Variant report

Variant	esv1799275
Chromosome Location	chr1:211751816-211754866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:799)
CpG islands
(count:489)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:799 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:211752854-211753252	HepG2	liver:	n/a	n/a
2	ATF1	chr1:211752422-211753356	K562	blood:	n/a	n/a
3	ATF2	chr1:211752231-211752766	GM12878	blood:	n/a	n/a
4	ATF2	chr1:211752810-211753285	GM12878	blood:	n/a	n/a
5	ATF3	chr1:211752831-211753225	K562	blood:	n/a	n/a
6	ATF3	chr1:211752145-211752722	A549	lung:	n/a	chr1:211752642-211752652 chr1:211752711-211752720
7	BACH1	chr1:211752827-211753014	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:211754622-211754624	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:211752419-211752460	K562	blood:	n/a	n/a
10	BCLAF1	chr1:211752191-211752685	GM12878	blood:	n/a	chr1:211752298-211752311 chr1:211752248-211752257 chr1:211752455-211752468
11	BCLAF1	chr1:211752744-211753311	GM12878	blood:	n/a	chr1:211752906-211752919 chr1:211753003-211753016 chr1:211753008-211753017
12	BHLHE40	chr1:211752320-211753462	HepG2	liver:	n/a	chr1:211752458-211752474
13	BHLHE40	chr1:211751039-211753381	GM12878	blood:	n/a	chr1:211751231-211751247 chr1:211751960-211751976 chr1:211752458-211752474 chr1:211751957-211751973 chr1:211751172-211751188
14	BHLHE40	chr1:211753820-211753860	K562	blood:	n/a	n/a
15	BHLHE40	chr1:211750870-211753535	K562	blood:	n/a	chr1:211751231-211751247 chr1:211751960-211751976 chr1:211752458-211752474 chr1:211751957-211751973 chr1:211751172-211751188
16	BHLHE40	chr1:211752489-211752588	A549	lung:	n/a	n/a
17	BRCA1	chr1:211752911-211753098	HepG2	liver:	n/a	n/a
18	BRCA1	chr1:211752430-211752734	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr1:211752888-211753516	K562	blood:	n/a	n/a
20	CBX3	chr1:211750976-211752035	K562	blood:	n/a	n/a
21	CBX3	chr1:211752100-211752732	K562	blood:	n/a	n/a
22	CCNT2	chr1:211750901-211753387	K562	blood:	n/a	chr1:211752711-211752720 chr1:211753013-211753022 chr1:211752738-211752747 chr1:211752838-211752847
23	CEBPB	chr1:211752743-211753440	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:211752309-211752706	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:211751548-211751845	K562	blood:	n/a	n/a
26	CEBPB	chr1:211751496-211751864	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:211753174-211753508	K562	blood:	n/a	n/a
28	CEBPB	chr1:211754791-211755264	IMR90	lung:	n/a	chr1:211754812-211754824
29	CEBPB	chr1:211750408-211751876	Hela-S3	cervix:	n/a	n/a
30	CEBPD	chr1:211752197-211752665	K562	blood:	n/a	n/a
31	CEBPD	chr1:211752330-211753183	HepG2	liver:	n/a	n/a
32	CEBPD	chr1:211752810-211753593	K562	blood:	n/a	n/a
33	CEBPD	chr1:211752384-211752673	HepG2	liver:	n/a	n/a
34	CEBPD	chr1:211752894-211753497	K562	blood:	n/a	n/a
35	CEBPD	chr1:211752829-211753141	HepG2	liver:	n/a	n/a
36	CHD1	chr1:211750902-211751988	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr1:211751737-211752579	GM12878	blood:	n/a	n/a
38	CHD1	chr1:211752885-211753281	GM12878	blood:	n/a	n/a
39	CHD1	chr1:211752268-211752468	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr1:211751157-211751930	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr1:211752359-211753320	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr1:211751868-211751871	GM12878	blood:	n/a	n/a
43	CHD2	chr1:211752391-211753310	HepG2	liver:	n/a	n/a
44	CHD2	chr1:211752383-211753290	K562	blood:	n/a	n/a
45	CHD2	chr1:211752248-211753347	GM12878	blood:	n/a	n/a
46	CHD2	chr1:211750845-211753328	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr1:211751060-211751996	K562	blood:	n/a	n/a
48	CREB1	chr1:211751738-211753229	A549	lung:	n/a	n/a
49	CREB1	chr1:211752419-211752775	A549	lung:	n/a	n/a
50	CREB1	chr1:211750869-211753695	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:211753152-211753202	GM06990	blood:	n/a
2	chr1:211753152-211753202	GM06990	blood:	n/a
3	chr1:211753152-211753202	NHDF-neo	bronchial:	n/a
4	chr1:211752571-211752621	HUVEC	blood vessel:	n/a
5	chr1:211752620-211752670	T-47D	breast:	n/a
6	chr1:211752511-211752561	T-47D	breast:	n/a
7	chr1:211752571-211752621	BJ	skin:	n/a
8	chr1:211752571-211752621	HL-60	blood:	n/a
9	chr1:211752895-211752945	GM12891	blood:	n/a
10	chr1:211751793-211751843	IMR90	lung:	fetal
11	chr1:211751907-211751957	NHBE	bronchial:	n/a
12	chr1:211752511-211752561	U87	brain:	n/a
13	chr1:211752571-211752621	HNPCEpiC	eye:	n/a
14	chr1:211752571-211752621	HMEC	breast:	n/a
15	chr1:211751907-211751957	SK-N-SH_RA	brain:	n/a
16	chr1:211752895-211752945	A549	lung:	n/a
17	chr1:211752620-211752670	NHBE	bronchial:	n/a
18	chr1:211751907-211751957	HRE	kidney:	n/a
19	chr1:211752895-211752945	SK-N-SH	brain:	n/a
20	chr1:211752571-211752621	IMR90	lung:	fetal
21	chr1:211753582-211753632	AoSMC	blood vessel:	n/a
22	chr1:211752620-211752670	Hepatocyte	liver:	n/a
23	chr1:211753152-211753202	Hela-S3	cervix:	n/a
24	chr1:211751907-211751957	AG09309	skin:	n/a
25	chr1:211752571-211752621	AG04449	skin:	fetal
26	chr1:211753152-211753202	AG10803	skin:	n/a
27	chr1:211752895-211752945	HCF	heart:	n/a
28	chr1:211753582-211753632	HRE	kidney:	n/a
29	chr1:211751793-211751843	K562	blood:	n/a
30	chr1:211751907-211751957	NH-A	brain:	n/a
31	chr1:211752895-211752945	HCM	heart:	n/a
32	chr1:211751907-211751957	Hela-S3	cervix:	n/a
