Variant report

Variant	nsv458957
Chromosome Location	chr20:26085338-26246086
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2314)
CpG islands
(count:1038)
Chromatin interactive
region (count:66)
LncRNA
region (count:186)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2314 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:26188665-26190661	K562	blood:	n/a	n/a
2	ARID3A	chr20:26188670-26190654	HepG2	liver:	n/a	n/a
3	ATF1	chr20:26210425-26210440	K562	blood:	n/a	n/a
4	ATF1	chr20:26206579-26206689	K562	blood:	n/a	n/a
5	ATF1	chr20:26202933-26202936	K562	blood:	n/a	n/a
6	ATF1	chr20:26204024-26204365	K562	blood:	n/a	n/a
7	ATF1	chr20:26210887-26211336	K562	blood:	n/a	n/a
8	ATF1	chr20:26200807-26200973	K562	blood:	n/a	n/a
9	ATF1	chr20:26207700-26208236	K562	blood:	n/a	n/a
10	ATF1	chr20:26213000-26213056	K562	blood:	n/a	n/a
11	ATF1	chr20:26202019-26202231	K562	blood:	n/a	n/a
12	ATF1	chr20:26207076-26207177	K562	blood:	n/a	n/a
13	ATF1	chr20:26209393-26209538	K562	blood:	n/a	n/a
14	ATF1	chr20:26201702-26201703	K562	blood:	n/a	n/a
15	ATF1	chr20:26212000-26212002	K562	blood:	n/a	n/a
16	ATF2	chr20:26188609-26189520	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr20:26188742-26189499	GM12878	blood:	n/a	n/a
18	ATF2	chr20:26189688-26190460	GM12878	blood:	n/a	n/a
19	ATF2	chr20:26188598-26189527	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr20:26189559-26190696	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr20:26188658-26189437	GM12878	blood:	n/a	n/a
22	ATF2	chr20:26190350-26190549	GM12878	blood:	n/a	n/a
23	ATF2	chr20:26189705-26190319	GM12878	blood:	n/a	n/a
24	ATF2	chr20:26189566-26190667	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr20:26189239-26189386	K562	blood:	n/a	n/a
26	ATF3	chr20:26189724-26190322	HepG2	liver:	n/a	n/a
27	ATF3	chr20:26188697-26190655	K562	blood:	n/a	chr20:26190344-26190352
28	ATF3	chr20:26188778-26189204	GM12878	blood:	n/a	n/a
29	ATF3	chr20:26188637-26190747	A549	lung:	n/a	chr20:26190344-26190352
30	ATF3	chr20:26190389-26190519	K562	blood:	n/a	n/a
31	ATF3	chr20:26189743-26190295	GM12878	blood:	n/a	n/a
32	ATF3	chr20:26188677-26189497	HepG2	liver:	n/a	n/a
33	ATF3	chr20:26188643-26190671	A549	lung:	n/a	chr20:26190344-26190352
34	ATF3	chr20:26188754-26189204	K562	blood:	n/a	n/a
35	ATF3	chr20:26188662-26189535	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF3	chr20:26189549-26190567	H1-hESC	embryonic stem cell:	n/a	chr20:26190344-26190352
37	ATF3	chr20:26190355-26190540	HepG2	liver:	n/a	n/a
38	ATF3	chr20:26189747-26190340	K562	blood:	n/a	n/a
39	ATF3	chr20:26189707-26190649	H1-hESC	embryonic stem cell:	n/a	chr20:26190344-26190352
40	ATF3	chr20:26189712-26190314	K562	blood:	n/a	n/a
41	BACH1	chr20:26188659-26190667	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr20:26203731-26203928	K562	blood:	n/a	n/a
