Variant report

Variant	nsv531527
Chromosome Location	chr12:39680812-40182822
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4355)
CpG islands
(count:2075)
Chromatin interactive
region (count:266)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:4355 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:39986074-39986631	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:39836907-39837197	K562	blood:	n/a	n/a
3	ARID3A	chr12:39928847-39929140	K562	blood:	n/a	n/a
4	ARID3A	chr12:39884993-39885007	K562	blood:	n/a	n/a
5	ARID3A	chr12:39941824-39941979	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:39713017-39713303	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:39795806-39796000	K562	blood:	n/a	n/a
8	ARID3A	chr12:39734843-39735216	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:39708632-39708643	K562	blood:	n/a	n/a
10	ARID3A	chr12:39836791-39838267	HepG2	liver:	n/a	n/a
11	ARID3A	chr12:39782854-39783156	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:39726981-39727045	K562	blood:	n/a	n/a
13	ARID3A	chr12:39928840-39929108	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:39820791-39821583	HepG2	liver:	n/a	n/a
15	ARID3A	chr12:40067214-40067268	K562	blood:	n/a	n/a
16	ARID3A	chr12:39835038-39836342	K562	blood:	n/a	chr12:39835387-39835403
17	ARID3A	chr12:39848930-39849020	K562	blood:	n/a	n/a
18	ARID3A	chr12:39835680-39836022	HepG2	liver:	n/a	n/a
19	ARID3A	chr12:39870885-39870932	K562	blood:	n/a	n/a
20	ARID3A	chr12:40019707-40020121	K562	blood:	n/a	n/a
21	ARID3A	chr12:39832346-39832912	K562	blood:	n/a	n/a
22	ARID3A	chr12:39811875-39812336	HepG2	liver:	n/a	n/a
23	ARID3A	chr12:39932499-39932672	K562	blood:	n/a	n/a
24	ATF1	chr12:39681654-39681982	K562	blood:	n/a	n/a
25	ATF1	chr12:39852846-39853261	K562	blood:	n/a	n/a
26	ATF1	chr12:40106808-40106910	K562	blood:	n/a	n/a
27	ATF1	chr12:39870962-39871125	K562	blood:	n/a	n/a
28	ATF1	chr12:39861151-39861342	K562	blood:	n/a	n/a
29	ATF1	chr12:39932360-39932733	K562	blood:	n/a	n/a
30	ATF1	chr12:40017728-40018001	K562	blood:	n/a	n/a
31	ATF1	chr12:40107344-40107573	K562	blood:	n/a	n/a
32	ATF1	chr12:39884692-39884945	K562	blood:	n/a	n/a
33	ATF2	chr12:40011528-40012131	GM12878	blood:	n/a	n/a
34	ATF2	chr12:40017634-40018151	GM12878	blood:	n/a	n/a
35	ATF2	chr12:39836804-39837331	GM12878	blood:	n/a	n/a
36	ATF2	chr12:39796699-39797138	GM12878	blood:	n/a	n/a
37	ATF2	chr12:40017642-40018058	GM12878	blood:	n/a	n/a
38	ATF2	chr12:39799352-39799893	GM12878	blood:	n/a	n/a
39	ATF2	chr12:39734914-39735478	GM12878	blood:	n/a	n/a
40	ATF2	chr12:39861004-39861752	GM12878	blood:	n/a	n/a
41	ATF2	chr12:39805997-39806276	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF2	chr12:39861088-39861613	GM12878	blood:	n/a	n/a
43	ATF2	chr12:40015033-40015558	GM12878	blood:	n/a	n/a
44	ATF2	chr12:40014910-40015547	GM12878	blood:	n/a	n/a
45	ATF2	chr12:39796658-39797164	GM12878	blood:	n/a	n/a
46	ATF2	chr12:40013016-40014468	GM12878	blood:	n/a	n/a
47	ATF2	chr12:40013030-40014309	GM12878	blood:	n/a	n/a
48	ATF3	chr12:39853035-39853260	K562	blood:	n/a	n/a
49	ATF3	chr12:39748780-39749070	K562	blood:	n/a	n/a
50	ATF3	chr12:39932340-39932621	K562	blood:	n/a	n/a

(count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:39836285-39836335	GM12891	blood:	n/a
2	chr12:39836285-39836335	GM12891	blood:	n/a
3	chr12:39836148-39836198	HPAEpiC	pulmonary alveolar:	n/a
4	chr12:39706834-39706884	HIPEpiC	eye:	n/a
5	chr12:40014132-40014182	GM12891	blood:	n/a
6	chr12:39706834-39706884	SKMC	muscle:	n/a
7	chr12:39706834-39706884	HCM	heart:	n/a
8	chr12:39763210-39763260	RPTEC	kidney:	n/a
9	chr12:39932673-39932723	HCPEpiC	choroid plexus:	n/a
10	chr12:40013596-40013646	AoSMC	blood vessel:	n/a
11	chr12:40020000-40020050	HPAEpiC	pulmonary alveolar:	n/a
12	chr12:40019768-40019818	LNCaP	prostate:	n/a
13	chr12:40020000-40020050	HL-60	blood:	n/a
14	chr12:40014061-40014111	GM12891	blood:	n/a
