Variant report

Variant	nsv932989
Chromosome Location	chr3:142204208-142423305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2407)
CpG islands
(count:2075)
Chromatin interactive
region (count:202)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2407 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:142382781-142383900	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:142337710-142338316	K562	blood:	n/a	n/a
3	ARID3A	chr3:142297425-142297909	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:142305620-142305987	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:142208918-142209055	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:142338059-142338176	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:142314945-142315362	K562	blood:	n/a	n/a
8	ARID3A	chr3:142297606-142297816	K562	blood:	n/a	n/a
9	ARID3A	chr3:142314492-142315669	HepG2	liver:	n/a	n/a
10	ATF1	chr3:142261070-142261144	K562	blood:	n/a	n/a
11	ATF1	chr3:142337691-142338316	K562	blood:	n/a	n/a
12	ATF2	chr3:142314925-142315425	GM12878	blood:	n/a	n/a
13	ATF2	chr3:142297296-142297906	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr3:142297242-142298410	GM12878	blood:	n/a	n/a
15	ATF2	chr3:142296665-142297253	GM12878	blood:	n/a	n/a
16	ATF2	chr3:142314955-142315367	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr3:142305623-142306010	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr3:142297369-142298083	GM12878	blood:	n/a	n/a
19	ATF2	chr3:142314899-142315326	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr3:142297249-142297908	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr3:142297371-142298043	A549	lung:	n/a	chr3:142297742-142297751
22	ATF3	chr3:142297353-142297927	A549	lung:	n/a	chr3:142297742-142297751
23	ATF3	chr3:142314771-142315450	A549	lung:	n/a	chr3:142315426-142315435
24	ATF3	chr3:142314665-142315432	A549	lung:	n/a	n/a
25	BACH1	chr3:142371509-142372137	K562	blood:	n/a	n/a
26	BACH1	chr3:142314989-142315328	K562	blood:	n/a	n/a
27	BACH1	chr3:142371673-142372078	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr3:142296525-142296543	K562	blood:	n/a	n/a
29	BACH1	chr3:142297319-142297884	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr3:142314729-142315608	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr3:142239050-142239289	GM12878	blood:	n/a	chr3:142239207-142239218
32	BATF	chr3:142239093-142239336	GM12878	blood:	n/a	chr3:142239207-142239218
33	BATF	chr3:142297399-142297972	GM12878	blood:	n/a	n/a
34	BATF	chr3:142347753-142348011	GM12878	blood:	n/a	n/a
35	BATF	chr3:142347721-142347987	GM12878	blood:	n/a	n/a
36	BCL3	chr3:142297197-142298041	A549	lung:	n/a	chr3:142297368-142297381
37	BCL3	chr3:142314812-142315463	A549	lung:	n/a	n/a
38	BCL3	chr3:142314688-142315482	A549	lung:	n/a	n/a
39	BCL3	chr3:142297396-142298001	GM12878	blood:	n/a	n/a
40	BCL3	chr3:142297172-142298106	A549	lung:	n/a	chr3:142297368-142297381
41	BCLAF1	chr3:142297048-142298036	K562	blood:	n/a	chr3:142297368-142297381
42	BCLAF1	chr3:142314848-142315411	GM12878	blood:	n/a	n/a
43	BCLAF1	chr3:142297313-142298038	GM12878	blood:	n/a	chr3:142297368-142297381
44	BCLAF1	chr3:142297354-142298206	GM12878	blood:	n/a	chr3:142297368-142297381
45	BCLAF1	chr3:142297343-142298041	K562	blood:	n/a	chr3:142297368-142297381
46	BHLHE40	chr3:142371389-142372288	K562	blood:	n/a	n/a
47	BHLHE40	chr3:142370425-142370798	K562	blood:	n/a	n/a
48	BHLHE40	chr3:142297242-142298040	K562	blood:	n/a	n/a
49	BHLHE40	chr3:142314477-142315605	K562	blood:	n/a	n/a
50	BHLHE40	chr3:142297256-142298186	GM12878	blood:	n/a	n/a

(count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:142297641-142297691	SK-N-SH	brain:	n/a
2	chr3:142297641-142297691	SK-N-SH	brain:	n/a
3	chr3:142294184-142294234	AG09319	gingival:	n/a
4	chr3:142297641-142297691	NHDF-neo	bronchial:	n/a
5	chr3:142297635-142297685	U87	brain:	n/a
6	chr3:142315213-142315263	HCF	heart:	n/a
7	chr3:142340792-142340842	AG09319	gingival:	n/a
8	chr3:142297824-142297874	Hela-S3	cervix:	n/a
9	chr3:142314968-142315018	HRCEpiC	kidney:	n/a
10	chr3:142316082-142316132	HNPCEpiC	eye:	n/a
11	chr3:142315326-142315376	T-47D	breast:	n/a
12	chr3:142297824-142297874	ECC-1	luminal epithelium:	n/a
13	chr3:142298018-142298068	U87	brain:	n/a
14	chr3:142300190-142300240	Caco-2	colon:	n/a
15	chr3:142297905-142297955	SK-N-SH	brain:	n/a
16	chr3:142318115-142318165	U87	brain:	n/a
17	chr3:142314493-142314543	HNPCEpiC	eye:	n/a
18	chr3:142300190-142300240	Jurkat	blood:	n/a
19	chr3:142296671-142296721	T-47D	breast:	n/a
20	chr3:142297929-142297979	HEK293	kidney:	embryo
21	chr3:142297747-142297797	HCT-116	colon:	n/a
22	chr3:142297737-142297787	AG09319	gingival:	n/a
23	chr3:142297747-142297797	ECC-1	luminal epithelium:	n/a
24	chr3:142361468-142361518	HIPEpiC	eye:	n/a
25	chr3:142297747-142297797	SK-N-SH_RA	brain:	n/a
26	chr3:142340931-142340981	HepG2	liver:	n/a
27	chr3:142297224-142297274	ECC-1	luminal epithelium:	n/a
28	chr3:142297635-142297685	HRPEpiC	eye:	n/a
29	chr3:142315064-142315114	ECC-1	luminal epithelium:	n/a