33	chr1:211753582-211753632	HAEpiC	amniotic membrane:	n/a
34	chr1:211752895-211752945	SAEC	small airway:	n/a
35	chr1:211752571-211752621	HRE	kidney:	n/a
36	chr1:211753152-211753202	A549	lung:	n/a
37	chr1:211752571-211752621	ovcar-3	ovarian:	n/a
38	chr1:211752895-211752945	AG04449	skin:	fetal
39	chr1:211752620-211752670	NH-A	brain:	n/a
40	chr1:211752895-211752945	BE2_C	brain:	n/a
41	chr1:211751907-211751957	HRCEpiC	kidney:	n/a
42	chr1:211752511-211752561	AG09309	skin:	n/a
43	chr1:211753152-211753202	AG09319	gingival:	n/a
44	chr1:211752895-211752945	HRE	kidney:	n/a
45	chr1:211753152-211753202	IMR90	lung:	fetal
46	chr1:211753582-211753632	SK-N-SH	brain:	n/a
47	chr1:211751793-211751843	BJ	skin:	n/a
48	chr1:211753582-211753632	PFSK-1	brain:	n/a
49	chr1:211752620-211752670	Hela-S3	cervix:	n/a
50	chr1:211753582-211753632	HRPEpiC	eye:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:211749200..211754595-chr1:211816014..211824648,8	K562	blood:
2	chr1:211750915..211755112-chr1:211826013..211829699,5	K562	blood:
3	chr1:211750437..211753125-chr1:211823737..211827672,4	MCF-7	breast:
4	chr1:211751624..211752576-chr2:27435164..27436057,2	Hela-S3	cervix:
5	chr1:211752607..211754839-chr1:211771160..211773503,2	K562	blood:
6	chr1:211750433..211752019-chr1:211835257..211837969,2	K562	blood:
7	chr1:211750060..211753695-chr1:211824093..211827463,4	MCF-7	breast:
8	chr1:211752517..211753385-chr13:114145050..114145629,2	Hela-S3	cervix:
9	chr1:211498857..211501622-chr1:211752568..211754249,2	K562	blood:
10	chr1:211750794..211754252-chr1:211815868..211819773,4	MCF-7	breast:
11	chr1:211752671..211753306-chrX:123093276..123093877,2	Hela-S3	cervix:
12	chr1:211752607..211756285-chr1:211771490..211773503,3	K562	blood:
13	chr1:211429991..211432106-chr1:211750411..211752434,2	MCF-7	breast:
14	chr1:211751146..211751864-chr1:211798100..211799087,3	K562	blood:
15	chr1:211752053..211752664-chr2:98262083..98262626,2	HCT-116	colon:
16	chr1:211751822..211752607-chr7:35734035..35734698,2	Hela-S3	cervix:
17	chr1:211751583..211753296-chr1:211847712..211850652,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC30A1	TF binding region
SLC30A1	CpG island
ENSG00000117625	chromatin interactions
ENSG00000150401	chromatin interactions
ENSG00000228792	chromatin interactions
ENSG00000138074	chromatin interactions
ENSG00000231057	chromatin interactions
ENSG00000122557	chromatin interactions
ENSG00000135940	chromatin interactions
ENSG00000150403	chromatin interactions
ENSG00000138085	chromatin interactions
ENSG00000222080	chromatin interactions
ENSG00000117650	chromatin interactions
ENSG00000082512	chromatin interactions

Extended variants
information (count: 82 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376879993	chr1:211751832-211751833	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs577421431	chr1:211751850-211751851	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs143632069	chr1:211751908-211751909	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs115358595	chr1:211751925-211751926	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs113173086	chr1:211751974-211751975	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs575459232	chr1:211751984-211751985	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs201014656	chr1:211751987-211751988	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs562091419	chr1:211752147-211752148	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs11810058	chr1:211752148-211752149	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs547951877	chr1:211752193-211752194	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs559838003	chr1:211752214-211752215	Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs371444935	chr1:211752318-211752319	Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs533384187	chr1:211752348-211752349	Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs376041310	chr1:211752433-211752434	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs551918206	chr1:211752484-211752485	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs369681844	chr1:211752496-211752497	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs570135591	chr1:211752505-211752506	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs374111013	chr1:211752509-211752510	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs537778488	chr1:211752511-211752512	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs138036346	chr1:211752597-211752598	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs185927554	chr1:211752640-211752641	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs367918566	chr1:211752645-211752646	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs534276130	chr1:211752693-211752694	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs566384091	chr1:211752710-211752711	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs552656972	chr1:211752761-211752762	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs577293403	chr1:211752846-211752847	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs3041304	chr1:211752883-211752884	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs33941932	chr1:211752884-211752885	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs3041307	chr1:211752925-211752926	