Variant report

Variant	esv2762580
Chromosome Location	chr6:15105917-15159110
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:530)
CpG islands
(count:183)
Chromatin interactive
region (count:50)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:15106725-15107548	K562	blood:	n/a	n/a
2	ATF1	chr6:15121792-15121851	K562	blood:	n/a	n/a
3	ATF2	chr6:15137321-15137716	GM12878	blood:	n/a	n/a
4	ATF2	chr6:15151311-15151869	GM12878	blood:	n/a	n/a
5	ATF3	chr6:15144832-15145213	K562	blood:	n/a	n/a
6	ATF3	chr6:15133116-15133632	A549	lung:	n/a	n/a
7	BACH1	chr6:15131621-15131806	K562	blood:	n/a	n/a
8	BACH1	chr6:15109371-15109372	K562	blood:	n/a	n/a
9	BACH1	chr6:15122347-15122763	K562	blood:	n/a	n/a
10	BATF	chr6:15137326-15137576	GM12878	blood:	n/a	n/a
11	BATF	chr6:15150444-15150764	GM12878	blood:	n/a	chr6:15150606-15150617
12	BATF	chr6:15137335-15137660	GM12878	blood:	n/a	n/a
13	BATF	chr6:15151444-15151726	GM12878	blood:	n/a	n/a
14	BCL11A	chr6:15151369-15151810	GM12878	blood:	n/a	n/a
15	BCL3	chr6:15133100-15133556	A549	lung:	n/a	chr6:15133398-15133407
16	BCLAF1	chr6:15151355-15151858	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:15151358-15151813	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:15151478-15151810	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:15148768-15149053	HepG2	liver:	n/a	n/a
20	BHLHE40	chr6:15148784-15148998	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:15106719-15107788	K562	blood:	n/a	n/a
22	CBX3	chr6:15122363-15122748	K562	blood:	n/a	n/a
23	CBX3	chr6:15132935-15133974	HCT-116	colon:	n/a	n/a
24	CBX3	chr6:15132786-15134075	HCT-116	colon:	n/a	n/a
25	CBX3	chr6:15106008-15107878	K562	blood:	n/a	n/a
26	CCNT2	chr6:15107227-15107846	K562	blood:	n/a	chr6:15107707-15107716
27	CEBPB	chr6:15144715-15145302	HCT-116	colon:	n/a	chr6:15145015-15145026
28	CEBPB	chr6:15139096-15139310	IMR90	lung:	n/a	chr6:15139172-15139183
29	CEBPB	chr6:15148762-15149047	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:15144802-15145167	K562	blood:	n/a	chr6:15145015-15145026
31	CEBPB	chr6:15145011-15145062	H1-hESC	embryonic stem cell:	n/a	chr6:15145015-15145026
32	CEBPB	chr6:15156262-15156533	K562	blood:	n/a	n/a
33	CEBPB	chr6:15144839-15145278	A549	lung:	n/a	chr6:15145015-15145026
34	CEBPB	chr6:15133146-15133520	MCF-7	breast:	n/a	n/a
35	CEBPB	chr6:15139086-15139332	K562	blood:	n/a	chr6:15139172-15139183
36	CEBPB	chr6:15139144-15139206	Hela-S3	cervix:	n/a	chr6:15139172-15139183
37	CEBPB	chr6:15107164-15107551	K562	blood:	n/a	n/a
38	CEBPB	chr6:15144848-15145172	IMR90	lung:	n/a	chr6:15145015-15145026
39	CEBPB	chr6:15156263-15156475	IMR90	lung:	n/a	n/a
40	CEBPB	chr6:15134524-15134739	A549	lung:	n/a	n/a
41	CEBPB	chr6:15108802-15109097	K562	blood:	n/a	chr6:15108962-15108973 chr6:15108963-15108974 chr6:15108962-15108975
42	CEBPB	chr6:15156243-15156571	K562	blood:	n/a	n/a
43	CEBPB	chr6:15150602-15150767	HepG2	liver:	n/a	chr6:15150672-15150683 chr6:15150673-15150684 chr6:15150631-15150639 chr6:15150672-15150683 chr6:15150672-15150685 chr6:15150672-15150685
44	CEBPB	chr6:15144879-15145141	HepG2	liver:	n/a	chr6:15145015-15145026
45	CEBPB	chr6:15108799-15109127	HepG2	liver:	n/a	chr6:15108962-15108973 chr6:15108963-15108974 chr6:15108962-15108975
46	CEBPB	chr6:15132872-15133942	HCT-116	colon:	n/a	n/a
47	CEBPB	chr6:15134634-15134765	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:15108823-15109087	H1-hESC	embryonic stem cell:	n/a	chr6:15108962-15108973 chr6:15108963-15108974 chr6:15108962-15108975
49	CEBPB	chr6:15144941-15145213	A549	lung:	n/a	chr6:15145015-15145026
50	CEBPB	chr6:15109716-15109896	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:15149029-15149079	HUVEC	blood vessel:	n/a
2	chr6:15149029-15149079	AG04449	skin:	fetal
3	chr6:15143233-15143283	HRE	kidney:	n/a
4	chr6:15149029-15149079	GM12891	blood:	n/a
5	chr6:15133183-15133233	HL-60	blood:	n/a
6	chr6:15143233-15143283	HEEpiC	esophagus:	n/a
7	chr6:15149029-15149079	GM12892	blood:	n/a
8	chr6:15143233-15143283	CMK	blood:	n/a
9	chr6:15133183-15133233	HCT-116	colon:	n/a
10	chr6:15149029-15149079	H1-hESC	embryonic stem cell:	embryo
11	chr6:15149029-15149079	NT2-D1	testis:	n/a
12	chr6:15133183-15133233	HCM	heart:	n/a
13	chr6:15149029-15149079	HIPEpiC	eye:	n/a
14	chr6:15149029-15149079	HMEC	breast:	n/a
15	chr6:15143233-15143283	GM12878	blood:	n/a
16	chr6:15143233-15143283	IMR90	lung:	fetal
17	chr6:15133183-15133233	Jurkat	blood:	n/a
