Variant report

Variant	esv3338807
Chromosome Location	chr14:105069932-105072480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:105070922-105071333	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr14:105071194-105071232	HepG2	liver:	n/a	n/a
3	BHLHE40	chr14:105071080-105071347	K562	blood:	n/a	chr14:105071161-105071177
4	CCNT2	chr14:105071130-105071365	K562	blood:	n/a	n/a
5	CEBPB	chr14:105071172-105071282	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr14:105070967-105071403	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr14:105071022-105071273	A549	lung:	n/a	n/a
8	CTCF	chr14:105071195-105071244	H1-hESC	embryonic stem cell:	n/a	n/a
9	E2F4	chr14:105071040-105071381	K562	blood:	n/a	chr14:105071210-105071222 chr14:105071159-105071169 chr14:105071211-105071222
10	E2F6	chr14:105070999-105071396	K562	blood:	n/a	chr14:105071210-105071222 chr14:105071159-105071169 chr14:105071211-105071222
11	E2F6	chr14:105071006-105071304	K562	blood:	n/a	chr14:105071210-105071222 chr14:105071159-105071169 chr14:105071211-105071222
12	E2F6	chr14:105070999-105071277	K562	blood:	n/a	chr14:105071210-105071222 chr14:105071159-105071169 chr14:105071211-105071222
13	E2F6	chr14:105070663-105071480	H1-hESC	embryonic stem cell:	n/a	chr14:105071210-105071222 chr14:105071159-105071169 chr14:105071211-105071222
14	E2F6	chr14:105071031-105071401	A549	lung:	n/a	chr14:105071210-105071222 chr14:105071159-105071169 chr14:105071211-105071222
15	E2F6	chr14:105070802-105070970	K562	blood:	n/a	n/a
16	E2F6	chr14:105070827-105071416	A549	lung:	n/a	chr14:105071210-105071222 chr14:105071159-105071169 chr14:105071211-105071222
17	E2F6	chr14:105070424-105071512	H1-hESC	embryonic stem cell:	n/a	chr14:105071210-105071222 chr14:105071159-105071169 chr14:105071211-105071222
18	ELF1	chr14:105070333-105070644	K562	blood:	n/a	chr14:105070443-105070455 chr14:105070517-105070526 chr14:105070513-105070526
19	ELF1	chr14:105070349-105070619	K562	blood:	n/a	chr14:105070443-105070455 chr14:105070517-105070526 chr14:105070513-105070526
20	ELF1	chr14:105071104-105071334	K562	blood:	n/a	chr14:105071159-105071171
21	ETS1	chr14:105071092-105071238	K562	blood:	n/a	n/a
22	GABPA	chr14:105070628-105071491	H1-hESC	embryonic stem cell:	n/a	chr14:105071194-105071203 chr14:105071192-105071203
23	GABPA	chr14:105070679-105071460	H1-hESC	embryonic stem cell:	n/a	chr14:105071194-105071203 chr14:105071192-105071203
24	GATA3	chr14:105071859-105072186	SH-SY5Y	brain:	n/a	n/a
25	GTF2F1	chr14:105071022-105071325	H1-hESC	embryonic stem cell:	n/a	n/a
26	HCFC1	chr14:105071212-105071214	K562	blood:	n/a	n/a
27	HDAC2	chr14:105071100-105071308	K562	blood:	n/a	chr14:105071231-105071250
28	HMGN3	chr14:105071059-105071252	K562	blood:	n/a	n/a
29	JUND	chr14:105071106-105071365	H1-hESC	embryonic stem cell:	n/a	n/a
30	MAX	chr14:105071123-105071363	K562	blood:	n/a	n/a
31	MAX	chr14:105070591-105071520	H1-hESC	embryonic stem cell:	n/a	chr14:105071452-105071462
32	MAX	chr14:105070955-105071362	H1-hESC	embryonic stem cell:	n/a	n/a
33	MAX	chr14:105070642-105071493	H1-hESC	embryonic stem cell:	n/a	chr14:105071452-105071462
34	MAX	chr14:105071168-105071219	A549	lung:	n/a	n/a
35	MAX	chr14:105070714-105071485	ECC-1	luminal epithelium:	n/a	chr14:105071452-105071462
36	MAX	chr14:105071050-105071363	K562	blood:	n/a	n/a
37	MAX	chr14:105070688-105071455	ECC-1	luminal epithelium:	n/a	n/a
38	MAX	chr14:105070814-105071346	K562	blood:	n/a	n/a
39	MAX	chr14:105070984-105071469	A549	lung:	n/a	chr14:105071452-105071462
40	MAZ	chr14:105071071-105071341	K562	blood:	n/a	n/a
41	MAZ	chr14:105071216-105071240	HepG2	liver:	n/a	n/a
42	MXI1	chr14:105070933-105071431	H1-hESC	embryonic stem cell:	n/a	n/a
43	MXI1	chr14:105070985-105071477	IMR90	lung:	n/a	n/a
44	MXI1	chr14:105071113-105071336	HepG2	liver:	n/a	n/a
45	MYC	chr14:105071090-105071373	K562	blood:	n/a	n/a
46	MYC	chr14:105071148-105071303	H1-hESC	embryonic stem cell:	n/a	n/a
47	MYC	chr14:105071128-105071347	K562	blood:	n/a	n/a
48	MYC	chr14:105071230-105071247	K562	blood:	n/a	n/a
49	NFIC	chr14:105070747-105071258	ECC-1	luminal epithelium:	n/a	n/a
50	NRF1	chr14:105070978-105071423	SK-N-SH	brain:	n/a	chr14:105071194-105071203 chr14:105071192-105071203 chr14:105071192-105071203

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105071313-105071363	AoSMC	blood vessel:	n/a
2	chr14:105070864-105070914	GM19239	blood:	n/a
3	chr14:105071382-105071432	AG10803	skin:	n/a
4	chr14:105071313-105071363	NT2-D1	testis:	n/a
5	chr14:105070340-105070390	AG09319	gingival:	n/a
6	chr14:105071714-105071764	PrEC	prostate:	n/a
7	chr14:105071714-105071764	SK-N-SH_RA	brain:	n/a
8	chr14:105071695-105071745	ECC-1	luminal epithelium:	n/a
9	chr14:105071382-105071432	AG09309	skin:	n/a
10	chr14:105070998-105071048	ProgFib	skin:	n/a
11	chr14:105071714-105071764	HCPEpiC	choroid plexus:	n/a
12	chr14:105070749-105070799	GM19239	blood:	n/a
13	chr14:105071313-105071363	HCM	heart:	n/a
14	chr14:105070340-105070390	AG04450	lung:	fetal
15	chr14:105070864-105070914	NHDF-neo	bronchial:	n/a
16	chr14:105071714-105071764	AG09309	skin:	n/a
17	chr14:105071313-105071363	Hepatocyte	liver:	n/a
18	chr14:105070864-105070914	SKMC	muscle:	n/a
19	chr14:105071382-105071432	HCM	heart:	n/a
20	chr14:105070864-105070914	HCM	heart:	n/a
21	chr14:105070340-105070390	AG10803	skin:	n/a
