Variant report

Variant	esv3340384
Chromosome Location	chr8:1199645-1204643
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:673)
Chromatin interactive
region (count:1)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr8:1201577-1202272	GM12878	blood:	n/a	n/a
2	BCL3	chr8:1202523-1202866	GM12878	blood:	n/a	chr8:1202682-1202695
3	BCL3	chr8:1201626-1202699	GM12878	blood:	n/a	chr8:1202682-1202695
4	CTCF	chr8:1201748-1201810	GM19239	blood:	n/a	n/a
5	CTCF	chr8:1202155-1202201	GM19239	blood:	n/a	n/a
6	CTCF	chr8:1202441-1202492	MCF-7	breast:	n/a	n/a
7	CTCF	chr8:1202246-1202421	GM19239	blood:	n/a	n/a
8	CTCF	chr8:1202285-1202287	MCF-7	breast:	n/a	n/a
9	CTCF	chr8:1202504-1202525	GM19239	blood:	n/a	n/a
10	CTCF	chr8:1202117-1202150	GM19239	blood:	n/a	n/a
11	GATA2	chr8:1202795-1203589	SH-SY5Y	brain:	n/a	chr8:1203320-1203337
12	GATA3	chr8:1203109-1203906	SH-SY5Y	brain:	n/a	chr8:1203320-1203337
13	MAX	chr8:1202373-1202591	K562	blood:	n/a	n/a
14	MAX	chr8:1201696-1201697	A549	lung:	n/a	n/a
15	MAX	chr8:1201720-1201953	NB4	blood:	n/a	chr8:1201910-1201919
16	MAX	chr8:1201562-1201894	K562	blood:	n/a	chr8:1201679-1201688
17	MYC	chr8:1202453-1202498	MCF-7	breast:	n/a	n/a
18	MYC	chr8:1202319-1202339	MCF-7	breast:	n/a	n/a
19	MYC	chr8:1202357-1202434	MCF-7	breast:	n/a	n/a
20	MYC	chr8:1202098-1202491	MCF-7	breast:	n/a	n/a
21	MYC	chr8:1202348-1202517	GM12878	blood:	n/a	n/a
22	MYC	chr8:1202092-1202511	MCF-7	breast:	n/a	n/a
23	NFATC1	chr8:1201665-1202663	GM12878	blood:	n/a	n/a
24	NFATC1	chr8:1201607-1202038	GM12878	blood:	n/a	n/a
25	NR2C2	chr8:1201653-1202582	GM12878	blood:	n/a	n/a
26	PBX3	chr8:1201811-1202421	GM12878	blood:	n/a	n/a
27	POLR2A	chr8:1202021-1202525	MCF-7	breast:	n/a	n/a
28	POLR2A	chr8:1201763-1201892	MCF-7	breast:	n/a	n/a
29	POLR2A	chr8:1201748-1202597	MCF-7	breast:	n/a	n/a
30	POLR2A	chr8:1201974-1202007	HUVEC	blood vessel:	n/a	n/a
31	POLR2A	chr8:1202297-1202408	H1-hESC	embryonic stem cell:	n/a	n/a
32	SUZ12	chr8:1201683-1202587	H1-hESC	embryonic stem cell:	n/a	n/a
33	TCF3	chr8:1201767-1202378	GM12878	blood:	n/a	n/a
34	USF1	chr8:1201770-1202082	K562	blood:	n/a	n/a
35	USF1	chr8:1201526-1201750	K562	blood:	n/a	n/a
36	USF2	chr8:1201841-1202101	HepG2	liver:	n/a	n/a
37	USF2	chr8:1202376-1202583	HepG2	liver:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1204483-1204533	AG04449	skin:	fetal
2	chr8:1203598-1203648	AoSMC	blood vessel:	n/a
3	chr8:1204483-1204533	AG04449	skin:	fetal
4	chr8:1203598-1203648	AoSMC	blood vessel:	n/a