15	chr12:39836148-39836198	T-47D	breast:	n/a
16	chr12:40014132-40014182	SK-N-SH_RA	brain:	n/a
17	chr12:40013961-40014011	MCF-7	breast:	n/a
18	chr12:39837660-39837710	AoSMC	blood vessel:	n/a
19	chr12:39763210-39763260	HAEpiC	amniotic membrane:	n/a
20	chr12:39800627-39800677	Hela-S3	cervix:	n/a
21	chr12:40093094-40093144	SK-N-SH_RA	brain:	n/a
22	chr12:40014132-40014182	NH-A	brain:	n/a
23	chr12:39836347-39836397	HRE	kidney:	n/a
24	chr12:39932673-39932723	HCT-116	colon:	n/a
25	chr12:40019883-40019933	NB4	blood:	n/a
26	chr12:39787968-39788018	SK-N-SH	brain:	n/a
27	chr12:40146787-40146837	K562	blood:	n/a
28	chr12:40014292-40014342	K562	blood:	n/a
29	chr12:39836712-39836762	NHBE	bronchial:	n/a
30	chr12:39687917-39687967	HCM	heart:	n/a
31	chr12:39836712-39836762	AG09309	skin:	n/a
32	chr12:39836347-39836397	HMEC	breast:	n/a
33	chr12:39837362-39837412	AG04449	skin:	fetal
34	chr12:40020000-40020050	SK-N-MC	brain:	n/a
35	chr12:40013680-40013730	Jurkat	blood:	n/a
36	chr12:40019768-40019818	GM12878	blood:	n/a
37	chr12:39932673-39932723	MCF-7	breast:	n/a
38	chr12:39836347-39836397	GM12891	blood:	n/a
39	chr12:39836148-39836198	HepG2	liver:	n/a
40	chr12:39981136-39981186	IMR90	lung:	fetal
41	chr12:39836347-39836397	AG04449	skin:	fetal
42	chr12:40019883-40019933	H1-hESC	embryonic stem cell:	embryo
43	chr12:39981136-39981186	MCF10A-Er-Src	breast:	n/a
44	chr12:39836347-39836397	BJ	skin:	n/a
45	chr12:40013596-40013646	NHBE	bronchial:	n/a
46	chr12:40020000-40020050	SKMC	muscle:	n/a
47	chr12:39837362-39837412	T-47D	breast:	n/a
48	chr12:39763210-39763260	HepG2	liver:	n/a
49	chr12:39726715-39726765	Hela-S3	cervix:	n/a
50	chr12:39981136-39981186	NHDF-neo	bronchial:	n/a

(count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr12:39807954..39810429-chr12:39835327..39837986,3	MCF-7	breast:
2	chr12:39748533..39750921-chr12:39755964..39757616,2	K562	blood:
3	chr12:39768164..39770883-chr12:39771123..39773923,3	K562	blood:
4	chr12:39751967..39753839-chr12:39754682..39757326,2	K562	blood:
5	chr12:39835437..39837020-chr12:39841787..39843770,2	MCF-7	breast:
6	chr12:40015362..40017426-chr12:40020461..40022505,2	MCF-7	breast:
7	chr12:39933714..39935696-chr12:39937326..39938975,2	K562	blood:
8	chr12:39998727..40000314-chr12:40002624..40004346,2	MCF-7	breast:
9	chr12:39836717..39837250-chr15:72766168..72767135,2	Hela-S3	cervix:
10	chr12:39705679..39708570-chr12:39709976..39712207,2	MCF-7	breast:
11	chr12:39887806..39889912-chr12:39892327..39894419,2	K562	blood:
12	chr12:39708256..39710912-chr12:39833762..39835679,2	MCF-7	breast:
13	chr12:39749714..39751981-chr12:39755102..39756669,2	MCF-7	breast:
14	chr12:39707343..39709850-chr12:39833796..39835957,2	K562	blood:
15	chr12:39779513..39783139-chr12:39785165..39787752,3	K562	blood:
16	chr12:39835315..39837704-chr12:39933049..39935834,3	K562	blood:
17	chr12:39813929..39815788-chr12:39828871..39831420,2	K562	blood:
18	chr12:39998727..40000314-chr12:40002624..40004346,2	MCF-7	breast:
19	chr12:39701621..39703209-chr12:39709361..39712125,2	K562	blood:
20	chr12:39838865..39841148-chr12:39868533..39871402,3	K562	blood:
21	chr12:40158494..40159394-chr12:40706485..40707345,2	MCF-7	breast:
22	chr12:40161730..40164453-chr12:40368546..40370092,2	K562	blood:
23	chr12:39766807..39768997-chr12:39769052..39771333,2	MCF-7	breast:
24	chr12:39755090..39757754-chr12:39764621..39766612,2	MCF-7	breast:
25	chr12:40154023..40155558-chr12:40243257..40245766,2	MCF-7	breast:
26	chr12:40150704..40153291-chr12:40154955..40157099,2	K562	blood:
27	chr12:39989700..39991592-chr12:39994179..39996342,2	K562	blood:
28	chr12:39821875..39824994-chr12:39835535..39837994,3	MCF-7	breast:
29	chr12:39759047..39762172-chr12:39834495..39838400,6	MCF-7	breast:
30	chr12:40014171..40017168-chr12:40017549..40021409,3	K562	blood:
31	chr12:39771043..39772683-chr12:39784560..39786078,2	MCF-7	breast:
32	chr12:39742374..39745219-chr12:39747056..39748871,3	K562	blood:
33	chr12:39751967..39753839-chr12:39754682..39757326,2	K562	blood:
34	chr12:40165086..40168049-chr12:40212824..40214791,2	MCF-7	breast:
35	chr12:39815681..39818065-chr12:39831801..39835369,3	K562	blood:
36	chr12:39747712..39750921-chr12:39754829..39757616,3	K562	blood:
37	chr12:39790931..39794937-chr12:39833585..39836831,4	K562	blood:
38	chr12:39835345..39837836-chr12:39849615..39851379,2	MCF-7	breast:
39	chr12:39803978..39806554-chr12:39812297..39814697,2	MCF-7	breast:
40	chr12:39788415..39791571-chr12:39793998..39797026,3	K562	blood:
41	chr12:39796736..39799159-chr12:39806907..39808655,2	K562	blood:
42	chr12:39803978..39806554-chr12:39812297..39814697,2	MCF-7	breast:
43	chr12:39694207..39696152-chr12:39837237..39840087,2	K562	blood:
44	chr12:40158540..40159495-chr12:40351942..40352752,5	MCF-7	breast:
45	chr12:40010562..40012556-chr12:40014262..40016328,2	K562	blood:
46	chr12:39793372..39796238-chr12:39806830..39809770,2	K562	blood:
47	chr12:40158493..40159396-chr12:40384037..40384925,5	MCF-7	breast:
48	chr12:39804413..39806857-chr12:39807005..39809707,2	K562	blood:
49	chr12:39735428..39738305-chr12:39770401..39772553,2	K562	blood:
50	chr12:39975317..39977272-chr12:39980536..39983177,3	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRK2-2	chr12:40035446-40035663	uc_337_+
2	lnc-C12orf40-1	chr12:39942705-39943943	NONHSAT027707
3	lnc-ABCD2-5	chr12:39750402-39750697	NONHSAT027704
4	lnc-C12orf40-3	chr12:39721452-39721634	NONHSAT027702
5	lnc-C12orf40-3	chr12:39720075-39720147	NONHSAT027700
6	lnc-C12orf40-3	chr12:39721472-39721634	NONHSAT027700
7	lnc-C12orf40-3	chr12:39721472-39721634	NONHSAT027701
8	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027702
9	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027701
10	lnc-ABCD2-4	chr12:40148896-40150095	NONHSAT027710
11	lnc-C12orf40-1	chr12:39940682-39942476	NONHSAT027707
12	lnc-ABCD2-3	chr12:40035446-40035663	uc_337_-
13	lnc-ABCD2-5	chr12:39751050-39751089	NONHSAT027704
14	lnc-ABCD2-2	chr12:39933383-39933653	NONHSAT027706
15	lnc-C12orf40-3	chr12:39720338-39720424	NONHSAT027701
16	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027700

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	KIF21A	hsa-miR-186-5p	chr12:39687380-39687401
2	KIF21A	hsa-miR-186-5p	chr12:39688170-39688191
3	C12orf40	hsa-miR-1	chr12:40076763-40076785

Variant related genes	Relation type
KIF21A	TF binding region
C12orf40	TF binding region
ENSG00000270273	TF binding region
ENSG00000255991	TF binding region
ABCD2	TF binding region
ENSG00000252974	TF binding region
KIF21A	CpG island
C12orf40	CpG island
ENSG00000270273	CpG island
ENSG00000255991	CpG island
ABCD2	CpG island
ENSG00000252974	CpG island
ENSG00000151229	chromatin interactions
ENSG00000042429	chromatin interactions
ENSG00000180116	chromatin interactions
ENSG00000168522	chromatin interactions
ENSG00000188906	chromatin interactions
ENSG00000139116	chromatin interactions
ENSG00000199571	chromatin interactions
ENSG00000142676	chromatin interactions
ENSG00000198001	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000270273	chromatin interactions
ENSG00000172115	chromatin interactions
ENSG00000261423	chromatin interactions
ENSG00000252974	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000129317	chromatin interactions
ENSG00000116830	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000099875	chromatin interactions
ENSG00000173208	chromatin interactions
ENSG00000166012	chromatin interactions

Extended variants
information (count: 15626 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:15626 , 50 per page) page: 1 2 3 4 5 6 7 ... 313

