Variant report

Variant	nsv977110
Chromosome Location	chr16:12123355-12146787
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:419)
CpG islands
(count:977)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12132637-12133185	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12133673-12133920	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:12141895-12142057	K562	blood:	n/a	n/a
4	ARID3A	chr16:12130779-12131371	K562	blood:	n/a	n/a
5	ARID3A	chr16:12135563-12135772	K562	blood:	n/a	n/a
6	ATF1	chr16:12135426-12135668	K562	blood:	n/a	n/a
7	ATF1	chr16:12130924-12131227	K562	blood:	n/a	n/a
8	ATF1	chr16:12141814-12142122	K562	blood:	n/a	n/a
9	ATF2	chr16:12128063-12128394	GM12878	blood:	n/a	n/a
10	ATF2	chr16:12128089-12128384	GM12878	blood:	n/a	n/a
11	ATF2	chr16:12127661-12128046	GM12878	blood:	n/a	n/a
12	ATF3	chr16:12130879-12131248	K562	blood:	n/a	n/a
13	ATF3	chr16:12130915-12131113	K562	blood:	n/a	n/a
14	BACH1	chr16:12141911-12142249	K562	blood:	n/a	n/a
15	BACH1	chr16:12130974-12131171	K562	blood:	n/a	n/a
16	BATF	chr16:12127826-12128339	GM12878	blood:	n/a	n/a
17	BATF	chr16:12123988-12124229	GM12878	blood:	n/a	chr16:12124127-12124138
18	BATF	chr16:12128778-12129110	GM12878	blood:	n/a	chr16:12128977-12128988
19	BATF	chr16:12128854-12129036	GM12878	blood:	n/a	chr16:12128977-12128988
20	BATF	chr16:12127805-12128214	GM12878	blood:	n/a	n/a
21	BATF	chr16:12140954-12141193	GM12878	blood:	n/a	n/a
22	BATF	chr16:12123989-12124226	GM12878	blood:	n/a	chr16:12124127-12124138
23	BCL11A	chr16:12127760-12128251	GM12878	blood:	n/a	chr16:12128135-12128144
24	BCL11A	chr16:12128864-12129049	GM12878	blood:	n/a	chr16:12129018-12129027
25	BCL11A	chr16:12127800-12128279	GM12878	blood:	n/a	chr16:12128135-12128144
26	BCL11A	chr16:12127146-12127432	GM12878	blood:	n/a	n/a
27	BCL3	chr16:12137822-12138120	GM12878	blood:	n/a	n/a
28	BCL3	chr16:12140899-12141273	GM12878	blood:	n/a	n/a
29	BCL3	chr16:12140946-12141226	GM12878	blood:	n/a	n/a
30	BCLAF1	chr16:12127072-12127387	GM12878	blood:	n/a	n/a
31	BHLHE40	chr16:12130848-12131185	K562	blood:	n/a	n/a
32	BHLHE40	chr16:12132870-12133440	HepG2	liver:	n/a	n/a
33	BHLHE40	chr16:12127894-12128473	GM12878	blood:	n/a	n/a
34	BHLHE40	chr16:12141776-12142532	K562	blood:	n/a	n/a
35	BHLHE40	chr16:12132622-12132719	HepG2	liver:	n/a	n/a
36	BRCA1	chr16:12130961-12131173	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr16:12141793-12142206	K562	blood:	n/a	n/a
38	CBX3	chr16:12130757-12131312	K562	blood:	n/a	n/a
39	CEBPB	chr16:12132521-12132872	K562	blood:	n/a	n/a
40	CEBPB	chr16:12135448-12135773	A549	lung:	n/a	chr16:12135607-12135618
41	CEBPB	chr16:12135410-12135803	Hela-S3	cervix:	n/a	chr16:12135607-12135618
42	CEBPB	chr16:12130470-12130681	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr16:12132599-12132873	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr16:12132608-12132887	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr16:12127222-12128449	GM12878	blood:	n/a	n/a
46	CEBPB	chr16:12144567-12144661	K562	blood:	n/a	n/a
47	CEBPB	chr16:12135467-12135690	K562	blood:	n/a	chr16:12135607-12135618
48	CEBPB	chr16:12135413-12135800	K562	blood:	n/a	chr16:12135607-12135618
49	CEBPB	chr16:12132516-12132891	HepG2	liver:	n/a	n/a
50	CEBPB	chr16:12135422-12135779	HepG2	liver:	n/a	chr16:12135607-12135618

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12142497-12142547	HL-60	blood:	n/a
2	chr16:12142497-12142547	HL-60	blood:	n/a
3	chr16:12145724-12145774	AG04449	skin:	fetal
4	chr16:12145724-12145774	GM19239	blood:	n/a
5	chr16:12139025-12139075	HepG2	liver:	n/a
6	chr16:12135470-12135520	Hela-S3	cervix:	n/a
7	chr16:12136797-12136847	GM06990	blood:	n/a
8	chr16:12146129-12146179	BE2_C	brain:	n/a
9	chr16:12142497-12142547	LNCaP	prostate:	n/a
10	chr16:12145847-12145897	GM06990	blood:	n/a
11	chr16:12137030-12137080	RPTEC	kidney:	n/a
12	chr16:12146023-12146073	LNCaP	prostate:	n/a
13	chr16:12145724-12145774	HCT-116	colon:	n/a
14	chr16:12139025-12139075	GM12892	blood:	n/a
15	chr16:12146074-12146124	AG10803	skin:	n/a
16	chr16:12145847-12145897	SK-N-SH_RA	brain:	n/a
17	chr16:12136938-12136988	HRCEpiC	kidney:	n/a
18	chr16:12137030-12137080	Hepatocyte	liver:	n/a
19	chr16:12136938-12136988	BE2_C	brain:	n/a
20	chr16:12142335-12142385	PANC-1	pancreas:	n/a
21	chr16:12145888-12145938	HNPCEpiC	eye:	n/a
22	chr16:12145888-12145938	GM19239	blood:	n/a
23	chr16:12139025-12139075	ProgFib	skin:	n/a
24	chr16:12146023-12146073	HCM	heart:	n/a
25	chr16:12135470-12135520	HAEpiC	amniotic membrane:	n/a
26	chr16:12146023-12146073	GM12878	blood:	n/a
27	chr16:12146074-12146124	Hepatocyte	liver:	n/a
28	chr16:12145724-12145774	HEEpiC	esophagus:	n/a
29	chr16:12137030-12137080	NB4	blood:	n/a
30	chr16:12136938-12136988	HCT-116	colon:	n/a
31	chr16:12142335-12142385	Hela-S3	cervix:	n/a
32	chr16:12137030-12137080	LNCaP	prostate:	n/a
33	chr16:12146129-12146179	SAEC	small airway:	n/a
34	chr16:12136797-12136847	Jurkat	blood:	n/a
