Variant report

Variant	nsv890370
Chromosome Location	chr8:11755513-11900847
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2554)
CpG islands
(count:3912)
Chromatin interactive
region (count:59)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2554 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11799803-11800003	K562	blood:	n/a	n/a
2	ARID3A	chr8:11872669-11872691	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:11801213-11801488	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:11813783-11814113	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:11758928-11760170	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:11769447-11769628	K562	blood:	n/a	n/a
7	ARID3A	chr8:11767366-11767469	HepG2	liver:	n/a	n/a
8	ATF1	chr8:11807083-11807365	K562	blood:	n/a	n/a
9	ATF1	chr8:11793688-11793744	K562	blood:	n/a	n/a
10	ATF1	chr8:11799573-11800081	K562	blood:	n/a	n/a
11	ATF2	chr8:11754354-11755726	GM12878	blood:	n/a	n/a
12	ATF2	chr8:11759720-11760180	GM12878	blood:	n/a	n/a
13	ATF2	chr8:11754279-11755628	GM12878	blood:	n/a	n/a
14	ATF3	chr8:11801205-11801445	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr8:11801205-11801436	K562	blood:	n/a	n/a
16	ATF3	chr8:11759787-11760027	K562	blood:	n/a	n/a
17	BACH1	chr8:11816433-11816692	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:11815300-11815374	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:11766653-11766839	K562	blood:	n/a	n/a
20	BACH1	chr8:11791553-11791787	K562	blood:	n/a	n/a
21	BACH1	chr8:11759765-11760312	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr8:11764476-11764781	GM12878	blood:	n/a	n/a
23	BATF	chr8:11895971-11896326	GM12878	blood:	n/a	n/a
24	BATF	chr8:11768607-11768792	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:11783650-11783829	GM12878	blood:	n/a	n/a
26	BCL3	chr8:11822405-11822652	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:11801183-11801540	HepG2	liver:	n/a	chr8:11801359-11801372
28	BHLHE40	chr8:11815181-11815494	K562	blood:	n/a	n/a
29	BHLHE40	chr8:11806929-11807352	K562	blood:	n/a	n/a
30	BHLHE40	chr8:11759086-11760250	HepG2	liver:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
31	BHLHE40	chr8:11801158-11801425	A549	lung:	n/a	chr8:11801359-11801372
32	BHLHE40	chr8:11801130-11801571	K562	blood:	n/a	chr8:11801359-11801372
33	BHLHE40	chr8:11799584-11800147	K562	blood:	n/a	n/a
34	BHLHE40	chr8:11815192-11815513	HepG2	liver:	n/a	n/a
35	BHLHE40	chr8:11759743-11760084	GM12878	blood:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
36	BHLHE40	chr8:11812950-11813081	K562	blood:	n/a	n/a
37	BHLHE40	chr8:11801171-11801545	GM12878	blood:	n/a	chr8:11801359-11801372
38	BHLHE40	chr8:11759739-11760276	K562	blood:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
39	BHLHE40	chr8:11793297-11793881	K562	blood:	n/a	n/a
40	BHLHE40	chr8:11769211-11769482	K562	blood:	n/a	n/a
41	BHLHE40	chr8:11816398-11816683	K562	blood:	n/a	n/a
42	BRCA1	chr8:11801145-11801480	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr8:11801202-11801448	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr8:11759696-11760000	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr8:11759673-11760101	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr8:11759068-11759443	HepG2	liver:	n/a	n/a
47	BRCA1	chr8:11759733-11760090	HepG2	liver:	n/a	n/a
48	CBX3	chr8:11839401-11840135	HCT-116	colon:	n/a	n/a
49	CBX3	chr8:11799688-11800155	K562	blood:	n/a	n/a
50	CBX3	chr8:11796176-11796816	K562	blood:	n/a	n/a

(count:3912 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11895252-11895302	HRE	kidney:	n/a
2	chr8:11771345-11771395	MCF10A-Er-Src	breast:	n/a
3	chr8:11853878-11853928	A549	lung:	n/a
4	chr8:11771244-11771294	HIPEpiC	eye:	n/a
5	chr8:11853878-11853928	HRE	kidney:	n/a
6	chr8:11760061-11760111	HUVEC	blood vessel:	n/a
7	chr8:11813211-11813261	AG10803	skin:	n/a
8	chr8:11835607-11835657	HRCEpiC	kidney:	n/a
9	chr8:11895252-11895302	HRE	kidney:	n/a
10	chr8:11771345-11771395	MCF10A-Er-Src	breast:	n/a
11	chr8:11853878-11853928	A549	lung:	n/a
12	chr8:11771244-11771294	HIPEpiC	eye:	n/a
13	chr8:11853878-11853928	HRE	kidney:	n/a
14	chr8:11760061-11760111	HUVEC	blood vessel:	n/a
15	chr8:11813211-11813261	AG10803	skin:	n/a
16	chr8:11835607-11835657	HRCEpiC	kidney:	n/a
17	chr8:11872659-11872709	HEEpiC	esophagus:	n/a
18	chr8:11795262-11795312	PrEC	prostate:	n/a
19	chr8:11833039-11833089	AG04450	lung:	fetal
20	chr8:11795273-11795323	GM06990	blood:	n/a
21	chr8:11853878-11853928	HMEC	breast:	n/a
22	chr8:11838843-11838893	SKMC	muscle:	n/a
23	chr8:11794716-11794766	SAEC	small airway:	n/a
