Variant report

Variant	esv2422416
Chromosome Location	chr12:124009676-124085689
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2323)
CpG islands
(count:1343)
Chromatin interactive
region (count:149)
LncRNA
region (count:10)
Mature miRNA
region (count: 1)
miRNA target
sites (count:2)

(count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124055889-124056158	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:124017367-124017624	K562	blood:	n/a	n/a
3	ARID3A	chr12:124066707-124067005	K562	blood:	n/a	n/a
4	ARID3A	chr12:124066719-124067024	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:124055016-124055130	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:124018494-124018555	K562	blood:	n/a	n/a
7	ARID3A	chr12:124068840-124069198	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:124080339-124081019	HepG2	liver:	n/a	n/a
9	ATF1	chr12:124068826-124069223	K562	blood:	n/a	n/a
10	ATF2	chr12:124068634-124069051	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr12:124068668-124069206	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr12:124068622-124069127	GM12878	blood:	n/a	n/a
13	ATF2	chr12:124068644-124069075	GM12878	blood:	n/a	n/a
14	ATF3	chr12:124055844-124056086	K562	blood:	n/a	n/a
15	ATF3	chr12:124066738-124067088	K562	blood:	n/a	n/a
16	ATF3	chr12:124055837-124056188	HepG2	liver:	n/a	n/a
17	ATF3	chr12:124068610-124069255	A549	lung:	n/a	n/a
18	ATF3	chr12:124055748-124056205	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr12:124068575-124069116	A549	lung:	n/a	n/a
20	ATF3	chr12:124055844-124056095	HepG2	liver:	n/a	n/a
21	BACH1	chr12:124081790-124081812	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr12:124068749-124069490	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr12:124069419-124069441	K562	blood:	n/a	n/a
24	BACH1	chr12:124018798-124018914	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr12:124019171-124019340	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr12:124066841-124067190	K562	blood:	n/a	n/a
27	BCL11A	chr12:124016656-124016943	GM12878	blood:	n/a	chr12:124016835-124016844
28	BCL3	chr12:124017686-124018120	A549	lung:	n/a	chr12:124018049-124018058 chr12:124017704-124017717
29	BCL3	chr12:124015207-124015490	GM12878	blood:	n/a	n/a
30	BCL3	chr12:124068512-124069173	A549	lung:	n/a	chr12:124069073-124069082
31	BCL3	chr12:124068562-124069521	A549	lung:	n/a	chr12:124069073-124069082
32	BCLAF1	chr12:124068545-124069449	GM12878	blood:	n/a	chr12:124069073-124069082
33	BCLAF1	chr12:124068709-124069153	K562	blood:	n/a	chr12:124069073-124069082
34	BCLAF1	chr12:124016596-124017027	GM12878	blood:	n/a	chr12:124016835-124016844
35	BCLAF1	chr12:124068617-124069381	GM12878	blood:	n/a	chr12:124069073-124069082
36	BHLHE40	chr12:124066728-124067308	K562	blood:	n/a	n/a
37	BHLHE40	chr12:124068738-124069187	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:124017508-124017986	HepG2	liver:	n/a	chr12:124017636-124017652
39	BHLHE40	chr12:124017548-124018031	GM12878	blood:	n/a	chr12:124017636-124017652
40	BHLHE40	chr12:124054989-124054991	K562	blood:	n/a	n/a