22	chr14:105071714-105071764	SKMC	muscle:	n/a
23	chr14:105071313-105071363	NHDF-neo	bronchial:	n/a
24	chr14:105070998-105071048	HCF	heart:	n/a
25	chr14:105071313-105071363	GM19239	blood:	n/a
26	chr14:105070340-105070390	MCF10A-Er-Src	breast:	n/a
27	chr14:105070864-105070914	SK-N-MC	brain:	n/a
28	chr14:105070340-105070390	ECC-1	luminal epithelium:	n/a
29	chr14:105071695-105071745	ovcar-3	ovarian:	n/a
30	chr14:105070864-105070914	HEEpiC	esophagus:	n/a
31	chr14:105071313-105071363	HIPEpiC	eye:	n/a
32	chr14:105070864-105070914	LNCaP	prostate:	n/a
33	chr14:105070749-105070799	HMEC	breast:	n/a
34	chr14:105071695-105071745	BJ	skin:	n/a
35	chr14:105071313-105071363	AG09309	skin:	n/a
36	chr14:105071695-105071745	GM12878	blood:	n/a
37	chr14:105070749-105070799	HUVEC	blood vessel:	n/a
38	chr14:105070864-105070914	RPTEC	kidney:	n/a
39	chr14:105071313-105071363	HCPEpiC	choroid plexus:	n/a
40	chr14:105070340-105070390	HepG2	liver:	n/a
41	chr14:105070749-105070799	HEK293	kidney:	embryo
42	chr14:105071313-105071363	NH-A	brain:	n/a
43	chr14:105070864-105070914	HUVEC	blood vessel:	n/a
44	chr14:105070749-105070799	CMK	blood:	n/a
45	chr14:105070864-105070914	A549	lung:	n/a
46	chr14:105070864-105070914	HIPEpiC	eye:	n/a
47	chr14:105071313-105071363	HEK293	kidney:	embryo
48	chr14:105071313-105071363	MCF-7	breast:	n/a
49	chr14:105070998-105071048	HNPCEpiC	eye:	n/a
50	chr14:105071313-105071363	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:105067674..105070275-chr14:105105172..105108009,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf180-2	chr14:105071099-105072888	NONHSAT040264
2	lnc-C14orf180-2	chr14:105070351-105071697	ucscGeneNc_uc001yrr_2

Variant related genes	Relation type
TMEM179	TF binding region
TMEM179	CpG island

Extended variants
information (count: 105 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533401548	chr14:105069942-105069943	Enhancers Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs549785036	chr14:105069943-105069944	Enhancers Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs180700013	chr14:105069953-105069954	Enhancers Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs186354412	chr14:105069957-105069958	Enhancers Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs569981494	chr14:105069959-105069960	Enhancers Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs113957753	chr14:105069975-105069976	Enhancers Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs533135864	chr14:105069979-105069980	Enhancers Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs548776740	chr14:105069998-105069999	Enhancers Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs367575798	chr14:105070012-105070013	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534432919	chr14:105070028-105070029	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557701286	chr14:105070038-105070039	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571140551	chr14:105070058-105070059	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28547458	chr14:105070093-105070094	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs10220597	chr14:105070146-105070147	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534687196	chr14:105070164-105070165	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189733395	chr14:105070180-105070181	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs117099437	chr14:105070256-105070257	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72713829	chr14:105070332-105070333	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556020517	chr14:105070344-105070345	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572539428	chr14:105070389-105070390	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs35526829	chr14:105070400-105070401	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs541524626	chr14:105070429-105070430	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs564635823	chr14:105070431-105070432	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs181786829	chr14:105070441-105070442	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs559161943	chr14:105070442-105070443	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs8015839	chr14:105070485-105070486	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs147602995	chr14:105070502-105070503	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs555208545	chr14:105070520-105070521	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs72713830	chr14:105070542-105070543	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs113060596	chr14:105070560-105070561	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs150105944	chr14:105070566-105070567	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs551165482	chr14:105070569-105070570	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs571364486	chr14:105070596-105070597	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs112573850	chr14:105070619-105070620	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs145473820	chr14:105070640-105070641	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs373066395	chr14:105070782-105070783	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs3803313	chr14:105070791-105070792	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs112480105	