Variant report

Variant	nsv585776
Chromosome Location	chr20:26146163-26246086
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2123)
CpG islands
(count:1039)
Chromatin interactive
region (count:64)
LncRNA
region (count:182)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2123 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:26188665-26190661	K562	blood:	n/a	n/a
2	ARID3A	chr20:26188670-26190654	HepG2	liver:	n/a	n/a
3	ATF1	chr20:26202019-26202231	K562	blood:	n/a	n/a
4	ATF1	chr20:26201702-26201703	K562	blood:	n/a	n/a
5	ATF1	chr20:26207700-26208236	K562	blood:	n/a	n/a
6	ATF1	chr20:26213000-26213056	K562	blood:	n/a	n/a
7	ATF1	chr20:26202933-26202936	K562	blood:	n/a	n/a
8	ATF1	chr20:26210425-26210440	K562	blood:	n/a	n/a
9	ATF1	chr20:26210887-26211336	K562	blood:	n/a	n/a
10	ATF1	chr20:26206579-26206689	K562	blood:	n/a	n/a
11	ATF1	chr20:26204024-26204365	K562	blood:	n/a	n/a
12	ATF1	chr20:26212000-26212002	K562	blood:	n/a	n/a
13	ATF1	chr20:26207076-26207177	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	ATF2	chr20:26189688-26190460	GM12878	blood:	n/a	n/a
17	ATF2	chr20:26188742-26189499	GM12878	blood:	n/a	n/a
18	ATF2	chr20:26188658-26189437	GM12878	blood:	n/a	n/a
19	ATF2	chr20:26188598-26189527	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr20:26189566-26190667	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr20:26188609-26189520	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr20:26189559-26190696	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr20:26189705-26190319	GM12878	blood:	n/a	n/a
24	ATF2	chr20:26190350-26190549	GM12878	blood:	n/a	n/a
25	ATF3	chr20:26188754-26189204	K562	blood:	n/a	n/a
26	ATF3	chr20:26188643-26190671	A549	lung:	n/a	chr20:26190344-26190352
27	ATF3	chr20:26189747-26190340	K562	blood:	n/a	n/a
28	ATF3	chr20:26190355-26190540	HepG2	liver:	n/a	n/a
29	ATF3	chr20:26189743-26190295	GM12878	blood:	n/a	n/a
30	ATF3	chr20:26188637-26190747	A549	lung:	n/a	chr20:26190344-26190352
31	ATF3	chr20:26189724-26190322	HepG2	liver:	n/a	n/a
32	ATF3	chr20:26190389-26190519	K562	blood:	n/a	n/a
33	ATF3	chr20:26189712-26190314	K562	blood:	n/a	n/a
34	ATF3	chr20:26188677-26189497	HepG2	liver:	n/a	n/a
35	ATF3	chr20:26188662-26189535	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF3	chr20:26189707-26190649	H1-hESC	embryonic stem cell:	n/a	chr20:26190344-26190352
37	ATF3	chr20:26189549-26190567	H1-hESC	embryonic stem cell:	n/a	chr20:26190344-26190352
38	ATF3	chr20:26188697-26190655	K562	blood:	n/a	chr20:26190344-26190352
39	ATF3	chr20:26189239-26189386	K562	blood:	n/a	n/a
40	ATF3	chr20:26188778-26189204	GM12878	blood:	n/a	n/a
41	BACH1	chr20:26188668-26190665	K562	blood:	n/a	n/a
42	BACH1	chr20:26203731-26203928	K562	blood:	n/a	n/a
43	BACH1	chr20:26188659-26190667	H1-hESC	embryonic stem cell:	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	chr20:26188682-26189216	GM12878	blood:	n/a	chr20:26188715-26188728 chr20:26188719-26188732 chr20:26189177-26189186
47	BCL11A	chr20:26189727-26190296	GM12878	blood:	n/a	n/a
48	BCL11A	chr20:26189735-26190289	H1-hESC	embryonic stem cell:	n/a	n/a
49	BCL3	chr20:26188531-26190586	A549	lung:	n/a	chr20:26188715-26188728 chr20:26188719-26188732 chr20:26189177-26189186
50	BCL3	chr20:26188680-26189512	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	chr20:26190354-26190404	PFSK-1	brain:	n/a
2	chr20:26190347-26190397	CMK	blood:	n/a
3	chr20:26190354-26190404	PFSK-1	brain:	n/a
4	chr20:26190347-26190397	CMK	blood:	n/a
5	chr20:26188943-26188993	PANC-1	pancreas:	n/a
6	chr20:26189240-26189290	HRCEpiC	kidney:	n/a
7	chr20:26189240-26189290	K562	blood:	n/a
8	chr20:26188971-26189021	HRPEpiC	eye:	n/a
9	chr20:26188919-26188969	HCM	heart:	n/a
10	chr20:26188908-26188958	NT2-D1	testis:	n/a
11	chr20:26188943-26188993	SK-N-SH	brain:	n/a
12	chr20:26188943-26188993	HRE	kidney:	n/a
13	chr20:26188997-26189047	AG09309	skin:	n/a
14	chr20:26190347-26190397	AG04449	skin:	fetal
15	chr20:26186908-26186958	SKMC	muscle:	n/a
16	chr20:26188943-26188993	HNPCEpiC	eye:	n/a
17	chr20:26188971-26189021	HCM	heart:	n/a
18	chr20:26189665-26189715	ProgFib	skin:	n/a
19	chr20:26186545-26186595	HRE	kidney:	n/a
20	chr20:26190347-26190397	HAEpiC	amniotic membrane:	n/a
