Variant report

Variant	nsv890353
Chromosome Location	chr8:11097804-11110503
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	chr8:11104377-11104780	K562	blood:	n/a	n/a
2	ATF2	chr8:11105843-11106307	GM12878	blood:	n/a	n/a
3	ATF2	chr8:11104317-11104796	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:11108513-11108819	GM12878	blood:	n/a	n/a
5	BATF	chr8:11108550-11108789	GM12878	blood:	n/a	n/a
6	BATF	chr8:11105909-11106255	GM12878	blood:	n/a	n/a
7	BATF	chr8:11105906-11106241	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:11108541-11108828	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:11108560-11108800	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:11105929-11106232	GM12878	blood:	n/a	chr8:11106049-11106058
11	BCL3	chr8:11105899-11106156	GM12878	blood:	n/a	chr8:11106049-11106058
12	BCLAF1	chr8:11108482-11108814	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:11101751-11101988	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:11108519-11108884	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:11101696-11102061	K562	blood:	n/a	n/a
16	BHLHE40	chr8:11109568-11109569	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:11108693-11108715	K562	blood:	n/a	n/a
18	CEBPB	chr8:11100478-11100708	HepG2	liver:	n/a	chr8:11100569-11100580
19	CEBPB	chr8:11099511-11099685	HepG2	liver:	n/a	chr8:11099541-11099552
20	CEBPB	chr8:11101766-11101943	K562	blood:	n/a	chr8:11101916-11101927 chr8:11101916-11101929 chr8:11101916-11101927
21	CTCF	chr8:11104540-11104690	GM12872	blood:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
22	CTCF	chr8:11104180-11104330	GM12870	blood:	n/a	n/a
23	CTCF	chr8:11104545-11104609	Kidney_OC	kidney:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
24	CTCF	chr8:11104220-11104370	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr8:11104460-11104610	GM12868	blood:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
26	CTCF	chr8:11104222-11104318	A549	lung:	n/a	n/a
27	CTCF	chr8:11104520-11104670	HA-sp	spinal cord:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
28	CTCF	chr8:11104527-11104618	GM13976	blood:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
29	CTCF	chr8:11104500-11104650	HPAF	blood vessel:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
30	CTCF	chr8:11104540-11104690	HRPEpiC	eye:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
31	CTCF	chr8:11104540-11104690	GM12870	blood:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
32	CTCF	chr8:11104220-11104370	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr8:11104500-11104650	SK-N-SH_RA	brain:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
34	CTCF	chr8:11104480-11104630	HL-60	blood:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
35	CTCF	chr8:11104438-11104713	H1-hESC	embryonic stem cell:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
36	CTCF	chr8:11104223-11104327	GM12891	blood:	n/a	n/a
37	CTCF	chr8:11104518-11104952	H1-hESC	embryonic stem cell:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
38	CTCF	chr8:11104520-11104670	A549	lung:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
39	CTCF	chr8:11104170-11105070	A549	lung:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
40	CTCF	chr8:11104540-11104690	GM12865	blood:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
41	CTCF	chr8:11104432-11104714	K562	blood:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
42	CTCF	chr8:11104439-11104686	A549	lung:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
43	CTCF	chr8:11104460-11104610	RPTEC	kidney:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
44	CTCF	chr8:11104564-11104677	NHEK	skin:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
45	CTCF	chr8:11103974-11105079	SK-N-SH	brain:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
46	CTCF	chr8:11099120-11099270	A549	lung:	n/a	n/a
47	CTCF	chr8:11104140-11104290	AG10803	skin:	n/a	n/a
48	CTCF	chr8:11104520-11104670	HPAF	blood vessel:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
49	CTCF	chr8:11104540-11104690	BE2_C	brain:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596
50	CTCF	chr8:11104509-11104702	A549	lung:	n/a	chr8:11104576-11104589 chr8:11104574-11104590 chr8:11104578-11104586 chr8:11104573-11104591 chr8:11104575-11104596

No.	Distal block	Cell Line	Cell type
1	chr8:11104163..11104968-chr8:11410930..11412030,3	K562	blood:
2	chr8:11104140..11105082-chr8:11136652..11137703,3	MCF-7	breast:
3	chr8:11101887..11103674-chr8:11105009..11107051,2	K562	blood:
4	chr8:11101887..11103674-chr8:11105009..11107051,2	K562	blood:
5	chr8:11084951..11086615-chr8:11108350..11109872,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00529-1	chr8:11105135-11105298	ENSG00000236827.1

Variant related genes	Relation type
RPL19P13	TF binding region
ENSG00000254774	chromatin interactions

