Variant report

Variant	nsv538094
Chromosome Location	chr6:1757776-1907505
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:112)
LncRNA
region (count:69)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:1769402..1771120-chr6:1775658..1777745,2	K562	blood:
2	chr6:1640395..1643139-chr6:1772426..1774181,2	MCF-7	breast:
3	chr6:1901619..1903388-chr6:1908460..1910593,2	MCF-7	breast:
4	chr6:1612642..1614747-chr6:1828037..1830665,2	MCF-7	breast:
5	chr6:1879945..1882331-chr6:1886412..1889066,2	K562	blood:
6	chr6:1839372..1842046-chr6:1850595..1852706,2	MCF-7	breast:
7	chr6:1640135..1642323-chr6:1758348..1760880,2	MCF-7	breast:
8	chr6:1858177..1860635-chr6:1865077..1867804,2	MCF-7	breast:
9	chr6:1769402..1771120-chr6:1775658..1777745,2	K562	blood:
10	chr6:1792364..1794850-chr6:1794950..1797651,3	K562	blood:
11	chr6:1606384..1611793-chr6:1762059..1766159,7	MCF-7	breast:
12	chr6:1843508..1846277-chr6:1850765..1853357,2	MCF-7	breast:
13	chr6:1641157..1641856-chr6:1767705..1768705,2	MCF-7	breast:
14	chr6:1612582..1614145-chr6:1846859..1849142,2	MCF-7	breast:
15	chr6:1816700..1818272-chr6:1821927..1824699,2	MCF-7	breast:
16	chr6:1845499..1849284-chr6:1851999..1854046,3	K562	blood:
17	chr6:1755526..1758374-chr6:1765956..1768528,2	MCF-7	breast:
18	chr6:1860563..1862869-chr6:1864416..1866746,2	K562	blood:
19	chr6:1839714..1842732-chr6:1843630..1846250,4	MCF-7	breast:
20	chr6:1820101..1824094-chr6:1824755..1828299,3	MCF-7	breast:
21	chr6:1839588..1841532-chr6:1851475..1853574,2	MCF-7	breast:
22	chr6:1839588..1841532-chr6:1851475..1853574,2	MCF-7	breast:
23	chr6:1839372..1842046-chr6:1850595..1852706,2	MCF-7	breast:
24	chr6:1879945..1882331-chr6:1886412..1889066,2	K562	blood:
25	chr6:1772266..1774519-chr6:1779951..1781505,2	K562	blood:
26	chr6:1772266..1774519-chr6:1779951..1781505,2	K562	blood:
27	chr6:1806875..1808412-chr6:1811634..1813547,2	K562	blood:
28	chr6:1839714..1842732-chr6:1843630..1846250,4	MCF-7	breast:
29	chr6:1759044..1762047-chr6:1765205..1768245,4	MCF-7	breast:
30	chr6:1767654..1768676-chr6:1832751..1833553,3	MCF-7	breast:
31	chr6:1755526..1758374-chr6:1765956..1768528,2	MCF-7	breast:
32	chr6:1841908..1843510-chr6:1844738..1846986,2	MCF-7	breast:
33	chr6:1814803..1816537-chr6:1819747..1822348,2	K562	blood:
34	chr6:1876778..1878814-chr6:1880634..1882553,2	K562	blood:
35	chr6:1827013..1828622-chr6:1829332..1831596,2	MCF-7	breast:
36	chr6:1612577..1614591-chr6:1838798..1840944,2	MCF-7	breast:
37	chr6:1610120..1613038-chr6:1790645..1792806,2	MCF-7	breast:
38	chr6:1641242..1642170-chr6:1838518..1839870,7	MCF-7	breast:
39	chr6:1876778..1878814-chr6:1880634..1882553,2	K562	blood:
40	chr6:1831250..1835471-chr6:1835503..1841068,8	MCF-7	breast:
41	chr6:1791638..1793487-chr6:1817770..1820087,2	MCF-7	breast:
42	chr6:1838007..1840315-chr6:1844075..1845612,2	MCF-7	breast:
43	chr6:1792364..1794850-chr6:1795241..1797651,2	K562	blood:
44	chr6:1609985..1612105-chr6:1773959..1776813,2	MCF-7	breast:
45	chr6:1608691..1612262-chr6:1889207..1891694,3	MCF-7	breast:
46	chr6:1783810..1786283-chr6:1790693..1792568,2	K562	blood:
47	chr6:1868113..1870293-chr6:1878428..1880757,2	MCF-7	breast:
48	chr6:1820101..1824094-chr6:1824755..1828299,3	MCF-7	breast:
49	chr6:1762522..1764369-chr6:1837443..1839225,2	MCF-7	breast:
50	chr6:1756824..1758512-chr6:1760303..1761859,2	MCF-7	breast:

