Variant report

Variant	esv16022
Chromosome Location	chr1:150601192-150602306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:542)
CpG islands
(count:855)
Chromatin interactive
region (count:22)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:542 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:150601424-150602376	K562	blood:	n/a	n/a
2	ARID3A	chr1:150601473-150602498	HepG2	liver:	n/a	n/a
3	ATF1	chr1:150601465-150602490	K562	blood:	n/a	n/a
4	ATF2	chr1:150601379-150602622	GM12878	blood:	n/a	n/a
5	ATF2	chr1:150601343-150602594	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:150601512-150602577	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:150601226-150602547	GM12878	blood:	n/a	n/a
8	ATF3	chr1:150601482-150602554	K562	blood:	n/a	chr1:150602144-150602152 chr1:150602271-150602280 chr1:150602141-150602154 chr1:150602142-150602152
9	BCL3	chr1:150601297-150602440	A549	lung:	n/a	n/a
10	BCLAF1	chr1:150601254-150602114	GM12878	blood:	n/a	n/a
11	BCLAF1	chr1:150602142-150602650	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:150601456-150602391	K562	blood:	n/a	n/a
13	BHLHE40	chr1:150601364-150602363	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:150601560-150602437	HepG2	liver:	n/a	n/a
15	BRCA1	chr1:150601519-150601923	GM12878	blood:	n/a	n/a
16	BRCA1	chr1:150602208-150602325	HepG2	liver:	n/a	n/a
17	BRCA1	chr1:150601414-150602262	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr1:150601634-150601961	HepG2	liver:	n/a	n/a
19	BRCA1	chr1:150601377-150602501	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr1:150601506-150602578	K562	blood:	n/a	n/a
21	CCNT2	chr1:150601627-150602042	K562	blood:	n/a	chr1:150602003-150602012
22	CEBPB	chr1:150601277-150601973	MCF-7	breast:	n/a	n/a
23	CEBPB	chr1:150601501-150602335	K562	blood:	n/a	n/a
24	CEBPB	chr1:150601366-150602329	A549	lung:	n/a	n/a
25	CEBPB	chr1:150601474-150602469	K562	blood:	n/a	n/a
26	CEBPB	chr1:150601504-150602310	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:150601665-150601852	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:150601503-150602371	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:150601564-150602315	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:150601538-150602335	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:150601501-150602334	HepG2	liver:	n/a	n/a
32	CEBPD	chr1:150601745-150602572	K562	blood:	n/a	n/a
33	CEBPD	chr1:150601403-150601727	HepG2	liver:	n/a	n/a
34	CEBPD	chr1:150601745-150602501	HepG2	liver:	n/a	n/a
35	CEBPZ	chr1:150601464-150602397	HepG2	liver:	n/a	n/a
36	CHD1	chr1:150601316-150602085	H1-hESC	embryonic stem cell:	n/a	chr1:150601858-150601868
37	CHD1	chr1:150601057-150602437	GM12878	blood:	n/a	chr1:150601858-150601868
38	CHD2	chr1:150601325-150602472	GM12878	blood:	n/a	chr1:150601858-150601868
39	CHD2	chr1:150601205-150602504	Hela-S3	cervix:	n/a	chr1:150601858-150601868
40	CHD2	chr1:150601284-150602498	K562	blood:	n/a	chr1:150601858-150601868
41	CHD2	chr1:150601369-150602481	H1-hESC	embryonic stem cell:	n/a	chr1:150601858-150601868
42	CHD2	chr1:150601443-150602430	HepG2	liver:	n/a	chr1:150601858-150601868
43	CREB1	chr1:150601376-150602467	A549	lung:	n/a	n/a
44	CREB1	chr1:150601440-150602292	A549	lung:	n/a	n/a
45	CREB1	chr1:150601291-150602550	K562	blood:	n/a	n/a
46	CREB1	chr1:150601435-150601940	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr1:150601374-150602496	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr1:150601371-150602459	K562	blood:	n/a	n/a
49	CREB1	chr1:150601115-150602677	GM12878	blood:	n/a	n/a
50	CREB1	chr1:150601976-150602423	H1-hESC	embryonic stem cell:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:150602196-150602246	SK-N-SH_RA	brain:	n/a
2	chr1:150602196-150602246	SK-N-SH_RA	brain:	n/a
3	chr1:150602100-150602150	HNPCEpiC	eye:	n/a
4	chr1:150601613-150601663	AoSMC	blood vessel:	n/a
5	chr1:150601949-150601999	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:150602200-150602250	HEEpiC	esophagus:	n/a
7	chr1:150601648-150601698	AG09309	skin:	n/a
8	chr1:150601493-150601543	AG09309	skin:	n/a
9	chr1:150601613-150601663	GM06990	blood:	n/a
10	chr1:150601613-150601663	GM19239	blood:	n/a
11	chr1:150602100-150602150	SKMC	muscle:	n/a
12	chr1:150601711-150601761	IMR90	lung:	fetal
13	chr1:150602196-150602246	AG09319	gingival:	n/a