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535908816	chr12:39680843-39680844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560820114	chr12:39680853-39680854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531294598	chr12:39680880-39680881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1512943	chr12:39680881-39680882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs572555306	chr12:39680895-39680896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146512267	chr12:39680956-39680957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182717534	chr12:39680965-39680966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576787951	chr12:39680975-39680976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544161702	chr12:39680981-39680982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11171662	chr12:39680995-39680996	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs187940910	chr12:39681013-39681014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541861576	chr12:39681031-39681032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559998689	chr12:39681041-39681042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527424877	chr12:39681066-39681067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532831458	chr12:39681070-39681071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74088333	chr12:39681096-39681097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs141037605	chr12:39681181-39681182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531489443	chr12:39681267-39681268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191323087	chr12:39681287-39681288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184193756	chr12:39681475-39681476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566268684	chr12:39681520-39681521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535485698	chr12:39681524-39681525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555232783	chr12:39681530-39681531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547829949	chr12:39681538-39681539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144769499	chr12:39681605-39681606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138640470	chr12:39681630-39681631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368865263	chr12:39681650-39681651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558367910	chr12:39681678-39681679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187118699	chr12:39681716-39681717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536894615	chr12:39681743-39681744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537709497	chr12:39681792-39681793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556096379	chr12:39681811-39681812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555001173	chr12:39681829-39681830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192331615	chr12:39681832-39681833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113277078	chr12:39681833-39681834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572027940	chr12:39681934-39681935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372343125	chr12:39681955-39681956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184437518	chr12:39681966-39681967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563905647	chr12:39681997-39681998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146528711	chr12:39682019-39682020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531424730	chr12:39682033-39682034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543267193	chr12:39682044-39682045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561846337	chr12:39682108-39682109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371367569	chr12:39682142-39682143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs137922496	chr12:39682196-39682197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10670433	chr12:39682246-39682247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376834651	chr12:39682247-39682248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72516159	chr12:39682248-39682249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397816885	chr12:39682249-39682250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547452949	chr12:39682260-39682261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:4028 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39674800-39690200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:39681200-39682000	Enhancers	Hela-S3	cervix
