Variant report

Variant	esv1836726
Chromosome Location	chr1:211736470-211752981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1337)
CpG islands
(count:673)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1337 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:211751183-211751451	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:211748069-211748373	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:211751176-211751327	K562	blood:	n/a	n/a
4	ARID3A	chr1:211752854-211753252	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:211740042-211740230	HepG2	liver:	n/a	n/a
6	ATF1	chr1:211752422-211753356	K562	blood:	n/a	n/a
7	ATF2	chr1:211752231-211752766	GM12878	blood:	n/a	n/a
8	ATF2	chr1:211752810-211753285	GM12878	blood:	n/a	n/a
9	ATF2	chr1:211739700-211740211	GM12878	blood:	n/a	n/a
10	ATF2	chr1:211751006-211751542	GM12878	blood:	n/a	n/a
11	ATF3	chr1:211750701-211751745	A549	lung:	n/a	chr1:211751215-211751224
12	ATF3	chr1:211752145-211752722	A549	lung:	n/a	chr1:211752642-211752652 chr1:211752711-211752720
13	ATF3	chr1:211751091-211751348	K562	blood:	n/a	chr1:211751215-211751224
14	ATF3	chr1:211752831-211753225	K562	blood:	n/a	n/a
15	BACH1	chr1:211739722-211739898	K562	blood:	n/a	n/a
16	BACH1	chr1:211752827-211753014	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:211751332-211751657	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:211752419-211752460	K562	blood:	n/a	n/a
19	BATF	chr1:211751153-211751360	GM12878	blood:	n/a	n/a
20	BATF	chr1:211739673-211740188	GM12878	blood:	n/a	n/a
21	BATF	chr1:211739709-211740124	GM12878	blood:	n/a	n/a
22	BATF	chr1:211740975-211741301	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:211739675-211740136	GM12878	blood:	n/a	n/a
24	BCL3	chr1:211739797-211740117	GM12878	blood:	n/a	n/a
25	BCLAF1	chr1:211751020-211751546	GM12878	blood:	n/a	chr1:211751211-211751220
26	BCLAF1	chr1:211739673-211740287	GM12878	blood:	n/a	n/a
27	BCLAF1	chr1:211752744-211753311	GM12878	blood:	n/a	chr1:211752906-211752919 chr1:211753003-211753016 chr1:211753008-211753017
28	BCLAF1	chr1:211752191-211752685	GM12878	blood:	n/a	chr1:211752298-211752311 chr1:211752248-211752257 chr1:211752455-211752468
29	BCLAF1	chr1:211751059-211751498	GM12878	blood:	n/a	chr1:211751211-211751220
30	BHLHE40	chr1:211739809-211740116	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:211752489-211752588	A549	lung:	n/a	n/a
32	BHLHE40	chr1:211751039-211753381	GM12878	blood:	n/a	chr1:211751231-211751247 chr1:211751960-211751976 chr1:211752458-211752474 chr1:211751957-211751973 chr1:211751172-211751188
33	BHLHE40	chr1:211752320-211753462	HepG2	liver:	n/a	chr1:211752458-211752474
34	BHLHE40	chr1:211750870-211753535	K562	blood:	n/a	chr1:211751231-211751247 chr1:211751960-211751976 chr1:211752458-211752474 chr1:211751957-211751973 chr1:211751172-211751188
35	BHLHE40	chr1:211746139-211746212	GM12878	blood:	n/a	n/a
36	BRCA1	chr1:211752911-211753098	HepG2	liver:	n/a	n/a
37	BRCA1	chr1:211750530-211751763	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr1:211751314-211751496	HepG2	liver:	n/a	n/a
39	BRCA1	chr1:211752430-211752734	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr1:211752100-211752732	K562	blood:	n/a	n/a
41	CBX3	chr1:211752888-211753516	K562	blood:	n/a	n/a
42	CBX3	chr1:211750976-211752035	K562	blood:	n/a	n/a
43	CCNT2	chr1:211750901-211753387	K562	blood:	n/a	chr1:211752711-211752720 chr1:211753013-211753022 chr1:211752738-211752747 chr1:211752838-211752847
44	CEBPB	chr1:211751206-211751450	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr1:211740157-211740209	K562	blood:	n/a	chr1:211740166-211740179
46	CEBPB	chr1:211752309-211752706	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr1:211746856-211747208	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr1:211751555-211751797	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:211748057-211748418	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr1:211746937-211747149	A549	lung:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:211751793-211751843	PFSK-1	brain:	n/a
2	chr1:211752571-211752621	SK-N-MC	brain:	n/a
3	chr1:211751793-211751843	PFSK-1	brain:	n/a
4	chr1:211752571-211752621	SK-N-MC	brain:	n/a
5	chr1:211752620-211752670	CMK	blood:	n/a
6	chr1:211750967-211751017	HRE	kidney:	n/a
7	chr1:211751122-211751172	SK-N-MC	brain:	n/a
8	chr1:211751907-211751957	HCF	heart:	n/a
9	chr1:211752511-211752561	LNCaP	prostate:	n/a
10	chr1:211749023-211749073	ovcar-3	ovarian:	n/a
11	chr1:211750839-211750889	HAEpiC	amniotic membrane:	n/a
12	chr1:211752620-211752670	HCF	heart:	n/a
13	chr1:211750967-211751017	NB4	blood:	n/a
