Variant report

Variant	esv3438502
Chromosome Location	chr1:247093554-247096502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:247095108-247095660	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:247095395-247095787	K562	blood:	n/a	n/a
3	ATF1	chr1:247095033-247095724	K562	blood:	n/a	n/a
4	ATF2	chr1:247094857-247095646	GM12878	blood:	n/a	n/a
5	ATF2	chr1:247095024-247095628	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:247095002-247095491	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:247095033-247095564	GM12878	blood:	n/a	n/a
8	ATF3	chr1:247094993-247095380	K562	blood:	n/a	n/a
9	ATF3	chr1:247095382-247095733	K562	blood:	n/a	n/a
10	BACH1	chr1:247094957-247095580	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:247094361-247094561	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:247095543-247095730	K562	blood:	n/a	n/a
13	BCL3	chr1:247094121-247094620	A549	lung:	n/a	n/a
14	BCL3	chr1:247094844-247095304	A549	lung:	n/a	chr1:247094899-247094912 chr1:247094899-247094908 chr1:247095150-247095163 chr1:247094900-247094913 chr1:247095042-247095055
15	BCL3	chr1:247095009-247095589	A549	lung:	n/a	chr1:247095150-247095163 chr1:247095042-247095055
16	BCLAF1	chr1:247094981-247095724	K562	blood:	n/a	chr1:247095150-247095163 chr1:247095042-247095055
17	BCLAF1	chr1:247094844-247095801	K562	blood:	n/a	chr1:247094899-247094912 chr1:247094899-247094908 chr1:247095150-247095163 chr1:247094900-247094913 chr1:247095042-247095055
18	BCLAF1	chr1:247094834-247095750	GM12878	blood:	n/a	chr1:247094899-247094912 chr1:247094837-247094846 chr1:247094899-247094908 chr1:247095150-247095163 chr1:247094900-247094913 chr1:247095042-247095055
19	BCLAF1	chr1:247094885-247095739	GM12878	blood:	n/a	chr1:247094899-247094912 chr1:247094899-247094908 chr1:247095150-247095163 chr1:247094900-247094913 chr1:247095042-247095055
20	BHLHE40	chr1:247094349-247094505	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:247094859-247095823	K562	blood:	n/a	chr1:247095671-247095687 chr1:247095618-247095634 chr1:247095039-247095055 chr1:247094898-247094914 chr1:247095045-247095061
22	BHLHE40	chr1:247094197-247094622	K562	blood:	n/a	n/a
23	BHLHE40	chr1:247094920-247095681	HepG2	liver:	n/a	chr1:247095618-247095634 chr1:247095039-247095055 chr1:247095045-247095061
24	BHLHE40	chr1:247094801-247095686	GM12878	blood:	n/a	chr1:247095618-247095634 chr1:247095039-247095055 chr1:247094898-247094914 chr1:247095045-247095061
25	BRCA1	chr1:247094989-247095724	H1-hESC	embryonic stem cell:	n/a	chr1:247095343-247095352
26	BRCA1	chr1:247094889-247095752	Hela-S3	cervix:	n/a	chr1:247095343-247095352
27	BRCA1	chr1:247095057-247095650	HepG2	liver:	n/a	chr1:247095343-247095352
28	BRCA1	chr1:247094411-247094465	GM12878	blood:	n/a	n/a
29	BRCA1	chr1:247095014-247095828	GM12878	blood:	n/a	chr1:247095343-247095352
30	CBX3	chr1:247095052-247095609	K562	blood:	n/a	n/a
31	CBX3	chr1:247093268-247093833	K562	blood:	n/a	n/a
32	CBX3	chr1:247094818-247095865	K562	blood:	n/a	n/a
33	CBX3	chr1:247094156-247094715	K562	blood:	n/a	n/a
34	CCNT2	chr1:247094335-247095866	K562	blood:	n/a	n/a
35	CEBPB	chr1:247095175-247095726	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:247094536-247094751	A549	lung:	n/a	n/a
37	CEBPB	chr1:247095078-247095762	K562	blood:	n/a	n/a
38	CEBPB	chr1:247094589-247095810	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:247094522-247094718	K562	blood:	n/a	n/a
40	CEBPB	chr1:247095462-247095742	K562	blood:	n/a	n/a
41	CEBPB	chr1:247095228-247095790	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr1:247094214-247095828	Hela-S3	cervix:	n/a	n/a
43	CEBPD	chr1:247094918-247095929	K562	blood:	n/a	n/a
44	CEBPD	chr1:247094913-247095371	HepG2	liver:	n/a	n/a
45	CHD1	chr1:247094917-247095740	GM12878	blood:	n/a	chr1:247095150-247095160 chr1:247095343-247095352
46	CHD1	chr1:247094160-247094570	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr1:247094240-247094662	GM12878	blood:	n/a	n/a
48	CHD1	chr1:247094996-247095227	H1-hESC	embryonic stem cell:	n/a	chr1:247095150-247095160
49	CHD2	chr1:247094192-247095932	Hela-S3	cervix:	n/a	chr1:247095150-247095160 chr1:247094705-247094715 chr1:247095343-247095352
50	CHD2	chr1:247094410-247095843	HepG2	liver:	n/a	chr1:247095150-247095160 chr1:247094705-247094715 chr1:247095343-247095352

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:247094486-247094536	IMR90	lung:	fetal
