Variant report

Variant	nsv522814
Chromosome Location	chr6:76375321-76405700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:76383585-76383961	HepG2	liver:	n/a	n/a
2	ATF3	chr6:76400719-76401129	HCT-116	colon:	n/a	n/a
3	BHLHE40	chr6:76397729-76398031	K562	blood:	n/a	n/a
4	CEBPB	chr6:76383580-76384058	A549	lung:	n/a	n/a
5	CEBPB	chr6:76400745-76401117	MCF-7	breast:	n/a	chr6:76400914-76400925
6	CEBPB	chr6:76383586-76384024	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr6:76383701-76383950	K562	blood:	n/a	n/a
8	CEBPB	chr6:76383602-76383982	A549	lung:	n/a	n/a
9	CEBPB	chr6:76383670-76384002	K562	blood:	n/a	n/a
10	CEBPB	chr6:76400734-76401054	K562	blood:	n/a	chr6:76400914-76400925
11	CEBPB	chr6:76400814-76401136	ECC-1	luminal epithelium:	n/a	chr6:76400914-76400925
12	CEBPB	chr6:76396873-76397089	K562	blood:	n/a	n/a
13	CEBPB	chr6:76401962-76402326	MCF-7	breast:	n/a	chr6:76402141-76402152
14	CEBPB	chr6:76400797-76401054	A549	lung:	n/a	chr6:76400914-76400925
15	CEBPB	chr6:76403289-76403630	A549	lung:	n/a	chr6:76403486-76403499
16	CEBPB	chr6:76400838-76401046	H1-hESC	embryonic stem cell:	n/a	chr6:76400914-76400925
17	CEBPB	chr6:76400740-76401106	IMR90	lung:	n/a	chr6:76400914-76400925
18	CEBPB	chr6:76403222-76403604	MCF-7	breast:	n/a	chr6:76403486-76403499
19	CEBPB	chr6:76382532-76382723	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr6:76383753-76383989	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr6:76381598-76381917	HepG2	liver:	n/a	chr6:76381756-76381767 chr6:76381754-76381765
22	CEBPB	chr6:76400745-76401104	K562	blood:	n/a	chr6:76400914-76400925
23	CEBPB	chr6:76383017-76383259	HepG2	liver:	n/a	chr6:76383095-76383106
24	CEBPB	chr6:76400625-76401191	HCT-116	colon:	n/a	chr6:76400914-76400925
25	CEBPB	chr6:76400741-76401177	A549	lung:	n/a	chr6:76400914-76400925
26	CEBPB	chr6:76400858-76401116	ECC-1	luminal epithelium:	n/a	chr6:76400914-76400925
27	CEBPB	chr6:76383698-76383973	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:76403299-76403704	MCF-7	breast:	n/a	chr6:76403486-76403499
29	CEBPB	chr6:76383646-76383968	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr6:76400739-76401100	HepG2	liver:	n/a	chr6:76400914-76400925
31	CEBPB	chr6:76403319-76403629	HepG2	liver:	n/a	chr6:76403486-76403499
32	CEBPB	chr6:76383743-76383944	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr6:76401984-76402296	HepG2	liver:	n/a	chr6:76402141-76402152
34	CEBPB	chr6:76400675-76401277	HCT-116	colon:	n/a	chr6:76400914-76400925
35	CEBPB	chr6:76400748-76401106	Hela-S3	cervix:	n/a	chr6:76400914-76400925
36	CEBPB	chr6:76381652-76381945	A549	lung:	n/a	chr6:76381756-76381767 chr6:76381754-76381765
37	CEBPB	chr6:76403280-76403671	IMR90	lung:	n/a	chr6:76403486-76403499
38	CEBPB	chr6:76400753-76401106	A549	lung:	n/a	chr6:76400914-76400925
39	CEBPB	chr6:76403351-76403657	K562	blood:	n/a	chr6:76403486-76403499
40	CEBPB	chr6:76383590-76384030	HepG2	liver:	n/a	n/a
41	CEBPB	chr6:76402022-76402164	K562	blood:	n/a	chr6:76402141-76402152
42	CEBPB	chr6:76400863-76400978	K562	blood:	n/a	chr6:76400914-76400925
43	CEBPB	chr6:76403252-76403625	Hela-S3	cervix:	n/a	chr6:76403486-76403499
44	CTCF	chr6:76397360-76397510	HepG2	liver:	n/a	n/a
45	CTCF	chr6:76403360-76403510	HCM	heart:	n/a	n/a
46	CTCF	chr6:76403340-76403490	GM12870	blood:	n/a	n/a
47	CTCF	chr6:76403360-76403510	GM12873	blood:	n/a	n/a
48	CTCF	chr6:76389072-76389090	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:76397373-76397522	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:76403416-76403499	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:76402073..76403999-chr6:76420565..76422699,2	MCF-7	breast:
2	chr6:76405218..76407618-chr6:76430939..76433858,2	MCF-7	breast:
3	chr6:76310342..76312305-chr6:76373129..76377244,3	K562	blood:
4	chr6:76404187..76405990-chr6:76505413..76507332,2	MCF-7	breast:
5	chr6:76384444..76386029-chr6:76458187..76459716,2	MCF-7	breast:
6	chr6:76373474..76375579-chr6:76380760..76383330,2	K562	blood:
7	chr6:76363284..76364897-chr6:76389536..76391998,2	MCF-7	breast:
8	chr6:76402029..76404149-chr6:76408590..76410105,2	MCF-7	breast:
9	chr6:76386546..76388318-chr6:76399041..76401218,2	K562	blood:
10	chr6:76373474..76375579-chr6:76380760..76383330,2	K562	blood:
11	chr6:76371815..76374314-chr6:76380785..76382399,2	MCF-7	breast:
12	chr6:76359039..76361608-chr6:76376741..76379401,2	MCF-7	breast:
13	chr6:76354799..76357581-chr6:76387845..76390206,2	K562	blood:
14	chr6:76370677..76372880-chr6:76377007..76378733,2	K562	blood:
15	chr6:76369769..76371871-chr6:76379242..76380946,2	K562	blood:
16	chr6:76310717..76312305-chr6:76374454..76377244,2	K562	blood:
17	chr6:76386546..76388318-chr6:76399041..76401218,2	K562	blood:
18	chr6:76397986..76399777-chr6:76458759..76460559,2	MCF-7	breast:

Variant related genes	Relation type
SENP6	TF binding region
ENSG00000196586	chromatin interactions
ENSG00000112701	chromatin interactions

Extended variants
information (count: 1236 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1236 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2647415	chr6:76375321-76375322	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533688951	chr6:76375441-76375442	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551742362	chr6:76375470-76375471	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs189632385	chr6:76375472-76375473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs2647416	chr6:76375540-76375541	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs549133816	chr6:76375572-76375573	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs148308644	chr6:76375618-76375619	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534367368	chr6:76375629-76375630	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs180678931	chr6:76375630-76375631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs571114515	chr6:76375638-76375639	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs185985240	chr6:76375646-76375647	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141404218	chr6:76375666-76375667	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs575109238	chr6:76375671-76375672	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372278833	chr6:76375683-76375684	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567559859	chr6:76375698-76375699	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs191281621	chr6:76375718-76375719	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573955705	chr6:76375790-76375791	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35277437	chr6:76375803-76375804	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs150909980	chr6:76375824-76375825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs181343502	chr6:76375842-76375843	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs571967865	chr6:76375868-76375869	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34716703	chr6:76375869-76375870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532994132	chr6:76375871-76375872	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs397705606	chr6:76375873-76375874	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200170034	chr6:76375876-76375877	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375490878	chr6:76375899-76375900	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368927758	chr6:76375910-76375911	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35867662	chr6:76375912-76375913	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372461786	chr6:76375914-76375915	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs375780685	chr6:76375929-76375930	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs199816111	chr6:76375950-76375951	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs34726946	chr6:76375952-76375953	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs34214349	chr6:76375962-76375963	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185574103	chr6:76375971-76375972	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545732180	chr6:76375973-76375974	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563956066	chr6:76376024-76376025	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552958056	chr6:76376088-76376089	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs531156815	chr6:76376113-76376114	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs74674923	chr6:76376114-76376115	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs190447298	chr6:76376120-76376121	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183038302	chr6:76376129-76376130	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs528198505	chr6:76376196-76376197	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs546330023	chr6:76376296-76376297	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs368066186	chr6:76376311-76376312	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs201762586	chr6:76376399-76376400	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs538219477	chr6:76376452-76376453	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374458449	chr6:76376489-76376490	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs550493481	chr6:76376492-76376493	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs147285994	chr6:76376526-76376527	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs199660674	chr6:76376551-76376552	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76320200-76391600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:76330600-76381600	Weak transcription	Stomach Mucosa	stomach
3	chr6:76330600-76390400	Weak transcription	Gastric	stomach
4	chr6:76332800-76389000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:76333200-76391000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr6:76335400-76388800	Weak transcription	Small Intestine	intestine
7	chr6:76339400-76402000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:76340200-76390400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:76340400-76390400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr6:76342200-76387200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:76342800-76391200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr6:76351400-76390400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:76354400-76377600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr6:76354600-76391200	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:76356800-76391800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:76357200-76390000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:76358200-76388000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr6:76358200-76392200	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr6:76358400-76375400	Strong transcription	Fetal Intestine Large	intestine
20	chr6:76358400-76391000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr6:76361800-76380600	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr6:76362000-76387600	Weak transcription	Esophagus	oesophagus
23	chr6:76362000-76389800	Weak transcription	Spleen	Spleen
24	chr6:76364400-76392200	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr6:76364800-76378800	Strong transcription	Primary hematopoietic stem cells	blood
26	chr6:76364800-76392400	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr6:76366200-76382400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr6:76366400-76392400	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr6:76366600-76375400	Strong transcription	Primary T cells from cord blood	blood
30	chr6:76366600-76392400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:76366800-76378800	Strong transcription	Dnd41	blood
32	chr6:76366800-76382200	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr6:76366800-76391000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:76367200-76378000	Strong transcription	Primary B cells from peripheral blood	blood
35	chr6:76367400-76375600	Strong transcription	Fetal Muscle Trunk	muscle
36	chr6:76368000-76389800	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr6:76368200-76382200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr6:76368200-76392200	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr6:76368400-76375600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:76368400-76377600	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr6:76368400-76381000	Strong transcription	HepG2	liver
42	chr6:76368400-76382400	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr6:76368400-76384600	Strong transcription	Fetal Thymus	thymus
44	chr6:76368600-76375400	Strong transcription	Colon Smooth Muscle	Colon
45	chr6:76368600-76377800	Strong transcription	Skeletal Muscle Female	skeletal muscle
46	chr6:76368600-76379600	Strong transcription	HSMM	muscle
47	chr6:76368600-76391800	Strong transcription	Fetal Lung	lung
48	chr6:76368800-76375600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr6:76368800-76377000	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr6:76368800-76381800	Strong transcription	Placenta	Placenta

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