	skin:	fetal
9	chr3:105601834-105601884	HUVEC	blood vessel:	n/a
10	chr3:105587719-105587769	LNCaP	prostate:	n/a
11	chr3:105587721-105587771	HRE	kidney:	n/a
12	chr3:105587814-105587864	NHDF-neo	bronchial:	n/a
13	chr3:105587814-105587864	HMEC	breast:	n/a
14	chr3:105588211-105588261	MCF-7	breast:	n/a
15	chr3:105587721-105587771	PrEC	prostate:	n/a
16	chr3:105588068-105588118	PFSK-1	brain:	n/a
17	chr3:105588068-105588118	HAEpiC	amniotic membrane:	n/a
18	chr3:105588247-105588297	Hela-S3	cervix:	n/a
19	chr3:105587981-105588031	T-47D	breast:	n/a
20	chr3:105586684-105586734	HepG2	liver:	n/a
21	chr3:105583527-105583577	HCF	heart:	n/a
22	chr3:105586684-105586734	HIPEpiC	eye:	n/a
23	chr3:105591430-105591480	GM19239	blood:	n/a
24	chr3:105588068-105588118	HCF	heart:	n/a
25	chr3:105601834-105601884	NT2-D1	testis:	n/a
26	chr3:105588247-105588297	HCM	heart:	n/a
27	chr3:105587981-105588031	Caco-2	colon:	n/a
28	chr3:105588247-105588297	HCF	heart:	n/a
29	chr3:105601834-105601884	HCPEpiC	choroid plexus:	n/a
30	chr3:105587814-105587864	K562	blood:	n/a
31	chr3:105587981-105588031	HRCEpiC	kidney:	n/a
32	chr3:105588014-105588064	K562	blood:	n/a
33	chr3:105588020-105588070	SKMC	muscle:	n/a
34	chr3:105588068-105588118	HEEpiC	esophagus:	n/a
35	chr3:105587981-105588031	AoSMC	blood vessel:	n/a
36	chr3:105587814-105587864	HCM	heart:	n/a
37	chr3:105555131-105555181	AG09319	gingival:	n/a
38	chr3:105586684-105586734	SKMC	muscle:	n/a
39	chr3:105555131-105555181	GM19239	blood:	n/a
40	chr3:105588020-105588070	Caco-2	colon:	n/a
41	chr3:105587719-105587769	HMEC	breast:	n/a
42	chr3:105586684-105586734	AG04450	lung:	fetal
43	chr3:105587719-105587769	HCM	heart:	n/a
44	chr3:105583527-105583577	BE2_C	brain:	n/a
45	chr3:105587981-105588031	AG09319	gingival:	n/a
46	chr3:105591430-105591480	NHDF-neo	bronchial:	n/a
47	chr3:105591430-105591480	SK-N-MC	brain:	n/a
48	chr3:105583527-105583577	A549	lung:	n/a
49	chr3:105588208-105588258	IMR90	lung:	fetal
50	chr3:105587981-105588031	GM12878	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:105643011..105645255-chr3:105645507..105647155,2	MCF-7	breast:
2	chr3:105578910..105582345-chr3:105586229..105588462,4	MCF-7	breast:
3	chr3:105552906..105555738-chr3:105560216..105562214,2	K562	blood:
4	chr3:105595423..105598244-chr3:105600923..105603422,2	K562	blood:
5	chr3:105580037..105582399-chr3:105585433..105589052,3	MCF-7	breast:
6	chr3:105567530..105570429-chr3:105573055..105575422,2	MCF-7	breast:
7	chr3:105571306..105573447-chr3:105586296..105588296,2	MCF-7	breast:
8	chr3:105595423..105598244-chr3:105600923..105603422,2	K562	blood:
9	chr3:105579577..105582453-chr3:105582537..105585477,2	MCF-7	breast:
10	chr3:105587379..105589688-chr3:105590274..105592993,2	K562	blood:
11	chr1:121483899..121485401-chr3:105625252..105628201,2	MCF-7	breast:
12	chr3:105584001..105586223-chr3:105590379..105592467,2	MCF-7	breast:
13	chr3:105577086..105579511-chr3:105584750..105588658,3	K562	blood:
14	chr3:105603078..105603677-chr3:105774410..105775125,2	MCF-7	breast:
15	chr3:105552676..105554224-chr3:105555679..105557862,2	K562	blood:
16	chr3:105552906..105555738-chr3:105560216..105562214,2	K562	blood:
17	chr17:57913805..57916301-chr3:105586626..105589272,2	MCF-7	breast:
18	chr3:105594821..105597024-chr3:105599746..105602672,2	K562	blood:
19	chr3:105594821..105597024-chr3:105599746..105602672,2	K562	blood:
20	chr3:105553976..105556329-chr3:105573888..105575863,2	MCF-7	breast:
21	chr3:105584001..105586223-chr3:105590379..105592467,2	MCF-7	breast:
22	chr3:105581787..105584079-chr3:105585457..105588306,3	K562	blood:
23	chr3:105552724..105554590-chr3:105555325..105557862,2	K562	blood:
24	chr12:100660714..100661219-chr3:105587461..105588148,2	NB4	blood:
25	chr3:105579577..105582453-chr3:105582537..105585477,2	MCF-7	breast:
26	chr3:105553976..105556329-chr3:105573888..105575863,2	MCF-7	breast:
27	chr3:105567530..105570429-chr3:105573055..105575422,2	MCF-7	breast:
28	chr3:42641686..42642395-chr3:105587711..105588497,2	Hela-S3	cervix:
29	chr3:105533973..105536078-chr3:105552694..105554794,2	K562	blood:
30	chr3:105525619..105527234-chr3:105585628..105587643,2	MCF-7	breast:
31	chr3:105552724..105554590-chr3:105555325..105557862,2	K562	blood:
32	chr3:105586396..105588232-chr3:105595370..105598050,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CBLB-1	chr3:105599338-105599421	NONHSAT090971
2	lnc-CBLB-1	chr3:105592595-105592642	NONHSAT090971
