Variant report

Variant	esv3437857
Chromosome Location	chr14:103999749-104002547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:367)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:103999980-104000130	WERI-Rb-1	eye:	n/a	chr14:104000021-104000034 chr14:104000054-104000072 chr14:104000056-104000069
2	MAZ	chr14:104001932-104002052	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr14:104002541-104005753	K562	blood:	n/a	n/a
4	POLR2A	chr14:104001437-104006198	GM12892	blood:	n/a	n/a
5	POLR2A	chr14:104001880-104006121	HepG2	liver:	n/a	n/a
6	POLR2A	chr14:104001271-104002613	GM12892	blood:	n/a	n/a
7	POLR2A	chr14:104000848-104006103	A549	lung:	n/a	n/a
8	POLR2A	chr14:104000500-104000683	K562	blood:	n/a	n/a
9	POLR2A	chr14:104001664-104002140	PANC-1	pancreas:	n/a	n/a
10	POLR2A	chr14:104000735-104000802	HepG2	liver:	n/a	n/a
11	POLR2A	chr14:103999999-104000279	GM12878	blood:	n/a	n/a
12	POLR2A	chr14:104001219-104001433	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr14:104000743-104000799	GM12878	blood:	n/a	n/a
14	POLR2A	chr14:104001560-104002044	GM12891	blood:	n/a	n/a
15	POLR2A	chr14:104001244-104001397	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr14:104002407-104002463	MCF-7	breast:	n/a	n/a
17	POLR2A	chr14:104000593-104000789	GM12878	blood:	n/a	n/a
18	POLR2A	chr14:104001864-104002188	K562	blood:	n/a	n/a
19	POLR2A	chr14:104001793-104004867	K562	blood:	n/a	n/a
20	POLR2A	chr14:104001456-104003265	GM18505	blood:	n/a	n/a
21	POLR2A	chr14:104002017-104002024	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr14:104001266-104005805	HepG2	liver:	n/a	n/a
23	POLR2A	chr14:104000317-104001163	GM12892	blood:	n/a	n/a
24	POLR2A	chr14:104001457-104002833	GM12878	blood:	n/a	n/a
25	POLR2A	chr14:104001771-104001931	A549	lung:	n/a	n/a
26	POLR2A	chr14:104001985-104003490	HepG2	liver:	n/a	n/a
27	POLR2A	chr14:104002291-104005622	PANC-1	pancreas:	n/a	n/a
28	POLR2A	chr14:104002461-104003397	K562	blood:	n/a	n/a
29	POLR2A	chr14:104001646-104001680	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr14:104000467-104000591	HepG2	liver:	n/a	n/a
31	POLR2A	chr14:104000553-104001589	HepG2	liver:	n/a	n/a
32	POLR2A	chr14:104002054-104002800	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr14:104001184-104001189	HepG2	liver:	n/a	n/a
34	POLR2A	chr14:104001444-104006090	SK-N-MC	brain:	n/a	n/a
35	POLR2A	chr14:104001658-104001735	K562	blood:	n/a	n/a
36	POLR2A	chr14:104000871-104001204	GM12878	blood:	n/a	n/a
37	POLR2A	chr14:104002329-104002705	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr14:104001670-104002041	A549	lung:	n/a	n/a
39	POLR2A	chr14:104001055-104005415	GM12892	blood:	n/a	n/a
40	POLR2A	chr14:104002388-104002398	MCF-7	breast:	n/a	n/a
41	POLR2A	chr14:104002364-104002610	HepG2	liver:	n/a	n/a
42	POLR2A	chr14:104000331-104000514	K562	blood:	n/a	n/a
43	POLR2A	chr14:104001238-104001360	MCF-7	breast:	n/a	n/a
44	POLR2A	chr14:104000132-104000227	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr14:104001348-104001601	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr14:104001672-104002855	GM12878	blood:	n/a	n/a
47	POLR2A	chr14:104000103-104006105	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr14:104001718-104002114	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr14:104001327-104001406	K562	blood:	n/a	n/a
50	POLR2A	chr14:104001811-104001981	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104001005-104001055	AG09309	skin:	n/a
2	chr14:104001005-104001055	AG09309	skin:	n/a
3	chr14:104000955-104001005	NT2-D1	testis:	n/a
4	chr14:104001005-104001055	NT2-D1	testis:	n/a
5	chr14:104000447-104000497	HRE	kidney:	n/a
6	chr14:104001089-104001139	IMR90	lung:	fetal
7	chr14:104000460-104000510	BJ	skin:	n/a
8	chr14:104000505-104000555	GM12891	blood:	n/a
9	chr14:104001089-104001139	Hepatocyte	liver:	n/a
10	chr14:104000505-104000555	PrEC	prostate:	n/a
11	chr14:104000955-104001005	U87	brain:	n/a
12	chr14:104001005-104001055	H1-hESC	embryonic stem cell:	embryo
13	chr14:104000505-104000555	AG09309	skin:	n/a
14	chr14:104000460-104000510	U87	brain:	n/a
15	chr14:104000447-104000497	GM12878	blood:	n/a
16	chr14:104000460-104000510	K562	blood:	n/a
17	chr14:104001089-104001139	MCF-7	breast:	n/a
18	chr14:104000447-104000497	IMR90	lung:	fetal
19	chr14:104001005-104001055	BE2_C	brain:	n/a
20	chr14:104000460-104000510	Hepatocyte	liver:	n/a
21	chr14:104001005-104001055	HRPEpiC	eye:	n/a
22	chr14:104000955-104001005	HNPCEpiC	eye:	n/a
23	chr14:104000447-104000497	HCF	heart:	n/a
24	chr14:104000955-104001005	AG09309	skin:	n/a
25	chr14:104000460-104000510	GM12891	blood:	n/a
26	chr14:104000447-104000497	HEEpiC	esophagus:	n/a
27	chr14:104000955-104001005	MCF10A-Er-Src	breast:	n/a
28	chr14:104000955-104001005	NH-A	brain:	n/a
29	chr14:104000955-104001005	HIPEpiC	eye:	n/a
30	chr14:104000460-104000510	GM06990	blood:	n/a
31	chr14:104000447-104000497	AoSMC	blood vessel:	n/a
32	chr14:104001005-104001055	GM12892	blood:	n/a