(count:69 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf195-34	chr6:1775932-1776037	NONHSAT106547
2	lnc-C6orf195-34	chr6:1767197-1772399	NONHSAT106546
3	lnc-FOXC1-9	chr6:1889013-1889114	NONHSAT106553
4	lnc-C6orf195-34	chr6:1794049-1794262	NONHSAT106547
5	lnc-FOXC1-9	chr6:1904182-1904425	NONHSAT106556
6	lnc-FOXC1-9	chr6:1904182-1906085	NONHSAT106555
7	lnc-FOXC1-9	chr6:1887520-1887676	NONHSAT106554
8	lnc-FOXC1-9	chr6:1889266-1889326	NONHSAT106557
9	lnc-FOXC1-9	chr6:1888251-1888407	NONHSAT106556
10	lnc-C6orf195-34	chr6:1774271-1774764	NONHSAT106546
11	lnc-FOXC1-9	chr6:1889051-1889142	NONHSAT106557
12	lnc-C6orf195-34	chr6:1805934-1806156	NONHSAT106546
13	lnc-FOXC1-9	chr6:1888144-1888204	NONHSAT106553
14	lnc-FOXC1-9	chr6:1888144-1888204	NONHSAT106552
15	lnc-FOXC1-9	chr6:1888320-1888411	NONHSAT106554
16	lnc-FOXC1-9	chr6:1903452-1903695	NONHSAT106552
17	lnc-FOXC1-9	chr6:1889051-1889142	NONHSAT106556
18	lnc-FOXC1-9	chr6:1889013-1889114	NONHSAT106552
19	lnc-FOXC1-9	chr6:1904213-1905355	NONHSAT106552
20	lnc-FOXC1-9	chr6:1902860-1902931	NONHSAT106552
21	lnc-FOXC1-9	chr6:1904943-1906085	NONHSAT106556
22	lnc-FOXC1-9	chr6:1888875-1888935	NONHSAT106556
23	lnc-FOXC1-9	chr6:1888144-1888204	NONHSAT106554
24	lnc-FOXC1-9	chr6:1889744-1889845	NONHSAT106557
25	lnc-FOXC1-9	chr6:1903590-1903661	NONHSAT106556
26	lnc-C6orf195-34	chr6:1774271-1774764	NONHSAT106547
27	lnc-FOXC1-9	chr6:1888535-1888595	NONHSAT106553
28	lnc-C6orf195-34	chr6:1806137-1806933	NONHSAT106547
29	lnc-FOXC1-9	chr6:1901061-1901106	NONHSAT106552
30	lnc-FOXC1-9	chr6:1907481-1908235	NONHSAT106557
31	lnc-FOXC1-9	chr6:1887520-1887676	NONHSAT106553
32	lnc-FOXC1-9	chr6:1889013-1889114	NONHSAT106554
33	lnc-FOXC1-9	chr6:1888716-1888829	NONHSAT106553
34	lnc-FOXC1-9	chr6:1888320-1888411	NONHSAT106552
35	lnc-FOXC1-9	chr6:1906751-1907505	NONHSAT106554
36	lnc-FOXC1-9	chr6:1888535-1888595	NONHSAT106552
37	lnc-FOXC1-9	chr6:1889266-1889326	NONHSAT106555
38	lnc-FOXC1-9	chr6:1888251-1888407	NONHSAT106555
39	lnc-FOXC1-9	chr6:1888875-1888935	NONHSAT106555
40	lnc-FOXC1-9	chr6:1888716-1888829	NONHSAT106552
41	lnc-FOXC1-9	chr6:1889447-1889560	NONHSAT106555
42	lnc-FOXC1-9	chr6:1889266-1889326	NONHSAT106556
43	lnc-FOXC1-9	chr6:1889744-1889845	NONHSAT106556
44	lnc-FOXC1-9	chr6:1903590-1903661	NONHSAT106555
45	lnc-FOXC1-9	chr6:1901791-1901836	NONHSAT106556
46	lnc-FOXC1-9	chr6:1888320-1888411	NONHSAT106553
47	lnc-FOXC1-9	chr6:1889744-1889845	NONHSAT106555
48	lnc-FOXC1-9	chr6:1888875-1888935	NONHSAT106557
49	lnc-FOXC1-9	chr6:1889447-1889560	NONHSAT106556
50	lnc-FOXC1-9	chr6:1888535-1888595	NONHSAT106554

