Variant report

Variant	nsv1007194
Chromosome Location	chr1:246813090-246855424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:460)
CpG islands
(count:122)
Chromatin interactive
region (count:38)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246852848-246853159	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:246852892-246853051	K562	blood:	n/a	n/a
3	BCLAF1	chr1:246852778-246853195	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:246852897-246853121	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:246852917-246853125	K562	blood:	n/a	n/a
6	BHLHE40	chr1:246853014-246853018	A549	lung:	n/a	n/a
7	BRCA1	chr1:246852771-246853091	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr1:246852786-246853158	K562	blood:	n/a	n/a
9	CCNT2	chr1:246813221-246813364	K562	blood:	n/a	n/a
10	CEBPB	chr1:246841004-246841227	K562	blood:	n/a	chr1:246841092-246841103
11	CEBPB	chr1:246852842-246853219	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:246840956-246841203	HepG2	liver:	n/a	chr1:246841092-246841103
13	CEBPB	chr1:246840959-246841470	Hela-S3	cervix:	n/a	chr1:246841092-246841103
14	CHD1	chr1:246852925-246853046	GM12878	blood:	n/a	n/a
15	CHD2	chr1:246852907-246853158	GM12878	blood:	n/a	n/a
16	CHD2	chr1:246847933-246847946	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr1:246830022-246830030	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr1:246845140-246845290	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr1:246852940-246853090	GM12875	blood:	n/a	n/a
20	CTCF	chr1:246852863-246853119	ECC-1	luminal epithelium:	n/a	n/a
21	CTCF	chr1:246850400-246850550	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr1:246852887-246853119	Fibrobl	skin:	n/a	n/a
23	CTCF	chr1:246852927-246853097	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:246852900-246853050	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr1:246852900-246853050	HMF	breast:	n/a	n/a
26	CTCF	chr1:246852920-246853070	GM06990	blood:	n/a	n/a
27	CTCF	chr1:246850360-246850510	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr1:246852821-246853131	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr1:246852900-246853050	SAEC	small airway:	n/a	n/a
30	CTCF	chr1:246852610-246852674	GM19239	blood:	n/a	n/a
31	CTCF	chr1:246852880-246853030	HPF	lung:	n/a	n/a
32	CTCF	chr1:246850420-246850570	BE2_C	brain:	n/a	n/a
33	CTCF	chr1:246852900-246853050	GM12872	blood:	n/a	n/a
34	CTCF	chr1:246852909-246853118	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:246852920-246853070	GM12866	blood:	n/a	n/a
36	CTCF	chr1:246852940-246853090	HEK293	kidney:	n/a	n/a
37	CTCF	chr1:246852880-246853030	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr1:246852900-246853050	GM12878	blood:	n/a	n/a
39	CTCF	chr1:246852360-246852510	GM12870	blood:	n/a	n/a
40	CTCF	chr1:246852900-246853050	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr1:246850386-246850569	HepG2	liver:	n/a	n/a
42	CTCF	chr1:246832559-246832742	GM12878	blood:	n/a	chr1:246832637-246832655 chr1:246832632-246832653 chr1:246832638-246832654
43	CTCF	chr1:246852861-246853078	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr1:246845180-246845330	BE2_C	brain:	n/a	n/a
45	CTCF	chr1:246850300-246850450	GM12867	blood:	n/a	n/a
46	CTCF	chr1:246852540-246852690	GM12871	blood:	n/a	n/a
47	CTCF	chr1:246852920-246853070	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr1:246853280-246853430	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr1:246852940-246853090	GM12869	blood:	n/a	n/a
50	CTCF	chr1:246852920-246853070	GM12870	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246831331-246831381	GM06990	blood:	n/a
2	chr1:246831331-246831381	SK-N-MC	brain:	n/a
3	chr1:246843900-246843950	Hepatocyte	liver:	n/a
4	chr1:246831331-246831381	Hela-S3	cervix:	n/a
5	chr1:246831331-246831381	U87	brain:	n/a
6	chr1:246843900-246843950	Jurkat	blood:	n/a
7	chr1:246831331-246831381	BJ	skin:	n/a
8	chr1:246831331-246831381	AG04450	lung:	fetal
9	chr1:246843900-246843950	HRE	kidney:	n/a
10	chr1:246831331-246831381	NT2-D1	testis:	n/a
11	chr1:246831331-246831381	HEK293	kidney:	embryo
12	chr1:246843900-246843950	ovcar-3	ovarian:	n/a
13	chr1:246843900-246843950	HepG2	liver:	n/a
14	chr1:246843900-246843950	NHDF-neo	bronchial:	n/a
15	chr1:246843900-246843950	MCF-7	breast:	n/a
16	chr1:246843900-246843950	AG10803	skin:	n/a
17	chr1:246831331-246831381	HL-60	blood:	n/a
18	chr1:246843900-246843950	HEK293	kidney:	embryo
19	chr1:246831331-246831381	T-47D	breast:	n/a
20	chr1:246831331-246831381	HRE	kidney:	n/a