chr14:105070850-105070851	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs556132914	chr14:105070864-105070865	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs377119267	chr14:105070921-105070922	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs370868904	chr14:105070950-105070951	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs375287943	chr14:105070967-105070968	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs146294994	chr14:105071024-105071025	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs372300989	chr14:105071046-105071047	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs12433571	chr14:105071055-105071056	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs368299377	chr14:105071084-105071085	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs372353213	chr14:105071094-105071095	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs374532765	chr14:105071097-105071098	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs546419481	chr14:105071108-105071109	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs139040111	chr14:105071113-105071114	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
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
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20932292	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	21980252	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105063800-105070000	Enhancers	Fetal Brain Male	brain
2	chr14:105065200-105070800	Weak transcription	Right Atrium	heart
3	chr14:105065400-105070000	Weak transcription	Fetal Heart	heart
4	chr14:105066800-105070400	Weak transcription	Pancreas	Pancrea
5	chr14:105068600-105070000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr14:105069000-105071800	Bivalent/Poised TSS	Brain Anterior Caudate	brain
7	chr14:105069000-105071800	Active TSS	Brain Inferior Temporal Lobe	brain
8	chr14:105069400-105070000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
9	chr14:105069400-105070200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:105069400-105070400	Active TSS	Brain Angular Gyrus	brain
11	chr14:105069400-105071800	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr14:105069600-105070400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
13	chr14:105069800-105070000	Active TSS	Brain Germinal Matrix	brain
14	chr14:105069800-105070000	Enhancers	Fetal Brain Female	brain
15	chr14:105070000-105070200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr14:105070000-105070200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
17	chr14:105070000-105070400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:105070000-105070400	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr14:105070000-105070800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
20	chr14:105070000-105070800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
21	chr14:105070000-105070800	Flanking Active TSS	Fetal Brain Male	brain
22	chr14:105070000-105070800	Flanking Active TSS	Fetal Brain Female	brain
23	chr14:105070000-105071000	Enhancers	Fetal Heart	heart
24	chr14:105070200-105070400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:105070200-105070400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
26	chr14:105070200-105070600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
27	chr14:105070200-105070600	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:105070200-105070600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr14:105070200-105070600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
30	chr14:105070200-105070600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
31	chr14:105070200-105070800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr14:105070200-105070800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr14:105070200-105070800	Bivalent Enhancer	Fetal Intestine Small	intestine
34	chr14:105070200-105070800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr14:105070200-105070800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
36	chr14:105070200-105071000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr14:105070200-105071000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
38	chr14:105070200-105071200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr14:105070200-105071800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
40	chr14:105070400-105070600	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr14:105070400-105070600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr14:105070400-105070600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr14:105070400-105070600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
44	chr14:105070400-105070600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
45	chr14:105070400-105070600	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
46	chr14:105070400-105070600	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
47	chr14:105070400-105070800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
48	chr14:105070400-105070800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
49	chr14:105070400-105070800	Bivalent Enhancer	Primary T cells from cord blood	blood
50	chr14:105070400-105070800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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