21	chr20:26188963-26189013	ECC-1	luminal epithelium:	n/a
22	chr20:26188639-26188689	BJ	skin:	n/a
23	chr20:26189510-26189560	HRCEpiC	kidney:	n/a
24	chr20:26189240-26189290	GM12878	blood:	n/a
25	chr20:26186545-26186595	SKMC	muscle:	n/a
26	chr20:26188976-26189026	Jurkat	blood:	n/a
27	chr20:26189510-26189560	NB4	blood:	n/a
28	chr20:26188976-26189026	Caco-2	colon:	n/a
29	chr20:26186545-26186595	NHDF-neo	bronchial:	n/a
30	chr20:26190328-26190378	Jurkat	blood:	n/a
31	chr20:26188976-26189026	LNCaP	prostate:	n/a
32	chr20:26188943-26188993	GM06990	blood:	n/a
33	chr20:26190347-26190397	GM12891	blood:	n/a
34	chr20:26186908-26186958	GM12892	blood:	n/a
35	chr20:26188976-26189026	SK-N-SH_RA	brain:	n/a
36	chr20:26186908-26186958	HRCEpiC	kidney:	n/a
37	chr20:26190328-26190378	AG09319	gingival:	n/a
38	chr20:26190347-26190397	GM12892	blood:	n/a
39	chr20:26190354-26190404	AoSMC	blood vessel:	n/a
40	chr20:26188997-26189047	HRCEpiC	kidney:	n/a
41	chr20:26190347-26190397	HEEpiC	esophagus:	n/a
42	chr20:26188908-26188958	GM19239	blood:	n/a
43	chr20:26190347-26190397	SKMC	muscle:	n/a
44	chr20:26190347-26190397	ECC-1	luminal epithelium:	n/a
45	chr20:26188943-26188993	NHDF-neo	bronchial:	n/a
46	chr20:26188639-26188689	K562	blood:	n/a
47	chr20:26190354-26190404	GM12892	blood:	n/a
48	chr20:26188908-26188958	HPAEpiC	pulmonary alveolar:	n/a
49	chr20:26188971-26189021	NHDF-neo	bronchial:	n/a
50	chr20:26188971-26189021	NH-A	brain:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:133013729..133016735-chr20:26188305..26190826,4	MCF-7	breast:
2	chr20:26206073..26206971-chr3:75991464..75992265,2	MCF-7	breast:
3	chr20:26208095..26209894-chr3:75988198..75990401,2	MCF-7	breast:
4	chr2:133014709..133015762-chr20:26188882..26190143,12	MCF-7	breast:
5	chr20:26208071..26209607-chr3:75987301..75988916,2	K562	blood:
6	chr2:133013667..133017081-chr20:26187658..26190834,11	MCF-7	breast:
7	chr2:133014681..133015764-chr20:26189070..26190458,26	MCF-7	breast:
8	chr12:127649141..127652032-chr20:26188488..26190208,4	K562	blood:
9	chr20:26199924..26201625-chr3:75995563..75997738,2	MCF-7	breast:
10	chr20:26188275..26190944-chr21:9825018..9827152,38	MCF-7	breast:
11	chr1:17866319..17866839-chr20:26189992..26190745,2	MCF-7	breast:
12	chr1:109756113..109757974-chr20:26187645..26190102,2	MCF-7	breast:
13	chr20:26192921..26195094-chr20:26197740..26199404,2	K562	blood:
14	chr2:133015211..133015762-chr20:26189170..26190019,2	MCF-7	breast:
15	chr16:33961300..33961956-chr20:26188840..26189578,6	MCF-7	breast:
16	chr20:26188413..26189362-chr8:101964386..101965001,2	MCF-7	breast:
17	chr16:33961305..33961892-chr20:26188839..26189533,2	MCF-7	breast:
18	chr12:127649002..127652005-chr20:26189997..26191614,3	K562	blood:
19	chr19:56154889..56155389-chr20:26189706..26190477,2	K562	blood:
20	chr16:33961325..33966193-chr20:26187372..26191793,13	K562	blood:
21	chr2:75937839..75938339-chr20:26189314..26190135,2	MCF-7	breast:
22	chr16:33964537..33965670-chr20:26188912..26190067,3	K562	blood:
23	chr16:33959793..33967555-chr20:26187372..26191632,15	K562	blood:
24	chr17:73256462..73259302-chr20:26189013..26191624,2	MCF-7	breast:
25	chr2:133011277..133016757-chr20:26187363..26191986,20	K562	blood:
26	chr13:63647679..63650483-chr20:26148365..26151073,2	K562	blood:
27	chr20:26201563..26203476-chr3:75993448..75995749,2	K562	blood:
28	chr18:8406500..8407500-chr20:26188735..26189378,2	MCF-7	breast:
29	chr2:133014633..133016102-chr20:26188637..26190095,17	MCF-7	breast:
30	chr12:20703970..20704942-chr20:26190011..26190793,2	K562	blood:
31	chr20:26188344..26189679-chr21:9825010..9826530,20	HCT-116	colon:
32	chr16:33961286..33962956-chr20:26188880..26190564,2	MCF-7	breast:
33	chr16:33960878..33961871-chr20:26188853..26189656,7	MCF-7	breast:
34	chr20:26188341..26189368-chr21:9825099..9826092,4	MCF-7	breast:
35	chr16:33960778..33961976-chr20:26188545..26190262,6	K562	blood:
36	chr20:26189322..26189965-chr3:72495919..72496919,2	MCF-7	breast:
37	chr12:20703907..20704890-chr20:26188413..26189402,2	MCF-7	breast:
38	chr20:26187350..26191964-chr21:9824053..9828992,54	K562	blood:
39	chr20:26188433..26190277-chr3:193787174..193790154,2	K562	blood:
40	chr16:33960800..33961892-chr20:26188687..26190008,21	MCF-7	breast:
41	chr20:26190004..26190733-chr8:67687205..67687727,4	MCF-7	breast:
42	chr20:26188395..26190565-chr6:74228700..74231505,2	MCF-7	breast:
43	chr20:26189053..26190595-chr8:67624606..67626126,2	MCF-7	breast:
44	chr12:20704427..20705972-chr20:26188595..26190576,2	MCF-7	breast:
45	chr13:63647812..63648534-chr20:26148535..26149113,2	MCF-7	breast:
46	chr20:26201915..26204776-chr3:75992954..75996738,5	MCF-7	breast:
47	chr20:26188271..26189555-chr21:9824988..9827433,58	MCF-7	breast:
48	chr2:133011277..133017359-chr20:26187383..26191986,21	K562	blood:
49	chr20:26188254..26190671-chr21:9824984..9827890,92	MCF-7	breast:
50	chr2:133014738..133015584-chr20:26189167..26190034,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182B-6	chr20:26188781-26188874	ENSG00000227195.4
2	lnc-FAM182B-6	chr20:26189806-26189884	ENSG00000227195.4
3	lnc-FAM182B-6	chr20:26167655-26168473	ENSG00000227195
4	lnc-FAM182B-6	chr20:26172429-26172536	XLOC_013715
5	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
6	lnc-FAM182B-6	chr20:26188310-26188679	ENSG00000227195.4
7	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
8	lnc-FAM182B-6	chr20:26168346-26168473	ENSG00000227195.4
9	lnc-FAM182B-6	chr20:26189783-26189897	ENSG00000227195.4
10	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
11	lnc-FAM182B-6	chr20:26231899-26232102	ENSG00000227195.4
12	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
13	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
14	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
15	lnc-FAM182B-6	chr20:26168268-26168473	ENSG00000227195.4
16	lnc-FAM182B-6	chr20:26188310-26188714	ENSG00000227195.4
17	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
18	lnc-FAM182B-6	chr20:26172765-26172868	ENSG00000227195.4
19	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
20	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
21	lnc-FAM182B-6	chr20:26188781-26188874	ENSG00000227195.4
22	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
23	lnc-FAM182A-2	chr20:26171625-26171691	XLOC_013504
24	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
25	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
26	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
27	lnc-FAM182B-6	chr20:26181094-26181178	ENSG00000227195.4
28	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
29	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
30	lnc-FAM182B-6	chr20:26168346-26168473	ENSG00000227195.4
31	lnc-FAM182B-6	chr20:26172769-26172868	XLOC_013715
32	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
33	lnc-FAM182B-6	chr20:26172429-26172536	ENSG00000227195.4
34	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
35	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
36	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
37	lnc-FAM182B-6	chr20:26189759-26189869	ENSG00000227195
38	lnc-FAM182B-6	chr20:26172769-26172868	ENSG00000227195.4
39	lnc-FAM182B-6	chr20:26180085-26180159	ENSG00000227195.4
40	lnc-FAM182B-6	chr20:26174934-26175080	ENSG00000227195.4
41	lnc-FAM182B-6	chr20:26168271-26168473	ENSG00000227195.4
42	lnc-FAM182B-6	chr20:26174934-26174953	XLOC_013715
43	lnc-FAM182B-6	chr20:26174934-26175080	ENSG00000227195.4
44	lnc-FAM182B-6	chr20:26168274-26168473	ENSG00000227195.4
45	lnc-FAM182B-6	chr20:26188310-26188703	ENSG00000227195.4
46	lnc-FAM182B-6	chr20:26188939-26189080	ENSG00000227195.4
47	lnc-FAM182B-6	chr20:26189501-26189527	ENSG00000227195
48	lnc-FAM182B-6	chr20:26172769-26173473	ENSG00000227195.4
49	lnc-FAM182B-6	chr20:26170599-26170755	ENSG00000227195.4
50	lnc-FAM182B-6	chr20:26168268-26168716	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
ENSG00000264063	chromatin interactions
ENSG00000188130	chromatin interactions
ENSG00000163602	chromatin interactions
ENSG00000074964	chromatin interactions
ENSG00000005436	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000256663	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000207986	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000163046	chromatin interactions
ENSG00000125445	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000230102	chromatin interactions
