Variant report

Variant	esv33119
Chromosome Location	chr14:65421491-65434429
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:376)
CpG islands
(count:123)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr14:65427450-65427452	K562	blood:	n/a	n/a
2	BHLHE40	chr14:65426924-65426991	K562	blood:	n/a	chr14:65426948-65426969 chr14:65426953-65426962 chr14:65426954-65426963 chr14:65426955-65426964 chr14:65426952-65426965 chr14:65426954-65426963
3	CEBPB	chr14:65433346-65434170	MCF-7	breast:	n/a	n/a
4	CHD2	chr14:65427459-65427870	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr14:65430490-65430594	GM10266	blood:	n/a	n/a
6	CTCF	chr14:65427497-65427707	MCF-7	breast:	n/a	chr14:65427579-65427592
7	CTCF	chr14:65430520-65430670	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr14:65426020-65426170	AoAF	blood vessel:	n/a	n/a
9	CTCF	chr14:65426009-65426083	GM12891	blood:	n/a	n/a
10	CTCF	chr14:65427520-65427670	HA-sp	spinal cord:	n/a	chr14:65427579-65427592
11	CTCF	chr14:65427948-65428010	Pancreas_OC	pancreas:	n/a	n/a
12	CTCF	chr14:65427540-65427690	GM12868	blood:	n/a	chr14:65427579-65427592
13	CTCF	chr14:65427548-65427625	HUVEC	blood vessel:	n/a	chr14:65427579-65427592
14	CTCF	chr14:65430420-65430570	GM12872	blood:	n/a	n/a
15	CTCF	chr14:65427560-65427710	AG09319	gingival:	n/a	chr14:65427579-65427592
16	CTCF	chr14:65427518-65427661	GM12878	blood:	n/a	chr14:65427579-65427592
17	CTCF	chr14:65427540-65427690	HEEpiC	esophagus:	n/a	chr14:65427579-65427592
18	CTCF	chr14:65427509-65427595	LNCaP	prostate:	n/a	chr14:65427579-65427592
19	CTCF	chr14:65427600-65427750	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr14:65427520-65427670	AG04449	skin:	n/a	chr14:65427579-65427592
21	CTCF	chr14:65427513-65427647	A549	lung:	n/a	chr14:65427579-65427592
22	CTCF	chr14:65430318-65430640	K562	blood:	n/a	n/a
23	CTCF	chr14:65427480-65427630	GM12872	blood:	n/a	chr14:65427579-65427592
24	CTCF	chr14:65427490-65427730	GM12878	blood:	n/a	chr14:65427579-65427592
25	CTCF	chr14:65430450-65430586	NHEK	skin:	n/a	n/a
26	CTCF	chr14:65427436-65427706	K562	blood:	n/a	chr14:65427579-65427592
27	CTCF	chr14:65430400-65430550	HMF	breast:	n/a	n/a
28	CTCF	chr14:65430440-65430590	A549	lung:	n/a	n/a
29	CTCF	chr14:65427536-65427659	Gliobla	brain:	n/a	chr14:65427579-65427592
30	CTCF	chr14:65430560-65430710	RPTEC	kidney:	n/a	n/a
31	CTCF	chr14:65426020-65426170	NB4	blood:	n/a	n/a
32	CTCF	chr14:65430460-65430610	MCF-7	breast:	n/a	n/a
33	CTCF	chr14:65430429-65430625	GM12878	blood:	n/a	n/a
34	CTCF	chr14:65427500-65427650	GM06990	blood:	n/a	chr14:65427579-65427592
35	CTCF	chr14:65427493-65427705	GM12892	blood:	n/a	chr14:65427579-65427592
36	CTCF	chr14:65427440-65427590	GM12873	blood:	n/a	n/a
37	CTCF	chr14:65430260-65430410	GM12865	blood:	n/a	n/a
38	CTCF	chr14:65430420-65430570	GM12866	blood:	n/a	n/a
39	CTCF	chr14:65427520-65427670	HAc	cerebellar:	n/a	chr14:65427579-65427592
40	CTCF	chr14:65427500-65427650	HCFaa	heart:	n/a	chr14:65427579-65427592
41	CTCF	chr14:65427540-65427690	SAEC	small airway:	n/a	chr14:65427579-65427592
42	CTCF	chr14:65427383-65428058	H1-hESC	embryonic stem cell:	n/a	chr14:65427579-65427592
43	CTCF	chr14:65427420-65427570	RPTEC	kidney:	n/a	n/a
44	CTCF	chr14:65427579-65427658	Fibrobl	skin:	n/a	chr14:65427579-65427592
45	CTCF	chr14:65430480-65430630	K562	blood:	n/a	n/a
46	CTCF	chr14:65427900-65428050	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr14:65426060-65426210	HepG2	liver:	n/a	n/a
48	CTCF	chr14:65430497-65430566	Gliobla	brain:	n/a	n/a
49	CTCF	chr14:65430394-65430635	GM12891	blood:	n/a	n/a
50	CTCF	chr14:65427962-65428012	GM19238	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65427659-65427709	NT2-D1	testis:	n/a
2	chr14:65427659-65427709	NT2-D1	testis:	n/a
3	chr14:65427659-65427709	A549	lung:	n/a
4	chr14:65421784-65421834	HL-60	blood:	n/a
5	chr14:65427659-65427709	RPTEC	kidney:	n/a
6	chr14:65427659-65427709	CMK	blood:	n/a
7	chr14:65427659-65427709	Caco-2	colon:	n/a
8	chr14:65421784-65421834	Hepatocyte	liver:	n/a
