Variant report

Variant	esv3358491
Chromosome Location	chr14:104173249-104175747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:158)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:158 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:104175260-104175410	HMEC	breast:	n/a	chr14:104175362-104175375 chr14:104175361-104175382 chr14:104175359-104175377
2	CTCF	chr14:104175280-104175430	BE2_C	brain:	n/a	chr14:104175362-104175375 chr14:104175361-104175382 chr14:104175359-104175377
3	CTCF	chr14:104174240-104174390	HCPEpiC	choroid plexus:	n/a	chr14:104174342-104174355 chr14:104174347-104174355
4	CTCF	chr14:104174200-104174350	HMEC	breast:	n/a	n/a
5	CTCF	chr14:104175333-104175401	NHEK	skin:	n/a	chr14:104175362-104175375 chr14:104175361-104175382 chr14:104175359-104175377
6	CTCF	chr14:104173860-104174010	NHDF-neo	bronchial:	n/a	n/a
7	CTCF	chr14:104174300-104174450	AG04449	skin:	n/a	chr14:104174342-104174355 chr14:104174347-104174355
8	CTCF	chr14:104174020-104174170	BE2_C	brain:	n/a	n/a
9	CTCF	chr14:104174060-104174210	NHDF-neo	bronchial:	n/a	n/a
10	CTCF	chr14:104175320-104175451	LNCaP	prostate:	n/a	chr14:104175362-104175375 chr14:104175361-104175382 chr14:104175359-104175377
11	CTCF	chr14:104174240-104174390	NHEK	skin:	n/a	chr14:104174342-104174355 chr14:104174347-104174355
12	CTCF	chr14:104174314-104174340	GM10248	blood:	n/a	n/a
13	HMGN3	chr14:104175425-104175665	K562	blood:	n/a	chr14:104175633-104175640
14	POLR2A	chr14:104174161-104174523	A549	lung:	n/a	n/a
15	POLR2A	chr14:104173289-104173714	A549	lung:	n/a	n/a
16	POLR2A	chr14:104174981-104175878	GM12891	blood:	n/a	n/a
17	POLR2A	chr14:104173762-104174854	HL-60	blood:	n/a	n/a
18	POLR2A	chr14:104173365-104173711	MCF-7	breast:	n/a	n/a
19	POLR2A	chr14:104174685-104174889	MCF-7	breast:	n/a	n/a
20	POLR2A	chr14:104174963-104175735	U87	brain:	n/a	n/a
21	POLR2A	chr14:104175062-104175262	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr14:104173268-104173756	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr14:104161532-104176510	SK-N-MC	brain:	n/a	n/a
24	POLR2A	chr14:104173947-104174861	GM12892	blood:	n/a	n/a
25	POLR2A	chr14:104174138-104174477	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr14:104174948-104175259	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr14:104173114-104173679	GM12891	blood:	n/a	n/a
28	POLR2A	chr14:104173401-104173756	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr14:104175117-104175275	HepG2	liver:	n/a	n/a
30	POLR2A	chr14:104175397-104175567	A549	lung:	n/a	n/a
31	POLR2A	chr14:104175141-104175308	GM12878	blood:	n/a	n/a
32	POLR2A	chr14:104173368-104173572	HCT-116	colon:	n/a	n/a
33	POLR2A	chr14:104173272-104173278	K562	blood:	n/a	n/a
34	POLR2A	chr14:104174882-104174893	K562	blood:	n/a	n/a
35	POLR2A	chr14:104173473-104174872	GM18951	blood:	n/a	n/a
36	POLR2A	chr14:104175240-104175998	GM12892	blood:	n/a	n/a
37	POLR2A	chr14:104173334-104173483	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr14:104174107-104174595	HepG2	liver:	n/a	n/a
39	POLR2A	chr14:104173847-104173862	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr14:104174068-104174133	GM12878	blood:	n/a	n/a
41	POLR2A	chr14:104175024-104175626	GM12878	blood:	n/a	n/a
42	POLR2A	chr14:104173845-104174885	GM12878	blood:	n/a	n/a
43	POLR2A	chr14:104175225-104175612	GM12891	blood:	n/a	n/a
44	POLR2A	chr14:104172912-104173627	A549	lung:	n/a	n/a
45	POLR2A	chr14:104173682-104174175	U87	brain:	n/a	n/a
46	POLR2A	chr14:104173297-104173664	GM12891	blood:	n/a	n/a
47	POLR2A	chr14:104173845-104173863	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr14:104175217-104175243	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr14:104174159-104174190	GM12878	blood:	n/a	n/a
50	POLR2A	chr14:104174982-104175188	ECC-1	luminal epithelium:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104173299-104173349	ECC-1	luminal epithelium:	n/a
2	chr14:104173299-104173349	AG04450	lung:	fetal
3	chr14:104173299-104173349	NHBE	bronchial:	n/a
4	chr14:104175555-104175605	PANC-1	pancreas:	n/a
5	chr14:104173299-104173349	MCF10A-Er-Src	breast:	n/a
6	chr14:104173299-104173349	HCPEpiC	choroid plexus:	n/a
7	chr14:104173299-104173349	HNPCEpiC	eye:	n/a
8	chr14:104175555-104175605	PFSK-1	brain:	n/a
9	chr14:104173299-104173349	HRCEpiC	kidney:	n/a
10	chr14:104173299-104173349	HIPEpiC	eye:	n/a
11	chr14:104173299-104173349	IMR90	lung:	fetal
12	chr14:104173299-104173349	K562	blood:	n/a
13	chr14:104175555-104175605	SAEC	small airway:	n/a
14	chr14:104173299-104173349	U87	brain:	n/a
15	chr14:104173299-104173349	ovcar-3	ovarian:	n/a
16	chr14:104175555-104175605	HRCEpiC	kidney:	n/a
17	chr14:104175555-104175605	ECC-1	luminal epithelium:	n/a
18	chr14:104173299-104173349	HL-60	blood:	n/a
19	chr14:104173299-104173349	SK-N-MC	brain:	n/a
20	chr14:104173299-104173349	HAEpiC	amniotic membrane:	n/a
21	chr14:104175555-104175605	HPAEpiC	pulmonary alveolar:	n/a
22	chr14:104173299-104173349	CMK	blood:	n/a
23	chr14:104175555-104175605	BJ	skin:	n/a
24	chr14:104175555-104175605	Jurkat	blood:	n/a
25	chr14:104173299-104173349	HCT-116	colon:	n/a
26	chr14:104175555-104175605	GM12891	blood:	n/a
27	chr14:104173299-104173349	SAEC	small airway:	n/a
