Variant report

Variant	nsv1000686
Chromosome Location	chr3:118752098-118818041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:684)
CpG islands
(count:794)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:118753735-118753935	K562	blood:	n/a	n/a
2	ATF1	chr3:118817076-118817276	K562	blood:	n/a	n/a
3	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr3:118753664-118753967	GM12878	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
5	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
6	CCNT2	chr3:118753087-118754043	K562	blood:	n/a	n/a
7	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
8	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
9	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
10	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
12	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
14	CREB1	chr3:118753090-118753994	A549	lung:	n/a	n/a
15	CTBP2	chr3:118753482-118754214	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr3:118817461-118817789	A549	lung:	n/a	chr3:118817652-118817670
17	CTCF	chr3:118817580-118817730	HMF	breast:	n/a	chr3:118817652-118817670
18	CTCF	chr3:118817466-118817852	HepG2	liver:	n/a	chr3:118817652-118817670
19	CTCF	chr3:118817500-118817650	RPTEC	kidney:	n/a	n/a
20	CTCF	chr3:118753380-118753530	GM12864	blood:	n/a	n/a
21	CTCF	chr3:118817655-118817686	NHEK	skin:	n/a	n/a
22	CTCF	chr3:118817580-118817730	AG04450	lung:	n/a	chr3:118817652-118817670
23	CTCF	chr3:118753480-118753630	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr3:118817580-118817730	HL-60	blood:	n/a	chr3:118817652-118817670
25	CTCF	chr3:118817576-118817753	ProgFib	skin:	n/a	chr3:118817652-118817670
26	CTCF	chr3:118754020-118754170	AG09309	skin:	n/a	n/a
27	CTCF	chr3:118753760-118753910	BE2_C	brain:	n/a	n/a
28	CTCF	chr3:118753491-118754113	K562	blood:	n/a	n/a
29	CTCF	chr3:118753760-118753910	GM12870	blood:	n/a	n/a
30	CTCF	chr3:118753740-118753890	GM12871	blood:	n/a	n/a
31	CTCF	chr3:118803940-118804090	GM12873	blood:	n/a	n/a
32	CTCF	chr3:118817580-118817730	HEEpiC	esophagus:	n/a	chr3:118817652-118817670
33	CTCF	chr3:118753720-118753870	GM12864	blood:	n/a	n/a
34	CTCF	chr3:118753521-118753966	HepG2	liver:	n/a	n/a
35	CTCF	chr3:118770467-118770489	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr3:118753580-118753870	NHEK	skin:	n/a	n/a
37	CTCF	chr3:118753439-118754040	ProgFib	skin:	n/a	n/a
38	CTCF	chr3:118753460-118753610	HEK293	kidney:	n/a	n/a
39	CTCF	chr3:118753580-118753730	HFF	foreskin:	n/a	n/a
40	CTCF	chr3:118754000-118754001	GM13977	blood:	n/a	n/a
41	CTCF	chr3:118753690-118753932	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr3:118817534-118817780	Lung_OC	lung:	n/a	chr3:118817652-118817670
43	CTCF	chr3:118753700-118753850	Caco-2	colon:	n/a	n/a
44	CTCF	chr3:118817580-118817730	SAEC	small airway:	n/a	chr3:118817652-118817670
