Variant report

Variant	nsv9452
Chromosome Location	chr16:69976026-70008199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:549)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr16:69977094-69977496	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr16:69977076-69977449	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr16:69977211-69977432	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr16:69980218-69980446	K562	blood:	n/a	n/a
5	CEBPD	chr16:69999210-69999421	HepG2	liver:	n/a	n/a
6	CEBPD	chr16:69999182-69999502	HepG2	liver:	n/a	n/a
7	CTCF	chr16:69985083-69985092	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr16:69985093-69985109	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr16:70006981-70007209	GM12892	blood:	n/a	n/a
10	CTCF	chr16:70007000-70007150	GM12872	blood:	n/a	n/a
11	CTCF	chr16:69977689-69977745	GM20000	blood:	n/a	n/a
12	CTCF	chr16:69992952-69992983	LNCaP	prostate:	n/a	n/a
13	CTCF	chr16:69991793-69991895	GM13976	blood:	n/a	n/a
14	CTCF	chr16:70007036-70007155	GM19238	blood:	n/a	n/a
15	CTCF	chr16:70007025-70007190	GM12878	blood:	n/a	n/a
16	CTCF	chr16:69991772-69991788	GM13976	blood:	n/a	n/a
17	CTCF	chr16:70007043-70007167	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr16:69994228-69994248	LNCaP	prostate:	n/a	n/a
19	CTCF	chr16:70007030-70007169	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr16:70007040-70007153	GM19239	blood:	n/a	n/a
21	CTCF	chr16:70000364-70000446	LNCaP	prostate:	n/a	n/a
22	CTCF	chr16:69992990-69993094	LNCaP	prostate:	n/a	n/a
23	CTCF	chr16:70007049-70007166	K562	blood:	n/a	n/a
24	CTCF	chr16:69985065-69985141	A549	lung:	n/a	n/a
25	CTCF	chr16:70007040-70007190	GM12864	blood:	n/a	n/a
26	CTCF	chr16:70007066-70007207	LNCaP	prostate:	n/a	n/a
27	CTCF	chr16:70007048-70007160	Gliobla	brain:	n/a	n/a
28	CTCF	chr16:70007020-70007170	GM06990	blood:	n/a	n/a
29	CTCF	chr16:69995267-69995309	LNCaP	prostate:	n/a	n/a
30	CTCF	chr16:70002225-70002358	GM13976	blood:	n/a	n/a
31	CTCF	chr16:70007040-70007190	GM12873	blood:	n/a	n/a
32	CTCF	chr16:70007046-70007140	MCF-7	breast:	n/a	n/a
33	CTCF	chr16:69985041-69985053	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr16:69984957-69985245	A549	lung:	n/a	n/a
35	CTCF	chr16:70002243-70002328	LNCaP	prostate:	n/a	n/a
36	CTCF	chr16:69984991-69985236	Gliobla	brain:	n/a	n/a
37	CTCF	chr16:70007034-70007184	GM12891	blood:	n/a	n/a
38	CTCF	chr16:70007020-70007170	GM12869	blood:	n/a	n/a
39	CTCF	chr16:70007080-70007230	HEK293	kidney:	n/a	n/a
40	CTCF	chr16:70007042-70007166	A549	lung:	n/a	n/a
41	CTCF	chr16:70007004-70007185	GM19240	blood:	n/a	n/a
42	CTCF	chr16:69993730-69993820	GM13976	blood:	n/a	n/a
43	CTCF	chr16:70004499-70004526	Lung_OC	lung:	n/a	n/a
44	CTCF	chr16:70007087-70007113	NHEK	skin:	n/a	n/a
45	CTCF	chr16:69977620-69977743	GM13976	blood:	n/a	n/a
46	EBF1	chr16:69999357-69999621	GM12878	blood:	n/a	chr16:69999507-69999516
47	EBF1	chr16:69999391-69999669	GM12878	blood:	n/a	chr16:69999507-69999516
48	ELF1	chr16:69999204-69999374	HepG2	liver:	n/a	chr16:69999324-69999336
49	EP300	chr16:69977129-69977475	H1-hESC	embryonic stem cell:	n/a	n/a
50	FOSL2	chr16:69984871-69985512	HepG2	liver:	n/a	chr16:69985134-69985142 chr16:69984930-69984939