2	chr1:247094486-247094536	IMR90	lung:	fetal
3	chr1:247095607-247095657	HRCEpiC	kidney:	n/a
4	chr1:247095660-247095710	HUVEC	blood vessel:	n/a
5	chr1:247095607-247095657	GM06990	blood:	n/a
6	chr1:247094486-247094536	SK-N-SH	brain:	n/a
7	chr1:247095483-247095533	HCM	heart:	n/a
8	chr1:247094386-247094436	MCF-7	breast:	n/a
9	chr1:247096088-247096138	HRPEpiC	eye:	n/a
10	chr1:247093553-247093603	BJ	skin:	n/a
11	chr1:247095483-247095533	NHBE	bronchial:	n/a
12	chr1:247094143-247094193	BE2_C	brain:	n/a
13	chr1:247093553-247093603	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:247094143-247094193	U87	brain:	n/a
15	chr1:247094694-247094744	HIPEpiC	eye:	n/a
16	chr1:247093553-247093603	MCF-7	breast:	n/a
17	chr1:247094143-247094193	HepG2	liver:	n/a
18	chr1:247094143-247094193	HCPEpiC	choroid plexus:	n/a
19	chr1:247095483-247095533	ProgFib	skin:	n/a
20	chr1:247095607-247095657	AG09319	gingival:	n/a
21	chr1:247095660-247095710	K562	blood:	n/a
22	chr1:247095226-247095276	GM12878	blood:	n/a
23	chr1:247093553-247093603	HMEC	breast:	n/a
24	chr1:247094694-247094744	GM12891	blood:	n/a
25	chr1:247096025-247096075	BJ	skin:	n/a
26	chr1:247094486-247094536	GM12891	blood:	n/a
27	chr1:247094386-247094436	GM06990	blood:	n/a
28	chr1:247095660-247095710	A549	lung:	n/a
29	chr1:247096025-247096075	SK-N-SH	brain:	n/a
30	chr1:247096088-247096138	PFSK-1	brain:	n/a
31	chr1:247093553-247093603	AG04450	lung:	fetal
32	chr1:247094694-247094744	NB4	blood:	n/a
33	chr1:247094143-247094193	HEEpiC	esophagus:	n/a
34	chr1:247094486-247094536	Hepatocyte	liver:	n/a
35	chr1:247094143-247094193	Hepatocyte	liver:	n/a
36	chr1:247094143-247094193	SKMC	muscle:	n/a
37	chr1:247095483-247095533	BE2_C	brain:	n/a
38	chr1:247095607-247095657	AG04449	skin:	fetal
39	chr1:247095607-247095657	AG04450	lung:	fetal
40	chr1:247096088-247096138	AG09319	gingival:	n/a
41	chr1:247095607-247095657	HAEpiC	amniotic membrane:	n/a
42	chr1:247095660-247095710	ovcar-3	ovarian:	n/a
43	chr1:247094386-247094436	PFSK-1	brain:	n/a
44	chr1:247095660-247095710	NH-A	brain:	n/a
45	chr1:247093553-247093603	HAEpiC	amniotic membrane:	n/a
46	chr1:247095660-247095710	MCF10A-Er-Src	breast:	n/a
47	chr1:247096025-247096075	AG10803	skin:	n/a
48	chr1:247094486-247094536	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:247094386-247094436	A549	lung:	n/a
50	chr1:247096088-247096138	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:247092146..247096759-chr1:247274350..247278356,6	MCF-7	breast:
2	chr1:246871057..246874045-chr1:247092351..247094206,2	MCF-7	breast:
3	chr1:247095732..247098585-chr1:247108516..247110039,2	K562	blood:
4	chr1:247056860..247058918-chr1:247092602..247094534,2	MCF-7	breast:
5	chr1:247093791..247096097-chr1:247493835..247497465,5	K562	blood:
6	chr1:247094550..247095484-chr1:247241843..247242470,2	MCF-7	breast:
7	chr1:247092719..247096472-chr1:247266171..247268660,3	MCF-7	breast:
8	chr1:247093731..247095297-chr1:247494500..247497465,3	K562	blood:
9	chr1:247095350..247097520-chr1:247156671..247158364,2	K562	blood:
10	chr1:247094698..247095429-chr16:2204826..2205626,2	HCT-116	colon:
11	chr1:247093046..247095250-chr1:247265472..247268873,4	MCF-7	breast:
12	chr1:247093552..247097819-chr1:247240197..247243590,5	MCF-7	breast:
13	chr1:247093657..247096650-chr1:247335096..247337981,2	K562	blood:
14	chr1:247094403..247095339-chr8:134309571..134310460,2	Hela-S3	cervix:
15	chr1:247046300..247048217-chr1:247091357..247094558,3	K562	blood:
16	chr1:247094834..247095447-chr11:61582600..61583201,2	Hela-S3	cervix:
17	chr1:247093628..247096678-chr1:247168698..247172076,4	MCF-7	breast:
18	chr1:247092059..247094068-chr1:247274280..247275871,2	K562	blood:
19	chr1:247092592..247095168-chr1:247240880..247243272,2	K562	blood:
20	chr1:247094242..247096736-chr1:249153131..249154703,2	K562	blood:
21	chr1:247092220..247095330-chr1:247240373..247243272,3	K562	blood:
22	chr1:247092987..247095907-chr22:39713891..39716269,2	K562	blood:
23	chr1:247094499..247095162-chr17:8339191..8339716,2	Hela-S3	cervix:
24	chr1:247095122..247095967-chr11:32913877..32914747,2	Hela-S3	cervix:
25	chr1:247093881..247096879-chr1:247169993..247171703,3	K562	blood:

Variant related genes	Relation type
AHCTF1	TF binding region
AHCTF1	CpG island
ENSG00000221953	chromatin interactions
