Variant report

Variant	esv3435213
Chromosome Location	chr8:11865908-11900957
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	chr8:11872669-11872691	HepG2	liver:	n/a	n/a
2	BATF	chr8:11895971-11896326	GM12878	blood:	n/a	n/a
3	CCNT2	chr8:11872580-11872794	K562	blood:	n/a	n/a
4	CTCF	chr8:11872605-11872867	GM19240	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
5	CTCF	chr8:11889431-11889487	GM10248	blood:	n/a	n/a
6	CTCF	chr8:11872595-11872884	GM10248	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
7	CTCF	chr8:11872543-11872869	A549	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
8	CTCF	chr8:11872563-11872926	K562	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
9	CTCF	chr8:11872540-11872810	GM12866	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
10	CTCF	chr8:11872640-11872790	HRE	kidney:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
11	CTCF	chr8:11872461-11873003	A549	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
12	CTCF	chr8:11872640-11872790	HVMF	connective:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
13	CTCF	chr8:11872585-11872957	MCF-7	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
14	CTCF	chr8:11872680-11872830	HEK293	kidney:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
15	CTCF	chr8:11872640-11872790	Caco-2	colon:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
16	CTCF	chr8:11872740-11872890	AG10803	skin:	n/a	n/a
17	CTCF	chr8:11872618-11872868	GM13977	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
18	CTCF	chr8:11872640-11872837	Lung_OC	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
19	CTCF	chr8:11872583-11872909	Spleen_OC	spleen:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
20	CTCF	chr8:11872640-11872790	HCM	heart:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
21	CTCF	chr8:11872660-11872810	BE2_C	brain:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
22	CTCF	chr8:11872640-11872790	AG09319	gingival:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
23	CTCF	chr8:11872640-11872790	HCPEpiC	choroid plexus:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
24	CTCF	chr8:11872660-11872810	MCF-7	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
25	CTCF	chr8:11872640-11872790	AG04450	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
26	CTCF	chr8:11872553-11872908	HepG2	liver:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
27	CTCF	chr8:11872427-11873106	K562	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
28	CTCF	chr8:11872640-11872790	K562	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
29	CTCF	chr8:11872618-11872885	H1-hESC	embryonic stem cell:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
30	CTCF	chr8:11872660-11872810	GM12864	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
31	CTCF	chr8:11872760-11872910	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr8:11872640-11872790	GM12874	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
33	CTCF	chr8:11872660-11872810	GM12868	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
34	CTCF	chr8:11872613-11872877	Fibrobl	skin:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
35	CTCF	chr8:11872367-11873042	A549	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
36	CTCF	chr8:11872583-11872907	GM12892	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
37	CTCF	chr8:11872660-11872810	HCT-116	colon:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
38	CTCF	chr8:11872609-11872888	A549	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
39	CTCF	chr8:11872606-11872874	K562	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
40	CTCF	chr8:11872660-11872810	SAEC	small airway:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
41	CTCF	chr8:11872660-11872810	GM12865	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
42	CTCF	chr8:11872645-11872849	MCF-7	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
43	CTCF	chr8:11872621-11872890	Hela-S3	cervix:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
44	CTCF	chr8:11872660-11872810	GM12871	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
45	CTCF	chr8:11872640-11872790	SAEC	small airway:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
46	CTCF	chr8:11872760-11872910	GM12878	blood:	n/a	n/a
47	CTCF	chr8:11872840-11872990	HMEC	breast:	n/a	n/a
48	CTCF	chr8:11872640-11872790	GM12872	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
49	CTCF	chr8:11872640-11872790	HMF	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
50	CTCF	chr8:11872640-11872790	HUVEC	blood vessel:	n/a	chr8:11872722-11872738 chr8:11872721-11872739

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11882982-11883032	Caco-2	colon:	n/a
2	chr8:11882982-11883032	Caco-2	colon:	n/a
3	chr8:11872882-11872932	AG10803	skin:	n/a
4	chr8:11870063-11870113	CMK	blood:	n/a
5	chr8:11882962-11883012	NHDF-neo	bronchial:	n/a
6	chr8:11870063-11870113	HEK293	kidney:	embryo
7	chr8:11882962-11883012	SKMC	muscle:	n/a
8	chr8:11895252-11895302	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:11876646-11876696	HRE	kidney:	n/a
10	chr8:11872882-11872932	Hepatocyte	liver:	n/a
11	chr8:11882897-11882947	HCPEpiC	choroid plexus:	n/a
12	chr8:11870338-11870388	GM12892	blood:	n/a
