Variant report

Variant	esv3339225
Chromosome Location	chr13:50366351-50367299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:631)
CpG islands
(count:671)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50366846-50367514	HepG2	liver:	n/a	n/a
2	ATF2	chr13:50366738-50367057	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr13:50366842-50367554	GM12878	blood:	n/a	n/a
4	ATF2	chr13:50366922-50367551	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr13:50366713-50367215	GM12878	blood:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
6	ATF3	chr13:50366747-50367052	H1-hESC	embryonic stem cell:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
7	ATF3	chr13:50366730-50367199	HepG2	liver:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
8	ATF3	chr13:50366712-50367018	K562	blood:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
9	ATF3	chr13:50366740-50366957	GM12878	blood:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
10	ATF3	chr13:50366758-50367176	HepG2	liver:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
11	BACH1	chr13:50366820-50367599	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr13:50366705-50367096	A549	lung:	n/a	n/a
13	BHLHE40	chr13:50366529-50367473	GM12878	blood:	n/a	n/a
14	BHLHE40	chr13:50365474-50367685	HepG2	liver:	n/a	chr13:50366364-50366380 chr13:50366375-50366391 chr13:50366423-50366439 chr13:50366367-50366383
15	BHLHE40	chr13:50366566-50367565	K562	blood:	n/a	n/a
16	BRCA1	chr13:50367029-50367219	HepG2	liver:	n/a	n/a
17	BRCA1	chr13:50366994-50367517	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr13:50366766-50367665	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr13:50366737-50367385	K562	blood:	n/a	n/a
20	CCNT2	chr13:50366034-50367396	K562	blood:	n/a	chr13:50366046-50366055
21	CEBPB	chr13:50366807-50367734	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr13:50366935-50367179	HepG2	liver:	n/a	n/a
23	CEBPD	chr13:50366425-50366737	HepG2	liver:	n/a	n/a
24	CEBPD	chr13:50366876-50367347	HepG2	liver:	n/a	n/a
25	CHD1	chr13:50365648-50366511	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr13:50366903-50367142	H1-hESC	embryonic stem cell:	n/a	chr13:50367048-50367058
27	CHD1	chr13:50366902-50367627	GM12878	blood:	n/a	chr13:50367048-50367058
28	CHD2	chr13:50365471-50367514	GM12878	blood:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
29	CHD2	chr13:50366642-50367694	HepG2	liver:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
30	CHD2	chr13:50366604-50367762	H1-hESC	embryonic stem cell:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
31	CHD2	chr13:50365461-50367498	Hela-S3	cervix:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
32	CHD2	chr13:50366562-50367411	K562	blood:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
33	CREB1	chr13:50366032-50367805	GM12878	blood:	n/a	n/a
34	CREB1	chr13:50366582-50367861	HepG2	liver:	n/a	n/a
35	CREB1	chr13:50365934-50367817	HepG2	liver:	n/a	n/a
36	CREB1	chr13:50366559-50367841	K562	blood:	n/a	n/a
37	CREB1	chr13:50366592-50367928	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr13:50366541-50367836	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr13:50366579-50367288	A549	lung:	n/a	n/a
40	CTCF	chr13:50366716-50366947	HepG2	liver:	n/a	n/a
41	CTCF	chr13:50366740-50366890	AG10803	skin:	n/a	n/a
42	CTCF	chr13:50366760-50366910	GM12872	blood:	n/a	n/a
43	CTCF	chr13:50366740-50366890	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr13:50366680-50366830	BE2_C	brain:	n/a	n/a
45	CTCF	chr13:50366740-50366890	GM12874	blood:	n/a	n/a
46	CTCF	chr13:50366780-50366930	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr13:50366708-50366893	GM10248	blood:	n/a	n/a
48	CTCF	chr13:50366700-50366850	GM12878	blood:	n/a	n/a
49	CTCF	chr13:50366708-50366898	GM13977	blood:	n/a	n/a
50	CTCF	chr13:50366760-50366910	SAEC	small airway:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50367057-50367107	H1-hESC	embryonic stem cell:	embryo
2	chr13:50366546-50366596	HRE	kidney:	n/a
3	chr13:50367279-50367329	LNCaP	prostate:	n/a
4	chr13:50367057-50367107	HCF	heart:	n/a
5	chr13:50367095-50367145	BJ	skin:	n/a
6	chr13:50367095-50367145	HL-60	blood:	n/a
7	chr13:50367114-50367164	BE2_C	brain:	n/a
8	chr13:50367279-50367329	GM19239	blood:	n/a
9	chr13:50367057-50367107	NB4	blood:	n/a
10	chr13:50366559-50366609	HNPCEpiC	eye:	n/a
11	chr13:50367064-50367114	HIPEpiC	eye:	n/a
12	chr13:50366648-50366698	PFSK-1	brain:	n/a
13	chr13:50367057-50367107	PrEC	prostate:	n/a
14	chr13:50367173-50367223	Hela-S3	cervix:	n/a
15	chr13:50367173-50367223	HCM	heart:	n/a
16	chr13:50367057-50367107	NHDF-neo	bronchial:	n/a
17	chr13:50367060-50367110	PFSK-1	brain:	n/a
18	chr13:50367114-50367164	GM19239	blood:	n/a
19	chr13:50367064-50367114	ovcar-3	ovarian:	n/a
20	chr13:50366546-50366596	GM06990	blood:	n/a
21	chr13:50367064-50367114	HPAEpiC	pulmonary alveolar:	n/a
22	chr13:50366648-50366698	AG09319	gingival:	n/a
23	chr13:50366648-50366698	NH-A	brain:	n/a
24	chr13:50367295-50367345	HPAEpiC	pulmonary alveolar:	n/a
25	chr13:50367279-50367329	PANC-1	pancreas:	n/a
26	chr13:50367057-50367107	GM19239	blood:	n/a
27	chr13:50367114-50367164	RPTEC	kidney:	n/a
28	chr13:50367064-50367114	HEK293	kidney:	embryo
29	chr13:50366648-50366698	HRE	kidney:	n/a
30	chr13:50366546-50366596	MCF-7	breast:	n/a