45	CTCF	chr3:118753760-118753910	HCFaa	heart:	n/a	n/a
46	CTCF	chr3:118753820-118753970	A549	lung:	n/a	n/a
47	CTCF	chr3:118753200-118753350	HRE	kidney:	n/a	n/a
48	CTCF	chr3:118753720-118753870	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:118753584-118753947	T-47D	breast:	n/a	n/a
50	CTCF	chr3:118753720-118753870	GM12875	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118753005-118753055	HL-60	blood:	n/a
2	chr3:118753005-118753055	HL-60	blood:	n/a
3	chr3:118792317-118792367	PrEC	prostate:	n/a
4	chr3:118753005-118753055	Hela-S3	cervix:	n/a
5	chr3:118753871-118753921	ovcar-3	ovarian:	n/a
6	chr3:118792317-118792367	AG10803	skin:	n/a
7	chr3:118753707-118753757	HCF	heart:	n/a
8	chr3:118753610-118753660	ECC-1	luminal epithelium:	n/a
9	chr3:118753610-118753660	HRCEpiC	kidney:	n/a
10	chr3:118753660-118753710	MCF10A-Er-Src	breast:	n/a
11	chr3:118754376-118754426	NH-A	brain:	n/a
12	chr3:118753871-118753921	SK-N-SH	brain:	n/a
13	chr3:118792317-118792367	HCPEpiC	choroid plexus:	n/a
14	chr3:118753738-118753788	HCPEpiC	choroid plexus:	n/a
15	chr3:118754376-118754426	IMR90	lung:	fetal
16	chr3:118753871-118753921	HRCEpiC	kidney:	n/a
17	chr3:118792317-118792367	GM19239	blood:	n/a
18	chr3:118753707-118753757	SKMC	muscle:	n/a
19	chr3:118753610-118753660	ProgFib	skin:	n/a
20	chr3:118757898-118757948	IMR90	lung:	fetal
21	chr3:118754376-118754426	SK-N-SH	brain:	n/a
22	chr3:118753705-118753755	NH-A	brain:	n/a
23	chr3:118754376-118754426	ProgFib	skin:	n/a
24	chr3:118754097-118754147	PrEC	prostate:	n/a
25	chr3:118753714-118753764	A549	lung:	n/a
26	chr3:118754376-118754426	ovcar-3	ovarian:	n/a
27	chr3:118753707-118753757	SK-N-SH	brain:	n/a
28	chr3:118757898-118757948	ovcar-3	ovarian:	n/a
29	chr3:118753660-118753710	GM12891	blood:	n/a
30	chr3:118792317-118792367	T-47D	breast:	n/a
31	chr3:118754376-118754426	CMK	blood:	n/a
32	chr3:118753660-118753710	HUVEC	blood vessel:	n/a
33	chr3:118753738-118753788	HRPEpiC	eye:	n/a
34	chr3:118753707-118753757	K562	blood:	n/a
35	chr3:118753871-118753921	U87	brain:	n/a
36	chr3:118753660-118753710	CMK	blood:	n/a
37	chr3:118753610-118753660	HMEC	breast:	n/a
38	chr3:118753871-118753921	A549	lung:	n/a
39	chr3:118753705-118753755	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:118753660-118753710	GM19239	blood:	n/a
41	chr3:118753871-118753921	HNPCEpiC	eye:	n/a
42	chr3:118753660-118753710	MCF-7	breast:	n/a
43	chr3:118753610-118753660	HepG2	liver:	n/a
44	chr3:118753705-118753755	CMK	blood:	n/a
45	chr3:118753005-118753055	HepG2	liver:	n/a
46	chr3:118753707-118753757	NHDF-neo	bronchial:	n/a
47	chr3:118754097-118754147	GM19239	blood:	n/a
48	chr3:118753610-118753660	NB4	blood:	n/a
49	chr3:118754097-118754147	SAEC	small airway:	n/a
50	chr3:118753714-118753764	AG04450	lung:	fetal

