Variant report

Variant	esv2762762
Chromosome Location	chr8:105189986-105247833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:273)
CpG islands
(count:549)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:105235242-105235626	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr8:105235838-105236141	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr8:105235221-105235500	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr8:105213207-105213368	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:105238181-105238219	HepG2	liver:	n/a	chr8:105238189-105238200 chr8:105238186-105238203
6	CEBPB	chr8:105200046-105200279	HepG2	liver:	n/a	chr8:105200154-105200165
7	CEBPB	chr8:105235232-105235543	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr8:105200098-105200302	A549	lung:	n/a	chr8:105200154-105200165
9	CEBPB	chr8:105218860-105219093	MCF-7	breast:	n/a	n/a
10	CEBPB	chr8:105234414-105234818	A549	lung:	n/a	chr8:105234647-105234660 chr8:105234649-105234660 chr8:105234647-105234660 chr8:105234647-105234660 chr8:105234649-105234660
11	CHD1	chr8:105235097-105235911	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr8:105235250-105236397	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr8:105235317-105235718	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr8:105235163-105235814	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr8:105235240-105236295	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr8:105235810-105235988	Fibrobl	skin:	n/a	n/a
17	CTCF	chr8:105236120-105236270	NHEK	skin:	n/a	n/a
18	CTCF	chr8:105235846-105235850	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:105235840-105235990	GM12871	blood:	n/a	n/a
20	CTCF	chr8:105235411-105235531	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:105236000-105236150	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr8:105194917-105194956	MCF-7	breast:	n/a	n/a
23	CTCF	chr8:105236220-105236370	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr8:105236080-105236230	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr8:105235320-105235470	HMEC	breast:	n/a	n/a
26	CTCF	chr8:105235780-105235930	GM12874	blood:	n/a	n/a
27	CTCF	chr8:105236302-105236315	Fibrobl	skin:	n/a	n/a
28	CTCF	chr8:105236200-105236350	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr8:105236020-105236170	GM12866	blood:	n/a	n/a
30	CTCF	chr8:105236200-105236350	AG10803	skin:	n/a	n/a
31	CTCF	chr8:105235800-105235968	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:105236100-105236250	AG09319	gingival:	n/a	n/a
33	CTCF	chr8:105236160-105236310	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr8:105235720-105235870	AG09319	gingival:	n/a	n/a
35	CTCF	chr8:105236160-105236310	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:105235818-105236013	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:105236020-105236170	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr8:105235540-105235690	NHEK	skin:	n/a	chr8:105235571-105235584
39	CTCF	chr8:105235820-105235970	SAEC	small airway:	n/a	n/a
40	CTCF	chr8:105244620-105244770	GM12866	blood:	n/a	n/a
41	CTCF	chr8:105236280-105236430	HAc	cerebellar:	n/a	n/a
42	CTCF	chr8:105235060-105235210	BJ	skin:	n/a	n/a
43	CTCF	chr8:105235851-105235984	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:105236017-105236022	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:105235820-105235970	HAc	cerebellar:	n/a	n/a
46	CTCF	chr8:105236220-105236470	BJ	skin:	n/a	n/a
47	CTCF	chr8:105236120-105236270	HRE	kidney:	n/a	n/a
48	CTCF	chr8:105213034-105213085	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:105236160-105236310	HMF	breast:	n/a	n/a
50	CTCF	chr8:105236200-105236350	HBMEC	blood vessel:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:105235943-105235993	SK-N-MC	brain:	n/a
2	chr8:105235715-105235765	GM06990	blood:	n/a
3	chr8:105235385-105235435	GM12892	blood:	n/a
4	chr8:105235606-105235656	H1-hESC	embryonic stem cell:	embryo
5	chr8:105236155-105236205	HAEpiC	amniotic membrane:	n/a
6	chr8:105244257-105244307	HUVEC	blood vessel:	n/a
7	chr8:105238428-105238478	AG10803	skin:	n/a
8	chr8:105235978-105236028	NH-A	brain:	n/a
9	chr8:105235943-105235993	HepG2	liver:	n/a
10	chr8:105238428-105238478	A549	lung:	n/a
11	chr8:105235606-105235656	HNPCEpiC	eye:	n/a
12	chr8:105235184-105235234	BE2_C	brain:	n/a
13	chr8:105235715-105235765	BJ	skin:	n/a
14	chr8:105236155-105236205	HNPCEpiC	eye:	n/a
15	chr8:105235943-105235993	NT2-D1	testis:	n/a
16	chr8:105238428-105238478	HIPEpiC	eye:	n/a
17	chr8:105244257-105244307	ECC-1	luminal epithelium:	n/a
18	chr8:105235978-105236028	NHDF-neo	bronchial:	n/a
19	chr8:105238428-105238478	T-47D	breast:	n/a
20	chr8:105238428-105238478	GM06990	blood:	n/a
21	chr8:105235606-105235656	HIPEpiC	eye:	n/a
22	chr8:105235943-105235993	HCPEpiC	choroid plexus:	n/a
23	chr8:105235385-105235435	HEK293	kidney:	embryo
24	chr8:105235978-105236028	HUVEC	blood vessel:	n/a
25	chr8:105235606-105235656	HCPEpiC	choroid plexus:	n/a
26	chr8:105235978-105236028	A549	lung:	n/a
27	chr8:105235606-105235656	K562	blood:	n/a
28	chr8:105244257-105244307	HRPEpiC	eye:	n/a
29	chr8:105244257-105244307	K562	blood:	n/a
30	chr8:105235184-105235234	HMEC	breast:	n/a
31	chr8:105235184-105235234	Hepatocyte	liver:	n/a
