Variant report

Variant	nsv564681
Chromosome Location	chr14:44733804-45149546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1253)
CpG islands
(count:305)
Chromatin interactive
region (count:50)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:44786027-44786367	K562	blood:	n/a	n/a
2	ARID3A	chr14:44786011-44786505	HepG2	liver:	n/a	n/a
3	ATF1	chr14:44786110-44786462	K562	blood:	n/a	n/a
4	ATF1	chr14:44918300-44918537	K562	blood:	n/a	n/a
5	ATF3	chr14:44786091-44786377	K562	blood:	n/a	n/a
6	ATF3	chr14:44786197-44786335	K562	blood:	n/a	n/a
7	ATF3	chr14:44786000-44786531	HCT-116	colon:	n/a	n/a
8	ATF3	chr14:44786106-44786596	HCT-116	colon:	n/a	n/a
9	ATF3	chr14:44786082-44786534	A549	lung:	n/a	n/a
10	ATF3	chr14:44786185-44786384	HepG2	liver:	n/a	n/a
11	BACH1	chr14:44862483-44862496	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr14:44786178-44786410	GM12878	blood:	n/a	n/a
13	BATF	chr14:44786155-44786410	GM12878	blood:	n/a	n/a
14	BCL11A	chr14:44974131-44974349	GM12878	blood:	n/a	n/a
15	BCL3	chr14:44786061-44786449	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:44918875-44919187	HepG2	liver:	n/a	n/a
17	BHLHE40	chr14:44918215-44918640	K562	blood:	n/a	n/a
18	BHLHE40	chr14:44786136-44786463	HepG2	liver:	n/a	n/a
19	BHLHE40	chr14:44918841-44919166	HepG2	liver:	n/a	n/a
20	BHLHE40	chr14:44786155-44786484	K562	blood:	n/a	n/a
21	BRCA1	chr14:45104768-45104769	GM12878	blood:	n/a	n/a
22	BRCA1	chr14:44887139-44887316	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr14:44785944-44786626	HCT-116	colon:	n/a	n/a
24	CCNT2	chr14:44870973-44871349	K562	blood:	n/a	n/a
25	CCNT2	chr14:44918261-44918573	K562	blood:	n/a	n/a
26	CEBPB	chr14:44865484-44865848	HepG2	liver:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
27	CEBPB	chr14:45126502-45126841	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr14:44865514-44865808	IMR90	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
29	CEBPB	chr14:44859620-44859752	H1-hESC	embryonic stem cell:	n/a	chr14:44859701-44859712
30	CEBPB	chr14:44932945-44933181	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:44859595-44859755	HepG2	liver:	n/a	chr14:44859701-44859712
32	CEBPB	chr14:44822869-44823209	HepG2	liver:	n/a	chr14:44823024-44823035
33	CEBPB	chr14:44804471-44804773	IMR90	lung:	n/a	chr14:44804642-44804653
34	CEBPB	chr14:44937972-44938311	HepG2	liver:	n/a	chr14:44937995-44938006 chr14:44937995-44938008 chr14:44937995-44938008 chr14:44938138-44938149 chr14:44937995-44938008 chr14:44938159-44938170
35	CEBPB	chr14:45082337-45082720	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:45080960-45081587	MCF-7	breast:	n/a	chr14:45081396-45081407
37	CEBPB	chr14:45081026-45081565	A549	lung:	n/a	chr14:45081396-45081407
38	CEBPB	chr14:44937993-44938273	Hela-S3	cervix:	n/a	chr14:44937995-44938006 chr14:44937995-44938008 chr14:44937995-44938008 chr14:44938138-44938149 chr14:44937995-44938008 chr14:44938159-44938170
39	CEBPB	chr14:44862132-44862411	HepG2	liver:	n/a	chr14:44862299-44862316 chr14:44862302-44862315
40	CEBPB	chr14:44865547-44865773	H1-hESC	embryonic stem cell:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
41	CEBPB	chr14:45080999-45081511	Hela-S3	cervix:	n/a	chr14:45081396-45081407
42	CEBPB	chr14:44865478-44865918	MCF-7	breast:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
43	CEBPB	chr14:45068081-45068271	IMR90	lung:	n/a	chr14:45068217-45068228
44	CEBPB	chr14:44822861-44823165	K562	blood:	n/a	chr14:44823024-44823035
45	CEBPB	chr14:44865476-44865832	A549	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
46	CEBPB	chr14:44822866-44823194	H1-hESC	embryonic stem cell:	n/a	chr14:44823024-44823035
47	CEBPB	chr14:44801504-44801816	IMR90	lung:	n/a	chr14:44801651-44801662 chr14:44801651-44801664
48	CEBPB	chr14:45147074-45147280	HepG2	liver:	n/a	chr14:45147163-45147174 chr14:45147216-45147227
49	CEBPB	chr14:45089415-45090042	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr14:44957012-44957082	HepG2	liver:	n/a	chr14:44957022-44957033

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44976233-44976283	Hepatocyte	liver:	n/a
