Variant report

Variant	esv2756603
Chromosome Location	chr16:46529399-46610199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:353)
CpG islands
(count:671)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr16:46530690-46530890	K562	blood:	n/a	n/a
2	BACH1	chr16:46530728-46530816	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr16:46588341-46588614	GM12878	blood:	n/a	n/a
4	BHLHE40	chr16:46607758-46607783	K562	blood:	n/a	n/a
5	BHLHE40	chr16:46603093-46603220	K562	blood:	n/a	n/a
6	CEBPB	chr16:46534572-46534639	HepG2	liver:	n/a	n/a
7	CEBPB	chr16:46607214-46607273	K562	blood:	n/a	n/a
8	CEBPB	chr16:46607698-46607727	IMR90	lung:	n/a	n/a
9	CEBPB	chr16:46553053-46553266	Hela-S3	cervix:	n/a	chr16:46553164-46553181 chr16:46553167-46553180
10	CEBPB	chr16:46553020-46553329	HepG2	liver:	n/a	chr16:46553164-46553181 chr16:46553167-46553180
11	CTCF	chr16:46588269-46588645	K562	blood:	n/a	n/a
12	CTCF	chr16:46587940-46588090	AG04450	lung:	n/a	n/a
13	CTCF	chr16:46588332-46588648	MCF-7	breast:	n/a	n/a
14	CTCF	chr16:46588325-46588615	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr16:46588360-46588510	HPF	lung:	n/a	n/a
16	CTCF	chr16:46543827-46543902	GM20000	blood:	n/a	n/a
17	CTCF	chr16:46588260-46588410	WI-38	lung:	n/a	n/a
18	CTCF	chr16:46588400-46588550	HMF	breast:	n/a	n/a
19	CTCF	chr16:46588143-46588647	K562	blood:	n/a	n/a
20	CTCF	chr16:46588323-46588544	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr16:46588322-46588562	GM10266	blood:	n/a	n/a
22	CTCF	chr16:46588360-46588510	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr16:46588322-46588569	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr16:46588340-46588490	WI-38	lung:	n/a	n/a
25	CTCF	chr16:46588380-46588530	GM12869	blood:	n/a	n/a
26	CTCF	chr16:46588360-46588510	BE2_C	brain:	n/a	n/a
27	CTCF	chr16:46588331-46588578	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr16:46588308-46588592	GM13977	blood:	n/a	n/a
29	CTCF	chr16:46588360-46588510	AG10803	skin:	n/a	n/a
30	CTCF	chr16:46588271-46588540	ECC-1	luminal epithelium:	n/a	n/a
31	CTCF	chr16:46588284-46588525	A549	lung:	n/a	n/a
32	CTCF	chr16:46588420-46588570	AG09309	skin:	n/a	n/a
33	CTCF	chr16:46588268-46588745	MCF-7	breast:	n/a	n/a
34	CTCF	chr16:46608898-46608987	MCF-7	breast:	n/a	chr16:46608943-46608952
35	CTCF	chr16:46588310-46588630	A549	lung:	n/a	n/a
36	CTCF	chr16:46588380-46588530	GM12865	blood:	n/a	n/a
37	CTCF	chr16:46588053-46588739	A549	lung:	n/a	n/a
38	CTCF	chr16:46588302-46588637	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr16:46588400-46588550	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr16:46588380-46588530	AG09319	gingival:	n/a	n/a
41	CTCF	chr16:46588320-46588470	GM12878	blood:	n/a	n/a
42	CTCF	chr16:46588400-46588550	HVMF	connective:	n/a	n/a
43	CTCF	chr16:46588029-46588841	SK-N-SH	brain:	n/a	n/a
44	CTCF	chr16:46588380-46588530	GM12871	blood:	n/a	n/a
45	CTCF	chr16:46588360-46588510	HL-60	blood:	n/a	n/a
46	CTCF	chr16:46559670-46559748	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr16:46588297-46588593	Medullo	brain:	n/a	n/a
48	CTCF	chr16:46588360-46588510	Caco-2	colon:	n/a	n/a
49	CTCF	chr16:46588380-46588530	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr16:46588400-46588550	GM12873	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46603321-46603371	HepG2	liver:	n/a
2	chr16:46603015-46603065	ovcar-3	ovarian:	n/a
3	chr16:46602737-46602787	GM19239	blood:	n/a
4	chr16:46603015-46603065	HCF	heart:	n/a
5	chr16:46603021-46603071	SK-N-SH_RA	brain:	n/a
6	chr16:46588509-46588559	GM12878	blood:	n/a
7	chr16:46603015-46603065	HIPEpiC	eye:	n/a
8	chr16:46603259-46603309	SAEC	small airway:	n/a
9	chr16:46604297-46604347	SK-N-SH_RA	brain:	n/a
10	chr16:46588509-46588559	BJ	skin:	n/a
11	chr16:46588509-46588559	MCF-7	breast:	n/a
12	chr16:46602737-46602787	HCPEpiC	choroid plexus:	n/a
13	chr16:46602737-46602787	AG09319	gingival:	n/a
14	chr16:46603021-46603071	Hepatocyte	liver:	n/a
15	chr16:46603059-46603109	HEEpiC	esophagus:	n/a
16	chr16:46607688-46607738	U87	brain:	n/a
17	chr16:46607688-46607738	NHDF-neo	bronchial:	n/a
18	chr16:46603321-46603371	HRPEpiC	eye:	n/a
19	chr16:46603191-46603241	Caco-2	colon:	n/a
20	chr16:46607903-46607953	AG09309	skin:	n/a
21	chr16:46603259-46603309	T-47D	breast:	n/a
22	chr16:46603259-46603309	GM12891	blood:	n/a
23	chr16:46607688-46607738	SK-N-MC	brain:	n/a
24	chr16:46604297-46604347	Jurkat	blood:	n/a
25	chr16:46607688-46607738	K562	blood:	n/a
26	chr16:46602737-46602787	SAEC	small airway:	n/a
27	chr16:46607903-46607953	PANC-1	pancreas:	n/a
28	chr16:46602737-46602787	SK-N-SH	brain:	n/a
29	chr16:46607688-46607738	RPTEC	kidney:	n/a
30	chr16:46588509-46588559	PrEC	prostate:	n/a
31	chr16:46603015-46603065	SK-N-SH	brain:	n/a
32	chr16:46588509-46588559	SAEC	small airway:	n/a
33	chr16:46588509-46588559	HCPEpiC	choroid plexus:	n/a
34	chr16:46607903-46607953	SK-N-MC	brain:	n/a
35	chr16:46603259-46603309	HMEC	breast:	n/a
