Variant report

Variant	nsv916688
Chromosome Location	chr12:119801814-120044407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1664)
CpG islands
(count:1464)
Chromatin interactive
region (count:109)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1664 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:119850974-119851341	K562	blood:	n/a	chr12:119850980-119850996
2	ARID3A	chr12:119951518-119951521	K562	blood:	n/a	n/a
3	ARID3A	chr12:119851024-119851322	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:119982854-119983066	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:119938133-119938298	K562	blood:	n/a	n/a
6	ARID3A	chr12:119992403-119992909	K562	blood:	n/a	n/a
7	ARID3A	chr12:119882282-119882529	K562	blood:	n/a	n/a
8	ARID3A	chr12:120030131-120030463	K562	blood:	n/a	n/a
9	ARID3A	chr12:119803212-119803732	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:119882317-119882590	HepG2	liver:	n/a	n/a
11	ATF1	chr12:119992486-119992706	K562	blood:	n/a	n/a
12	ATF1	chr12:120039746-120039978	K562	blood:	n/a	n/a
13	ATF1	chr12:120030081-120030307	K562	blood:	n/a	n/a
14	ATF2	chr12:119882197-119882678	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr12:119848173-119848584	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr12:119882302-119882566	K562	blood:	n/a	n/a
17	ATF3	chr12:119882230-119882687	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr12:119895046-119895404	K562	blood:	n/a	n/a
19	BACH1	chr12:119894800-119895706	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr12:119886603-119886864	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr12:120040022-120040213	K562	blood:	n/a	n/a
22	BACH1	chr12:120032405-120032497	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr12:119835465-119835564	K562	blood:	n/a	n/a
24	BATF	chr12:119813500-119813772	GM12878	blood:	n/a	chr12:119813647-119813658
25	BATF	chr12:119813452-119813791	GM12878	blood:	n/a	chr12:119813647-119813658
26	BCL3	chr12:119917040-119917391	GM12878	blood:	n/a	chr12:119917213-119917222 chr12:119917357-119917365 chr12:119917214-119917223
27	BCL3	chr12:119917163-119917405	GM12878	blood:	n/a	chr12:119917213-119917222 chr12:119917357-119917365 chr12:119917214-119917223
28	BCLAF1	chr12:119882236-119882543	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:119882283-119882584	K562	blood:	n/a	n/a
30	BHLHE40	chr12:119950793-119950979	K562	blood:	n/a	n/a
31	BHLHE40	chr12:119992330-119992998	K562	blood:	n/a	n/a
32	BHLHE40	chr12:120012870-120012874	K562	blood:	n/a	n/a
33	BHLHE40	chr12:120030079-120030363	K562	blood:	n/a	n/a
34	BHLHE40	chr12:119901361-119901436	K562	blood:	n/a	n/a
35	BHLHE40	chr12:119882284-119882587	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:120039820-120039920	K562	blood:	n/a	n/a
37	BHLHE40	chr12:119851086-119851312	K562	blood:	n/a	n/a
38	CBX3	chr12:119882266-119882589	K562	blood:	n/a	n/a
39	CBX3	chr12:119882253-119882595	K562	blood:	n/a	n/a
40	CBX3	chr12:119941249-119941643	HCT-116	colon:	n/a	n/a
41	CBX3	chr12:119882135-119882790	HCT-116	colon:	n/a	n/a
42	CBX3	chr12:119882162-119882790	HCT-116	colon:	n/a	n/a
43	CCNT2	chr12:120030063-120030429	K562	blood:	n/a	n/a
44	CCNT2	chr12:119992469-119992784	K562	blood:	n/a	n/a
45	CEBPB	chr12:119913496-119913814	A549	lung:	n/a	chr12:119913646-119913657
46	CEBPB	chr12:119803466-119803681	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:120036160-120036182	IMR90	lung:	n/a	n/a
48	CEBPB	chr12:120028509-120028709	HepG2	liver:	n/a	chr12:120028630-120028641
49	CEBPB	chr12:119933283-119933483	IMR90	lung:	n/a	n/a
50	CEBPB	chr12:120026946-120027240	A549	lung:	n/a	chr12:120027077-120027088 chr12:120027062-120027079 chr12:120027067-120027078 chr12:120027076-120027089

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:120033862-120033912	IMR90	lung:	fetal
2	chr12:119895394-119895444	U87	brain:	n/a
3	chr12:120031137-120031187	HAEpiC	amniotic membrane:	n/a
4	chr12:120031649-120031699	HCM	heart:	n/a
5	chr12:119836173-119836223	RPTEC	kidney:	n/a
6	chr12:120027629-120027679	HMEC	breast:	n/a
7	chr12:120032374-120032424	Hela-S3	cervix:	n/a
8	chr12:119836215-119836265	PANC-1	pancreas:	n/a
9	chr12:120032623-120032673	GM12892	blood:	n/a
10	chr12:119818931-119818981	HRE	kidney:	n/a
11	chr12:120032142-120032192	HepG2	liver:	n/a
12	chr12:119828513-119828563	LNCaP	prostate:	n/a
13	chr12:119836129-119836179	AG04449	skin:	fetal
14	chr12:120036581-120036631	U87	brain:	n/a
15	chr12:120032790-120032840	AG04450	lung:	fetal
16	chr12:120032623-120032673	Hepatocyte	liver:	n/a
17	chr12:119836173-119836223	NT2-D1	testis:	n/a
18	chr12:119935697-119935747	RPTEC	kidney:	n/a
19	chr12:120030707-120030757	HCM	heart:	n/a
20	chr12:120027629-120027679	SK-N-SH	brain:	n/a
21	chr12:119836173-119836223	GM06990	blood:	n/a
22	chr12:119818931-119818981	HRPEpiC	eye:	n/a
23	chr12:119836173-119836223	NH-A	brain:	n/a
24	chr12:120031649-120031699	T-47D	breast:	n/a
25	chr12:120030707-120030757	HUVEC	blood vessel:	n/a
