Variant report

Variant	esv3341980
Chromosome Location	chr1:45097165-45099063
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:305)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:45097471-45097705	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:45097236-45097496	K562	blood:	n/a	n/a
3	ATF3	chr1:45097428-45097829	GM12878	blood:	n/a	chr1:45097629-45097638 chr1:45097618-45097638
4	ATF3	chr1:45097465-45097884	K562	blood:	n/a	chr1:45097629-45097638 chr1:45097618-45097638
5	ATF3	chr1:45097482-45097896	HepG2	liver:	n/a	chr1:45097629-45097638 chr1:45097618-45097638
6	BACH1	chr1:45097271-45097638	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr1:45097352-45098014	K562	blood:	n/a	chr1:45097582-45097591 chr1:45097428-45097441
8	BCLAF1	chr1:45097250-45097990	GM12878	blood:	n/a	chr1:45097582-45097591 chr1:45097428-45097441
9	BHLHE40	chr1:45097173-45098067	GM12878	blood:	n/a	chr1:45097629-45097638 chr1:45097629-45097638
10	BHLHE40	chr1:45097441-45097818	A549	lung:	n/a	chr1:45097629-45097638 chr1:45097629-45097638
11	BHLHE40	chr1:45096913-45098690	K562	blood:	n/a	chr1:45097629-45097638 chr1:45097629-45097638
12	BHLHE40	chr1:45097185-45098093	HepG2	liver:	n/a	chr1:45097629-45097638 chr1:45097629-45097638
13	BRCA1	chr1:45097849-45097996	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr1:45097338-45097731	HepG2	liver:	n/a	n/a
15	BRCA1	chr1:45097771-45097840	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr1:45097166-45097462	GM12878	blood:	n/a	n/a
17	CBX3	chr1:45096976-45097668	K562	blood:	n/a	n/a
18	CBX3	chr1:45097885-45098793	K562	blood:	n/a	n/a
19	CBX3	chr1:45096665-45097743	K562	blood:	n/a	n/a
20	CCNT2	chr1:45098232-45098560	K562	blood:	n/a	n/a
21	CCNT2	chr1:45097147-45098030	K562	blood:	n/a	n/a
22	CEBPB	chr1:45097705-45097717	Hela-S3	cervix:	n/a	n/a
23	CEBPD	chr1:45097381-45097928	HepG2	liver:	n/a	n/a
24	CEBPD	chr1:45096946-45097761	K562	blood:	n/a	n/a
25	CHD1	chr1:45097499-45098011	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr1:45097221-45098095	GM12878	blood:	n/a	chr1:45097389-45097399
27	CHD2	chr1:45097223-45098045	GM12878	blood:	n/a	chr1:45097389-45097399
28	CHD2	chr1:45097349-45097630	HepG2	liver:	n/a	chr1:45097389-45097399
29	CHD2	chr1:45097354-45098150	Hela-S3	cervix:	n/a	chr1:45097389-45097399
30	CHD2	chr1:45097087-45097906	K562	blood:	n/a	chr1:45097389-45097399
31	CHD2	chr1:45098389-45098663	K562	blood:	n/a	n/a
32	CHD2	chr1:45097241-45097774	H1-hESC	embryonic stem cell:	n/a	chr1:45097389-45097399
33	CREB1	chr1:45097244-45098252	GM12878	blood:	n/a	n/a
34	CREB1	chr1:45097461-45097756	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr1:45097363-45098038	A549	lung:	n/a	n/a
36	CREB1	chr1:45097025-45098290	HepG2	liver:	n/a	n/a
37	CTCF	chr1:45097220-45097370	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr1:45097300-45097450	HBMEC	blood vessel:	n/a	chr1:45097384-45097397
39	CTCF	chr1:45097372-45097550	K562	blood:	n/a	chr1:45097384-45097397
40	CTCF	chr1:45097220-45097370	GM12867	blood:	n/a	n/a
41	CTCF	chr1:45097719-45097769	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr1:45097380-45097530	HUVEC	blood vessel:	n/a	chr1:45097384-45097397
43	CUX1	chr1:45098460-45098659	K562	blood:	n/a	n/a
44	E2F4	chr1:45097276-45097677	MCF10A-Er-Src	breast:	n/a	chr1:45097578-45097588
45	E2F4	chr1:45097116-45098099	K562	blood:	n/a	chr1:45097578-45097588
46	E2F6	chr1:45097137-45098231	K562	blood:	n/a	chr1:45097578-45097588
47	E2F6	chr1:45097176-45097726	A549	lung:	n/a	chr1:45097578-45097588
48	E2F6	chr1:45097557-45097847	K562	blood:	n/a	chr1:45097578-45097588
49	E2F6	chr1:45096999-45098702	K562	blood:	n/a	chr1:45098651-45098660 chr1:45098246-45098257 chr1:45097578-45097588 chr1:45098246-45098257
50	EBF1	chr1:45098424-45098481	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:45098125-45098175	HRCEpiC	kidney:	n/a
2	chr1:45097499-45097549	LNCaP	prostate:	n/a
3	chr1:45097282-45097332	GM12891	blood:	n/a
4	chr1:45097931-45097981	HL-60	blood:	n/a
5	chr1:45097282-45097332	H1-hESC	embryonic stem cell:	embryo
6	chr1:45098125-45098175	MCF-7	breast:	n/a
7	chr1:45098125-45098175	U87	brain:	n/a
8	chr1:45097499-45097549	NB4	blood:	n/a
9	chr1:45097931-45097981	Jurkat	blood:	n/a
10	chr1:45097962-45098012	AoSMC	blood vessel:	n/a
11	chr1:45098125-45098175	AoSMC	blood vessel:	n/a
