Variant report

Variant	nsv974810
Chromosome Location	chr16:46642280-46653079
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	ATF2	chr16:46645891-46646515	GM12878	blood:	n/a	n/a
2	CREB1	chr16:46645850-46646474	GM12878	blood:	n/a	n/a
3	CREB1	chr16:46645962-46646444	GM12878	blood:	n/a	n/a
4	CTCF	chr16:46646240-46646390	GM12864	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
5	CTCF	chr16:46646360-46646510	GM12871	blood:	n/a	chr16:46646361-46646369
6	CTCF	chr16:46646240-46646390	GM12865	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
7	CTCF	chr16:46646220-46646370	GM12866	blood:	n/a	chr16:46646361-46646369
8	CTCF	chr16:46646300-46646450	GM12864	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
9	CTCF	chr16:46646300-46646450	GM12869	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
10	CTCF	chr16:46645540-46645690	AoAF	blood vessel:	n/a	n/a
11	CTCF	chr16:46646280-46646430	GM12868	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
12	CTCF	chr16:46646300-46646450	GM12878	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
13	CTCF	chr16:46646280-46646430	GM12873	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
14	CTCF	chr16:46646340-46646490	GM12873	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
15	CTCF	chr16:46646360-46646510	GM12865	blood:	n/a	chr16:46646361-46646369
16	CTCF	chr16:46646360-46646510	GM06990	blood:	n/a	chr16:46646361-46646369
17	CTCF	chr16:46646320-46646470	GM12873	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
18	CTCF	chr16:46652554-46652647	GM10248	blood:	n/a	n/a
19	CTCF	chr16:46646300-46646450	GM12872	blood:	n/a	chr16:46646361-46646369 chr16:46646351-46646372 chr16:46646357-46646373
20	EP300	chr16:46652566-46652738	GM12878	blood:	n/a	n/a
21	MAFF	chr16:46642173-46642319	HepG2	liver:	n/a	chr16:46642184-46642202
22	MAFK	chr16:46642098-46642326	HepG2	liver:	n/a	chr16:46642185-46642201 chr16:46642190-46642201 chr16:46642185-46642200 chr16:46642190-46642201
23	MYC	chr16:46644496-46644562	MCF-7	breast:	n/a	n/a
24	PAX5	chr16:46652467-46652783	GM12878	blood:	n/a	n/a
25	POLR2A	chr16:46647322-46647584	K562	blood:	n/a	n/a
26	POLR2A	chr16:46645908-46646082	K562	blood:	n/a	n/a
27	POLR2A	chr16:46647773-46647930	K562	blood:	n/a	n/a
28	POLR2A	chr16:46647479-46647712	K562	blood:	n/a	n/a
29	POLR2A	chr16:46645929-46646979	GM12892	blood:	n/a	n/a
30	POLR2A	chr16:46644880-46645139	K562	blood:	n/a	n/a
31	POLR2A	chr16:46646869-46647216	K562	blood:	n/a	n/a
32	POLR2A	chr16:46643999-46644023	HepG2	liver:	n/a	n/a
33	POLR2A	chr16:46647432-46647559	K562	blood:	n/a	n/a
34	POLR2A	chr16:46647278-46647747	K562	blood:	n/a	n/a
35	POLR2A	chr16:46644308-46644373	K562	blood:	n/a	n/a
36	POLR2A	chr16:46650232-46650559	K562	blood:	n/a	n/a
37	POLR2A	chr16:46643694-46643869	K562	blood:	n/a	n/a
38	POLR2A	chr16:46642213-46642304	K562	blood:	n/a	n/a
39	RUNX3	chr16:46652426-46652837	GM12878	blood:	n/a	n/a
40	RUNX3	chr16:46652427-46652741	GM12878	blood:	n/a	n/a
41	TBP	chr16:46646195-46646268	GM12878	blood:	n/a	n/a
42	TCF12	chr16:46647381-46647845	SK-N-SH	brain:	n/a	n/a
43	ZNF384	chr16:46644415-46644507	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46651918-46651968	AG04450	lung:	fetal
2	chr16:46651918-46651968	HNPCEpiC	eye:	n/a
3	chr16:46648124-46648174	NH-A	brain:	n/a
4	chr16:46648124-46648174	Caco-2	colon:	n/a
5	chr16:46651918-46651968	HRPEpiC	eye:	n/a
6	chr16:46651918-46651968	PFSK-1	brain:	n/a
7	chr16:46648124-46648174	AG09309	skin:	n/a
8	chr16:46648124-46648174	HL-60	blood:	n/a
9	chr16:46651918-46651968	LNCaP	prostate:	n/a
10	chr16:46651918-46651968	HCM	heart:	n/a
11	chr16:46651918-46651968	HepG2	liver:	n/a
12	chr16:46651918-46651968	ovcar-3	ovarian:	n/a
13	chr16:46648124-46648174	GM12891	blood:	n/a
14	chr16:46648124-46648174	GM06990	blood:	n/a
15	chr16:46648124-46648174	HRPEpiC	eye:	n/a
16	chr16:46648124-46648174	K562	blood:	n/a
17	chr16:46648124-46648174	U87	brain:	n/a
18	chr16:46651918-46651968	MCF-7	breast:	n/a
19	chr16:46651918-46651968	H1-hESC	embryonic stem cell:	embryo
20	chr16:46648124-46648174	MCF10A-Er-Src	breast:	n/a
21	chr16:46651918-46651968	AG10803	skin:	n/a
22	chr16:46648124-46648174	ProgFib	skin:	n/a
23	chr16:46648124-46648174	BE2_C	brain:	n/a
24	chr16:46651918-46651968	RPTEC	kidney:	n/a
25	chr16:46648124-46648174	AoSMC	blood vessel:	n/a
26	chr16:46651918-46651968	ECC-1	luminal epithelium:	n/a
27	chr16:46651918-46651968	HEK293	kidney:	embryo
28	chr16:46651918-46651968	IMR90	lung:	fetal
29	chr16:46651918-46651968	GM12891	blood:	n/a
30	chr16:46648124-46648174	NT2-D1	testis:	n/a
31	chr16:46648124-46648174	HCM	heart:	n/a
32	chr16:46651918-46651968	K562	blood:	n/a
33	chr16:46651918-46651968	SK-N-SH	brain:	n/a
34	chr16:46648124-46648174	HMEC	breast:	n/a
