Variant report

Variant	nsv428686
Chromosome Location	chr20:26124000-26233848
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2230)
CpG islands
(count:1039)
Chromatin interactive
region (count:66)
LncRNA
region (count:182)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2230 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:26188670-26190654	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:26188665-26190661	K562	blood:	n/a	n/a
3	ATF1	chr20:26207700-26208236	K562	blood:	n/a	n/a
4	ATF1	chr20:26209393-26209538	K562	blood:	n/a	n/a
5	ATF1	chr20:26201702-26201703	K562	blood:	n/a	n/a
6	ATF1	chr20:26213000-26213056	K562	blood:	n/a	n/a
7	ATF1	chr20:26206579-26206689	K562	blood:	n/a	n/a
8	ATF1	chr20:26200807-26200973	K562	blood:	n/a	n/a
9	ATF1	chr20:26204024-26204365	K562	blood:	n/a	n/a
10	ATF1	chr20:26212000-26212002	K562	blood:	n/a	n/a
11	ATF1	chr20:26210425-26210440	K562	blood:	n/a	n/a
12	ATF1	chr20:26210887-26211336	K562	blood:	n/a	n/a
13	ATF1	chr20:26202933-26202936	K562	blood:	n/a	n/a
14	ATF1	chr20:26207076-26207177	K562	blood:	n/a	n/a
15	ATF1	chr20:26202019-26202231	K562	blood:	n/a	n/a
16	ATF2	chr20:26189559-26190696	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr20:26188742-26189499	GM12878	blood:	n/a	n/a
18	ATF2	chr20:26188598-26189527	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr20:26189688-26190460	GM12878	blood:	n/a	n/a
20	ATF2	chr20:26190350-26190549	GM12878	blood:	n/a	n/a
21	ATF2	chr20:26188658-26189437	GM12878	blood:	n/a	n/a
22	ATF2	chr20:26189705-26190319	GM12878	blood:	n/a	n/a
23	ATF2	chr20:26189566-26190667	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr20:26188609-26189520	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr20:26189743-26190295	GM12878	blood:	n/a	n/a
26	ATF3	chr20:26188677-26189497	HepG2	liver:	n/a	n/a
27	ATF3	chr20:26189712-26190314	K562	blood:	n/a	n/a
28	ATF3	chr20:26188662-26189535	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF3	chr20:26190355-26190540	HepG2	liver:	n/a	n/a
30	ATF3	chr20:26189724-26190322	HepG2	liver:	n/a	n/a
31	ATF3	chr20:26189239-26189386	K562	blood:	n/a	n/a
32	ATF3	chr20:26188637-26190747	A549	lung:	n/a	chr20:26190344-26190352
33	ATF3	chr20:26188778-26189204	GM12878	blood:	n/a	n/a
34	ATF3	chr20:26189549-26190567	H1-hESC	embryonic stem cell:	n/a	chr20:26190344-26190352
35	ATF3	chr20:26188697-26190655	K562	blood:	n/a	chr20:26190344-26190352
36	ATF3	chr20:26189747-26190340	K562	blood:	n/a	n/a
37	ATF3	chr20:26189707-26190649	H1-hESC	embryonic stem cell:	n/a	chr20:26190344-26190352
38	ATF3	chr20:26188643-26190671	A549	lung:	n/a	chr20:26190344-26190352
39	ATF3	chr20:26190389-26190519	K562	blood:	n/a	n/a
40	ATF3	chr20:26188754-26189204	K562	blood:	n/a	n/a
41	BACH1	chr20:26188668-26190665	K562	blood:	n/a	n/a
42	BACH1	chr20:26188659-26190667	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr20:26203731-26203928	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	BCL11A	chr20:26189727-26190296	GM12878	blood:	n/a	n/a
47	BCL11A	chr20:26141604-26141853	H1-hESC	embryonic stem cell:	n/a	n/a
48	BCL11A	chr20:26189735-26190289	H1-hESC	embryonic stem cell:	n/a	n/a
49	BCL11A	chr20:26188682-26189216	GM12878	blood:	n/a	chr20:26188715-26188728 chr20:26188719-26188732 chr20:26189177-26189186
50	BCL3	chr20:26188670-26189518	GM12878	blood:	n/a	chr20:26188715-26188728 chr20:26188719-26188732 chr20:26189177-26189186