41	BHLHE40	chr12:124016448-124016532	K562	blood:	n/a	n/a
42	BHLHE40	chr12:124018423-124019050	HepG2	liver:	n/a	n/a
43	BHLHE40	chr12:124068701-124069166	HepG2	liver:	n/a	n/a
44	BHLHE40	chr12:124017420-124018105	K562	blood:	n/a	chr12:124017636-124017652
45	BHLHE40	chr12:124018484-124018487	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:124068739-124069124	K562	blood:	n/a	n/a
47	BHLHE40	chr12:124030246-124030390	K562	blood:	n/a	n/a
48	BRCA1	chr12:124069298-124069309	HepG2	liver:	n/a	n/a
49	BRCA1	chr12:124017418-124017970	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr12:124017817-124017913	HepG2	liver:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124017975-124018025	BE2_C	brain:	n/a
2	chr12:124017975-124018025	BE2_C	brain:	n/a
3	chr12:124068794-124068844	CMK	blood:	n/a
4	chr12:124068984-124069034	HMEC	breast:	n/a
5	chr12:124068991-124069041	PrEC	prostate:	n/a
6	chr12:124019284-124019334	Jurkat	blood:	n/a
7	chr12:124018993-124019043	AoSMC	blood vessel:	n/a
8	chr12:124017975-124018025	HRCEpiC	kidney:	n/a
9	chr12:124069649-124069699	NHDF-neo	bronchial:	n/a
10	chr12:124068866-124068916	PANC-1	pancreas:	n/a
11	chr12:124069168-124069218	SK-N-SH_RA	brain:	n/a
12	chr12:124021914-124021964	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:124068794-124068844	U87	brain:	n/a
14	chr12:124017613-124017663	GM12878	blood:	n/a
15	chr12:124014409-124014459	H1-hESC	embryonic stem cell:	embryo
16	chr12:124043090-124043140	HEEpiC	esophagus:	n/a
17	chr12:124043090-124043140	GM19239	blood:	n/a
18	chr12:124066860-124066910	RPTEC	kidney:	n/a
19	chr12:124068984-124069034	HUVEC	blood vessel:	n/a
20	chr12:124018993-124019043	HIPEpiC	eye:	n/a
21	chr12:124082333-124082383	Hepatocyte	liver:	n/a
22	chr12:124068984-124069034	PrEC	prostate:	n/a
23	chr12:124018492-124018542	NT2-D1	testis:	n/a
24	chr12:124069758-124069808	GM12892	blood:	n/a
25	chr12:124082333-124082383	HEEpiC	esophagus:	n/a
26	chr12:124068991-124069041	NT2-D1	testis:	n/a
27	chr12:124069758-124069808	HIPEpiC	eye:	n/a
28	chr12:124021914-124021964	H1-hESC	embryonic stem cell:	embryo
29	chr12:124069168-124069218	T-47D	breast:	n/a
30	chr12:124017613-124017663	AG10803	skin:	n/a
31	chr12:124014409-124014459	HRCEpiC	kidney:	n/a
32	chr12:124043090-124043140	HCM	heart:	n/a
33	chr12:124066860-124066910	BJ	skin:	n/a
34	chr12:124069324-124069374	SK-N-MC	brain:	n/a
35	chr12:124069475-124069525	GM12891	blood:	n/a
36	chr12:124043090-124043140	AG09319	gingival:	n/a
37	chr12:124069758-124069808	SKMC	muscle:	n/a
38	chr12:124021914-124021964	AG10803	skin:	n/a
39	chr12:124018492-124018542	GM19239	blood:	n/a
40	chr12:124069168-124069218	HCM	heart:	n/a
41	chr12:124069324-124069374	HRE	kidney:	n/a
42	chr12:124068903-124068953	GM12891	blood:	n/a
43	chr12:124068794-124068844	PANC-1	pancreas:	n/a
44	chr12:124069324-124069374	T-47D	breast:	n/a
45	chr12:124018993-124019043	MCF10A-Er-Src	breast:	n/a
46	chr12:124068984-124069034	HRE	kidney:	n/a
47	chr12:124069649-124069699	U87	brain:	n/a
48	chr12:124068794-124068844	K562	blood:	n/a
49	chr12:124014409-124014459	SKMC	muscle:	n/a
50	chr12:124082333-124082383	AG09319	gingival:	n/a