3	lnc-CD47-8	chr3:105565135-105569968	NONHSAT090970
4	lnc-CBLB-1	chr3:105599339-105599421	XLOC_003197
5	lnc-CBLB-1	chr3:105592596-105592642	XLOC_003197
6	lnc-CBLB-1	chr3:105597125-105597287	NONHSAT090971
7	lnc-CBLB-1	chr3:105597126-105597287	XLOC_003197

No data

Variant related genes	Relation type
CBLB	TF binding region
CBLB	CpG island
ENSG00000062716	chromatin interactions
ENSG00000114423	chromatin interactions
ENSG00000093183	chromatin interactions
ENSG00000136021	chromatin interactions
ENSG00000166153	chromatin interactions
ENSG00000114857	chromatin interactions

Extended variants
information (count: 3051 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3051 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7651784	chr3:105554580-105554581	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115173306	chr3:105554648-105554649	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs115773759	chr3:105554779-105554780	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs73196327	chr3:105554780-105554781	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs140894298	chr3:105554803-105554804	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs150449562	chr3:105554862-105554863	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs557709004	chr3:105554885-105554886	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs138345033	chr3:105554958-105554959	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs533655106	chr3:105554972-105554973	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs555465797	chr3:105554974-105554975	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs573763051	chr3:105555008-105555009	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs544252477	chr3:105555020-105555021	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs149215112	chr3:105555068-105555069	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs575885778	chr3:105555138-105555139	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs371492010	chr3:105555192-105555193	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs546434520	chr3:105555211-105555212	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs9838768	chr3:105555217-105555218	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs571517141	chr3:105555233-105555234	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs181928594	chr3:105555274-105555275	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs77390246	chr3:105555311-105555312	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs539480480	chr3:105555332-105555333	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs75835413	chr3:105555343-105555344	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs558118965	chr3:105555387-105555388	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs186298119	chr3:105555394-105555395	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs116432649	chr3:105555409-105555410	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115889109	chr3:105555427-105555428	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs573120944	chr3:105555434-105555435	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs117971325	chr3:105555443-105555444	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566562218	chr3:105555482-105555483	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs534026046	chr3:105555487-105555488	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs188027009	chr3:105555508-105555509	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs534310726	chr3:105555521-105555522	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs368339970	chr3:105555576-105555577	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs562949684	chr3:105555601-105555602	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs567416229	chr3:105555605-105555606	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs532247324	chr3:105555637-105555638	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs555852847	chr3:105555716-105555717	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs113010548	chr3:105555765-105555766	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs577516901	chr3:105555786-105555787	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs34209714	chr3:105555812-105555813	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs397783927	chr3:105555826-105555827	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs547932437	chr3:105555850-105555851	