Variant report

Variant	esv2829993
Chromosome Location	chr14:19700048-20425051
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3216)
CpG islands
(count:3478)
Chromatin interactive
region (count:5)
LncRNA
region (count:134)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3216 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

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	chr14:20388271-20388560	K562	blood:	n/a	n/a
5	ATF1	chr14:19795048-19796237	K562	blood:	n/a	n/a
6	ATF1	chr14:20319622-20319703	K562	blood:	n/a	n/a
7	ATF1	chr14:20325048-20325100	K562	blood:	n/a	n/a
8	ATF1	chr14:19792967-19794009	K562	blood:	n/a	n/a
9	ATF1	chr14:20374096-20374405	K562	blood:	n/a	n/a
10	BACH1	chr14:19795663-19796213	K562	blood:	n/a	n/a
11	BACH1	chr14:20348120-20348235	K562	blood:	n/a	n/a
12	BATF	chr14:20031700-20032016	GM12878	blood:	n/a	n/a
13	BATF	chr14:20025214-20025459	GM12878	blood:	n/a	n/a
14	BATF	chr14:19921485-19921738	GM12878	blood:	n/a	n/a
15	BATF	chr14:20131255-20131487	GM12878	blood:	n/a	n/a
16	BATF	chr14:19986920-19987123	GM12878	blood:	n/a	n/a
17	BATF	chr14:20085953-20086237	GM12878	blood:	n/a	n/a
18	BATF	chr14:20026256-20026650	GM12878	blood:	n/a	n/a
19	BATF	chr14:19937525-19937845	GM12878	blood:	n/a	chr14:19937698-19937709
20	BATF	chr14:19937503-19937859	GM12878	blood:	n/a	chr14:19937698-19937709
21	BATF	chr14:20025031-20025541	GM12878	blood:	n/a	n/a
22	BATF	chr14:19748478-19748726	GM12878	blood:	n/a	n/a
23	BATF	chr14:19827024-19827305	GM12878	blood:	n/a	n/a
24	BCL11A	chr14:19747728-19747905	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:19746165-19746357	GM12878	blood:	n/a	n/a
26	BCL11A	chr14:19776347-19776520	GM12878	blood:	n/a	n/a
27	BCL11A	chr14:19827039-19827376	GM12878	blood:	n/a	n/a
28	BCL11A	chr14:19937474-19937874	GM12878	blood:	n/a	n/a
29	BCL11A	chr14:19829015-19829207	GM12878	blood:	n/a	n/a
30	BCL11A	chr14:19937603-19937812	GM12878	blood:	n/a	n/a
31	BCL11A	chr14:20025076-20025493	GM12878	blood:	n/a	chr14:20025351-20025360
32	BCL11A	chr14:19824315-19824574	GM12878	blood:	n/a	n/a
33	BCL11A	chr14:19826185-19826607	GM12878	blood:	n/a	n/a
34	BCL11A	chr14:19819837-19820033	GM12878	blood:	n/a	n/a
35	BCL11A	chr14:19920793-19920958	GM12878	blood:	n/a	n/a
36	BCL11A	chr14:19753894-19754206	GM12878	blood:	n/a	n/a
37	BCL11A	chr14:19748407-19748711	GM12878	blood:	n/a	n/a
38	BCL11A	chr14:20084307-20084477	GM12878	blood:	n/a	n/a
39	BCL11A	chr14:19748843-19749025	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:19921178-19921362	GM12878	blood:	n/a	n/a
41	BCL11A	chr14:19821581-19821893	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:19747489-19747677	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:19827491-19827723	GM12878	blood:	n/a	n/a
44	BCL11A	chr14:19826657-19827003	GM12878	blood:	n/a	n/a
45	BHLHE40	chr14:19973726-19973967	HepG2	liver:	n/a	n/a
46	BHLHE40	chr14:19978638-19978868	HepG2	liver:	n/a	n/a
47	BHLHE40	chr14:19925145-19925472	HepG2	liver:	n/a	n/a
48	BHLHE40	chr14:19932458-19932823	HepG2	liver:	n/a	chr14:19932665-19932681 chr14:19932534-19932550
49	BHLHE40	chr14:19921007-19921253	HepG2	liver:	n/a	n/a
50	BHLHE40	chr14:19937479-19937774	HepG2	liver:	n/a	n/a