33	chr14:104000505-104000555	HEK293	kidney:	embryo
34	chr14:104000955-104001005	PrEC	prostate:	n/a
35	chr14:104001005-104001055	GM12891	blood:	n/a
36	chr14:104000955-104001005	IMR90	lung:	fetal
37	chr14:104000505-104000555	SAEC	small airway:	n/a
38	chr14:104001005-104001055	HAEpiC	amniotic membrane:	n/a
39	chr14:104001005-104001055	SKMC	muscle:	n/a
40	chr14:104000505-104000555	SK-N-SH	brain:	n/a
41	chr14:104000447-104000497	NH-A	brain:	n/a
42	chr14:104000447-104000497	BE2_C	brain:	n/a
43	chr14:104000447-104000497	ProgFib	skin:	n/a
44	chr14:104000505-104000555	GM12878	blood:	n/a
45	chr14:104000505-104000555	U87	brain:	n/a
46	chr14:104001005-104001055	HMEC	breast:	n/a
47	chr14:104001005-104001055	BJ	skin:	n/a
48	chr14:104000955-104001005	H1-hESC	embryonic stem cell:	embryo
49	chr14:104000460-104000510	H1-hESC	embryonic stem cell:	embryo
50	chr14:104001089-104001139	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:103858408..103860033-chr14:103999938..104001765,2	K562	blood:
2	chr14:104002192..104004863-chr14:104043017..104044904,2	K562	blood:
3	chr14:103793692..103795249-chr14:104002201..104004870,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TRMT61A	hsa-miR-342-3p	chr14:104002332-104002354

Variant related genes	Relation type
ENSG00000260285	TF binding region
ENSG00000260285	CpG island

Extended variants
information (count: 156 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:156 , 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	rs200623062	chr14:103999750-103999751	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs190674866	chr14:103999766-103999767	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs566495068	chr14:103999778-103999779	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs538219359	chr14:103999814-103999815	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs181773998	chr14:103999951-103999952	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs575149123	chr14:104000019-104000020	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs185403458	chr14:104000052-104000053	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs554382346	chr14:104000053-104000054	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs574288030	chr14:104000063-104000064	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs570176796	chr14:104000107-104000108	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs189717544	chr14:104000116-104000117	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs150574331	chr14:104000148-104000149	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2756127	chr14:104000183-104000184	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs545049230	chr14:104000208-104000209	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs2756126	chr14:104000251-104000252	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs531191177	chr14:104000321-104000322	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs374237454	chr14:104000340-104000341	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551289543	chr14:104000372-104000373	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs941836	chr14:104000373-104000374	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs76445448	chr14:104000380-104000381	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs546688079	chr14:104000387-104000388	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs566415129	chr14:104000405-104000406	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs538631221	chr14:104000424-104000425	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs529692209	chr14:104000446-104000447	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs558089257	chr14:104000461-104000462	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568502292	chr14:104000469-104000470	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs537794250	chr14:104000511-104000512	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs554423137	chr14:104000517-104000518	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs2236281	chr14:104000518-104000519	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs540020422	chr14:104000522-104000523	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs553455651	chr14:104000524-104000525	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs573212950	chr14:104000563-104000564	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs8012232	chr14:104000572-104000573	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs565320466	chr14:104000589-104000590	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs376268180	chr14:104000602-104000603	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544953720	chr14:104000619-104000620	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561529955	chr14:104000630-104000631	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530336049	chr14:104000634-104000635	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546828898	chr14:104000648-104000649	