Variant report

Variant	esv3326233
Chromosome Location	chr8:91690825-91708859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:91691471-91691520	HepG2	liver:	n/a	n/a
2	CBX3	chr8:91691242-91691856	K562	blood:	n/a	n/a
3	CEBPB	chr8:91693393-91693523	A549	lung:	n/a	n/a
4	CHD1	chr8:91694481-91694518	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr8:91707060-91707210	RPTEC	kidney:	n/a	n/a
6	CTCF	chr8:91707044-91707149	Fibrobl	skin:	n/a	n/a
7	CTCF	chr8:91704600-91704750	HPF	lung:	n/a	n/a
8	CTCF	chr8:91704620-91704770	HRPEpiC	eye:	n/a	n/a
9	CTCF	chr8:91698393-91698451	GM10248	blood:	n/a	n/a
10	E2F6	chr8:91694244-91694663	H1-hESC	embryonic stem cell:	n/a	n/a
11	EP300	chr8:91691347-91691557	K562	blood:	n/a	n/a
12	EP300	chr8:91703888-91704594	MCF-7	breast:	n/a	n/a
13	EP300	chr8:91704001-91704841	MCF-7	breast:	n/a	n/a
14	EP300	chr8:91704887-91705663	MCF-7	breast:	n/a	chr8:91705468-91705477 chr8:91705223-91705232
15	EP300	chr8:91694695-91694953	SK-N-SH_RA	brain:	n/a	n/a
16	ESR1	chr8:91704134-91704446	T-47D	breast:	n/a	chr8:91704218-91704235
17	ESR1	chr8:91704075-91704394	T-47D	breast:	n/a	chr8:91704218-91704235
18	ESR1	chr8:91704068-91704424	T-47D	breast:	n/a	chr8:91704218-91704235
19	FOS	chr8:91705046-91705475	HUVEC	blood vessel:	n/a	chr8:91705310-91705320 chr8:91705224-91705232 chr8:91705310-91705320 chr8:91705225-91705232 chr8:91705222-91705233 chr8:91705223-91705233 chr8:91705311-91705319 chr8:91705224-91705232
20	FOS	chr8:91691474-91691903	HUVEC	blood vessel:	n/a	n/a
21	FOS	chr8:91705098-91705412	MCF10A-Er-Src	breast:	n/a	chr8:91705310-91705320 chr8:91705224-91705232 chr8:91705310-91705320 chr8:91705225-91705232 chr8:91705222-91705233 chr8:91705223-91705233 chr8:91705311-91705319 chr8:91705224-91705232
22	FOSL2	chr8:91705018-91705516	A549	lung:	n/a	chr8:91705310-91705320 chr8:91705224-91705232 chr8:91705310-91705320 chr8:91705225-91705232 chr8:91705223-91705233 chr8:91705311-91705319 chr8:91705224-91705232
23	FOSL2	chr8:91691508-91691855	HepG2	liver:	n/a	n/a
24	FOSL2	chr8:91706872-91707369	SK-N-SH	brain:	n/a	chr8:91706904-91706913
25	FOSL2	chr8:91705005-91705667	MCF-7	breast:	n/a	chr8:91705310-91705320 chr8:91705224-91705232 chr8:91705310-91705320 chr8:91705225-91705232 chr8:91705311-91705319 chr8:91705223-91705233 chr8:91705224-91705232
26	FOSL2	chr8:91704904-91705607	MCF-7	breast:	n/a	chr8:91705310-91705320 chr8:91705224-91705232 chr8:91705310-91705320 chr8:91705225-91705232 chr8:91705223-91705233 chr8:91705311-91705319 chr8:91705224-91705232
27	FOXA2	chr8:91696148-91696791	A549	lung:	n/a	n/a
28	FOXA2	chr8:91697045-91697553	A549	lung:	n/a	n/a
29	FOXM1	chr8:91703906-91705767	MCF-7	breast:	n/a	n/a
30	FOXM1	chr8:91704016-91704677	MCF-7	breast:	n/a	n/a
31	GATA2	chr8:91691399-91691753	HUVEC	blood vessel:	n/a	n/a
32	GATA3	chr8:91703947-91704533	MCF-7	breast:	n/a	n/a
33	GATA3	chr8:91703898-91704630	MCF-7	breast:	n/a	n/a
34	GATA3	chr8:91704955-91705764	MCF-7	breast:	n/a	n/a
35	GATA3	chr8:91703759-91704938	MCF-7	breast:	n/a	n/a
36	GATA3	chr8:91690401-91691018	MCF-7	breast:	n/a	chr8:91690764-91690775 chr8:91690477-91690488 chr8:91690758-91690766 chr8:91690759-91690768
37	GATA3	chr8:91690657-91690982	MCF-7	breast:	n/a	chr8:91690764-91690775 chr8:91690758-91690766 chr8:91690759-91690768
38	GATA3	chr8:91704871-91705652	MCF-7	breast:	n/a	n/a
39	GATA3	chr8:91705017-91705484	MCF-7	breast:	n/a	n/a
40	GATA3	chr8:91705097-91705458	MCF-7	breast:	n/a	n/a
41	GATA3	chr8:91703885-91704785	MCF-7	breast:	n/a	n/a
42	GATA3	chr8:91690441-91691661	MCF-7	breast:	n/a	chr8:91690764-91690775 chr8:91690477-91690488 chr8:91690758-91690766 chr8:91690759-91690768
43	HDAC2	chr8:91704067-91704900	MCF-7	breast:	n/a	chr8:91704087-91704096 chr8:91704791-91704805 chr8:91704410-91704419
44	IRF1	chr8:91693689-91693846	K562	blood:	n/a	n/a
45	JUN	chr8:91705097-91705496	HUVEC	blood vessel:	n/a	chr8:91705310-91705320 chr8:91705224-91705232 chr8:91705310-91705320 chr8:91705225-91705232 chr8:91705223-91705233 chr8:91705311-91705319 chr8:91705224-91705232