12	chr1:45098125-45098175	SKMC	muscle:	n/a
13	chr1:45097931-45097981	A549	lung:	n/a
14	chr1:45097282-45097332	HCF	heart:	n/a
15	chr1:45098125-45098175	NB4	blood:	n/a
16	chr1:45097962-45098012	Hepatocyte	liver:	n/a
17	chr1:45097962-45098012	HUVEC	blood vessel:	n/a
18	chr1:45098125-45098175	NHDF-neo	bronchial:	n/a
19	chr1:45097282-45097332	NT2-D1	testis:	n/a
20	chr1:45097962-45098012	SAEC	small airway:	n/a
21	chr1:45097282-45097332	AG09319	gingival:	n/a
22	chr1:45097962-45098012	Hela-S3	cervix:	n/a
23	chr1:45097499-45097549	HAEpiC	amniotic membrane:	n/a
24	chr1:45098125-45098175	H1-hESC	embryonic stem cell:	embryo
25	chr1:45097282-45097332	SK-N-MC	brain:	n/a
26	chr1:45097282-45097332	HEK293	kidney:	embryo
27	chr1:45097282-45097332	AG04450	lung:	fetal
28	chr1:45097931-45097981	HEK293	kidney:	embryo
29	chr1:45097499-45097549	PANC-1	pancreas:	n/a
30	chr1:45097931-45097981	HAEpiC	amniotic membrane:	n/a
31	chr1:45097282-45097332	MCF10A-Er-Src	breast:	n/a
32	chr1:45097931-45097981	NHBE	bronchial:	n/a
33	chr1:45097499-45097549	U87	brain:	n/a
34	chr1:45097931-45097981	AG04450	lung:	fetal
35	chr1:45097282-45097332	NH-A	brain:	n/a
36	chr1:45097282-45097332	PFSK-1	brain:	n/a
37	chr1:45097282-45097332	HEEpiC	esophagus:	n/a
38	chr1:45097962-45098012	HMEC	breast:	n/a
39	chr1:45098125-45098175	HIPEpiC	eye:	n/a
40	chr1:45097282-45097332	GM19239	blood:	n/a
41	chr1:45097962-45098012	PFSK-1	brain:	n/a
42	chr1:45098125-45098175	GM12891	blood:	n/a
43	chr1:45097931-45097981	K562	blood:	n/a
44	chr1:45098125-45098175	GM06990	blood:	n/a
45	chr1:45097931-45097981	Caco-2	colon:	n/a
46	chr1:45097931-45097981	HRE	kidney:	n/a
47	chr1:45097962-45098012	AG09309	skin:	n/a
48	chr1:45097499-45097549	SK-N-SH_RA	brain:	n/a
49	chr1:45098125-45098175	HL-60	blood:	n/a
50	chr1:45097499-45097549	MCF10A-Er-Src	breast:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45097084..45097952-chr10:103578351..103578852,2	Hela-S3	cervix:
2	chr1:44440424..44442164-chr1:45096404..45098062,2	K562	blood:
3	chr1:44459804..44461997-chr1:45097523..45099408,2	MCF-7	breast:
4	chr1:44818922..44822604-chr1:45096121..45099112,6	K562	blood:
5	chr1:45096122..45099489-chr1:45284877..45287072,3	K562	blood:
6	chr1:45097570..45100220-chr1:45105727..45109004,3	MCF-7	breast:
7	chr1:45096334..45100885-chr1:45195106..45197628,6	K562	blood:
8	chr1:45097493..45098414-chr6:43543365..43544009,2	HCT-116	colon:
9	chr1:45096184..45099066-chr1:45264568..45266380,3	K562	blood:
10	chr1:44676967..44680043-chr1:45097059..45099100,3	K562	blood:
11	chr1:45097355..45098136-chr19:3572542..3573373,2	Hela-S3	cervix:
12	chr1:45089432..45094163-chr1:45095736..45099125,6	MCF-7	breast:
13	chr1:45097189..45098175-chr2:101618808..101619704,2	HCT-116	colon:
14	chr1:45095169..45100377-chr1:45133934..45142864,15	K562	blood:
15	chr1:45096767..45097715-chr13:52585858..52586559,2	NB4	blood:
16	chr1:45096334..45099417-chr1:45195073..45197438,5	K562	blood:
17	chr1:45097288..45098193-chr12:49110421..49111318,2	HCT-116	colon:
18	chr1:44677773..44680547-chr1:45095385..45099072,4	K562	blood:
19	chr1:45097395..45098344-chr11:8703634..8704499,2	NB4	blood:
20	chr1:44444668..44446709-chr1:45098219..45100033,2	K562	blood:
21	chr1:45096002..45100159-chr1:45110119..45116077,6	MCF-7	breast:
22	chr1:44482218..44484038-chr1:45097268..45099139,2	K562	blood:
23	chr1:45077147..45081258-chr1:45096476..45100107,4	MCF-7	breast:
24	chr1:45097094..45097610-chr3:152879896..152880538,2	Hela-S3	cervix:
25	chr1:45095364..45099259-chr1:45185766..45189852,13	K562	blood:
26	chr1:45086647..45106769-chr1:45179099..45192041,56	K562	blood:
27	chr1:45051849..45053627-chr1:45094986..45097347,2	K562	blood:

No data

Variant related genes	Relation type
RNF220	TF binding region
RNF220	CpG island
ENSG00000178028	chromatin interactions
ENSG00000198520	chromatin interactions
ENSG00000124571	chromatin interactions
ENSG00000159214	chromatin interactions
ENSG00000173846	chromatin interactions
ENSG00000226009	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000129315	chromatin interactions
ENSG00000064961	chromatin interactions
ENSG00000126106	chromatin interactions
ENSG00000117410	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000196517	chromatin interactions
ENSG00000181467	chromatin interactions