14	chr1:211752620-211752670	Caco-2	colon:	n/a
15	chr1:211750967-211751017	LNCaP	prostate:	n/a
16	chr1:211750967-211751017	ECC-1	luminal epithelium:	n/a
17	chr1:211750967-211751017	HCT-116	colon:	n/a
18	chr1:211752895-211752945	HepG2	liver:	n/a
19	chr1:211751127-211751177	HCT-116	colon:	n/a
20	chr1:211752511-211752561	GM12891	blood:	n/a
21	chr1:211750839-211750889	ProgFib	skin:	n/a
22	chr1:211751122-211751172	HepG2	liver:	n/a
23	chr1:211751122-211751172	HAEpiC	amniotic membrane:	n/a
24	chr1:211752511-211752561	BE2_C	brain:	n/a
25	chr1:211749023-211749073	CMK	blood:	n/a
26	chr1:211751122-211751172	MCF-7	breast:	n/a
27	chr1:211749023-211749073	BJ	skin:	n/a
28	chr1:211750967-211751017	SKMC	muscle:	n/a
29	chr1:211751122-211751172	GM12878	blood:	n/a
30	chr1:211750839-211750889	Hepatocyte	liver:	n/a
31	chr1:211752511-211752561	GM19239	blood:	n/a
32	chr1:211751127-211751177	GM06990	blood:	n/a
33	chr1:211750839-211750889	CMK	blood:	n/a
34	chr1:211749023-211749073	K562	blood:	n/a
35	chr1:211750839-211750889	HIPEpiC	eye:	n/a
36	chr1:211750839-211750889	AG09309	skin:	n/a
37	chr1:211752511-211752561	AoSMC	blood vessel:	n/a
38	chr1:211750839-211750889	GM12892	blood:	n/a
39	chr1:211750839-211750889	HEEpiC	esophagus:	n/a
40	chr1:211751127-211751177	HUVEC	blood vessel:	n/a
41	chr1:211752571-211752621	PrEC	prostate:	n/a
42	chr1:211751793-211751843	HNPCEpiC	eye:	n/a
43	chr1:211752895-211752945	GM12891	blood:	n/a
44	chr1:211752620-211752670	HEEpiC	esophagus:	n/a
45	chr1:211750967-211751017	SAEC	small airway:	n/a
46	chr1:211749023-211749073	AoSMC	blood vessel:	n/a
47	chr1:211752511-211752561	HCF	heart:	n/a
48	chr1:211749023-211749073	NT2-D1	testis:	n/a
49	chr1:211750967-211751017	AoSMC	blood vessel:	n/a
50	chr1:211752511-211752561	HCM	heart:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:211751583..211753296-chr1:211847712..211850652,2	MCF-7	breast:
2	chr1:211750781..211751639-chr1:211798078..211798633,2	MCF-7	breast:
3	chr1:211751624..211752576-chr2:27435164..27436057,2	Hela-S3	cervix:
4	chr1:211750437..211753125-chr1:211823737..211827672,4	MCF-7	breast:
5	chr1:211715064..211716989-chr1:211735008..211737498,2	MCF-7	breast:
6	chr1:211752607..211756285-chr1:211771490..211773503,3	K562	blood:
7	chr1:211735884..211738489-chr1:211748516..211752343,3	MCF-7	breast:
8	chr1:211736674..211739531-chr1:211847084..211848830,2	K562	blood:
9	chr1:211694132..211696485-chr1:211743577..211746464,2	MCF-7	breast:
10	chr1:211697121..211699374-chr1:211746833..211748555,2	K562	blood:
11	chr1:211735413..211738313-chr1:211738485..211740150,2	MCF-7	breast:
12	chr1:211751146..211751864-chr1:211798100..211799087,3	K562	blood:
13	chr1:211752607..211754839-chr1:211771160..211773503,2	K562	blood:
14	chr1:211431710..211433363-chr1:211744568..211747446,2	K562	blood:
15	chr1:211750915..211755112-chr1:211826013..211829699,5	K562	blood:
16	chr1:211750433..211752019-chr1:211835257..211837969,2	K562	blood:
17	chr1:211741510..211743942-chr1:211802313..211805190,2	K562	blood:
18	chr1:211498857..211501622-chr1:211752568..211754249,2	K562	blood:
19	chr1:211743190..211745097-chr1:211827808..211829565,2	MCF-7	breast:
20	chr1:211746810..211749692-chr1:211783974..211785917,2	MCF-7	breast:
21	chr1:211750794..211754252-chr1:211815868..211819773,4	MCF-7	breast:
22	chr1:211429991..211432106-chr1:211750411..211752434,2	MCF-7	breast:
23	chr1:211721060..211723722-chr1:211744392..211746338,2	K562	blood:
24	chr1:211752671..211753306-chrX:123093276..123093877,2	Hela-S3	cervix:
25	chr1:211698404..211701104-chr1:211743081..211745100,2	MCF-7	breast:
26	chr1:211735413..211738313-chr1:211738485..211740150,2	MCF-7	breast:
27	chr1:211715152..211718143-chr1:211748506..211750792,2	K562	blood:
28	chr1:211747427..211749600-chr1:211810215..211812897,2	K562	blood:
29	chr1:211750816..211751334-chr1:211828394..211828945,2	MCF-7	breast:
30	chr1:211752517..211753385-chr13:114145050..114145629,2	Hela-S3	cervix:
31	chr1:211729557..211732599-chr1:211743450..211747456,3	K562	blood:
32	chr1:211733190..211735497-chr1:211740773..211743674,2	K562	blood:
33	chr1:211686187..211688121-chr1:211747912..211750697,2	K562	blood:
34	chr1:211745327..211748451-chr1:211846943..211849410,3	K562	blood:
35	chr1:211710767..211712862-chr1:211741822..211743757,2	MCF-7	breast:
36	chr1:211738614..211743299-chr1:211744203..211747378,6	K562	blood:
37	chr1:211742646..211744909-chr1:211759048..211760986,2	K562	blood:
38	chr1:211738614..211743299-chr1:211744203..211747378,6	K562	blood:
39	chr1:211751822..211752607-chr7:35734035..35734698,2	Hela-S3	cervix:
40	chr1:211749200..211754595-chr1:211816014..211824648,8	K562	blood:
41	chr1:211750683..211751727-chr1:211803429..211804168,3	K562	blood:
42	chr1:211692734..211695713-chr1:211744143..211747035,2	MCF-7	breast:
43	chr1:211431188..211433363-chr1:211744568..211747070,2	K562	blood:
44	chr1:211750060..211753695-chr1:211824093..211827463,4	MCF-7	breast:
45	chr1:211752053..211752664-chr2:98262083..98262626,2	HCT-116	colon:
46	chr1:211750650..211751428-chr1:211803176..211803710,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLC30A1	hsa-miR-193b-3p	chr1:211748500-211748521

Variant related genes	Relation type
SLC30A1	TF binding region
SLC30A1	CpG island
ENSG00000138074	chromatin interactions
ENSG00000231057	chromatin interactions
ENSG00000150401	chromatin interactions
ENSG00000228792	chromatin interactions
ENSG00000222080	chromatin interactions
ENSG00000135940	chromatin interactions
ENSG00000170385	chromatin interactions
ENSG00000082512	chromatin interactions
ENSG00000138085	chromatin interactions
ENSG00000150403	chromatin interactions
ENSG00000122557	chromatin interactions
ENSG00000117625	chromatin interactions
ENSG00000117650	chromatin interactions

Extended variants
information (count: 574 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:574 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7530862	chr1:211736470-211736471	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182142622	chr1:211736471-211736472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs17639435	chr1:211736538-211736539	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs148826653	chr1:211736554-211736555	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551568042	chr1:211736556-211736557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563176581	chr1:211736615-211736616	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530596821	chr1:211736663-211736664	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548911811	chr1:211736731-211736732	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142506199	chr1:211736733-211736734	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs532713447	chr1:211736739-211736740	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73075127	chr1:211736759-211736760	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs553821039	chr1:211736784-211736785	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs374267051	chr1:211736789-211736790	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs191140390	chr1:211736826-211736827	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs566184884	chr1:211736829-211736830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572078483	chr1:211736921-211736922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539584746	chr1:211736924-211736925	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545768797	chr1:211736928-211736929	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs558264202	chr1:211736949-211736950	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12091351	chr1:211737006-211737007	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs372821392	chr1:211737012-211737013	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs556104607	chr1:211737013-211737014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs57771290	chr1:211737038-211737039	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs541043805	chr1:211737047-211737048	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374596071	chr1:211737053-211737054	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559053047	chr1:211737064-211737065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577549524	chr1:211737076-211737077	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544731046	chr1:211737098-211737099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563041051	chr1:211737101-211737102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530658561	chr1:211737112-211737113	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548724553	chr1:211737113-211737114	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs561237225	chr1:211737114-211737115	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528344473	chr1:211737208-211737209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs377531359	chr1:211737222-211737223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561448604	chr1:211737234-211737235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369125668	chr1:211737235-211737236	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559590643	chr1:211737252-211737253	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181832322	chr1:211737280-211737281	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs150969970	