Variant report

Variant	nsv1037731
Chromosome Location	chr14:19877060-20425497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2149)
CpG islands
(count:2870)
Chromatin interactive
region (count:5)
LncRNA
region (count:124)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2149 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20346227-20346537	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:20346241-20346527	K562	blood:	n/a	n/a
3	ARID3A	chr14:20387153-20387455	HepG2	liver:	n/a	n/a
4	ATF1	chr14:20319622-20319703	K562	blood:	n/a	n/a
5	ATF1	chr14:20374096-20374405	K562	blood:	n/a	n/a
6	ATF1	chr14:20325048-20325100	K562	blood:	n/a	n/a
7	ATF1	chr14:20388271-20388560	K562	blood:	n/a	n/a
8	BACH1	chr14:20348120-20348235	K562	blood:	n/a	n/a
9	BATF	chr14:20131255-20131487	GM12878	blood:	n/a	n/a
10	BATF	chr14:19921485-19921738	GM12878	blood:	n/a	n/a
11	BATF	chr14:19937525-19937845	GM12878	blood:	n/a	chr14:19937698-19937709
12	BATF	chr14:20026256-20026650	GM12878	blood:	n/a	n/a
13	BATF	chr14:20085953-20086237	GM12878	blood:	n/a	n/a
14	BATF	chr14:19986920-19987123	GM12878	blood:	n/a	n/a
15	BATF	chr14:20031700-20032016	GM12878	blood:	n/a	n/a
16	BATF	chr14:20025214-20025459	GM12878	blood:	n/a	n/a
17	BATF	chr14:19937503-19937859	GM12878	blood:	n/a	chr14:19937698-19937709
18	BATF	chr14:20025031-20025541	GM12878	blood:	n/a	n/a
19	BCL11A	chr14:20084307-20084477	GM12878	blood:	n/a	n/a
20	BCL11A	chr14:19920793-19920958	GM12878	blood:	n/a	n/a
21	BCL11A	chr14:20025076-20025493	GM12878	blood:	n/a	chr14:20025351-20025360
22	BCL11A	chr14:19937474-19937874	GM12878	blood:	n/a	n/a
23	BCL11A	chr14:19937603-19937812	GM12878	blood:	n/a	n/a
24	BCL11A	chr14:19921178-19921362	GM12878	blood:	n/a	n/a
25	BHLHE40	chr14:20136685-20136689	K562	blood:	n/a	n/a
26	BHLHE40	chr14:19984674-19984958	HepG2	liver:	n/a	n/a
27	BHLHE40	chr14:19937479-19937774	HepG2	liver:	n/a	n/a
28	BHLHE40	chr14:19933072-19933376	HepG2	liver:	n/a	n/a
29	BHLHE40	chr14:19921007-19921253	HepG2	liver:	n/a	n/a
30	BHLHE40	chr14:19925145-19925472	HepG2	liver:	n/a	n/a
31	BHLHE40	chr14:19973726-19973967	HepG2	liver:	n/a	n/a
32	BHLHE40	chr14:19978638-19978868	HepG2	liver:	n/a	n/a
33	BHLHE40	chr14:19932458-19932823	HepG2	liver:	n/a	chr14:19932665-19932681 chr14:19932534-19932550
34	BHLHE40	chr14:19918428-19918670	HepG2	liver:	n/a	n/a
35	CBX3	chr14:19925121-19925504	K562	blood:	n/a	n/a
36	CBX3	chr14:19937708-19938010	K562	blood:	n/a	n/a
37	CBX3	chr14:19925184-19925431	K562	blood:	n/a	n/a
38	CBX3	chr14:19937536-19938018	K562	blood:	n/a	n/a
39	CEBPB	chr14:20347421-20347704	K562	blood:	n/a	n/a
40	CEBPB	chr14:19877398-19877707	K562	blood:	n/a	n/a
41	CEBPB	chr14:20144535-20144743	IMR90	lung:	n/a	chr14:20144569-20144580
42	CEBPB	chr14:20279888-20280102	A549	lung:	n/a	n/a
43	CEBPB	chr14:20353091-20353443	IMR90	lung:	n/a	n/a
44	CEBPB	chr14:20374855-20375196	IMR90	lung:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
45	CEBPB	chr14:20420582-20420802	HepG2	liver:	n/a	chr14:20420660-20420671
46	CEBPB	chr14:20346421-20346658	HepG2	liver:	n/a	chr14:20346574-20346585
47	CEBPB	chr14:20245850-20246106	IMR90	lung:	n/a	chr14:20245944-20245955
48	CEBPB	chr14:20374865-20375205	K562	blood:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
49	CEBPB	chr14:20365988-20366164	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:20394073-20394339	HepG2	liver:	n/a	chr14:20394191-20394202

(count:2870 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:19932946-19932996	A549	lung:	n/a
2	chr14:19932946-19932996	NHDF-neo	bronchial:	n/a
3	chr14:20344394-20344444	ProgFib	skin:	n/a
4	chr14:19932946-19932996	A549	lung:	n/a
5	chr14:19932946-19932996	NHDF-neo	bronchial:	n/a
6	chr14:20344394-20344444	ProgFib	skin:	n/a
7	chr14:20344394-20344444	IMR90	lung:	fetal
8	chr14:19890087-19890137	SK-N-SH_RA	brain:	n/a
