Variant report

Variant	esv3323980
Chromosome Location	chr15:45458085-45460633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:305)
Chromatin interactive
region (count:38)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45459687-45459941	K562	blood:	n/a	n/a
2	ARID3A	chr15:45459297-45459300	K562	blood:	n/a	n/a
3	ARID3A	chr15:45459757-45459773	HepG2	liver:	n/a	n/a
4	ATF3	chr15:45459029-45459297	K562	blood:	n/a	chr15:45459163-45459172
5	BACH1	chr15:45459461-45459883	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr15:45459523-45459793	GM12878	blood:	n/a	n/a
7	BCLAF1	chr15:45458947-45459967	GM12878	blood:	n/a	chr15:45459191-45459204 chr15:45459123-45459136
8	BHLHE40	chr15:45459057-45459957	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:45458677-45459264	K562	blood:	n/a	n/a
10	BHLHE40	chr15:45459621-45459920	K562	blood:	n/a	n/a
11	BRCA1	chr15:45459103-45459895	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr15:45459551-45459919	K562	blood:	n/a	n/a
13	CCNT2	chr15:45458624-45459873	K562	blood:	n/a	n/a
14	CEBPB	chr15:45459114-45459907	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr15:45458722-45459400	HepG2	liver:	n/a	n/a
16	CEBPD	chr15:45460052-45460356	HepG2	liver:	n/a	n/a
17	CHD1	chr15:45458743-45459753	GM12878	blood:	n/a	n/a
18	CHD1	chr15:45458815-45459662	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr15:45459669-45459750	HepG2	liver:	n/a	n/a
20	CHD2	chr15:45458726-45459992	K562	blood:	n/a	n/a
21	CHD2	chr15:45458880-45459914	GM12878	blood:	n/a	n/a
22	CHD2	chr15:45459007-45459872	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr15:45459201-45459324	HepG2	liver:	n/a	n/a
24	CHD2	chr15:45458807-45459983	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr15:45457927-45458124	GM12878	blood:	n/a	n/a
26	CREB1	chr15:45458933-45459434	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr15:45458876-45459449	K562	blood:	n/a	n/a
28	CREB1	chr15:45459533-45459849	A549	lung:	n/a	n/a
29	CREB1	chr15:45458983-45459379	A549	lung:	n/a	n/a
30	CREB1	chr15:45458940-45459469	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr15:45458956-45459981	GM12878	blood:	n/a	n/a
32	CREB1	chr15:45458622-45459982	HepG2	liver:	n/a	n/a
33	CTBP2	chr15:45458764-45459988	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr15:45459620-45459770	MCF-7	breast:	n/a	n/a
35	CTCF	chr15:45459840-45459990	A549	lung:	n/a	n/a
36	CTCF	chr15:45459642-45459888	GM10266	blood:	n/a	n/a
37	CTCF	chr15:45460380-45460530	GM12875	blood:	n/a	n/a
38	CTCF	chr15:45459660-45459810	AG09319	gingival:	n/a	n/a
39	CTCF	chr15:45459700-45459850	GM12867	blood:	n/a	n/a
40	CTCF	chr15:45459643-45459856	Medullo	brain:	n/a	n/a
41	CTCF	chr15:45459641-45459878	LNCaP	prostate:	n/a	n/a
42	CTCF	chr15:45459680-45459830	K562	blood:	n/a	n/a
43	CTCF	chr15:45460420-45460570	GM12872	blood:	n/a	n/a
44	CTCF	chr15:45459030-45459156	GM12891	blood:	n/a	n/a
45	CTCF	chr15:45459680-45459830	AG09309	skin:	n/a	n/a
46	CTCF	chr15:45459080-45459230	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr15:45459185-45459187	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:45459000-45459150	GM12874	blood:	n/a	n/a
49	CTCF	chr15:45459013-45459152	GM10248	blood:	n/a	n/a
50	CTCF	chr15:45459640-45459790	HFF-Myc	foreskin:	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	chr15:45459300-45459350	HCT-116	colon:	n/a
2	chr15:45458906-45458956	MCF-7	breast:	n/a
3	chr15:45458818-45458868	PFSK-1	brain:	n/a
4	chr15:45459300-45459350	LNCaP	prostate:	n/a
5	chr15:45458818-45458868	BJ	skin:	n/a
6	chr15:45459467-45459517	HEEpiC	esophagus:	n/a
7	chr15:45459467-45459517	Hela-S3	cervix:	n/a
8	chr15:45459406-45459456	HCF	heart:	n/a
9	chr15:45458818-45458868	NHDF-neo	bronchial:	n/a
10	chr15:45459467-45459517	Jurkat	blood:	n/a
11	chr15:45459467-45459517	SKMC	muscle:	n/a
12	chr15:45458906-45458956	HEK293	kidney:	embryo
13	chr15:45458818-45458868	SK-N-MC	brain:	n/a
14	chr15:45459467-45459517	AoSMC	blood vessel:	n/a
15	chr15:45458818-45458868	ProgFib	skin:	n/a
16	chr15:45459300-45459350	ECC-1	luminal epithelium:	n/a
17	chr15:45458818-45458868	HMEC	breast:	n/a
18	chr15:45459300-45459350	Hela-S3	cervix:	n/a
19	chr15:45459406-45459456	Caco-2	colon:	n/a
20	chr15:45458906-45458956	ovcar-3	ovarian:	n/a
21	chr15:45459300-45459350	GM12892	blood:	n/a
22	chr15:45459300-45459350	HepG2	liver:	n/a