ENSG00000227237	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000260260	chromatin interactions
ENSG00000222326	chromatin interactions
ENSG00000188295	chromatin interactions
ENSG00000197472	chromatin interactions
ENSG00000162714	chromatin interactions
ENSG00000166579	chromatin interactions
ENSG00000196418	chromatin interactions
ENSG00000135747	chromatin interactions
ENSG00000206630	chromatin interactions
ENSG00000100316	chromatin interactions
ENSG00000171163	chromatin interactions
ENSG00000104419	chromatin interactions
ENSG00000263764	chromatin interactions

Extended variants
information (count: 111 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:111 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7512439	chr1:247093593-247093594	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374133415	chr1:247093618-247093619	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs548590031	chr1:247093730-247093731	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs570794200	chr1:247093736-247093737	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs368212406	chr1:247093737-247093738	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs534298671	chr1:247093836-247093837	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs548117279	chr1:247093845-247093846	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs79921823	chr1:247093875-247093876	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs564591272	chr1:247093886-247093887	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs2029789	chr1:247093888-247093889	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs75379026	chr1:247093900-247093901	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs191802152	chr1:247093920-247093921	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs182432605	chr1:247093960-247093961	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs556437164	chr1:247093961-247093962	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs576634025	chr1:247094015-247094016	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs535920845	chr1:247094016-247094017	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs555883756	chr1:247094106-247094107	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs572500107	chr1:247094189-247094190	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs186720154	chr1:247094203-247094204	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs564444203	chr1:247094205-247094206	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs200512569	chr1:247094249-247094250	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs73146640	chr1:247094263-247094264	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs534579122	chr1:247094278-247094279	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs546666663	chr1:247094280-247094281	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs78510255	chr1:247094302-247094303	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs35494760	chr1:247094305-247094306	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs386641790	chr1:247094324-247094325	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs77855548	chr1:247094354-247094355	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs80056231	chr1:247094355-247094356	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs148056251	chr1:247094358-247094359	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs528116595	chr1:247094370-247094371	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs140851502	chr1:247094386-247094387	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs41267539	chr1:247094393-247094394	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs150139369	chr1:247094405-247094406	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs114778821	chr1:247094446-247094447	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs570299748	chr1:247094484-247094485	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs61854047	chr1:247094486-247094487	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs536037532	chr1:247094508-247094509	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs555942778	chr1:247094538-247094539	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs572560433	chr1:247094546-247094547	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs113177866	chr1:247094568-247094569	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs535024624	chr1:247094571-247094572	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs557817726	chr1:247094577-247094578	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs577891160	chr1:247094637-247094638	Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs138217683	chr1:247094670-247094671	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