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70004872-70004922	HIPEpiC	eye:	n/a
2	chr16:69997368-69997418	AoSMC	blood vessel:	n/a
3	chr16:69984927-69984977	K562	blood:	n/a
4	chr16:69999425-69999475	Hepatocyte	liver:	n/a
5	chr16:69999859-69999909	MCF10A-Er-Src	breast:	n/a
6	chr16:69976228-69976278	Hela-S3	cervix:	n/a
7	chr16:69984927-69984977	CMK	blood:	n/a
8	chr16:69997368-69997418	HUVEC	blood vessel:	n/a
9	chr16:69984889-69984939	A549	lung:	n/a
10	chr16:69999859-69999909	K562	blood:	n/a
11	chr16:69999425-69999475	SK-N-SH	brain:	n/a
12	chr16:69976040-69976090	RPTEC	kidney:	n/a
13	chr16:69999859-69999909	ProgFib	skin:	n/a
14	chr16:69999859-69999909	NHDF-neo	bronchial:	n/a
15	chr16:69984889-69984939	HRE	kidney:	n/a
16	chr16:69984889-69984939	SK-N-SH_RA	brain:	n/a
17	chr16:69976228-69976278	Hepatocyte	liver:	n/a
18	chr16:69999425-69999475	GM12891	blood:	n/a
19	chr16:69999859-69999909	HPAEpiC	pulmonary alveolar:	n/a
20	chr16:69999425-69999475	SKMC	muscle:	n/a
21	chr16:69984927-69984977	GM12892	blood:	n/a
22	chr16:69976228-69976278	HRPEpiC	eye:	n/a
23	chr16:69984889-69984939	SAEC	small airway:	n/a
24	chr16:69984927-69984977	HL-60	blood:	n/a
25	chr16:69976228-69976278	SK-N-SH	brain:	n/a
26	chr16:70004872-70004922	AG09309	skin:	n/a
27	chr16:69984927-69984977	HNPCEpiC	eye:	n/a
28	chr16:69976040-69976090	HCT-116	colon:	n/a
29	chr16:69999859-69999909	GM12892	blood:	n/a
30	chr16:69999425-69999475	AG10803	skin:	n/a
31	chr16:69997368-69997418	PANC-1	pancreas:	n/a
32	chr16:70004872-70004922	MCF-7	breast:	n/a
33	chr16:69988428-69988478	HIPEpiC	eye:	n/a
34	chr16:69999425-69999475	U87	brain:	n/a
35	chr16:69976228-69976278	AG04450	lung:	fetal
36	chr16:69988428-69988478	GM19239	blood:	n/a
37	chr16:69999425-69999475	NH-A	brain:	n/a
38	chr16:69976228-69976278	GM12891	blood:	n/a
39	chr16:70004872-70004922	Caco-2	colon:	n/a
40	chr16:69976040-69976090	PANC-1	pancreas:	n/a
41	chr16:70004872-70004922	BJ	skin:	n/a
42	chr16:69999859-69999909	Hepatocyte	liver:	n/a
43	chr16:69988428-69988478	U87	brain:	n/a
44	chr16:69976040-69976090	Jurkat	blood:	n/a
45	chr16:69999859-69999909	HNPCEpiC	eye:	n/a
46	chr16:69976040-69976090	U87	brain:	n/a
47	chr16:69999425-69999475	MCF-7	breast:	n/a
48	chr16:69999425-69999475	Hela-S3	cervix:	n/a
49	chr16:70004872-70004922	GM19239	blood:	n/a
50	chr16:69999859-69999909	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:69970218..69972832-chr16:69974384..69976612,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WWP2-3	chr16:69985376-69987715	NONHSAT143377

No data

Variant related genes	Relation type
CLEC18A	TF binding region
CLEC18A	CpG island
ENSG00000198373	chromatin interactions