9	chr14:20136693-20136743	HCPEpiC	choroid plexus:	n/a
10	chr14:19887082-19887132	HepG2	liver:	n/a
11	chr14:20295616-20295666	GM19239	blood:	n/a
12	chr14:19960920-19960970	U87	brain:	n/a
13	chr14:19890601-19890651	GM06990	blood:	n/a
14	chr14:19890601-19890651	PrEC	prostate:	n/a
15	chr14:19932946-19932996	Hepatocyte	liver:	n/a
16	chr14:20106919-20106969	HMEC	breast:	n/a
17	chr14:20148103-20148153	AG10803	skin:	n/a
18	chr14:20012038-20012088	U87	brain:	n/a
19	chr14:20134518-20134568	Jurkat	blood:	n/a
20	chr14:19962440-19962490	HAEpiC	amniotic membrane:	n/a
21	chr14:19949555-19949605	ECC-1	luminal epithelium:	n/a
22	chr14:19925080-19925130	HRCEpiC	kidney:	n/a
23	chr14:19960920-19960970	Caco-2	colon:	n/a
24	chr14:20147187-20147237	RPTEC	kidney:	n/a
25	chr14:19962440-19962490	MCF-7	breast:	n/a
26	chr14:20148125-20148175	GM12892	blood:	n/a
27	chr14:20247697-20247747	CMK	blood:	n/a
28	chr14:20020024-20020074	HEEpiC	esophagus:	n/a
29	chr14:20387292-20387342	NH-A	brain:	n/a
30	chr14:20344394-20344444	GM12892	blood:	n/a
31	chr14:20403239-20403289	HEK293	kidney:	embryo
32	chr14:20106919-20106969	HUVEC	blood vessel:	n/a
33	chr14:19962440-19962490	HRCEpiC	kidney:	n/a
34	chr14:19888434-19888484	HAEpiC	amniotic membrane:	n/a
35	chr14:19960920-19960970	HEK293	kidney:	embryo
36	chr14:20012038-20012088	ECC-1	luminal epithelium:	n/a
37	chr14:20215980-20216030	Jurkat	blood:	n/a
38	chr14:19932946-19932996	GM12892	blood:	n/a
39	chr14:20389177-20389227	AG09309	skin:	n/a
40	chr14:20020668-20020718	SK-N-SH_RA	brain:	n/a
41	chr14:20139478-20139528	ovcar-3	ovarian:	n/a
42	chr14:19888629-19888679	PrEC	prostate:	n/a
43	chr14:20146694-20146744	HIPEpiC	eye:	n/a
44	chr14:20403845-20403895	MCF10A-Er-Src	breast:	n/a
45	chr14:20134518-20134568	NHDF-neo	bronchial:	n/a
46	chr14:20020024-20020074	NHBE	bronchial:	n/a
47	chr14:19890087-19890137	HUVEC	blood vessel:	n/a
48	chr14:20020024-20020074	HepG2	liver:	n/a
49	chr14:20344394-20344444	BJ	skin:	n/a
50	chr14:19887082-19887132	PFSK-1	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20378405..20379102-chr22:33621834..33622612,2	MCF-7	breast:
2	chr14:20421291..20423829-chr14:20424473..20427279,2	MCF-7	breast:
3	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:
4	chr14:20330082..20332945-chr14:20336237..20338891,2	K562	blood:
5	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:

(count:124 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEM-2	chr14:19921591-19921738	ENSG00000244306
2	lnc-POTEM-1	chr14:19968877-19972292	ENSG00000257931
3	lnc-POTEM-1	chr14:19955880-19955945	ENSG00000257931
4	lnc-POTEM-2	chr14:19880209-19884029	NONHSAT035503
5	lnc-POTEM-2	chr14:19925240-19925305	ENSG00000244306
6	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT035520
7	lnc-POTEM-2	chr14:19883543-19884029	ENSG00000244306
8	lnc-POTEM-2	chr14:19894700-19894790	ENSG00000244306
9	lnc-OR4N2-1	chr14:20150010-20150118	ENSG00000257395
10	lnc-POTEM-2	chr14:19923013-19923123	NONHSAT035521
11	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT140152
12	lnc-POTEM-2	chr14:19925240-19925345	ENSG00000244306
13	lnc-POTEM-6	chr14:19887445-19887497	ENSG00000257898.1
14	lnc-POTEM-2	chr14:19921591-19921738	ENSG00000244306
15	lnc-POTEM-1	chr14:19963420-19963645	ENSG00000257931.2
16	lnc-POTEM-2	chr14:19894700-19894790	ENSG00000244306
17	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT035521
18	lnc-POTEM-2	chr14:19881070-19881410	ucscGeneNc_uc001vxa_1
19	lnc-POTEM-2	chr14:19919492-19919581	ENSG00000244306
20	lnc-POTEM-2	chr14:19892138-19892361	ENSG00000244306
21	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
22	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
23	lnc-POTEM-2	chr14:19880596-19880882	ENSG00000244306
24	lnc-POTEM-1	chr14:19932012-19932316	ENSG00000257931
25	lnc-POTEM-2	chr14:19919492-19919629	NR_110526
