Variant report

Variant	nsv976760
Chromosome Location	chr12:120577931-120587880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:147 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:120580420-120580570	HCPEpiC	choroid plexus:	n/a	n/a
2	CTCF	chr12:120580380-120580530	GM12871	blood:	n/a	n/a
3	CTCF	chr12:120578535-120578558	H1-hESC	embryonic stem cell:	n/a	n/a
4	NR3C1	chr12:120579978-120580505	A549	lung:	n/a	chr12:120580181-120580202 chr12:120580184-120580200 chr12:120580184-120580200 chr12:120580179-120580205 chr12:120580182-120580203 chr12:120580184-120580200 chr12:120580179-120580205 chr12:120580184-120580199 chr12:120580185-120580199 chr12:120580184-120580200 chr12:120580179-120580205 chr12:120580185-120580199 chr12:120580183-120580201 chr12:120580179-120580205 chr12:120580179-120580205
5	NR3C1	chr12:120580132-120580398	A549	lung:	n/a	chr12:120580181-120580202 chr12:120580184-120580200 chr12:120580184-120580200 chr12:120580179-120580205 chr12:120580182-120580203 chr12:120580184-120580200 chr12:120580179-120580205 chr12:120580184-120580199 chr12:120580185-120580199 chr12:120580184-120580200 chr12:120580179-120580205 chr12:120580185-120580199 chr12:120580183-120580201 chr12:120580179-120580205 chr12:120580179-120580205
6	NR3C1	chr12:120580046-120580458	A549	lung:	n/a	chr12:120580181-120580202 chr12:120580184-120580200 chr12:120580184-120580200 chr12:120580179-120580205 chr12:120580182-120580203 chr12:120580184-120580200 chr12:120580179-120580205 chr12:120580184-120580199 chr12:120580185-120580199 chr12:120580184-120580200 chr12:120580179-120580205 chr12:120580185-120580199 chr12:120580183-120580201 chr12:120580179-120580205 chr12:120580179-120580205
7	POLR2A	chr12:120587532-120587620	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr12:120583131-120583464	PFSK-1	brain:	n/a	n/a
9	POLR2A	chr12:120578325-120578326	K562	blood:	n/a	n/a
10	POLR2A	chr12:120578056-120578320	GM12891	blood:	n/a	n/a
11	POLR2A	chr12:120578424-120578766	GM12878	blood:	n/a	n/a
12	POLR2A	chr12:120578568-120579743	K562	blood:	n/a	n/a
13	POLR2A	chr12:120585996-120586193	ECC-1	luminal epithelium:	n/a	n/a
14	POLR2A	chr12:120578374-120578384	K562	blood:	n/a	n/a
15	POLR2A	chr12:120586341-120586597	K562	blood:	n/a	n/a
16	POLR2A	chr12:120578159-120578631	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr12:120582993-120583349	GM12892	blood:	n/a	n/a
18	POLR2A	chr12:120579184-120579603	K562	blood:	n/a	n/a
19	POLR2A	chr12:120580218-120580592	K562	blood:	n/a	n/a
20	POLR2A	chr12:120579225-120579455	GM12878	blood:	n/a	n/a
21	POLR2A	chr12:120579237-120579558	HepG2	liver:	n/a	n/a
22	POLR2A	chr12:120585720-120586381	K562	blood:	n/a	n/a
23	POLR2A	chr12:120577897-120578975	K562	blood:	n/a	n/a
24	POLR2A	chr12:120584658-120585383	K562	blood:	n/a	n/a
25	POLR2A	chr12:120584401-120584422	K562	blood:	n/a	n/a
26	POLR2A	chr12:120579484-120579490	A549	lung:	n/a	n/a
27	POLR2A	chr12:120585460-120585481	HepG2	liver:	n/a	n/a
28	POLR2A	chr12:120579233-120579698	GM12891	blood:	n/a	n/a
29	POLR2A	chr12:120583015-120583495	GM12892	blood:	n/a	n/a
30	POLR2A	chr12:120582426-120583395	K562	blood:	n/a	n/a
31	POLR2A	chr12:120584455-120584507	K562	blood:	n/a	n/a
32	POLR2A	chr12:120579289-120579425	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr12:120581041-120581440	HepG2	liver:	n/a	n/a
34	POLR2A	chr12:120584644-120584769	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr12:120584894-120585189	HepG2	liver:	n/a	n/a