21	chr1:246843900-246843950	AoSMC	blood vessel:	n/a
22	chr1:246843900-246843950	AG09309	skin:	n/a
23	chr1:246831331-246831381	NHBE	bronchial:	n/a
24	chr1:246831331-246831381	NHDF-neo	bronchial:	n/a
25	chr1:246843900-246843950	SKMC	muscle:	n/a
26	chr1:246831331-246831381	H1-hESC	embryonic stem cell:	embryo
27	chr1:246831331-246831381	HepG2	liver:	n/a
28	chr1:246843900-246843950	HAEpiC	amniotic membrane:	n/a
29	chr1:246831331-246831381	A549	lung:	n/a
30	chr1:246843900-246843950	K562	blood:	n/a
31	chr1:246843900-246843950	NT2-D1	testis:	n/a
32	chr1:246843900-246843950	BJ	skin:	n/a
33	chr1:246843900-246843950	NB4	blood:	n/a
34	chr1:246831331-246831381	RPTEC	kidney:	n/a
35	chr1:246843900-246843950	HRPEpiC	eye:	n/a
36	chr1:246843900-246843950	AG04449	skin:	fetal
37	chr1:246831331-246831381	PANC-1	pancreas:	n/a
38	chr1:246843900-246843950	MCF10A-Er-Src	breast:	n/a
39	chr1:246831331-246831381	HIPEpiC	eye:	n/a
40	chr1:246831331-246831381	IMR90	lung:	fetal
41	chr1:246831331-246831381	ovcar-3	ovarian:	n/a
42	chr1:246831331-246831381	ECC-1	luminal epithelium:	n/a
43	chr1:246843900-246843950	Caco-2	colon:	n/a
44	chr1:246843900-246843950	PFSK-1	brain:	n/a
45	chr1:246843900-246843950	RPTEC	kidney:	n/a
46	chr1:246831331-246831381	ProgFib	skin:	n/a
47	chr1:246831331-246831381	SK-N-SH	brain:	n/a
48	chr1:246831331-246831381	K562	blood:	n/a
49	chr1:246843900-246843950	NHBE	bronchial:	n/a
50	chr1:246831331-246831381	HUVEC	blood vessel:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246813415..246815262-chr1:246816849..246818678,2	K562	blood:
2	chr1:246853196..246855742-chr1:246886661..246889205,4	MCF-7	breast:
3	chr1:246834302..246836576-chr1:246850858..246853240,2	K562	blood:
4	chr1:246805689..246809236-chr1:246811706..246814341,4	K562	blood:
5	chr1:246817586..246818454-chr1:246829878..246830575,2	K562	blood:
6	chr1:246801219..246803848-chr1:246819940..246821442,2	MCF-7	breast:
7	chr1:246272101..246273950-chr1:246817056..246818596,2	K562	blood:
8	chr1:246834497..246836021-chr1:246836490..246838405,2	K562	blood:
9	chr1:246833383..246835466-chr1:246835764..246838210,2	K562	blood:
10	chr1:246819262..246822483-chr1:246827489..246830691,4	K562	blood:
11	chr1:246826840..246829651-chr1:246886042..246887576,2	MCF-7	breast:
12	chr1:246834497..246836021-chr1:246836490..246838405,2	K562	blood:
13	chr1:246848698..246850576-chr1:246851787..246854723,2	MCF-7	breast:
14	chr1:246817289..246819425-chr1:246820924..246823201,2	MCF-7	breast:
15	chr1:246852892..246854672-chr1:246916760..246919420,2	MCF-7	breast:
16	chr1:246817289..246819425-chr1:246820924..246823201,2	MCF-7	breast:
17	chr1:246810760..246814409-chr1:246816683..246820922,4	K562	blood:
18	chr1:246817628..246820326-chr1:246894643..246896981,2	MCF-7	breast:
19	chr1:246704378..246705938-chr1:246830141..246833108,2	K562	blood:
20	chr1:246852764..246853288-chr1:246862284..246863046,2	MCF-7	breast:
21	chr1:246834302..246836576-chr1:246850858..246853240,2	K562	blood:
22	chr1:246828128..246831058-chr1:246844118..246846484,2	K562	blood:
23	chr1:246817586..246818454-chr1:246829878..246830575,2	K562	blood:
24	chr1:246842065..246844479-chr1:246852979..246855083,3	K562	blood:
25	chr1:246813415..246815262-chr1:246816849..246818678,2	K562	blood:
26	chr1:246810760..246814409-chr1:246816683..246820922,4	K562	blood:
27	chr1:246815669..246818664-chr1:246820426..246822139,2	K562	blood:
28	chr1:246803588..246807692-chr1:246815416..246819511,4	K562	blood:
29	chr1:246774160..246776210-chr1:246811520..246814004,2	K562	blood:
30	chr1:246722538..246724149-chr1:246820776..246822354,2	K562	blood:
31	chr1:246819262..246822483-chr1:246827489..246830691,4	K562	blood:
32	chr1:246811207..246813895-chr1:246830093..246833035,2	K562	blood:
33	chr1:246855312..246858038-chr1:246858334..246859912,2	K562	blood:
34	chr1:246853163..246855096-chr1:246886538..246888986,3	MCF-7	breast:
35	chr1:246833383..246835466-chr1:246835764..246838210,2	K562	blood:
36	chr1:246822078..246824863-chr1:247030582..247033303,2	K562	blood:
37	chr1:246811207..246813895-chr1:246830093..246833035,2	K562	blood:
38	chr1:246815669..246818664-chr1:246820426..246822139,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNST-1	chr1:246854769-246855123	NONHSAT010718
2	lnc-CNST-1	chr1:246854770-246855175	XLOC_000642
3	lnc-CNST-1	chr1:246845410-246848377	ENSG00000260698.1
4	lnc-CNST-1	chr1:246853034-246853516	XLOC_000642
5	lnc-SCCPDH-3	chr1:246830010-246830784	NONHSAT010714
6	lnc-CNST-1	chr1:246853349-246853516	XLOC_000642
7	lnc-SCCPDH-3	chr1:246831385-246831658	NONHSAT010714