ENSG00000221288	chromatin interactions
ENSG00000171425	chromatin interactions
ENSG00000125447	chromatin interactions
ENSG00000104205	chromatin interactions
ENSG00000263970	chromatin interactions
ENSG00000239776	chromatin interactions
ENSG00000256642	chromatin interactions
ENSG00000031698	chromatin interactions
ENSG00000200434	chromatin interactions
CDK1	Mature miRNA region
HSPG2	Mature miRNA region
JUND	Mature miRNA region
JUNB	Mature miRNA region
TCEAL1	Mature miRNA region
SLC16A1	miRNA target sites
NXT2	miRNA target sites

Extended variants
information (count: 2733 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:2733 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs845982	chr20:26146163-26146164	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376877203	chr20:26146167-26146168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369867133	chr20:26146168-26146169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374533602	chr20:26146179-26146180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367675492	chr20:26146182-26146183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183416060	chr20:26146192-26146193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs80285445	chr20:26146217-26146218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78319104	chr20:26146220-26146221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377556226	chr20:26146235-26146236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375683644	chr20:26146239-26146240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs74709425	chr20:26146244-26146245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200030996	chr20:26146263-26146264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371370891	chr20:26146267-26146268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373925099	chr20:26146271-26146272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201229864	chr20:26146277-26146278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370716922	chr20:26146283-26146284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375241457	chr20:26146284-26146285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376022779	chr20:26146287-26146288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35684021	chr20:26146302-26146303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs386813625	chr20:26146305-26146306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs386813626	chr20:26146307-26146308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376356196	chr20:26146310-26146311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75503185	chr20:26146320-26146321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554443026	chr20:26146326-26146327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143306550	chr20:26146345-26146346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs199931720	chr20:26146347-26146348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149107320	chr20:26146366-26146367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111574294	chr20:26146368-26146369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540494916	chr20:26146372-26146373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560190950	chr20:26146387-26146388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576903497	chr20:26146398-26146399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76323506	chr20:26146405-26146406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74576919	chr20:26146406-26146407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75781621	chr20:26146449-26146450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74694367	chr20:26146480-26146481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77195701	chr20:26146481-26146482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73350672	chr20:26146497-26146498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73350674	chr20:26146522-26146523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs367672646	chr20:26146550-26146551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79324382	chr20:26146551-26146552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73350676	chr20:26146591-26146592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs202188393	