46	rs563225195	chr1:247094761-247094762	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs568054756	chr1:247094775-247094776	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs374471218	chr1:247094869-247094870	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
49	rs559032029	chr1:247094899-247094900	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
50	rs528127298	chr1:247094905-247094906	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Bipolar disorder	19114987	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:247069800-247093800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:247070000-247093600	Weak transcription	Aorta	Aorta
3	chr1:247078400-247093600	Weak transcription	Fetal Kidney	kidney
4	chr1:247087400-247093600	Weak transcription	Brain Angular Gyrus	brain
5	chr1:247089400-247093600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr1:247089600-247093800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:247092800-247093600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr1:247092800-247093600	Enhancers	Fetal Heart	heart
9	chr1:247092800-247093800	Transcr. at gene 5' and 3'	Dnd41	blood
10	chr1:247092800-247094000	Enhancers	Primary T cells fromperipheralblood	blood
11	chr1:247092800-247094000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:247092800-247095800	Active TSS	A549	lung
13	chr1:247093000-247093600	Enhancers	Fetal Brain Male	brain
14	chr1:247093000-247093600	Active TSS	K562	blood
15	chr1:247093000-247093800	Enhancers	Small Intestine	intestine
16	chr1:247093000-247095800	Active TSS	HSMM	muscle
17	chr1:247093000-247096200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:247093000-247096200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:247093000-247096200	Active TSS	GM12878-XiMat	blood
20	chr1:247093200-247093600	Transcr. at gene 5' and 3'	HMEC	breast
21	chr1:247093200-247094400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr1:247093200-247094400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr1:247093200-247095800	Active TSS	Ovary	ovary
24	chr1:247093400-247093600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:247093400-247093600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:247093400-247093600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:247093400-247093600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:247093400-247093600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:247093400-247093600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr1:247093400-247093600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr1:247093400-247093600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr1:247093400-247093600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr1:247093400-247093600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr1:247093400-247093600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:247093400-247093600	Enhancers	Liver	Liver
36	chr1:247093400-247093600	Enhancers	Brain Cingulate Gyrus	brain
37	chr1:247093400-247093600	Flanking Active TSS	Colonic Mucosa	Colon
38	chr1:247093400-247093600	Enhancers	Esophagus	oesophagus
39	chr1:247093400-247093600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr1:247093400-247093600	Flanking Active TSS	Fetal Brain Female	brain
41	chr1:247093400-247093600	Enhancers	Fetal Intestine Large	intestine
42	chr1:247093400-247093600	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
43	chr1:247093400-247093600	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr1:247093400-247093600	Enhancers	Fetal Muscle Leg	muscle
45	chr1:247093400-247093600	Enhancers	Fetal Thymus	thymus
46	chr1:247093400-247093600	Flanking Active TSS	Psoas Muscle	Psoas
47	chr1:247093400-247093600	Flanking Active TSS	Right Atrium	heart
48	chr1:247093400-247093600	Flanking Active TSS	HepG2	liver
49	chr1:247093400-247093600	Flanking Active TSS	NHDF-Ad	bronchial
50	chr1:247093400-247093600	Transcr. at gene 5' and 3'	NHEK	skin

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