8	lnc-TFB2M-5	chr1:246831977-246832419	NONHSAT010715
9	lnc-TFB2M-1	chr1:246830009-246830785	ENSG00000245759
10	lnc-CNST-1	chr1:246853023-246853757	NONHSAT010718
11	lnc-TFB2M-1	chr1:246831384-246831638	ENSG00000245759
12	lnc-CNST-1	chr1:246854770-246855123	XLOC_000642
13	lnc-CNST-1	chr1:246846453-246846487	XLOC_000642

No data

Variant related genes	Relation type
ENSG00000260698	TF binding region
ENSG00000235021	TF binding region
ENSG00000260698	CpG island
ENSG00000235021	CpG island
ENSG00000235021	chromatin interactions
ENSG00000143653	chromatin interactions
ENSG00000260698	chromatin interactions
ENSG00000228879	chromatin interactions
ACVR2A	miRNA target sites
BRD3	miRNA target sites

Extended variants
information (count: 1927 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1927 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189506660	chr1:246813110-246813111	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs139608281	chr1:246813127-246813128	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552801727	chr1:246813192-246813193	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573100012	chr1:246813230-246813231	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144427713	chr1:246813231-246813232	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564966033	chr1:246813237-246813238	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530604485	chr1:246813238-246813239	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544292593	chr1:246813244-246813245	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560977179	chr1:246813273-246813274	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548835880	chr1:246813302-246813303	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565363222	chr1:246813416-246813417	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111461639	chr1:246813435-246813436	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147833394	chr1:246813464-246813465	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544930906	chr1:246813465-246813466	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139643591	chr1:246813474-246813475	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3124085	chr1:246813477-246813478	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181512122	chr1:246813482-246813483	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144772352	chr1:246813531-246813532	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571720329	chr1:246813552-246813553	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185997098	chr1:246813554-246813555	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563951727	chr1:246813555-246813556	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550620221	chr1:246813625-246813626	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567423239	chr1:246813653-246813654	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536239474	chr1:246813686-246813687	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553129906	chr1:246813691-246813692	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573075176	chr1:246813694-246813695	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531155558	chr1:246813727-246813728	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535052894	chr1:246813736-246813737	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538582562	chr1:246813740-246813741	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558832030	chr1:246813742-246813743	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575306468	chr1:246813752-246813753	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190016026	chr1:246813831-246813832	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560964948	chr1:246813866-246813867	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370202236	chr1:246813943-246813944	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs66876655	chr1:246813978-246813979	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10693662	chr1:246813997-246813998	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111629356	chr1:246814037-246814038	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540218154	chr1:246814128-246814129	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs3129559	chr1:246814137-246814138	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs199917839	chr1:246814168-246814169	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143629106	chr1:246814247-246814248	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs117917284	chr1:246814294-246814295	