Variant report

Variant	nsv551875
Chromosome Location	chr10:91681344-92297943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3145)
CpG islands
(count:916)
Chromatin interactive
region (count:64)
LncRNA
region (count:62)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3145 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:91846748-91847513	GM12878	blood:	n/a	n/a
2	ATF2	chr10:91890317-91890862	GM12878	blood:	n/a	n/a
3	ATF2	chr10:91890093-91890911	GM12878	blood:	n/a	n/a
4	ATF2	chr10:91927258-91927862	GM12878	blood:	n/a	n/a
5	ATF2	chr10:92180364-92180842	GM12878	blood:	n/a	n/a
6	ATF2	chr10:91806823-91807702	GM12878	blood:	n/a	n/a
7	ATF2	chr10:91752309-91752672	GM12878	blood:	n/a	n/a
8	ATF2	chr10:92079033-92079660	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr10:91927400-91927804	GM12878	blood:	n/a	n/a
10	ATF2	chr10:92079277-92079707	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr10:91846872-91847473	GM12878	blood:	n/a	n/a
12	ATF2	chr10:91806614-91807664	GM12878	blood:	n/a	n/a
13	ATF2	chr10:91719469-91719945	GM12878	blood:	n/a	n/a
14	ATF3	chr10:92079201-92079608	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr10:92079291-92079622	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr10:92079146-92079685	HCT-116	colon:	n/a	n/a
17	ATF3	chr10:91986779-91987513	HCT-116	colon:	n/a	n/a
18	ATF3	chr10:92073505-92074222	HCT-116	colon:	n/a	n/a
19	ATF3	chr10:91986749-91987509	HCT-116	colon:	n/a	n/a
20	ATF3	chr10:91939363-91939912	HCT-116	colon:	n/a	n/a
21	ATF3	chr10:91982032-91982513	HCT-116	colon:	n/a	n/a
22	BACH1	chr10:92076070-92076080	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr10:92079099-92079716	H1-hESC	embryonic stem cell:	n/a	chr10:92079432-92079446
24	BACH1	chr10:92184912-92184933	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr10:91890152-91890374	GM12878	blood:	n/a	n/a
26	BATF	chr10:91719496-91719906	GM12878	blood:	n/a	n/a
27	BATF	chr10:91689122-91689475	GM12878	blood:	n/a	n/a
28	BATF	chr10:91719389-91719943	GM12878	blood:	n/a	n/a
29	BATF	chr10:92079240-92079608	GM12878	blood:	n/a	chr10:92079435-92079446 chr10:92079436-92079446
30	BATF	chr10:92079259-92079651	GM12878	blood:	n/a	chr10:92079435-92079446 chr10:92079436-92079446
31	BATF	chr10:91986969-91987320	GM12878	blood:	n/a	chr10:91987115-91987126 chr10:91987112-91987122 chr10:91987116-91987126
32	BATF	chr10:91752392-91752637	GM12878	blood:	n/a	n/a
33	BATF	chr10:91714636-91715272	GM12878	blood:	n/a	n/a
34	BATF	chr10:92180389-92180682	GM12878	blood:	n/a	n/a
35	BATF	chr10:91846967-91847391	GM12878	blood:	n/a	chr10:91847191-91847202
36	BATF	chr10:91846926-91847379	GM12878	blood:	n/a	chr10:91847191-91847202
37	BATF	chr10:91811356-91811631	GM12878	blood:	n/a	n/a
38	BATF	chr10:91959364-91959521	GM12878	blood:	n/a	n/a
39	BATF	chr10:91890157-91890885	GM12878	blood:	n/a	chr10:91890837-91890847
40	BATF	chr10:91871473-91871730	GM12878	blood:	n/a	chr10:91871572-91871582
41	BATF	chr10:91927387-91927750	GM12878	blood:	n/a	n/a
42	BATF	chr10:91927485-91927777	GM12878	blood:	n/a	n/a
43	BATF	chr10:91806923-91807482	GM12878	blood:	n/a	n/a
44	BATF	chr10:91752336-91752655	GM12878	blood:	n/a	n/a
45	BATF	chr10:92180437-92180697	GM12878	blood:	n/a	n/a
46	BATF	chr10:91806747-91807472	GM12878	blood:	n/a	n/a
47	BCL11A	chr10:91752342-91752657	GM12878	blood:	n/a	n/a
48	BCL11A	chr10:91806776-91807612	GM12878	blood:	n/a	n/a
49	BCL11A	chr10:91846899-91847461	GM12878	blood:	n/a	n/a
50	BCL11A	chr10:91890115-91890841	GM12878	blood:	n/a	chr10:91890270-91890279

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:91919031-91919081	HCF	heart:	n/a
2	chr10:91919031-91919081	HCF	heart:	n/a
3	chr10:91738461-91738511	Hepatocyte	liver:	n/a
4	chr10:92063013-92063063	PrEC	prostate:	n/a
5	chr10:91738528-91738578	HRE	kidney:	n/a
6	chr10:92213389-92213439	GM12878	blood:	n/a
7	chr10:92153495-92153545	ovcar-3	ovarian:	n/a
8	chr10:91738791-91738841	SK-N-SH_RA	brain:	n/a
9	chr10:92079600-92079650	H1-hESC	embryonic stem cell:	embryo
10	chr10:91738461-91738511	NHDF-neo	bronchial:	n/a
11	chr10:91737463-91737513	A549	lung:	n/a
12	chr10:91852861-91852911	NT2-D1	testis:	n/a
13	chr10:91919031-91919081	SK-N-SH	brain:	n/a