31	chr13:50367095-50367145	A549	lung:	n/a
32	chr13:50367114-50367164	BJ	skin:	n/a
33	chr13:50367173-50367223	IMR90	lung:	fetal
34	chr13:50367295-50367345	AG10803	skin:	n/a
35	chr13:50367114-50367164	MCF-7	breast:	n/a
36	chr13:50367173-50367223	GM19239	blood:	n/a
37	chr13:50366648-50366698	AG04450	lung:	fetal
38	chr13:50366559-50366609	HCT-116	colon:	n/a
39	chr13:50367064-50367114	HRCEpiC	kidney:	n/a
40	chr13:50367095-50367145	MCF10A-Er-Src	breast:	n/a
41	chr13:50366648-50366698	SKMC	muscle:	n/a
42	chr13:50367057-50367107	HUVEC	blood vessel:	n/a
43	chr13:50367279-50367329	SK-N-MC	brain:	n/a
44	chr13:50367295-50367345	MCF10A-Er-Src	breast:	n/a
45	chr13:50367095-50367145	ovcar-3	ovarian:	n/a
46	chr13:50367060-50367110	CMK	blood:	n/a
47	chr13:50366559-50366609	Hela-S3	cervix:	n/a
48	chr13:50367295-50367345	Caco-2	colon:	n/a
49	chr13:50366559-50366609	HRE	kidney:	n/a
50	chr13:50366546-50366596	HMEC	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:50263387..50265868-chr13:50365424..50368677,3	K562	blood:
2	chr13:50261767..50269137-chr13:50365068..50368535,12	MCF-7	breast:
3	chr12:57472055..57474451-chr13:50366783..50368850,2	K562	blood:
4	chr13:50365087..50367801-chr13:50569333..50572997,5	MCF-7	breast:
5	chr13:50366691..50367418-chr3:40350564..40351423,2	NB4	blood:
6	chr13:50278979..50281390-chr13:50365910..50368755,2	MCF-7	breast:
7	chr13:50242498..50244504-chr13:50366051..50367551,2	MCF-7	breast:
8	chr13:50262508..50268089-chr13:50363531..50368771,13	MCF-7	breast:
9	chr13:50365136..50367359-chr13:50509492..50511604,3	MCF-7	breast:
10	chr13:50366632..50367555-chr15:65588352..65589049,2	Hela-S3	cervix:
11	chr10:104210318..104210821-chr13:50367293..50367793,2	NB4	blood:
12	chr13:50263387..50266299-chr13:50365424..50368132,3	K562	blood:
13	chr13:50365172..50367900-chr13:50655465..50657230,2	K562	blood:
14	chr13:50366438..50367362-chr9:91925263..91926169,2	NB4	blood:
15	chr13:50366935..50367602-chr14:73524591..73525438,2	NB4	blood:
16	chr13:50367116..50367723-chr7:128170990..128171600,2	NB4	blood:

No data

Variant related genes	Relation type
KPNA3	TF binding region
KPNA3	CpG island
ENSG00000231607	chromatin interactions
ENSG00000123178	chromatin interactions
ENSG00000203547	chromatin interactions
ENSG00000119707	chromatin interactions
ENSG00000204977	chromatin interactions
ENSG00000102753	chromatin interactions
ENSG00000269609	chromatin interactions
ENSG00000123179	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000114784	chromatin interactions
ENSG00000176124	chromatin interactions
ENSG00000123975	chromatin interactions
ENSG00000264864	chromatin interactions
ENSG00000166881	chromatin interactions
ENSG00000273270	chromatin interactions

Extended variants
information (count: 48 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:48 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544446767	chr13:50366370-50366371	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs562741723	chr13:50366510-50366511	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs533475975	chr13:50366541-50366542	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs369465748	chr13:50366549-50366550	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs200563678	chr13:50366555-50366556	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs560589166	chr13:50366561-50366562	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs374104014	chr13:50366653-50366654	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs200365157	chr13:50366665-50366666	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs199509096	chr13:50366672-50366673	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs374334924	chr13:50366674-50366675	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs377544239	chr13:50366680-50366681	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs375322361	chr13:50366681-50366682	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs567760110	chr13:50366686-50366687	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs376163982	chr13:50366687-50366688	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs538338299	chr13:50366696-50366697	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs550028434	chr13:50366709-50366710	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs571451190	chr13:50366714-50366715	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs532345061	chr13:50366718-50366719	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs538803285	chr13:50366721-50366722	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs554127749	chr13:50366737-50366738	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs572197359	chr13:50366740-50366741	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs201124891	chr13:50366743-50366744	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs536251158	chr13:50366765-50366766	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs372727234	chr13:50366785-50366786	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs192550050	chr13:50366818-50366819	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs576135766	chr13:50366832-50366833	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs543095139	chr13:50366833-50366834	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs145162947	chr13:50366848-50366849	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs12870739	chr13:50366869-50366870	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs118042815	chr13:50366983-50366984	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