13	chr8:11882982-11883032	LNCaP	prostate:	n/a
14	chr8:11872141-11872191	A549	lung:	n/a
15	chr8:11882962-11883012	Jurkat	blood:	n/a
16	chr8:11882897-11882947	GM12878	blood:	n/a
17	chr8:11882982-11883032	HCPEpiC	choroid plexus:	n/a
18	chr8:11882962-11883012	AG04450	lung:	fetal
19	chr8:11895252-11895302	IMR90	lung:	fetal
20	chr8:11872778-11872828	Hepatocyte	liver:	n/a
21	chr8:11876646-11876696	MCF-7	breast:	n/a
22	chr8:11870338-11870388	HUVEC	blood vessel:	n/a
23	chr8:11882962-11883012	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:11882962-11883012	RPTEC	kidney:	n/a
25	chr8:11882897-11882947	A549	lung:	n/a
26	chr8:11870338-11870388	HCT-116	colon:	n/a
27	chr8:11870338-11870388	AG04449	skin:	fetal
28	chr8:11872778-11872828	Caco-2	colon:	n/a
29	chr8:11872141-11872191	ECC-1	luminal epithelium:	n/a
30	chr8:11876646-11876696	RPTEC	kidney:	n/a
31	chr8:11872659-11872709	Hela-S3	cervix:	n/a
32	chr8:11872141-11872191	CMK	blood:	n/a
33	chr8:11872882-11872932	A549	lung:	n/a
34	chr8:11872882-11872932	U87	brain:	n/a
35	chr8:11870063-11870113	K562	blood:	n/a
36	chr8:11872778-11872828	ProgFib	skin:	n/a
37	chr8:11870338-11870388	GM19239	blood:	n/a
38	chr8:11870338-11870388	Hela-S3	cervix:	n/a
39	chr8:11895252-11895302	MCF-7	breast:	n/a
40	chr8:11870338-11870388	IMR90	lung:	fetal
41	chr8:11872778-11872828	GM12878	blood:	n/a
42	chr8:11895252-11895302	RPTEC	kidney:	n/a
43	chr8:11870338-11870388	ovcar-3	ovarian:	n/a
44	chr8:11876646-11876696	PANC-1	pancreas:	n/a
45	chr8:11872778-11872828	NHBE	bronchial:	n/a
46	chr8:11872778-11872828	BE2_C	brain:	n/a
47	chr8:11872882-11872932	SK-N-SH	brain:	n/a
48	chr8:11870063-11870113	ProgFib	skin:	n/a
49	chr8:11872141-11872191	T-47D	breast:	n/a
50	chr8:11895252-11895302	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
2	chr11:64863606..64864139-chr8:11882400..11882963,2	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000255016	TF binding region
ENSG00000254507	TF binding region
ENSG00000255098	TF binding region
OR7E160P	TF binding region
ENSG00000255016	CpG island
ENSG00000254507	CpG island
ENSG00000255098	CpG island
OR7E160P	CpG island
ENSG00000149823	chromatin interactions

Extended variants
information (count: 1191 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530469382	chr8:11866812-11866813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552241891	chr8:11866860-11866861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570490098	chr8:11866861-11866862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7823991	chr8:11866862-11866863	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs546902491	chr8:11866863-11866864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568736359	chr8:11866879-11866880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536166169	chr8:11866893-11866894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557347068	chr8:11866897-11866898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs386722355	chr8:11866906-11866907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138780537	chr8:11866907-11866908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558208851	chr8:11866908-11866909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573278035	chr8:11866912-11866913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566399012	chr8:11866915-11866916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541186520	chr8:11866920-11866921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368822152	chr8:11866934-11866935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185861986	chr8:11866939-11866940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192441543	chr8:11866950-11866951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373041660	chr8:11866962-11866963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541716151	chr8:11866990-11866991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs28657064	chr8:11867041-11867042	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs28495388	chr8:11867046-11867047	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs377064443	chr8:11867058-11867059	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs149415907	chr8:11867060-11867061	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs548744920	chr8:11867072-11867073	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs545512154	chr8:11867077-11867078	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs564182763	chr8:11867079-11867080	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs528192674	chr8:11867085-11867086	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs111765751	chr8:11867097-11867098	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs562270659	chr8:11867106-11867107	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs529559900	chr8:11867113-11867114	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs551287794	chr8:11867125-11867126	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs187666323	chr8:11867133-11867134	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs138483844	chr8:11867139-11867140	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs190637691	chr8:11867151-11867152	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs371430231	