Variant report

Variant	nsv482712
Chromosome Location	chr20:26111091-26279775
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2844)
CpG islands
(count:1039)
Chromatin interactive
region (count:66)
LncRNA
region (count:186)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2844 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

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	chr20:26210887-26211336	K562	blood:	n/a	n/a
4	ATF1	chr20:26204024-26204365	K562	blood:	n/a	n/a
5	ATF1	chr20:26212000-26212002	K562	blood:	n/a	n/a
6	ATF1	chr20:26213000-26213056	K562	blood:	n/a	n/a
7	ATF1	chr20:26207076-26207177	K562	blood:	n/a	n/a
8	ATF1	chr20:26210425-26210440	K562	blood:	n/a	n/a
9	ATF1	chr20:26259878-26260247	K562	blood:	n/a	n/a
10	ATF1	chr20:26201702-26201703	K562	blood:	n/a	n/a
11	ATF1	chr20:26207700-26208236	K562	blood:	n/a	n/a
12	ATF1	chr20:26202019-26202231	K562	blood:	n/a	n/a
13	ATF1	chr20:26202933-26202936	K562	blood:	n/a	n/a
14	ATF1	chr20:26200807-26200973	K562	blood:	n/a	n/a
15	ATF1	chr20:26209393-26209538	K562	blood:	n/a	n/a
16	ATF1	chr20:26269527-26269727	K562	blood:	n/a	n/a
17	ATF1	chr20:26206579-26206689	K562	blood:	n/a	n/a
18	ATF2	chr20:26189566-26190667	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr20:26188742-26189499	GM12878	blood:	n/a	n/a
20	ATF2	chr20:26189559-26190696	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr20:26188598-26189527	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr20:26190350-26190549	GM12878	blood:	n/a	n/a
23	ATF2	chr20:26189688-26190460	GM12878	blood:	n/a	n/a
24	ATF2	chr20:26189705-26190319	GM12878	blood:	n/a	n/a
25	ATF2	chr20:26188609-26189520	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr20:26188658-26189437	GM12878	blood:	n/a	n/a
27	ATF3	chr20:26189724-26190322	HepG2	liver:	n/a	n/a
28	ATF3	chr20:26188754-26189204	K562	blood:	n/a	n/a
29	ATF3	chr20:26189549-26190567	H1-hESC	embryonic stem cell:	n/a	chr20:26190344-26190352
30	ATF3	chr20:26189712-26190314	K562	blood:	n/a	n/a
31	ATF3	chr20:26188697-26190655	K562	blood:	n/a	chr20:26190344-26190352
32	ATF3	chr20:26188637-26190747	A549	lung:	n/a	chr20:26190344-26190352
33	ATF3	chr20:26189707-26190649	H1-hESC	embryonic stem cell:	n/a	chr20:26190344-26190352
34	ATF3	chr20:26189747-26190340	K562	blood:	n/a	n/a
35	ATF3	chr20:26189743-26190295	GM12878	blood:	n/a	n/a
36	ATF3	chr20:26188778-26189204	GM12878	blood:	n/a	n/a
37	ATF3	chr20:26188643-26190671	A549	lung:	n/a	chr20:26190344-26190352
38	ATF3	chr20:26188677-26189497	HepG2	liver:	n/a	n/a
39	ATF3	chr20:26190389-26190519	K562	blood:	n/a	n/a
40	ATF3	chr20:26188662-26189535	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF3	chr20:26189239-26189386	K562	blood:	n/a	n/a
42	ATF3	chr20:26190355-26190540	HepG2	liver:	n/a	n/a
43	BACH1	chr20:26266555-26266850	K562	blood:	n/a	n/a
44	BACH1	chr20:26268242-26268311	K562	blood:	n/a	n/a
45	BACH1	chr20:26277375-26277379	K562	blood:	n/a	n/a
46	BACH1	chr20:26203731-26203928	K562	blood:	n/a	n/a
47	BACH1	chr20:26188668-26190665	K562	blood:	n/a	n/a
48	BACH1	chr20:26188659-26190667	H1-hESC	embryonic stem cell:	n/a	n/a
49	BATF	chr20:26188677-26189220	GM12878	blood:	n/a	n/a
50	BATF	chr20:26264552-26264856	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:26188943-26188993	U87	brain:	n/a
2	chr20:26186545-26186595	PrEC	prostate:	n/a
3	chr20:26188943-26188993	U87	brain:	n/a
4	chr20:26186545-26186595	PrEC	prostate:	n/a
5	chr20:26189665-26189715	GM12892	blood:	n/a
6	chr20:26189240-26189290	HCT-116	colon:	n/a
7	chr20:26189240-26189290	NHBE	bronchial:	n/a
8	chr20:26188963-26189013	SKMC	muscle:	n/a
9	chr20:26188908-26188958	HL-60	blood:	n/a
10	chr20:26190328-26190378	MCF-7	breast:	n/a
11	chr20:26186545-26186595	LNCaP	prostate:	n/a
12	chr20:26188943-26188993	SAEC	small airway:	n/a
13	chr20:26188943-26188993	AG04449	skin:	fetal
14	chr20:26186908-26186958	HEK293	kidney:	embryo
15	chr20:26186545-26186595	SK-N-MC	brain:	n/a
16	chr20:26188997-26189047	HEEpiC	esophagus:	n/a
17	chr20:26188639-26188689	HepG2	liver:	n/a
18	chr20:26189240-26189290	HRPEpiC	eye:	n/a
19	chr20:26188976-26189026	AG10803	skin:	n/a
20	chr20:26188919-26188969	NHDF-neo	bronchial:	n/a
21	chr20:26188997-26189047	PANC-1	pancreas:	n/a
22	chr20:26189665-26189715	ovcar-3	ovarian:	n/a
23	chr20:26189665-26189715	T-47D	breast:	n/a
24	chr20:26189665-26189715	HEEpiC	esophagus:	n/a
25	chr20:26188971-26189021	HAEpiC	amniotic membrane:	n/a
26	chr20:26190354-26190404	HCM	heart:	n/a