5	chr8:1200583-1200633	PANC-1	pancreas:	n/a
6	chr8:1204530-1204580	HCM	heart:	n/a
7	chr8:1200861-1200911	SK-N-MC	brain:	n/a
8	chr8:1200896-1200946	HUVEC	blood vessel:	n/a
9	chr8:1204530-1204580	GM12891	blood:	n/a
10	chr8:1203186-1203236	HNPCEpiC	eye:	n/a
11	chr8:1202533-1202583	PrEC	prostate:	n/a
12	chr8:1202762-1202812	ovcar-3	ovarian:	n/a
13	chr8:1203598-1203648	HMEC	breast:	n/a
14	chr8:1202533-1202583	HEEpiC	esophagus:	n/a
15	chr8:1200861-1200911	NT2-D1	testis:	n/a
16	chr8:1200861-1200911	ovcar-3	ovarian:	n/a
17	chr8:1200525-1200575	NHDF-neo	bronchial:	n/a
18	chr8:1202762-1202812	BE2_C	brain:	n/a
19	chr8:1203186-1203236	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:1200583-1200633	ovcar-3	ovarian:	n/a
21	chr8:1201838-1201888	HCPEpiC	choroid plexus:	n/a
22	chr8:1203598-1203648	Caco-2	colon:	n/a
23	chr8:1200896-1200946	NB4	blood:	n/a
24	chr8:1202762-1202812	IMR90	lung:	fetal
25	chr8:1200525-1200575	SK-N-SH	brain:	n/a
26	chr8:1203186-1203236	HIPEpiC	eye:	n/a
27	chr8:1200896-1200946	PANC-1	pancreas:	n/a
28	chr8:1202762-1202812	HRPEpiC	eye:	n/a
29	chr8:1202533-1202583	AG04449	skin:	fetal
30	chr8:1204530-1204580	AoSMC	blood vessel:	n/a
31	chr8:1201838-1201888	BJ	skin:	n/a
32	chr8:1203598-1203648	PFSK-1	brain:	n/a
33	chr8:1204483-1204533	HCM	heart:	n/a
34	chr8:1203598-1203648	AG09309	skin:	n/a
35	chr8:1200583-1200633	PFSK-1	brain:	n/a
36	chr8:1204530-1204580	HRE	kidney:	n/a
37	chr8:1203186-1203236	MCF10A-Er-Src	breast:	n/a
38	chr8:1203598-1203648	SK-N-SH	brain:	n/a
39	chr8:1201838-1201888	T-47D	breast:	n/a
40	chr8:1202533-1202583	NHDF-neo	bronchial:	n/a
41	chr8:1202762-1202812	H1-hESC	embryonic stem cell:	embryo
42	chr8:1200896-1200946	HCT-116	colon:	n/a
43	chr8:1200525-1200575	Caco-2	colon:	n/a
44	chr8:1203186-1203236	NHDF-neo	bronchial:	n/a
45	chr8:1200583-1200633	U87	brain:	n/a
46	chr8:1200583-1200633	HAEpiC	amniotic membrane:	n/a
47	chr8:1203598-1203648	SK-N-SH_RA	brain:	n/a
48	chr8:1200896-1200946	RPTEC	kidney:	n/a
49	chr8:1204530-1204580	A549	lung:	n/a
50	chr8:1200896-1200946	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:1201588..1203243-chr8:1212763..1215262,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLGAP2-7	chr8:1199822-1199999	l_3529_chr8:1197061-1199999_testes
2	lnc-FBXO25-5	chr8:1200380-1200572	XLOC_006683
3	lnc-FBXO25-5	chr8:1200373-1200572	ENSG00000254269
4	lnc-FBXO25-5	chr8:1200323-1200572	NONHSAT124640
5	lnc-FBXO25-5	chr8:1200380-1200572	XLOC_006683