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566570334	chr14:104000664-104000665	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182243351	chr14:104000684-104000685	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551851733	chr14:104000687-104000688	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568539308	chr14:104000702-104000703	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537433844	chr14:104000727-104000728	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565896533	chr14:104000750-104000751	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368697873	chr14:104000768-104000769	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11350625	chr14:104000803-104000804	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs398078003	chr14:104000804-104000805	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs397716144	chr14:104000805-104000806	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548095702	chr14:104000834-104000835	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Basal cell lymphoma	17053054	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
Cancer	17160897	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:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103995800-104001400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr14:103996200-104000200	Weak transcription	Aorta	Aorta
3	chr14:103996400-104000400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:103996400-104000800	Genic enhancers	Fetal Intestine Large	intestine
5	chr14:103996600-104000600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:103996600-104001200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:103996600-104002800	Genic enhancers	Fetal Stomach	stomach
8	chr14:103996800-103999800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr14:103996800-104000400	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr14:103996800-104000800	Genic enhancers	Fetal Intestine Small	intestine
11	chr14:103996800-104002200	Strong transcription	H9 Cell Line	embryonic stem cell
12	chr14:103996800-104002200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr14:103996800-104002800	Weak transcription	HSMMtube	muscle
14	chr14:103996800-104004000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:103996800-104004000	Genic enhancers	Fetal Muscle Trunk	muscle
16	chr14:103996800-104004600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr14:103996800-104005000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:103996800-104023400	Weak transcription	Primary B cells from cord blood	blood
19	chr14:103997000-104000600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr14:103997000-104001600	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr14:103997000-104003400	Strong transcription	NHLF	lung
22	chr14:103997000-104004800	Weak transcription	Psoas Muscle	Psoas
23	chr14:103997200-103999800	Weak transcription	Left Ventricle	heart
24	chr14:103997200-104000200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr14:103997200-104001000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr14:103997200-104002600	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr14:103997200-104003000	Strong transcription	Fetal Brain Female	brain
28	chr14:103997200-104003200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr14:103997200-104003400	Strong transcription	NHEK	skin
30	chr14:103997200-104004000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
31	chr14:103997200-104004600	Weak transcription	Fetal Heart	heart
32	chr14:103997200-104005400	Weak transcription	Fetal Lung	lung
33	chr14:103997400-104000200	Weak transcription	Osteobl	bone
34	chr14:103997400-104000800	Weak transcription	Stomach Mucosa	stomach
35	chr14:103997400-104002000	Strong transcription	H1 Cell Line	embryonic stem cell
36	chr14:103997400-104002800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr14:103997400-104003600	Weak transcription	NH-A	brain
38	chr14:103997400-104005000	Weak transcription	GM12878-XiMat	blood
39	chr14:103997600-104001800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr14:103997600-104003200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr14:103997600-104003400	Strong transcription	Brain Germinal Matrix	brain
42	chr14:103997600-104006800	Weak transcription	Small Intestine	intestine
43	chr14:103997600-104013000	Weak transcription	K562	blood
44	chr14:103997800-103999800	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr14:103997800-104002600	Strong transcription	Right Ventricle	heart
46	chr14:103997800-104003000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr14:103997800-104003000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr14:103997800-104003400	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr14:103997800-104004600	Weak transcription	Brain Angular Gyrus	brain
50	chr14:103997800-104004800	Weak transcription	Hela-S3	cervix

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