35	chr16:12145724-12145774	SAEC	small airway:	n/a
36	chr16:12146074-12146124	PANC-1	pancreas:	n/a
37	chr16:12146129-12146179	AoSMC	blood vessel:	n/a
38	chr16:12145724-12145774	GM12891	blood:	n/a
39	chr16:12136822-12136872	Caco-2	colon:	n/a
40	chr16:12142497-12142547	HEEpiC	esophagus:	n/a
41	chr16:12142335-12142385	MCF10A-Er-Src	breast:	n/a
42	chr16:12136797-12136847	SAEC	small airway:	n/a
43	chr16:12142497-12142547	Hela-S3	cervix:	n/a
44	chr16:12135470-12135520	HL-60	blood:	n/a
45	chr16:12146129-12146179	NH-A	brain:	n/a
46	chr16:12136822-12136872	AG10803	skin:	n/a
47	chr16:12146129-12146179	SK-N-SH_RA	brain:	n/a
48	chr16:12145847-12145897	NHDF-neo	bronchial:	n/a
49	chr16:12142335-12142385	ProgFib	skin:	n/a
50	chr16:12135470-12135520	HIPEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12141844..12143563-chr16:12144575..12146387,2	K562	blood:
2	chr16:12070167..12072046-chr16:12129596..12132350,2	K562	blood:
3	chr16:12118157..12118838-chr16:12130477..12131347,2	MCF-7	breast:
4	chr16:12073934..12076136-chr16:12129849..12132030,2	K562	blood:
5	chr16:12070192..12071929-chr16:12142370..12144393,2	MCF-7	breast:
6	chr16:12008162..12010269-chr16:12142729..12146819,3	K562	blood:
7	chr16:12068621..12072204-chr16:12129850..12134239,5	MCF-7	breast:
8	chr16:12126814..12127314-chr20:39765771..39766517,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
SNX29	TF binding region
SNX29	CpG island
ENSG00000266163	chromatin interactions
ENSG00000048471	chromatin interactions
ENSG00000260488	chromatin interactions
ENSG00000124181	chromatin interactions
ENSG00000234719	chromatin interactions
ENSG00000103342	chromatin interactions

Extended variants
information (count: 1249 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1249 , 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	rs546094054	chr16:12123392-12123393	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565106830	chr16:12123394-12123395	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530914086	chr16:12123405-12123406	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529730588	chr16:12123414-12123415	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148696061	chr16:12123428-12123429	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200950086	chr16:12123451-12123452	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576077145	chr16:12123453-12123454	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562694637	chr16:12123466-12123467	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs56970661	chr16:12123467-12123468	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530264082	chr16:12123498-12123499	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547168929	chr16:12123524-12123525	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142208405	chr16:12123556-12123557	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538926596	chr16:12123559-12123560	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs151204169	chr16:12123569-12123570	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192127322	chr16:12123612-12123613	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369128477	chr16:12123642-12123643	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184082896	chr16:12123655-12123656	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188568993	chr16:12123680-12123681	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554192435	chr16:12123695-12123696	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574150017	chr16:12123696-12123697	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533654436	chr16:12123698-12123699	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553652400	chr16:12123700-12123701	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190772655	chr16:12123701-12123702	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201292466	chr16:12123729-12123730	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576990147	chr16:12123741-12123742	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs168411	chr16:12123744-12123745	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs548421248	chr16:12123746-12123747	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183087307	chr16:12123785-12123786	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35128101	chr16:12123802-12123803	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs67937896	chr16:12123803-12123804	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs374794953	chr16:12123893-12123894	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs531998999	chr16:12123904-12123905	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs561269208	chr16:12123961-12123962	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs116684576	chr16:12123982-12123983	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs547128311	chr16:12123984-12123985	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs560450415	chr16:12124004-12124005	