Variant report

Variant	nsv1063412
Chromosome Location	chr16:82806653-82826507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr16:82819586-82819857	GM12878	blood:	n/a	n/a
2	CEBPB	chr16:82810502-82810653	K562	blood:	n/a	chr16:82810606-82810617
3	CEBPB	chr16:82816457-82816749	H1-hESC	embryonic stem cell:	n/a	chr16:82816601-82816612
4	CEBPB	chr16:82810463-82810760	A549	lung:	n/a	chr16:82810606-82810617
5	CEBPB	chr16:82810451-82810782	IMR90	lung:	n/a	chr16:82810606-82810617
6	CEBPB	chr16:82810428-82810778	HepG2	liver:	n/a	chr16:82810606-82810617
7	E2F6	chr16:82816144-82816740	H1-hESC	embryonic stem cell:	n/a	n/a
8	E2F6	chr16:82816253-82816573	H1-hESC	embryonic stem cell:	n/a	n/a
9	EBF1	chr16:82810223-82810240	GM12878	blood:	n/a	n/a
10	EBF1	chr16:82806654-82807179	GM12878	blood:	n/a	chr16:82807019-82807028
11	EGR1	chr16:82825881-82826026	K562	blood:	n/a	chr16:82825966-82825980 chr16:82825966-82825979 chr16:82825968-82825978 chr16:82825967-82825978 chr16:82825969-82825978 chr16:82825965-82825980 chr16:82825966-82825979 chr16:82825967-82825978 chr16:82825968-82825977 chr16:82825968-82825978
12	EP300	chr16:82816247-82816832	H1-hESC	embryonic stem cell:	n/a	n/a
13	EP300	chr16:82813914-82814233	SK-N-SH_RA	brain:	n/a	n/a
14	GATA3	chr16:82818942-82819142	SH-SY5Y	brain:	n/a	n/a
15	GTF2F1	chr16:82816363-82816595	H1-hESC	embryonic stem cell:	n/a	n/a
16	IRF3	chr16:82810621-82810640	GM12878	blood:	n/a	n/a
17	JUND	chr16:82816343-82816535	H1-hESC	embryonic stem cell:	n/a	n/a
18	MAFK	chr16:82822551-82822862	HepG2	liver:	n/a	n/a
19	MAFK	chr16:82807259-82807300	IMR90	lung:	n/a	n/a
20	MAFK	chr16:82822585-82822830	IMR90	lung:	n/a	n/a
21	MAX	chr16:82816178-82816717	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAX	chr16:82810173-82810373	NB4	blood:	n/a	n/a
23	MAX	chr16:82816198-82816800	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAX	chr16:82821973-82822044	NB4	blood:	n/a	n/a
25	MAX	chr16:82816197-82816487	H1-hESC	embryonic stem cell:	n/a	n/a
26	MXI1	chr16:82816338-82816781	H1-hESC	embryonic stem cell:	n/a	n/a
27	MYC	chr16:82821909-82822042	H1-hESC	embryonic stem cell:	n/a	n/a
28	MYC	chr16:82816261-82816514	H1-hESC	embryonic stem cell:	n/a	n/a
29	NANOG	chr16:82816374-82816822	H1-hESC	embryonic stem cell:	n/a	chr16:82816510-82816519
30	POLR2A	chr16:82816282-82816458	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr16:82818665-82818701	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr16:82816261-82816749	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr16:82816901-82816905	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr16:82816852-82816868	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr16:82817912-82818038	A549	lung:	n/a	n/a
36	POLR2A	chr16:82819506-82819524	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr16:82816772-82816818	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr16:82816276-82816532	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr16:82816558-82816789	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr16:82816304-82816578	H1-hESC	embryonic stem cell:	n/a	n/a
41	RAD21	chr16:82816431-82817009	H1-hESC	embryonic stem cell:	n/a	n/a
42	REST	chr16:82811347-82811587	H1-hESC	embryonic stem cell:	n/a	n/a
43	REST	chr16:82811261-82811598	PFSK-1	brain:	n/a	n/a
44	REST	chr16:82816420-82816648	H1-hESC	embryonic stem cell:	n/a	chr16:82816572-82816592 chr16:82816580-82816590 chr16:82816572-82816592 chr16:82816625-82816632
45	REST	chr16:82811300-82811597	H1-hESC	embryonic stem cell:	n/a	n/a
46	REST	chr16:82811268-82811642	SK-N-SH	brain:	n/a	n/a
47	REST	chr16:82811329-82811630	SK-N-SH	brain:	n/a	n/a
48	REST	chr16:82811333-82811603	PFSK-1	brain:	n/a	n/a
49	REST	chr16:82811372-82811665	MCF-7	breast:	n/a	n/a
50	RUNX3	chr16:82806743-82806958	GM12878	blood:	n/a	chr16:82806859-82806868 chr16:82806859-82806868