18	chr6:15143233-15143283	ovcar-3	ovarian:	n/a
19	chr6:15149029-15149079	HRCEpiC	kidney:	n/a
20	chr6:15149029-15149079	PFSK-1	brain:	n/a
21	chr6:15143233-15143283	AoSMC	blood vessel:	n/a
22	chr6:15143233-15143283	A549	lung:	n/a
23	chr6:15143233-15143283	GM12891	blood:	n/a
24	chr6:15133183-15133233	HMEC	breast:	n/a
25	chr6:15133183-15133233	PFSK-1	brain:	n/a
26	chr6:15143233-15143283	AG10803	skin:	n/a
27	chr6:15133183-15133233	AG10803	skin:	n/a
28	chr6:15143233-15143283	BJ	skin:	n/a
29	chr6:15149029-15149079	HL-60	blood:	n/a
30	chr6:15143233-15143283	H1-hESC	embryonic stem cell:	embryo
31	chr6:15149029-15149079	AG10803	skin:	n/a
32	chr6:15143233-15143283	NB4	blood:	n/a
33	chr6:15143233-15143283	NH-A	brain:	n/a
34	chr6:15143233-15143283	PFSK-1	brain:	n/a
35	chr6:15133183-15133233	GM12892	blood:	n/a
36	chr6:15133183-15133233	HIPEpiC	eye:	n/a
37	chr6:15133183-15133233	ovcar-3	ovarian:	n/a
38	chr6:15143233-15143283	SAEC	small airway:	n/a
39	chr6:15149029-15149079	AG04450	lung:	fetal
40	chr6:15149029-15149079	Hela-S3	cervix:	n/a
41	chr6:15149029-15149079	AG09309	skin:	n/a
42	chr6:15143233-15143283	Hela-S3	cervix:	n/a
43	chr6:15133183-15133233	RPTEC	kidney:	n/a
44	chr6:15143233-15143283	HRPEpiC	eye:	n/a
45	chr6:15143233-15143283	SK-N-SH	brain:	n/a
46	chr6:15149029-15149079	GM12878	blood:	n/a
47	chr6:15143233-15143283	NT2-D1	testis:	n/a
48	chr6:15133183-15133233	GM12891	blood:	n/a
49	chr6:15149029-15149079	HCT-116	colon:	n/a
50	chr6:15133183-15133233	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:15092731..15095339-chr6:15106274..15108820,2	K562	blood:
2	chr6:15133229..15135738-chr6:15147564..15149146,2	K562	blood:
3	chr6:15156210..15158890-chr6:15211476..15214661,3	K562	blood:
4	chr6:15131659..15133367-chr6:15138303..15139913,2	K562	blood:
5	chr6:15143787..15146280-chr6:15158034..15160190,2	K562	blood:
6	chr6:15107869..15110295-chr6:15242346..15245809,3	K562	blood:
7	chr6:15110076..15111884-chr6:15115512..15117432,2	K562	blood:
8	chr6:15134521..15137153-chr6:15210415..15211932,2	K562	blood:
9	chr6:15106983..15108831-chr6:15151531..15154353,2	K562	blood:
10	chr6:15105604..15108959-chr6:15245974..15248979,5	K562	blood:
11	chr6:15102630..15105132-chr6:15106724..15108823,2	K562	blood:
12	chr6:14778863..14781243-chr6:15107030..15109161,2	K562	blood:
13	chr6:15092995..15095757-chr6:15118674..15121139,2	K562	blood:
14	chr6:15148839..15151214-chr6:15151716..15153395,2	MCF-7	breast:
15	chr6:15119436..15121863-chr6:15121946..15124173,2	K562	blood:
16	chr6:15143619..15146318-chr6:15151883..15153386,2	MCF-7	breast:
17	chr6:15133229..15135738-chr6:15147564..15149146,2	K562	blood:
18	chr6:15125739..15127625-chr6:15128414..15130165,2	MCF-7	breast:
19	chr6:15132794..15134906-chr6:15135026..15137692,3	K562	blood:
20	chr6:15106983..15108831-chr6:15151531..15154353,2	K562	blood:
21	chr6:15096022..15098594-chr6:15145992..15148961,2	K562	blood:
22	chr6:15136573..15138156-chr6:15245614..15247177,2	K562	blood:
23	chr6:15155665..15157322-chr6:15249355..15251263,2	K562	blood:
24	chr6:15132794..15134906-chr6:15135026..15137692,3	K562	blood:
25	chr6:15103877..15106260-chr6:15135421..15138243,2	K562	blood:
26	chr6:15125739..15127625-chr6:15128414..15130165,2	MCF-7	breast:
27	chr6:15106427..15109667-chr6:15111584..15114479,3	K562	blood:
28	chr6:15088965..15090791-chr6:15157951..15160766,2	K562	blood:
29	chr6:15099407..15102397-chr6:15106486..15108344,2	K562	blood:
30	chr6:15136761..15139272-chr6:15149097..15150701,2	MCF-7	breast:
31	chr6:14918253..14920493-chr6:15156735..15158710,2	MCF-7	breast:
32	chr6:15103632..15105300-chr6:15106507..15108224,2	K562	blood:
33	chr6:15130172..15131963-chr6:15134360..15137201,2	K562	blood:
34	chr6:15143619..15146318-chr6:15151883..15153386,2	MCF-7	breast:
35	chr6:15084562..15086829-chr6:15124067..15125929,2	K562	blood:
36	chr6:15144340..15146667-chr6:15148737..15150328,2	K562	blood:
37	chr6:15086616..15088953-chr6:15137602..15139748,2	K562	blood:
38	chr6:15110076..15111884-chr6:15115512..15117432,2	K562	blood:
39	chr6:15143787..15146280-chr6:15158034..15160190,2	K562	blood:
40	chr6:14882855..14884940-chr6:15106180..15108933,2	K562	blood:
41	chr6:15131659..15133367-chr6:15138303..15139913,2	K562	blood:
42	chr6:15147856..15151805-chr6:15244004..15248641,4	MCF-7	breast:
43	chr6:15119436..15121863-chr6:15121946..15124173,2	K562	blood:
44	chr6:15069920..15071454-chr6:15106788..15108446,2	K562	blood:
45	chr6:15130172..15131963-chr6:15134360..15137201,2	K562	blood:
46	chr6:15120083..15121964-chr6:15210438..15212064,2	K562	blood:
47	chr6:15158330..15160167-chr6:15160268..15162625,2	K562	blood:
48	chr6:15093162..15095883-chr6:15107253..15109539,2	MCF-7	breast:
49	chr6:15106242..15108900-chr6:15209959..15212920,4	K562	blood:
50	chr6:15069954..15071516-chr6:15106946..15109346,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-JARID2-3	chr6:15113199-15113450	NONHSAT107865

No data

Variant related genes	Relation type
ENSG00000216754	TF binding region
ENSG00000264687	TF binding region
RN7SL332P	TF binding region
ENSG00000216754	CpG island
ENSG00000264687	CpG island
RN7SL332P	CpG island
ENSG00000264687	chromatin interactions
ENSG00000242989	chromatin interactions
ENSG00000234261	chromatin interactions
ENSG00000008083	chromatin interactions
ENSG00000235488	chromatin interactions
ENSG00000271888	chromatin interactions
ENSG00000216754	chromatin interactions

Extended variants
information (count: 2066 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2066 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375125052	chr6:15105937-15105938	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs563085281	chr6:15105954-15105955	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs576644112	chr6:15105974-15105975	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs150769078	chr6:15105998-15105999	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs542366598	chr6:15106059-15106060	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs562144159	chr6:15106080-15106081	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs368650703	chr6:15106082-15106083	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs572554808	chr6:15106119-15106120	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs199702928	chr6:15106148-15106149	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs114170483	chr6:15106155-15106156	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs149792796	chr6:15106183-15106184	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs35548607	chr6:15106207-15106208	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs530323206	chr6:15106208-15106209	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs146808169	chr6:15106247-15106248	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs562963928	chr6:15106248-15106249	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs137862733	chr6:15106282-15106283	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs35111027	chr6:15106295-15106296	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs70993083	chr6:15106296-15106297	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs9383022	chr6:15106310-15106311	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs551991406	chr6:15106325-15106326	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs578229942	chr6:15106337-15106338	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs181258560	chr6:15106369-15106370	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs374971404	chr6:15106421-15106422	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs548364167	chr6:15106434-15106435	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs568392993	chr6:15106634-15106635	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs537328082	chr6:15106682-15106683	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs557259025	chr6:15106683-15106684	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs144181873	chr6:15106705-15106706	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs560516049	chr6:15106707-15106708	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs538975320	chr6:15106733-15106734	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs558790863	chr6:15106884-15106885	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs572491525	chr6:15106901-15106902	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs541307576	chr6:15106942-15106943	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs555119918	chr6:15106948-15106949	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs185273762	chr6:15106980-15106981	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs543730998	chr6:15107012-15107013	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs570702885	chr6:15107015-15107016	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs563595093	chr6:15107034-15107035	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs543738289	