(count:3478 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:19890601-19890651	HCF	heart:	n/a
2	chr14:19890601-19890651	HCF	heart:	n/a
3	chr14:20215980-20216030	A549	lung:	n/a
4	chr14:20106919-20106969	SK-N-SH	brain:	n/a
5	chr14:20136822-20136872	HRE	kidney:	n/a
6	chr14:19950047-19950097	CMK	blood:	n/a
7	chr14:20020762-20020812	GM12891	blood:	n/a
8	chr14:20344083-20344133	HRE	kidney:	n/a
9	chr14:19959522-19959572	K562	blood:	n/a
10	chr14:19950047-19950097	ProgFib	skin:	n/a
11	chr14:19746900-19746950	HCM	heart:	n/a
12	chr14:20146694-20146744	HRPEpiC	eye:	n/a
13	chr14:19855384-19855434	IMR90	lung:	fetal
14	chr14:20134518-20134568	AG04449	skin:	fetal
15	chr14:20020762-20020812	NT2-D1	testis:	n/a
16	chr14:20137365-20137415	HEEpiC	esophagus:	n/a
17	chr14:20139478-20139528	MCF-7	breast:	n/a
18	chr14:20135228-20135278	LNCaP	prostate:	n/a
19	chr14:20136822-20136872	A549	lung:	n/a
20	chr14:20403239-20403289	GM12891	blood:	n/a
21	chr14:19747134-19747184	A549	lung:	n/a
22	chr14:19888434-19888484	HepG2	liver:	n/a
23	chr14:20135228-20135278	AG09309	skin:	n/a
24	chr14:19949555-19949605	T-47D	breast:	n/a
25	chr14:19964024-19964074	HRPEpiC	eye:	n/a
26	chr14:19719117-19719167	BJ	skin:	n/a
27	chr14:20148103-20148153	K562	blood:	n/a
28	chr14:19719117-19719167	GM19239	blood:	n/a
29	chr14:20387292-20387342	SAEC	small airway:	n/a
30	chr14:19890601-19890651	LNCaP	prostate:	n/a
31	chr14:19828288-19828338	U87	brain:	n/a
32	chr14:19962440-19962490	PANC-1	pancreas:	n/a
33	chr14:20147652-20147702	MCF10A-Er-Src	breast:	n/a
34	chr14:19960976-19961026	AG10803	skin:	n/a
35	chr14:20020668-20020718	SK-N-SH_RA	brain:	n/a
36	chr14:19950047-19950097	BE2_C	brain:	n/a
37	chr14:19855384-19855434	HCPEpiC	choroid plexus:	n/a
38	chr14:20020024-20020074	PANC-1	pancreas:	n/a
39	chr14:19950047-19950097	AG09309	skin:	n/a
40	chr14:20215980-20216030	ovcar-3	ovarian:	n/a
41	chr14:20247697-20247747	HMEC	breast:	n/a
42	chr14:20137365-20137415	ECC-1	luminal epithelium:	n/a
43	chr14:20147187-20147237	CMK	blood:	n/a
44	chr14:19855113-19855163	SK-N-SH_RA	brain:	n/a
45	chr14:20136693-20136743	LNCaP	prostate:	n/a
46	chr14:20012038-20012088	NHDF-neo	bronchial:	n/a
47	chr14:20344083-20344133	HAEpiC	amniotic membrane:	n/a
48	chr14:19858845-19858895	BE2_C	brain:	n/a
49	chr14:19949555-19949605	HMEC	breast:	n/a
50	chr14:19828288-19828338	AG09309	skin:	n/a