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187056579	chr16:12124009-12124010	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191782107	chr16:12124032-12124033	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569533251	chr16:12124045-12124046	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538152661	chr16:12124075-12124076	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547744233	chr16:12124087-12124088	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567733346	chr16:12124092-12124093	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561918943	chr16:12124133-12124134	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147903503	chr16:12124169-12124170	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553811146	chr16:12124171-12124172	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73515646	chr16:12124174-12124175	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs184277167	chr16:12124180-12124181	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556129459	chr16:12124184-12124185	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141616970	chr16:12124190-12124191	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574992685	chr16:12124192-12124193	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
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
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12071400-12130800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr16:12071800-12140200	Weak transcription	Fetal Intestine Small	intestine
3	chr16:12098400-12136000	Weak transcription	Fetal Stomach	stomach
4	chr16:12099600-12135200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr16:12099600-12141200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr16:12101800-12123600	Weak transcription	Lung	lung
7	chr16:12101800-12129800	Weak transcription	Aorta	Aorta
8	chr16:12102000-12124200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr16:12105200-12142200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr16:12105800-12124200	Weak transcription	Primary T cells from cord blood	blood
11	chr16:12108600-12128400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr16:12109800-12124200	Weak transcription	Left Ventricle	heart
13	chr16:12109800-12142200	Weak transcription	Gastric	stomach
14	chr16:12112000-12124200	Weak transcription	HSMMtube	muscle
15	chr16:12112000-12129200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr16:12112000-12142200	Weak transcription	NHLF	lung
17	chr16:12112000-12144000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr16:12113200-12129200	Weak transcription	Ovary	ovary
19	chr16:12115200-12140600	Weak transcription	Thymus	Thymus
20	chr16:12116200-12141000	Weak transcription	Primary hematopoietic stem cells	blood
21	chr16:12116800-12129600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr16:12116800-12130800	Weak transcription	Fetal Kidney	kidney
23	chr16:12117200-12140400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr16:12117400-12183400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr16:12118200-12140400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr16:12118400-12130800	Weak transcription	Right Ventricle	heart
27	chr16:12118600-12129400	Weak transcription	NHDF-Ad	bronchial
28	chr16:12118600-12130800	Weak transcription	Duodenum Mucosa	Duodenum
29	chr16:12118600-12130800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr16:12118800-12128400	Weak transcription	Adipose Nuclei	Adipose
31	chr16:12118800-12129600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr16:12119200-12146400	Weak transcription	Fetal Lung	lung
33	chr16:12119400-12129600	Weak transcription	Stomach Mucosa	stomach
34	chr16:12119400-12142000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr16:12119600-12130800	Weak transcription	Pancreas	Pancrea
36	chr16:12119600-12148400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr16:12119800-12130800	Weak transcription	HepG2	liver
38	chr16:12120200-12132600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr16:12120400-12123800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr16:12120400-12128200	Weak transcription	Placenta	Placenta
41	chr16:12120600-12124200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr16:12121000-12142200	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr16:12121200-12124200	Weak transcription	Brain Anterior Caudate	brain
44	chr16:12121200-12124400	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr16:12121200-12125200	Weak transcription	Brain Germinal Matrix	brain
46	chr16:12121200-12130800	Weak transcription	Fetal Muscle Leg	muscle
47	chr16:12121200-12130800	Weak transcription	Spleen	Spleen
48	chr16:12121200-12132600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr16:12121400-12123800	Weak transcription	Brain Substantia Nigra	brain
50	chr16:12121400-12124200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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