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:26190347-26190397	AG04450	lung:	fetal
2	chr20:26188943-26188993	GM06990	blood:	n/a
3	chr20:26190347-26190397	AG04450	lung:	fetal
4	chr20:26188943-26188993	GM06990	blood:	n/a
5	chr20:26188963-26189013	GM19239	blood:	n/a
6	chr20:26188919-26188969	LNCaP	prostate:	n/a
7	chr20:26186908-26186958	ECC-1	luminal epithelium:	n/a
8	chr20:26188639-26188689	T-47D	breast:	n/a
9	chr20:26189510-26189560	Caco-2	colon:	n/a
10	chr20:26190347-26190397	ECC-1	luminal epithelium:	n/a
11	chr20:26188639-26188689	NHDF-neo	bronchial:	n/a
12	chr20:26192541-26192591	Hela-S3	cervix:	n/a
13	chr20:26188971-26189021	A549	lung:	n/a
14	chr20:26189665-26189715	HCF	heart:	n/a
15	chr20:26186908-26186958	Hela-S3	cervix:	n/a
16	chr20:26188919-26188969	ovcar-3	ovarian:	n/a
17	chr20:26186545-26186595	HEEpiC	esophagus:	n/a
18	chr20:26188963-26189013	NH-A	brain:	n/a
19	chr20:26186908-26186958	NHBE	bronchial:	n/a
20	chr20:26188943-26188993	AG10803	skin:	n/a
21	chr20:26189240-26189290	GM12892	blood:	n/a
22	chr20:26188963-26189013	HIPEpiC	eye:	n/a
23	chr20:26188639-26188689	HCM	heart:	n/a
24	chr20:26189240-26189290	AG09309	skin:	n/a
25	chr20:26188639-26188689	HUVEC	blood vessel:	n/a
26	chr20:26189240-26189290	RPTEC	kidney:	n/a
27	chr20:26189510-26189560	MCF-7	breast:	n/a
28	chr20:26188997-26189047	HEK293	kidney:	embryo
29	chr20:26186908-26186958	HEK293	kidney:	embryo
30	chr20:26189665-26189715	BE2_C	brain:	n/a
31	chr20:26188971-26189021	SK-N-SH	brain:	n/a
32	chr20:26188976-26189026	HPAEpiC	pulmonary alveolar:	n/a
33	chr20:26192541-26192591	HEK293	kidney:	embryo
34	chr20:26190354-26190404	GM12878	blood:	n/a
35	chr20:26188963-26189013	HRE	kidney:	n/a
36	chr20:26192541-26192591	HIPEpiC	eye:	n/a
37	chr20:26186908-26186958	HNPCEpiC	eye:	n/a
38	chr20:26190328-26190378	GM19239	blood:	n/a
39	chr20:26188908-26188958	SK-N-SH	brain:	n/a
40	chr20:26192541-26192591	GM12878	blood:	n/a
41	chr20:26188943-26188993	PrEC	prostate:	n/a
42	chr20:26189665-26189715	AG09309	skin:	n/a
43	chr20:26192541-26192591	HRE	kidney:	n/a
44	chr20:26190354-26190404	Caco-2	colon:	n/a
45	chr20:26188976-26189026	HRE	kidney:	n/a
46	chr20:26189240-26189290	AG04449	skin:	fetal
47	chr20:26189510-26189560	AoSMC	blood vessel:	n/a
48	chr20:26190347-26190397	GM12892	blood:	n/a
49	chr20:26192541-26192591	RPTEC	kidney:	n/a
50	chr20:26189665-26189715	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:26199924..26201625-chr3:75995563..75997738,2	MCF-7	breast:
2	chr20:26192921..26195094-chr20:26197740..26199404,2	K562	blood:
3	chr20:26188341..26189368-chr21:9825099..9826092,4	MCF-7	breast:
4	chr16:33961286..33962956-chr20:26188880..26190564,2	MCF-7	breast:
5	chr2:133013729..133016735-chr20:26188305..26190826,4	MCF-7	breast:
6	chr13:63637188..63639152-chr20:26145559..26148373,3	K562	blood:
7	chr20:26189964..26190759-chr22:50700113..50700613,2	MCF-7	breast:
8	chr20:26187251..26191978-chr21:9823998..9829001,56	K562	blood:
9	chr12:127649141..127652032-chr20:26188488..26190208,4	K562	blood:
10	chr12:20704427..20705972-chr20:26188595..26190576,2	MCF-7	breast:
11	chr20:26189053..26190595-chr8:67624606..67626126,2	MCF-7	breast:
12	chr20:26188947..26190833-chr6:26156720..26159562,2	MCF-7	breast:
13	chr20:26201563..26203476-chr3:75993448..75995749,2	K562	blood:
14	chr20:26188271..26189555-chr21:9824988..9827433,58	MCF-7	breast:
15	chr20:26188275..26190944-chr21:9825018..9827152,38	MCF-7	breast:
16	chr20:26187273..26191752-chr21:9823988..9828758,49	MCF-7	breast:
17	chr16:33960878..33961871-chr20:26188853..26189656,7	MCF-7	breast:
18	chr20:26188251..26190477-chr21:9825050..9827838,61	MCF-7	breast:
19	chr17:73256462..73259302-chr20:26189013..26191624,2	MCF-7	breast:
20	chr2:133011277..133016757-chr20:26187363..26191986,20	K562	blood:
21	chr20:26131190..26134756-chr7:57619861..57622623,3	K562	blood:
22	chr2:133014718..133015708-chr20:26189240..26189953,2	MCF-7	breast:
23	chr18:8406500..8407500-chr20:26188735..26189378,2	MCF-7	breast:
24	chr2:133014709..133015762-chr20:26188882..26190143,12	MCF-7	breast:
25	chr16:33960778..33961976-chr20:26188545..26190262,6	K562	blood:
26	chr12:127649002..127652005-chr20:26189997..26191614,3	K562	blood:
27	chr16:33961305..33961892-chr20:26188839..26189533,2	MCF-7	breast:
28	chr16:33960780..33961953-chr20:26188513..26190294,8	MCF-7	breast:
29	chr20:26188254..26190671-chr21:9824984..9827890,92	MCF-7	breast:
30	chr2:133014633..133016102-chr20:26188637..26190095,17	MCF-7	breast:
31	chr13:63637281..63639152-chr20:26145559..26147940,2	K562	blood:
32	chr20:26208095..26209894-chr3:75988198..75990401,2	MCF-7	breast:
33	chr12:20703907..20704890-chr20:26188413..26189402,2	MCF-7	breast:
34	chr20:26188275..26190975-chr21:9824996..9827903,45	K562	blood:
35	chr20:26190004..26190733-chr8:67687205..67687727,4	MCF-7	breast:
36	chr2:133013667..133017081-chr20:26187658..26190834,11	MCF-7	breast:
37	chr2:133015211..133015762-chr20:26189170..26190019,2	MCF-7	breast:
38	chr20:26192921..26195094-chr20:26197740..26199404,2	K562	blood:
39	chr2:133014727..133015757-chr20:26189158..26190413,12	MCF-7	breast:
40	chr16:33961325..33966193-chr20:26187372..26191793,13	K562	blood:
41	chr2:133014681..133015764-chr20:26189070..26190458,26	MCF-7	breast:
42	chr1:17866319..17866839-chr20:26189992..26190745,2	MCF-7	breast:
43	chr2:133014738..133015584-chr20:26189167..26190034,2	NB4	blood:
44	chr20:26206073..26206971-chr3:75991464..75992265,2	MCF-7	breast:
45	chr1:109756113..109757974-chr20:26187645..26190102,2	MCF-7	breast:
46	chr20:26201915..26204776-chr3:75992954..75996738,5	MCF-7	breast:
47	chr2:75937839..75938339-chr20:26189314..26190135,2	MCF-7	breast:
48	chr20:26188344..26189679-chr21:9825010..9826530,20	HCT-116	colon:
49	chr20:26208071..26209607-chr3:75987301..75988916,2	K562	blood:
50	chr20:26188433..26190277-chr3:193787174..193790154,2	K562	blood:

(count:182 , 50 per page) page: 1 2 3 4

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
2	lnc-FAM182B-6	chr20:26180085-26180161	ENSG00000227195.4
3	lnc-FAM182B-6	chr20:26174934-26174953	XLOC_013715
4	lnc-FAM182B-5	chr20:26160090-26160098	XLOC_013714
5	lnc-FAM182B-6	chr20:26188781-26188874	ENSG00000227195.4
6	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
7	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
8	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
9	lnc-FAM182B-6	chr20:26168268-26168473	ENSG00000227195.4
10	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
11	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
12	lnc-FAM182B-6	chr20:26168430-26168473	ENSG00000227195.4
13	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
14	lnc-FAM182B-6	chr20:26190379-26190480	ENSG00000227195.4
15	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
16	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
17	lnc-FAM182B-6	chr20:26189900-26189978	ENSG00000227195.4
18	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
19	lnc-FAM182B-6	chr20:26188310-26188703	ENSG00000227195.4
20	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
21	lnc-FAM182B-6	chr20:26172307-26172399	ENSG00000227195.4
22	lnc-FAM182B-6	chr20:26180832-26180952	ENSG00000227195.4
23	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195
24	lnc-FAM182B-6	chr20:26190379-26190475	ENSG00000227195.4
25	lnc-FAM182A-2	chr20:26171625-26171691	XLOC_013504
26	lnc-FAM182B-6	chr20:26180085-26180159	XLOC_013715
27	lnc-FAM182B-6	chr20:26172769-26172868	XLOC_013715
28	lnc-FAM182B-6	chr20:26189900-26189942	ENSG00000227195.4
29	lnc-FAM182B-6	chr20:26168346-26168473	ENSG00000227195.4
30	lnc-FAM182B-6	chr20:26189806-26189884	ENSG00000227195.4
31	lnc-FAM182B-6	chr20:26180832-26180952	ENSG00000227195.4
32	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
33	lnc-FAM182B-6	chr20:26172307-26172399	ENSG00000227195.4
34	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
35	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
36	lnc-FAM182B-6	chr20:26168268-26168473	ENSG00000227195.4
37	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
38	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195
39	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
40	lnc-FAM182B-6	chr20:26189783-26189897	ENSG00000227195.4
41	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
42	lnc-FAM182B-6	chr20:26174934-26175080	ENSG00000227195.4
43	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
44	lnc-FAM182B-6	chr20:26231899-26232141	ENSG00000227195.4
45	lnc-FAM182B-6	chr20:26188310-26188679	ENSG00000227195.4
46	lnc-FAM182B-6	chr20:26175022-26175080	ENSG00000227195.4
47	lnc-FAM182B-6	chr20:26168268-26168473	ENSG00000227195.4
48	lnc-FAM182B-6	chr20:26168268-26168473	ENSG00000227195.4
49	lnc-FAM182B-6	chr20:26181094-26181178	ENSG00000227195.4
50	lnc-FAM182B-6	chr20:26180832-26180948	ENSG00000227195.4

