Variant report

Variant	esv11736
Chromosome Location	chr1:70820591-70825114
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:522)
CpG islands
(count:427)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:522 , 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	chr1:70820195-70820764	HepG2	liver:	n/a	n/a
2	ATF1	chr1:70820250-70820932	K562	blood:	n/a	n/a
3	ATF2	chr1:70820050-70820998	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr1:70820141-70820996	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:70820087-70821010	GM12878	blood:	n/a	n/a
6	ATF2	chr1:70820147-70821014	GM12878	blood:	n/a	n/a
7	ATF2	chr1:70824692-70825437	GM12878	blood:	n/a	n/a
8	ATF2	chr1:70824764-70825364	GM12878	blood:	n/a	n/a
9	ATF3	chr1:70820304-70820984	K562	blood:	n/a	n/a
10	ATF3	chr1:70820197-70820779	K562	blood:	n/a	n/a
11	BACH1	chr1:70820165-70820756	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr1:70824957-70825220	GM12878	blood:	n/a	n/a
13	BATF	chr1:70824988-70825262	GM12878	blood:	n/a	n/a
14	BATF	chr1:70820354-70820915	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:70824918-70825245	GM12878	blood:	n/a	n/a
16	BCL3	chr1:70820307-70820906	A549	lung:	n/a	n/a
17	BCLAF1	chr1:70824864-70825313	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:70819954-70820929	GM12878	blood:	n/a	n/a
19	BCLAF1	chr1:70820154-70820934	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:70820266-70820936	K562	blood:	n/a	n/a
21	BHLHE40	chr1:70819246-70820872	GM12878	blood:	n/a	chr1:70820349-70820365
22	BHLHE40	chr1:70820079-70820939	K562	blood:	n/a	chr1:70820349-70820365
23	BHLHE40	chr1:70824688-70825278	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:70820037-70820896	HepG2	liver:	n/a	chr1:70820349-70820365
25	BRCA1	chr1:70820094-70820991	GM12878	blood:	n/a	chr1:70820407-70820416
26	BRCA1	chr1:70819787-70820855	HepG2	liver:	n/a	chr1:70820407-70820416
27	BRCA1	chr1:70820007-70820985	H1-hESC	embryonic stem cell:	n/a	chr1:70820407-70820416
28	BRCA1	chr1:70819134-70820943	Hela-S3	cervix:	n/a	chr1:70820407-70820416
29	CBX3	chr1:70819972-70821023	K562	blood:	n/a	n/a
30	CBX3	chr1:70820193-70820883	K562	blood:	n/a	n/a
31	CCNT2	chr1:70820124-70820880	K562	blood:	n/a	n/a
32	CEBPB	chr1:70820151-70820907	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:70824848-70825445	GM12878	blood:	n/a	n/a
34	CEBPB	chr1:70821728-70822035	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:70820185-70820878	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:70820131-70821081	GM12878	blood:	n/a	chr1:70820981-70820989
37	CEBPB	chr1:70821687-70822129	K562	blood:	n/a	n/a
38	CEBPB	chr1:70820222-70820908	K562	blood:	n/a	n/a
39	CEBPB	chr1:70820266-70820892	K562	blood:	n/a	n/a
40	CEBPB	chr1:70821676-70822117	HepG2	liver:	n/a	n/a
41	CEBPD	chr1:70820207-70820727	HepG2	liver:	n/a	n/a
42	CEBPD	chr1:70820133-70820818	K562	blood:	n/a	n/a
43	CHD1	chr1:70819051-70821083	H1-hESC	embryonic stem cell:	n/a	chr1:70820407-70820416
44	CHD1	chr1:70819287-70821036	GM12878	blood:	n/a	chr1:70820407-70820416
45	CHD2	chr1:70819179-70820959	GM12878	blood:	n/a	chr1:70820407-70820416
46	CHD2	chr1:70819179-70820997	Hela-S3	cervix:	n/a	chr1:70820407-70820416
47	CHD2	chr1:70819276-70821003	K562	blood:	n/a	chr1:70820407-70820416
48	CHD2	chr1:70819624-70820891	H1-hESC	embryonic stem cell:	n/a	chr1:70820407-70820416
49	CHD2	chr1:70819383-70820925	HepG2	liver:	n/a	chr1:70820407-70820416
50	CREB1	chr1:70819969-70821133	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70824341-70824391	PFSK-1	brain:	n/a
2	chr1:70820640-70820690	AG04449	skin:	fetal
3	chr1:70824341-70824391	HMEC	breast:	n/a
4	chr1:70820640-70820690	PFSK-1	brain:	n/a
5	chr1:70820718-70820768	Hepatocyte	liver:	n/a
6	chr1:70820790-70820840	A549	lung:	n/a
7	chr1:70820718-70820768	RPTEC	kidney:	n/a
8	chr1:70820718-70820768	GM06990	blood:	n/a
9	chr1:70820607-70820657	GM12891	blood:	n/a
10	chr1:70820640-70820690	HRPEpiC	eye:	n/a
11	chr1:70820718-70820768	AoSMC	blood vessel:	n/a
12	chr1:70820790-70820840	HUVEC	blood vessel:	n/a
13	chr1:70820607-70820657	HNPCEpiC	eye:	n/a
14	chr1:70820718-70820768	SK-N-SH	brain:	n/a
15	chr1:70820790-70820840	RPTEC	kidney:	n/a
16	chr1:70820607-70820657	PrEC	prostate:	n/a
17	chr1:70820736-70820786	PFSK-1	brain:	n/a
18	chr1:70824341-70824391	AG09319	gingival:	n/a
19	chr1:70820607-70820657	HCT-116	colon:	n/a
20	chr1:70821806-70821856	HRCEpiC	kidney:	n/a
