Variant report

Variant	esv3521596
Chromosome Location	chr13:95244837-95249504
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:483)
CpG islands
(count:732)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95248619-95248622	K562	blood:	n/a	n/a
2	ARID3A	chr13:95248325-95248633	HepG2	liver:	n/a	n/a
3	ATF2	chr13:95248125-95248762	GM12878	blood:	n/a	n/a
4	ATF2	chr13:95248225-95248680	GM12878	blood:	n/a	n/a
5	ATF3	chr13:95248222-95248650	HepG2	liver:	n/a	n/a
6	ATF3	chr13:95248249-95248522	GM12878	blood:	n/a	n/a
7	ATF3	chr13:95248194-95248815	GM12878	blood:	n/a	n/a
8	ATF3	chr13:95248210-95248634	K562	blood:	n/a	n/a
9	ATF3	chr13:95248149-95248623	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr13:95248221-95248684	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr13:95248214-95248644	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr13:95247943-95248770	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:95247337-95247432	GM12878	blood:	n/a	n/a
14	BHLHE40	chr13:95247900-95248769	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:95248282-95248736	K562	blood:	n/a	n/a
16	BRCA1	chr13:95248019-95248732	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr13:95248050-95248670	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr13:95248285-95248689	HepG2	liver:	n/a	n/a
19	BRCA1	chr13:95248303-95248654	GM12878	blood:	n/a	n/a
20	CCNT2	chr13:95248258-95248681	K562	blood:	n/a	n/a
21	CEBPB	chr13:95244619-95244897	K562	blood:	n/a	n/a
22	CEBPB	chr13:95248025-95248798	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr13:95248101-95248745	GM12878	blood:	n/a	n/a
24	CEBPD	chr13:95248209-95248773	HepG2	liver:	n/a	n/a
25	CHD1	chr13:95247736-95248435	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr13:95247742-95248805	GM12878	blood:	n/a	n/a
27	CHD2	chr13:95248078-95248790	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr13:95247696-95248746	GM12878	blood:	n/a	n/a
29	CHD2	chr13:95247539-95247694	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr13:95247989-95248661	K562	blood:	n/a	n/a
31	CHD2	chr13:95248331-95248800	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr13:95248299-95248666	HepG2	liver:	n/a	n/a
33	CREB1	chr13:95248132-95248837	HepG2	liver:	n/a	n/a
34	CREB1	chr13:95248253-95248619	A549	lung:	n/a	n/a
35	CREB1	chr13:95248294-95248546	A549	lung:	n/a	n/a
36	CTCF	chr13:95248500-95248650	AG09319	gingival:	n/a	n/a
37	CTCF	chr13:95248420-95248570	HPF	lung:	n/a	n/a
38	CTCF	chr13:95248500-95248591	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr13:95248500-95248650	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr13:95248500-95248650	AG04449	skin:	n/a	n/a
41	CTCF	chr13:95248500-95248650	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr13:95248400-95248550	HPF	lung:	n/a	n/a
43	CTCF	chr13:95248660-95248810	HRE	kidney:	n/a	n/a
44	CTCF	chr13:95248480-95248630	GM12878	blood:	n/a	n/a
45	CTCF	chr13:95248500-95248650	HMF	breast:	n/a	n/a
46	CTCF	chr13:95248560-95248710	GM12865	blood:	n/a	n/a
47	CTCF	chr13:95248520-95248670	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr13:95248423-95248637	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr13:95246800-95246950	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr13:95248500-95248650	AG10803	skin:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95248662-95248712	GM12891	blood:	n/a