30	chr3:142297641-142297691	HCF	heart:	n/a
31	chr3:142297771-142297821	HRCEpiC	kidney:	n/a
32	chr3:142361468-142361518	ovcar-3	ovarian:	n/a
33	chr3:142315064-142315114	PFSK-1	brain:	n/a
34	chr3:142297900-142297950	LNCaP	prostate:	n/a
35	chr3:142297737-142297787	T-47D	breast:	n/a
36	chr3:142294184-142294234	HCT-116	colon:	n/a
37	chr3:142297848-142297898	HMEC	breast:	n/a
38	chr3:142383107-142383157	HCT-116	colon:	n/a
39	chr3:142315064-142315114	MCF10A-Er-Src	breast:	n/a
40	chr3:142361468-142361518	BE2_C	brain:	n/a
41	chr3:142314968-142315018	HCM	heart:	n/a
42	chr3:142297929-142297979	HCF	heart:	n/a
43	chr3:142297900-142297950	BE2_C	brain:	n/a
44	chr3:142297848-142297898	NH-A	brain:	n/a
45	chr3:142294184-142294234	HCF	heart:	n/a
46	chr3:142315220-142315270	HepG2	liver:	n/a
47	chr3:142314968-142315018	H1-hESC	embryonic stem cell:	embryo
48	chr3:142298018-142298068	HRE	kidney:	n/a
49	chr3:142297900-142297950	Hela-S3	cervix:	n/a
50	chr3:142315207-142315257	NHDF-neo	bronchial:	n/a

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr3:142280626..142282527-chr3:142296623..142299039,2	K562	blood:
2	chr3:142294568..142300006-chr3:142310942..142319455,13	MCF-7	breast:
3	chr3:142366648..142369083-chr3:142371257..142373675,2	K562	blood:
4	chr3:142251000..142253225-chr3:142255307..142257885,2	MCF-7	breast:
5	chr3:142255246..142257071-chr3:142259760..142261943,2	K562	blood:
6	chr3:142297403..142299294-chr3:142720282..142722143,3	MCF-7	breast:
7	chr3:142297625..142299268-chr3:142441632..142444151,3	K562	blood:
8	chr3:142296730..142299279-chr3:142395182..142397447,2	MCF-7	breast:
9	chr3:142327574..142330140-chr3:142335677..142337995,2	MCF-7	breast:
10	chr3:142415071..142417481-chr3:142424230..142426565,2	K562	blood:
11	chr3:142305364..142306466-chr3:142399184..142400223,7	MCF-7	breast:
12	chr3:142387225..142389939-chr3:142390380..142394474,3	MCF-7	breast:
13	chr17:41399646..41402633-chr3:142404029..142407052,5	K562	blood:
14	chr3:142210650..142212164-chr3:142212182..142213935,2	K562	blood:
15	chr3:142223658..142226531-chr3:142293631..142295358,2	K562	blood:
16	chr3:142294183..142301262-chr3:142311308..142318922,13	MCF-7	breast:
17	chr3:142316986..142319598-chr3:142354070..142355822,2	MCF-7	breast:
18	chr3:142418554..142422462-chr3:142423148..142426338,3	K562	blood:
19	chr3:142360347..142363924-chr3:142363947..142367785,4	K562	blood:
20	chr3:142217843..142219879-chr3:142296547..142298953,2	MCF-7	breast:
21	chr3:142366648..142369083-chr3:142371257..142373675,2	K562	blood:
22	chr3:142226820..142229052-chr3:142234427..142237247,3	K562	blood:
23	chr3:142409223..142411101-chr3:142411877..142413945,2	MCF-7	breast:
24	chr3:142296660..142299430-chr3:142300614..142303082,3	MCF-7	breast:
25	chr3:142229095..142231741-chr3:142253840..142256348,2	MCF-7	breast:
26	chr3:142267438..142270247-chr3:142280572..142282585,2	MCF-7	breast:
27	chr17:41380707..41383716-chr3:142404049..142407051,3	MCF-7	breast:
28	chr3:142255246..142257071-chr3:142259760..142261943,2	K562	blood:
29	chr3:142319541..142323718-chr3:142324179..142327610,6	MCF-7	breast:
30	chr3:142312134..142313647-chr3:142313760..142315366,2	MCF-7	breast:
31	chr3:142217843..142219879-chr3:142296547..142298953,2	MCF-7	breast:
32	chr3:142262100..142263612-chr3:142267272..142269416,2	K562	blood:
33	chr3:142305688..142306265-chr3:142712595..142713344,2	MCF-7	breast:
34	chr3:142297466..142299799-chr3:142313558..142315620,3	K562	blood:
35	chr3:142360507..142362272-chr3:142381303..142382879,2	K562	blood:
36	chr3:142314095..142315702-chr3:142384843..142386495,2	MCF-7	breast:
37	chr3:142296526..142298782-chr3:142343605..142345141,2	MCF-7	breast:
38	chr3:142226820..142229052-chr3:142234427..142237247,3	K562	blood:
39	chr3:142314277..142316663-chr3:142382049..142384101,2	MCF-7	breast:
40	chr18:45456991..45457971-chr3:142297413..142297998,2	Hela-S3	cervix:
41	chr12:46753334..46754030-chr3:142297866..142298600,2	Hela-S3	cervix:
42	chr3:142246869..142249118-chr3:142259250..142261613,2	K562	blood:
43	chr3:142297466..142299799-chr3:142313558..142315620,3	K562	blood:
44	chr3:142295888..142299099-chr3:142720440..142723490,3	K562	blood:
45	chr3:142282794..142284400-chr3:142286449..142288968,2	K562	blood:
46	chr3:142280626..142282527-chr3:142296623..142299039,2	K562	blood:
47	chr3:142336924..142339246-chr3:142443118..142445487,2	MCF-7	breast:
48	chr3:142316986..142319598-chr3:142354070..142355822,2	MCF-7	breast:
49	chr3:142294703..142296575-chr3:142522509..142525334,2	MCF-7	breast:
50	chr3:142305389..142306193-chr3:142623757..142624589,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLS1-1	chr3:142300147-142300816	NONHSAT092476
2	lnc-ATR-1	chr3:142375400-142375587	ENSG00000239641.1
3	lnc-ATR-1	chr3:142373626-142373783	ENSG00000239641.1
4	lnc-TRPC1-1	chr3:142392439-142392746	NONHSAT092479
5	lnc-PLS1-1	chr3:142301137-142301241	NONHSAT092476
6	lnc-PLS1-1	chr3:142299752-142299835	NONHSAT092476

No data

Variant related genes	Relation type
RPL6P9	TF binding region