2	chr14:45071625-45071675	LNCaP	prostate:	n/a
3	chr14:44976457-44976507	ECC-1	luminal epithelium:	n/a
4	chr14:45071625-45071675	HNPCEpiC	eye:	n/a
5	chr14:44853952-44854002	IMR90	lung:	fetal
6	chr14:45071625-45071675	SK-N-MC	brain:	n/a
7	chr14:45133024-45133074	GM12878	blood:	n/a
8	chr14:45133024-45133074	GM12891	blood:	n/a
9	chr14:44976457-44976507	LNCaP	prostate:	n/a
10	chr14:44976457-44976507	HCPEpiC	choroid plexus:	n/a
11	chr14:45071625-45071675	NT2-D1	testis:	n/a
12	chr14:44976233-44976283	GM19239	blood:	n/a
13	chr14:45071625-45071675	NHBE	bronchial:	n/a
14	chr14:45071625-45071675	GM12892	blood:	n/a
15	chr14:44976457-44976507	HepG2	liver:	n/a
16	chr14:44976233-44976283	AG09309	skin:	n/a
17	chr14:45071625-45071675	ProgFib	skin:	n/a
18	chr14:44976233-44976283	NH-A	brain:	n/a
19	chr14:45133024-45133074	HEK293	kidney:	embryo
20	chr14:44976233-44976283	BE2_C	brain:	n/a
21	chr14:44853952-44854002	GM12891	blood:	n/a
22	chr14:44976233-44976283	AG04449	skin:	fetal
23	chr14:44976233-44976283	ProgFib	skin:	n/a
24	chr14:45071625-45071675	SKMC	muscle:	n/a
25	chr14:45071625-45071675	HCM	heart:	n/a
26	chr14:44853952-44854002	MCF10A-Er-Src	breast:	n/a
27	chr14:45071625-45071675	HRPEpiC	eye:	n/a
28	chr14:45133024-45133074	K562	blood:	n/a
29	chr14:45133024-45133074	HCT-116	colon:	n/a
30	chr14:44853952-44854002	Jurkat	blood:	n/a
31	chr14:44976457-44976507	NHDF-neo	bronchial:	n/a
32	chr14:45133024-45133074	IMR90	lung:	fetal
33	chr14:44976233-44976283	Hela-S3	cervix:	n/a
34	chr14:45071625-45071675	K562	blood:	n/a
35	chr14:45133024-45133074	SKMC	muscle:	n/a
36	chr14:44976233-44976283	LNCaP	prostate:	n/a
37	chr14:44976457-44976507	HRCEpiC	kidney:	n/a
38	chr14:44853952-44854002	HRPEpiC	eye:	n/a
39	chr14:44976233-44976283	NHDF-neo	bronchial:	n/a
40	chr14:45133024-45133074	AG04449	skin:	fetal
41	chr14:45133024-45133074	U87	brain:	n/a
42	chr14:45071625-45071675	AoSMC	blood vessel:	n/a
43	chr14:45133024-45133074	AoSMC	blood vessel:	n/a
44	chr14:44853952-44854002	HepG2	liver:	n/a
45	chr14:44853952-44854002	HAEpiC	amniotic membrane:	n/a
46	chr14:44976233-44976283	GM12878	blood:	n/a
47	chr14:44976233-44976283	H1-hESC	embryonic stem cell:	embryo
48	chr14:45133024-45133074	LNCaP	prostate:	n/a
49	chr14:45133024-45133074	Jurkat	blood:	n/a
50	chr14:44976457-44976507	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:44980119..44981640-chr17:41463656..41466583,4	K562	blood:
2	chr14:44978619..44981639-chr17:41463816..41468065,6	K562	blood:
3	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
4	chr14:44799704..44802515-chr14:44803665..44805548,2	K562	blood:
5	chr14:44755644..44758887-chr14:44761125..44763162,3	K562	blood:
6	chr14:45117709..45119759-chr14:45126176..45128721,2	MCF-7	breast:
7	chr14:44838296..44838875-chr14:45126583..45127520,3	MCF-7	breast:
8	chr14:44922572..44923387-chr14:45126451..45127121,2	MCF-7	breast:
9	chr14:44980118..44981638-chr17:41465259..41467724,2	MCF-7	breast:
10	chr11:62607619..62609217-chr14:44980118..44981639,2	K562	blood:
11	chr14:44922572..44923387-chr14:45126451..45127121,2	MCF-7	breast:
12	chr14:44972455..44975189-chr14:45002674..45004244,2	MCF-7	breast:
13	chr14:44838296..44838875-chr14:45126583..45127520,3	MCF-7	breast:
14	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
15	chr14:45071494..45073529-chr14:45073607..45075703,2	MCF-7	breast:
16	chr14:44978638..44981619-chrX:77931842..77933343,2	K562	blood:
17	chr14:44795723..44798432-chr14:44798850..44801579,2	MCF-7	breast:
18	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
19	chr14:44799704..44802515-chr14:44803665..44805548,2	K562	blood:
20	chr14:44785511..44787603-chr14:44801475..44804165,2	MCF-7	breast:
21	chr14:44785511..44787603-chr14:44801475..44804165,2	MCF-7	breast:
22	chr14:45082497..45084291-chr14:45088461..45090212,2	MCF-7	breast:
23	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
24	chr14:44980118..44981638-chr17:41380370..41382247,2	MCF-7	breast:
25	chr14:44755644..44758887-chr14:44761125..44763162,3	K562	blood:
26	chr14:45105348..45106907-chr14:45108669..45111586,2	MCF-7	breast:
27	chr14:44838612..44839205-chr14:44974588..44975472,2	MCF-7	breast:
28	chr14:44980139..44981640-chr17:41398653..41400867,3	K562	blood:
29	chr14:44795723..44798432-chr14:44798850..44801579,2	MCF-7	breast:
30	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
31	chr14:45105348..45106907-chr14:45108669..45111586,2	MCF-7	breast:
32	chr14:45117709..45119759-chr14:45126176..45128721,2	MCF-7	breast:
33	chr14:45126668..45127459-chr14:45315563..45316088,2	MCF-7	breast:
34	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
35	chr14:44980119..44981639-chr17:41463633..41465366,4	MCF-7	breast:
36	chr14:44856514..44860245-chr14:44862169..44864602,3	K562	blood:
37	chr14:45071494..45073529-chr14:45073607..45075703,2	MCF-7	breast:
38	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
39	chr14:44972455..44975189-chr14:45002674..45004244,2	MCF-7	breast:
40	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
41	chr1:17231477..17232007-chr14:44939008..44939528,2	Hela-S3	cervix:
42	chr14:44803036..44805789-chr14:44807681..44809917,2	MCF-7	breast:
43	chr14:45082497..45084291-chr14:45088461..45090212,2	MCF-7	breast:
44	chr14:44980118..44981640-chr17:41398653..41402673,7	K562	blood:
45	chr14:44980137..44981640-chr17:41380487..41382264,3	K562	blood:
46	chr14:44857399..44860693-chr14:44862169..44864634,3	K562	blood:
47	chr14:44838612..44839205-chr14:44974588..44975472,2	MCF-7	breast:
48	chr14:44754776..44756782-chr14:44760420..44763272,3	MCF-7	breast:
49	chr14:44803036..44805789-chr14:44807681..44809917,2	MCF-7	breast:
50	chr14:44948272..44949206-chr8:143706277..143707059,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-1	chr14:44862812-44862997	XLOC_011006
2	lnc-FSCB-1	chr14:44949713-44949833	XLOC_011007
3	lnc-C14orf28-1	chr14:44976610-44976672	ENSG00000258747.1
4	lnc-FSCB-1	chr14:44913926-44914025	NONHSAT036608
5	lnc-C14orf28-1	chr14:44977855-44977932	NONHSAT036614
6	lnc-FSCB-1	chr14:44947923-44948054	ENSG00000258487
7	lnc-C14orf28-1	chr14:44978530-44978686	ENSG00000258747.1
8	lnc-C14orf28-1	chr14:45007477-45007691	NONHSAT036614
9	lnc-C14orf28-1	chr14:44976612-44976672	ENSG00000258747.1
10	lnc-FSCB-1	chr14:44861745-44861893	ENSG00000259126
11	lnc-FSCB-1	chr14:44947921-44948054	XLOC_011007
12	lnc-FSCB-1	chr14:44947932-44948054	NONHSAT036608
13	lnc-FSCB-1	chr14:44949713-44949821	ENSG00000258487
14	lnc-FSCB-1	chr14:44861702-44861893	XLOC_011006
15	lnc-FSCB-1	chr14:44915851-44915996	ENSG00000258487
16	lnc-FSCB-1	chr14:44947932-44948054	ENSG00000258487
17	lnc-FSCB-1	chr14:44913910-44914002	XLOC_011006
18	lnc-FSCB-1	chr14:44949713-44949833	XLOC_011007
19	lnc-FSCB-1	chr14:44862209-44862941	XLOC_011006
20	lnc-FSCB-2	chr14:44853680-44853748	ENSG00000258969
21	lnc-FSCB-1	chr14:44949713-44949820	ENSG00000258487
22	lnc-FSCB-1	chr14:44949713-44949737	NONHSAT036608
23	lnc-FSCB-1	chr14:44947932-44948054	XLOC_011007
24	lnc-FSCB-1	chr14:44947932-44948054	XLOC_011007
25	lnc-FSCB-1	chr14:44862821-44862919	ENSG00000259126
26	lnc-FSCB-1	chr14:44913950-44914025	ENSG00000258487
27	lnc-C14orf28-1	chr14:45007477-45007716	ENSG00000258747.1
28	lnc-FSCB-1	chr14:44936162-44936372	XLOC_011007
29	lnc-C14orf28-1	chr14:45007477-45007714	ENSG00000258747.1
30	lnc-FSCB-1	chr14:44862812-44862914	ENSG00000259126
31	lnc-C14orf28-1	chr14:44976560-44976672	NONHSAT036614
32	lnc-FSCB-1	chr14:44936161-44936372	ENSG00000258487
33	lnc-C14orf28-1	chr14:44977855-44977932	ENSG00000258747.1
34	lnc-C14orf28-1	chr14:44978172-44978434	ENSG00000258747.1
35	lnc-FSCB-1	chr14:44936293-44936372	XLOC_011007
36	lnc-FSCB-1	chr14:44861734-44861893	ENSG00000259126
37	lnc-FSCB-5	chr14:44760200-44760921	NONHSAT036604
38	lnc-C14orf28-1	chr14:44978206-44978434	ENSG00000258747.1

No data

Variant related genes	Relation type
FSCB	TF binding region
ENSG00000238501	TF binding region
ENSG00000258487	TF binding region
ENSG00000259148	TF binding region
ENSG00000258969	TF binding region
ENSG00000258747	TF binding region
ENSG00000259126	TF binding region
FSCB	CpG island
ENSG00000238501	CpG island
ENSG00000258487	CpG island