36	chr16:46607903-46607953	HCF	heart:	n/a
37	chr16:46607688-46607738	BJ	skin:	n/a
38	chr16:46607688-46607738	AG10803	skin:	n/a
39	chr16:46607903-46607953	Jurkat	blood:	n/a
40	chr16:46603015-46603065	PFSK-1	brain:	n/a
41	chr16:46607903-46607953	GM12878	blood:	n/a
42	chr16:46588509-46588559	K562	blood:	n/a
43	chr16:46603059-46603109	GM12891	blood:	n/a
44	chr16:46603015-46603065	HCM	heart:	n/a
45	chr16:46607903-46607953	Caco-2	colon:	n/a
46	chr16:46603021-46603071	NHDF-neo	bronchial:	n/a
47	chr16:46588509-46588559	RPTEC	kidney:	n/a
48	chr16:46603259-46603309	HepG2	liver:	n/a
49	chr16:46603059-46603109	Hepatocyte	liver:	n/a
50	chr16:46607688-46607738	SKMC	muscle:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:46589331..46591714-chr16:46654314..46656100,2	K562	blood:
2	chr16:46598432..46601412-chr16:46613348..46615647,2	K562	blood:
3	chr16:46588378..46588920-chr16:46662972..46663507,2	K562	blood:
4	chr16:46511252..46512930-chr16:46534367..46536672,2	K562	blood:
5	chr16:46603053..46604562-chr16:46606887..46609535,2	MCF-7	breast:
6	chr16:46530274..46532917-chr16:46535064..46536684,2	K562	blood:
7	chr16:46588077..46588805-chr16:46640597..46641513,2	MCF-7	breast:
8	chr16:46530274..46532917-chr16:46535064..46536684,2	K562	blood:
9	chr11:125334060..125334821-chr16:46593821..46594420,2	HCT-116	colon:
10	chr16:46601237..46602830-chr16:46605603..46608385,2	K562	blood:
11	chr16:46607322..46610381-chr16:46616231..46620606,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ORC6-4	chr16:46605449-46606048	NONHSAT142252

No data

Variant related genes	Relation type
RNU6-845P	TF binding region
ENSG00000261356	TF binding region
ANKRD26P1	TF binding region
ENSG00000260251	TF binding region
RNU6-845P	CpG island
ENSG00000261356	CpG island
ANKRD26P1	CpG island
ENSG00000260251	CpG island
ENSG00000171241	chromatin interactions
ENSG00000261239	chromatin interactions
ENSG00000260251	chromatin interactions

Extended variants
information (count: 696 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576380789	chr16:46534426-46534427	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs543909066	chr16:46534470-46534471	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs117130137	chr16:46534518-46534519	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531033209	chr16:46534572-46534573	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs574880099	chr16:46534591-46534592	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs542310370	chr16:46534619-46534620	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs144283627	chr16:46534637-46534638	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561663402	chr16:46534651-46534652	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112527425	chr16:46534652-46534653	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs147390892	chr16:46534671-46534672	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571556290	chr16:46534723-46534724	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139445819	chr16:46534769-46534770	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs551115632	chr16:46534774-46534775	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560223594	chr16:46534798-46534799	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536484655	chr16:46534825-46534826	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs548073868	chr16:46534832-46534833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs543712004	chr16:46534893-46534894	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373334149	chr16:46534904-46534905	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144986759	chr16:46534956-46534957	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533844461	chr16:46534969-46534970	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs16945380	chr16:46534977-46534978	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs183855199	chr16:46534990-46534991	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532329779	chr16:46535006-46535007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149211399	chr16:46535088-46535089	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs565871476	chr16:46535113-46535114	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs77621215	chr16:46535115-46535116	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574183001	chr16:46535119-46535120	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543249947	chr16:46535121-46535122	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs561322092	chr16:46535157-46535158	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573340542	chr16:46535180-46535181	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs142467025	chr16:46535204-46535205	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565201911	chr16:46535217-46535218	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs565548406	chr16:46535224-46535225	