46	JUND	chr8:91691576-91691747	H1-hESC	embryonic stem cell:	n/a	chr8:91691640-91691651
47	JUND	chr8:91705017-91705721	MCF-7	breast:	n/a	chr8:91705310-91705320 chr8:91705224-91705232 chr8:91705310-91705320 chr8:91705225-91705232 chr8:91705223-91705233 chr8:91705311-91705319 chr8:91705224-91705232
48	JUND	chr8:91691540-91691740	K562	blood:	n/a	chr8:91691640-91691651
49	JUND	chr8:91691554-91691829	HepG2	liver:	n/a	chr8:91691640-91691651
50	JUND	chr8:91706878-91707327	SK-N-SH	brain:	n/a	chr8:91706904-91706913

No.	Distal block	Cell Line	Cell type
1	chr8:91594033..91595914-chr8:91702199..91704842,2	MCF-7	breast:
2	chr8:91657081..91659555-chr8:91692442..91695453,3	K562	blood:
3	chr8:91658760..91661338-chr8:91707449..91709669,2	K562	blood:
4	chr8:91703809..91704698-chr8:91766212..91767104,5	MCF-7	breast:
5	chr8:91704605..91706263-chr8:91708143..91710693,2	MCF-7	breast:
6	chr8:91653608..91662753-chr8:91702053..91707757,26	MCF-7	breast:
7	chr8:91704062..91704591-chr8:91899605..91900389,2	MCF-7	breast:
8	chr8:91708540..91711261-chr8:91799440..91801904,2	MCF-7	breast:
9	chr8:91705691..91710257-chr8:91923411..91927074,5	MCF-7	breast:
10	chr8:91703840..91704698-chr8:91766212..91767104,2	MCF-7	breast:
11	chr8:91656752..91660080-chr8:91707988..91711450,4	MCF-7	breast:
12	chr8:91652169..91654028-chr8:91698689..91701594,2	MCF-7	breast:
13	chr8:91703897..91704427-chr8:91924931..91925718,2	MCF-7	breast:
14	chr8:91632919..91634479-chr8:91696741..91698675,2	MCF-7	breast:
15	chr8:91657324..91660204-chr8:91691658..91693612,2	MCF-7	breast:
16	chr8:91659065..91661571-chr8:91690814..91693630,2	K562	blood:
17	chr8:91703619..91705136-chr8:91710451..91712123,2	MCF-7	breast:
18	chr8:91703739..91707372-chr8:91708045..91711511,5	K562	blood:
19	chr8:91705203..91706049-chr8:91766185..91766752,2	MCF-7	breast:
20	chr8:91649679..91651282-chr8:91705770..91708113,2	MCF-7	breast:
21	chr8:91655789..91659978-chr8:91686080..91690997,6	K562	blood:
22	chr8:91703653..91704652-chr8:91899599..91900269,2	MCF-7	breast:
23	chr8:91657079..91658654-chr8:91690664..91693571,2	MCF-7	breast:
24	chr8:91687150..91691411-chr8:91769036..91770944,3	MCF-7	breast:
25	chr8:91702608..91708143-chr8:91763380..91770972,10	MCF-7	breast:
26	chr8:91655961..91659913-chr8:91697811..91701494,3	K562	blood:
27	chr8:91704605..91706263-chr8:91708143..91710693,2	MCF-7	breast:
28	chr8:91703739..91707372-chr8:91708045..91711511,5	K562	blood:
29	chr8:91681513..91683796-chr8:91702436..91704437,2	MCF-7	breast:
30	chr8:91704726..91706793-chr8:91760204..91762419,3	MCF-7	breast:
31	chr8:91656308..91659290-chr8:91694293..91696671,3	MCF-7	breast:
32	chr8:91655723..91658520-chr8:91691444..91693877,2	K562	blood:
33	chr8:91707268..91708794-chr8:91715848..91717475,2	K562	blood:
34	chr8:91655311..91659894-chr8:91701508..91706218,8	K562	blood:
35	chr8:91699039..91701699-chr8:91701924..91705332,3	MCF-7	breast:
36	chr8:91704437..91707166-chr8:91906109..91908383,2	MCF-7	breast:
37	chr8:91699039..91701699-chr8:91701924..91705332,3	MCF-7	breast:
38	chr8:91704585..91708027-chr8:91711099..91715067,9	MCF-7	breast:
39	chr8:91707642..91709593-chr8:91712850..91714825,2	MCF-7	breast:
40	chr8:91701605..91703833-chr8:91894006..91896640,2	MCF-7	breast:
41	chr8:91682939..91685904-chr8:91705283..91708247,3	MCF-7	breast:
42	chr8:91682168..91683156-chr8:91704088..91704602,2	MCF-7	breast:
43	chr8:91703063..91706391-chr8:91765504..91767653,3	MCF-7	breast:
44	chr8:91656804..91661563-chr8:91708196..91711491,5	MCF-7	breast:
45	chr8:91656428..91660411-chr8:91700903..91705938,6	MCF-7	breast:
46	chr8:91700595..91702835-chr8:91924612..91926709,2	MCF-7	breast:
47	chr8:91703935..91704591-chr8:91899605..91900403,3	MCF-7	breast:
48	chr8:91655211..91656811-chr8:91701508..91704271,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-122A3.2.1-1	chr8:91702672-91702803	NONHSAT127661
2	lnc-RP11-122A3.2.1-1	chr8:91696179-91696258	NONHSAT127662
3	lnc-RP11-122A3.2.1-1	chr8:91696044-91696258	NONHSAT127661

Variant related genes	Relation type
ENSG00000254182	TF binding region
ENSG00000180694	chromatin interactions
