Variant report

Variant	nsv902314
Chromosome Location	chr14:104163901-104170465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:454)
CpG islands
(count:427)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:454 , 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	BCL3	chr14:104164891-104165665	A549	lung:	n/a	n/a
2	BCL3	chr14:104165009-104166292	A549	lung:	n/a	n/a
3	BCL3	chr14:104166274-104166748	A549	lung:	n/a	n/a
4	BCL3	chr14:104162417-104164861	A549	lung:	n/a	chr14:104162570-104162579
5	BCL3	chr14:104169265-104169771	A549	lung:	n/a	n/a
6	BCL3	chr14:104170100-104170653	A549	lung:	n/a	n/a
7	BCL3	chr14:104165184-104165614	K562	blood:	n/a	n/a
8	BCL3	chr14:104168808-104169518	A549	lung:	n/a	n/a
9	BCL3	chr14:104163354-104164480	A549	lung:	n/a	n/a
10	BCL3	chr14:104165387-104165703	GM12878	blood:	n/a	n/a
11	BCL3	chr14:104164233-104164473	GM12878	blood:	n/a	n/a
12	CCNT2	chr14:104165060-104165284	K562	blood:	n/a	n/a
13	CCNT2	chr14:104166717-104166917	K562	blood:	n/a	n/a
14	CCNT2	chr14:104167552-104167762	K562	blood:	n/a	n/a
15	CEBPB	chr14:104167192-104167298	K562	blood:	n/a	n/a
16	CHD2	chr14:104164440-104164476	K562	blood:	n/a	n/a
17	CHD2	chr14:104164389-104164391	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr14:104166604-104166802	K562	blood:	n/a	n/a
19	CTCF	chr14:104165394-104165479	MCF-7	breast:	n/a	n/a
20	CTCF	chr14:104164960-104165110	NHEK	skin:	n/a	n/a
21	EBF1	chr14:104165339-104165548	GM12878	blood:	n/a	n/a
22	ELF1	chr14:104164708-104166141	MCF-7	breast:	n/a	n/a
23	ELF1	chr14:104164969-104165645	GM12878	blood:	n/a	n/a
24	FOXA1	chr14:104165164-104165475	T-47D	breast:	n/a	n/a
25	GABPA	chr14:104165039-104165668	MCF-7	breast:	n/a	chr14:104165398-104165407
26	HA-E2F1	chr14:104165082-104165712	MCF-7	breast:	n/a	n/a
27	HMGN3	chr14:104164240-104164525	K562	blood:	n/a	n/a
28	HMGN3	chr14:104167218-104167832	K562	blood:	n/a	n/a
29	HMGN3	chr14:104165122-104165888	K562	blood:	n/a	n/a
30	JUND	chr14:104165032-104165867	A549	lung:	n/a	n/a
31	JUND	chr14:104163962-104165779	MCF-7	breast:	n/a	n/a
32	JUND	chr14:104163854-104164629	A549	lung:	n/a	n/a
33	JUND	chr14:104166421-104166997	A549	lung:	n/a	chr14:104166683-104166694
34	MAFF	chr14:104170136-104170466	K562	blood:	n/a	chr14:104170296-104170314
35	MAFF	chr14:104170269-104170316	HepG2	liver:	n/a	chr14:104170296-104170314
36	MAFK	chr14:104170180-104170372	HepG2	liver:	n/a	chr14:104170297-104170312
37	MAFK	chr14:104170157-104170603	K562	blood:	n/a	chr14:104170297-104170312
38	MAFK	chr14:104170248-104170455	HepG2	liver:	n/a	chr14:104170297-104170312
39	MAX	chr14:104164922-104165836	MCF-7	breast:	n/a	chr14:104165397-104165407
40	MAX	chr14:104165059-104165715	ECC-1	luminal epithelium:	n/a	chr14:104165397-104165407
41	MAX	chr14:104169980-104170710	HUVEC	blood vessel:	n/a	n/a
42	MAX	chr14:104165119-104165653	ECC-1	luminal epithelium:	n/a	chr14:104165397-104165407
43	MTA3	chr14:104168191-104168783	GM12878	blood:	n/a	n/a
44	MTA3	chr14:104162445-104165839	GM12878	blood:	n/a	n/a
45	MTA3	chr14:104169145-104170692	GM12878	blood:	n/a	n/a
46	MTA3	chr14:104165883-104166861	GM12878	blood:	n/a	n/a