chr8:11867158-11867159	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs551498951	chr8:11867159-11867160	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs182879074	chr8:11867160-11867161	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs187226365	chr8:11867163-11867164	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs555485562	chr8:11867202-11867203	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143013861	chr8:11867206-11867207	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546694849	chr8:11867223-11867224	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs55798133	chr8:11867248-11867249	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs55805862	chr8:11867252-11867253	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535302408	chr8:11867256-11867257	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139058606	chr8:11867264-11867265	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575473040	chr8:11867273-11867274	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111989634	chr8:11867281-11867282	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192643562	chr8:11867284-11867285	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377619741	chr8:11867289-11867290	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370720455	chr8:11867308-11867309	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:143)

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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	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:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11866800-11867200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:11867000-11867200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:11867000-11867400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:11867000-11869800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:11867200-11868000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:11868000-11869800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:11869000-11869200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr8:11869800-11870200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:11869800-11870400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr8:11870200-11871000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:11870400-11872800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:11870800-11871200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:11871000-11871200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:11871200-11872800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:11871400-11871600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:11871400-11871800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:11871400-11872600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
18	chr8:11871600-11871800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:11871600-11871800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr8:11871600-11871800	Enhancers	Stomach Smooth Muscle	stomach
21	chr8:11871600-11872000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr8:11871600-11872000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:11871600-11872000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:11871600-11872000	Bivalent Enhancer	Fetal Stomach	stomach
25	chr8:11871600-11872000	Enhancers	HMEC	breast
26	chr8:11871800-11872000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr8:11871800-11872200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
28	chr8:11871800-11872200	Enhancers	Colon Smooth Muscle	Colon
29	chr8:11871800-11872400	Enhancers	Primary B cells from cord blood	blood
30	chr8:11871800-11872400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr8:11871800-11872400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:11871800-11872600	Active TSS	H9 Cell Line	embryonic stem cell
33	chr8:11871800-11872600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr8:11871800-11872600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr8:11871800-11872600	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr8:11871800-11872600	Active TSS	Brain Anterior Caudate	brain
37	chr8:11871800-11872600	Active TSS	Stomach Smooth Muscle	stomach
38	chr8:11871800-11872800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
39	chr8:11871800-11873000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:11872000-11872200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:11872000-11872200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:11872000-11872200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:11872000-11872200	Enhancers	Primary hematopoietic stem cells	blood
44	chr8:11872000-11872200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr8:11872000-11872200	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr8:11872000-11872200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr8:11872000-11872200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:11872000-11872200	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr8:11872000-11872200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr8:11872000-11872200	Enhancers	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links