14	chr1:150601613-150601663	HRCEpiC	kidney:	n/a
15	chr1:150601789-150601839	NHDF-neo	bronchial:	n/a
16	chr1:150602196-150602246	HepG2	liver:	n/a
17	chr1:150601648-150601698	SAEC	small airway:	n/a
18	chr1:150602200-150602250	AG09309	skin:	n/a
19	chr1:150601727-150601777	HCM	heart:	n/a
20	chr1:150601807-150601857	GM12892	blood:	n/a
21	chr1:150601949-150601999	ovcar-3	ovarian:	n/a
22	chr1:150602200-150602250	RPTEC	kidney:	n/a
23	chr1:150601949-150601999	HAEpiC	amniotic membrane:	n/a
24	chr1:150601727-150601777	HCT-116	colon:	n/a
25	chr1:150601789-150601839	HRE	kidney:	n/a
26	chr1:150601493-150601543	ovcar-3	ovarian:	n/a
27	chr1:150601743-150601793	H1-hESC	embryonic stem cell:	embryo
28	chr1:150602029-150602079	HIPEpiC	eye:	n/a
29	chr1:150602029-150602079	PFSK-1	brain:	n/a
30	chr1:150601613-150601663	Caco-2	colon:	n/a
31	chr1:150601613-150601663	AG09309	skin:	n/a
32	chr1:150602200-150602250	NH-A	brain:	n/a
33	chr1:150601711-150601761	AG09319	gingival:	n/a
34	chr1:150601949-150601999	NHBE	bronchial:	n/a
35	chr1:150602100-150602150	AG09309	skin:	n/a
36	chr1:150601493-150601543	ProgFib	skin:	n/a
37	chr1:150601648-150601698	CMK	blood:	n/a
38	chr1:150601949-150601999	MCF-7	breast:	n/a
39	chr1:150601743-150601793	HepG2	liver:	n/a
40	chr1:150602200-150602250	HCT-116	colon:	n/a
41	chr1:150602029-150602079	HCM	heart:	n/a
42	chr1:150601613-150601663	K562	blood:	n/a
43	chr1:150601949-150601999	GM19239	blood:	n/a
44	chr1:150601949-150601999	HIPEpiC	eye:	n/a
45	chr1:150601727-150601777	NHDF-neo	bronchial:	n/a
46	chr1:150602196-150602246	NT2-D1	testis:	n/a
47	chr1:150601493-150601543	Jurkat	blood:	n/a
48	chr1:150602200-150602250	Jurkat	blood:	n/a
49	chr1:150601613-150601663	SK-N-SH_RA	brain:	n/a
50	chr1:150601743-150601793	BJ	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150600086..150604497-chr1:150798595..150803015,4	MCF-7	breast:
2	chr1:150459471..150461027-chr1:150601141..150603564,2	K562	blood:
3	chr1:150458113..150460742-chr1:150599904..150603804,4	MCF-7	breast:
4	chr1:45987145..45987741-chr1:150601221..150601934,2	Hela-S3	cervix:
5	chr1:150538995..150557554-chr1:150581886..150604495,126	K562	blood:
6	chr1:150600704..150602423-chr1:150722921..150725680,2	MCF-7	breast:
7	chr1:150600280..150603071-chr17:56707754..56709707,2	MCF-7	breast:
8	chr1:150523106..150526873-chr1:150601148..150603781,4	K562	blood:
9	chr1:150532182..150537720-chr1:150588719..150604935,28	MCF-7	breast:
10	chr1:150549047..150553046-chr1:150599453..150603954,9	MCF-7	breast:
11	chr1:150533703..150535548-chr1:150601310..150603343,2	K562	blood:
12	chr1:150600402..150602469-chr12:6642434..6645132,2	MCF-7	breast:
13	chr1:150601091..150602624-chr1:150945367..150947119,2	MCF-7	breast:
14	chr1:150600957..150603301-chr1:150669104..150670860,3	MCF-7	breast:
15	chr1:150547986..150553838-chr1:150598744..150606232,19	K562	blood:
16	chr1:150520854..150524966-chr1:150599341..150603058,4	K562	blood:
17	chr1:150600649..150603708-chr1:150666872..150671304,5	K562	blood:
18	chr1:150601356..150602327-chr16:71929417..71930053,2	Hela-S3	cervix:
19	chr1:150600620..150604710-chr1:150667156..150670884,6	K562	blood:
20	chr1:150526992..150529114-chr1:150602291..150603866,2	MCF-7	breast:
21	chr1:150531290..150540028-chr1:150591374..150603951,29	MCF-7	breast:
22	chr1:150548752..150555486-chr1:150599368..150605834,15	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAMTSL4-7	chr1:150602100-150609632	NONHSAT006322
2	lnc-ENSA-1	chr1:150602026-150602088	NONHSAT006320

No data

Variant related genes	Relation type
ENSA	TF binding region
ENSA	CpG island
ENSG00000143418	chromatin interactions
ENSG00000143382	chromatin interactions
ENSG00000264584	chromatin interactions
ENSG00000163131	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000143374	chromatin interactions
ENSG00000264508	chromatin interactions
ENSG00000143437	chromatin interactions
ENSG00000143457	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000182149	chromatin interactions
ENSG00000231073	chromatin interactions
ENSG00000111640	chromatin interactions
ENSG00000225996	chromatin interactions
ENSG00000203804	chromatin interactions
ENSG00000264553	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000255966	chromatin interactions

Extended variants