21	chr1:70820640-70820690	HIPEpiC	eye:	n/a
22	chr1:70820640-70820690	HL-60	blood:	n/a
23	chr1:70820607-70820657	K562	blood:	n/a
24	chr1:70821806-70821856	PANC-1	pancreas:	n/a
25	chr1:70820640-70820690	HCF	heart:	n/a
26	chr1:70824341-70824391	ovcar-3	ovarian:	n/a
27	chr1:70820736-70820786	AG10803	skin:	n/a
28	chr1:70820790-70820840	HCM	heart:	n/a
29	chr1:70820790-70820840	PrEC	prostate:	n/a
30	chr1:70820736-70820786	PANC-1	pancreas:	n/a
31	chr1:70820736-70820786	HRPEpiC	eye:	n/a
32	chr1:70820790-70820840	MCF10A-Er-Src	breast:	n/a
33	chr1:70821806-70821856	BJ	skin:	n/a
34	chr1:70820607-70820657	NH-A	brain:	n/a
35	chr1:70820790-70820840	IMR90	lung:	fetal
36	chr1:70821806-70821856	HRE	kidney:	n/a
37	chr1:70820736-70820786	ECC-1	luminal epithelium:	n/a
38	chr1:70824341-70824391	HIPEpiC	eye:	n/a
39	chr1:70824341-70824391	RPTEC	kidney:	n/a
40	chr1:70820718-70820768	GM12878	blood:	n/a
41	chr1:70824341-70824391	BE2_C	brain:	n/a
42	chr1:70820790-70820840	HIPEpiC	eye:	n/a
43	chr1:70820736-70820786	IMR90	lung:	fetal
44	chr1:70820790-70820840	HRE	kidney:	n/a
45	chr1:70820718-70820768	HAEpiC	amniotic membrane:	n/a
46	chr1:70821806-70821856	HNPCEpiC	eye:	n/a
47	chr1:70820640-70820690	SK-N-SH	brain:	n/a
48	chr1:70820607-70820657	IMR90	lung:	fetal
49	chr1:70824341-70824391	NH-A	brain:	n/a
50	chr1:70820640-70820690	GM12878	blood:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:70820369..70820909-chr16:4103767..4104269,2	Hela-S3	cervix:
2	chr1:70820288..70821043-chr14:55878152..55878652,2	Hela-S3	cervix:
3	chr1:70670191..70673421-chr1:70819814..70822311,3	K562	blood:
4	chr1:70819013..70822302-chr1:70824014..70829303,9	MCF-7	breast:
5	chr1:70686924..70688596-chr1:70820161..70821739,2	MCF-7	breast:
6	chr1:70819841..70820741-chr21:33765342..33765918,2	Hela-S3	cervix:
7	chr1:70819013..70822302-chr1:70824014..70829303,9	MCF-7	breast:
8	chr1:70820399..70820978-chr19:1039823..1040333,2	Hela-S3	cervix:
9	chr1:70819015..70821620-chr1:70875663..70878848,3	MCF-7	breast:
10	chr1:70686799..70689606-chr1:70818481..70820974,3	K562	blood:
11	chr1:70820240..70820765-chr21:36228154..36229153,2	Hela-S3	cervix:
12	chr1:70820419..70821379-chr6:31794911..31795554,2	Hela-S3	cervix:
13	chr1:70686799..70688622-chr1:70819236..70822047,3	K562	blood:
14	chr1:70814842..70821925-chr1:70874223..70879265,8	K562	blood:
15	chr1:70820369..70820950-chr20:18487901..18488870,2	Hela-S3	cervix:
16	chr1:70820317..70820900-chr2:204103295..204104099,2	Hela-S3	cervix:
17	chr1:70819774..70820742-chr19:2268884..2269581,2	Hela-S3	cervix:
18	chr1:70820321..70821295-chr16:67693740..67694256,2	Hela-S3	cervix:
19	chr1:70820185..70820796-chr5:57755458..57756161,2	Hela-S3	cervix:
20	chr1:40506025..40506869-chr1:70820330..70820998,2	Hela-S3	cervix:
21	chr1:70819966..70820788-chr12:46765760..46766512,2	Hela-S3	cervix:
22	chr1:70820287..70820857-chr20:33543072..33543925,2	Hela-S3	cervix:
23	chr1:70685799..70687948-chr1:70819964..70821804,2	MCF-7	breast:
24	chr1:70820223..70820900-chr8:22925930..22926635,2	Hela-S3	cervix:
25	chr1:70820288..70821087-chr12:13044176..13045013,2	Hela-S3	cervix:
26	chr1:70820102..70820781-chr15:65903328..65904070,2	Hela-S3	cervix:
27	chr1:70820291..70820901-chr2:219433432..219434034,2	Hela-S3	cervix:
28	chr1:70818087..70822177-chr1:70874224..70879265,8	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-9	chr1:70820493-70820790	NR_027404
2	lnc-CTH-9	chr1:70820511-70820891	NONHSAT003856

No data

Variant related genes	Relation type
HHLA3	TF binding region
ANKRD13C	TF binding region
HHLA3	CpG island
ANKRD13C	CpG island
ENSG00000074621	chromatin interactions
ENSG00000013588	chromatin interactions
ENSG00000120889	chromatin interactions
ENSG00000104904	chromatin interactions
ENSG00000197568	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000119004	chromatin interactions
ENSG00000162104	chromatin interactions
ENSG00000228988	chromatin interactions
ENSG00000138614	chromatin interactions
ENSG00000101310	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000256073	chromatin interactions
ENSG00000066557	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000145632	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000226088	chromatin interactions
ENSG00000159216	chromatin interactions
ENSG00000126775	chromatin interactions
ENSG00000144580	chromatin interactions
ENSG00000102977	chromatin interactions
ENSG00000167476	chromatin interactions