24	chr8:11790559-11790609	NH-A	brain:	n/a
25	chr8:11838532-11838582	ProgFib	skin:	n/a
26	chr8:11772119-11772169	LNCaP	prostate:	n/a
27	chr8:11895252-11895302	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:11832261-11832311	RPTEC	kidney:	n/a
29	chr8:11841980-11842030	Hepatocyte	liver:	n/a
30	chr8:11872141-11872191	HAEpiC	amniotic membrane:	n/a
31	chr8:11772734-11772784	H1-hESC	embryonic stem cell:	embryo
32	chr8:11790639-11790689	HRE	kidney:	n/a
33	chr8:11759863-11759913	HepG2	liver:	n/a
34	chr8:11870063-11870113	SK-N-SH_RA	brain:	n/a
35	chr8:11772568-11772618	Caco-2	colon:	n/a
36	chr8:11872882-11872932	CMK	blood:	n/a
37	chr8:11770970-11771020	CMK	blood:	n/a
38	chr8:11870063-11870113	HCT-116	colon:	n/a
39	chr8:11872659-11872709	Jurkat	blood:	n/a
40	chr8:11795262-11795312	GM12892	blood:	n/a
41	chr8:11872659-11872709	MCF10A-Er-Src	breast:	n/a
42	chr8:11833039-11833089	NHBE	bronchial:	n/a
43	chr8:11832261-11832311	CMK	blood:	n/a
44	chr8:11795262-11795312	U87	brain:	n/a
45	chr8:11772119-11772169	HEEpiC	esophagus:	n/a
46	chr8:11760061-11760111	SK-N-MC	brain:	n/a
47	chr8:11770970-11771020	AG09309	skin:	n/a
48	chr8:11841980-11842030	AG09309	skin:	n/a
49	chr8:11839764-11839814	GM12891	blood:	n/a
50	chr8:11882962-11883012	SK-N-SH	brain:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
2	chr8:11851923..11853652-chr8:11853797..11856578,2	K562	blood:
3	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
4	chr8:11759912..11760480-chr8:11816112..11816711,2	K562	blood:
5	chr8:11718467..11721222-chr8:11754378..11756104,3	K562	blood:
6	chr8:11723911..11726339-chr8:11798413..11801274,2	K562	blood:
7	chr8:11622652..11623752-chr8:11800899..11801806,5	MCF-7	breast:
8	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
9	chr8:11622903..11623629-chr8:11815893..11817036,5	K562	blood:
10	chr8:11746436..11748896-chr8:11754900..11757322,2	K562	blood:
11	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
12	chr8:11702698..11703665-chr8:11759456..11760160,2	MCF-7	breast:
13	chr8:11699877..11702780-chr8:11758303..11760780,3	K562	blood:
14	chr8:11619764..11620442-chr8:11816053..11817012,3	K562	blood:
15	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
16	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
17	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
18	chr8:11612285..11613206-chr8:11801217..11801735,2	MCF-7	breast:
19	chr8:11718857..11721432-chr8:11753489..11755957,2	K562	blood:
20	chr8:11752267..11756149-chr8:11756562..11759200,3	MCF-7	breast:
21	chr8:11710424..11713168-chr8:11798660..11801424,2	K562	blood:
22	chr8:11768991..11769997-chr8:11800815..11801744,4	MCF-7	breast:
23	chr8:11662199..11664746-chr8:11796348..11798802,2	K562	blood:
24	chr8:11711030..11711819-chr8:11759482..11760312,2	MCF-7	breast:
25	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
26	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
27	chr8:11424253..11424822-chr8:11800849..11801372,2	K562	blood:
28	chr8:11768991..11769997-chr8:11800815..11801744,4	MCF-7	breast:
29	chr8:11724650..11727565-chr8:11758155..11761309,4	MCF-7	breast:
30	chr8:11744571..11746987-chr8:11757045..11759456,2	MCF-7	breast:
31	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
32	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
33	chr8:11421778..11422656-chr8:11816114..11817045,3	MCF-7	breast:
34	chr8:11421685..11422256-chr8:11800840..11801381,2	K562	blood:
35	chr11:64863606..64864139-chr8:11882400..11882963,2	Hela-S3	cervix:
36	chr8:11603020..11605526-chr8:11757590..11759777,2	K562	blood:
37	chr8:11830756..11832686-chr8:11834027..11835713,2	K562	blood:
38	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
39	chr8:11622750..11623420-chr8:11815244..11815854,2	MCF-7	breast:
40	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
41	chr8:11724862..11726557-chr8:11758521..11760693,2	MCF-7	breast:
42	chr8:11759912..11760480-chr8:11816112..11816711,2	K562	blood:
43	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
44	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
45	chr8:11759679..11760322-chr8:11800851..11801844,2	K562	blood:
46	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
47	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
48	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
49	chr8:11424139..11425217-chr8:11815416..11817027,6	K562	blood:
50	chr8:11658805..11661004-chr8:11802756..11805427,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB135-1	chr8:11856596-11856977	NONHSAT125105
2	lnc-CTSB-2	chr8:11777409-11778318	NONHSAT125102
3	lnc-DEFB134-1	chr8:11860909-11861591	NONHSAT125106