information (count: 51 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:51 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386635378	chr1:150601203-150601204	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
2	rs184222578	chr1:150601204-150601205	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
3	rs587642584	chr1:150601221-150601222	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs587699905	chr1:150601270-150601271	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
5	rs587757890	chr1:150601284-150601285	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
6	rs587647594	chr1:150601298-150601299	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
7	rs190024592	chr1:150601377-150601378	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
8	rs587711000	chr1:150601421-150601422	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
9	rs41266901	chr1:150601422-150601423	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs587646347	chr1:150601454-150601455	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
11	rs372855492	chr1:150601464-150601465	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
12	rs587594676	chr1:150601468-150601469	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
13	rs375460829	chr1:150601510-150601511	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
14	rs201267816	chr1:150601513-150601514	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
15	rs200916561	chr1:150601516-150601517	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
16	rs371698688	chr1:150601521-150601522	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
17	rs41266903	chr1:150601529-150601530	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
18	rs587606221	chr1:150601537-150601538	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
19	rs74800622	chr1:150601542-150601543	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
20	rs374974585	chr1:150601567-150601568	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
21	rs587655461	chr1:150601595-150601596	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
22	rs367856217	chr1:150601600-150601601	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
23	rs372022946	chr1:150601618-150601619	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
24	rs587741475	chr1:150601626-150601627	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
25	rs376923966	chr1:150601627-150601628	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
26	rs369597675	chr1:150601657-150601658	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
27	rs369514379	chr1:150601668-150601669	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
28	rs587611627	chr1:150601727-150601728	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
29	rs148024395	chr1:150601748-150601749	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
30	rs77115129	chr1:150601751-150601752	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
31	rs587744963	chr1:150601762-150601763	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
32	rs587620271	chr1:150601775-150601776	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
33	rs181236187	chr1:150601783-150601784	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
34	rs587759689	chr1:150601833-150601834	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
35	rs373509426	chr1:150601835-150601836	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
36	rs376720538	chr1:150601838-150601839	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
37	rs112523257	chr1:150601840-150601841	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
38	rs587770057	chr1:150601856-150601857	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
39	rs79906755	chr1:150601861-150601862	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
40	rs376642323	chr1:150601877-150601878	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
41	rs199580689	chr1:150601929-150601930	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
42	rs369922289	chr1:150601930-150601931	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
43	rs148754482	chr1:150601936-150601937	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
44	rs376153418	chr1:150601955-150601956	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