28	chr14:104175555-104175605	H1-hESC	embryonic stem cell:	embryo
29	chr14:104175555-104175605	Hepatocyte	liver:	n/a
30	chr14:104173299-104173349	HRPEpiC	eye:	n/a
31	chr14:104173299-104173349	BJ	skin:	n/a
32	chr14:104175555-104175605	CMK	blood:	n/a
33	chr14:104175555-104175605	GM12878	blood:	n/a
34	chr14:104175555-104175605	K562	blood:	n/a
35	chr14:104175555-104175605	AoSMC	blood vessel:	n/a
36	chr14:104175555-104175605	HCT-116	colon:	n/a
37	chr14:104175555-104175605	LNCaP	prostate:	n/a
38	chr14:104173299-104173349	AG09309	skin:	n/a
39	chr14:104173299-104173349	Caco-2	colon:	n/a
40	chr14:104173299-104173349	SKMC	muscle:	n/a
41	chr14:104173299-104173349	RPTEC	kidney:	n/a
42	chr14:104173299-104173349	PrEC	prostate:	n/a
43	chr14:104173299-104173349	LNCaP	prostate:	n/a
44	chr14:104173299-104173349	AG10803	skin:	n/a
45	chr14:104175555-104175605	RPTEC	kidney:	n/a
46	chr14:104175555-104175605	ovcar-3	ovarian:	n/a
47	chr14:104173299-104173349	GM06990	blood:	n/a
48	chr14:104173299-104173349	H1-hESC	embryonic stem cell:	embryo
49	chr14:104173299-104173349	AG04449	skin:	fetal
50	chr14:104175555-104175605	BE2_C	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:149857743..149859653-chr14:104171587..104173631,2	MCF-7	breast:
2	chr14:104172426..104175375-chr14:104213214..104215800,2	K562	blood:
3	chr14:104092924..104097008-chr14:104171636..104177946,5	K562	blood:
4	chr14:104093558..104096899-chr14:104170639..104176222,7	MCF-7	breast:
5	chr14:104151812..104156751-chr14:104171759..104176142,6	K562	blood:
6	chr14:104146923..104148909-chr14:104171106..104173857,2	K562	blood:
7	chr14:104092924..104095729-chr14:104175116..104177946,2	K562	blood:

No data

Variant related genes	Relation type
XRCC3	TF binding region
ENSG00000269963	TF binding region
ENSG00000224997	TF binding region
XRCC3	CpG island
ENSG00000269963	CpG island
ENSG00000224997	CpG island
ENSG00000088808	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000270108	chromatin interactions
ENSG00000126214	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000184260	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373084327	chr14:104173251-104173252	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs72563150	chr14:104173280-104173281	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs566655808	chr14:104173285-104173286	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs374684710	chr14:104173300-104173301	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs111750986	chr14:104173305-104173306	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs377685108	chr14:104173364-104173365	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs371455247	chr14:104173395-104173396	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs577087507	chr14:104173417-104173418	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs374120119	chr14:104173425-104173426	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs368062647	chr14:104173428-104173429	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs3212057	chr14:104173465-104173466	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs374354789	chr14:104173485-104173486	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs370617343	chr14:104173500-104173501	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs574258303	chr14:104173503-104173504	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs372383657	chr14:104173525-104173526	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs61995794	chr14:104173605-104173606	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs3212056	chr14:104173624-104173625	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs553338577	chr14:104173654-104173655	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs3212055	chr14:104173666-104173667	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs573366867	chr14:104173672-104173673	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs545161347	chr14:104173681-104173682	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs186566754	chr14:104173757-104173758	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs552802332	chr14:104173801-104173802	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs3212054	chr14:104173823-104173824	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs544231043	chr14:104173845-104173846	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs542231695	chr14:104173846-104173847	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs147766261	chr14:104173849-104173850	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs190108216	chr14:104173851-104173852	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs3212053	chr14:104173857-104173858	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs183113811	chr14:104173858-104173859	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs3212052	chr14:104173863-104173864	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs566584050	chr14:104173868-104173869	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs532350773	chr14:104173889-104173890	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs562071516	chr14:104173929-104173930	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs376249796	