43	BACH1	chr20:26188668-26190665	K562	blood:	n/a	n/a
44	BATF	chr20:26189721-26190303	GM12878	blood:	n/a	n/a
45	BATF	chr20:26188677-26189220	GM12878	blood:	n/a	n/a
46	BATF	chr20:26086012-26086209	GM12878	blood:	n/a	n/a
47	BATF	chr20:26104768-26105049	GM12878	blood:	n/a	n/a
48	BCL11A	chr20:26120133-26120429	GM12878	blood:	n/a	n/a
49	BCL11A	chr20:26188682-26189216	GM12878	blood:	n/a	chr20:26188715-26188728 chr20:26188719-26188732 chr20:26189177-26189186
50	BCL11A	chr20:26189727-26190296	GM12878	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:26188976-26189026	HRPEpiC	eye:	n/a
2	chr20:26188976-26189026	HRPEpiC	eye:	n/a
3	chr20:26192541-26192591	AG04449	skin:	fetal
4	chr20:26188976-26189026	ovcar-3	ovarian:	n/a
5	chr20:26192541-26192591	AG09309	skin:	n/a
6	chr20:26188997-26189047	U87	brain:	n/a
7	chr20:26188997-26189047	NB4	blood:	n/a
8	chr20:26192541-26192591	HAEpiC	amniotic membrane:	n/a
9	chr20:26192541-26192591	GM12891	blood:	n/a
10	chr20:26192541-26192591	Caco-2	colon:	n/a
11	chr20:26190328-26190378	BJ	skin:	n/a
12	chr20:26189240-26189290	A549	lung:	n/a
13	chr20:26188976-26189026	BJ	skin:	n/a
14	chr20:26189665-26189715	GM12892	blood:	n/a
15	chr20:26190354-26190404	SK-N-SH_RA	brain:	n/a
16	chr20:26186545-26186595	AoSMC	blood vessel:	n/a
17	chr20:26186908-26186958	HMEC	breast:	n/a
18	chr20:26188919-26188969	MCF-7	breast:	n/a
19	chr20:26189510-26189560	GM12891	blood:	n/a
20	chr20:26189665-26189715	NB4	blood:	n/a
21	chr20:26189665-26189715	ovcar-3	ovarian:	n/a
22	chr20:26188919-26188969	NB4	blood:	n/a
23	chr20:26186908-26186958	SK-N-SH_RA	brain:	n/a
24	chr20:26186545-26186595	SK-N-SH	brain:	n/a
25	chr20:26188943-26188993	HRPEpiC	eye:	n/a
26	chr20:26188919-26188969	HCPEpiC	choroid plexus:	n/a
27	chr20:26188976-26189026	HL-60	blood:	n/a
28	chr20:26190328-26190378	GM12891	blood:	n/a
29	chr20:26188971-26189021	HIPEpiC	eye:	n/a
30	chr20:26189240-26189290	HRPEpiC	eye:	n/a
31	chr20:26188963-26189013	T-47D	breast:	n/a
32	chr20:26190328-26190378	SKMC	muscle:	n/a
33	chr20:26188639-26188689	HMEC	breast:	n/a
34	chr20:26188908-26188958	ECC-1	luminal epithelium:	n/a
35	chr20:26188943-26188993	HEEpiC	esophagus:	n/a
36	chr20:26190347-26190397	Hepatocyte	liver:	n/a
37	chr20:26190354-26190404	MCF10A-Er-Src	breast:	n/a
38	chr20:26186908-26186958	A549	lung:	n/a
39	chr20:26192541-26192591	NT2-D1	testis:	n/a
40	chr20:26188908-26188958	AG09309	skin:	n/a
41	chr20:26188963-26189013	GM06990	blood:	n/a
42	chr20:26189665-26189715	RPTEC	kidney:	n/a
43	chr20:26186908-26186958	HEK293	kidney:	embryo
44	chr20:26189240-26189290	Hela-S3	cervix:	n/a
45	chr20:26190347-26190397	HRPEpiC	eye:	n/a
46	chr20:26188908-26188958	SAEC	small airway:	n/a
47	chr20:26188908-26188958	PrEC	prostate:	n/a
48	chr20:26188919-26188969	PrEC	prostate:	n/a
49	chr20:26192541-26192591	HCF	heart:	n/a
50	chr20:26188997-26189047	H1-hESC	embryonic stem cell:	embryo