chr6:15107052-15107053	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs531991383	chr6:15107066-15107067	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs545775627	chr6:15107078-15107079	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs559230355	chr6:15107156-15107157	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs1884120	chr6:15107204-15107205	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs548118633	chr6:15107223-15107224	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs568277762	chr6:15107231-15107232	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs530696204	chr6:15107254-15107255	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs139050338	chr6:15107279-15107280	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs549766992	chr6:15107347-15107348	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs570716673	chr6:15107350-15107351	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs538695359	chr6:15107379-15107380	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD

Chromatin state (count:274 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15087400-15117600	Weak transcription	Right Atrium	heart
2	chr6:15090400-15109000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:15104800-15106600	Weak transcription	K562	blood
4	chr6:15106600-15106800	Enhancers	K562	blood
5	chr6:15106800-15108000	Flanking Active TSS	K562	blood
6	chr6:15107000-15107800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr6:15107400-15108200	Enhancers	Fetal Stomach	stomach
8	chr6:15107400-15109200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:15107800-15108800	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr6:15108000-15108400	Enhancers	Fetal Brain Female	brain
11	chr6:15108000-15109200	Enhancers	K562	blood
12	chr6:15108400-15109200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr6:15108400-15110600	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr6:15108600-15110000	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr6:15108800-15109400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr6:15108800-15109400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:15109000-15109400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr6:15109000-15109400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr6:15109000-15109400	Enhancers	Fetal Lung	lung
20	chr6:15109000-15109400	Enhancers	Pancreas	Pancrea
21	chr6:15109000-15109600	Enhancers	Primary B cells from cord blood	blood
22	chr6:15109000-15109600	Enhancers	Fetal Intestine Large	intestine
23	chr6:15109000-15110000	Enhancers	Fetal Brain Male	brain
24	chr6:15109000-15110400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:15109200-15109600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr6:15109200-15111000	Weak transcription	K562	blood
27	chr6:15109400-15115800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:15109400-15116200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:15109600-15109800	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr6:15110600-15114800	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr6:15111000-15112000	Enhancers	K562	blood
32	chr6:15111400-15112000	Enhancers	Fetal Thymus	thymus
33	chr6:15112000-15113800	Weak transcription	K562	blood
34	chr6:15113800-15114200	Enhancers	K562	blood
35	chr6:15114800-15116200	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr6:15115800-15116200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:15115800-15116200	Weak transcription	Aorta	Aorta
38	chr6:15115800-15116400	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr6:15116200-15116400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr6:15116200-15116400	Enhancers	Aorta	Aorta
41	chr6:15116400-15117200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr6:15116400-15132000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:15117000-15117400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:15117200-15117600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr6:15121400-15122400	Enhancers	Fetal Thymus	thymus
46	chr6:15121600-15122000	Enhancers	Thymus	Thymus
47	chr6:15121800-15122800	Enhancers	K562	blood
48	chr6:15122000-15122800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:15128600-15130200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:15128800-15129200	Enhancers	Primary monocytes fromperipheralblood	blood

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