ENSG00000187147	chromatin interactions
ENSG00000117411	chromatin interactions
ENSG00000253710	chromatin interactions
ENSG00000117419	chromatin interactions
ENSG00000071082	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000198408	chromatin interactions
ENSG00000170734	chromatin interactions
ENSG00000166441	chromatin interactions

Extended variants
information (count: 75 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:75 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61598786	chr1:45097280-45097281	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
2	rs74554154	chr1:45097317-45097318	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
3	rs533368247	chr1:45097319-45097320	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
4	rs373614925	chr1:45097388-45097389	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
5	rs181687097	chr1:45097392-45097393	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
6	rs113103937	chr1:45097399-45097400	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
7	rs535541271	chr1:45097452-45097453	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
8	rs115545367	chr1:45097513-45097514	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
9	rs568700514	chr1:45097540-45097541	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
10	rs537606753	chr1:45097565-45097566	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
11	rs558034968	chr1:45097566-45097567	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
12	rs114477934	chr1:45097584-45097585	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
13	rs115027833	chr1:45097589-45097590	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
14	rs553471970	chr1:45097592-45097593	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
15	rs573808716	chr1:45097617-45097618	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
16	rs115428399	chr1:45097639-45097640	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
17	rs562311035	chr1:45097681-45097682	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
18	rs575920485	chr1:45097733-45097734	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
19	rs544435179	chr1:45097777-45097778	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
20	rs454469	chr1:45097778-45097779	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
21	rs564824801	chr1:45097786-45097787	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
22	rs533428108	chr1:45097851-45097852	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
23	rs111993242	chr1:45097931-45097932	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
24	rs374630875	chr1:45097936-45097937	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
25	rs190080079	chr1:45097985-45097986	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
26	rs374860495	chr1:45097987-45097988	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
27	rs199845330	chr1:45097991-45097992	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
28	rs370364812	chr1:45097994-45097995	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
29	rs113387399	chr1:45098012-45098013	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
30	rs112178669	chr1:45098014-45098015	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
31	rs199738126	chr1:45098016-45098017	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
32	rs370355938	chr1:45098034-45098035	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
33	rs373810509	chr1:45098053-45098054	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
34	rs375363320	chr1:45098070-45098071	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
35	rs369357360	chr1:45098074-45098075	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
36	rs371084669	chr1:45098147-45098148	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
37	rs538065128	chr1:45098155-45098156	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
38	rs551251436	chr1:45098156-45098157	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
39	rs571551415	chr1:45098158-45098159	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
40	rs533822471	chr1:45098160-45098161	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
41	rs553850464	chr1:45098183-45098184	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