ENSG00000246792	chromatin interactions
ENSG00000254182	chromatin interactions

Extended variants
information (count: 569 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374982249	chr8:91690883-91690884	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs35547810	chr8:91690923-91690924	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533148675	chr8:91690963-91690964	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs111564610	chr8:91691005-91691006	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs568975928	chr8:91691007-91691008	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs564940890	chr8:91691142-91691143	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs532185461	chr8:91691164-91691165	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs570459574	chr8:91691171-91691172	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551315795	chr8:91691175-91691176	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs141632358	chr8:91691183-91691184	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs534240291	chr8:91691192-91691193	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs547194756	chr8:91691195-91691196	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs555770432	chr8:91691200-91691201	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs10090406	chr8:91691270-91691271	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs144516352	chr8:91691303-91691304	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs527777637	chr8:91691312-91691313	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs10091274	chr8:91691313-91691314	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs148023003	chr8:91691322-91691323	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553948403	chr8:91691331-91691332	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572053424	chr8:91691400-91691401	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs118002695	chr8:91691407-91691408	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs77619176	chr8:91691419-91691420	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs531649507	chr8:91691421-91691422	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs150580951	chr8:91691492-91691493	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs538043454	chr8:91691493-91691494	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs556678885	chr8:91691504-91691505	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs187957337	chr8:91691597-91691598	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs112726404	chr8:91691618-91691619	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs140623854	chr8:91691630-91691631	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs4637779	chr8:91691631-91691632	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs539095778	chr8:91691670-91691671	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs551452937	chr8:91691786-91691787	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs192195421	chr8:91691796-91691797	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs144550076	chr8:91691819-91691820	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs553991037	chr8:91691869-91691870	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs567832645	chr8:91691885-91691886	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs182777087	chr8:91691899-91691900	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556940876	chr8:91691945-91691946	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs571857618	chr8:91691992-91691993	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs539268980	chr8:91691999-91692000	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs7846120	chr8:91692011-91692012	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs543072546	chr8:91692018-91692019	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs112062593	chr8:91692022-91692023	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs147450923	chr8:91692075-91692076	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576210429	chr8:91692096-91692097	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs187136405	chr8:91692107-91692108	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs564878165	chr8:91692172-91692173	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs191676494	chr8:91692178-91692179	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs75297678	chr8:91692203-91692204	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200424488	chr8:91692206-91692207	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91683800-91691000	Weak transcription	Placenta	Placenta