ENSG00000259148	CpG island
ENSG00000258969	CpG island
ENSG00000258747	CpG island
ENSG00000259126	CpG island
ENSG00000259126	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000259148	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000188825	chromatin interactions
B4GALT1	miRNA target sites
FAM134B	miRNA target sites

Extended variants
information (count: 6109 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6109 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8021486	chr14:44733804-44733805	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574462282	chr14:44733816-44733817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77965275	chr14:44733889-44733890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191695480	chr14:44733922-44733923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572438558	chr14:44733992-44733993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561410869	chr14:44733995-44733996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150569130	chr14:44734003-44734004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563959847	chr14:44734118-44734119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182552971	chr14:44734168-44734169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544096796	chr14:44734173-44734174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6572245	chr14:44734184-44734185	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs6572246	chr14:44734194-44734195	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs138448774	chr14:44734233-44734234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559442845	chr14:44734250-44734251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532862700	chr14:44734260-44734261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570319812	chr14:44734315-44734316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551195331	chr14:44734418-44734419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569477352	chr14:44734441-44734442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530733485	chr14:44734450-44734451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528702597	chr14:44734451-44734452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533245617	chr14:44734454-44734455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548817110	chr14:44734477-44734478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568372605	chr14:44734478-44734479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535884377	chr14:44734546-44734547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149281522	chr14:44734640-44734641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566193211	chr14:44734685-44734686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570518022	chr14:44734701-44734702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539538667	chr14:44734748-44734749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558402843	chr14:44734794-44734795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576684307	chr14:44734831-44734832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186835580	chr14:44734853-44734854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546622431	chr14:44734877-44734878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191658669	chr14:44734884-44734885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144420227	chr14:44734902-44734903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs17654500	chr14:44734929-44734930	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs183757662	chr14:44734944-44734945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544674011	chr14:44734951-44734952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187793435	chr14:44734952-44734953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530578226	chr14:44734959-44734960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs60903115	chr14:44743025-44743026	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs570882148	chr14:44743054-44743055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78891717	