ENSG00000116754	chromatin interactions
ENSG00000100983	chromatin interactions
ENSG00000131236	chromatin interactions
ENSG00000064687	chromatin interactions

Extended variants
information (count: 162 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:162 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372256171	chr1:70820592-70820593	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	27 gene(s)	Overlapped CNVs	n/a
2	rs375221939	chr1:70820611-70820612	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	Overlapped CNVs	n/a
3	rs369713202	chr1:70820621-70820622	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	Overlapped CNVs	n/a
4	rs111439828	chr1:70820626-70820627	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	Overlapped CNVs	n/a
5	rs145621079	chr1:70820628-70820629	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	Overlapped CNVs	n/a
6	rs372108058	chr1:70820633-70820634	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	Overlapped CNVs	n/a
7	rs376021762	chr1:70820658-70820659	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	Overlapped CNVs	n/a
8	rs369236367	chr1:70820664-70820665	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	Overlapped CNVs	n/a
9	rs139629563	chr1:70820688-70820689	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	Overlapped CNVs	n/a
10	rs201691903	chr1:70820709-70820710	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	26 gene(s)	Overlapped CNVs	n/a
11	rs542471494	chr1:70820716-70820717	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	26 gene(s)	Overlapped CNVs	n/a
12	rs199616884	chr1:70820789-70820790	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	19 gene(s)	Overlapped CNVs	n/a
13	rs372400412	chr1:70820790-70820791	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	Overlapped CNVs	n/a
14	rs200918239	chr1:70820794-70820795	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	Overlapped CNVs	n/a
15	rs368043207	chr1:70820799-70820800	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
16	rs17131261	chr1:70820802-70820803	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs375666043	chr1:70820816-70820817	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
18	rs373844538	chr1:70820830-70820831	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
19	rs530784979	chr1:70820848-70820849	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
20	rs149664135	chr1:70820867-70820868	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	17 gene(s)	Overlapped CNVs	n/a
21	rs55863806	chr1:70820880-70820881	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs368213512	chr1:70820928-70820929	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
23	rs564632124	chr1:70820941-70820942	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
24	rs533265580	chr1:70820951-70820952	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs76708515	chr1:70820988-70820989	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs182375563	chr1:70820998-70820999	Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs536160193	chr1:70821017-70821018	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs549672590	chr1:70821077-70821078	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs568889052	chr1:70821101-70821102	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs537872030	chr1:70821118-70821119	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs557443767	chr1:70821142-70821143	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs145463589	chr1:70821229-70821230	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs112116431	chr1:70821240-70821241	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs4650040	chr1:70821245-70821246	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs577712575	chr1:70821261-70821262	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs533639413	chr1:70821266-70821267	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs553940899	chr1:70821271-70821272	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs4650041	chr1:70821307-70821308	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs148823695	chr1:70821313-70821314	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs535280002	chr1:70821318-70821319	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs10622503	chr1:70821328-70821329	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs550399131	chr1:70821330-70821331	