No data

Variant related genes	Relation type
ENSG00000254269	TF binding region
ENSG00000254160	TF binding region
ENSG00000254269	CpG island
ENSG00000254160	CpG island
CDCA3	miRNA target sites

Extended variants
information (count: 437 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:437 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117332333	chr8:1199647-1199648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139697127	chr8:1199654-1199655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182544387	chr8:1199657-1199658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149418136	chr8:1199675-1199676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549499827	chr8:1199682-1199683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185714782	chr8:1199689-1199690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569390898	chr8:1199712-1199713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545241758	chr8:1199791-1199792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560649480	chr8:1199792-1199793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191952817	chr8:1199799-1199800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144837556	chr8:1199802-1199803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535013126	chr8:1199803-1199804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115820326	chr8:1199817-1199818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183755737	chr8:1199839-1199840	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs575824919	chr8:1199848-1199849	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs527812200	chr8:1199858-1199859	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs78432553	chr8:1199866-1199867	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs577410968	chr8:1199906-1199907	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs567704222	chr8:1199922-1199923	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs201017080	chr8:1199941-1199942	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs7013470	chr8:1199943-1199944	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs571540527	chr8:1199947-1199948	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs113254926	chr8:1199950-1199951	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs573144103	chr8:1199961-1199962	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs189159000	chr8:1199973-1199974	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs192245169	chr8:1199985-1199986	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs182441849	chr8:1199988-1199989	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs529867183	chr8:1199990-1199991	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs73531966	chr8:1199996-1199997	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs187136936	chr8:1199999-1200000	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs560501469	chr8:1200005-1200006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553716092	chr8:1200009-1200010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6989858	chr8:1200041-1200042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376681341	chr8:1200055-1200056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10108098	chr8:1200093-1200094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs191622398	chr8:1200100-1200101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs151132996	chr8:1200115-1200116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548632981	chr8:1200128-1200129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs13269338	chr8:1200131-1200132	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs542966709	chr8:1200138-1200139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13269349	chr8:1200139-1200140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs77972347	chr8:1200156-1200157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6990056	chr8:1200198-1200199	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs545662992	chr8:1200200-1200201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553402847	chr8:1200208-1200209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566154919	chr8:1200216-1200217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573172125	chr8:1200217-1200218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112927047	chr8:1200218-1200219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542184867	chr8:1200219-1200220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141150987	chr8:1200228-1200229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
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
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
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Breast cancer	20932292	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Congenital diaphragmatic hernia	21064195	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1197200-1201800	Weak transcription	Gastric	stomach
2	chr8:1197400-1201600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:1197400-1202000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr8:1197400-1202000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr8:1199000-1201600	Weak transcription	Pancreas	Pancrea
6	chr8:1199200-1200200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:1199400-1201800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr8:1200200-1200600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:1200200-1200600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:1200600-1201800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:1200600-1206400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:1201400-1201600	Weak transcription	Spleen	Spleen
13	chr8:1201600-1202400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:1201600-1202400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:1201600-1202600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
16	chr8:1201600-1202800	ZNF genes & repeats	Pancreas	Pancrea
17	chr8:1201800-1202000	ZNF genes & repeats	Spleen	Spleen
18	chr8:1201800-1202400	Strong transcription	H9 Cell Line	embryonic stem cell
19	chr8:1201800-1202600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:1201800-1202600	ZNF genes & repeats	Fetal Kidney	kidney
21	chr8:1201800-1202800	ZNF genes & repeats	Gastric	stomach
22	chr8:1202000-1202200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr8:1202000-1202200	Bivalent/Poised TSS	Fetal Brain Male	brain
24	chr8:1202000-1202600	ZNF genes & repeats	Fetal Lung	lung
25	chr8:1202000-1203400	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr8:1202200-1202600	Enhancers	Brain Anterior Caudate	brain
27	chr8:1202200-1202600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr8:1202400-1202600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
29	chr8:1202400-1202800	Enhancers	Brain Angular Gyrus	brain
30	chr8:1202600-1203600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr8:1202600-1204000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr8:1202600-1204200	Weak transcription	Brain Anterior Caudate	brain
33	chr8:1202600-1207200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr8:1202600-1209200	Weak transcription	Fetal Lung	lung
35	chr8:1202800-1204000	Weak transcription	Brain Angular Gyrus	brain
36	chr8:1202800-1210800	Weak transcription	Gastric	stomach
37	chr8:1203000-1203800	Enhancers	Fetal Brain Male	brain
38	chr8:1203000-1204000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr8:1203400-1203800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr8:1203800-1204600	Bivalent Enhancer	Fetal Brain Male	brain
41	chr8:1203800-1205000	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr8:1204000-1204200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
43	chr8:1204000-1205000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr8:1204000-1205200	Enhancers	Brain Angular Gyrus	brain
45	chr8:1204200-1205000	Enhancers	Brain Anterior Caudate	brain

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