23	chr15:45458906-45458956	Hela-S3	cervix:	n/a
24	chr15:45458818-45458868	MCF10A-Er-Src	breast:	n/a
25	chr15:45459300-45459350	Hepatocyte	liver:	n/a
26	chr15:45459467-45459517	Caco-2	colon:	n/a
27	chr15:45459467-45459517	AG04449	skin:	fetal
28	chr15:45458906-45458956	GM12892	blood:	n/a
29	chr15:45459300-45459350	GM06990	blood:	n/a
30	chr15:45458818-45458868	HCF	heart:	n/a
31	chr15:45459300-45459350	HRE	kidney:	n/a
32	chr15:45459406-45459456	MCF10A-Er-Src	breast:	n/a
33	chr15:45459406-45459456	T-47D	breast:	n/a
34	chr15:45459300-45459350	HAEpiC	amniotic membrane:	n/a
35	chr15:45459467-45459517	HL-60	blood:	n/a
36	chr15:45459467-45459517	T-47D	breast:	n/a
37	chr15:45458818-45458868	K562	blood:	n/a
38	chr15:45459467-45459517	NB4	blood:	n/a
39	chr15:45459467-45459517	NH-A	brain:	n/a
40	chr15:45459406-45459456	U87	brain:	n/a
41	chr15:45459300-45459350	SK-N-MC	brain:	n/a
42	chr15:45459406-45459456	Hepatocyte	liver:	n/a
43	chr15:45458818-45458868	HRE	kidney:	n/a
44	chr15:45458818-45458868	AG04449	skin:	fetal
45	chr15:45459467-45459517	HCM	heart:	n/a
46	chr15:45458818-45458868	SK-N-SH	brain:	n/a
47	chr15:45459467-45459517	NHDF-neo	bronchial:	n/a
48	chr15:45458906-45458956	NHDF-neo	bronchial:	n/a
49	chr15:45459406-45459456	ProgFib	skin:	n/a
50	chr15:45458906-45458956	ECC-1	luminal epithelium:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:45457346..45461990-chr15:45488766..45494297,11	MCF-7	breast:
2	chr15:45459070..45459878-chr15:65588119..65588621,2	Hela-S3	cervix:
3	chr15:45457159..45458711-chr15:45469879..45471937,2	MCF-7	breast:
4	chr15:45457925..45460364-chr15:45492288..45495049,4	MCF-7	breast:
5	chr15:45456315..45459130-chr15:45878271..45881206,2	K562	blood:
6	chr15:45457610..45461525-chr15:45477333..45480560,5	MCF-7	breast:
7	chr15:45458863..45459698-chr16:30076064..30076687,2	Hela-S3	cervix:
8	chr15:45444706..45447350-chr15:45459510..45461724,2	K562	blood:
9	chr15:45458222..45460718-chr15:45477355..45481212,4	K562	blood:
10	chr15:45458146..45462463-chr15:45465556..45468797,6	MCF-7	breast:
11	chr1:28974918..28975657-chr15:45458791..45459483,2	Hela-S3	cervix:
12	chr15:45459071..45462844-chr15:45693635..45696532,4	K562	blood:
13	chr15:45457588..45459238-chr15:45747257..45749159,2	K562	blood:
14	chr11:62608445..62609565-chr15:45458977..45459729,4	Hela-S3	cervix:
15	chr1:151254368..151255147-chr15:45459225..45460088,2	Hela-S3	cervix:
16	chr15:45458064..45460777-chr15:45570184..45573179,2	MCF-7	breast:
17	chr15:45457064..45458836-chr15:45462821..45464924,2	MCF-7	breast:
18	chr15:45458782..45460452-chr15:45469150..45471146,2	MCF-7	breast:
19	chr15:45458745..45459668-chr6:33393132..33393783,2	NB4	blood:
20	chr15:45459519..45461778-chr15:45469004..45470564,2	K562	blood:
21	chr15:45458776..45462841-chr15:45467209..45473486,10	K562	blood:
22	chr15:45459092..45459965-chr15:75134556..75135332,2	Hela-S3	cervix:
23	chr15:45457999..45463256-chr15:45488727..45493013,8	K562	blood:
24	chr15:45456638..45458886-chr15:45696035..45698478,2	K562	blood:
25	chr15:45458882..45460694-chr15:45692968..45695992,3	MCF-7	breast:
26	chr15:45457813..45459796-chr15:45472458..45474302,2	MCF-7	breast:
27	chr15:45459427..45462384-chr15:45693635..45696116,3	K562	blood:
28	chr15:45458639..45462602-chr15:45463163..45466877,10	K562	blood:
29	chr15:45457736..45460170-chr15:45478587..45480947,2	MCF-7	breast:
30	chr15:45456567..45458793-chr15:45475778..45478216,2	MCF-7	breast:
31	chr15:45457899..45460285-chr15:45489261..45492223,4	MCF-7	breast:
32	chr12:49245617..49246517-chr15:45459356..45460000,2	Hela-S3	cervix:
33	chr15:45459774..45461695-chr15:45467150..45468709,2	K562	blood:
34	chr15:45449920..45453086-chr15:45456416..45459415,4	K562	blood:
35	chr15:45459088..45459735-chr5:134240707..134241290,2	Hela-S3	cervix:
36	chr15:45457607..45459113-chr15:45748789..45750442,2	K562	blood:
37	chr15:45458639..45463256-chr15:45489443..45493548,9	K562	blood:
38	chr15:45457275..45460718-chr15:45477484..45481344,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHF-2	chr15:45459684-45459724	ENSG00000259539.1

No data

Variant related genes	Relation type
ENSG00000259539	TF binding region
ENSG00000259519	TF binding region
ENSG00000259539	CpG island
ENSG00000259519	CpG island
ENSG00000260170	chromatin interactions
ENSG00000171763	chromatin interactions
ENSG00000174243	chromatin interactions
