Variant report

Variant	esv1842993
Chromosome Location	chr16:70251428-70283736
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:923)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:923 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr16:70266179-70266523	GM12878	blood:	n/a	n/a
2	BATF	chr16:70269207-70269408	GM12878	blood:	n/a	n/a
3	BATF	chr16:70272645-70272986	GM12878	blood:	n/a	n/a
4	BATF	chr16:70277954-70278184	GM12878	blood:	n/a	n/a
5	BATF	chr16:70275352-70275629	GM12878	blood:	n/a	n/a
6	BATF	chr16:70269196-70269455	GM12878	blood:	n/a	n/a
7	BATF	chr16:70275330-70275612	GM12878	blood:	n/a	n/a
8	BATF	chr16:70252521-70252845	GM12878	blood:	n/a	chr16:70252736-70252746
9	BATF	chr16:70259711-70260057	GM12878	blood:	n/a	n/a
10	BATF	chr16:70265769-70265977	GM12878	blood:	n/a	n/a
11	BATF	chr16:70266143-70266490	GM12878	blood:	n/a	n/a
12	BATF	chr16:70274531-70275234	GM12878	blood:	n/a	n/a
13	BATF	chr16:70272693-70272978	GM12878	blood:	n/a	n/a
14	BATF	chr16:70274761-70275229	GM12878	blood:	n/a	n/a
15	BATF	chr16:70270340-70270551	GM12878	blood:	n/a	n/a
16	BCL11A	chr16:70273183-70273430	GM12878	blood:	n/a	n/a
17	BCL11A	chr16:70253466-70253640	GM12878	blood:	n/a	n/a
18	BCL11A	chr16:70266128-70266474	GM12878	blood:	n/a	n/a
19	BCL11A	chr16:70267253-70267439	GM12878	blood:	n/a	n/a
20	BCL11A	chr16:70274544-70275641	GM12878	blood:	n/a	n/a
21	BCL11A	chr16:70264796-70265164	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:70274796-70275305	GM12878	blood:	n/a	n/a
23	BCL11A	chr16:70252607-70252876	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:70256979-70257253	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:70252674-70252910	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:70256507-70256821	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:70272703-70272967	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:70274569-70274791	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:70260079-70260328	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:70266040-70266508	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:70265235-70265407	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:70272603-70273149	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:70256901-70257158	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:70275340-70275579	GM12878	blood:	n/a	n/a
35	BHLHE40	chr16:70277485-70277753	HepG2	liver:	n/a	n/a
36	BHLHE40	chr16:70256452-70256822	HepG2	liver:	n/a	n/a
37	BHLHE40	chr16:70254336-70254859	HepG2	liver:	n/a	n/a
38	BHLHE40	chr16:70254937-70255237	HepG2	liver:	n/a	n/a
39	BHLHE40	chr16:70256978-70257194	HepG2	liver:	n/a	n/a
40	BHLHE40	chr16:70264795-70265113	HepG2	liver:	n/a	n/a
41	BHLHE40	chr16:70260045-70260625	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:70264195-70264243	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr16:70262826-70262837	GM13976	blood:	n/a	n/a
44	CTCF	chr16:70262795-70262824	GM13976	blood:	n/a	n/a
45	CTCF	chr16:70277514-70277570	GM13977	blood:	n/a	n/a
46	CTCF	chr16:70267965-70268030	GM13976	blood:	n/a	n/a