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:82816457-82816507	GM12878	blood:	n/a
2	chr16:82816457-82816507	HCT-116	colon:	n/a
3	chr16:82816457-82816507	NT2-D1	testis:	n/a
4	chr16:82816457-82816507	GM19239	blood:	n/a
5	chr16:82816457-82816507	GM12891	blood:	n/a
6	chr16:82816457-82816507	U87	brain:	n/a
7	chr16:82816457-82816507	HAEpiC	amniotic membrane:	n/a
8	chr16:82816457-82816507	HRE	kidney:	n/a
9	chr16:82816457-82816507	SAEC	small airway:	n/a
10	chr16:82816457-82816507	MCF10A-Er-Src	breast:	n/a
11	chr16:82816457-82816507	GM12892	blood:	n/a
12	chr16:82816457-82816507	Hela-S3	cervix:	n/a
13	chr16:82816457-82816507	NHBE	bronchial:	n/a
14	chr16:82816457-82816507	ECC-1	luminal epithelium:	n/a
15	chr16:82816457-82816507	Jurkat	blood:	n/a
16	chr16:82816457-82816507	NHDF-neo	bronchial:	n/a
17	chr16:82816457-82816507	IMR90	lung:	fetal
18	chr16:82816457-82816507	NH-A	brain:	n/a
19	chr16:82816457-82816507	SKMC	muscle:	n/a
20	chr16:82816457-82816507	LNCaP	prostate:	n/a
21	chr16:82816457-82816507	HEK293	kidney:	embryo
22	chr16:82816457-82816507	SK-N-MC	brain:	n/a
23	chr16:82816457-82816507	ovcar-3	ovarian:	n/a
24	chr16:82816457-82816507	SK-N-SH	brain:	n/a
25	chr16:82816457-82816507	Hepatocyte	liver:	n/a
26	chr16:82816457-82816507	HCPEpiC	choroid plexus:	n/a
27	chr16:82816457-82816507	PANC-1	pancreas:	n/a
28	chr16:82816457-82816507	HRCEpiC	kidney:	n/a
29	chr16:82816457-82816507	BJ	skin:	n/a
30	chr16:82816457-82816507	AG09319	gingival:	n/a
31	chr16:82816457-82816507	AG04449	skin:	fetal
32	chr16:82816457-82816507	GM06990	blood:	n/a
33	chr16:82816457-82816507	AoSMC	blood vessel:	n/a
34	chr16:82816457-82816507	HIPEpiC	eye:	n/a
35	chr16:82816457-82816507	SK-N-SH_RA	brain:	n/a
36	chr16:82816457-82816507	HCM	heart:	n/a
37	chr16:82816457-82816507	AG10803	skin:	n/a
38	chr16:82816457-82816507	AG04450	lung:	fetal
39	chr16:82816457-82816507	H1-hESC	embryonic stem cell:	embryo
40	chr16:82816457-82816507	HL-60	blood:	n/a
41	chr16:82816457-82816507	MCF-7	breast:	n/a
42	chr16:82816457-82816507	HMEC	breast:	n/a
43	chr16:82816457-82816507	AG09309	skin:	n/a
44	chr16:82816457-82816507	NB4	blood:	n/a
45	chr16:82816457-82816507	K562	blood:	n/a
46	chr16:82816457-82816507	A549	lung:	n/a
47	chr16:82816457-82816507	ProgFib	skin:	n/a
48	chr16:82816457-82816507	PFSK-1	brain:	n/a
49	chr16:82816457-82816507	HepG2	liver:	n/a
50	chr16:82816457-82816507	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:82810032..82812890-chr16:82813373..82816205,2	K562	blood:
2	chr16:82810032..82812890-chr16:82813373..82816205,2	K562	blood:
3	chr16:82800736..82802731-chr16:82823544..82826539,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSD17B2-2	chr16:82806924-82807094	ENSG00000260862.1

No data

Variant related genes	Relation type
ENSG00000260862	TF binding region
ENSG00000260862	CpG island