26	lnc-POTEM-2	chr14:19912755-19913184	ENSG00000244306
27	lnc-POTEM-2	chr14:19925240-19925300	ENSG00000244306
28	lnc-POTEM-2	chr14:19884775-19884897	ENSG00000244306
29	lnc-POTEM-1	chr14:19955880-19955945	ENSG00000257931.2
30	lnc-POTEM-2	chr14:19891517-19892052	ENSG00000244306
31	lnc-POTEM-2	chr14:19919138-19919273	ENSG00000244306
32	lnc-POTEM-2	chr14:19893856-19894790	ENSG00000244306
33	lnc-OR4N2-1	chr14:20149579-20149748	ENSG00000257395
34	lnc-POTEM-2	chr14:19919492-19919629	NONHSAT035503
35	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT035520
36	lnc-POTEM-2	chr14:19923009-19923123	ENSG00000244306
37	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
38	lnc-POTEM-2	chr14:19921591-19921738	ENSG00000244306
39	lnc-POTEM-2	chr14:19883801-19884029	ENSG00000244306
40	lnc-POTEM-2	chr14:19923013-19923123	ENSG00000244306
41	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
42	lnc-POTEM-2	chr14:19923013-19923123	NR_110526
43	lnc-POTEM-4	chr14:20145803-20146140	ENSG00000259069.1
44	lnc-OR4N2-1	chr14:20151685-20152898	ENSG00000257395
45	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
46	lnc-POTEM-2	chr14:19918476-19918662	ENSG00000244306
47	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
48	lnc-POTEM-2	chr14:19923013-19923068	NONHSAT035522
49	lnc-POTEM-2	chr14:19894700-19894790	ENSG00000244306
50	lnc-OR4N2-4	chr14:19894369-19894691	ENSG00000215394

No data

Variant related genes	Relation type
ENSG00000259016	TF binding region
OR4K5	TF binding region
ENSG00000244306	TF binding region
ENSG00000257142	TF binding region
ENSG00000259069	TF binding region
OR4K4P	TF binding region
ENSG00000257884	TF binding region
ENSG00000258324	TF binding region
OR4K3	TF binding region
ARHGAP42P4	TF binding region
ENSG00000238492	TF binding region
OR4K16P	TF binding region
ENSG00000257846	TF binding region
BMS1P18	TF binding region
OR11H2	TF binding region
ENSG00000257357	TF binding region
ENSG00000257868	TF binding region
OR4N2	TF binding region
ENSG00000258027	TF binding region
OR4K1	TF binding region
MED15P6	TF binding region
OR4M1	TF binding region
OR11K2P	TF binding region
ENSG00000257395	TF binding region
OR4N1P	TF binding region
ENSG00000257493	TF binding region
OR4Q3	TF binding region
ENSG00000258276	TF binding region
OR4H12P	TF binding region
ENSG00000257931	TF binding region
OR4K6P	TF binding region
GRAMD4P4	TF binding region
ENSG00000257751	TF binding region
RNU6-1268P	TF binding region
ENSG00000257977	TF binding region
ENSG00000257432	TF binding region
POTEM	TF binding region
OR4K2	TF binding region
ENSG00000259016	CpG island
OR4K5	CpG island
ENSG00000244306	CpG island
ENSG00000257142	CpG island
ENSG00000259069	CpG island
OR4K4P	CpG island
ENSG00000257884	CpG island
ENSG00000258324	CpG island
OR4K3	CpG island
ARHGAP42P4	CpG island
ENSG00000238492	CpG island
OR4K16P	CpG island
ENSG00000257846	CpG island
BMS1P18	CpG island
OR11H2	CpG island
ENSG00000257357	CpG island
ENSG00000257868	CpG island
OR4N2	CpG island
ENSG00000258027	CpG island
OR4K1	CpG island
MED15P6	CpG island
OR4M1	CpG island
OR11K2P	CpG island
ENSG00000257395	CpG island
OR4N1P	CpG island
ENSG00000257493	CpG island
OR4Q3	CpG island
ENSG00000258276	CpG island
OR4H12P	CpG island
ENSG00000257931	CpG island
OR4K6P	CpG island
GRAMD4P4	CpG island
ENSG00000257751	CpG island
RNU6-1268P	CpG island
ENSG00000257977	CpG island
ENSG00000257432	CpG island
POTEM	CpG island
OR4K2	CpG island
ENSG00000176290	chromatin interactions
ENSG00000258822	chromatin interactions

Extended variants