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs545528677	chr16:46535314-46535315	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs118098722	chr16:46535320-46535321	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563010769	chr16:46535323-46535324	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530131675	chr16:46535348-46535349	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548614997	chr16:46535389-46535390	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529715819	chr16:46535457-46535458	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs369969318	chr16:46535458-46535459	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs151297046	chr16:46535510-46535511	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533952486	chr16:46535534-46535535	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552212053	chr16:46535608-46535609	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570393884	chr16:46535610-46535611	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537485185	chr16:46535632-46535633	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563831764	chr16:46535633-46535634	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34253469	chr16:46535644-46535645	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555733878	chr16:46535677-46535678	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376320920	chr16:46535809-46535810	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34829003	chr16:46535823-46535824	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46552600-46553800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr16:46558600-46559200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr16:46581800-46583000	Enhancers	Fetal Lung	lung
4	chr16:46588400-46588600	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr16:46588400-46588600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr16:46588400-46588600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
7	chr16:46588400-46588600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr16:46588400-46588600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr16:46588400-46588600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr16:46588400-46588600	Enhancers	Adipose Nuclei	Adipose
11	chr16:46588400-46588600	Active TSS	K562	blood
12	chr16:46588400-46588800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr16:46588400-46588800	Active TSS	Muscle Satellite Cultured Cells	--
14	chr16:46588400-46588800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr16:46588400-46588800	Active TSS	Brain Angular Gyrus	brain
16	chr16:46588400-46588800	Active TSS	Brain Cingulate Gyrus	brain
17	chr16:46588400-46588800	Enhancers	Fetal Muscle Trunk	muscle
18	chr16:46588400-46588800	Enhancers	Stomach Mucosa	stomach
19	chr16:46588400-46588800	Active TSS	HepG2	liver
20	chr16:46588400-46588800	Active TSS	NHDF-Ad	bronchial
21	chr16:46588600-46588800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr16:46588600-46588800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
23	chr16:46588600-46588800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr16:46588600-46588800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr16:46588600-46588800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr16:46588600-46588800	Flanking Active TSS	K562	blood
27	chr16:46588800-46589400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr16:46588800-46589600	Weak transcription	NHDF-Ad	bronchial
29	chr16:46588800-46590800	Weak transcription	K562	blood
30	chr16:46589600-46591600	Enhancers	NHDF-Ad	bronchial
31	chr16:46589800-46590000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr16:46589800-46590200	Enhancers	Osteobl	bone
33	chr16:46589800-46590400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr16:46590200-46594000	Weak transcription	Osteobl	bone
35	chr16:46590400-46591400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr16:46590800-46591000	Bivalent/Poised TSS	HepG2	liver
37	chr16:46590800-46591000	Flanking Active TSS	K562	blood
38	chr16:46591000-46591200	Enhancers	K562	blood
39	chr16:46591000-46591600	Bivalent Enhancer	HepG2	liver
40	chr16:46591200-46591600	Flanking Active TSS	K562	blood
41	chr16:46591400-46592000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr16:46591600-46592000	Enhancers	K562	blood
43	chr16:46594000-46594200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr16:46594000-46594200	Enhancers	Osteobl	bone
45	chr16:46599800-46600000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr16:46600000-46602000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr16:46600400-46602800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr16:46601400-46603000	Weak transcription	Right Atrium	heart
49	chr16:46602000-46602600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr16:46602600-46603600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links