RNA5SP143	TF binding region
ATR	TF binding region
PLS1-AS1	TF binding region
RN7SKP25	TF binding region
PLS1	TF binding region
RPL6P9	CpG island
RNA5SP143	CpG island
ATR	CpG island
PLS1-AS1	CpG island
RN7SKP25	CpG island
PLS1	CpG island
ENSG00000113048	chromatin interactions
ENSG00000241570	chromatin interactions
ENSG00000144935	chromatin interactions
ENSG00000242390	chromatin interactions
ENSG00000141985	chromatin interactions
ENSG00000120756	chromatin interactions
ENSG00000175040	chromatin interactions
ENSG00000175054	chromatin interactions
ENSG00000065150	chromatin interactions
ENSG00000176845	chromatin interactions
ENSG00000153395	chromatin interactions
ENSG00000117298	chromatin interactions
ENSG00000170634	chromatin interactions
ENSG00000188582	chromatin interactions
ENSG00000041880	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000156599	chromatin interactions
ENSG00000268129	chromatin interactions
ENSG00000129696	chromatin interactions
ENSG00000103275	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000091527	chromatin interactions
ENSG00000182768	chromatin interactions
ENSG00000213654	chromatin interactions
ENSG00000252745	chromatin interactions
ENSG00000114127	chromatin interactions
ENSG00000049883	chromatin interactions
ENSG00000198242	chromatin interactions
ENSG00000114126	chromatin interactions
ENSG00000199319	chromatin interactions
ENSG00000175387	chromatin interactions
ENSG00000163714	chromatin interactions

Extended variants
information (count: 7620 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:7620 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188019155	chr3:142204256-142204257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574566452	chr3:142204261-142204262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370574498	chr3:142204263-142204264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114790050	chr3:142204344-142204345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75534481	chr3:142204356-142204357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113572604	chr3:142204385-142204386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78820355	chr3:142204412-142204413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113409577	chr3:142204462-142204463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532338514	chr3:142204464-142204465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368264270	chr3:142204556-142204557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115554685	chr3:142204564-142204565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538299432	chr3:142204568-142204569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141818887	chr3:142204607-142204608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73238200	chr3:142204634-142204635	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs575367174	chr3:142204641-142204642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181408425	chr3:142204661-142204662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186172776	chr3:142204687-142204688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572545232	chr3:142204707-142204708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73238201	chr3:142204728-142204729	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs370109224	chr3:142204803-142204804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566880284	chr3:142204819-142204820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533684726	chr3:142204881-142204882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143699668	chr3:142204885-142204886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150036529	chr3:142204901-142204902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370721446	chr3:142204902-142204903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544267628	chr3:142204943-142204944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113044235	chr3:142204976-142204977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562970754	chr3:142204986-142204987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530302385	chr3:142205023-142205024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145813077	chr3:142205026-142205027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531521925	chr3:142205028-142205029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560766253	chr3:142205038-142205039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112378911	chr3:142205060-142205061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527939655	chr3:142205116-142205117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148992283	chr3:142205173-142205174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570822672	chr3:142205174-142205175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192083099	chr3:142205195-142205196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537973201	chr3:142205247-142205248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550225995	