No data

Variant related genes	Relation type
DEFB136	TF binding region
OR7E161P	TF binding region
ENSG00000255016	TF binding region
ENSG00000255174	TF binding region
DEFB134	TF binding region
ENSG00000254507	TF binding region
DEFB135	TF binding region
ENSG00000255098	TF binding region
OR7E160P	TF binding region
OR7E158P	TF binding region
ENSG00000255144	TF binding region
DEFB136	CpG island
OR7E161P	CpG island
ENSG00000255016	CpG island
ENSG00000255174	CpG island
DEFB134	CpG island
ENSG00000254507	CpG island
DEFB135	CpG island
ENSG00000255098	CpG island
OR7E160P	CpG island
OR7E158P	CpG island
ENSG00000255144	CpG island
ENSG00000164733	chromatin interactions
ENSG00000205884	chromatin interactions
ENSG00000255144	chromatin interactions
ENSG00000255046	chromatin interactions
ENSG00000079459	chromatin interactions
ENSG00000205883	chromatin interactions
ENSG00000205882	chromatin interactions
ENSG00000149823	chromatin interactions

Extended variants
information (count: 7166 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:7166 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9644757	chr8:11755513-11755514	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548599000	chr8:11755521-11755522	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563651886	chr8:11755561-11755562	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs569911509	chr8:11755569-11755570	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs530900188	chr8:11755570-11755571	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs150678154	chr8:11755571-11755572	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs7831946	chr8:11755599-11755600	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs535226729	chr8:11755673-11755674	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs558239942	chr8:11755674-11755675	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs186161047	chr8:11755696-11755697	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs578154636	chr8:11755712-11755713	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs190673549	chr8:11755722-11755723	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs139840399	chr8:11755726-11755727	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs143904311	chr8:11755747-11755748	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs181703822	chr8:11755752-11755753	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs146870043	chr8:11755753-11755754	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs558431562	chr8:11755791-11755792	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs527509078	chr8:11755792-11755793	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs7819276	chr8:11755804-11755805	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs541260634	chr8:11755812-11755813	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs559268822	chr8:11755820-11755821	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs140818325	chr8:11755832-11755833	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs542364778	chr8:11755848-11755849	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563739504	chr8:11755854-11755855	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs7832347	chr8:11755872-11755873	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs74688660	chr8:11755891-11755892	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs62493566	chr8:11755904-11755905	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs77531698	chr8:11755927-11755928	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531794388	chr8:11755928-11755929	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201731290	chr8:11755965-11755966	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs143201363	chr8:11755982-11755983	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529451845	chr8:11755984-11755985	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs547889731	chr8:11755995-11755996	Weak transcription Enhancers Genic enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs569364037	chr8:11756012-11756013	Weak transcription Enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536694027	chr8:11756015-11756016	Weak transcription Enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs370145625	chr8:11756018-11756019	Weak transcription Enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs145448462	chr8:11756029-11756030	Weak transcription Enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs376228572	chr8:11756030-11756031	Weak transcription Enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7819301	