36	POLR2A	chr12:120586278-120586693	K562	blood:	n/a	n/a
37	POLR2A	chr12:120582938-120583176	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr12:120587378-120587572	HepG2	liver:	n/a	n/a
39	POLR2A	chr12:120583019-120583396	GM12878	blood:	n/a	n/a
40	POLR2A	chr12:120582655-120583327	GM12892	blood:	n/a	n/a
41	POLR2A	chr12:120582333-120582522	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr12:120582769-120582823	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr12:120586137-120586155	K562	blood:	n/a	n/a
44	POLR2A	chr12:120582373-120583350	HepG2	liver:	n/a	n/a
45	POLR2A	chr12:120578318-120578905	HepG2	liver:	n/a	n/a
46	POLR2A	chr12:120578158-120578166	K562	blood:	n/a	n/a
47	POLR2A	chr12:120578193-120578317	K562	blood:	n/a	n/a
48	POLR2A	chr12:120579536-120579591	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr12:120582629-120583380	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr12:120587385-120587637	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:120578192-120578242	HCF	heart:	n/a
2	chr12:120578192-120578242	SKMC	muscle:	n/a
3	chr12:120578192-120578242	GM12878	blood:	n/a
4	chr12:120578192-120578242	MCF-7	breast:	n/a
5	chr12:120578192-120578242	HEK293	kidney:	embryo
6	chr12:120578192-120578242	NH-A	brain:	n/a
7	chr12:120578192-120578242	HRE	kidney:	n/a
8	chr12:120578192-120578242	HMEC	breast:	n/a
9	chr12:120578192-120578242	LNCaP	prostate:	n/a
10	chr12:120578192-120578242	ProgFib	skin:	n/a
11	chr12:120578192-120578242	BE2_C	brain:	n/a
12	chr12:120578192-120578242	Hepatocyte	liver:	n/a
13	chr12:120578192-120578242	HCT-116	colon:	n/a
14	chr12:120578192-120578242	Hela-S3	cervix:	n/a
15	chr12:120578192-120578242	HIPEpiC	eye:	n/a
16	chr12:120578192-120578242	NT2-D1	testis:	n/a
17	chr12:120578192-120578242	HAEpiC	amniotic membrane:	n/a
18	chr12:120578192-120578242	SK-N-SH	brain:	n/a
19	chr12:120578192-120578242	GM12892	blood:	n/a
20	chr12:120578192-120578242	H1-hESC	embryonic stem cell:	embryo
21	chr12:120578192-120578242	PrEC	prostate:	n/a
22	chr12:120578192-120578242	K562	blood:	n/a
23	chr12:120578192-120578242	GM19239	blood:	n/a
24	chr12:120578192-120578242	AG09309	skin:	n/a
25	chr12:120578192-120578242	NHDF-neo	bronchial:	n/a
26	chr12:120578192-120578242	PANC-1	pancreas:	n/a
27	chr12:120578192-120578242	HCM	heart:	n/a
28	chr12:120578192-120578242	NHBE	bronchial:	n/a
29	chr12:120578192-120578242	A549	lung:	n/a
30	chr12:120578192-120578242	HRCEpiC	kidney:	n/a
31	chr12:120578192-120578242	HUVEC	blood vessel:	n/a
32	chr12:120578192-120578242	HepG2	liver:	n/a
33	chr12:120578192-120578242	Jurkat	blood:	n/a
34	chr12:120578192-120578242	HPAEpiC	pulmonary alveolar:	n/a
35	chr12:120578192-120578242	AG04450	lung:	fetal
36	chr12:120578192-120578242	U87	brain:	n/a
37	chr12:120578192-120578242	PFSK-1	brain:	n/a
38	chr12:120578192-120578242	GM06990	blood:	n/a
39	chr12:120578192-120578242	SAEC	small airway:	n/a
40	chr12:120578192-120578242	IMR90	lung:	fetal
41	chr12:120578192-120578242	T-47D	breast:	n/a
42	chr12:120578192-120578242	Caco-2	colon:	n/a
43	chr12:120578192-120578242	HNPCEpiC	eye:	n/a
44	chr12:120578192-120578242	AG09319	gingival:	n/a
45	chr12:120578192-120578242	MCF10A-Er-Src	breast:	n/a
46	chr12:120578192-120578242	AoSMC	blood vessel:	n/a
47	chr12:120578192-120578242	BJ	skin:	n/a
48	chr12:120578192-120578242	ECC-1	luminal epithelium:	n/a
49	chr12:120578192-120578242	AG10803	skin:	n/a
50	chr12:120578192-120578242	AG04449	skin:	fetal

