Variant report

Variant	nsv891436
Chromosome Location	chr8:126283766-126345076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:101)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:126342754..126344650-chr8:126346334..126348343,3	K562	blood:
2	chr8:126290403..126294435-chr8:126303618..126306610,4	K562	blood:
3	chr8:126315465..126318192-chr8:126341334..126342938,2	K562	blood:
4	chr8:126283879..126287098-chr8:126289140..126291457,3	K562	blood:
5	chr8:126322775..126325077-chr8:126329486..126331781,2	K562	blood:
6	chr8:126288880..126291551-chr8:126340107..126343091,2	K562	blood:
7	chr8:126295600..126298519-chr8:126310859..126313125,2	K562	blood:
8	chr8:126322775..126325077-chr8:126329486..126331781,2	K562	blood:
9	chr8:126303707..126305559-chr8:126307667..126310106,2	K562	blood:
10	chr8:126335232..126337186-chr8:126341576..126343163,2	K562	blood:
11	chr8:126287173..126289298-chr8:126442431..126444189,2	MCF-7	breast:
12	chr8:126318641..126321559-chr8:126341791..126343679,2	MCF-7	breast:
13	chr8:126319216..126321150-chr8:126442622..126444295,2	MCF-7	breast:
14	chr8:126290287..126294135-chr8:126298870..126301775,4	K562	blood:
15	chr8:126290403..126294435-chr8:126303618..126306610,4	K562	blood:
16	chr8:126285610..126287271-chr8:126288882..126290405,2	MCF-7	breast:
17	chr8:126303707..126305559-chr8:126307667..126310106,2	K562	blood:
18	chr8:126314491..126316142-chr8:126318788..126320646,2	K562	blood:
19	chr8:126291720..126294435-chr8:126303942..126305549,2	K562	blood:
20	chr8:126338417..126342692-chr8:126345063..126348300,5	K562	blood:
21	chr8:126306226..126307841-chr8:126440492..126443071,2	K562	blood:
22	chr8:126298759..126300267-chr8:126304142..126306532,2	MCF-7	breast:
23	chr8:126316293..126317813-chr8:126318662..126321423,2	K562	blood:
24	chr8:126290473..126292876-chr8:126294905..126297324,3	K562	blood:
25	chr8:126313139..126314893-chr8:126441960..126444560,2	MCF-7	breast:
26	chr8:126343351..126345120-chr8:126444427..126447046,2	K562	blood:
27	chr8:126315465..126318192-chr8:126341334..126342938,2	K562	blood:
28	chr8:126289014..126291245-chr8:126440114..126442015,2	MCF-7	breast:
29	chr8:126233282..126235149-chr8:126318935..126321777,2	MCF-7	breast:
30	chr8:126322882..126325288-chr8:126341226..126344036,2	MCF-7	breast:
31	chr8:126322565..126325543-chr8:126398051..126400754,2	K562	blood:
32	chr8:126131877..126132657-chr8:126292156..126292668,2	K562	blood:
33	chr8:126310853..126313276-chr8:126316044..126318835,2	MCF-7	breast:
34	chr8:126272432..126274189-chr8:126283876..126286401,2	MCF-7	breast:
35	chr8:126306802..126309917-chr8:126312229..126314853,3	MCF-7	breast:
36	chr2:56773723..56776584-chr8:126325913..126327457,2	MCF-7	breast:
37	chr8:126291720..126294435-chr8:126303942..126305549,2	K562	blood:
38	chr8:126294613..126297401-chr8:126298251..126300790,2	K562	blood:
39	chr8:126290287..126294135-chr8:126298870..126301775,4	K562	blood:
40	chr8:126326305..126327912-chr8:126330901..126332474,2	MCF-7	breast:
41	chr8:126320818..126322361-chr8:126441952..126443721,2	K562	blood:
42	chr8:126287704..126290628-chr8:126303543..126305382,2	MCF-7	breast:
43	chr8:126287701..126290542-chr8:126297201..126298945,2	MCF-7	breast:
44	chr8:126285610..126287271-chr8:126288882..126290405,2	MCF-7	breast:
45	chr8:126283799..126286168-chr8:126444764..126446499,2	MCF-7	breast:
46	chr8:126318394..126322454-chr8:126322882..126325184,6	K562	blood:
47	chr8:126280606..126282810-chr8:126295937..126297699,2	MCF-7	breast:
48	chr8:126305198..126307115-chr8:126309185..126311282,2	MCF-7	breast:
49	chr8:126322882..126325288-chr8:126341226..126344036,2	MCF-7	breast:
50	chr8:126344683..126349065-chr8:126441599..126445443,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000173334	chromatin interactions
ENSG00000242170	chromatin interactions