chr8:11756048-11756049	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs73663043	chr8:11756070-11756071	Weak transcription Enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs186824557	chr8:11756123-11756124	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs574561853	chr8:11756129-11756130	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs542007409	chr8:11756147-11756148	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs557496071	chr8:11756178-11756179	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191207192	chr8:11756179-11756180	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs148862586	chr8:11756182-11756183	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs143492679	chr8:11756183-11756184	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs528458054	chr8:11756191-11756192	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs73546801	chr8:11756212-11756213	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs55991488	chr8:11756226-11756227	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:146)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Osteosarcoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11738000-11755800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:11745800-11759600	Weak transcription	Right Atrium	heart
3	chr8:11749800-11759400	Weak transcription	NHEK	skin
4	chr8:11753400-11756400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr8:11753600-11756800	Enhancers	Primary B cells from cord blood	blood
6	chr8:11754000-11756200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:11754200-11755600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr8:11754200-11755800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:11754200-11756200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr8:11754200-11756200	Flanking Active TSS	GM12878-XiMat	blood
11	chr8:11754400-11755600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:11754400-11755600	Enhancers	NH-A	brain
13	chr8:11754400-11755800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr8:11754400-11756000	Enhancers	Muscle Satellite Cultured Cells	--
15	chr8:11754400-11756000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr8:11754400-11756000	Enhancers	NHDF-Ad	bronchial
17	chr8:11754400-11756200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:11754400-11756600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr8:11754600-11755600	Enhancers	Fetal Kidney	kidney
20	chr8:11754600-11755800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
21	chr8:11754600-11756000	Enhancers	Placenta	Placenta
22	chr8:11754600-11756200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr8:11754800-11755600	Enhancers	NHLF	lung
24	chr8:11754800-11756000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr8:11754800-11756000	Enhancers	Fetal Intestine Small	intestine
26	chr8:11754800-11756800	Enhancers	Fetal Intestine Large	intestine
27	chr8:11754800-11759600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:11755000-11755600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr8:11755000-11755600	Flanking Active TSS	Liver	Liver
30	chr8:11755000-11755800	Enhancers	Osteobl	bone
31	chr8:11755000-11756000	Enhancers	K562	blood
32	chr8:11755000-11756200	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr8:11755000-11756800	Enhancers	Primary B cells from peripheral blood	blood
34	chr8:11755000-11757000	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr8:11755000-11759000	Weak transcription	Ovary	ovary
36	chr8:11755000-11759600	Weak transcription	Esophagus	oesophagus
37	chr8:11755000-11759600	Weak transcription	Pancreas	Pancrea
38	chr8:11755000-11760000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr8:11755200-11755600	Enhancers	Adipose Nuclei	Adipose
40	chr8:11755200-11756200	Enhancers	Duodenum Mucosa	Duodenum
41	chr8:11755200-11759200	Weak transcription	A549	lung
42	chr8:11755200-11759400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:11755200-11759400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr8:11755200-11759400	Weak transcription	Stomach Mucosa	stomach
45	chr8:11755200-11759600	Weak transcription	Left Ventricle	heart
46	chr8:11755400-11755600	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr8:11755400-11755800	Enhancers	HepG2	liver
48	chr8:11755400-11756000	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr8:11755400-11756000	Enhancers	Spleen	Spleen
50	chr8:11755400-11759200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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