Variant report

Variant	nsv890934
Chromosome Location	chr8:58037522-58112053
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:301)
CpG islands
(count:1040)
Chromatin interactive
region (count:16)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:58049285-58049314	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr8:58105853-58106191	K562	blood:	n/a	n/a
3	CBX3	chr8:58105849-58106177	K562	blood:	n/a	n/a
4	CCNT2	chr8:58105900-58106102	K562	blood:	n/a	n/a
5	CEBPB	chr8:58053880-58054182	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr8:58061157-58061275	K562	blood:	n/a	n/a
7	CEBPB	chr8:58061093-58061371	HepG2	liver:	n/a	chr8:58061133-58061146
8	CEBPB	chr8:58053845-58054196	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:58053930-58054161	K562	blood:	n/a	n/a
10	CEBPB	chr8:58059648-58059906	MCF-7	breast:	n/a	chr8:58059752-58059765 chr8:58059752-58059763
11	CEBPB	chr8:58053895-58054196	IMR90	lung:	n/a	n/a
12	CEBPB	chr8:58053850-58054200	A549	lung:	n/a	n/a
13	CEBPB	chr8:58061084-58061385	IMR90	lung:	n/a	chr8:58061133-58061146
14	CHD2	chr8:58105531-58106370	K562	blood:	n/a	n/a
15	CTCF	chr8:58094880-58095030	GM12871	blood:	n/a	n/a
16	CTCF	chr8:58094820-58094970	GM12873	blood:	n/a	n/a
17	CTCF	chr8:58094820-58094970	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr8:58094800-58094950	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:58094880-58095030	AG09309	skin:	n/a	n/a
20	CTCF	chr8:58094840-58094990	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr8:58057966-58058146	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr8:58094880-58095030	HCT-116	colon:	n/a	n/a
23	CTCF	chr8:58077023-58077061	GM10248	blood:	n/a	n/a
24	CTCF	chr8:58094715-58095113	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:58094720-58095010	HVMF	connective:	n/a	n/a
26	CTCF	chr8:58077022-58077077	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:58094840-58094990	HRE	kidney:	n/a	n/a
28	CTCF	chr8:58094829-58095024	LNCaP	prostate:	n/a	n/a
29	CTCF	chr8:58094880-58095030	Caco-2	colon:	n/a	n/a
30	CTCF	chr8:58094820-58094970	NHEK	skin:	n/a	n/a
31	CTCF	chr8:58058040-58058190	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:58094780-58094930	AG09309	skin:	n/a	n/a
33	CTCF	chr8:58094781-58095030	A549	lung:	n/a	n/a
34	CTCF	chr8:58101060-58101210	HEK293	kidney:	n/a	n/a
35	CTCF	chr8:58094882-58094957	HepG2	liver:	n/a	n/a
36	CTCF	chr8:58100977-58101320	K562	blood:	n/a	n/a
37	CTCF	chr8:58094830-58095032	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:58058300-58058319	GM13976	blood:	n/a	n/a
39	CTCF	chr8:58094854-58094974	GM20000	blood:	n/a	n/a
40	CTCF	chr8:58094900-58095050	HCM	heart:	n/a	n/a
41	CTCF	chr8:58058011-58058097	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr8:58062327-58062355	Fibrobl	skin:	n/a	n/a
43	CTCF	chr8:58094880-58095030	GM06990	blood:	n/a	n/a
44	CTCF	chr8:58094688-58095149	A549	lung:	n/a	n/a
45	CTCF	chr8:58094840-58094990	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr8:58094862-58094976	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr8:58058000-58058150	GM06990	blood:	n/a	n/a
48	CTCF	chr8:58094720-58094870	HFF	foreskin:	n/a	n/a
49	CTCF	chr8:58057995-58058139	GM12878	blood:	n/a	n/a
50	CTCF	chr8:58094875-58095005	GM10248	blood:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58054756-58054806	GM12878	blood:	n/a
2	chr8:58059068-58059118	HCM	heart:	n/a
3	chr8:58053663-58053713	HCM	heart:	n/a
4	chr8:58054756-58054806	GM12878	blood:	n/a
5	chr8:58059068-58059118	HCM	heart:	n/a
6	chr8:58053663-58053713	HCM	heart:	n/a
7	chr8:58056175-58056225	H1-hESC	embryonic stem cell:	embryo
8	chr8:58055168-58055218	NHDF-neo	bronchial:	n/a
9	chr8:58055876-58055926	AoSMC	blood vessel:	n/a
10	chr8:58056751-58056801	SAEC	small airway:	n/a
11	chr8:58057665-58057715	NHBE	bronchial:	n/a
12	chr8:58056113-58056163	HEK293	kidney:	embryo
13	chr8:58059068-58059118	AG09309	skin:	n/a
14	chr8:58106598-58106648	NHDF-neo	bronchial:	n/a
15	chr8:58057665-58057715	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:58106094-58106144	GM19239	blood:	n/a
17	chr8:58053663-58053713	Caco-2	colon:	n/a
18	chr8:58055591-58055641	HepG2	liver:	n/a
19	chr8:58056751-58056801	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:58106598-58106648	HRCEpiC	kidney:	n/a
21	chr8:58056751-58056801	MCF10A-Er-Src	breast:	n/a
22	chr8:58054756-58054806	GM12892	blood:	n/a
23	chr8:58056751-58056801	Hepatocyte	liver:	n/a
24	chr8:58106598-58106648	NH-A	brain:	n/a
25	chr8:58106155-58106205	T-47D	breast:	n/a
26	chr8:58053663-58053713	NHBE	bronchial:	n/a
27	chr8:58055591-58055641	HRE	kidney:	n/a
28	chr8:58106520-58106570	A549	lung:	n/a
29	chr8:58055876-58055926	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:58055876-58055926	GM12892	blood:	n/a
31	chr8:58056175-58056225	SK-N-MC	brain:	n/a
32	chr8:58056175-58056225	SK-N-SH	brain:	n/a
33	chr8:58106155-58106205	BE2_C	brain:	n/a
34	chr8:58059068-58059118	Hela-S3	cervix:	n/a
35	chr8:58059068-58059118	HL-60	blood:	n/a
36	chr8:58057665-58057715	GM06990	blood:	n/a
37	chr8:58056113-58056163	MCF-7	breast:	n/a
38	chr8:58055168-58055218	LNCaP	prostate:	n/a
39	chr8:58053663-58053713	ProgFib	skin:	n/a
40	chr8:58054756-58054806	HCM	heart:	n/a
41	chr8:58106155-58106205	HRE	kidney:	n/a
42	chr8:58056501-58056551	HCM	heart:	n/a
43	chr8:58059068-58059118	H1-hESC	embryonic stem cell:	embryo
44	chr8:58056026-58056076	Caco-2	colon:	n/a
45	chr8:58055168-58055218	AG10803	skin:	n/a
46	chr8:58056751-58056801	HRCEpiC	kidney:	n/a
47	chr8:58056026-58056076	BE2_C	brain:	n/a
48	chr8:58055591-58055641	ProgFib	skin:	n/a
49	chr8:58106520-58106570	Hepatocyte	liver:	n/a
50	chr8:58056026-58056076	AG04450	lung:	fetal