27	chr20:26188639-26188689	HIPEpiC	eye:	n/a
28	chr20:26188943-26188993	A549	lung:	n/a
29	chr20:26186908-26186958	AG09309	skin:	n/a
30	chr20:26189510-26189560	SK-N-SH_RA	brain:	n/a
31	chr20:26186908-26186958	HRCEpiC	kidney:	n/a
32	chr20:26189510-26189560	GM06990	blood:	n/a
33	chr20:26192541-26192591	AG09319	gingival:	n/a
34	chr20:26188971-26189021	AG09319	gingival:	n/a
35	chr20:26188997-26189047	HNPCEpiC	eye:	n/a
36	chr20:26192541-26192591	IMR90	lung:	fetal
37	chr20:26190347-26190397	BJ	skin:	n/a
38	chr20:26188963-26189013	SK-N-SH	brain:	n/a
39	chr20:26189510-26189560	MCF10A-Er-Src	breast:	n/a
40	chr20:26188639-26188689	HL-60	blood:	n/a
41	chr20:26190328-26190378	SK-N-SH	brain:	n/a
42	chr20:26189510-26189560	Hepatocyte	liver:	n/a
43	chr20:26189510-26189560	LNCaP	prostate:	n/a
44	chr20:26189240-26189290	Caco-2	colon:	n/a
45	chr20:26188943-26188993	HCM	heart:	n/a
46	chr20:26188919-26188969	H1-hESC	embryonic stem cell:	embryo
47	chr20:26188963-26189013	SK-N-SH_RA	brain:	n/a
48	chr20:26189510-26189560	AG04450	lung:	fetal
49	chr20:26188963-26189013	A549	lung:	n/a
50	chr20:26188943-26188993	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:26188254..26190671-chr21:9824984..9827890,92	MCF-7	breast:
2	chr20:26199924..26201625-chr3:75995563..75997738,2	MCF-7	breast:
3	chr12:20703970..20704942-chr20:26190011..26190793,2	K562	blood:
4	chr20:26188413..26189362-chr8:101964386..101965001,2	MCF-7	breast:
5	chr20:26192921..26195094-chr20:26197740..26199404,2	K562	blood:
6	chr16:33961286..33962956-chr20:26188880..26190564,2	MCF-7	breast:
7	chr20:26208071..26209607-chr3:75987301..75988916,2	K562	blood:
8	chr2:133014681..133015764-chr20:26189070..26190458,26	MCF-7	breast:
9	chr16:33961325..33966193-chr20:26187372..26191793,13	K562	blood:
10	chr2:133014709..133015762-chr20:26188882..26190143,12	MCF-7	breast:
11	chr20:26189964..26190759-chr22:50700113..50700613,2	MCF-7	breast:
12	chr20:26188341..26189368-chr21:9825099..9826092,4	MCF-7	breast:
13	chr20:26188251..26190477-chr21:9825050..9827838,61	MCF-7	breast:
14	chr20:26206073..26206971-chr3:75991464..75992265,2	MCF-7	breast:
15	chr20:26189322..26189965-chr3:72495919..72496919,2	MCF-7	breast:
16	chr13:63637281..63639152-chr20:26145559..26147940,2	K562	blood:
17	chr2:133014718..133015708-chr20:26189240..26189953,2	MCF-7	breast:
18	chr17:73256462..73259302-chr20:26189013..26191624,2	MCF-7	breast:
19	chr2:133014738..133015584-chr20:26189167..26190034,2	NB4	blood:
20	chr20:26201563..26203476-chr3:75993448..75995749,2	K562	blood:
21	chr12:127649002..127652005-chr20:26189997..26191614,3	K562	blood:
22	chr20:26188275..26190975-chr21:9824996..9827903,45	K562	blood:
23	chr20:26189053..26190595-chr8:67624606..67626126,2	MCF-7	breast:
24	chr20:26188275..26190944-chr21:9825018..9827152,38	MCF-7	breast:
25	chr2:133013667..133017081-chr20:26187658..26190834,11	MCF-7	breast:
26	chr16:33960800..33961892-chr20:26188687..26190008,21	MCF-7	breast:
27	chr13:63647812..63648534-chr20:26148535..26149113,2	MCF-7	breast:
28	chr16:33959793..33967555-chr20:26187372..26191632,15	K562	blood:
29	chr2:133015211..133015762-chr20:26189170..26190019,2	MCF-7	breast:
30	chr2:133015237..133015768-chr20:26189161..26190454,3	K562	blood:
31	chr20:26188395..26190565-chr6:74228700..74231505,2	MCF-7	breast:
32	chr20:26190004..26190733-chr8:67687205..67687727,4	MCF-7	breast:
33	chr19:56154889..56155389-chr20:26189706..26190477,2	K562	blood:
34	chr16:33961300..33961956-chr20:26188840..26189578,6	MCF-7	breast:
35	chr2:75937839..75938339-chr20:26189314..26190135,2	MCF-7	breast:
36	chr13:63647679..63650483-chr20:26148365..26151073,2	K562	blood:
37	chr16:33964537..33965670-chr20:26188912..26190067,3	K562	blood:
38	chr20:26187350..26191964-chr21:9824053..9828992,54	K562	blood:
39	chr20:26187251..26191978-chr21:9823998..9829001,56	K562	blood:
40	chr20:26131190..26134756-chr7:57619861..57622623,3	K562	blood:
41	chr16:33960780..33961953-chr20:26188513..26190294,8	MCF-7	breast:
42	chr1:109756113..109757974-chr20:26187645..26190102,2	MCF-7	breast:
43	chr20:26130778..26134198-chr7:57619861..57623955,5	K562	blood:
44	chr2:133013729..133016735-chr20:26188305..26190826,4	MCF-7	breast:
45	chr2:133011277..133016757-chr20:26187363..26191986,20	K562	blood:
46	chr20:26188433..26190277-chr3:193787174..193790154,2	K562	blood:
47	chr20:26208095..26209894-chr3:75988198..75990401,2	MCF-7	breast:
48	chr20:26187273..26191752-chr21:9823988..9828758,49	MCF-7	breast:
49	chr20:26188344..26189679-chr21:9825010..9826530,20	HCT-116	colon:
50	chr20:26188271..26189555-chr21:9824988..9827433,58	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
2	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
3	lnc-FAM182B-6	chr20:26168268-26168473	ENSG00000227195.4
4	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
5	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195
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	chr20:26180085-26180159	ENSG00000227195.4
10	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
11	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
12	lnc-FAM182B-6	chr20:26180832-26180952	ENSG00000227195.4
13	lnc-FAM182A-5	chr20:26122024-26122582	NONHSAT079227
14	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
15	lnc-FAM182B-6	chr20:26168430-26168473	ENSG00000227195.4
16	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
17	lnc-FAM182B-6	chr20:26189900-26190098	ENSG00000227195.4
18	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
19	lnc-FAM182B-6	chr20:26188310-26188422	ENSG00000227195.4
20	lnc-FAM182B-6	chr20:26168271-26168473	ENSG00000227195.4
21	lnc-FAM182B-6	chr20:26188781-26188874	ENSG00000227195.4
22	lnc-FAM182B-6	chr20:26172429-26172536	XLOC_013715
23	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
24	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
25	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
26	lnc-FAM182B-6	chr20:26168271-26168473	ENSG00000227195.4
27	lnc-FAM182B-6	chr20:26168445-26168473	ENSG00000227195.4
28	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
29	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
30	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
31	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
32	lnc-FAM182B-6	chr20:26189783-26189897	ENSG00000227195.4
33	lnc-FAM182B-6	chr20:26180832-26180952	ENSG00000227195.4
34	lnc-FAM182B-6	chr20:26174934-26175080	ENSG00000227195.4
35	lnc-FAM182B-6	chr20:26168271-26168473	ENSG00000227195.4
36	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
37	lnc-FAM182B-6	chr20:26174934-26175080	ENSG00000227195.4
38	lnc-FAM182B-6	chr20:26189783-26189825	ENSG00000227195.4
39	lnc-FAM182B-6	chr20:26189783-26189882	ENSG00000227195.4
40	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
41	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195
42	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
43	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
44	lnc-FAM182B-4	chr20:26113523-26113633	XLOC_013713
45	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
46	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
47	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
48	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
49	lnc-FAM182A-2	chr20:26171625-26171691	XLOC_013504
50	lnc-FAM182B-6	chr20:26180085-26180161	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
ENSG00000230440	CpG island
ENSG00000238129	CpG island
MIR663A	CpG island
ENSG00000163046	chromatin interactions
ENSG00000171425	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000188130	chromatin interactions
ENSG00000263970	chromatin interactions
ENSG00000163602	chromatin interactions
ENSG00000239776	chromatin interactions
ENSG00000200434	chromatin interactions
ENSG00000125447	chromatin interactions
ENSG00000031698	chromatin interactions
ENSG00000207986	chromatin interactions
ENSG00000125445	chromatin interactions
ENSG00000221288	chromatin interactions
ENSG00000230102	chromatin interactions
ENSG00000256663	chromatin interactions
ENSG00000005436	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000256642	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000074964	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000104205	chromatin interactions
ENSG00000164924	chromatin interactions
HSPG2	Mature miRNA region
JUNB	Mature miRNA region
CDK1	Mature miRNA region
TCEAL1	Mature miRNA region
JUND	Mature miRNA region
NXT2	miRNA target sites
SLC16A1	miRNA target sites

Extended variants