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:120580347..120581938-chr12:120583213..120585871,2	MCF-7	breast:
2	chr12:120576167..120578821-chr12:120637302..120640400,3	K562	blood:
3	chr12:120584903..120587679-chr12:120593088..120596006,3	MCF-7	breast:
4	chr12:120578652..120580296-chr12:120582169..120584083,2	K562	blood:
5	chr12:120553303..120556316-chr12:120578604..120582371,4	MCF-7	breast:
6	chr12:120582632..120586450-chr12:120589165..120596666,6	K562	blood:
7	chr12:120562054..120563752-chr12:120583178..120584938,2	K562	blood:
8	chr12:120583085..120585428-chr12:120589677..120591389,2	MCF-7	breast:
9	chr12:120576095..120579770-chr12:120584354..120586008,3	K562	blood:
10	chr12:120575018..120577152-chr12:120580218..120582213,2	MCF-7	breast:
11	chr12:120580898..120582942-chr12:120588270..120591019,2	MCF-7	breast:
12	chr12:120575987..120578062-chr12:120634816..120636487,2	K562	blood:
13	chr12:120585916..120589195-chr12:120646328..120649433,3	MCF-7	breast:
14	chr12:120574814..120578175-chr12:120636472..120639249,3	MCF-7	breast:
15	chr12:120587776..120590251-chr12:120726393..120729476,3	MCF-7	breast:
16	chr12:120577537..120579959-chr12:120630858..120632870,2	MCF-7	breast:
17	chr12:120587276..120588807-chr12:120602039..120603973,2	K562	blood:
18	chr12:120577345..120580147-chr12:120592811..120595731,2	K562	blood:
19	chr12:120577301..120580617-chr12:120600923..120603365,3	K562	blood:
20	chr12:120575608..120577582-chr12:120580676..120583270,2	K562	blood:
21	chr12:120578652..120580296-chr12:120582169..120584083,2	K562	blood:
22	chr12:120553957..120557976-chr12:120571615..120578270,6	MCF-7	breast:
23	chr12:120568428..120573002-chr12:120580087..120584233,4	MCF-7	breast:
24	chr12:120576335..120579124-chr12:120728555..120730059,2	MCF-7	breast:
25	chr12:120582133..120585365-chr12:120589813..120593363,4	K562	blood:
26	chr12:120581381..120583584-chr12:120728691..120731043,3	K562	blood:
27	chr12:120578342..120580518-chr12:120725654..120728594,2	MCF-7	breast:
28	chr12:120569171..120570951-chr12:120586181..120588091,2	MCF-7	breast:
29	chr12:120582613..120586889-chr12:120637591..120639948,3	K562	blood:
30	chr12:120581480..120583324-chr12:120594712..120597351,2	MCF-7	breast:
31	chr12:120573274..120575306-chr12:120582972..120584710,2	K562	blood:
32	chr12:120582633..120584337-chr12:120595846..120597580,2	K562	blood:
33	chr12:120580347..120581938-chr12:120583213..120585871,2	MCF-7	breast:
34	chr12:120559688..120561260-chr12:120583869..120585789,2	K562	blood:
35	chr12:120581778..120584149-chr12:120629758..120631422,2	K562	blood:
36	chr12:120582806..120587342-chr12:120631625..120635566,4	K562	blood:
37	chr12:120577095..120579573-chr12:120622728..120624803,2	K562	blood:

No data

Variant related genes	Relation type
GCN1L1	TF binding region
GCN1L1	CpG island
ENSG00000202538	chromatin interactions
ENSG00000111737	chromatin interactions
ENSG00000266704	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000089154	chromatin interactions
ENSG00000089157	chromatin interactions
ENSG00000255857	chromatin interactions

Extended variants
information (count: 409 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531894895	chr12:120577991-120577992	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs545250956	chr12:120578014-120578015	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs2240315	chr12:120578070-120578071	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs73412812	chr12:120578139-120578140	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs34156806	chr12:120578155-120578156	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs12301083	chr12:120578199-120578200	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567724241	chr12:120578255-120578256	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs112371363	chr12:120578308-120578309	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs117491083	chr12:120578329-120578330	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs185524518	chr12:120578353-120578354	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs4611268	chr12:120578375-120578376	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs538937213	chr12:120578389-120578390	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs533239394	chr12:120578400-120578401	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs543540648	chr12:120578492-120578493	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs115677480	chr12:120578493-120578494	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs565714451	chr12:120578557-120578558	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs534590547	chr12:120578558-120578559	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs2240316	chr12:120578581-120578582	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs113755527	chr12:120578582-120578583	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs4643128	chr12:120578586-120578587	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs141557121	chr12:120578603-120578604	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs190429497	chr12:120578620-120578621	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs202163851	chr12:120578627-120578628	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs556344382	chr12:120578641-120578642	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs191977759	chr12:120578650-120578651	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs200089590	chr12:120578663-120578664	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs368998511	chr12:120578672-120578673	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs565221525	chr12:120578680-120578681	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs373441523	chr12:120578684-120578685	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs111838318	chr12:120578714-120578715	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs371127784	chr12:120578726-120578727	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs374519389	chr12:120578765-120578766	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs35572885	chr12:120578770-120578771	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs541410880	chr12:120578771-120578772	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs377633057	chr12:120578773-120578774	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs184219578	chr12:120578774-120578775	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs202017755	chr12:120578789-120578790	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs566246941	chr12:120578792-120578793	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs373966395	chr12:120578804-120578805	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs550250831	chr12:120578825-120578826	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs368144298	chr12:120578837-120578838	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs370530493	chr12:120578850-120578851	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs540671476	chr12:120578877-120578878	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs532331670	chr12:120578909-120578910	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs552528995	chr12:120578922-120578923	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs565976127	chr12:120578926-120578927	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs562023085	chr12:120578967-120578968	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs373996416	chr12:120578980-120578981	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs577653512	chr12:120578984-120578985	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs139657781	chr12:120578990-120578991	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Medulloblastoma	16783165	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

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120556800-120578200	Weak transcription	Fetal Heart	heart
2	chr12:120563000-120580200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:120563000-120580200	Strong transcription	A549	lung
4	chr12:120563000-120588000	Strong transcription	HSMM	muscle
5	chr12:120563000-120596800	Strong transcription	Stomach Smooth Muscle	stomach
6	chr12:120563000-120605600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr12:120563000-120629800	Strong transcription	Fetal Stomach	stomach
8	chr12:120563000-120630200	Strong transcription	Fetal Muscle Leg	muscle
9	chr12:120563200-120602800	Strong transcription	Brain Germinal Matrix	brain
10	chr12:120563200-120630400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:120563400-120616200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr12:120563400-120629200	Strong transcription	Fetal Intestine Small	intestine
13	chr12:120563400-120630200	Strong transcription	Fetal Thymus	thymus
14	chr12:120563600-120580400	Strong transcription	Pancreas	Pancrea
15	chr12:120563600-120583600	Strong transcription	Fetal Brain Female	brain
16	chr12:120563600-120596400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:120563600-120602400	Strong transcription	Cortex derived primary cultured neurospheres	brain
18	chr12:120563600-120603600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:120563600-120603800	Strong transcription	Sigmoid Colon	Sigmoid Colon
20	chr12:120563600-120605600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr12:120563600-120626000	Strong transcription	Brain Cingulate Gyrus	brain
22	chr12:120563600-120626200	Strong transcription	Placenta Amnion	Placenta Amnion
23	chr12:120563600-120629000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr12:120563600-120630200	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr12:120563600-120630200	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr12:120563600-120630200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr12:120563600-120630200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:120563600-120630200	Strong transcription	Fetal Muscle Trunk	muscle
29	chr12:120563800-120581000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr12:120563800-120582600	Strong transcription	Liver	Liver
31	chr12:120563800-120602600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr12:120563800-120602600	Strong transcription	Primary T cells from cord blood	blood
33	chr12:120563800-120602600	Strong transcription	Brain Inferior Temporal Lobe	brain
34	chr12:120563800-120602800	Strong transcription	Dnd41	blood
35	chr12:120563800-120603600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr12:120563800-120629800	Strong transcription	H1 Cell Line	embryonic stem cell
37	chr12:120563800-120630000	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr12:120563800-120630200	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr12:120564000-120580800	Strong transcription	HMEC	breast
40	chr12:120564000-120581200	Strong transcription	NHEK	skin
41	chr12:120564000-120583400	Strong transcription	Hela-S3	cervix
42	chr12:120564000-120603600	Strong transcription	Brain Angular Gyrus	brain
43	chr12:120564000-120603800	Strong transcription	Thymus	Thymus
44	chr12:120564200-120594200	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr12:120564200-120624400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr12:120564200-120629600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr12:120564400-120579200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr12:120564400-120597000	Strong transcription	HepG2	liver
49	chr12:120564400-120602600	Strong transcription	Brain Hippocampus Middle	brain
50	chr12:120564400-120602600	Strong transcription	Placenta	Placenta

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