47	MXI1	chr14:104164989-104164995	HepG2	liver:	n/a	n/a
48	MYC	chr14:104165308-104165559	MCF-7	breast:	n/a	chr14:104165397-104165407
49	MYC	chr14:104165238-104165648	MCF-7	breast:	n/a	chr14:104165397-104165407
50	MYC	chr14:104170186-104170535	HUVEC	blood vessel:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104164402-104164452	HRPEpiC	eye:	n/a
2	chr14:104165052-104165102	HRCEpiC	kidney:	n/a
3	chr14:104165052-104165102	AG04449	skin:	fetal
4	chr14:104165401-104165451	SAEC	small airway:	n/a
5	chr14:104165183-104165233	ProgFib	skin:	n/a
6	chr14:104167610-104167660	RPTEC	kidney:	n/a
7	chr14:104165183-104165233	GM12891	blood:	n/a
8	chr14:104165183-104165233	PrEC	prostate:	n/a
9	chr14:104165052-104165102	RPTEC	kidney:	n/a
10	chr14:104165183-104165233	SK-N-SH	brain:	n/a
11	chr14:104165401-104165451	NHDF-neo	bronchial:	n/a
12	chr14:104164402-104164452	Hepatocyte	liver:	n/a
13	chr14:104165183-104165233	PFSK-1	brain:	n/a
14	chr14:104165401-104165451	AG04450	lung:	fetal
15	chr14:104165401-104165451	HCM	heart:	n/a
16	chr14:104167610-104167660	HRPEpiC	eye:	n/a
17	chr14:104167610-104167660	AG09309	skin:	n/a
18	chr14:104165183-104165233	K562	blood:	n/a
19	chr14:104165277-104165327	NH-A	brain:	n/a
20	chr14:104165052-104165102	HCT-116	colon:	n/a
21	chr14:104164402-104164452	HRE	kidney:	n/a
22	chr14:104164402-104164452	HEK293	kidney:	embryo
23	chr14:104165052-104165102	HEEpiC	esophagus:	n/a
24	chr14:104164402-104164452	Jurkat	blood:	n/a
25	chr14:104165183-104165233	HPAEpiC	pulmonary alveolar:	n/a
26	chr14:104165277-104165327	HCM	heart:	n/a
27	chr14:104165475-104165525	AG10803	skin:	n/a
28	chr14:104165401-104165451	GM06990	blood:	n/a
29	chr14:104165401-104165451	HCT-116	colon:	n/a
30	chr14:104164402-104164452	ECC-1	luminal epithelium:	n/a
31	chr14:104165183-104165233	NB4	blood:	n/a
32	chr14:104165277-104165327	HRE	kidney:	n/a
33	chr14:104167610-104167660	HMEC	breast:	n/a
34	chr14:104165183-104165233	HEK293	kidney:	embryo
35	chr14:104165401-104165451	HRPEpiC	eye:	n/a
36	chr14:104165475-104165525	HEEpiC	esophagus:	n/a
37	chr14:104165475-104165525	HNPCEpiC	eye:	n/a
38	chr14:104165277-104165327	HEK293	kidney:	embryo
39	chr14:104165277-104165327	HNPCEpiC	eye:	n/a
40	chr14:104164402-104164452	NB4	blood:	n/a
41	chr14:104165401-104165451	NB4	blood:	n/a
42	chr14:104165183-104165233	SK-N-MC	brain:	n/a
43	chr14:104165475-104165525	NHBE	bronchial:	n/a
44	chr14:104165475-104165525	HCM	heart:	n/a
45	chr14:104164402-104164452	BE2_C	brain:	n/a
46	chr14:104165052-104165102	HCM	heart:	n/a
47	chr14:104164402-104164452	H1-hESC	embryonic stem cell:	embryo
48	chr14:104165277-104165327	NHDF-neo	bronchial:	n/a
49	chr14:104165052-104165102	PFSK-1	brain:	n/a
50	chr14:104165277-104165327	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:103986573..103988930-chr14:104167446..104169282,2	K562	blood:
2	chr14:104094584..104096859-chr14:104165203..104168753,3	MCF-7	breast:
3	chr14:104093531..104096163-chr14:104161716..104165608,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-73M18.2.1-4	chr14:104167538-104167881	NONHSAT040200
2	lnc-RP11-73M18.2.1-4	chr14:104166259-104167064	NONHSAT040200