35	chr16:46651918-46651968	Hela-S3	cervix:	n/a
36	chr16:46651918-46651968	SK-N-MC	brain:	n/a
37	chr16:46651918-46651968	GM12878	blood:	n/a
38	chr16:46648124-46648174	GM12892	blood:	n/a
39	chr16:46648124-46648174	HEEpiC	esophagus:	n/a
40	chr16:46651918-46651968	HRE	kidney:	n/a
41	chr16:46651918-46651968	U87	brain:	n/a
42	chr16:46651918-46651968	NH-A	brain:	n/a
43	chr16:46648124-46648174	NHDF-neo	bronchial:	n/a
44	chr16:46648124-46648174	HRCEpiC	kidney:	n/a
45	chr16:46651918-46651968	NHDF-neo	bronchial:	n/a
46	chr16:46648124-46648174	SK-N-SH	brain:	n/a
47	chr16:46651918-46651968	PANC-1	pancreas:	n/a
48	chr16:46651918-46651968	HL-60	blood:	n/a
49	chr16:46651918-46651968	A549	lung:	n/a
50	chr16:46651918-46651968	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:46651769..46655217-chr16:46661271..46664188,4	K562	blood:
2	chr16:46642369..46643957-chr16:46648260..46651071,2	K562	blood:
3	chr16:46638622..46640277-chr16:46650672..46652723,2	K562	blood:
4	chr16:46649901..46653063-chr16:46653348..46656157,4	K562	blood:
5	chr16:46650731..46653063-chr16:46653686..46656157,4	K562	blood:
6	chr16:46636261..46637898-chr16:46641523..46644415,2	K562	blood:

Variant related genes	Relation type
SHCBP1	TF binding region
SHCBP1	CpG island
ENSG00000171241	chromatin interactions

Extended variants
information (count: 350 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34559393	chr16:46642286-46642287	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs186594524	chr16:46642326-46642327	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs539181685	chr16:46642391-46642392	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557299553	chr16:46642434-46642435	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs8052092	chr16:46642456-46642457	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538111070	chr16:46642493-46642494	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs34823071	chr16:46642515-46642516	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559103016	chr16:46642560-46642561	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149851174	chr16:46642601-46642602	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575069470	chr16:46642607-46642608	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs542404289	chr16:46642641-46642642	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs533672951	chr16:46642687-46642688	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs371970316	chr16:46642769-46642770	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572556308	chr16:46642801-46642802	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567136181	chr16:46642802-46642803	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs145842187	chr16:46642804-46642805	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569981861	chr16:46642818-46642819	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs535944487	chr16:46642886-46642887	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531733251	chr16:46642925-46642926	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs537886631	chr16:46642940-46642941	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148587866	chr16:46643155-46643156	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs71380960	chr16:46643163-46643164	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs530719021	chr16:46643164-46643165	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71380961	chr16:46643186-46643187	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562013699	chr16:46643188-46643189	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs71380962	chr16:46643193-46643194	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192377303	chr16:46643278-46643279	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567312316	chr16:46643324-46643325	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs138770609	chr16:46643354-46643355	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs71158875	chr16:46643380-46643381	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs571563950	chr16:46643413-46643414	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs7205598	chr16:46643456-46643457	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368893580	chr16:46643463-46643464	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112797488	chr16:46643521-46643522	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs141286865	chr16:46643625-46643626	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs183155583	chr16:46643649-46643650	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534679184	chr16:46643653-46643654	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537808703	chr16:46643726-46643727	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs537039400	