14	chr10:92063013-92063063	MCF10A-Er-Src	breast:	n/a
15	chr10:92213236-92213286	Hela-S3	cervix:	n/a
16	chr10:91738791-91738841	PFSK-1	brain:	n/a
17	chr10:91738461-91738511	GM12891	blood:	n/a
18	chr10:92079600-92079650	HRCEpiC	kidney:	n/a
19	chr10:92079600-92079650	AG10803	skin:	n/a
20	chr10:91738713-91738763	K562	blood:	n/a
21	chr10:91738528-91738578	K562	blood:	n/a
22	chr10:92123669-92123719	CMK	blood:	n/a
23	chr10:92153495-92153545	HPAEpiC	pulmonary alveolar:	n/a
24	chr10:91738461-91738511	H1-hESC	embryonic stem cell:	embryo
25	chr10:91919031-91919081	IMR90	lung:	fetal
26	chr10:92123669-92123719	H1-hESC	embryonic stem cell:	embryo
27	chr10:92213389-92213439	U87	brain:	n/a
28	chr10:91919031-91919081	CMK	blood:	n/a
29	chr10:92153495-92153545	K562	blood:	n/a
30	chr10:91852861-91852911	NHDF-neo	bronchial:	n/a
31	chr10:91738461-91738511	HCT-116	colon:	n/a
32	chr10:92153495-92153545	RPTEC	kidney:	n/a
33	chr10:92079600-92079650	HMEC	breast:	n/a
34	chr10:91738791-91738841	HAEpiC	amniotic membrane:	n/a
35	chr10:91717815-91717865	NHBE	bronchial:	n/a
36	chr10:92213389-92213439	MCF-7	breast:	n/a
37	chr10:92079600-92079650	HIPEpiC	eye:	n/a
38	chr10:91738713-91738763	AoSMC	blood vessel:	n/a
39	chr10:92153495-92153545	AG09309	skin:	n/a
40	chr10:91858201-91858251	HRPEpiC	eye:	n/a
41	chr10:91858201-91858251	NH-A	brain:	n/a
42	chr10:92063013-92063063	HIPEpiC	eye:	n/a
43	chr10:92213236-92213286	GM06990	blood:	n/a
44	chr10:91738713-91738763	ECC-1	luminal epithelium:	n/a
45	chr10:91738528-91738578	ovcar-3	ovarian:	n/a
46	chr10:91738791-91738841	SAEC	small airway:	n/a
47	chr10:92213236-92213286	GM12892	blood:	n/a
48	chr10:92213389-92213439	Jurkat	blood:	n/a
49	chr10:91919031-91919081	MCF-7	breast:	n/a
50	chr10:92063013-92063063	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:91886442..91889438-chr10:91891894..91894771,2	MCF-7	breast:
2	chr10:91900968..91904082-chr10:91905876..91909843,4	MCF-7	breast:
3	chr10:91931353..91933621-chr10:91948075..91950614,2	K562	blood:
4	chr10:91908451..91909024-chr10:92048226..92048868,2	MCF-7	breast:
5	chr10:92064760..92066679-chr10:92166883..92168806,2	MCF-7	breast:
6	chr10:91908033..91909093-chr10:92411955..92412824,3	MCF-7	breast:
7	chr10:92184835..92186685-chr10:92187388..92189622,2	MCF-7	breast:
8	chr10:92047473..92050346-chr10:92165247..92168101,3	MCF-7	breast:
9	chr10:92184835..92186685-chr10:92187388..92189622,2	MCF-7	breast:
10	chr10:92048060..92049321-chr10:92352261..92353257,6	MCF-7	breast:
11	chr10:91967172..91968882-chr10:91972156..91974992,2	MCF-7	breast:
12	chr10:91968000..91970356-chr10:91975660..91978114,2	MCF-7	breast:
13	chr10:92264610..92266324-chr17:57922453..57924071,2	MCF-7	breast:
14	chr10:92196966..92197656-chr10:92339492..92340259,2	MCF-7	breast:
15	chr10:91967172..91968882-chr10:91972156..91974992,2	MCF-7	breast:
16	chr10:92255876..92258347-chr10:92261128..92263614,2	MCF-7	breast:
17	chr10:92064760..92066679-chr10:92166883..92168806,2	MCF-7	breast:
18	chr10:92197334..92197860-chr10:92338992..92339734,2	MCF-7	breast:
19	chr10:92079088..92081474-chr10:92085377..92088671,3	MCF-7	breast:
20	chr10:91679148..91682138-chr10:91965404..91969772,3	MCF-7	breast:
21	chr10:91718660..91720369-chr10:91722902..91725645,2	MCF-7	breast:
22	chr10:91905536..91908500-chr10:91908685..91910985,2	K562	blood:
23	chr10:91905536..91908500-chr10:91908685..91910985,2	K562	blood:
24	chr10:91908037..91908636-chr10:92339006..92340002,2	MCF-7	breast:
25	chr10:92255876..92258347-chr10:92261128..92263614,2	MCF-7	breast:
26	chr10:91404738..91406321-chr10:91777135..91780059,2	MCF-7	breast:
27	chr10:91722915..91725484-chr10:91726332..91728860,2	MCF-7	breast:
28	chr10:91938353..91941143-chr10:91951885..91953423,2	MCF-7	breast:
29	chr10:92248193..92249705-chr10:92254263..92256644,2	MCF-7	breast:
30	chr10:91907918..91908914-chr10:92477743..92478315,2	MCF-7	breast:
31	chr10:92047856..92048792-chr10:92412267..92413265,3	MCF-7	breast:
32	chr10:91718660..91720369-chr10:91722902..91725645,2	MCF-7	breast:
33	chr10:92079088..92081474-chr10:92085377..92088671,3	MCF-7	breast:
34	chr10:91968000..91970356-chr10:91975660..91978114,2	MCF-7	breast:
35	chr10:92177056..92178628-chr10:92179037..92181377,2	MCF-7	breast:
36	chr10:92051318..92054074-chr10:92099394..92101764,2	MCF-7	breast:
37	chr10:92177056..92178628-chr10:92179037..92181377,2	MCF-7	breast:
38	chr10:91685460..91687042-chr10:91688949..91691797,2	MCF-7	breast:
39	chr10:91553240..91554032-chr10:91898333..91899226,2	MCF-7	breast:
40	chr10:91900968..91904082-chr10:91905876..91909843,4	MCF-7	breast:
41	chr10:92047878..92048766-chr10:92339403..92340022,2	MCF-7	breast:
42	chr10:92051318..92054074-chr10:92099394..92101764,2	MCF-7	breast:
43	chr10:91722915..91725484-chr10:91726332..91728860,2	MCF-7	breast:
44	chr10:91679148..91682138-chr10:91965404..91969772,3	MCF-7	breast:
45	chr10:91553149..91554039-chr10:91898323..91899074,3	MCF-7	breast:
46	chr10:91585659..91588157-chr10:92199771..92201481,2	MCF-7	breast:
47	chr10:91886442..91889438-chr10:91891894..91894771,2	MCF-7	breast:
48	chr10:91982612..91984620-chr10:91985971..91988082,2	MCF-7	breast:
49	chr10:91908451..91909024-chr10:92048226..92048868,2	MCF-7	breast:
50	chr10:91982612..91984620-chr10:91985971..91988082,2	MCF-7	breast:

(count:62 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPP30-10	chr10:92235756-92235809	NONHSAT015587
2	lnc-RPP30-6	chr10:92214455-92214580	XLOC_008556
3	lnc-RPP30-10	chr10:92249010-92249108	NONHSAT015590
4	lnc-RPP30-9	chr10:92212454-92213123	NONHSAT015591
5	lnc-RPP30-6	chr10:92213927-92214072	ENSG00000224750
6	lnc-RPP30-10	chr10:92252523-92252705	NONHSAT015589
7	lnc-PANK1-8	chr10:91923408-91923717	NONHSAT015582
8	lnc-RPP30-10	chr10:92235756-92235809	NONHSAT015590
9	lnc-RPP30-6	chr10:92213926-92214072	XLOC_008556
10	lnc-PANK1-7	chr10:91705612-91705740	NONHSAT015579
11	lnc-HTR7-2	chr10:92152691-92152776	NONHSAT015585
12	lnc-RPP30-5	chr10:92225673-92225745	XLOC_008557
13	lnc-RPP30-10	chr10:92204435-92204560	NONHSAT015590
14	lnc-RPP30-10	chr10:92235756-92235809	NONHSAT015589
15	lnc-RPP30-6	chr10:92290369-92290873	XLOC_008556
16	lnc-HTR7-2	chr10:92153725-92153791	NONHSAT015585
17	lnc-RPP30-6	chr10:92214437-92214580	XLOC_008556
18	lnc-RPP30-6	chr10:92245776-92245829	XLOC_008556
19	lnc-HTR7-1	chr10:92211437-92211590	XLOC_008901
20	lnc-RPP30-10	chr10:92210509-92211238	NONHSAT015588
21	lnc-HTR7-1	chr10:92166207-92166352	XLOC_008901
22	lnc-KIF20B-8	chr10:91924526-91924552	NONHSAT015584
23	lnc-KIF20B-8	chr10:91939472-91939926	NONHSAT015584
24	lnc-HTR7-1	chr10:92287031-92287196	XLOC_008901
25	lnc-RPP30-10	chr10:92204417-92204560	NONHSAT015588
26	lnc-RPP30-6	chr10:92259030-92259128	XLOC_008556
27	lnc-PANK1-7	chr10:91705952-91706174	NONHSAT015579
28	lnc-RPP30-9	chr10:92217602-92217689	NONHSAT015591
29	lnc-HTR7-1	chr10:92163745-92163811	XLOC_008901
30	lnc-HTR7-2	chr10:92152258-92152545	NONHSAT015585
31	lnc-HTR7-2	chr10:92201417-92201570	NONHSAT015585
32	lnc-RPP30-6	chr10:92262543-92262725	XLOC_008556
33	lnc-PANK1-4	chr10:91715972-91716194	XLOC_008900
34	lnc-RPP30-6	chr10:92214455-92214580	XLOC_008556
35	lnc-RPP30-10	chr10:92249010-92251177	NONHSAT015587
36	lnc-RPP30-6	chr10:92245776-92245829	ENSG00000224750
37	lnc-RPP30-10	chr10:92249010-92249108	NONHSAT015589
38	lnc-RPP30-6	chr10:92245776-92245829	XLOC_008556
39	lnc-RPP30-6	chr10:92245776-92245829	XLOC_008556
40	lnc-RPP30-6	chr10:92259030-92261197	ENSG00000224750
41	lnc-RPP30-10	chr10:92280349-92280853	NONHSAT015590
42	lnc-HTR7-2	chr10:92156187-92156332	NONHSAT015585
43	lnc-RPP30-10	chr10:92203906-92204052	ucscGeneNc_uc001kgy_2
44	lnc-RPP30-6	chr10:92259030-92259128	XLOC_008556
45	lnc-HTR7-2	chr10:92277011-92277176	NONHSAT015585
46	lnc-KIF20B-5	chr10:91923670-91923893	XLOC_008555
47	lnc-PANK1-4	chr10:91715632-91715760	XLOC_008900
48	lnc-HTR7-1	chr10:92162278-92162565	XLOC_008901
49	lnc-RPP30-10	chr10:92204435-92204560	NONHSAT015589
50	lnc-PANK1-4	chr10:91716906-91717130	XLOC_008900

No data

Variant related genes	Relation type
SNRPD2P1	TF binding region
ENSG00000238291	TF binding region
RN7SKP143	TF binding region
ENSG00000224750	TF binding region
ENSG00000226159	TF binding region
SNRPD2P1	CpG island
ENSG00000238291	CpG island
RN7SKP143	CpG island
ENSG00000224750	CpG island
ENSG00000226159	CpG island
ENSG00000249962	chromatin interactions