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs567301508	chr1:246814353-246814354	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs375765352	chr1:246814363-246814364	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs12750060	chr1:246814372-246814373	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530963703	chr1:246814374-246814375	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs3124086	chr1:246814376-246814377	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs567408919	chr1:246814413-246814414	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs566099505	chr1:246814439-246814440	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs199541587	chr1:246814447-246814448	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Oral cancer	21386901	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246755400-246832800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr1:246780800-246813400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:246784200-246833800	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr1:246789200-246839200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr1:246795600-246813600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr1:246796000-246831200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:246796200-246822000	Weak transcription	Brain Substantia Nigra	brain
8	chr1:246801000-246826400	Weak transcription	HMEC	breast
9	chr1:246801000-246829000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr1:246801600-246842800	Weak transcription	Fetal Kidney	kidney
11	chr1:246801800-246817200	Weak transcription	A549	lung
12	chr1:246802000-246814600	Weak transcription	Fetal Brain Female	brain
13	chr1:246803400-246817200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:246803400-246822000	Weak transcription	Psoas Muscle	Psoas
15	chr1:246804200-246833400	Strong transcription	Liver	Liver
16	chr1:246804600-246833800	Strong transcription	Primary T cells from cord blood	blood
17	chr1:246804800-246834200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr1:246805200-246813400	Strong transcription	Fetal Thymus	thymus
19	chr1:246805200-246816000	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr1:246805200-246819400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:246805200-246825200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr1:246805400-246814000	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr1:246805400-246837600	Weak transcription	Small Intestine	intestine
24	chr1:246805800-246813400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:246807200-246820600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr1:246808200-246817400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:246808400-246817000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr1:246809600-246813400	Strong transcription	Primary hematopoietic stem cells	blood
29	chr1:246809600-246818400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr1:246809800-246814200	Strong transcription	Primary B cells from peripheral blood	blood
31	chr1:246810200-246813600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:246810200-246819200	Strong transcription	Dnd41	blood
33	chr1:246810400-246813400	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr1:246810400-246813400	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr1:246810400-246815400	Strong transcription	Primary B cells from cord blood	blood
36	chr1:246810600-246828200	Weak transcription	Fetal Heart	heart
37	chr1:246810800-246814000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:246811000-246813200	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr1:246811000-246814000	Weak transcription	Right Ventricle	heart
40	chr1:246811000-246814200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr1:246811000-246815400	Weak transcription	Fetal Brain Male	brain
42	chr1:246811000-246817200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr1:246811000-246817200	Weak transcription	Ovary	ovary
44	chr1:246811000-246820000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr1:246811000-246820000	Weak transcription	Esophagus	oesophagus
46	chr1:246811000-246820000	Weak transcription	Fetal Intestine Small	intestine
47	chr1:246811000-246820400	Weak transcription	Lung	lung
48	chr1:246811000-246828600	Weak transcription	Brain Anterior Caudate	brain
49	chr1:246811000-246835000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:246811200-246814000	Weak transcription	Right Atrium	heart

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