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58098067..58099836-chr8:58101928..58103636,2	K562	blood:
2	chr8:58057960..58058531-chr8:58255912..58256499,2	MCF-7	breast:
3	chr8:58094338..58095391-chr8:58255624..58256416,4	MCF-7	breast:
4	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
5	chr8:58048196..58050433-chr8:58051015..58053775,2	K562	blood:
6	chr8:58094799..58095495-chr8:58255642..58256690,5	MCF-7	breast:
7	chr8:58048196..58050433-chr8:58051015..58053775,2	K562	blood:
8	chr8:58104914..58107604-chr8:58109994..58112221,3	K562	blood:
9	chr8:58076519..58079288-chr8:58083789..58085655,2	K562	blood:
10	chr8:58076519..58079288-chr8:58083789..58085655,2	K562	blood:
11	chr8:58098067..58099836-chr8:58101928..58103636,2	K562	blood:
12	chr8:58094506..58095013-chr8:58135741..58136318,2	MCF-7	breast:
13	chr8:57905221..57907345-chr8:58041168..58043040,2	MCF-7	breast:
14	chr8:58083900..58086328-chr8:58091891..58093782,2	K562	blood:
15	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
16	chr8:58083900..58086328-chr8:58091891..58093782,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58106149-58106248	ENSG00000253301.1
2	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
3	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
4	lnc-FAM110B-8	chr8:58055271-58055444	NONHSAT126727
5	lnc-FAM110B-8	chr8:58063159-58063293	NONHSAT126727
6	lnc-FAM110B-8	chr8:58106179-58106275	ENSG00000253301.1

No data

Variant related genes	Relation type
RNA5SP266	TF binding region
ENSG00000220984	TF binding region
ENSG00000253301	TF binding region
RNA5SP266	CpG island
ENSG00000220984	CpG island
ENSG00000253301	CpG island
ENSG00000253871	chromatin interactions
ENSG00000253301	chromatin interactions
ENSG00000104331	chromatin interactions