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:118603251..118604473-chr3:118817204..118818111,6	K562	blood:
2	chr3:118601857..118602685-chr3:118817256..118818095,2	MCF-7	breast:
3	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
4	chr3:116489803..116490556-chr3:118816385..118817077,2	K562	blood:
5	chr3:118753444..118753993-chr3:118815481..118816221,2	MCF-7	breast:
6	chr20:55795723..55796346-chr3:118817504..118818179,2	MCF-7	breast:
7	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
8	chr3:118600900..118602263-chr3:118817111..118818102,7	MCF-7	breast:
9	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
10	chr3:118603151..118604416-chr3:118816830..118818388,23	MCF-7	breast:
11	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
12	chr3:118600918..118601876-chr3:118816856..118817797,3	K562	blood:
13	chr3:118604102..118604821-chr3:118803607..118804317,2	MCF-7	breast:
14	chr3:118600892..118601643-chr3:118803705..118804296,2	K562	blood:
15	chr3:118603511..118604421-chr3:118817152..118818248,5	MCF-7	breast:
16	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:

No data

Variant related genes	Relation type
IGSF11	TF binding region
IGSF11	CpG island
ENSG00000144847	chromatin interactions

Extended variants
information (count: 853 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:853 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534713683	chr3:118752098-118752099	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373531799	chr3:118752129-118752130	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578047070	chr3:118752175-118752176	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557932712	chr3:118752214-118752215	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144797907	chr3:118752231-118752232	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184181291	chr3:118752235-118752236	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563505875	chr3:118752249-118752250	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575492249	chr3:118752304-118752305	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542982232	chr3:118752314-118752315	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561160895	chr3:118752326-118752327	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577654992	chr3:118752345-118752346	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76372346	chr3:118752346-118752347	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35860	chr3:118752395-118752396	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs564862440	chr3:118752405-118752406	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532129261	chr3:118752442-118752443	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550239535	chr3:118752446-118752447	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138462415	chr3:118752476-118752477	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537244915	chr3:118752489-118752490	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199940894	chr3:118752543-118752544	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144033382	chr3:118752544-118752545	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35815349	chr3:118752551-118752552	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562425424	chr3:118752581-118752582	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567874842	chr3:118752665-118752666	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146541567	chr3:118752678-118752679	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138756612	chr3:118752704-118752705	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576054744	chr3:118752719-118752720	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149379334	chr3:118752727-118752728	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76469364	chr3:118752754-118752755	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535724390	chr3:118752763-118752764	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575554996	chr3:118752777-118752778	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370049687	chr3:118752782-118752783	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565415376	chr3:118752828-118752829	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144660100	chr3:118752836-118752837	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573069473	chr3:118752901-118752902	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116056208	chr3:118752939-118752940	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564756064	chr3:118752945-118752946	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556021357	chr3:118752952-118752953	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550308998	chr3:118752961-118752962	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75166470	chr3:118752968-118752969	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148513649	chr3:118753032-118753033	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs547823405	chr3:118753068-118753069	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs549183304	chr3:118753072-118753073	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs567822012	chr3:118753095-118753096	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs528813042	chr3:118753125-118753126	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs117145695	chr3:118753135-118753136	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs571589708	chr3:118753196-118753197	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs539029314	chr3:118753200-118753201	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557343256	chr3:118753205-118753206	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs79392388	chr3:118753298-118753299	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs200219429	chr3:118753354-118753355	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118739400-118753000	Weak transcription	Pancreas	Pancrea
2	chr3:118751000-118753200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:118751000-118754000	Active TSS	Brain Hippocampus Middle	brain
4	chr3:118751000-118754200	Active TSS	Brain Anterior Caudate	brain
5	chr3:118751000-118754200	Active TSS	Brain Cingulate Gyrus	brain
6	chr3:118751000-118754200	Active TSS	Brain Substantia Nigra	brain
7	chr3:118751000-118754400	Active TSS	Brain Angular Gyrus	brain
8	chr3:118751000-118754400	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr3:118751200-118754200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr3:118751400-118753200	Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr3:118751400-118753200	Active TSS	Fetal Brain Female	brain
12	chr3:118751400-118754200	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr3:118751400-118754200	Active TSS	Ovary	ovary
14	chr3:118751600-118752200	Flanking Active TSS	Brain Germinal Matrix	brain
15	chr3:118751600-118754200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr3:118751800-118752800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr3:118751800-118754000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr3:118752200-118752400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
19	chr3:118752200-118752400	Active TSS	Brain Germinal Matrix	brain
20	chr3:118752200-118752400	Bivalent/Poised TSS	Fetal Brain Male	brain
21	chr3:118752200-118752400	Enhancers	Fetal Heart	heart
22	chr3:118752200-118752600	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr3:118752200-118753200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr3:118752200-118754400	Active TSS	Stomach Smooth Muscle	stomach
25	chr3:118752200-118754400	Active TSS	A549	lung
26	chr3:118752400-118752600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr3:118752400-118752600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
28	chr3:118752400-118752600	Flanking Active TSS	Brain Germinal Matrix	brain
29	chr3:118752400-118752800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr3:118752400-118753000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
31	chr3:118752400-118754000	Weak transcription	Fetal Heart	heart
32	chr3:118752400-118754000	Active TSS	Rectal Smooth Muscle	rectum
33	chr3:118752400-118754400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
34	chr3:118752600-118752800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
35	chr3:118752600-118753000	Active TSS	Primary T helper cells fromperipheralblood	blood
36	chr3:118752600-118753200	Active TSS	Brain Germinal Matrix	brain
37	chr3:118752600-118753400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
38	chr3:118752600-118754400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
39	chr3:118752800-118753000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
40	chr3:118752800-118753000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
41	chr3:118752800-118753000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr3:118752800-118753000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:118752800-118753000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr3:118752800-118753000	Bivalent Enhancer	Fetal Intestine Large	intestine
45	chr3:118752800-118753000	Bivalent Enhancer	Fetal Lung	lung
46	chr3:118752800-118753000	Enhancers	Placenta Amnion	Placenta Amnion
47	chr3:118752800-118753000	Active TSS	Right Atrium	heart
48	chr3:118752800-118753000	Enhancers	Right Ventricle	heart
49	chr3:118752800-118753200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
50	chr3:118752800-118753200	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain

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