32	chr8:105235943-105235993	H1-hESC	embryonic stem cell:	embryo
33	chr8:105235978-105236028	ProgFib	skin:	n/a
34	chr8:105244257-105244307	Hela-S3	cervix:	n/a
35	chr8:105244257-105244307	MCF10A-Er-Src	breast:	n/a
36	chr8:105236155-105236205	T-47D	breast:	n/a
37	chr8:105235715-105235765	SAEC	small airway:	n/a
38	chr8:105244257-105244307	CMK	blood:	n/a
39	chr8:105235184-105235234	GM12878	blood:	n/a
40	chr8:105236155-105236205	Hepatocyte	liver:	n/a
41	chr8:105235715-105235765	HMEC	breast:	n/a
42	chr8:105235385-105235435	PrEC	prostate:	n/a
43	chr8:105235385-105235435	HNPCEpiC	eye:	n/a
44	chr8:105235385-105235435	HRE	kidney:	n/a
45	chr8:105235978-105236028	HCT-116	colon:	n/a
46	chr8:105235943-105235993	Caco-2	colon:	n/a
47	chr8:105236155-105236205	GM19239	blood:	n/a
48	chr8:105235715-105235765	GM19239	blood:	n/a
49	chr8:105235184-105235234	LNCaP	prostate:	n/a
50	chr8:105235943-105235993	HUVEC	blood vessel:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:105234317..105237730-chr8:105237758..105240241,3	MCF-7	breast:
2	chr8:105242316..105245331-chr8:105245427..105248797,3	K562	blood:
3	chr8:105234081..105236200-chr8:105240839..105243210,2	MCF-7	breast:
4	chr8:105173950..105176285-chr8:105193428..105195940,2	MCF-7	breast:
5	chr8:105241452..105243816-chr8:105245427..105247630,2	K562	blood:
6	chr8:105241452..105243816-chr8:105245427..105247630,2	K562	blood:
7	chr8:105242800..105244338-chr8:105249845..105251737,2	MCF-7	breast:
8	chr8:105225180..105227788-chr8:105237415..105240052,2	MCF-7	breast:
9	chr8:105207373..105209743-chr8:105210313..105212333,2	MCF-7	breast:
10	chr6:107307364..107309085-chr8:105230341..105231858,2	MCF-7	breast:
11	chr8:105225180..105227788-chr8:105237415..105240052,2	MCF-7	breast:
12	chr8:105242316..105245331-chr8:105245427..105248797,3	K562	blood:
13	chr8:105185671..105187346-chr8:105198346..105200773,2	MCF-7	breast:
14	chr8:105207373..105209743-chr8:105210313..105212333,2	MCF-7	breast:

No data

Variant related genes	Relation type
RIMS2	TF binding region
RIMS2	CpG island
ENSG00000176406	chromatin interactions

Extended variants
information (count: 1768 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:1768 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573612826	chr8:105189990-105189991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554836113	chr8:105190013-105190014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76379322	chr8:105190042-105190043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559072044	chr8:105190090-105190091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577408771	chr8:105190202-105190203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117509322	chr8:105190209-105190210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563146220	chr8:105190211-105190212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530689330	chr8:105190233-105190234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145691527	chr8:105190267-105190268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140205202	chr8:105190276-105190277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561919578	chr8:105190330-105190331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529335618	chr8:105190334-105190335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547563215	chr8:105190343-105190344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76832295	chr8:105190351-105190352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539941134	chr8:105190416-105190417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537754052	chr8:105190477-105190478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570276640	chr8:105190503-105190504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs57992869	chr8:105190556-105190557	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556050835	chr8:105190600-105190601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573556031	chr8:105190662-105190663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74720285	chr8:105190673-105190674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79457613	chr8:105190728-105190729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577274873	chr8:105190734-105190735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188560868	chr8:105190758-105190759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563109775	chr8:105190770-105190771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575430404	chr8:105190798-105190799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577385208	chr8:105190856-105190857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190568497	chr8:105190879-105190880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561276172	chr8:105190899-105190900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72685033	chr8:105190902-105190903	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs547766351	chr8:105190950-105190951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182399441	chr8:105190958-105190959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542669722	chr8:105190988-105190989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533429674	chr8:105190991-105190992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551935892	