ENSG00000152782	chromatin interactions
ENSG00000232936	chromatin interactions
MLL2	miRNA target sites
HMGA2	miRNA target sites
MLL3	miRNA target sites
BCL11B	miRNA target sites
TGFBR2	miRNA target sites

Extended variants
information (count: 20490 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:20490 , 50 per page) page: 1 2 3 4 5 6 7 ... 410

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1296513	chr10:91681344-91681345	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567691403	chr10:91681369-91681370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143081336	chr10:91681373-91681374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541521738	chr10:91681417-91681418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148232714	chr10:91681465-91681466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188227748	chr10:91681476-91681477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369343449	chr10:91681490-91681491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376227940	chr10:91681491-91681492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575073195	chr10:91681493-91681494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141199100	chr10:91681497-91681498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191769827	chr10:91681502-91681503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78494040	chr10:91681556-91681557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533119217	chr10:91681570-91681571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147359712	chr10:91681597-91681598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540522296	chr10:91681658-91681659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34624848	chr10:91681699-91681700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115012719	chr10:91681715-91681716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529302018	chr10:91681744-91681745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183811570	chr10:91681758-91681759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569404843	chr10:91681802-91681803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188188528	chr10:91681805-91681806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191438274	chr10:91681819-91681820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184341603	chr10:91681847-91681848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538231009	chr10:91681916-91681917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7078093	chr10:91682009-91682010	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs566314755	chr10:91682090-91682091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116729666	chr10:91682102-91682103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534282594	chr10:91682208-91682209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1274128	chr10:91682281-91682282	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs76627692	chr10:91682319-91682320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543996186	chr10:91682323-91682324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112800109	chr10:91682342-91682343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577775330	chr10:91682360-91682361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546678176	chr10:91682363-91682364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7903627	chr10:91682446-91682447	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs377038202	chr10:91682501-91682502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573932088	chr10:91682504-91682505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182032972	chr10:91682510-91682511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562963732	chr10:91682544-91682545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531888222	chr10:91682637-91682638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1274129	chr10:91682681-91682682	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs147207922	chr10:91682701-91682702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527903730	chr10:91682710-91682711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570982323	