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:26201915..26204776-chr3:75992954..75996738,5	MCF-7	breast:
2	chr20:26199924..26201625-chr3:75995563..75997738,2	MCF-7	breast:
3	chr2:133014709..133015762-chr20:26188882..26190143,12	MCF-7	breast:
4	chr20:26201563..26203476-chr3:75993448..75995749,2	K562	blood:
5	chr2:133014727..133015757-chr20:26189158..26190413,12	MCF-7	breast:
6	chr2:133013729..133016735-chr20:26188305..26190826,4	MCF-7	breast:
7	chr20:26208095..26209894-chr3:75988198..75990401,2	MCF-7	breast:
8	chr2:133015211..133015762-chr20:26189170..26190019,2	MCF-7	breast:
9	chr20:26188433..26190277-chr3:193787174..193790154,2	K562	blood:
10	chr2:133014681..133015764-chr20:26189070..26190458,26	MCF-7	breast:
11	chr20:26188947..26190833-chr6:26156720..26159562,2	MCF-7	breast:
12	chr16:33964537..33965670-chr20:26188912..26190067,3	K562	blood:
13	chr20:26187273..26191752-chr21:9823988..9828758,49	MCF-7	breast:
14	chr2:133014718..133015708-chr20:26189240..26189953,2	MCF-7	breast:
15	chr12:20703970..20704942-chr20:26190011..26190793,2	K562	blood:
16	chr20:26188395..26190565-chr6:74228700..74231505,2	MCF-7	breast:
17	chr20:26187350..26191964-chr21:9824053..9828992,54	K562	blood:
18	chr18:8406500..8407500-chr20:26188735..26189378,2	MCF-7	breast:
19	chr19:56154889..56155389-chr20:26189706..26190477,2	K562	blood:
20	chr16:33960878..33961871-chr20:26188853..26189656,7	MCF-7	breast:
21	chr20:26206073..26206971-chr3:75991464..75992265,2	MCF-7	breast:
22	chr20:26188251..26190477-chr21:9825050..9827838,61	MCF-7	breast:
23	chr2:133011277..133016757-chr20:26187363..26191986,20	K562	blood:
24	chr1:109756113..109757974-chr20:26187645..26190102,2	MCF-7	breast:
25	chr16:33961305..33961892-chr20:26188839..26189533,2	MCF-7	breast:
26	chr20:26187252..26191975-chr21:9823984..9828995,56	MCF-7	breast:
27	chr20:26188341..26189368-chr21:9825099..9826092,4	MCF-7	breast:
28	chr13:63637188..63639152-chr20:26145559..26148373,3	K562	blood:
29	chr2:133011277..133017359-chr20:26187383..26191986,21	K562	blood:
30	chr13:63637281..63639152-chr20:26145559..26147940,2	K562	blood:
31	chr20:26188275..26190944-chr21:9825018..9827152,38	MCF-7	breast:
32	chr13:63647679..63650483-chr20:26148365..26151073,2	K562	blood:
33	chr17:73256462..73259302-chr20:26189013..26191624,2	MCF-7	breast:
34	chr2:133013667..133017081-chr20:26187658..26190834,11	MCF-7	breast:
35	chr2:75937839..75938339-chr20:26189314..26190135,2	MCF-7	breast:
36	chr20:26131190..26134756-chr7:57619861..57622623,3	K562	blood:
37	chr20:26187251..26191978-chr21:9823998..9829001,56	K562	blood:
38	chr16:33960778..33961976-chr20:26188545..26190262,6	K562	blood:
39	chr2:133015237..133015768-chr20:26189161..26190454,3	K562	blood:
40	chr20:26130778..26134198-chr7:57619861..57623955,5	K562	blood:
41	chr16:33961300..33961956-chr20:26188840..26189578,6	MCF-7	breast:
42	chr20:26189964..26190759-chr22:50700113..50700613,2	MCF-7	breast:
43	chr20:26188275..26190975-chr21:9824996..9827903,45	K562	blood:
44	chr12:20703907..20704890-chr20:26188413..26189402,2	MCF-7	breast:
45	chr2:133014633..133016102-chr20:26188637..26190095,17	MCF-7	breast:
46	chr20:26188344..26189679-chr21:9825010..9826530,20	HCT-116	colon:
47	chr20:26189053..26190595-chr8:67624606..67626126,2	MCF-7	breast:
48	chr20:26190004..26190733-chr8:67687205..67687727,4	MCF-7	breast:
49	chr12:20704427..20705972-chr20:26188595..26190576,2	MCF-7	breast:
50	chr16:33959793..33967555-chr20:26187372..26191632,15	K562	blood:

(count:186 , 50 per page) page: 1 2 3 4

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
2	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
3	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
4	lnc-FAM182B-6	chr20:26168285-26168473	ENSG00000227195.4
5	lnc-FAM182B-6	chr20:26188310-26188422	ENSG00000227195.4
6	lnc-FAM182B-6	chr20:26189501-26189527	ENSG00000227195
7	lnc-FAM182B-6	chr20:26172450-26172536	ENSG00000227195.4
8	lnc-FAM182B-6	chr20:26174934-26175080	ENSG00000227195.4
9	lnc-FAM182B-6	chr20:26174934-26175080	ENSG00000227195.4
10	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
11	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
12	lnc-FAM182B-6	chr20:26168268-26168473	ENSG00000227195.4
13	lnc-FAM182B-6	chr20:26181094-26181178	ENSG00000227195.4
14	lnc-FAM182B-4	chr20:26114675-26114834	XLOC_013713
15	lnc-FAM182B-6	chr20:26175022-26175080	ENSG00000227195.4
16	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
17	lnc-FAM182B-6	chr20:26168268-26168473	ENSG00000227195.4
18	lnc-FAM182B-6	chr20:26167556-26168177	ENSG00000227195.4
19	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
20	lnc-FAM182B-6	chr20:26172429-26172497	ENSG00000227195.4
21	lnc-FAM182B-6	chr20:26172429-26172532	ENSG00000227195.4
22	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
23	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
24	lnc-FAM182B-6	chr20:26174934-26175080	ENSG00000227195.4
25	lnc-FAM182B-6	chr20:26168268-26168473	ENSG00000227195.4
26	lnc-FAM182B-6	chr20:26189783-26189882	ENSG00000227195.4
27	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
28	lnc-FAM182B-6	chr20:26168475-26168735	ENSG00000227195.4
29	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
30	lnc-FAM182B-6	chr20:26172765-26172868	ENSG00000227195.4
31	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
32	lnc-FAM182B-6	chr20:26189806-26189884	ENSG00000227195.4
33	lnc-FAM182B-6	chr20:26189783-26189897	ENSG00000227195.4
34	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
35	lnc-FAM182A-5	chr20:26122024-26122582	NONHSAT079227
36	lnc-FAM182B-6	chr20:26180832-26180952	ENSG00000227195.4
37	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
38	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
39	lnc-FAM182B-6	chr20:26172307-26172399	ENSG00000227195.4
40	lnc-FAM182B-6	chr20:26172307-26172399	ENSG00000227195.4
41	lnc-FAM182B-6	chr20:26189783-26189897	ENSG00000227195.4
42	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
43	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
44	lnc-FAM182B-6	chr20:26188310-26188703	ENSG00000227195.4
45	lnc-FAM182B-6	chr20:26189900-26189942	ENSG00000227195.4
46	lnc-FAM182B-6	chr20:26168271-26168473	ENSG00000227195.4
47	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
48	lnc-FAM182B-6	chr20:26168346-26168473	ENSG00000227195.4
49	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
50	lnc-FAM182B-6	chr20:26231899-26232141	ENSG00000227195.4

miRNA name	Chromosome Location	mirBase accession
hsa-miR-663a	chr20:26188879-26188900	MIMAT0003326

No data

Variant related genes	Relation type
ENSG00000230440	TF binding region
ENSG00000238129	TF binding region
MIR663A	TF binding region
NCOR1P1	TF binding region
ENSG00000230440	CpG island
ENSG00000238129	CpG island
MIR663A	CpG island
NCOR1P1	CpG island
ENSG00000264462	chromatin interactions
ENSG00000163602	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000163046	chromatin interactions
ENSG00000171425	chromatin interactions
ENSG00000263970	chromatin interactions
ENSG00000188130	chromatin interactions
ENSG00000074964	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000239776	chromatin interactions
ENSG00000207986	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000256642	chromatin interactions
ENSG00000031698	chromatin interactions
ENSG00000104205	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000125445	chromatin interactions
ENSG00000200434	chromatin interactions
ENSG00000125447	chromatin interactions
ENSG00000256663	chromatin interactions
ENSG00000221288	chromatin interactions
ENSG00000230102	chromatin interactions
ENSG00000005436	chromatin interactions
CDK1	Mature miRNA region
JUNB	Mature miRNA region
JUND	Mature miRNA region
TCEAL1	Mature miRNA region
HSPG2	Mature miRNA region
NXT2	miRNA target sites
SLC16A1	miRNA target sites