chr3:142205292-142205293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568991354	chr3:142205334-142205335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73238202	chr3:142205344-142205345	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs554488699	chr3:142205361-142205362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544897794	chr3:142205385-142205386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80033927	chr3:142205407-142205408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116385099	chr3:142205422-142205423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181702226	chr3:142205428-142205429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538029171	chr3:142205432-142205433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533803457	chr3:142205443-142205444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145070181	chr3:142205461-142205462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374168970	chr3:142205462-142205463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
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
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
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:4028 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142167400-142234600	Weak transcription	Psoas Muscle	Psoas
2	chr3:142198400-142214400	Weak transcription	Stomach Mucosa	stomach
3	chr3:142199200-142204400	Strong transcription	Skeletal Muscle Male	skeletal muscle
4	chr3:142199200-142216000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:142200000-142215200	Weak transcription	NHLF	lung
6	chr3:142200000-142223200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:142200200-142206400	Weak transcription	HepG2	liver
8	chr3:142200400-142204400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr3:142200400-142243800	Weak transcription	Fetal Heart	heart
10	chr3:142200600-142204400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr3:142200600-142204800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr3:142200600-142205400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr3:142200600-142205400	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr3:142200600-142208200	Weak transcription	NHDF-Ad	bronchial
15	chr3:142200600-142210000	Weak transcription	HUVEC	blood vessel
16	chr3:142200600-142271800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr3:142200800-142204400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr3:142200800-142206400	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr3:142200800-142213400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr3:142200800-142214000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr3:142200800-142219800	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr3:142201000-142204600	Strong transcription	Duodenum Smooth Muscle	Duodenum
23	chr3:142201000-142206600	Weak transcription	NH-A	brain
24	chr3:142201000-142218200	Strong transcription	Adipose Nuclei	Adipose
25	chr3:142201000-142218600	Strong transcription	Fetal Thymus	thymus
26	chr3:142201000-142239600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr3:142201000-142240600	Weak transcription	Fetal Brain Male	brain
28	chr3:142201200-142210000	Weak transcription	Brain Germinal Matrix	brain
29	chr3:142201200-142218000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr3:142201200-142226800	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr3:142201400-142217000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr3:142201600-142204400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr3:142201600-142204400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr3:142201600-142205000	Strong transcription	Primary B cells from cord blood	blood
35	chr3:142201600-142205000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr3:142201600-142216000	Strong transcription	Primary T cells from cord blood	blood
37	chr3:142201600-142216000	Strong transcription	GM12878-XiMat	blood
38	chr3:142201600-142218600	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr3:142201600-142219000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr3:142201600-142273200	Weak transcription	Esophagus	oesophagus
41	chr3:142201800-142205400	Strong transcription	Primary hematopoietic stem cells	blood
42	chr3:142201800-142208400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr3:142201800-142218000	Strong transcription	Duodenum Mucosa	Duodenum
44	chr3:142201800-142240600	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr3:142201800-142243600	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr3:142201800-142273800	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr3:142202000-142204800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr3:142202000-142221200	Strong transcription	Primary B cells from peripheral blood	blood
49	chr3:142202000-142223800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr3:142202000-142231000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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