42	rs116379330	chr1:45098229-45098230	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
43	rs536215630	chr1:45098277-45098278	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
44	rs112971499	chr1:45098294-45098295	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
45	rs369660764	chr1:45098295-45098296	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
46	rs556298047	chr1:45098296-45098297	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
47	rs200806733	chr1:45098297-45098298	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
48	rs181289398	chr1:45098301-45098302	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
49	rs565851588	chr1:45098328-45098329	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs565007546	chr1:45098341-45098342	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45083400-45097200	Weak transcription	Gastric	stomach
2	chr1:45093600-45097200	Enhancers	NHLF	lung
3	chr1:45093800-45097200	Enhancers	NHDF-Ad	bronchial
4	chr1:45096200-45097200	Enhancers	Brain Substantia Nigra	brain
5	chr1:45096400-45097200	Weak transcription	Lung	lung
6	chr1:45096600-45097400	Flanking Active TSS	Dnd41	blood
7	chr1:45096600-45097400	Flanking Active TSS	K562	blood
8	chr1:45096800-45097200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr1:45096800-45097200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:45096800-45097200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr1:45096800-45097200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:45096800-45097200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:45096800-45097200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:45096800-45097200	Flanking Active TSS	Colon Smooth Muscle	Colon
15	chr1:45096800-45097200	Enhancers	Placenta Amnion	Placenta Amnion
16	chr1:45096800-45097400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr1:45096800-45097400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr1:45096800-45097400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:45096800-45097400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr1:45096800-45097400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
21	chr1:45096800-45097400	Flanking Active TSS	Adipose Nuclei	Adipose
22	chr1:45096800-45097400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
23	chr1:45096800-45097400	Flanking Active TSS	GM12878-XiMat	blood
24	chr1:45096800-45097400	Flanking Active TSS	Hela-S3	cervix
25	chr1:45096800-45097600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
26	chr1:45096800-45097600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr1:45096800-45098200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:45096800-45098400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr1:45096800-45098400	Active TSS	Fetal Kidney	kidney
30	chr1:45096800-45098400	Active TSS	Rectal Smooth Muscle	rectum
31	chr1:45096800-45099000	Active TSS	A549	lung
32	chr1:45097000-45097200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr1:45097000-45097200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr1:45097000-45097200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:45097000-45097200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:45097000-45097200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:45097000-45097200	Flanking Active TSS	H9 Cell Line	embryonic stem cell
38	chr1:45097000-45097200	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:45097000-45097200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:45097000-45097200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr1:45097000-45097200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:45097000-45097200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:45097000-45097200	Flanking Active TSS	Primary T cells from cord blood	blood
44	chr1:45097000-45097200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
45	chr1:45097000-45097200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr1:45097000-45097200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:45097000-45097200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr1:45097000-45097200	Enhancers	Aorta	Aorta
49	chr1:45097000-45097200	Enhancers	Esophagus	oesophagus
50	chr1:45097000-45097200	Flanking Active TSS	Fetal Brain Female	brain

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