9	chr14:65427659-65427709	SK-N-SH_RA	brain:	n/a
10	chr14:65427659-65427709	HEK293	kidney:	embryo
11	chr14:65427659-65427709	SAEC	small airway:	n/a
12	chr14:65427659-65427709	NB4	blood:	n/a
13	chr14:65427659-65427709	GM19239	blood:	n/a
14	chr14:65421784-65421834	HPAEpiC	pulmonary alveolar:	n/a
15	chr14:65421784-65421834	SK-N-SH_RA	brain:	n/a
16	chr14:65421784-65421834	PFSK-1	brain:	n/a
17	chr14:65427659-65427709	GM06990	blood:	n/a
18	chr14:65427659-65427709	HRCEpiC	kidney:	n/a
19	chr14:65427659-65427709	HMEC	breast:	n/a
20	chr14:65421784-65421834	A549	lung:	n/a
21	chr14:65421784-65421834	NB4	blood:	n/a
22	chr14:65427659-65427709	Hepatocyte	liver:	n/a
23	chr14:65421784-65421834	NHDF-neo	bronchial:	n/a
24	chr14:65421784-65421834	H1-hESC	embryonic stem cell:	embryo
25	chr14:65427659-65427709	HRE	kidney:	n/a
26	chr14:65427659-65427709	ovcar-3	ovarian:	n/a
27	chr14:65421784-65421834	AG04449	skin:	fetal
28	chr14:65427659-65427709	AG04449	skin:	fetal
29	chr14:65421784-65421834	GM19239	blood:	n/a
30	chr14:65427659-65427709	H1-hESC	embryonic stem cell:	embryo
31	chr14:65421784-65421834	IMR90	lung:	fetal
32	chr14:65427659-65427709	HUVEC	blood vessel:	n/a
33	chr14:65421784-65421834	LNCaP	prostate:	n/a
34	chr14:65421784-65421834	HCT-116	colon:	n/a
35	chr14:65427659-65427709	HCF	heart:	n/a
36	chr14:65427659-65427709	ECC-1	luminal epithelium:	n/a
37	chr14:65427659-65427709	Hela-S3	cervix:	n/a
38	chr14:65421784-65421834	BJ	skin:	n/a
39	chr14:65427659-65427709	IMR90	lung:	fetal
40	chr14:65421784-65421834	AG09319	gingival:	n/a
41	chr14:65421784-65421834	ovcar-3	ovarian:	n/a
42	chr14:65421784-65421834	HEK293	kidney:	embryo
43	chr14:65421784-65421834	HepG2	liver:	n/a
44	chr14:65421784-65421834	BE2_C	brain:	n/a
45	chr14:65421784-65421834	SK-N-SH	brain:	n/a
46	chr14:65421784-65421834	NHBE	bronchial:	n/a
47	chr14:65427659-65427709	SKMC	muscle:	n/a
48	chr14:65427659-65427709	PFSK-1	brain:	n/a
49	chr14:65427659-65427709	AG10803	skin:	n/a
50	chr14:65421784-65421834	GM12891	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:65409449..65411345-chr14:65418260..65421533,3	MCF-7	breast:
2	chr14:65424121..65427590-chr14:65430879..65434090,3	MCF-7	breast:
3	chr14:65408109..65412260-chr14:65433845..65436986,6	MCF-7	breast:
4	chr14:65427868..65430496-chr14:65442543..65444279,2	MCF-7	breast:
5	chr14:65415735..65418064-chr14:65418807..65421614,2	MCF-7	breast:
6	chr14:65380772..65382817-chr14:65433113..65436626,3	MCF-7	breast:
7	chr14:65379731..65383710-chr14:65424558..65427647,5	MCF-7	breast:
8	chr14:65221708..65223520-chr14:65425560..65427904,2	MCF-7	breast:
9	chr14:65433037..65434817-chr14:65446366..65448711,2	MCF-7	breast:
10	chr14:65428039..65432050-chr14:65432116..65435145,5	MCF-7	breast:
11	chr14:65432320..65436010-chr14:65436140..65441261,16	MCF-7	breast:
12	chr14:65380020..65382161-chr14:65421775..65424244,2	MCF-7	breast:
13	chr14:65422306..65424138-chr14:65425780..65427345,2	K562	blood:
14	chr14:65407129..65411344-chr14:65424634..65427852,4	MCF-7	breast:
15	chr14:65426410..65429284-chr14:65447447..65450019,2	MCF-7	breast:
16	chr14:65428039..65432050-chr14:65432116..65435145,5	MCF-7	breast:
17	chr14:65380807..65382570-chr14:65419701..65422531,2	MCF-7	breast:
18	chr14:65422306..65424138-chr14:65425780..65427345,2	K562	blood:
19	chr14:65381132..65383613-chr14:65427775..65429554,2	MCF-7	breast:
20	chr14:65409296..65411152-chr14:65426645..65429491,2	MCF-7	breast:
21	chr14:65422596..65425109-chr14:65437838..65439509,2	MCF-7	breast:
22	chr14:65433002..65436926-chr14:65451032..65453686,3	MCF-7	breast:
23	chr14:65426546..65429390-chr14:65452046..65455184,4	MCF-7	breast:

No data

Variant related genes	Relation type
RAB15	TF binding region
RAB15	CpG island
ENSG00000257365	chromatin interactions
ENSG00000176153	chromatin interactions
ENSG00000125954	chromatin interactions
ENSG00000139998	chromatin interactions
ENSG00000258289	chromatin interactions

Extended variants