chr8:105190992-105190993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570125425	chr8:105190993-105190994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371098724	chr8:105190998-105190999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560891649	chr8:105191004-105191005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549404902	chr8:105191007-105191008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528056774	chr8:105191014-105191015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148113345	chr8:105191030-105191031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535013216	chr8:105191040-105191041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573601950	chr8:105191057-105191058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149388513	chr8:105191096-105191097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577235833	chr8:105191104-105191105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73301323	chr8:105191116-105191117	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556666222	chr8:105191144-105191145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575336728	chr8:105191157-105191158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555997794	chr8:105191294-105191295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542766725	chr8:105191329-105191330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
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
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
Multiple myeloma	16461302	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
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
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:105188400-105211800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:105188600-105190800	Enhancers	NHEK	skin
3	chr8:105188800-105190200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:105188800-105190400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:105188800-105192800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:105189600-105190000	Weak transcription	HMEC	breast
7	chr8:105190000-105191000	Enhancers	HMEC	breast
8	chr8:105190200-105190600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr8:105190400-105190600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:105190400-105190800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:105190600-105191800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:105190800-105196200	Weak transcription	NHEK	skin
13	chr8:105191000-105196200	Weak transcription	HMEC	breast
14	chr8:105192200-105192600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr8:105192200-105192800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:105192600-105193800	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr8:105192800-105193200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:105192800-105196000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:105193200-105197400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:105195200-105196200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr8:105196000-105196400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:105196200-105196600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:105196200-105196600	Enhancers	HMEC	breast
24	chr8:105196200-105196800	Enhancers	NHEK	skin
25	chr8:105202200-105205000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:105204400-105206000	Enhancers	Placenta Amnion	Placenta Amnion
27	chr8:105205000-105205200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:105205000-105205200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:105205200-105210800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:105206000-105207200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr8:105207800-105208000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:105208000-105209800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr8:105209800-105210600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:105210400-105211600	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr8:105210400-105213600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr8:105210600-105211400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:105210800-105213200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:105210800-105214000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr8:105211400-105212000	Enhancers	HMEC	breast
40	chr8:105211400-105213200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:105211400-105213200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:105211600-105211800	Enhancers	NHEK	skin
43	chr8:105211600-105213200	Enhancers	Placenta Amnion	Placenta Amnion
44	chr8:105211800-105212200	Enhancers	Muscle Satellite Cultured Cells	--
45	chr8:105211800-105212400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:105211800-105212400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr8:105211800-105212400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr8:105211800-105212400	Enhancers	NH-A	brain
49	chr8:105211800-105212400	Flanking Active TSS	NHEK	skin
50	chr8:105211800-105213200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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