No data

Variant related genes	Relation type
XRCC3	TF binding region
KLC1	TF binding region
ENSG00000269910	TF binding region
XRCC3	CpG island
KLC1	CpG island
ENSG00000269910	CpG island
ENSG00000126214	chromatin interactions
ENSG00000166165	chromatin interactions

Extended variants
information (count: 395 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs861540	chr14:104163901-104163902	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs3212127	chr14:104163913-104163914	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs551092637	chr14:104163938-104163939	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs571332532	chr14:104163991-104163992	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs540271138	chr14:104164015-104164016	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs45625536	chr14:104164018-104164019	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs536717537	chr14:104164020-104164021	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs75104408	chr14:104164021-104164022	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs573515775	chr14:104164031-104164032	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs3212126	chr14:104164041-104164042	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs34975865	chr14:104164074-104164075	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs553300152	chr14:104164082-104164083	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs78863423	chr14:104164085-104164086	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs545239247	chr14:104164150-104164151	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs559884792	chr14:104164176-104164177	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs186232444	chr14:104164180-104164181	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs150768508	chr14:104164194-104164195	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs377198655	chr14:104164199-104164200	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs528769172	chr14:104164223-104164224	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs578052355	chr14:104164253-104164254	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs3212125	chr14:104164267-104164268	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs563744794	chr14:104164277-104164278	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs11546528	chr14:104164280-104164281	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs529271454	chr14:104164314-104164315	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs542944317	chr14:104164326-104164327	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs117875015	chr14:104164327-104164328	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs3212124	chr14:104164328-104164329	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs3212123	chr14:104164347-104164348	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs3212122	chr14:104164352-104164353	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs11546527	chr14:104164381-104164382	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs571700552	chr14:104164391-104164392	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs530638739	chr14:104164418-104164419	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs574806963	chr14:104164436-104164437	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs567300930	chr14:104164437-104164438	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs536232000	chr14:104164443-104164444	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs552970909	chr14:104164453-104164454	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs536177608	chr14:104164456-104164457	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs566795325	chr14:104164481-104164482	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs538889498	chr14:104164496-104164497	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs3212121	chr14:104164522-104164523	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs575338872	chr14:104164532-104164533	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs118143436	chr14:104164534-104164535	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs557155704	chr14:104164546-104164547	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs3212120	chr14:104164550-104164551	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs140813869	chr14:104164570-104164571	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs559291946	chr14:104164581-104164582	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs528762137	chr14:104164583-104164584	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs77103957	chr14:104164596-104164597	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs565514723	chr14:104164597-104164598	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs532243901	chr14:104164602-104164603	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 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:394 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr14:104119200-104173000	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr14:104119400-104164600	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr14:104119400-104175200	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr14:104120000-104177000	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr14:104124600-104169800	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr14:104124600-104169800	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr14:104133400-104177200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
10	chr14:104135600-104177600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr14:104139800-104164400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr14:104146200-104174800	Weak transcription	K562	blood
13	chr14:104149200-104164600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:104152600-104178600	Weak transcription	Small Intestine	intestine
15	chr14:104153800-104164000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr14:104154400-104165200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr14:104157400-104167600	Genic enhancers	Placenta	Placenta
18	chr14:104157600-104164600	Strong transcription	Thymus	Thymus
19	chr14:104158200-104169000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr14:104158200-104170200	Genic enhancers	Fetal Muscle Leg	muscle
21	chr14:104158400-104167800	Strong transcription	Primary T cells from cord blood	blood
22	chr14:104158400-104171200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr14:104158400-104178000	Strong transcription	Dnd41	blood
24	chr14:104158600-104176400	Strong transcription	H9 Cell Line	embryonic stem cell
25	chr14:104158800-104165000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr14:104159800-104176200	Strong transcription	Sigmoid Colon	Sigmoid Colon
27	chr14:104160000-104164600	Enhancers	Fetal Brain Male	brain
28	chr14:104160200-104164000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr14:104160200-104167000	Strong transcription	HMEC	breast
30	chr14:104160800-104164000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
31	chr14:104161000-104167200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr14:104161000-104170600	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr14:104161000-104176600	Genic enhancers	Spleen	Spleen
34	chr14:104161200-104164000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr14:104161200-104164200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr14:104161200-104164400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr14:104161200-104164400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:104161200-104164400	Strong transcription	Hela-S3	cervix
39	chr14:104161200-104164800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr14:104161200-104165400	Genic enhancers	Fetal Stomach	stomach
41	chr14:104161200-104165600	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr14:104161200-104165800	Genic enhancers	Lung	lung
43	chr14:104161200-104166000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr14:104161200-104180000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr14:104161200-104180400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr14:104161400-104165600	Weak transcription	GM12878-XiMat	blood
47	chr14:104161600-104164600	Enhancers	Brain Substantia Nigra	brain
48	chr14:104161800-104164000	Genic enhancers	Muscle Satellite Cultured Cells	--
49	chr14:104161800-104164000	Enhancers	Brain Anterior Caudate	brain
50	chr14:104161800-104164200	Enhancers	Fetal Lung	lung

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