Extended variants
information (count: 895 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10504217	chr8:58037522-58037523	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191738985	chr8:58037558-58037559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148643155	chr8:58037627-58037628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72649115	chr8:58037631-58037632	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs570417378	chr8:58037633-58037634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72649117	chr8:58037639-58037640	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549961150	chr8:58037712-58037713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62512041	chr8:58038231-58038232	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185453011	chr8:58038260-58038261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576595071	chr8:58038263-58038264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150880410	chr8:58038277-58038278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529454007	chr8:58038297-58038298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527238213	chr8:58038298-58038299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189247072	chr8:58038302-58038303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565458828	chr8:58038339-58038340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564189684	chr8:58038366-58038367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143111824	chr8:58039370-58039371	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs553332610	chr8:58039377-58039378	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs570662682	chr8:58041109-58041110	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192943632	chr8:58041123-58041124	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs567379674	chr8:58041162-58041163	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536218029	chr8:58041220-58041221	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs553025901	chr8:58041245-58041246	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs112080497	chr8:58041265-58041266	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs113866613	chr8:58041266-58041267	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs575342805	chr8:58041322-58041323	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs184633273	chr8:58041323-58041324	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189752989	chr8:58041325-58041326	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs181006070	chr8:58041334-58041335	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs553197652	chr8:58041342-58041343	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566631180	chr8:58041345-58041346	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531530575	chr8:58041354-58041355	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs34332932	chr8:58041384-58041385	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542741809	chr8:58041407-58041408	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185267830	chr8:58041445-58041446	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189627931	chr8:58041455-58041456	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs112480460	chr8:58041456-58041457	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548416471	chr8:58041461-58041462	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186167495	chr8:58041463-58041464	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530973935	chr8:58041528-58041529	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190534637	chr8:58041556-58041557	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558865533	chr8:58041607-58041608	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs145590290	chr8:58041639-58041640	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529790819	chr8:58041674-58041675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546749884	chr8:58041679-58041680	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566335053	chr8:58041707-58041708	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538673750	chr8:58041711-58041712	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558524788	chr8:58041713-58041714	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs200473644	chr8:58041730-58041731	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112485834	chr8:58041737-58041738	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Bipolar disorder	19114987	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58036600-58037800	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr8:58038200-58038400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:58043200-58043800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:58043200-58043800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:58047000-58047600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr8:58054600-58055000	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr8:58054800-58055000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:58054800-58055000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
9	chr8:58054800-58055000	Bivalent Enhancer	Fetal Thymus	thymus
10	chr8:58054800-58055000	Enhancers	Pancreas	Pancrea
11	chr8:58054800-58055200	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
12	chr8:58054800-58055200	Bivalent Enhancer	Fetal Stomach	stomach
13	chr8:58054800-58055400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
14	chr8:58054800-58055600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr8:58054800-58055600	Active TSS	Brain Anterior Caudate	brain
16	chr8:58054800-58055600	Bivalent Enhancer	Placenta	Placenta
17	chr8:58054800-58055800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
18	chr8:58054800-58055800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
19	chr8:58054800-58056000	Enhancers	Lung	lung
20	chr8:58054800-58056200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr8:58054800-58056400	Active TSS	Brain Germinal Matrix	brain
22	chr8:58054800-58057000	Active TSS	Fetal Brain Female	brain
23	chr8:58055000-58055200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
24	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr8:58055000-58055200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
27	chr8:58055000-58055200	Flanking Active TSS	Brain Angular Gyrus	brain
28	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
29	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Right Ventricle	heart
30	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
31	chr8:58055000-58055400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:58055000-58055400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr8:58055000-58055400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:58055000-58055400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
35	chr8:58055000-58055400	Flanking Active TSS	Pancreas	Pancrea
36	chr8:58055000-58055400	Enhancers	Spleen	Spleen
37	chr8:58055000-58055400	Bivalent Enhancer	HMEC	breast
38	chr8:58055000-58055600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr8:58055000-58055600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr8:58055000-58055600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
41	chr8:58055000-58055600	Bivalent Enhancer	Left Ventricle	heart
42	chr8:58055000-58055600	Active TSS	Right Atrium	heart
43	chr8:58055000-58055600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
44	chr8:58055000-58055600	Bivalent Enhancer	Thymus	Thymus
45	chr8:58055000-58055800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr8:58055000-58056000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:58055000-58056000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr8:58055000-58056000	Bivalent Enhancer	Ovary	ovary
49	chr8:58055200-58055400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr8:58055200-58055400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood

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