ENSG00000259932	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000137857	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000140474	chromatin interactions
ENSG00000260035	chromatin interactions
ENSG00000171766	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000259520	chromatin interactions
ENSG00000104164	chromatin interactions
ENSG00000138606	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000132570	chromatin interactions

Extended variants
information (count: 79 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:79 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372448577	chr15:45458096-45458097	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs188589358	chr15:45458118-45458119	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs180727595	chr15:45458165-45458166	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs186164144	chr15:45458225-45458226	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs61030171	chr15:45458268-45458269	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs566530111	chr15:45458311-45458312	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs545431955	chr15:45458326-45458327	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs570878393	chr15:45458333-45458334	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs199937085	chr15:45458338-45458339	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs200548043	chr15:45458340-45458341	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs78549114	chr15:45458342-45458343	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs397743263	chr15:45458352-45458353	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs367650254	chr15:45458365-45458366	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs533429468	chr15:45458378-45458379	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs113102275	chr15:45458380-45458381	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs555221183	chr15:45458491-45458492	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs535407139	chr15:45458630-45458631	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs555233259	chr15:45458631-45458632	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs565600704	chr15:45458635-45458636	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs371339291	chr15:45458655-45458656	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs191885999	chr15:45458733-45458734	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs374935016	chr15:45458861-45458862	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs557709398	chr15:45458915-45458916	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs577681608	chr15:45458916-45458917	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs1706815	chr15:45458935-45458936	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs1648310	chr15:45458954-45458955	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs576698842	chr15:45459074-45459075	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs7182081	chr15:45459112-45459113	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs1648309	chr15:45459182-45459183	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs572748012	chr15:45459197-45459198	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
31	rs541082867	chr15:45459229-45459230	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs182512345	chr15:45459262-45459263	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs7182007	chr15:45459277-45459278	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs372062929	chr15:45459292-45459293	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs533294454	chr15:45459310-45459311	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs550246161	chr15:45459312-45459313	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs563378940	chr15:45459425-45459426	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
38	rs533229140	chr15:45459451-45459452	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
39	rs548722710	chr15:45459471-45459472	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
40	rs565661494	chr15:45459492-45459493	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs534573414	chr15:45459511-45459512	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
42	rs551126810	chr15:45459526-45459527	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