Extended variants
information (count: 839 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565012404	chr16:69976041-69976042	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs35580809	chr16:69976073-69976074	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574185486	chr16:69976080-69976081	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7184994	chr16:69976089-69976090	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs559665283	chr16:69976117-69976118	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533449021	chr16:69976198-69976199	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545256663	chr16:69976210-69976211	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375141130	chr16:69976215-69976216	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs563549418	chr16:69976230-69976231	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs576821508	chr16:69976234-69976235	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372156257	chr16:69976236-69976237	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530907827	chr16:69976239-69976240	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs80172760	chr16:69976295-69976296	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541244921	chr16:69976341-69976342	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529144430	chr16:69976454-69976455	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547613074	chr16:69976455-69976456	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs875011	chr16:69976479-69976480	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs182486668	chr16:69976512-69976513	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570938577	chr16:69976521-69976522	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs77405118	chr16:69976542-69976543	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs575987711	chr16:69976560-69976561	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188600132	chr16:69976565-69976566	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537033244	chr16:69976622-69976623	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111967888	chr16:69976640-69976641	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555210981	chr16:69976713-69976714	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140933904	chr16:69976718-69976719	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193265674	chr16:69976719-69976720	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185038164	chr16:69976721-69976722	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150133096	chr16:69976765-69976766	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188748395	chr16:69976766-69976767	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563987554	chr16:69976781-69976782	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575586019	chr16:69976788-69976789	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4985462	chr16:69976864-69976865	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs561078535	chr16:69976918-69976919	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572349644	chr16:69976938-69976939	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192219216	chr16:69976950-69976951	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183935818	chr16:69977012-69977013	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7190012	chr16:69977036-69977037	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs554558720	chr16:69977081-69977082	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533289418	chr16:69977087-69977088	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138596273	chr16:69977091-69977092	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs61059803	chr16:69977092-69977093	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536701454	chr16:69977097-69977098	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148891784	chr16:69977109-69977110	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77972055	chr16:69977152-69977153	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534303555	chr16:69977163-69977164	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188700288	chr16:69977185-69977186	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552577089	chr16:69977224-69977225	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577887877	chr16:69977279-69977280	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72785082	chr16:69977286-69977287	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20841430	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:69947600-69977200	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr16:69948200-69977400	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr16:69948400-69977400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr16:69957400-69977400	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr16:69957800-69977200	Strong transcription	Fetal Intestine Small	intestine
6	chr16:69959000-69976400	Strong transcription	Thymus	Thymus
7	chr16:69959000-69977200	Strong transcription	Fetal Intestine Large	intestine
8	chr16:69959000-69977600	Strong transcription	Primary T cells from cord blood	blood
9	chr16:69959400-69976200	Strong transcription	Sigmoid Colon	Sigmoid Colon
10	chr16:69961400-69976600	Weak transcription	Right Atrium	heart
11	chr16:69961400-69977000	Weak transcription	HSMM	muscle
12	chr16:69961600-69976800	Strong transcription	Spleen	Spleen
13	chr16:69962400-69976800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr16:69962400-69976800	Strong transcription	Rectal Mucosa Donor 29	rectum
15	chr16:69962600-69976800	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr16:69962800-69976200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr16:69962800-69976200	Strong transcription	Gastric	stomach
18	chr16:69963200-69976600	Strong transcription	Fetal Brain Female	brain
19	chr16:69963200-69977000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr16:69963400-69977200	Strong transcription	Primary B cells from peripheral blood	blood
21	chr16:69963600-69976400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr16:69963800-69976200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr16:69964200-69976400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr16:69964200-69976800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr16:69964400-69977400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr16:69964600-69976400	Strong transcription	Esophagus	oesophagus
27	chr16:69965000-69976200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr16:69965000-69976400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr16:69965200-69976200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr16:69967000-69976200	Strong transcription	Brain Anterior Caudate	brain
31	chr16:69967200-69977000	Strong transcription	Brain Substantia Nigra	brain
32	chr16:69970800-69977400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr16:69970800-69978800	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr16:69971200-69976400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr16:69971200-69977000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr16:69971600-69976800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr16:69971800-69977000	Weak transcription	HMEC	breast
38	chr16:69973200-69976200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr16:69973600-69977200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr16:69973600-69977200	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr16:69973800-69976600	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr16:69973800-69977000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr16:69973800-69977000	Weak transcription	Primary hematopoietic stem cells	blood
44	chr16:69974000-69976800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr16:69974000-69977000	Weak transcription	Dnd41	blood
46	chr16:69974400-69976800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr16:69974400-69976800	Weak transcription	Rectal Smooth Muscle	rectum
48	chr16:69974600-69976200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr16:69974600-69976200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr16:69974600-69976800	Weak transcription	GM12878-XiMat	blood

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