Extended variants
information (count: 4369 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:4369 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74712947	chr20:26094769-26094770	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs78871039	chr20:26094796-26094797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77352783	chr20:26094812-26094813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs569934177	chr20:26094816-26094817	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs535345012	chr20:26094822-26094823	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201506461	chr20:26094856-26094857	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs199801479	chr20:26094857-26094858	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs377501936	chr20:26094861-26094862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs373817583	chr20:26094862-26094863	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs201413725	chr20:26094863-26094864	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs200639100	chr20:26094884-26094885	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555354808	chr20:26094911-26094912	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs6138802	chr20:26094928-26094929	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs541004563	chr20:26094982-26094983	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs62211582	chr20:26094984-26094985	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs62211583	chr20:26094993-26094994	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs62211584	chr20:26094997-26094998	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs557920387	chr20:26095039-26095040	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs556762797	chr20:26097341-26097342	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs79423051	chr20:26097353-26097354	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs71332691	chr20:26097386-26097387	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs369430531	chr20:26097391-26097392	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs145395138	chr20:26097399-26097400	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs200099782	chr20:26097444-26097445	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs1937055	chr20:26097452-26097453	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs530789504	chr20:26097453-26097454	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs550318235	chr20:26097465-26097466	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs567217112	chr20:26097502-26097503	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs529759033	chr20:26097518-26097519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs141638410	chr20:26097579-26097580	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs376838338	chr20:26097580-26097581	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs566212475	chr20:26097584-26097585	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs370682943	chr20:26097614-26097615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs111388577	chr20:26097630-26097631	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs372939116	chr20:26097637-26097638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs534927324	chr20:26097656-26097657	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs201977595	chr20:26097660-26097661	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs150581808	chr20:26097678-26097679	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs571850368	chr20:26097692-26097693	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs79192888	chr20:26100808-26100809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556148727	chr20:26100833-26100834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371628573	chr20:26100836-26100837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374541290	chr20:26100843-26100844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200837851	chr20:26100853-26100854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs201928184	chr20:26100872-26100873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200071950	chr20:26100873-26100874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575984039	chr20:26100878-26100879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541827709	chr20:26100885-26100886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200617721	chr20:26100916-26100917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555538853	chr20:26100919-26100920	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:46)

Disease	PMID	Source
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:26100800-26101400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr20:26116000-26116400	Active TSS	K562	blood
3	chr20:26116000-26116800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr20:26116800-26125400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr20:26124600-26125400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr20:26125200-26125400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr20:26125400-26125600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr20:26125400-26125600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr20:26137600-26140000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr20:26140000-26141400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr20:26140000-26141400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr20:26140000-26141400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr20:26140400-26140600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr20:26140400-26141400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr20:26140600-26141200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr20:26140600-26143000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr20:26141200-26141400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr20:26141400-26141600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr20:26141400-26141600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
20	chr20:26141400-26141600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr20:26141400-26141800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr20:26141400-26141800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr20:26141400-26142200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr20:26141400-26142200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr20:26141600-26142000	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr20:26141600-26142000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr20:26141600-26142000	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr20:26141600-26142000	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr20:26141800-26142200	Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr20:26141800-26143200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr20:26142000-26142200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr20:26142000-26142200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr20:26142000-26142200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr20:26142000-26142600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr20:26142000-26142600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
36	chr20:26142200-26142600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr20:26142200-26142600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr20:26142200-26142600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr20:26142200-26143200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr20:26142200-26143800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr20:26142200-26146200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr20:26142400-26142600	Enhancers	H9 Cell Line	embryonic stem cell
43	chr20:26142400-26142600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr20:26142600-26142800	Enhancers	Muscle Satellite Cultured Cells	--
45	chr20:26142600-26143200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr20:26142600-26143800	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr20:26142600-26144000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr20:26142600-26145600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr20:26142800-26143200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr20:26143000-26144000	Weak transcription	Muscle Satellite Cultured Cells	--

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