47	CTCF	chr16:70261723-70261744	GM13976	blood:	n/a	n/a
48	CTCF	chr16:70276360-70276510	GM12869	blood:	n/a	n/a
49	EBF1	chr16:70269220-70269389	GM12878	blood:	n/a	n/a
50	EBF1	chr16:70254306-70254538	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70283421-70283471	BE2_C	brain:	n/a
2	chr16:70283421-70283471	ovcar-3	ovarian:	n/a
3	chr16:70283421-70283471	HCT-116	colon:	n/a
4	chr16:70259186-70259236	AoSMC	blood vessel:	n/a
5	chr16:70259186-70259236	NB4	blood:	n/a
6	chr16:70283421-70283471	BJ	skin:	n/a
7	chr16:70259186-70259236	Hela-S3	cervix:	n/a
8	chr16:70259186-70259236	NH-A	brain:	n/a
9	chr16:70283421-70283471	U87	brain:	n/a
10	chr16:70259186-70259236	HCM	heart:	n/a
11	chr16:70283421-70283471	A549	lung:	n/a
12	chr16:70283421-70283471	HRPEpiC	eye:	n/a
13	chr16:70283421-70283471	NB4	blood:	n/a
14	chr16:70259186-70259236	HL-60	blood:	n/a
15	chr16:70259186-70259236	HMEC	breast:	n/a
16	chr16:70259186-70259236	SAEC	small airway:	n/a
17	chr16:70259186-70259236	HIPEpiC	eye:	n/a
18	chr16:70259186-70259236	HUVEC	blood vessel:	n/a
19	chr16:70259186-70259236	HEK293	kidney:	embryo
20	chr16:70283421-70283471	GM19239	blood:	n/a
21	chr16:70283421-70283471	HUVEC	blood vessel:	n/a
22	chr16:70259186-70259236	MCF-7	breast:	n/a
23	chr16:70283421-70283471	GM06990	blood:	n/a
24	chr16:70259186-70259236	PrEC	prostate:	n/a
25	chr16:70259186-70259236	NHDF-neo	bronchial:	n/a
26	chr16:70259186-70259236	Hepatocyte	liver:	n/a
27	chr16:70283421-70283471	HCM	heart:	n/a
28	chr16:70283421-70283471	Hepatocyte	liver:	n/a
29	chr16:70259186-70259236	H1-hESC	embryonic stem cell:	embryo
30	chr16:70259186-70259236	LNCaP	prostate:	n/a
31	chr16:70259186-70259236	AG04449	skin:	fetal
32	chr16:70259186-70259236	MCF10A-Er-Src	breast:	n/a
33	chr16:70259186-70259236	SK-N-MC	brain:	n/a
34	chr16:70283421-70283471	K562	blood:	n/a
35	chr16:70259186-70259236	HRPEpiC	eye:	n/a
36	chr16:70259186-70259236	ProgFib	skin:	n/a
37	chr16:70259186-70259236	T-47D	breast:	n/a
38	chr16:70283421-70283471	NHBE	bronchial:	n/a
39	chr16:70259186-70259236	HepG2	liver:	n/a
40	chr16:70259186-70259236	GM06990	blood:	n/a
41	chr16:70283421-70283471	HEK293	kidney:	embryo
42	chr16:70259186-70259236	GM12891	blood:	n/a
43	chr16:70283421-70283471	SK-N-SH_RA	brain:	n/a
44	chr16:70259186-70259236	HNPCEpiC	eye:	n/a
45	chr16:70283421-70283471	IMR90	lung:	fetal
46	chr16:70283421-70283471	HL-60	blood:	n/a
47	chr16:70283421-70283471	PrEC	prostate:	n/a
48	chr16:70283421-70283471	Caco-2	colon:	n/a
49	chr16:70259186-70259236	ovcar-3	ovarian:	n/a
50	chr16:70259186-70259236	HCPEpiC	choroid plexus:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70283625..70285831-chr16:70321379..70323186,2	K562	blood:
2	chr16:70278247..70283453-chr16:70284015..70287841,6	MCF-7	breast:
3	chr16:70279273..70282169-chr16:70284255..70286204,3	K562	blood:
4	chr16:70279244..70282169-chr16:70284255..70286230,4	K562	blood:
5	chr16:70191657..70193675-chr16:70283732..70285560,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DDX19B-2	chr16:70273803-70273904	NONHSAT143414
2	lnc-DDX19B-2	chr16:70280560-70282018	NONHSAT143414