chr10:91682753-91682754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567982939	chr10:91682783-91682784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375000237	chr10:91682887-91682888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1274130	chr10:91682901-91682902	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs143641903	chr10:91682911-91682912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112694706	chr10:91682912-91682913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187032200	chr10:91682937-91682938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1756 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91674400-91685200	Enhancers	HMEC	breast
2	chr10:91674400-91685400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr10:91678400-91683400	Weak transcription	Primary B cells from cord blood	blood
4	chr10:91679000-91684600	Enhancers	Hela-S3	cervix
5	chr10:91679000-91685200	Enhancers	NHEK	skin
6	chr10:91679600-91684600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr10:91679600-91685200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr10:91679800-91684600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr10:91680200-91682000	Enhancers	A549	lung
10	chr10:91680400-91681400	Enhancers	Esophagus	oesophagus
11	chr10:91680400-91682000	Enhancers	Placenta Amnion	Placenta Amnion
12	chr10:91680600-91681400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr10:91680800-91681800	Weak transcription	Placenta	Placenta
14	chr10:91681200-91681400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr10:91681800-91682400	Enhancers	Placenta	Placenta
16	chr10:91683400-91684400	ZNF genes & repeats	Primary B cells from cord blood	blood
17	chr10:91683800-91684200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr10:91683800-91684200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr10:91684400-91686200	Weak transcription	Primary B cells from cord blood	blood
20	chr10:91684600-91686800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr10:91684600-91699600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr10:91685200-91686400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr10:91685200-91686400	Weak transcription	HMEC	breast
24	chr10:91685200-91686400	Weak transcription	NHEK	skin
25	chr10:91686200-91687000	Strong transcription	Primary B cells from cord blood	blood
26	chr10:91686400-91687000	Enhancers	NHEK	skin
27	chr10:91686400-91687200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr10:91686400-91687200	Enhancers	HMEC	breast
29	chr10:91686800-91687000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr10:91687000-91694000	Weak transcription	Primary B cells from cord blood	blood
31	chr10:91687200-91689600	Weak transcription	HMEC	breast
32	chr10:91687600-91687800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr10:91696800-91697200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr10:91697200-91697400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr10:91697200-91697400	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr10:91697200-91697600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr10:91697200-91700400	Enhancers	NHEK	skin
38	chr10:91697400-91698400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr10:91697600-91699800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr10:91697800-91698200	ZNF genes & repeats	Primary B cells from cord blood	blood
41	chr10:91698000-91698800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr10:91698200-91702000	Weak transcription	Primary B cells from cord blood	blood
43	chr10:91698400-91698600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr10:91698400-91702200	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr10:91698600-91701000	Enhancers	HMEC	breast
46	chr10:91698800-91699800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr10:91698800-91699800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr10:91699600-91700400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr10:91699600-91700400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr10:91699800-91700200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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