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs137909593	chr3:105555855-105555856	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs558397353	chr3:105555908-105555909	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs574295024	chr3:105555916-105555917	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs573445144	chr3:105555970-105555971	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs544810152	chr3:105555988-105555989	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs556628911	chr3:105556018-105556019	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116304607	chr3:105556026-105556027	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs578180003	chr3:105556034-105556035	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:2426 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105483200-105555200	Weak transcription	Placenta	Placenta
2	chr3:105511400-105566400	Weak transcription	Aorta	Aorta
3	chr3:105532200-105563000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:105533600-105560600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr3:105533800-105570000	Weak transcription	Dnd41	blood
6	chr3:105534200-105566200	Weak transcription	Brain Germinal Matrix	brain
7	chr3:105540800-105569600	Weak transcription	Fetal Thymus	thymus
8	chr3:105542600-105555400	Weak transcription	Brain Angular Gyrus	brain
9	chr3:105542600-105566000	Weak transcription	Fetal Stomach	stomach
10	chr3:105543000-105555600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:105543400-105555800	Weak transcription	HepG2	liver
12	chr3:105543400-105560800	Weak transcription	Fetal Muscle Trunk	muscle
13	chr3:105543400-105581200	Weak transcription	Gastric	stomach
14	chr3:105543600-105557200	Weak transcription	Fetal Intestine Large	intestine
15	chr3:105543800-105571000	Weak transcription	Lung	lung
16	chr3:105544200-105559200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr3:105544200-105584600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr3:105546600-105586200	Weak transcription	Esophagus	oesophagus
19	chr3:105546800-105560800	Weak transcription	Fetal Muscle Leg	muscle
20	chr3:105547200-105554600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr3:105547200-105554800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr3:105547200-105554800	Weak transcription	Ovary	ovary
23	chr3:105547200-105555000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr3:105547200-105557400	Weak transcription	Fetal Intestine Small	intestine
25	chr3:105547400-105557200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr3:105547800-105554600	Weak transcription	HMEC	breast
27	chr3:105547800-105554800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr3:105547800-105555400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr3:105547800-105557400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr3:105548400-105561200	Weak transcription	K562	blood
31	chr3:105548400-105561400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr3:105548600-105559600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr3:105549000-105554600	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr3:105549000-105555000	Weak transcription	Right Ventricle	heart
35	chr3:105549000-105560800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr3:105549000-105571800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr3:105549200-105555400	Weak transcription	Psoas Muscle	Psoas
38	chr3:105549200-105564400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:105549400-105557200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr3:105549600-105558000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:105549800-105554600	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr3:105549800-105554600	Weak transcription	Stomach Mucosa	stomach
43	chr3:105549800-105556000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:105550000-105562600	Weak transcription	HUVEC	blood vessel
45	chr3:105550000-105569600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr3:105550400-105554800	Weak transcription	Small Intestine	intestine
47	chr3:105550400-105555000	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr3:105550400-105555000	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr3:105550400-105555400	Weak transcription	Left Ventricle	heart
50	chr3:105551000-105556800	Enhancers	Primary T killer memory cells from peripheral blood	blood

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