Variant report

Variant	nsv883383
Chromosome Location	chr6:1775436-1918572
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:93)
LncRNA
region (count:65)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:1783810..1786283-chr6:1790693..1792568,2	K562	blood:
2	chr6:1839588..1841532-chr6:1851475..1853574,2	MCF-7	breast:
3	chr6:1791638..1793487-chr6:1817770..1820087,2	MCF-7	breast:
4	chr6:1868113..1870293-chr6:1878428..1880757,2	MCF-7	breast:
5	chr6:1831250..1835471-chr6:1835503..1841068,8	MCF-7	breast:
6	chr6:1833159..1835523-chr6:1854062..1855942,2	K562	blood:
7	chr6:1774055..1775958-chr6:1777177..1778698,2	K562	blood:
8	chr6:1687705..1689318-chr6:1909899..1912443,2	K562	blood:
9	chr6:1797246..1799087-chr6:1805136..1807218,2	K562	blood:
10	chr6:1641276..1642150-chr6:1832654..1833597,12	MCF-7	breast:
11	chr6:1918511..1920955-chr6:1921418..1923384,2	K562	blood:
12	chr6:1829103..1830910-chr6:1832147..1834124,2	MCF-7	breast:
13	chr6:1892981..1894808-chr6:1898634..1901101,2	K562	blood:
14	chr6:1792364..1794850-chr6:1795241..1797651,2	K562	blood:
15	chr6:1860563..1862869-chr6:1864416..1866746,2	K562	blood:
16	chr6:1856826..1858830-chr6:1861067..1863033,2	MCF-7	breast:
17	chr6:1893216..1895870-chr6:1897285..1899194,2	MCF-7	breast:
18	chr6:1814803..1816537-chr6:1819747..1822348,2	K562	blood:
19	chr6:1806875..1808412-chr6:1811634..1813547,2	K562	blood:
20	chr6:1613523..1614289-chr6:1838606..1839498,2	MCF-7	breast:
21	chr6:1773332..1775371-chr6:1778272..1781076,2	MCF-7	breast:
22	chr6:1769402..1771120-chr6:1775658..1777745,2	K562	blood:
23	chr6:1893216..1895870-chr6:1897285..1899194,2	MCF-7	breast:
24	chr6:1792364..1794850-chr6:1795241..1797651,2	K562	blood:
25	chr6:1609985..1612105-chr6:1773959..1776813,2	MCF-7	breast:
26	chr6:1827013..1828622-chr6:1829332..1831596,2	MCF-7	breast:
27	chr6:1860563..1862869-chr6:1864416..1866746,2	K562	blood:
28	chr6:1879945..1882331-chr6:1886412..1889066,2	K562	blood:
29	chr6:1901619..1903388-chr6:1908460..1910593,2	MCF-7	breast:
30	chr6:1839714..1842732-chr6:1843630..1846250,4	MCF-7	breast:
31	chr6:1610120..1613038-chr6:1790645..1792806,2	MCF-7	breast:
32	chr6:1845499..1849284-chr6:1851999..1854046,3	K562	blood:
33	chr6:1843508..1846277-chr6:1850765..1853357,2	MCF-7	breast:
34	chr6:1838007..1840315-chr6:1844075..1845612,2	MCF-7	breast:
35	chr6:1612577..1614591-chr6:1838798..1840944,2	MCF-7	breast:
36	chr6:1792364..1794850-chr6:1794950..1797651,3	K562	blood:
37	chr6:1797246..1799087-chr6:1805136..1807218,2	K562	blood:
38	chr6:1876778..1878814-chr6:1880634..1882553,2	K562	blood:
39	chr6:1608029..1610545-chr6:1915416..1919377,4	MCF-7	breast:
40	chr6:1608831..1611325-chr6:1793324..1795939,2	MCF-7	breast:
41	chr6:1791638..1793487-chr6:1817770..1820087,2	MCF-7	breast:
42	chr6:1611913..1614321-chr6:1833472..1836057,3	MCF-7	breast:
43	chr6:1641227..1642195-chr6:1832847..1833566,5	MCF-7	breast:
44	chr6:1839372..1842046-chr6:1850595..1852706,2	MCF-7	breast:
45	chr6:1814803..1816537-chr6:1819747..1822348,2	K562	blood:
46	chr6:1778842..1781326-chr6:1839801..1842724,2	MCF-7	breast:
47	chr6:1767654..1768676-chr6:1832751..1833553,3	MCF-7	breast:
48	chr6:1909308..1911195-chr6:1919277..1921722,2	K562	blood:
49	chr6:1868113..1870293-chr6:1878428..1880757,2	MCF-7	breast:
50	chr6:1879945..1882331-chr6:1886412..1889066,2	K562	blood:

(count:65 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXC1-9	chr6:1904182-1906085	NONHSAT106555
2	lnc-FOXC1-9	chr6:1889051-1889142	NONHSAT106557
3	lnc-C6orf195-34	chr6:1806137-1806933	NONHSAT106547
4	lnc-C6orf195-34	chr6:1794049-1794262	NONHSAT106547
5	lnc-FOXC1-9	chr6:1901061-1901106	NONHSAT106554
6	lnc-FOXC1-9	chr6:1889447-1889560	NONHSAT106555
7	lnc-FOXC1-9	chr6:1888320-1888411	NONHSAT106553
8	lnc-FOXC1-9	chr6:1888251-1888407	NONHSAT106555
9	lnc-FOXC1-9	chr6:1888535-1888595	NONHSAT106554
10	lnc-FOXC1-9	chr6:1888144-1888204	NONHSAT106554
11	lnc-FOXC1-9	chr6:1889266-1889326	NONHSAT106557
12	lnc-FOXC1-9	chr6:1901791-1901836	NONHSAT106555
13	lnc-FOXC1-9	chr6:1907309-1907388	NONHSAT106557
14	lnc-FOXC1-9	chr6:1901061-1901106	NONHSAT106552
15	lnc-FOXC1-9	chr6:1888535-1888595	NONHSAT106553
16	lnc-FOXC1-9	chr6:1901949-1902017	NONHSAT106557
17	lnc-FOXC1-9	chr6:1889744-1889845	NONHSAT106555
18	lnc-FOXC1-9	chr6:1888716-1888829	NONHSAT106552
19	lnc-FOXC1-9	chr6:1901791-1901836	NONHSAT106557
20	lnc-FOXC1-9	chr6:1902860-1902931	NONHSAT106552
21	lnc-FOXC1-9	chr6:1887520-1887676	NONHSAT106553
22	lnc-FOXC1-9	chr6:1888875-1888935	NONHSAT106555
23	lnc-FOXC1-9	chr6:1906579-1906658	NONHSAT106554
24	lnc-FOXC1-9	chr6:1889013-1889114	NONHSAT106554
25	lnc-FOXC1-9	chr6:1903452-1905355	NONHSAT106553
26	lnc-FOXC1-9	chr6:1906751-1907505	NONHSAT106554
27	lnc-FOXC1-9	chr6:1888535-1888595	NONHSAT106552
28	lnc-FOXC1-9	chr6:1887520-1887676	NONHSAT106554
29	lnc-FOXC1-9	chr6:1888144-1888204	NONHSAT106552
30	lnc-FOXC1-9	chr6:1889013-1889114	NONHSAT106553
31	lnc-FOXC1-9	chr6:1903590-1903661	NONHSAT106555
32	lnc-C6orf195-34	chr6:1805934-1806156	NONHSAT106546
33	lnc-FOXC1-9	chr6:1888320-1888411	NONHSAT106554
34	lnc-FOXC1-9	chr6:1889266-1889326	NONHSAT106555
35	lnc-FOXC1-9	chr6:1887520-1887676	NONHSAT106552
36	lnc-FOXC1-9	chr6:1904213-1905355	NONHSAT106552
37	lnc-FOXC1-9	chr6:1889051-1889142	NONHSAT106555
38	lnc-FOXC1-9	chr6:1902860-1902931	NONHSAT106554
39	lnc-FOXC1-9	chr6:1888144-1888204	NONHSAT106553
40	lnc-FOXC1-9	chr6:1888875-1888935	NONHSAT106556
41	lnc-FOXC1-9	chr6:1888320-1888411	NONHSAT106552
42	lnc-FOXC1-9	chr6:1907481-1908235	NONHSAT106557
43	lnc-FOXC1-9	chr6:1903452-1903695	NONHSAT106552
44	lnc-FOXC1-9	chr6:1889447-1889560	NONHSAT106557
45	lnc-FOXC1-9	chr6:1904943-1906085	NONHSAT106556
46	lnc-FOXC1-9	chr6:1888251-1888407	NONHSAT106557
47	lnc-C6orf195-34	chr6:1775932-1776037	NONHSAT106547
48	lnc-FOXC1-9	chr6:1888716-1888829	NONHSAT106553
49	lnc-FOXC1-9	chr6:1889051-1889142	NONHSAT106556
50	lnc-FOXC1-9	chr6:1889447-1889560	NONHSAT106556