information (count: 476 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11621450	chr14:65421516-65421517	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369706083	chr14:65421527-65421528	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs140347723	chr14:65421602-65421603	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs574455626	chr14:65421614-65421615	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs374092202	chr14:65421700-65421701	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs115539980	chr14:65421701-65421702	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs556583273	chr14:65421742-65421743	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs114582534	chr14:65421747-65421748	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs545727270	chr14:65421751-65421752	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs559236821	chr14:65421775-65421776	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546617763	chr14:65421785-65421786	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs566418059	chr14:65421787-65421788	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs55899531	chr14:65421810-65421811	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs541663509	chr14:65421832-65421833	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs561882689	chr14:65421852-65421853	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs150321771	chr14:65421944-65421945	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs550295426	chr14:65421950-65421951	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs78191394	chr14:65421959-65421960	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs532537801	chr14:65421960-65421961	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552573212	chr14:65421961-65421962	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs72728209	chr14:65422015-65422016	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs535282458	chr14:65422074-65422075	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs10134326	chr14:65422086-65422087	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs568633179	chr14:65422113-65422114	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs75724268	chr14:65422212-65422213	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs370753657	chr14:65422262-65422263	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs4902349	chr14:65422340-65422341	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs4902350	chr14:65422365-65422366	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs539066800	chr14:65422375-65422376	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs76815586	chr14:65422401-65422402	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs200511733	chr14:65422457-65422458	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs4902351	chr14:65422491-65422492	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs542098707	chr14:65422583-65422584	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561781272	chr14:65422601-65422602	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs575377134	chr14:65422616-65422617	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs942625	chr14:65422642-65422643	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs181743968	chr14:65422652-65422653	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs186359823	chr14:65422654-65422655	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs144927630	chr14:65422694-65422695	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs559688137	chr14:65422750-65422751	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs190324067	chr14:65422776-65422777	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs548840390	chr14:65422785-65422786	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs4902352	chr14:65422796-65422797	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs149060529	chr14:65422811-65422812	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs145740770	chr14:65422840-65422841	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs138686178	chr14:65422842-65422843	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs539106815	chr14:65422849-65422850	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs552735127	chr14:65422882-65422883	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs182187061	chr14:65422951-65422952	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs535413776	chr14:65422990-65422991	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	17440070	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65393400-65422200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr14:65399000-65428000	Weak transcription	NHLF	lung