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

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

(count:134 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4N2-3	chr14:20008836-20010958	ENSG00000258276
2	lnc-POTEM-2	chr14:19919138-19919273	ENSG00000244306
3	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT035503
4	lnc-POTEM-2	chr14:19918476-19918662	ENSG00000244306
5	lnc-POTEM-1	chr14:19968877-19972292	ENSG00000257931
6	lnc-OR4N2-4	chr14:19896785-19896872	XLOC_010749
7	lnc-POTEM-2	chr14:19883543-19884029	ENSG00000244306
8	lnc-POTEM-1	chr14:19963420-19963645	ENSG00000257931.2
9	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
10	lnc-POTEM-2	chr14:19919138-19919273	NONHSAT035503
11	lnc-POTEM-2	chr14:19925240-19925332	ENSG00000244306
12	lnc-POTEM-2	chr14:19925240-19925294	NONHSAT035522
13	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
14	lnc-POTEM-2	chr14:19921359-19921455	ENSG00000244306
15	lnc-POTEM-1	chr14:19955880-19955945	ENSG00000257931
16	lnc-POTEM-2	chr14:19921648-19921738	NONHSAT035522
17	lnc-POTEM-2	chr14:19925240-19925288	ENSG00000244306
18	lnc-POTEG-5	chr14:19859457-19859970	ENSG00000258188.1
19	lnc-POTEM-2	chr14:19911916-19913315	NONHSAT035515
20	lnc-OR4K14-1	chr14:20376255-20376808	NONHSAT035546
21	lnc-POTEM-2	chr14:19919138-19919273	ENSG00000244306
22	lnc-OR4N2-3	chr14:20008836-20010956	NR_110505
23	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT035521
24	lnc-POTEG-5	chr14:19812176-19812247	ENSG00000258188.1
25	lnc-POTEM-2	chr14:19894700-19894731	NONHSAT035499
26	lnc-POTEM-2	chr14:19880209-19884029	NONHSAT035503
27	lnc-POTEM-2	chr14:19925240-19925300	ENSG00000244306
28	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
29	lnc-POTEM-1	chr14:19944559-19944820	ENSG00000257931
30	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
31	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
32	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT140152
33	lnc-POTEM-2	chr14:19921359-19921470	NR_110526
34	lnc-POTEM-2	chr14:19912755-19913184	ENSG00000244306
35	lnc-POTEM-2	chr14:19919492-19919581	ENSG00000244306
36	lnc-POTEM-2	chr14:19894710-19894790	ENSG00000244306
37	lnc-POTEM-1	chr14:19963420-19963689	ENSG00000257931
38	lnc-POTEM-1	chr14:19932012-19932316	ENSG00000257931.2
39	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT140152
40	lnc-POTEM-2	chr14:19923013-19923123	NONHSAT035521
41	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT035503
42	lnc-POTEM-2	chr14:19894700-19894790	NONHSAT035503
43	lnc-OR4N2-4	chr14:19901742-19901892	ENSG00000215394
44	lnc-POTEM-2	chr14:19923013-19923068	NONHSAT035522
45	lnc-POTEM-2	chr14:19894700-19894790	NR_110526
46	lnc-POTEM-2	chr14:19921591-19921738	NR_110526
47	lnc-OR4N2-1	chr14:20149579-20149748	ENSG00000257395
48	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT035520
49	lnc-POTEM-2	chr14:19925240-19925348	ENSG00000244306
50	lnc-POTEM-2	chr14:19894700-19894790	ENSG00000244306

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
ENSG00000257573	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
OR11H13P	TF binding region
ENSG00000258027	TF binding region
OR4K1	TF binding region
ENSG00000258198	TF binding region
MED15P6	TF binding region
OR4M1	TF binding region
ENSG00000258781	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
ENSG00000271632	TF binding region
OR4H12P	TF binding region
ENSG00000257931	TF binding region
OR4K6P	TF binding region
ENSG00000257310	TF binding region
GRAMD4P4	TF binding region
ENSG00000257751	TF binding region
RNU6-1268P	TF binding region
ENSG00000257749	TF binding region
ENSG00000258188	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
ENSG00000257573	CpG island
ENSG00000257846	CpG island
BMS1P18	CpG island
OR11H2	CpG island
ENSG00000257357	CpG island
ENSG00000257868	CpG island
OR4N2	CpG island
OR11H13P	CpG island
ENSG00000258027	CpG island
OR4K1	CpG island
ENSG00000258198	CpG island
MED15P6	CpG island
OR4M1	CpG island
ENSG00000258781	CpG island
OR11K2P	CpG island
ENSG00000257395	CpG island
OR4N1P	CpG island
ENSG00000257493	CpG island
OR4Q3	CpG island
ENSG00000258276	CpG island
ENSG00000271632	CpG island
OR4H12P	CpG island
ENSG00000257931	CpG island
OR4K6P	CpG island
ENSG00000257310	CpG island
GRAMD4P4	CpG island
ENSG00000257751	CpG island
RNU6-1268P	CpG island
ENSG00000257749	CpG island
ENSG00000258188	CpG island
ENSG00000257977	CpG island
ENSG00000257432	CpG island
POTEM	CpG island
OR4K2	CpG island
ENSG00000176290	chromatin interactions
ENSG00000258822	chromatin interactions

Extended variants
information (count: 8590 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:8590 , 50 per page) page: 1 2 3 4 5 6 7 ... 172