26	chr12:119836129-119836179	HCPEpiC	choroid plexus:	n/a
27	chr12:119836173-119836223	Hepatocyte	liver:	n/a
28	chr12:119836215-119836265	HRE	kidney:	n/a
29	chr12:120032142-120032192	CMK	blood:	n/a
30	chr12:120031137-120031187	HUVEC	blood vessel:	n/a
31	chr12:120031137-120031187	GM19239	blood:	n/a
32	chr12:119850737-119850787	MCF-7	breast:	n/a
33	chr12:120027629-120027679	HAEpiC	amniotic membrane:	n/a
34	chr12:120027629-120027679	HRPEpiC	eye:	n/a
35	chr12:120033155-120033205	ECC-1	luminal epithelium:	n/a
36	chr12:119850737-119850787	Jurkat	blood:	n/a
37	chr12:120033032-120033082	NHDF-neo	bronchial:	n/a
38	chr12:119935697-119935747	Jurkat	blood:	n/a
39	chr12:120032623-120032673	A549	lung:	n/a
40	chr12:119935697-119935747	HepG2	liver:	n/a
41	chr12:120033032-120033082	SK-N-SH	brain:	n/a
42	chr12:119935697-119935747	T-47D	breast:	n/a
43	chr12:120032142-120032192	HIPEpiC	eye:	n/a
44	chr12:120029973-120030023	HRCEpiC	kidney:	n/a
45	chr12:120031137-120031187	H1-hESC	embryonic stem cell:	embryo
46	chr12:119895394-119895444	AG04449	skin:	fetal
47	chr12:120027629-120027679	A549	lung:	n/a
48	chr12:119850737-119850787	HCT-116	colon:	n/a
49	chr12:120032623-120032673	MCF-7	breast:	n/a
50	chr12:120032374-120032424	GM19239	blood:	n/a

(count:109 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:119608735..119609705-chr12:119917084..119918539,5	MCF-7	breast:
2	chr12:119883491..119884533-chr12:119982499..119983404,3	K562	blood:
3	chr12:119937705..119938674-chr12:119982968..119983529,3	K562	blood:
4	chr12:119913085..119915232-chr12:119915354..119917050,2	MCF-7	breast:
5	chr12:119882046..119882879-chr17:57181976..57182614,2	MCF-7	breast:
6	chr12:119633765..119636889-chr12:119849565..119852732,3	MCF-7	breast:
7	chr12:119885749..119887582-chr12:119923275..119926037,2	MCF-7	breast:
8	chr12:119982545..119983214-chr12:120086741..120087696,2	MCF-7	breast:
9	chr12:119850762..119851328-chr12:119881955..119882815,2	MCF-7	breast:
10	chr12:119982938..119983443-chr12:120086752..120087363,2	K562	blood:
11	chr12:119883274..119886371-chr12:119915842..119918823,3	MCF-7	breast:
12	chr12:119901170..119903751-chr12:119912148..119914468,2	MCF-7	breast:
13	chr12:119765671..119766355-chr12:119850911..119851698,3	K562	blood:
14	chr12:119884170..119886669-chr12:119907722..119909768,2	MCF-7	breast:
15	chr12:119856526..119857034-chr12:119982637..119983547,2	MCF-7	breast:
16	chr12:119858170..119861303-chr12:119864595..119866483,3	K562	blood:
17	chr12:119856554..119857225-chr12:120086612..120087366,2	MCF-7	breast:
18	chr12:119915459..119919519-chr12:119922678..119926603,4	MCF-7	breast:
19	chr12:119850295..119851264-chr12:119982488..119983086,2	MCF-7	breast:
20	chr12:119765655..119766458-chr12:119850699..119851560,2	MCF-7	breast:
21	chr12:119891011..119892854-chr12:119894450..119896303,2	K562	blood:
22	chr12:119609091..119609670-chr12:119949327..119950008,5	MCF-7	breast:
23	chr12:119894048..119897189-chr12:119897417..119901557,3	MCF-7	breast:
24	chr12:119883274..119886371-chr12:119915842..119918823,3	MCF-7	breast:
25	chr12:120016298..120018977-chr12:120030984..120032575,2	K562	blood:
26	chr12:119886069..119888446-chr12:119896498..119898792,2	MCF-7	breast:
27	chr12:119616454..119617961-chr12:119842773..119844959,2	MCF-7	breast:
28	chr12:119861971..119864906-chr12:119864949..119866973,2	K562	blood:
29	chr12:119884170..119886669-chr12:119907722..119909768,2	MCF-7	breast:
30	chr12:119998389..120000299-chr12:120029371..120031363,2	K562	blood:
31	chr12:119917727..119918526-chr12:119981821..119982376,2	MCF-7	breast:
32	chr12:120003654..120005469-chr12:120012916..120015894,2	K562	blood:
33	chr12:119151694..119152462-chr12:119850745..119851652,2	MCF-7	breast:
34	chr12:119882153..119882880-chr12:119982540..119983422,6	MCF-7	breast:
35	chr12:119944949..119947122-chr12:119948391..119950597,2	MCF-7	breast:
36	chr12:119901170..119903751-chr12:119912148..119914468,2	MCF-7	breast:
37	chr12:119615640..119617708-chr12:119848864..119850771,2	MCF-7	breast:
38	chr12:119896737..119898402-chr12:119901770..119903919,2	MCF-7	breast:
39	chr12:119885749..119887582-chr12:119923275..119926037,2	MCF-7	breast:
40	chr12:119992598..119995393-chr12:120116736..120118887,2	K562	blood:
41	chr12:119881958..119882695-chr12:119909939..119910747,2	MCF-7	breast:
42	chr12:119882040..119882723-chr12:119918595..119919451,2	MCF-7	breast:
43	chr12:119937781..119938725-chr12:119982582..119983300,3	MCF-7	breast:
44	chr12:119946564..119947475-chr16:85786654..85787465,2	MCF-7	breast:
45	chr12:119850762..119851328-chr12:119881955..119882815,2	MCF-7	breast:
46	chr12:119937781..119938725-chr12:119982582..119983300,3	MCF-7	breast:
47	chr12:119458483..119459134-chr12:119850426..119851166,2	MCF-7	breast:
48	chr12:119957963..119959771-chr12:119961069..119962984,2	K562	blood:
49	chr12:119896737..119898402-chr12:119901770..119903919,2	MCF-7	breast:
50	chr12:119894048..119897189-chr12:119897417..119901557,3	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSPB8-7	chr12:119867381-119867531	NONHSAT031079
2	lnc-CIT-1	chr12:119991353-119991450	ENSG00000248636
3	lnc-CIT-1	chr12:119991353-119991450	ENSG00000248636
4	lnc-HSPB8-5	chr12:119829841-119830126	l_741_chr12:119826869-119830126_testes
5	lnc-CIT-8	chr12:119892024-119894478	l_742_NR_024345
6	lnc-HSPB8-7	chr12:119885559-119885717	NONHSAT031079
7	lnc-HSPB8-7	chr12:119866488-119866567	NONHSAT031079
8	lnc-CIT-1	chr12:120031987-120032306	ENSG00000248636
9	lnc-CIT-1	chr12:120031987-120032045	ENSG00000248636
10	lnc-CIT-1	chr12:119825796-119826133	ENSG00000248636
11	lnc-CIT-1	chr12:120031987-120032602	NONHSAT031083
12	lnc-CIT-1	chr12:119991363-119991450	NONHSAT031083
13	lnc-HSPB8-5	chr12:119827076-119827542	l_741_chr12:119826869-119830126_testes
14	lnc-HSPB8-5	chr12:119826870-119826981	l_741_chr12:119826869-119830126_testes
15	lnc-CIT-1	chr12:119825796-119826072	ENSG00000248636

No data

Variant related genes	Relation type
ENSG00000222647	TF binding region
TMEM233	TF binding region
ENSG00000248636	TF binding region
ENSG00000222647	CpG island
TMEM233	CpG island
ENSG00000248636	CpG island
ENSG00000222647	chromatin interactions
ENSG00000111725	chromatin interactions
ENSG00000152137	chromatin interactions
ENSG00000224982	chromatin interactions
ENSG00000248636	chromatin interactions
EIF2C3	miRNA target sites
ZCCHC11	miRNA target sites
MIDN	miRNA target sites

Extended variants
information (count: 5940 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:5940 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140052728	chr12:119801846-119801847	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs577803357	chr12:119801884-119801885	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs534153231	chr12:119801927-119801928	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs181539569	chr12:119801933-119801934	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs150010300	chr12:119802007-119802008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184165678	chr12:119802021-119802022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188467641	chr12:119802083-119802084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574268704	chr12:119802103-119802104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181021817	chr12:119802104-119802105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185952473	chr12:119802121-119802122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576551778	chr12:119802123-119802124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112958324	chr12:119802143-119802144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12708370	chr12:119802149-119802150	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs565412154	chr12:119802160-119802161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531759306	chr12:119802164-119802165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547294683	chr12:119802218-119802219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541881271	chr12:119802224-119802225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145594229	chr12:119802286-119802287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117681883	chr12:119802319-119802320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79526688	chr12:119802400-119802401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550098968	chr12:119802426-119802427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569542245	chr12:119802432-119802433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538283722	chr12:119802482-119802483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551835316	chr12:119802559-119802560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565461228	chr12:119802564-119802565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192037362	chr12:119802565-119802566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370105271	chr12:119802583-119802584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147688396	chr12:119802585-119802586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574227135	chr12:119802655-119802656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536542119	chr12:119802659-119802660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117930651	chr12:119802815-119802816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111725861	chr12:119802856-119802857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142353140	chr12:119802865-119802866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565347062	chr12:119802869-119802870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572586173	chr12:119802900-119802901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541178396	chr12:119802915-119802916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374226806	chr12:119802916-119802917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76255428	