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs397980464	chr1:70821336-70821337	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs7367309	chr1:70821337-70821338	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs7366585	chr1:70821339-70821340	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs7367311	chr1:70821345-70821346	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs7366586	chr1:70821347-70821348	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs571779006	chr1:70821360-70821361	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs143520031	chr1:70821375-70821376	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs148003858	chr1:70821470-70821471	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	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
Papillary thyroid carcinoma	21436994	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
Breast cancer	17603634	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
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	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
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70817000-70821000	Active TSS	Fetal Brain Female	brain
2	chr1:70817600-70820600	Active TSS	Brain Angular Gyrus	brain
3	chr1:70817600-70821200	Active TSS	NHLF	lung
4	chr1:70817600-70821400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:70817600-70821600	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr1:70817600-70822000	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr1:70817800-70820800	Active TSS	GM12878-XiMat	blood
8	chr1:70817800-70821400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:70818000-70820600	Active TSS	NH-A	brain
10	chr1:70818000-70820800	Active TSS	Muscle Satellite Cultured Cells	--
11	chr1:70818000-70820800	Active TSS	Fetal Kidney	kidney
12	chr1:70818000-70820800	Active TSS	K562	blood
13	chr1:70818000-70820800	Active TSS	NHDF-Ad	bronchial
14	chr1:70818000-70821200	Active TSS	Brain Hippocampus Middle	brain
15	chr1:70818000-70821400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:70818000-70821400	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr1:70818000-70821400	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr1:70818000-70821800	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr1:70818200-70821000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr1:70818200-70821000	Active TSS	Ovary	ovary
21	chr1:70818200-70821000	Active TSS	HSMM	muscle
22	chr1:70818200-70821200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:70818200-70821200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr1:70818200-70821200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:70818200-70821200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr1:70818200-70821200	Active TSS	Aorta	Aorta
27	chr1:70818200-70821200	Active TSS	Psoas Muscle	Psoas
28	chr1:70818200-70821200	Active TSS	Right Atrium	heart
29	chr1:70818200-70821200	Active TSS	Stomach Smooth Muscle	stomach
30	chr1:70818200-70821400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:70818200-70821400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr1:70818200-70821400	Active TSS	A549	lung
33	chr1:70818400-70820600	Active TSS	Fetal Thymus	thymus
34	chr1:70818400-70820800	Active TSS	NHEK	skin
35	chr1:70818400-70821000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:70818400-70821000	Active TSS	Fetal Intestine Large	intestine
37	chr1:70818400-70821200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr1:70818400-70821200	Active TSS	H1 Cell Line	embryonic stem cell
39	chr1:70818400-70821400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:70818600-70820800	Active TSS	Fetal Heart	heart
41	chr1:70818600-70820800	Active TSS	Thymus	Thymus
42	chr1:70818600-70820800	Active TSS	HSMMtube	muscle
43	chr1:70818600-70821000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:70818600-70821200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr1:70818600-70821200	Active TSS	Fetal Stomach	stomach
46	chr1:70818800-70820600	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr1:70818800-70820600	Active TSS	Fetal Muscle Leg	muscle
48	chr1:70818800-70820800	Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr1:70818800-70820800	Active TSS	Brain Cingulate Gyrus	brain
50	chr1:70818800-70820800	Active TSS	Fetal Brain Male	brain

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