chr20:26146608-26146609	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs73350678	chr20:26146630-26146631	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs78832111	chr20:26146665-26146666	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs78732537	chr20:26146679-26146680	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs375290211	chr20:26146688-26146689	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs200342947	chr20:26146691-26146692	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs62212068	chr20:26146714-26146715	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs34603306	chr20:26146724-26146725	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs62212069	chr20:26146744-26146745	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:26142200-26146200	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr20:26143800-26146200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr20:26144000-26146200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr20:26144000-26146200	Enhancers	NHEK	skin
5	chr20:26144000-26146200	Enhancers	Osteobl	bone
6	chr20:26144000-26146400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr20:26144800-26148400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr20:26144800-26148400	Weak transcription	NHLF	lung
9	chr20:26145400-26146200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr20:26145400-26146200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr20:26145400-26146200	Enhancers	NHDF-Ad	bronchial
12	chr20:26146000-26148000	Weak transcription	NH-A	brain
13	chr20:26146000-26150000	Weak transcription	HSMMtube	muscle
14	chr20:26146000-26151800	Weak transcription	HSMM	muscle
15	chr20:26146200-26146800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr20:26146200-26147200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr20:26146200-26148000	Weak transcription	NHEK	skin
18	chr20:26146200-26148200	Weak transcription	Osteobl	bone
19	chr20:26146200-26148400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr20:26146200-26148400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr20:26146400-26148000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr20:26146600-26147200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
23	chr20:26146800-26147000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr20:26147200-26149000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr20:26148000-26148800	Enhancers	NH-A	brain
26	chr20:26148000-26148800	Enhancers	NHEK	skin
27	chr20:26148000-26149000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr20:26148200-26151800	Enhancers	Osteobl	bone
29	chr20:26148400-26148800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr20:26148400-26148800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr20:26148400-26148800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr20:26148400-26148800	ZNF genes & repeats	NHLF	lung
33	chr20:26148600-26148800	Bivalent/Poised TSS	Right Atrium	heart
34	chr20:26148800-26149200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr20:26148800-26149800	Weak transcription	NH-A	brain
36	chr20:26148800-26150000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr20:26149000-26149400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr20:26149000-26149400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr20:26149400-26151400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr20:26149400-26151800	Enhancers	Muscle Satellite Cultured Cells	--
41	chr20:26149800-26150200	Enhancers	NH-A	brain
42	chr20:26150000-26150200	Enhancers	HSMMtube	muscle
43	chr20:26150000-26150400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr20:26150200-26150600	Weak transcription	HSMMtube	muscle
45	chr20:26150600-26151000	Enhancers	HSMMtube	muscle
46	chr20:26150800-26151000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr20:26151800-26152000	Enhancers	HSMM	muscle
48	chr20:26168000-26168400	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr20:26188200-26188600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr20:26188200-26188600	Weak transcription	Right Atrium	heart

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