31	rs375862943	chr13:50367001-50367002	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
32	rs545169244	chr13:50367055-50367056	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
33	rs560844764	chr13:50367093-50367094	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs527940217	chr13:50367114-50367115	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs117601312	chr13:50367128-50367129	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs561103861	chr13:50367144-50367145	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs531876269	chr13:50367150-50367151	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs550313668	chr13:50367169-50367170	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs571738971	chr13:50367187-50367188	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
40	rs532348785	chr13:50367190-50367191	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs79318178	chr13:50367205-50367206	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs555772450	chr13:50367216-50367217	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
43	rs184841079	chr13:50367234-50367235	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
44	rs7319286	chr13:50367251-50367252	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs549029481	chr13:50367261-50367262	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs369557932	chr13:50367268-50367269	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs73194416	chr13:50367273-50367274	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs77901110	chr13:50367280-50367281	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50364000-50367600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr13:50364200-50367800	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr13:50364600-50367600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:50364600-50367800	Active TSS	Aorta	Aorta
5	chr13:50364600-50368000	Active TSS	H1 Cell Line	embryonic stem cell
6	chr13:50364600-50368000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr13:50364600-50368000	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr13:50364800-50366600	Active TSS	Right Atrium	heart
9	chr13:50364800-50367600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr13:50364800-50367600	Active TSS	Colonic Mucosa	Colon
11	chr13:50364800-50367800	Active TSS	A549	lung
12	chr13:50364800-50368000	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr13:50365000-50367400	Active TSS	Cortex derived primary cultured neurospheres	brain
14	chr13:50365000-50367400	Active TSS	Fetal Intestine Large	intestine
15	chr13:50365000-50367400	Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr13:50365000-50367400	Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr13:50365000-50367400	Active TSS	HMEC	breast
18	chr13:50365000-50367400	Active TSS	NHLF	lung
19	chr13:50365000-50367600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr13:50365000-50367600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr13:50365000-50367600	Active TSS	Fetal Intestine Small	intestine
22	chr13:50365000-50367600	Active TSS	Fetal Kidney	kidney
23	chr13:50365000-50367600	Active TSS	GM12878-XiMat	blood
24	chr13:50365000-50367600	Active TSS	K562	blood
25	chr13:50365000-50367600	Active TSS	NHDF-Ad	bronchial
26	chr13:50365000-50367800	Active TSS	HSMMtube	muscle
27	chr13:50365000-50368000	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr13:50365000-50368000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr13:50365200-50367400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr13:50365200-50367400	Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr13:50365200-50367400	Active TSS	Muscle Satellite Cultured Cells	--
32	chr13:50365200-50367400	Active TSS	Fetal Thymus	thymus
33	chr13:50365200-50367400	Active TSS	HSMM	muscle
34	chr13:50365200-50367600	Active TSS	Fetal Muscle Trunk	muscle
35	chr13:50365200-50367600	Active TSS	Fetal Muscle Leg	muscle
36	chr13:50365200-50367600	Active TSS	Placenta	Placenta
37	chr13:50365200-50367600	Active TSS	Psoas Muscle	Psoas
38	chr13:50365200-50367600	Active TSS	Stomach Mucosa	stomach
39	chr13:50365200-50367800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr13:50365200-50368000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr13:50365200-50368000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr13:50365200-50368000	Active TSS	Right Ventricle	heart
43	chr13:50365400-50366600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
44	chr13:50365400-50367400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr13:50365400-50367400	Active TSS	Stomach Smooth Muscle	stomach
46	chr13:50365400-50367400	Active TSS	Hela-S3	cervix
47	chr13:50365400-50367400	Active TSS	Osteobl	bone
48	chr13:50365400-50367600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr13:50365400-50367600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr13:50365400-50367600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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