information (count: 6487 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:6487 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112347668	chr14:19878069-19878070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116111797	chr14:19878078-19878079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183610156	chr14:19878097-19878098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188704255	chr14:19878112-19878113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559792128	chr14:19878125-19878126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533415631	chr14:19878136-19878137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77774152	chr14:19878162-19878163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113754282	chr14:19878183-19878184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569860297	chr14:19878186-19878187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs72661549	chr14:19878187-19878188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374711775	chr14:19878193-19878194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200582753	chr14:19878221-19878222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549239757	chr14:19878222-19878223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567421667	chr14:19878232-19878233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368859796	chr14:19878404-19878405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs202062072	chr14:19878419-19878420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552511737	chr14:19878428-19878429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577223310	chr14:19878438-19878439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181141059	chr14:19878461-19878462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146196558	chr14:19878480-19878481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs28636498	chr14:19878503-19878504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368439428	chr14:19878563-19878564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373142970	chr14:19880223-19880224	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs560923600	chr14:19880393-19880394	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs377507852	chr14:19880408-19880409	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs546467886	chr14:19880419-19880420	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs571179833	chr14:19880436-19880437	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs370696599	chr14:19880480-19880481	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs532288359	chr14:19880800-19880801	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs550118999	chr14:19880808-19880809	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs568836455	chr14:19880859-19880860	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs535959905	chr14:19880867-19880868	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs554687445	chr14:19880882-19880883	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs375381403	chr14:19880904-19880905	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs367631003	chr14:19880917-19880918	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs370349132	chr14:19880934-19880935	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs375494041	chr14:19880941-19880942	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs368706431	chr14:19880959-19880960	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs567740807	chr14:19880974-19880975	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs535264547	chr14:19880980-19880981	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs553627635	chr14:19881006-19881007	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs2495118	chr14:19881022-19881023	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs61968489	chr14:19881057-19881058	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs578241919	chr14:19881125-19881126	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs545726236	chr14:19881166-19881167	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs202116778	chr14:19881184-19881185	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs557027508	chr14:19881189-19881190	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs376974029	chr14:19881205-19881206	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs575642388	chr14:19881232-19881233	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs542746624	chr14:19881296-19881297	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ependymoma	20639864	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:19878000-19878600	Enhancers	Dnd41	blood