No data

Variant related genes	Relation type
ENSG00000054598	chromatin interactions

Extended variants
information (count: 5676 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5676 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184094755	chr6:1757878-1757879	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557809950	chr6:1757886-1757887	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189686229	chr6:1757901-1757902	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537030612	chr6:1757906-1757907	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557716260	chr6:1757921-1757922	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574385874	chr6:1757970-1757971	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142271665	chr6:1757982-1757983	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150835437	chr6:1757990-1757991	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs6935246	chr6:1758012-1758013	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs76407725	chr6:1758025-1758026	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530845372	chr6:1758036-1758037	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374206733	chr6:1758038-1758039	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550538439	chr6:1758063-1758064	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563289508	chr6:1758069-1758070	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78153243	chr6:1758171-1758172	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1040530	chr6:1758179-1758180	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs565708862	chr6:1758185-1758186	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546228334	chr6:1758247-1758248	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529762164	chr6:1758250-1758251	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114439702	chr6:1758263-1758264	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139259419	chr6:1758277-1758278	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12529743	chr6:1758304-1758305	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1040531	chr6:1758314-1758315	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12213621	chr6:1758321-1758322	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74940759	chr6:1758384-1758385	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147699847	chr6:1758472-1758473	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538977726	chr6:1758501-1758502	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536501384	chr6:1758546-1758547	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs117440062	chr6:1758580-1758581	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs7746168	chr6:1758615-1758616	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545179215	chr6:1758633-1758634	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs58269467	chr6:1758655-1758656	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs575330249	chr6:1758669-1758670	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138717594	chr6:1758674-1758675	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs371768054	chr6:1758715-1758716	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544239335	chr6:1758754-1758755	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560905438	chr6:1758769-1758770	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111746725	chr6:1758784-1758785	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs548973668	chr6:1758813-1758814	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145265113	chr6:1758816-1758817	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs147636260	chr6:1758829-1758830	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551601263	chr6:1758875-1758876	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs571408915	chr6:1758933-1758934	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs540971583	chr6:1758934-1758935	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550601035	chr6:1758980-1758981	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs112048843	chr6:1759039-1759040	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs6914504	chr6:1759042-1759043	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs536966196	chr6:1759043-1759044	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565170132	chr6:1759052-1759053	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553422632	chr6:1759088-1759089	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Prader-willi syndrome	20588305	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2155 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:1738400-1762400	Weak transcription	Gastric	stomach
2	chr6:1738400-1768200	Weak transcription	Primary T cells from cord blood	blood
3	chr6:1749400-1761600	Weak transcription	Stomach Mucosa	stomach
4	chr6:1749800-1762400	Weak transcription	Colonic Mucosa	Colon
5	chr6:1749800-1779000	Weak transcription	Aorta	Aorta
6	chr6:1751200-1780400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr6:1756400-1760000	Strong transcription	HepG2	liver
8	chr6:1757000-1758000	Enhancers	Fetal Kidney	kidney
9	chr6:1757000-1758200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr6:1757000-1766000	Weak transcription	Right Atrium	heart
11	chr6:1757200-1758200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:1757200-1760200	Weak transcription	Fetal Intestine Small	intestine
13	chr6:1757200-1764000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:1757200-1766800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:1757200-1770600	Weak transcription	Lung	lung
16	chr6:1757400-1757800	Enhancers	Duodenum Mucosa	Duodenum
17	chr6:1757600-1757800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:1757600-1757800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr6:1757600-1762800	Weak transcription	Pancreas	Pancrea
20	chr6:1757800-1758400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:1757800-1762200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr6:1758000-1759400	Weak transcription	Fetal Kidney	kidney
23	chr6:1758200-1758800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr6:1758200-1759000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:1758200-1761600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr6:1758400-1758600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:1758400-1758600	Enhancers	K562	blood
28	chr6:1758600-1758800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr6:1758600-1758800	Enhancers	Small Intestine	intestine
30	chr6:1758600-1771400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr6:1758800-1759400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr6:1758800-1767800	Weak transcription	Small Intestine	intestine
33	chr6:1759400-1763000	Enhancers	Fetal Kidney	kidney
34	chr6:1760000-1761400	Weak transcription	HepG2	liver
35	chr6:1760200-1760400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:1760200-1760400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr6:1760200-1763000	Enhancers	Fetal Intestine Small	intestine
38	chr6:1760400-1761200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr6:1760400-1763000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr6:1760600-1760800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:1760600-1760800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr6:1760600-1761000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
43	chr6:1760600-1761600	Enhancers	Fetal Intestine Large	intestine
44	chr6:1760800-1762000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:1760800-1762800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:1760800-1763200	Enhancers	Brain Germinal Matrix	brain
47	chr6:1761000-1762000	Enhancers	HMEC	breast
48	chr6:1761000-1762600	Enhancers	Brain Hippocampus Middle	brain
49	chr6:1761000-1763000	Enhancers	Fetal Lung	lung
50	chr6:1761000-1768400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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