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs112120082	chr1:211752926-211752927	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs201380113	chr1:211752927-211752928	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs2358242	chr1:211752934-211752935	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs538472900	chr1:211752957-211752958	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs377760761	chr1:211753064-211753065	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs191416276	chr1:211753152-211753153	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs557156068	chr1:211753160-211753161	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs575325915	chr1:211753164-211753165	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs542955072	chr1:211753169-211753170	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs376614947	chr1:211753196-211753197	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs369912354	chr1:211753197-211753198	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs574091814	chr1:211753273-211753274	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs541408174	chr1:211753291-211753292	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs184065176	chr1:211753301-211753302	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs559901511	chr1:211753335-211753336	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs373778980	chr1:211753338-211753339	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs533500761	chr1:211753345-211753346	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs545149322	chr1:211753352-211753353	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs149499166	chr1:211753373-211753374	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs78531863	chr1:211753424-211753425	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs7543376	chr1:211753489-211753490	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211748600-211753200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:211749000-211753400	Active TSS	Aorta	Aorta
3	chr1:211749000-211753400	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr1:211749400-211753200	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr1:211749400-211753200	Active TSS	Fetal Stomach	stomach
6	chr1:211749400-211753200	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr1:211749400-211753400	Active TSS	Duodenum Smooth Muscle	Duodenum
8	chr1:211749600-211753000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr1:211749600-211753000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:211749600-211753000	Active TSS	GM12878-XiMat	blood
11	chr1:211749600-211753000	Active TSS	HMEC	breast
12	chr1:211749600-211753000	Active TSS	HSMMtube	muscle
13	chr1:211749600-211753000	Active TSS	NH-A	brain
14	chr1:211749600-211753000	Active TSS	NHLF	lung
15	chr1:211749600-211753200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:211749600-211753200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:211749600-211753200	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr1:211749600-211753200	Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr1:211749600-211753200	Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr1:211749600-211753200	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr1:211749600-211753200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:211749600-211753200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:211749600-211753200	Active TSS	Duodenum Mucosa	Duodenum
24	chr1:211749600-211753200	Active TSS	Fetal Intestine Large	intestine
25	chr1:211749600-211753200	Active TSS	Fetal Kidney	kidney
26	chr1:211749600-211753200	Active TSS	Rectal Smooth Muscle	rectum
27	chr1:211749600-211753200	Active TSS	A549	lung
28	chr1:211749600-211753200	Active TSS	Hela-S3	cervix
29	chr1:211749600-211753200	Active TSS	K562	blood
30	chr1:211749600-211753200	Active TSS	NHDF-Ad	bronchial
31	chr1:211749600-211753800	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr1:211749800-211752000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:211749800-211753000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:211749800-211753000	Active TSS	Fetal Muscle Leg	muscle
35	chr1:211749800-211753200	Active TSS	NHEK	skin
36	chr1:211749800-211753400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr1:211749800-211753400	Active TSS	Fetal Muscle Trunk	muscle
38	chr1:211750000-211752600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr1:211750000-211753000	Active TSS	Muscle Satellite Cultured Cells	--
40	chr1:211750000-211753000	Active TSS	Rectal Mucosa Donor 31	rectum
41	chr1:211750000-211753000	Active TSS	Osteobl	bone
42	chr1:211750000-211753200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:211750000-211753200	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr1:211750000-211753200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:211750000-211753200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr1:211750000-211753200	Active TSS	Liver	Liver
47	chr1:211750000-211753200	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr1:211750000-211753200	Active TSS	Colon Smooth Muscle	Colon
49	chr1:211750000-211753200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr1:211750000-211753200	Active TSS	HSMM	muscle

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