(count:149 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:123866701..123869300-chr12:124085669..124087764,2	K562	blood:
2	chr12:123867374..123868909-chr12:124067489..124069464,2	K562	blood:
3	chr12:124008463..124013124-chr12:124014349..124019990,8	MCF-7	breast:
4	chr12:124067363..124072745-chr12:124084857..124088217,7	K562	blood:
5	chr12:124072536..124074198-chr12:124117676..124120099,2	K562	blood:
6	chr12:124002890..124005569-chr12:124009063..124010830,3	MCF-7	breast:
7	chr12:124075051..124078239-chr12:124079848..124084285,5	K562	blood:
8	chr12:123752131..123754716-chr12:124081309..124084264,2	MCF-7	breast:
9	chr12:124018351..124020362-chr12:124063140..124065356,2	MCF-7	breast:
10	chr12:124057277..124059073-chr12:124064975..124067218,3	MCF-7	breast:
11	chr12:124015709..124018064-chr12:124066858..124069100,3	MCF-7	breast:
12	chr12:124008800..124013373-chr12:124015066..124019267,4	K562	blood:
13	chr12:123755058..123757440-chr12:124084744..124087456,3	K562	blood:
14	chr12:124068417..124069053-chr7:100026334..100026841,2	Hela-S3	cervix:
15	chr12:124017908..124019727-chr12:124073877..124075658,2	MCF-7	breast:
16	chr12:124047707..124050611-chr12:124054919..124057365,3	MCF-7	breast:
17	chr12:124041024..124043349-chr12:124054707..124057427,2	MCF-7	breast:
18	chr12:123873494..123875550-chr12:124015653..124017169,2	MCF-7	breast:
19	chr12:124066647..124068350-chr12:124118155..124119898,2	K562	blood:
20	chr12:123755495..123756252-chr12:124066408..124067146,2	K562	blood:
21	chr12:123749254..123749803-chr12:124066367..124067369,3	MCF-7	breast:
22	chr12:123941098..123944051-chr12:124068238..124070527,2	K562	blood:
23	chr12:123873330..123875210-chr12:124033719..124035422,2	MCF-7	breast:
24	chr12:124007811..124010230-chr12:124011879..124014265,2	MCF-7	breast:
25	chr12:123847169..123849970-chr12:124085128..124088523,3	K562	blood:
26	chr12:124061690..124064565-chr12:124067348..124070635,4	MCF-7	breast:
27	chr12:124018963..124020649-chr12:124025084..124027162,2	MCF-7	breast:
28	chr12:124068482..124069384-chr17:48045883..48046404,2	Hela-S3	cervix:
29	chr1:150334954..150337894-chr12:124054865..124057568,2	MCF-7	breast:
30	chr12:124080644..124082674-chr12:124097166..124099326,2	K562	blood:
31	chr12:123997284..124000079-chr12:124017073..124019484,2	MCF-7	breast:
32	chr12:124018963..124020649-chr12:124025084..124027162,2	MCF-7	breast:
33	chr12:123848402..123850885-chr12:124079862..124083002,3	MCF-7	breast:
34	chr12:124007811..124010230-chr12:124011879..124014265,2	MCF-7	breast:
35	chr12:123870366..123875219-chr12:124064500..124069174,6	K562	blood:
36	chr12:124017444..124019100-chr12:124084646..124086674,2	MCF-7	breast:
37	chr12:124072094..124074168-chrX:128628423..128631086,2	MCF-7	breast:
38	chr12:123920837..123922890-chr12:124067881..124069805,2	K562	blood:
39	chr12:123847713..123850022-chr12:124067528..124071055,3	MCF-7	breast:
40	chr12:124024608..124026417-chr12:124031309..124033048,2	K562	blood:
41	chr12:124056030..124058750-chr12:124059393..124062222,4	K562	blood:
42	chr12:124003058..124006753-chr12:124009013..124012498,5	MCF-7	breast:
43	chr12:124061381..124063530-chr12:124065781..124068384,3	K562	blood:
44	chr12:124018609..124020737-chr12:124028286..124031087,2	MCF-7	breast:
45	chr12:123867386..123869300-chr12:124085669..124087822,2	K562	blood:
46	chr1:12652111..12654554-chr12:124037309..124039260,2	MCF-7	breast:
47	chr12:124018224..124020563-chr12:124065688..124070487,5	K562	blood:
48	chr12:124067363..124072745-chr12:124084857..124088217,7	K562	blood:
49	chr12:124065661..124069328-chr12:124081746..124084446,4	K562	blood:
50	chr12:124084893..124086565-chr12:124117453..124119818,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2B1-2	chr12:124062808-124062838	XLOC_010228
2	lnc-EIF2B1-1	chr12:124065632-124067714	NR_110049
3	lnc-EIF2B1-1	chr12:124068148-124068245	NR_110049
4	lnc-DDX55-1	chr12:124080952-124081554	expReg_chr12_11962_+
5	lnc-EIF2B1-1	chr12:124068759-124068874	NR_110049
6	lnc-EIF2B1-1	chr12:124068148-124068245	XLOC_010229
7	lnc-EIF2B1-1	chr12:124065613-124067714	XLOC_010229
8	lnc-EIF2B1-1	chr12:124066709-124068936	NONHSAT031599
9	lnc-EIF2B1-1	chr12:124068759-124068874	XLOC_010229
10	lnc-EIF2B1-2	chr12:124060445-124060779	XLOC_010228