No data

Variant related genes	Relation type
ENSG00000054598	chromatin interactions

Extended variants
information (count: 5478 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5478 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2318089	chr6:1775436-1775437	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142500608	chr6:1775452-1775453	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2016052	chr6:1775463-1775464	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs567835706	chr6:1775525-1775526	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs3778522	chr6:1775572-1775573	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533606537	chr6:1775634-1775635	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185935988	chr6:1775644-1775645	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564436355	chr6:1775688-1775689	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs722587	chr6:1775714-1775715	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs2015853	chr6:1775739-1775740	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs372113243	chr6:1775758-1775759	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188321072	chr6:1775776-1775777	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542444254	chr6:1775852-1775853	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs722585	chr6:1775863-1775864	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs551794821	chr6:1775867-1775868	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541202087	chr6:1775876-1775877	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564582919	chr6:1775917-1775918	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs7449919	chr6:1775929-1775930	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs181085742	chr6:1775930-1775931	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562454183	chr6:1775949-1775950	Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs531472992	chr6:1775969-1775970	Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs116147410	chr6:1776037-1776038	Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs567945838	chr6:1776085-1776086	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs79271533	chr6:1776139-1776140	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs3800055	chr6:1776141-1776142	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185879195	chr6:1776179-1776180	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs35900573	chr6:1776185-1776186	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs116631881	chr6:1776191-1776192	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs3800056	chr6:1776194-1776195	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs373398355	chr6:1776201-1776202	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190593455	chr6:1776211-1776212	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs183783738	chr6:1776269-1776270	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556080040	chr6:1776288-1776289	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs76175264	chr6:1776347-1776348	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs541613324	chr6:1776350-1776351	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7760202	chr6:1776354-1776355	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs7760204	chr6:1776360-1776361	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs7745811	chr6:1776376-1776377	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs7745817	chr6:1776383-1776384	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs529232049	chr6:1776385-1776386	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186858675	chr6:1776459-1776460	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141906124	chr6:1776462-1776463	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs527534217	chr6:1776506-1776507	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs574325864	chr6:1776509-1776510	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs75046865	chr6:1776544-1776545	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs570455500	chr6:1776556-1776557	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs114279860	chr6:1776573-1776574	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549820386	chr6:1776633-1776634	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543555639	chr6:1776659-1776660	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs569704420	chr6:1776682-1776683	Weak transcription Enhancers Genic enhancers	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	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1998 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:1749800-1779000	Weak transcription	Aorta	Aorta
2	chr6:1751200-1780400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr6:1762800-1801600	Weak transcription	Colonic Mucosa	Colon
4	chr6:1763000-1792600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr6:1768000-1778400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:1768000-1778600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:1768200-1777000	Weak transcription	Left Ventricle	heart
8	chr6:1768200-1778400	Weak transcription	Brain Anterior Caudate	brain
9	chr6:1768200-1803600	Weak transcription	Small Intestine	intestine
10	chr6:1768600-1778200	Weak transcription	Fetal Kidney	kidney
11	chr6:1768800-1779400	Weak transcription	Hela-S3	cervix
12	chr6:1770200-1776000	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr6:1770800-1792600	Weak transcription	Thymus	Thymus
14	chr6:1770800-1805600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr6:1771000-1776000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr6:1771200-1776200	Enhancers	Primary T cells from cord blood	blood
17	chr6:1771800-1785600	Weak transcription	Pancreas	Pancrea
18	chr6:1772000-1788400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr6:1772000-1798800	Weak transcription	Gastric	stomach
20	chr6:1772200-1788000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:1774400-1776400	Enhancers	Fetal Muscle Leg	muscle
22	chr6:1774400-1779800	Weak transcription	GM12878-XiMat	blood
23	chr6:1774600-1775600	Strong transcription	HepG2	liver
24	chr6:1774600-1775800	Enhancers	Fetal Stomach	stomach
25	chr6:1774600-1776200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:1774600-1777200	Weak transcription	Duodenum Mucosa	Duodenum
27	chr6:1774800-1778400	Weak transcription	Fetal Intestine Small	intestine
28	chr6:1774800-1789400	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr6:1775000-1778200	Weak transcription	Fetal Lung	lung
30	chr6:1775000-1780200	Weak transcription	Primary hematopoietic stem cells	blood
31	chr6:1775000-1780200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:1775000-1780200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:1775000-1797000	Weak transcription	Fetal Intestine Large	intestine
34	chr6:1775200-1778000	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr6:1775200-1780600	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr6:1775200-1781600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:1775400-1780800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr6:1775600-1777000	Genic enhancers	HepG2	liver
39	chr6:1775800-1778400	Weak transcription	Fetal Stomach	stomach
40	chr6:1776200-1776400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:1776200-1828800	Weak transcription	Primary T cells from cord blood	blood
42	chr6:1776400-1778400	Weak transcription	Fetal Muscle Leg	muscle
43	chr6:1776400-1780800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr6:1777000-1777600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr6:1777000-1782000	Strong transcription	HepG2	liver
46	chr6:1777200-1778000	Strong transcription	Duodenum Mucosa	Duodenum
47	chr6:1777200-1778200	Enhancers	Fetal Brain Female	brain
48	chr6:1777800-1779000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr6:1777800-1779200	Enhancers	Brain Substantia Nigra	brain
50	chr6:1778000-1778800	Enhancers	Brain Hippocampus Middle	brain

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