Extended variants
information (count: 2326 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:2326 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7011185	chr8:126283766-126283767	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559748262	chr8:126283813-126283814	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs74315899	chr8:126283820-126283821	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs558109360	chr8:126283852-126283853	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs193099125	chr8:126283867-126283868	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183147514	chr8:126283868-126283869	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs80081684	chr8:126283876-126283877	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs78545183	chr8:126283898-126283899	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs74457361	chr8:126283909-126283910	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs533524446	chr8:126283915-126283916	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547219895	chr8:126283916-126283917	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567100780	chr8:126283924-126283925	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188185884	chr8:126283927-126283928	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113657412	chr8:126283928-126283929	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs192418310	chr8:126283938-126283939	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs528973111	chr8:126283965-126283966	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs373044938	chr8:126283971-126283972	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs546074365	chr8:126283977-126283978	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs376465845	chr8:126283988-126283989	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs11779422	chr8:126284010-126284011	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs150755614	chr8:126284020-126284021	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs557599976	chr8:126284025-126284026	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571220303	chr8:126284028-126284029	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533878307	chr8:126284086-126284087	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376355063	chr8:126284110-126284111	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs183652829	chr8:126284139-126284140	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187941506	chr8:126284149-126284150	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541934565	chr8:126284160-126284161	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs111293055	chr8:126284188-126284189	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs367880647	chr8:126284193-126284194	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs115959683	chr8:126284223-126284224	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543430319	chr8:126284234-126284235	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs563967898	chr8:126284256-126284257	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34606312	chr8:126284257-126284258	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs564723757	chr8:126284278-126284279	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs372701477	chr8:126284287-126284288	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192368815	chr8:126284316-126284317	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs561559035	chr8:126284341-126284342	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs540963777	chr8:126284349-126284350	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112660679	chr8:126284356-126284357	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529521488	chr8:126284387-126284388	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs375536009	chr8:126284391-126284392	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548777779	chr8:126284395-126284396	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7844459	chr8:126284409-126284410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs7826327	chr8:126284419-126284420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs184910912	chr8:126284420-126284421	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559855230	chr8:126284426-126284427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570949224	chr8:126284446-126284447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533817083	chr8:126284466-126284467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs554071993	chr8:126284478-126284479	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:146)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Ovarian cancer	21240255	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1557 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126255400-126287800	Weak transcription	Primary B cells from cord blood	blood
2	chr8:126261400-126286000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr8:126262200-126288200	Weak transcription	Ovary	ovary
4	chr8:126264800-126310600	Weak transcription	Aorta	Aorta
5	chr8:126265600-126296600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:126272800-126283800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr8:126273600-126285200	Weak transcription	Stomach Mucosa	stomach
8	chr8:126275400-126284600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr8:126275600-126284600	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr8:126275600-126285200	Weak transcription	Primary T cells from cord blood	blood
11	chr8:126275600-126286000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:126275800-126289000	Weak transcription	Dnd41	blood
13	chr8:126276800-126285800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:126276800-126286000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:126277000-126285400	Weak transcription	Thymus	Thymus
16	chr8:126277000-126285800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr8:126278000-126286000	Weak transcription	Fetal Thymus	thymus
18	chr8:126278400-126285200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:126280000-126289800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:126280200-126285200	Weak transcription	Right Atrium	heart
21	chr8:126281200-126283800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:126281200-126285200	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr8:126281200-126285400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr8:126281400-126285200	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr8:126281400-126285200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr8:126281600-126285200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:126281600-126285200	Weak transcription	Esophagus	oesophagus
28	chr8:126281600-126286000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr8:126282800-126284000	Enhancers	Hela-S3	cervix
30	chr8:126282800-126286200	Enhancers	Placenta Amnion	Placenta Amnion
31	chr8:126283000-126285000	Weak transcription	Psoas Muscle	Psoas
32	chr8:126283000-126285200	Weak transcription	Left Ventricle	heart
33	chr8:126283200-126284600	Weak transcription	Fetal Heart	heart
34	chr8:126283400-126284000	Enhancers	HSMM	muscle
35	chr8:126283400-126284200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr8:126283400-126284200	Enhancers	NH-A	brain
37	chr8:126283400-126286400	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr8:126283400-126286800	Enhancers	HMEC	breast
39	chr8:126283400-126287000	Enhancers	Fetal Intestine Large	intestine
40	chr8:126283400-126288000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:126283400-126292600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:126283600-126283800	Enhancers	Brain Hippocampus Middle	brain
43	chr8:126283600-126283800	Enhancers	Brain Substantia Nigra	brain
44	chr8:126283600-126283800	Enhancers	Fetal Kidney	kidney
45	chr8:126283600-126284000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr8:126283600-126284000	Flanking Active TSS	K562	blood
47	chr8:126283600-126284200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr8:126283600-126284200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr8:126283600-126284200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr8:126283600-126284200	Flanking Active TSS	A549	lung

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