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

No data

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

Extended variants
information (count: 3530 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:3530 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs67012710	chr20:26124002-26124003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73105900	chr20:26124011-26124012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79983909	chr20:26124025-26124026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545352464	chr20:26124033-26124034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149804230	chr20:26124039-26124040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75104202	chr20:26124041-26124042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369977649	chr20:26124042-26124043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530800690	chr20:26124046-26124047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73107906	chr20:26124063-26124064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73906874	chr20:26124075-26124076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78666450	chr20:26124081-26124082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79667865	chr20:26124102-26124103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544736415	chr20:26124132-26124133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199517373	chr20:26124135-26124136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79586601	chr20:26124136-26124137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560999291	chr20:26124146-26124147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541252800	chr20:26124148-26124149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544966512	chr20:26124155-26124156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200657049	chr20:26124158-26124159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79485718	chr20:26124190-26124191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78433544	chr20:26124195-26124196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76036318	chr20:26124206-26124207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549091237	chr20:26124211-26124212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6138811	chr20:26124239-26124240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374816016	chr20:26124240-26124241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78137261	chr20:26124273-26124274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76620832	chr20:26124276-26124277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77367704	chr20:26124280-26124281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566451587	chr20:26124281-26124282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368885186	chr20:26124291-26124292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376945408	chr20:26124307-26124308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532465207	chr20:26124320-26124321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552173226	chr20:26124331-26124332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76620203	chr20:26124387-26124388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201860505	chr20:26124404-26124405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79852099	chr20:26124406-26124407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370906779	chr20:26124407-26124408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112777404	chr20:26124412-26124413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568877113	chr20:26124419-26124420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186059588	chr20:26124431-26124432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73107908	chr20:26124435-26124436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73107909	chr20:26124437-26124438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145822744	chr20:26124489-26124490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs67765774	chr20:26124501-26124502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114279630	chr20:26124507-26124508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201296620	chr20:26124510-26124511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140310091	chr20:26124522-26124523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201835783	chr20:26124524-26124525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375708193	chr20:26124529-26124530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536855942	chr20:26124532-26124533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:26116800-26125400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:26124600-26125400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr20:26125200-26125400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr20:26125400-26125600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr20:26125400-26125600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr20:26137600-26140000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr20:26140000-26141400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr20:26140000-26141400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr20:26140000-26141400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr20:26140400-26140600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr20:26140400-26141400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr20:26140600-26141200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr20:26140600-26143000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr20:26141200-26141400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr20:26141400-26141600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr20:26141400-26141600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chr20:26141400-26141600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr20:26141400-26141800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr20:26141400-26141800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr20:26141400-26142200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr20:26141400-26142200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr20:26141600-26142000	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr20:26141600-26142000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr20:26141600-26142000	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr20:26141600-26142000	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr20:26141800-26142200	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr20:26141800-26143200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr20:26142000-26142200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr20:26142000-26142200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr20:26142000-26142200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr20:26142000-26142600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr20:26142000-26142600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
33	chr20:26142200-26142600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr20:26142200-26142600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
35	chr20:26142200-26142600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr20:26142200-26143200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr20:26142200-26143800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr20:26142200-26146200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr20:26142400-26142600	Enhancers	H9 Cell Line	embryonic stem cell
40	chr20:26142400-26142600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr20:26142600-26142800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr20:26142600-26143200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr20:26142600-26143800	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr20:26142600-26144000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr20:26142600-26145600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr20:26142800-26143200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr20:26143000-26144000	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr20:26143200-26143800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr20:26143200-26143800	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr20:26143800-26144000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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