Extended variants
information (count: 607 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531268642	chr8:11099809-11099810	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs185900704	chr8:11099909-11099910	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs144491096	chr8:11099928-11099929	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs146647630	chr8:11099980-11099981	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs191054949	chr8:11099981-11099982	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs542949200	chr8:11100217-11100218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76878208	chr8:11100232-11100233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2117617	chr8:11100234-11100235	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs148823147	chr8:11100247-11100248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564584066	chr8:11100273-11100274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6601576	chr8:11100275-11100276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs150933586	chr8:11100305-11100306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546250590	chr8:11100307-11100308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559384773	chr8:11100372-11100373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114633746	chr8:11100374-11100375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547956639	chr8:11100389-11100390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140758416	chr8:11100398-11100399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530577687	chr8:11100404-11100405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376531135	chr8:11100420-11100421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552446495	chr8:11100425-11100426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4483111	chr8:11100427-11100428	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs183007844	chr8:11100432-11100433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546623242	chr8:11100441-11100442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17795704	chr8:11100443-11100444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs535965356	chr8:11100450-11100451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374360730	chr8:11100486-11100487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557143078	chr8:11100495-11100496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575804679	chr8:11100516-11100517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145892399	chr8:11100526-11100527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558331605	chr8:11100558-11100559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2736367	chr8:11100603-11100604	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs138804446	chr8:11100642-11100643	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs187580324	chr8:11100648-11100649	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs2572435	chr8:11100665-11100666	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs531100729	chr8:11100674-11100675	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs563188139	chr8:11100681-11100682	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs530623851	chr8:11100695-11100696	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs552128209	chr8:11100724-11100725	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs373510811	chr8:11100736-11100737	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs551001892	chr8:11100737-11100738	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs563923974	chr8:11100773-11100774	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs141366352	chr8:11100813-11100814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546459920	chr8:11100853-11100854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147006864	chr8:11100857-11100858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77536970	chr8:11100859-11100860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551056970	chr8:11100898-11100899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2572434	chr8:11100913-11100914	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs192528348	chr8:11100922-11100923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77514050	chr8:11100925-11100926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2736368	chr8:11100961-11100962	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:138)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11099800-11100000	Bivalent Enhancer	Stomach Mucosa	stomach
2	chr8:11100200-11100600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:11100600-11100800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
4	chr8:11100600-11101200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:11100800-11102400	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr8:11101000-11102400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr8:11101200-11102000	Enhancers	GM12878-XiMat	blood
8	chr8:11101200-11116000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:11101600-11101800	Enhancers	Primary B cells from peripheral blood	blood
10	chr8:11101600-11102000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr8:11102000-11105600	Weak transcription	GM12878-XiMat	blood
12	chr8:11102400-11108000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr8:11103600-11104400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:11103800-11104400	Enhancers	HMEC	breast
15	chr8:11104600-11104800	Enhancers	Rectal Smooth Muscle	rectum
16	chr8:11104600-11105000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr8:11104600-11105000	Enhancers	Colon Smooth Muscle	Colon
18	chr8:11104800-11106000	Weak transcription	Rectal Smooth Muscle	rectum
19	chr8:11105000-11106000	Weak transcription	Colon Smooth Muscle	Colon
20	chr8:11105600-11106600	Enhancers	GM12878-XiMat	blood
21	chr8:11105800-11106200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:11106000-11106600	Enhancers	Colon Smooth Muscle	Colon
23	chr8:11106000-11106600	Enhancers	Rectal Smooth Muscle	rectum
24	chr8:11106600-11107800	Weak transcription	GM12878-XiMat	blood
25	chr8:11106600-11110400	Weak transcription	Colon Smooth Muscle	Colon
26	chr8:11107600-11110800	Enhancers	Primary B cells from peripheral blood	blood
27	chr8:11107800-11108000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
28	chr8:11107800-11108000	Bivalent Enhancer	Right Ventricle	heart
29	chr8:11107800-11108400	Enhancers	GM12878-XiMat	blood
30	chr8:11108000-11108200	Bivalent Enhancer	Colonic Mucosa	Colon
31	chr8:11108000-11109800	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr8:11108000-11109800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr8:11108200-11108400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
34	chr8:11108200-11109000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr8:11108200-11109800	Enhancers	Primary B cells from cord blood	blood
36	chr8:11108400-11108600	Flanking Active TSS	GM12878-XiMat	blood
37	chr8:11108400-11108800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr8:11108400-11110000	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr8:11108600-11109000	Active TSS	GM12878-XiMat	blood
40	chr8:11109000-11109600	Flanking Active TSS	GM12878-XiMat	blood
41	chr8:11109600-11110000	Enhancers	GM12878-XiMat	blood
42	chr8:11110000-11111400	Weak transcription	GM12878-XiMat	blood
43	chr8:11110400-11112000	Enhancers	Colon Smooth Muscle	Colon

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