45	rs370041094	chr1:150601965-150601966	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
46	rs587736036	chr1:150601980-150601981	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
47	rs587594909	chr1:150602020-150602021	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
48	rs112688380	chr1:150602077-150602078	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
49	rs587670673	chr1:150602090-150602091	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
50	rs184709906	chr1:150602118-150602119	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Cancer	23975201	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150599000-150601200	Weak transcription	Gastric	stomach
2	chr1:150599200-150601200	Weak transcription	Lung	lung
3	chr1:150599800-150601200	Weak transcription	Ovary	ovary
4	chr1:150599800-150601200	Weak transcription	Small Intestine	intestine
5	chr1:150600200-150601200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:150600200-150601200	Enhancers	Stomach Mucosa	stomach
7	chr1:150600200-150601200	Flanking Active TSS	NHEK	skin
8	chr1:150600200-150601400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr1:150600200-150603000	Active TSS	Right Ventricle	heart
10	chr1:150600400-150601200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:150600400-150601200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:150600400-150601200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
13	chr1:150600400-150601200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
14	chr1:150600400-150601200	Flanking Active TSS	Fetal Brain Male	brain
15	chr1:150600400-150601200	Flanking Active TSS	Fetal Brain Female	brain
16	chr1:150600400-150601200	Flanking Active TSS	Fetal Lung	lung
17	chr1:150600400-150601200	Flanking Active TSS	Hela-S3	cervix
18	chr1:150600400-150601400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:150600400-150601400	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr1:150600400-150601400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
21	chr1:150600400-150601400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
22	chr1:150600400-150601400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
23	chr1:150600400-150601600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:150600400-150601600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:150600400-150603200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:150600400-150603400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:150600400-150603600	Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr1:150600400-150603800	Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr1:150600600-150601200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:150600600-150601200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr1:150600600-150601200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr1:150600600-150601200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
33	chr1:150600600-150601200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr1:150600600-150601200	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr1:150600600-150601200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr1:150600600-150601200	Flanking Active TSS	HMEC	breast
37	chr1:150600600-150601400	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr1:150600600-150601400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:150600600-150601400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr1:150600600-150601400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:150600600-150601400	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr1:150600600-150601400	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr1:150600600-150601400	Flanking Active TSS	Rectal Smooth Muscle	rectum
44	chr1:150600600-150601400	Flanking Active TSS	Stomach Smooth Muscle	stomach
45	chr1:150600600-150601400	Flanking Active TSS	Thymus	Thymus
46	chr1:150600600-150601400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr1:150600600-150601400	Flanking Active TSS	Osteobl	bone
48	chr1:150600600-150601600	Flanking Active TSS	Primary B cells from cord blood	blood
49	chr1:150600600-150602800	Active TSS	Esophagus	oesophagus
50	chr1:150600600-150603000	Active TSS	Breast Myoepithelial Primary Cells	Breast

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