chr1:211737322-211737323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs367767723	chr1:211737372-211737373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs551947979	chr1:211737376-211737377	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs570126429	chr1:211737387-211737388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs140768597	chr1:211737412-211737413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs116610286	chr1:211737418-211737419	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568148910	chr1:211737421-211737422	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567966513	chr1:211737543-211737544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371328430	chr1:211737638-211737639	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs9430071	chr1:211737647-211737648	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs577612351	chr1:211737715-211737716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs144639373	chr1:211737719-211737720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	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:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211733200-211738400	Weak transcription	HepG2	liver
2	chr1:211733400-211739800	Weak transcription	Hela-S3	cervix
3	chr1:211733800-211737800	Weak transcription	Fetal Intestine Small	intestine
4	chr1:211733800-211744800	Weak transcription	Fetal Intestine Large	intestine
5	chr1:211734400-211748000	Weak transcription	Placenta	Placenta
6	chr1:211736600-211736800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:211737800-211738800	Enhancers	Fetal Intestine Small	intestine
8	chr1:211738400-211738800	Enhancers	HepG2	liver
9	chr1:211738600-211738800	Active TSS	Stomach Smooth Muscle	stomach
10	chr1:211738800-211743800	Weak transcription	Fetal Intestine Small	intestine
11	chr1:211738800-211746000	Weak transcription	HepG2	liver
12	chr1:211738800-211748200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr1:211739400-211739600	Enhancers	GM12878-XiMat	blood
14	chr1:211739600-211740200	Flanking Active TSS	GM12878-XiMat	blood
15	chr1:211739800-211740200	Enhancers	Hela-S3	cervix
16	chr1:211739800-211740400	Enhancers	Liver	Liver
17	chr1:211740200-211741800	Enhancers	GM12878-XiMat	blood
18	chr1:211740200-211745800	Weak transcription	Hela-S3	cervix
19	chr1:211740400-211745400	Weak transcription	Liver	Liver
20	chr1:211741200-211741400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr1:211741200-211741400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr1:211741200-211741600	Enhancers	K562	blood
23	chr1:211741400-211744800	Weak transcription	Duodenum Mucosa	Duodenum
24	chr1:211741400-211745200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:211741400-211747400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr1:211741400-211747400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr1:211741600-211744800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:211741600-211747400	Weak transcription	K562	blood
29	chr1:211741800-211743800	Weak transcription	GM12878-XiMat	blood
30	chr1:211741800-211746600	Weak transcription	NH-A	brain
31	chr1:211742200-211745400	Weak transcription	Osteobl	bone
32	chr1:211742200-211747000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr1:211742200-211748800	Weak transcription	HSMMtube	muscle
34	chr1:211742400-211745800	Weak transcription	HSMM	muscle
35	chr1:211742400-211748600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr1:211742600-211746000	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr1:211742800-211744600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:211742800-211744600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:211742800-211745000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr1:211742800-211745400	Weak transcription	NHDF-Ad	bronchial
41	chr1:211743000-211744800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:211743000-211744800	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr1:211743000-211747200	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr1:211743200-211744800	Weak transcription	A549	lung
45	chr1:211743200-211745000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr1:211743200-211745000	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr1:211743200-211748400	Weak transcription	Fetal Lung	lung
48	chr1:211743400-211745000	Weak transcription	HMEC	breast
49	chr1:211743400-211745200	Weak transcription	Colonic Mucosa	Colon
50	chr1:211743400-211746000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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