information (count: 7744 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:7744 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113652379	chr20:26113533-26113534	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs200092343	chr20:26113534-26113535	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs375245697	chr20:26113543-26113544	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs11907719	chr20:26113569-26113570	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs544785979	chr20:26113575-26113576	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs41275518	chr20:26113587-26113588	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs368752799	chr20:26113597-26113598	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs12625696	chr20:26113626-26113627	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs577076915	chr20:26114686-26114687	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs567285193	chr20:26114719-26114720	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs537939706	chr20:26114720-26114721	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs556109428	chr20:26114760-26114761	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs576335883	chr20:26114770-26114771	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs542343261	chr20:26114793-26114794	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs562028617	chr20:26114849-26114850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs527525635	chr20:26114863-26114864	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs541178124	chr20:26114872-26114873	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs74377079	chr20:26114881-26114882	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs564379975	chr20:26114890-26114891	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs533230153	chr20:26114925-26114926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs549826653	chr20:26114954-26114955	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs78777440	chr20:26114973-26114974	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs34736689	chr20:26115005-26115006	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs76246686	chr20:26115036-26115037	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs146641626	chr20:26115083-26115084	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs377661684	chr20:26115095-26115096	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs111797158	chr20:26115096-26115097	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs565637706	chr20:26115104-26115105	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs148277333	chr20:26115119-26115120	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs188660218	chr20:26115129-26115130	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs79260792	chr20:26115143-26115144	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs547545887	chr20:26115193-26115194	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs191403481	chr20:26115199-26115200	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs182718135	chr20:26115204-26115205	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs556422543	chr20:26115209-26115210	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs35559867	chr20:26115432-26115433	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559410222	chr20:26115435-26115436	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs6138808	chr20:26115441-26115442	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs34548674	chr20:26115444-26115445	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs551037537	chr20:26115463-26115464	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs570742703	chr20:26115481-26115482	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs188912927	chr20:26115498-26115499	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs570206141	chr20:26115499-26115500	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs76835931	chr20:26115503-26115504	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs78906032	chr20:26115505-26115506	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs6138809	chr20:26115510-26115511	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs79290461	chr20:26115512-26115513	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs555439711	chr20:26115535-26115536	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs193250098	chr20:26115541-26115542	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs185376514	chr20:26115555-26115556	Inactive region	TF binding region	1 gene(s)	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:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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

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