43	rs571215890	chr15:45459558-45459559	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
44	rs200422486	chr15:45459564-45459565	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
45	rs557026731	chr15:45459583-45459584	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
46	rs577702953	chr15:45459604-45459605	Weak transcription 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	rs545242472	chr15:45459612-45459613	Weak transcription 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	rs113485725	chr15:45459632-45459633	Weak transcription 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	rs560301897	chr15:45459637-45459638	Weak transcription 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
50	rs7166354	chr15:45459718-45459719	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	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	chr15:45427600-45458600	Weak transcription	Right Atrium	heart
2	chr15:45440400-45458600	Weak transcription	Aorta	Aorta
3	chr15:45449400-45458600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:45451400-45458400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr15:45454800-45458600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:45455400-45458200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr15:45455400-45458200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr15:45455400-45458400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr15:45455400-45458600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr15:45455400-45458600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr15:45455400-45458600	Weak transcription	A549	lung
12	chr15:45455600-45458200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr15:45455600-45458600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr15:45455600-45458600	Weak transcription	Placenta	Placenta
15	chr15:45455800-45458200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:45455800-45458200	Weak transcription	Fetal Intestine Small	intestine
17	chr15:45455800-45458200	Weak transcription	NHDF-Ad	bronchial
18	chr15:45455800-45458600	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr15:45455800-45458600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr15:45455800-45458600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr15:45455800-45458600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr15:45455800-45458600	Weak transcription	Ovary	ovary
23	chr15:45455800-45458600	Weak transcription	Right Ventricle	heart
24	chr15:45455800-45458600	Weak transcription	HSMMtube	muscle
25	chr15:45455800-45458600	Weak transcription	K562	blood
26	chr15:45455800-45458800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr15:45456000-45458600	Weak transcription	Brain Cingulate Gyrus	brain
28	chr15:45456000-45458600	Weak transcription	NH-A	brain
29	chr15:45456000-45458600	Weak transcription	NHLF	lung
30	chr15:45456000-45458600	Weak transcription	Osteobl	bone
31	chr15:45456200-45458200	Enhancers	HepG2	liver
32	chr15:45456400-45458600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr15:45456600-45458600	Weak transcription	HSMM	muscle
34	chr15:45456600-45458600	Weak transcription	NHEK	skin
35	chr15:45457000-45458400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr15:45457000-45458600	Enhancers	Primary T cells fromperipheralblood	blood
37	chr15:45457000-45458600	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr15:45457000-45458600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr15:45457000-45458600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr15:45457000-45458600	Enhancers	Duodenum Mucosa	Duodenum
41	chr15:45457000-45458600	Enhancers	Fetal Lung	lung
42	chr15:45457000-45458600	Enhancers	Fetal Stomach	stomach
43	chr15:45457200-45458600	Enhancers	Primary B cells from peripheral blood	blood
44	chr15:45457200-45458600	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr15:45457200-45458600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr15:45457200-45458600	Enhancers	Fetal Brain Male	brain
47	chr15:45457200-45458800	Weak transcription	Gastric	stomach
48	chr15:45457400-45458200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr15:45457400-45458200	Genic enhancers	Esophagus	oesophagus
50	chr15:45457400-45458400	Enhancers	Left Ventricle	heart

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