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3908	chr12:124020960-124020981	MIMAT0018182

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TMED2	hsa-miR-7-5p	chr12:124081277-124081289
2	TMED2	hsa-miR-30a-5p	chr12:124081299-124081320

Variant related genes	Relation type
TMED2	TF binding region
MIR3908	TF binding region
RILPL1	TF binding region
ENSG00000247373	TF binding region
DDX55	TF binding region
TMED2	CpG island
MIR3908	CpG island
RILPL1	CpG island
ENSG00000247373	CpG island
DDX55	CpG island
ENSG00000051825	chromatin interactions
ENSG00000086598	chromatin interactions
ENSG00000267100	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000163125	chromatin interactions
ENSG00000206897	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000108813	chromatin interactions
ENSG00000111358	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000247373	chromatin interactions
ENSG00000108264	chromatin interactions
ENSG00000270113	chromatin interactions
ENSG00000039650	chromatin interactions
ENSG00000266655	chromatin interactions
ENSG00000188026	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000184209	chromatin interactions
ENSG00000256092	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000111361	chromatin interactions
ENSG00000139697	chromatin interactions
ENSG00000183955	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000150977	chromatin interactions
CD44	miRNA target sites
CD2AP	miRNA target sites

Extended variants
information (count: 2636 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2636 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550994698	chr12:124009676-124009677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs527640559	chr12:124009724-124009725	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150113590	chr12:124009729-124009730	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548666677	chr12:124009743-124009744	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs567368562	chr12:124009751-124009752	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs534792589	chr12:124009791-124009792	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs546609921	chr12:124009856-124009857	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs57883611	chr12:124009877-124009878	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs28833471	chr12:124009898-124009899	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs36117410	chr12:124009930-124009931	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs57022059	chr12:124009936-124009937	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs71088926	chr12:124009947-124009948	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs56688198	chr12:124009959-124009960	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs191192940	chr12:124010012-124010013	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs28775913	chr12:124010035-124010036	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533643695	chr12:124010038-124010039	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374115573	chr12:124010044-124010045	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549451761	chr12:124010045-124010046	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535964998	chr12:124010046-124010047	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs182242128	chr12:124010060-124010061	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs28491342	chr12:124010067-124010068	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573392184	chr12:124010072-124010073	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs367658444	chr12:124010105-124010106	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs28707421	chr12:124010185-124010186	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570115202	chr12:124010203-124010204	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs71088927	chr12:124010264-124010265	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374502947	chr12:124010265-124010266	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146247835	chr12:124010401-124010402	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs138103615	chr12:124010419-124010420	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562888378	chr12:124010444-124010445	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530086726	chr12:124010463-124010464	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs540250003	chr12:124010468-124010469	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545577980	chr12:124010476-124010477	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200832220	chr12:124010494-124010495	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs565432350	chr12:124010516-124010517	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs114643167	chr12:124010539-124010540	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs142645367	chr12:124010556-124010557	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201923718	chr12:124010563-124010564	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs376643338	chr12:124010567-124010568	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7298959	chr12:124010578-124010579	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546770810	chr12:124010579-124010580	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369811053	chr12:124010608-124010609	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186907258	chr12:124010630-124010631	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192759951	chr12:124010642-124010643	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs184612294	chr12:124010704-124010705	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201003186	chr12:124010862-124010863	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs201638675	chr12:124010864-124010865	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369055855	chr12:124010865-124010866	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192815952	chr12:124010898-124010899	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs59649594	chr12:124011045-124011046	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
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
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2489 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123944600-124012200	Strong transcription	Fetal Stomach	stomach
2	chr12:123970000-124016400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr12:123992600-124012800	Weak transcription	Thymus	Thymus
4	chr12:123993600-124011200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:123994400-124016200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr12:123994600-124016200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr12:123995200-124016400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr12:123999200-124015800	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr12:123999400-124016400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr12:124000200-124012400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr12:124000600-124009800	Strong transcription	Cortex derived primary cultured neurospheres	brain
12	chr12:124000600-124011400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr12:124000600-124015000	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr12:124001000-124016400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr12:124001200-124017400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr12:124001400-124017400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr12:124002000-124016800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr12:124003000-124015400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr12:124004600-124011200	Weak transcription	Psoas Muscle	Psoas
20	chr12:124004600-124016800	Weak transcription	Stomach Mucosa	stomach
21	chr12:124004800-124014600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr12:124004800-124016600	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr12:124005600-124015200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr12:124005600-124016000	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr12:124005600-124016400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr12:124005600-124016400	Weak transcription	Duodenum Mucosa	Duodenum
27	chr12:124005800-124012200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr12:124005800-124015800	Weak transcription	NHDF-Ad	bronchial
29	chr12:124005800-124016400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr12:124005800-124016600	Weak transcription	Fetal Kidney	kidney
31	chr12:124006000-124015000	Strong transcription	Fetal Muscle Leg	muscle
32	chr12:124006000-124015400	Weak transcription	Fetal Brain Male	brain
33	chr12:124006200-124017600	Weak transcription	Small Intestine	intestine
34	chr12:124006800-124016800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr12:124007200-124016600	Weak transcription	Primary T cells from cord blood	blood
36	chr12:124007800-124015200	Weak transcription	HUVEC	blood vessel
37	chr12:124007800-124016400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr12:124007800-124016600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr12:124007800-124017000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr12:124007800-124017400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:124008000-124014400	Weak transcription	HSMM	muscle
42	chr12:124008000-124015400	Weak transcription	Rectal Smooth Muscle	rectum
43	chr12:124008000-124016000	Weak transcription	Hela-S3	cervix
44	chr12:124008000-124016400	Weak transcription	Dnd41	blood
45	chr12:124008000-124017000	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr12:124008000-124017400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr12:124008200-124014200	Weak transcription	NHLF	lung
48	chr12:124008200-124015200	Weak transcription	Pancreas	Pancrea
49	chr12:124008200-124016600	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr12:124008200-124017200	Weak transcription	H9 Cell Line	embryonic stem cell

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