chr14:44743079-44743080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556812740	chr14:44743116-44743117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112382161	chr14:44743146-44743147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181826472	chr14:44743162-44743163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185962822	chr14:44743170-44743171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs554738476	chr14:44743202-44743203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190378206	chr14:44743244-44743245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76824543	chr14:44743246-44743247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559803646	chr14:44743285-44743286	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44733600-44734600	Enhancers	Fetal Intestine Small	intestine
2	chr14:44733600-44735000	Enhancers	Fetal Intestine Large	intestine
3	chr14:44743000-44743800	Enhancers	Fetal Heart	heart
4	chr14:44752200-44752800	Enhancers	NHDF-Ad	bronchial
5	chr14:44756800-44757200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr14:44760000-44761600	Enhancers	Fetal Heart	heart
7	chr14:44766000-44766200	Enhancers	Fetal Muscle Trunk	muscle
8	chr14:44770000-44771400	Enhancers	HUVEC	blood vessel
9	chr14:44770200-44771000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr14:44778000-44779600	Enhancers	HMEC	breast
11	chr14:44778200-44778400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr14:44778200-44779800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:44778400-44779400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:44778600-44779000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr14:44778600-44779200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr14:44779400-44780000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr14:44780000-44785200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr14:44784200-44787000	Enhancers	HUVEC	blood vessel
19	chr14:44785000-44786800	Enhancers	NHDF-Ad	bronchial
20	chr14:44785200-44787000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr14:44785200-44787000	Enhancers	HMEC	breast
22	chr14:44785400-44785600	Active TSS	NHEK	skin
23	chr14:44785400-44786000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:44785400-44786000	Enhancers	A549	lung
25	chr14:44785400-44786600	Enhancers	Hela-S3	cervix
26	chr14:44785600-44785800	Flanking Active TSS	NHEK	skin
27	chr14:44785600-44786800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:44785600-44786800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr14:44785600-44786800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr14:44785600-44786800	Enhancers	NH-A	brain
31	chr14:44785600-44787000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr14:44785800-44786800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr14:44785800-44786800	Enhancers	Fetal Intestine Large	intestine
34	chr14:44785800-44787000	Enhancers	NHEK	skin
35	chr14:44786000-44786400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr14:44786000-44786800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr14:44786000-44786800	Flanking Active TSS	A549	lung
38	chr14:44786000-44787000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr14:44786200-44786800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:44786200-44786800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr14:44786200-44786800	Enhancers	Lung	lung
42	chr14:44786400-44786600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr14:44786400-44786800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr14:44786400-44787000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr14:44786600-44787000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr14:44786800-44787000	Enhancers	A549	lung
47	chr14:44786800-44789000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr14:44787000-44787800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr14:44795000-44795200	Enhancers	NHDF-Ad	bronchial
50	chr14:44795000-44798600	Enhancers	Fetal Heart	heart

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