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200645918	chr14:19722366-19722367	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs568733014	chr14:19722395-19722396	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200661704	chr14:19722476-19722477	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559082504	chr14:19722490-19722491	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs368059237	chr14:19722498-19722499	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs567299092	chr14:19723296-19723297	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs558410795	chr14:19724253-19724254	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs375973457	chr14:19724668-19724669	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs201315014	chr14:19724670-19724671	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs61970866	chr14:19725214-19725215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs3001824	chr14:19737862-19737863	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs61970896	chr14:19737899-19737900	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs28882474	chr14:19737925-19737926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs61970897	chr14:19738080-19738081	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs28882242	chr14:19738105-19738106	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs1925985	chr14:19738180-19738181	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2495358	chr14:19739980-19739981	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs61970899	chr14:19740053-19740054	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs61970900	chr14:19740256-19740257	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs78360885	chr14:19740646-19740647	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs113004813	chr14:19740757-19740758	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs61970901	chr14:19740788-19740789	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs61970902	chr14:19741022-19741023	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs61970903	chr14:19741178-19741179	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs61970904	chr14:19741434-19741435	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs61970905	chr14:19741464-19741465	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs61970906	chr14:19741518-19741519	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs557441968	chr14:19741800-19741801	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs575314618	chr14:19741808-19741809	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs542783317	chr14:19741828-19741829	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs554500303	chr14:19741837-19741838	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs573173486	chr14:19741856-19741857	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs540537935	chr14:19741893-19741894	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs201810074	chr14:19742131-19742132	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs61970907	chr14:19742352-19742353	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs61970908	chr14:19742503-19742504	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs200110714	chr14:19742858-19742859	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs201402230	chr14:19744329-19744330	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs202147438	chr14:19744430-19744431	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs372324734	chr14:19744447-19744448	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs375880213	chr14:19744451-19744452	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs367964977	chr14:19744512-19744513	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs543945414	chr14:19744529-19744530	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs201294428	chr14:19744541-19744542	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs3001827	chr14:19744650-19744651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs78281641	chr14:19744672-19744673	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs79931929	chr14:19744677-19744678	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs112353993	chr14:19744690-19744691	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs374780693	chr14:19744728-19744729	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs369841132	chr14:19744871-19744872	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:19761400-19761600	Enhancers	Dnd41	blood
2	chr14:19763800-19764600	Weak transcription	Dnd41	blood
3	chr14:19764600-19764800	Enhancers	Dnd41	blood
4	chr14:19764800-19766400	Weak transcription	Dnd41	blood
5	chr14:19766400-19768200	Enhancers	Dnd41	blood
6	chr14:19768200-19771800	Weak transcription	Dnd41	blood
7	chr14:19771800-19772200	Active TSS	Dnd41	blood
8	chr14:19772200-19772600	Flanking Active TSS	Dnd41	blood
9	chr14:19772600-19772800	Active TSS	Dnd41	blood
10	chr14:19772800-19774000	Transcr. at gene 5' and 3'	Dnd41	blood
11	chr14:19774000-19775200	Weak transcription	Dnd41	blood
12	chr14:19775200-19775600	Flanking Active TSS	Dnd41	blood
13	chr14:19775600-19781000	Weak transcription	Dnd41	blood
14	chr14:19781000-19781200	Enhancers	Dnd41	blood
15	chr14:19781200-19783600	Weak transcription	Dnd41	blood
16	chr14:19783800-19784200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr14:19784000-19784200	Enhancers	Dnd41	blood
18	chr14:19785800-19786000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:19789600-19790400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr14:19792800-19794200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr14:19793000-19793200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
22	chr14:19793000-19793400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
23	chr14:19793000-19793800	ZNF genes & repeats	Fetal Lung	lung
24	chr14:19793000-19796000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr14:19793000-19796000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:19793000-19796000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr14:19793000-19796200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:19793200-19794400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
29	chr14:19793400-19795400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
30	chr14:19794000-19796000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr14:19794800-19795400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr14:19795000-19796200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr14:19795200-19795800	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr14:19795200-19796000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr14:19795400-19795600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr14:19795600-19795800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr14:19795800-19796000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr14:19795800-19796000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr14:19806400-19806800	Active TSS	Brain Substantia Nigra	brain
40	chr14:19806600-19807200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr14:19806800-19807400	Bivalent/Poised TSS	Brain Substantia Nigra	brain
42	chr14:19807200-19810800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr14:19810800-19811000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr14:19811000-19812800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr14:19812800-19813000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr14:19814600-19814800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:19814800-19817400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:19817400-19820200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:19818600-19823600	Weak transcription	Pancreas	Pancrea
50	chr14:19819400-19820200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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