2	chr14:19885600-19888800	Weak transcription	A549	lung
3	chr14:19887200-19890200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr14:19887400-19894400	Weak transcription	HepG2	liver
5	chr14:19888400-19888600	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr14:19888400-19889000	Enhancers	Placenta	Placenta
7	chr14:19888400-19891000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:19888600-19888800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
9	chr14:19888600-19889000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr14:19888600-19890400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr14:19888600-19891000	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
12	chr14:19888600-19891200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:19888800-19889000	ZNF genes & repeats	A549	lung
14	chr14:19888800-19889200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
15	chr14:19889000-19892600	Weak transcription	A549	lung
16	chr14:19889800-19891000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr14:19890000-19891000	ZNF genes & repeats	Dnd41	blood
18	chr14:19890200-19891200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr14:19890600-19891000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr14:19890800-19891000	ZNF genes & repeats	Fetal Kidney	kidney
21	chr14:19890800-19891200	ZNF genes & repeats	K562	blood
22	chr14:19891000-19891200	Enhancers	Dnd41	blood
23	chr14:19891000-19893000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr14:19891200-19894200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr14:19893000-19893200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr14:19916600-19920400	Weak transcription	HepG2	liver
27	chr14:19919800-19920400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr14:19920400-19920800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr14:19920400-19920800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr14:19920400-19920800	Enhancers	HepG2	liver
31	chr14:19920600-19920800	Enhancers	Dnd41	blood
32	chr14:19920800-19924400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr14:19920800-19924800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr14:19920800-19924800	Weak transcription	HepG2	liver
35	chr14:19921000-19921600	Weak transcription	Dnd41	blood
36	chr14:19921600-19922600	Enhancers	Dnd41	blood
37	chr14:19924400-19925200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr14:19924800-19925200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr14:19924800-19925200	Active TSS	HepG2	liver
40	chr14:19932800-19933400	Active TSS	HepG2	liver
41	chr14:19933000-19933400	Active TSS	A549	lung
42	chr14:20031400-20031800	Enhancers	HepG2	liver
43	chr14:20094600-20095000	Enhancers	Adipose Nuclei	Adipose
44	chr14:20094600-20095000	Enhancers	Placenta	Placenta
45	chr14:20136400-20136600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr14:20136400-20137600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
47	chr14:20136400-20137800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
48	chr14:20136400-20138000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:20136600-20136800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr14:20137200-20137800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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