chr16:46643774-46643775	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145071178	chr16:46643838-46643839	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs557531192	chr16:46643866-46643867	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201733391	chr16:46643867-46643868	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575052009	chr16:46643876-46643877	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77526846	chr16:46643878-46643879	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs536185738	chr16:46643883-46643884	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs185216804	chr16:46643926-46643927	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs6650585	chr16:46643931-46643932	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs553914277	chr16:46643932-46643933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs57308723	chr16:46643998-46643999	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556841729	chr16:46644007-46644008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46608000-46654200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr16:46609400-46646400	Weak transcription	Fetal Heart	heart
3	chr16:46614200-46650000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr16:46615200-46654400	Weak transcription	Fetal Kidney	kidney
5	chr16:46617200-46643800	Weak transcription	Fetal Stomach	stomach
6	chr16:46619600-46644600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr16:46620000-46654600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr16:46620800-46649800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr16:46621200-46647400	Weak transcription	NHDF-Ad	bronchial
10	chr16:46625200-46643000	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr16:46625200-46652400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr16:46625200-46653600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr16:46625400-46643400	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr16:46625400-46652200	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr16:46625400-46652800	Strong transcription	Dnd41	blood
16	chr16:46625600-46654600	Weak transcription	Left Ventricle	heart
17	chr16:46626600-46652200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr16:46627200-46646400	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr16:46627200-46651800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr16:46627400-46642400	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr16:46627400-46643000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
22	chr16:46627600-46654400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr16:46627800-46642600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr16:46627800-46646800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr16:46628200-46642400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr16:46628200-46654600	Weak transcription	Esophagus	oesophagus
27	chr16:46628600-46654000	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr16:46629000-46654600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr16:46629400-46654600	Weak transcription	Fetal Intestine Small	intestine
30	chr16:46629600-46646600	Weak transcription	Fetal Lung	lung
31	chr16:46630600-46643000	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr16:46630600-46643200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr16:46630800-46653400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr16:46631200-46654200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr16:46632000-46654200	Weak transcription	Fetal Brain Female	brain
36	chr16:46632200-46654800	Weak transcription	Pancreas	Pancrea
37	chr16:46633000-46649800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr16:46633200-46647200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr16:46633400-46654200	Weak transcription	Primary B cells from cord blood	blood
40	chr16:46633400-46654600	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr16:46634000-46648000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr16:46635600-46654200	Weak transcription	Placenta	Placenta
43	chr16:46637800-46644800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr16:46637800-46647200	Weak transcription	Brain Germinal Matrix	brain
45	chr16:46638000-46643800	Weak transcription	Fetal Muscle Trunk	muscle
46	chr16:46638000-46644600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr16:46638000-46644600	Weak transcription	Fetal Muscle Leg	muscle
48	chr16:46638000-46644800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr16:46638000-46644800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr16:46638000-46644800	Weak transcription	Thymus	Thymus

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