chr12:119803001-119803002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182209527	chr12:119803041-119803042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549794987	chr12:119803071-119803072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369944194	chr12:119803184-119803185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531953208	chr12:119803185-119803186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs151235138	chr12:119803201-119803202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565397113	chr12:119803313-119803314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374333162	chr12:119803314-119803315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534424030	chr12:119803321-119803322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140455731	chr12:119803326-119803327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567748814	chr12:119803332-119803333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145523241	chr12:119803346-119803347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556557542	chr12:119803349-119803350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119801000-119802000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:119801000-119802800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr12:119801000-119803800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr12:119801000-119803800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:119801200-119802400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:119801200-119802400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr12:119801200-119807800	Weak transcription	Fetal Heart	heart
8	chr12:119801400-119802800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr12:119801600-119802000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr12:119801600-119802000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr12:119801600-119802000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr12:119801600-119803000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr12:119801800-119806200	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr12:119801800-119806600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr12:119802000-119802600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr12:119802000-119803400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr12:119802000-119803600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:119802000-119804000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr12:119802400-119802800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:119802400-119803000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:119802600-119802800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr12:119802800-119806400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr12:119802800-119806400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr12:119802800-119806400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr12:119802800-119806600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr12:119803000-119806600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:119803000-119806800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr12:119803400-119803800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr12:119803400-119804600	Enhancers	HepG2	liver
30	chr12:119803600-119804600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:119803800-119804000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr12:119803800-119806400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr12:119804000-119806200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr12:119804000-119806200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr12:119804600-119806200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:119805800-119808000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:119806200-119807400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:119806200-119808200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr12:119806200-119808200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr12:119806200-119808400	Enhancers	Rectal Smooth Muscle	rectum
41	chr12:119806200-119809800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr12:119806400-119806600	Enhancers	Fetal Thymus	thymus
43	chr12:119806400-119807000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr12:119806400-119808400	Enhancers	H9 Cell Line	embryonic stem cell
45	chr12:119806400-119808400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr12:119806400-119808400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr12:119806400-119808600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr12:119806600-119807200	Weak transcription	Fetal Thymus	thymus
49	chr12:119806600-119807400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:119806600-119807400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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