2	chr8:91683800-91691600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:91684200-91691800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:91688800-91691800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:91688800-91693400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:91688800-91694000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:91689000-91691200	Weak transcription	Fetal Lung	lung
8	chr8:91689000-91691600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:91689000-91693400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:91689000-91693600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr8:91689400-91694000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr8:91689600-91691600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:91689800-91691600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr8:91689800-91691600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr8:91689800-91691600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr8:91690000-91691200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:91690000-91691400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr8:91690000-91691600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr8:91690400-91691600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr8:91690600-91691200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:91690600-91691200	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr8:91690800-91692000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:91691000-91691400	Enhancers	HepG2	liver
24	chr8:91691000-91692400	Enhancers	Placenta	Placenta
25	chr8:91691200-91692000	Enhancers	Placenta Amnion	Placenta Amnion
26	chr8:91691200-91692200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:91691200-91694600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:91691200-91694600	Enhancers	Fetal Lung	lung
29	chr8:91691400-91692200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr8:91691400-91692400	Flanking Active TSS	HepG2	liver
31	chr8:91691600-91692200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr8:91691600-91692200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr8:91691600-91692400	Enhancers	H1 Cell Line	embryonic stem cell
34	chr8:91691600-91692400	Enhancers	H9 Cell Line	embryonic stem cell
35	chr8:91691600-91695000	Enhancers	K562	blood
36	chr8:91691600-91695600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr8:91691600-91696000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr8:91691600-91696400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr8:91691600-91696400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr8:91691600-91696400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr8:91691800-91692000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:91691800-91692000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr8:91692000-91692400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:91692000-91692600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr8:91692200-91692600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr8:91692200-91694000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr8:91692200-91698600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr8:91692400-91692600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr8:91692400-91692600	Enhancers	HepG2	liver
50	chr8:91692400-91693800	Weak transcription	H1 Cell Line	embryonic stem cell

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