2	chr13:95245226-95245276	NHDF-neo	bronchial:	n/a
3	chr13:95248671-95248721	H1-hESC	embryonic stem cell:	embryo
4	chr13:95248439-95248489	U87	brain:	n/a
5	chr13:95248662-95248712	IMR90	lung:	fetal
6	chr13:95248662-95248712	SK-N-SH	brain:	n/a
7	chr13:95248882-95248932	PANC-1	pancreas:	n/a
8	chr13:95248671-95248721	K562	blood:	n/a
9	chr13:95248351-95248401	HPAEpiC	pulmonary alveolar:	n/a
10	chr13:95248888-95248938	HepG2	liver:	n/a
11	chr13:95248671-95248721	NHDF-neo	bronchial:	n/a
12	chr13:95248771-95248821	BJ	skin:	n/a
13	chr13:95248671-95248721	A549	lung:	n/a
14	chr13:95248351-95248401	PFSK-1	brain:	n/a
15	chr13:95248351-95248401	PANC-1	pancreas:	n/a
16	chr13:95248662-95248712	HCT-116	colon:	n/a
17	chr13:95248671-95248721	AG04450	lung:	fetal
18	chr13:95248351-95248401	GM12891	blood:	n/a
19	chr13:95248547-95248597	MCF10A-Er-Src	breast:	n/a
20	chr13:95248662-95248712	ECC-1	luminal epithelium:	n/a
21	chr13:95248457-95248507	HRE	kidney:	n/a
22	chr13:95248351-95248401	H1-hESC	embryonic stem cell:	embryo
23	chr13:95245226-95245276	IMR90	lung:	fetal
24	chr13:95248247-95248297	ProgFib	skin:	n/a
25	chr13:95248439-95248489	HRPEpiC	eye:	n/a
26	chr13:95245226-95245276	AG04449	skin:	fetal
27	chr13:95248671-95248721	NHBE	bronchial:	n/a
28	chr13:95248882-95248932	ProgFib	skin:	n/a
29	chr13:95248457-95248507	HEK293	kidney:	embryo
30	chr13:95248247-95248297	HMEC	breast:	n/a
31	chr13:95248247-95248297	HRE	kidney:	n/a
32	chr13:95248439-95248489	GM06990	blood:	n/a
33	chr13:95248888-95248938	NH-A	brain:	n/a
34	chr13:95248247-95248297	NT2-D1	testis:	n/a
35	chr13:95248771-95248821	K562	blood:	n/a
36	chr13:95248882-95248932	HRPEpiC	eye:	n/a
37	chr13:95248439-95248489	HRCEpiC	kidney:	n/a
38	chr13:95248247-95248297	HL-60	blood:	n/a
39	chr13:95248547-95248597	HRPEpiC	eye:	n/a
40	chr13:95248455-95248505	Jurkat	blood:	n/a
41	chr13:95248247-95248297	PANC-1	pancreas:	n/a
42	chr13:95248247-95248297	RPTEC	kidney:	n/a
43	chr13:95248457-95248507	SK-N-SH	brain:	n/a
44	chr13:95248547-95248597	AG04449	skin:	fetal
45	chr13:95248662-95248712	HEK293	kidney:	embryo
46	chr13:95248888-95248938	HCT-116	colon:	n/a
47	chr13:95248457-95248507	NHBE	bronchial:	n/a
48	chr13:95248455-95248505	NT2-D1	testis:	n/a
49	chr13:95248247-95248297	PrEC	prostate:	n/a
50	chr13:95248771-95248821	ProgFib	skin:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:95213304..95215332-chr13:95243591..95245923,2	K562	blood:
2	chr13:95247805..95248577-chr20:30192835..30193557,2	Hela-S3	cervix:
3	chr13:95248444..95249010-chr19:47291436..47292069,2	NB4	blood:
4	chr13:95247274..95249727-chr13:95251841..95255221,4	MCF-7	breast:
5	chr12:120728948..120729873-chr13:95247808..95248542,2	Hela-S3	cervix:
6	chr13:95247949..95248595-chr17:2206672..2207436,2	NB4	blood:
7	chr13:95239604..95244958-chr13:95245816..95249752,6	K562	blood:
8	chr11:62358993..62359769-chr13:95247964..95248584,2	NB4	blood:
9	chr13:95246267..95250128-chr13:95251933..95256020,6	MCF-7	breast:
10	chr13:95242784..95245986-chr13:95246161..95249973,6	MCF-7	breast:
11	chr13:95242101..95243874-chr13:95245900..95247690,2	K562	blood:
12	chr13:95242026..95244794-chr13:95245664..95248411,3	MCF-7	breast:
13	chr13:95245952..95249992-chr13:95252491..95255739,5	K562	blood:

No data

Variant related genes	Relation type
GPR180	TF binding region
TGDS	TF binding region
GPR180	CpG island
TGDS	CpG island
ENSG00000070366	chromatin interactions
ENSG00000255508	chromatin interactions
ENSG00000088451	chromatin interactions
ENSG00000149016	chromatin interactions
ENSG00000105281	chromatin interactions
ENSG00000167720	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000152749	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 177 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:177 , 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	rs531507619	chr13:95244855-95244856	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs550926036	chr13:95244869-95244870	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537150856	chr13:95244989-95244990	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567568397	chr13:95245000-95245001	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530144780	chr13:95245140-95245141	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188546236	chr13:95245185-95245186	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs193061279	chr13:95245186-95245187	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs147860116	chr13:95245224-95245225	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552363945	chr13:95245253-95245254	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs569489284	chr13:95245271-95245272	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs538170749	chr13:95245285-95245286	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555277225	chr13:95245322-95245323	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs184033149	chr13:95245323-95245324	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533829653	chr13:95245387-95245388	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77980634	chr13:95245428-95245429	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs187806769	chr13:95245431-95245432	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545972618	chr13:95245558-95245559	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs539381429	chr13:95245578-95245579	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562697605	chr13:95245585-95245586	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs567853806	chr13:95245619-95245620	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576253366	chr13:95245708-95245709	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552801451	chr13:95245730-95245731	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs201371929	chr13:95245761-95245762	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541746220	chr13:95245800-95245801	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs9561639	chr13:95245811-95245812	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562046786	chr13:95245872-95245873	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs530039208	chr13:95245914-95245915	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536474626	chr13:95245963-95245964	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs192373298	chr13:95245978-95245979	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560174510	chr13:95246001-95246002	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532473847	chr13:95246036-95246037	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs144478268	chr13:95246151-95246152	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs148461439	chr13:95246155-95246156	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112229637	chr13:95246166-95246167	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs34322805	chr13:95246168-95246169	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs538460217	chr13:95246199-95246200	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140382184	chr13:95246205-95246206	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs568773247	chr13:95246269-95246270	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs533726145	chr13:95246331-95246332	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183629205	chr13:95246342-95246343	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576982754	chr13:95246390-95246391	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1112370	chr13:95246440-95246441	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs556259812	chr13:95246459-95246460	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150355822	chr13:95246466-95246467	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542057792	chr13:95246482-95246483	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116277595	chr13:95246545-95246546	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572314449	chr13:95246547-95246548	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187987811	chr13:95246548-95246549	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs75716439	chr13:95246551-95246552	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532403444	chr13:95246592-95246593	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD

Chromatin state (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95219600-95245600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr13:95221400-95245800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr13:95222000-95245000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr13:95222000-95247200	Weak transcription	Fetal Brain Male	brain
5	chr13:95222200-95245000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr13:95222200-95245200	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr13:95223000-95245800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr13:95224200-95246400	Weak transcription	Fetal Heart	heart
9	chr13:95224200-95246400	Weak transcription	Stomach Mucosa	stomach
10	chr13:95225000-95247400	Weak transcription	Fetal Brain Female	brain
11	chr13:95226000-95245800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr13:95226200-95245400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr13:95226800-95246800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr13:95233000-95246600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr13:95233200-95246600	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr13:95233200-95247000	Weak transcription	Brain Cingulate Gyrus	brain
17	chr13:95233400-95247600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr13:95234400-95246800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr13:95234400-95246800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr13:95234400-95247000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr13:95234600-95247200	Weak transcription	Lung	lung
22	chr13:95234800-95246400	Weak transcription	Colon Smooth Muscle	Colon
23	chr13:95235000-95246800	Weak transcription	Spleen	Spleen
24	chr13:95235200-95246400	Weak transcription	Brain Anterior Caudate	brain
25	chr13:95235200-95246600	Weak transcription	Psoas Muscle	Psoas
26	chr13:95235200-95246800	Weak transcription	Right Ventricle	heart
27	chr13:95235200-95247000	Weak transcription	Ovary	ovary
28	chr13:95235200-95247400	Weak transcription	Gastric	stomach
29	chr13:95235400-95246400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr13:95235400-95246400	Weak transcription	Brain Hippocampus Middle	brain
31	chr13:95235600-95246800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr13:95235600-95246800	Weak transcription	Pancreas	Pancrea
33	chr13:95235600-95247000	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr13:95235600-95247400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr13:95235600-95247400	Weak transcription	Aorta	Aorta
36	chr13:95235600-95247400	Weak transcription	HSMMtube	muscle
37	chr13:95236600-95246400	Weak transcription	Brain Angular Gyrus	brain
38	chr13:95236600-95246600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr13:95237000-95246000	Weak transcription	A549	lung
40	chr13:95237000-95246400	Weak transcription	NHLF	lung
41	chr13:95237200-95245800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:95237600-95246600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr13:95237600-95246800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr13:95237800-95246400	Weak transcription	Primary hematopoietic stem cells	blood
45	chr13:95238000-95246800	Weak transcription	Left Ventricle	heart
46	chr13:95239200-95246400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr13:95240200-95245400	Strong transcription	Fetal Intestine Large	intestine
48	chr13:95240400-95245400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr13:95240600-95245400	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr13:95240800-95245200	Strong transcription	Rectal Mucosa Donor 29	rectum

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