No data

Variant related genes	Relation type
ENSG00000238734	TF binding region
ENSG00000269866	TF binding region
ENSG00000261556	TF binding region
ENSG00000238734	CpG island
ENSG00000269866	CpG island
ENSG00000261556	CpG island
ENSG00000223496	chromatin interactions

Extended variants
information (count: 1132 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1132 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545977478	chr16:70251433-70251434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564159061	chr16:70251434-70251435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576064130	chr16:70251454-70251455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200618042	chr16:70251479-70251480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543121174	chr16:70251548-70251549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561459685	chr16:70251553-70251554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528817634	chr16:70251614-70251615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546992638	chr16:70251772-70251773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559615266	chr16:70251780-70251781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533495155	chr16:70251785-70251786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575234503	chr16:70251826-70251827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140953118	chr16:70251869-70251870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3972050	chr16:70251900-70251901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570183601	chr16:70251901-70251902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537673611	chr16:70251912-70251913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557949207	chr16:70251925-70251926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3972051	chr16:70251937-70251938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552293061	chr16:70251939-70251940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3874610	chr16:70251954-70251955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540570141	chr16:70251960-70251961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564857290	chr16:70251989-70251990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572127114	chr16:70252015-70252016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549465759	chr16:70252026-70252027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3972042	chr16:70252046-70252047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3874611	chr16:70252052-70252053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11866101	chr16:70252074-70252075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567773340	chr16:70252082-70252083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554019018	chr16:70252088-70252089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371549639	chr16:70252089-70252090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534972840	chr16:70252112-70252113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2869139	chr16:70252124-70252125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188034916	chr16:70252134-70252135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2869140	chr16:70252144-70252145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572297882	chr16:70252154-70252155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2869141	chr16:70252168-70252169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539378160	chr16:70252169-70252170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56814555	chr16:70252188-70252189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2869142	chr16:70252202-70252203	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558053270	chr16:70252212-70252213	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2869143	chr16:70252217-70252218	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2869144	chr16:70252229-70252230	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2869145	chr16:70252243-70252244	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532735246	chr16:70252253-70252254	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2869146	chr16:70252275-70252276	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192607342	chr16:70252279-70252280	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs3972043	chr16:70252281-70252282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142160593	chr16:70252306-70252307	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2869147	chr16:70252307-70252308	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2869148	chr16:70252347-70252348	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2869149	chr16:70252348-70252349	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	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
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70226600-70252600	Weak transcription	Adipose Nuclei	Adipose
2	chr16:70231200-70252000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:70231400-70258600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr16:70232400-70284800	Weak transcription	Spleen	Spleen
5	chr16:70233200-70253600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr16:70233200-70283400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr16:70233200-70283600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr16:70233600-70253600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr16:70233800-70252200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr16:70234800-70260800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr16:70235600-70258600	Weak transcription	Pancreas	Pancrea
12	chr16:70235600-70284200	Weak transcription	Brain Cingulate Gyrus	brain
13	chr16:70236200-70258600	Weak transcription	Thymus	Thymus
14	chr16:70237000-70258600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr16:70237000-70258800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr16:70237200-70267200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr16:70237200-70284800	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr16:70238400-70253400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr16:70238400-70274600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr16:70238600-70252200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr16:70238600-70284800	Weak transcription	Esophagus	oesophagus
22	chr16:70238800-70252200	Weak transcription	Primary B cells from peripheral blood	blood
23	chr16:70238800-70253400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr16:70238800-70260400	Weak transcription	Fetal Brain Female	brain
25	chr16:70238800-70283400	Weak transcription	NHEK	skin
26	chr16:70238800-70283600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr16:70239000-70260600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr16:70239000-70266800	Weak transcription	Aorta	Aorta
29	chr16:70239200-70256800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr16:70239200-70260600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr16:70239600-70283400	Weak transcription	Brain Angular Gyrus	brain
32	chr16:70239800-70252200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr16:70239800-70253600	Weak transcription	Primary T cells from cord blood	blood
34	chr16:70239800-70259000	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr16:70240200-70253200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr16:70240200-70258600	Weak transcription	Gastric	stomach
37	chr16:70240200-70260800	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr16:70241000-70267600	Weak transcription	A549	lung
39	chr16:70241000-70283600	Weak transcription	Brain Germinal Matrix	brain
40	chr16:70241200-70255200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr16:70241200-70260600	Weak transcription	Fetal Thymus	thymus
42	chr16:70241200-70260600	Weak transcription	Osteobl	bone
43	chr16:70241400-70253600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr16:70242000-70253400	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr16:70242200-70253600	Weak transcription	HSMM	muscle
46	chr16:70242200-70260000	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr16:70242200-70272600	Weak transcription	Primary B cells from cord blood	blood
48	chr16:70242200-70283400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr16:70242400-70253800	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr16:70242400-70260000	Weak transcription	Duodenum Smooth Muscle	Duodenum

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