3	chr12:39681400-39681600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:39681400-39682200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr12:39681600-39687600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:39682000-39699200	Weak transcription	Hela-S3	cervix
7	chr12:39682400-39688800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr12:39683200-39696000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr12:39683400-39685600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr12:39683400-39686000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:39684400-39695400	Weak transcription	A549	lung
12	chr12:39684600-39688000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:39684600-39688200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:39685200-39697400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr12:39685200-39714400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr12:39685600-39688800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:39686000-39688200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:39686200-39686600	Enhancers	Brain Germinal Matrix	brain
19	chr12:39686400-39686600	Enhancers	Fetal Brain Male	brain
20	chr12:39686400-39699600	Weak transcription	HMEC	breast
21	chr12:39686600-39686800	Enhancers	Pancreas	Pancrea
22	chr12:39686600-39688000	Weak transcription	Brain Germinal Matrix	brain
23	chr12:39686600-39688400	Weak transcription	Fetal Brain Male	brain
24	chr12:39686600-39722400	Weak transcription	GM12878-XiMat	blood
25	chr12:39686600-39725400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr12:39686800-39729800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr12:39686800-39738800	Weak transcription	Pancreas	Pancrea
28	chr12:39687200-39696800	Weak transcription	Stomach Smooth Muscle	stomach
29	chr12:39687200-39726400	Weak transcription	Fetal Intestine Small	intestine
30	chr12:39687600-39688800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:39687600-39723800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr12:39687800-39688200	Enhancers	Brain Anterior Caudate	brain
33	chr12:39688000-39688400	Enhancers	Brain Germinal Matrix	brain
34	chr12:39688000-39688800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr12:39688000-39689600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:39688000-39690400	Weak transcription	Liver	Liver
37	chr12:39688200-39688600	Weak transcription	Brain Anterior Caudate	brain
38	chr12:39688200-39689000	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr12:39688200-39689200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:39688400-39688600	Enhancers	Fetal Brain Male	brain
41	chr12:39688400-39688800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr12:39688400-39688800	Enhancers	Brain Substantia Nigra	brain
43	chr12:39688400-39689000	Enhancers	Brain Angular Gyrus	brain
44	chr12:39688400-39689400	Enhancers	Brain Cingulate Gyrus	brain
45	chr12:39688400-39689400	Enhancers	Brain Hippocampus Middle	brain
46	chr12:39688400-39689400	Enhancers	Fetal Brain Female	brain
47	chr12:39688400-39694000	Weak transcription	Brain Germinal Matrix	brain
48	chr12:39688400-39709800	Weak transcription	Ovary	ovary
49	chr12:39688400-39724600	Weak transcription	Esophagus	oesophagus
50	chr12:39688400-39726400	Weak transcription	Aorta	Aorta

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