chr14:104173937-104173938	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs117655774	chr14:104173940-104173941	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs537106226	chr14:104173959-104173960	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs78815073	chr14:104173965-104173966	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs77467164	chr14:104174083-104174084	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs2368557	chr14:104174089-104174090	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs861530	chr14:104174123-104174124	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs115125943	chr14:104174126-104174127	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs115524130	chr14:104174137-104174138	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs559150274	chr14:104174138-104174139	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs3212050	chr14:104174150-104174151	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs142651063	chr14:104174152-104174153	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs560749291	chr14:104174178-104174179	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs146890075	chr14:104174187-104174188	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs539811850	chr14:104174219-104174220	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs560416150	chr14:104174234-104174235	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104117800-104176000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr14:104118800-104175600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr14:104119400-104175200	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr14:104120000-104177000	Strong transcription	HUES64 Cell Line	embryonic stem cell
5	chr14:104133400-104177200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
6	chr14:104135600-104177600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:104146200-104174800	Weak transcription	K562	blood
8	chr14:104152600-104178600	Weak transcription	Small Intestine	intestine
9	chr14:104158400-104178000	Strong transcription	Dnd41	blood
10	chr14:104158600-104176400	Strong transcription	H9 Cell Line	embryonic stem cell
11	chr14:104159800-104176200	Strong transcription	Sigmoid Colon	Sigmoid Colon
12	chr14:104161000-104176600	Genic enhancers	Spleen	Spleen
13	chr14:104161200-104180000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr14:104161200-104180400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr14:104162800-104177200	Strong transcription	HUES6 Cell Line	embryonic stem cell
16	chr14:104163400-104176800	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr14:104163400-104177200	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr14:104163600-104176200	Strong transcription	Osteobl	bone
19	chr14:104163600-104177200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr14:104163600-104177600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr14:104163800-104176200	Strong transcription	Fetal Brain Female	brain
22	chr14:104164000-104176000	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr14:104164000-104176600	Strong transcription	Brain Germinal Matrix	brain
24	chr14:104164200-104175200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr14:104164200-104176800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
26	chr14:104164200-104178600	Weak transcription	Fetal Heart	heart
27	chr14:104164400-104174600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr14:104164400-104177400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr14:104165200-104177000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:104165400-104174600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr14:104165400-104177200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr14:104165400-104180400	Strong transcription	Thymus	Thymus
33	chr14:104165600-104174800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:104165800-104174800	Strong transcription	NHEK	skin
35	chr14:104165800-104175000	Strong transcription	Rectal Mucosa Donor 29	rectum
36	chr14:104165800-104175200	Strong transcription	Colonic Mucosa	Colon
37	chr14:104165800-104176800	Strong transcription	Fetal Thymus	thymus
38	chr14:104166800-104175800	Strong transcription	Duodenum Mucosa	Duodenum
39	chr14:104166800-104176000	Strong transcription	NHLF	lung
40	chr14:104167000-104174800	Strong transcription	Muscle Satellite Cultured Cells	--
41	chr14:104167000-104174800	Weak transcription	Stomach Mucosa	stomach
42	chr14:104167200-104179600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr14:104167400-104176400	Strong transcription	Fetal Intestine Large	intestine
44	chr14:104167600-104174400	Weak transcription	Psoas Muscle	Psoas
45	chr14:104167600-104174800	Genic enhancers	Skeletal Muscle Male	skeletal muscle
46	chr14:104167600-104176200	Strong transcription	A549	lung
47	chr14:104167600-104176600	Strong transcription	Fetal Intestine Small	intestine
48	chr14:104167800-104178000	Weak transcription	Right Atrium	heart
49	chr14:104168400-104175200	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr14:104168400-104175400	Strong transcription	HepG2	liver

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