3	chr14:65401400-65432200	Weak transcription	HUVEC	blood vessel
4	chr14:65401600-65435000	Weak transcription	NH-A	brain
5	chr14:65406600-65438000	Weak transcription	Fetal Kidney	kidney
6	chr14:65409600-65428400	Strong transcription	Fetal Stomach	stomach
7	chr14:65410200-65425200	Weak transcription	HMEC	breast
8	chr14:65410400-65425400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr14:65410600-65421600	Weak transcription	Pancreas	Pancrea
10	chr14:65411000-65423200	Weak transcription	NHEK	skin
11	chr14:65411000-65437200	Weak transcription	Fetal Lung	lung
12	chr14:65411200-65425400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr14:65411200-65427600	Weak transcription	A549	lung
14	chr14:65411200-65435000	Weak transcription	Primary hematopoietic stem cells	blood
15	chr14:65411400-65425200	Weak transcription	Stomach Mucosa	stomach
16	chr14:65411400-65435000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:65411400-65438000	Weak transcription	Small Intestine	intestine
18	chr14:65412400-65438000	Weak transcription	Brain Substantia Nigra	brain
19	chr14:65413000-65426200	Weak transcription	Primary B cells from peripheral blood	blood
20	chr14:65413600-65423400	Strong transcription	Thymus	Thymus
21	chr14:65414200-65422800	Strong transcription	Spleen	Spleen
22	chr14:65414800-65424000	Weak transcription	HSMM	muscle
23	chr14:65414800-65425200	Strong transcription	Primary T cells from cord blood	blood
24	chr14:65415400-65428000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr14:65415400-65432400	Weak transcription	Ovary	ovary
26	chr14:65415400-65438200	Weak transcription	Aorta	Aorta
27	chr14:65415600-65427400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr14:65415600-65437600	Weak transcription	Colonic Mucosa	Colon
29	chr14:65415800-65422000	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr14:65415800-65427200	Strong transcription	Fetal Intestine Small	intestine
31	chr14:65415800-65427800	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr14:65415800-65427800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr14:65416000-65423400	Weak transcription	Fetal Thymus	thymus
34	chr14:65416000-65424000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr14:65416000-65425600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr14:65416000-65427400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr14:65416200-65421600	Weak transcription	HepG2	liver
38	chr14:65416200-65424600	Weak transcription	Primary B cells from cord blood	blood
39	chr14:65417000-65423600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr14:65417400-65426200	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr14:65417400-65426600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:65417600-65437200	Weak transcription	Adipose Nuclei	Adipose
43	chr14:65417800-65437600	Weak transcription	Rectal Smooth Muscle	rectum
44	chr14:65418000-65426600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:65418200-65421600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr14:65418200-65421800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr14:65418200-65428200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr14:65418200-65435400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr14:65418400-65424000	Weak transcription	Esophagus	oesophagus
50	chr14:65418400-65427400	Weak transcription	Primary T cells fromperipheralblood	blood

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