Extended variants
information (count: 1212 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1212 , 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	rs8060885	chr16:82806653-82806654	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565461284	chr16:82806659-82806660	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs535920649	chr16:82806692-82806693	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs566107939	chr16:82806694-82806695	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs533450242	chr16:82806701-82806702	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs554178131	chr16:82806702-82806703	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs138334036	chr16:82806794-82806795	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs538203110	chr16:82806814-82806815	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs556817820	chr16:82806825-82806826	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs149651231	chr16:82806831-82806832	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs373653501	chr16:82806841-82806842	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs376838613	chr16:82806855-82806856	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs7185673	chr16:82806863-82806864	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs560639890	chr16:82806876-82806877	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs572597131	chr16:82806885-82806886	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs572216699	chr16:82806917-82806918	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543125228	chr16:82806939-82806940	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs144388551	chr16:82806940-82806941	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs56219641	chr16:82807019-82807020	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs549868882	chr16:82807058-82807059	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs565202480	chr16:82807067-82807068	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs148778394	chr16:82807119-82807120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374074979	chr16:82807123-82807124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144807400	chr16:82807145-82807146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147488965	chr16:82807190-82807191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577690932	chr16:82807220-82807221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181957862	chr16:82807245-82807246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184950583	chr16:82807275-82807276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139925477	chr16:82807329-82807330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75858574	chr16:82807330-82807331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78794531	chr16:82807335-82807336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535033904	chr16:82807342-82807343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78042778	chr16:82807349-82807350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376375491	chr16:82807350-82807351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73604807	chr16:82807359-82807360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35646302	chr16:82807370-82807371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79046064	chr16:82807384-82807385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200574265	chr16:82807397-82807398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554487237	chr16:82807398-82807399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35479304	chr16:82807399-82807400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189761912	chr16:82807404-82807405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150226975	chr16:82807415-82807416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576427428	chr16:82807441-82807442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543822847	chr16:82807445-82807446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147677908	chr16:82807446-82807447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140932638	chr16:82807449-82807450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547281048	chr16:82807451-82807452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575794614	chr16:82807475-82807476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372176739	chr16:82807481-82807482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529840540	chr16:82807482-82807483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	17603634	CNVD
Prostate cancer	16573809	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 lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Non-small cell lung cancer	21829676	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16461572	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Alveolar capillary dysplasia	19500772	CNVD
VACTERL syndrome	21315191	CNVD
T-cell lymphomas	19863542	CNVD
Developmental delay	19490664	CNVD
Neuroblastoma	18923191	CNVD
Adrenocortical carcinoma	18281524	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82790200-82810400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr16:82793000-82815200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr16:82795800-82810800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr16:82796400-82810000	Weak transcription	HUVEC	blood vessel
5	chr16:82802000-82810400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr16:82803000-82807200	Enhancers	Left Ventricle	heart
7	chr16:82803800-82815600	Weak transcription	HSMM	muscle
8	chr16:82804400-82816600	Weak transcription	Brain Hippocampus Middle	brain
9	chr16:82805000-82807000	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr16:82805000-82811800	Enhancers	Primary B cells from peripheral blood	blood
11	chr16:82805400-82807200	Enhancers	HMEC	breast
12	chr16:82805600-82821600	Weak transcription	NHEK	skin
13	chr16:82805800-82806800	Enhancers	Right Ventricle	heart
14	chr16:82805800-82807000	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr16:82805800-82807200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr16:82806000-82807200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr16:82806000-82807200	Enhancers	Brain Angular Gyrus	brain
18	chr16:82806000-82813800	Weak transcription	Fetal Muscle Leg	muscle
19	chr16:82806200-82807000	Weak transcription	Fetal Heart	heart
20	chr16:82806200-82807200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr16:82806200-82811000	Weak transcription	Psoas Muscle	Psoas
22	chr16:82806200-82812800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr16:82806400-82806800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr16:82806400-82807200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr16:82806400-82807200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr16:82806600-82806800	Enhancers	Aorta	Aorta
27	chr16:82806600-82807000	Enhancers	HSMMtube	muscle
28	chr16:82806600-82807200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr16:82806800-82807200	Enhancers	NH-A	brain
30	chr16:82806800-82807400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr16:82806800-82813000	Weak transcription	Aorta	Aorta
32	chr16:82806800-82813000	Weak transcription	Right Ventricle	heart
33	chr16:82806800-82816200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr16:82807000-82815400	Weak transcription	HSMMtube	muscle
35	chr16:82807200-82809400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr16:82807200-82810000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr16:82807200-82810800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr16:82807200-82811400	Weak transcription	Left Ventricle	heart
39	chr16:82807200-82817800	Weak transcription	HMEC	breast
40	chr16:82808000-82824800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr16:82809400-82810000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr16:82809400-82810200	Enhancers	Primary B cells from cord blood	blood
43	chr16:82809400-82811000	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr16:82810000-82810200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr16:82810000-82810400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr16:82810000-82810600	Enhancers	Muscle Satellite Cultured Cells	--
47	chr16:82810000-82810600	Enhancers	HUVEC	blood vessel
48	chr16:82810200-82810600	Enhancers	Duodenum Mucosa	Duodenum
49	chr16:82810200-82815200	Weak transcription	Primary B cells from cord blood	blood
50	chr16:82810400-82810800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links