Variant report

Variant	esv1827883
Chromosome Location	chr16:74398758-74412222
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	ARID3A	chr16:74402200-74402343	K562	blood:	n/a	n/a
2	ATF1	chr16:74402006-74402375	K562	blood:	n/a	chr16:74402193-74402207
3	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
4	ATF3	chr16:74401853-74402428	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
5	ATF3	chr16:74401896-74402310	K562	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
6	ATF3	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
7	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
8	ATF3	chr16:74401940-74402325	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
9	BACH1	chr16:74402015-74402440	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
11	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
12	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
13	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
14	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
15	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
16	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
17	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
18	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
19	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
20	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
21	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
22	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
23	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
24	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
25	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
26	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
27	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
28	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
29	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
30	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
31	CHD2	chr16:74401780-74402403	GM12878	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
32	CHD2	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
33	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
34	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
35	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
36	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
37	CREB1	chr16:74402021-74402294	K562	blood:	n/a	n/a
38	CREB1	chr16:74401934-74402414	A549	lung:	n/a	n/a
39	CREB1	chr16:74402083-74402284	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr16:74401970-74402284	GM12878	blood:	n/a	n/a
41	CREB1	chr16:74402012-74402247	A549	lung:	n/a	n/a
42	CREB1	chr16:74401943-74402336	HepG2	liver:	n/a	n/a
43	CREB1	chr16:74401959-74402277	K562	blood:	n/a	n/a
44	CTCF	chr16:74402328-74402336	K562	blood:	n/a	n/a
45	CTCF	chr16:74402134-74402279	Lung_OC	lung:	n/a	n/a
46	CTCF	chr16:74401200-74401350	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr16:74401420-74401570	NHLF	lung:	n/a	n/a
48	CTCF	chr16:74402203-74402275	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr16:74402100-74402315	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr16:74402119-74402282	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74402329-74402379	NB4	blood:	n/a
2	chr16:74402336-74402386	GM12878	blood:	n/a
3	chr16:74400946-74400996	SK-N-SH_RA	brain:	n/a
4	chr16:74401547-74401597	Hela-S3	cervix:	n/a
5	chr16:74400946-74400996	AG09309	skin:	n/a
6	chr16:74402737-74402787	AG09309	skin:	n/a
7	chr16:74402737-74402787	SK-N-MC	brain:	n/a
8	chr16:74402737-74402787	HRPEpiC	eye:	n/a
9	chr16:74402336-74402386	T-47D	breast:	n/a
10	chr16:74401794-74401844	HNPCEpiC	eye:	n/a
11	chr16:74401986-74402036	SKMC	muscle:	n/a
12	chr16:74400946-74400996	SK-N-SH	brain:	n/a
13	chr16:74406059-74406109	A549	lung:	n/a
14	chr16:74402737-74402787	SKMC	muscle:	n/a
15	chr16:74406059-74406109	Hepatocyte	liver:	n/a
16	chr16:74406059-74406109	GM19239	blood:	n/a
17	chr16:74403516-74403566	HCM	heart:	n/a
18	chr16:74402329-74402379	MCF-7	breast:	n/a
19	chr16:74401986-74402036	AG09309	skin:	n/a
20	chr16:74401986-74402036	HRE	kidney:	n/a
21	chr16:74400946-74400996	AG04450	lung:	fetal
22	chr16:74403516-74403566	MCF-7	breast:	n/a
23	chr16:74400946-74400996	ovcar-3	ovarian:	n/a
24	chr16:74402336-74402386	HPAEpiC	pulmonary alveolar:	n/a
25	chr16:74406059-74406109	AG09309	skin:	n/a
26	chr16:74401986-74402036	GM19239	blood:	n/a
27	chr16:74401794-74401844	Hela-S3	cervix:	n/a
28	chr16:74401547-74401597	HAEpiC	amniotic membrane:	n/a
29	chr16:74402737-74402787	AG10803	skin:	n/a
30	chr16:74402329-74402379	GM12892	blood:	n/a
31	chr16:74401547-74401597	MCF10A-Er-Src	breast:	n/a
32	chr16:74402737-74402787	CMK	blood:	n/a
33	chr16:74402336-74402386	HRCEpiC	kidney:	n/a
34	chr16:74402737-74402787	SAEC	small airway:	n/a
35	chr16:74403516-74403566	SKMC	muscle:	n/a
36	chr16:74406059-74406109	NB4	blood:	n/a
37	chr16:74402336-74402386	PFSK-1	brain:	n/a
38	chr16:74406059-74406109	GM12892	blood:	n/a
39	chr16:74401547-74401597	PrEC	prostate:	n/a
40	chr16:74402336-74402386	HMEC	breast:	n/a
41	chr16:74402329-74402379	PrEC	prostate:	n/a
42	chr16:74406059-74406109	HEEpiC	esophagus:	n/a
43	chr16:74401794-74401844	SAEC	small airway:	n/a
44	chr16:74401794-74401844	MCF-7	breast:	n/a
45	chr16:74402737-74402787	HPAEpiC	pulmonary alveolar:	n/a
46	chr16:74401794-74401844	HUVEC	blood vessel:	n/a
47	chr16:74406059-74406109	U87	brain:	n/a
48	chr16:74401794-74401844	SK-N-MC	brain:	n/a
49	chr16:74401547-74401597	HPAEpiC	pulmonary alveolar:	n/a
50	chr16:74402329-74402379	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:74329306..74331523-chr16:74400690..74402975,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1
2	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681
3	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
4	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
5	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009

Variant related genes	Relation type
NPIPB15	TF binding region
ENSG00000261079	TF binding region
ENSG00000214331	TF binding region
NPIPB15	CpG island
ENSG00000261079	CpG island
ENSG00000214331	CpG island
ENSG00000261404	chromatin interactions
ENSG00000103035	chromatin interactions

Extended variants
information (count: 608 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11644724	chr16:74398758-74398759	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541345336	chr16:74398782-74398783	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555681075	chr16:74398797-74398798	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115962771	chr16:74398798-74398799	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370024423	chr16:74398808-74398809	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552295503	chr16:74398813-74398814	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11643683	chr16:74398820-74398821	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371358105	chr16:74398822-74398823	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573958041	chr16:74398825-74398826	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543368936	chr16:74398838-74398839	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563442936	chr16:74398861-74398862	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11644768	chr16:74398871-74398872	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529390466	chr16:74398888-74398889	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542700716	chr16:74398892-74398893	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542262468	chr16:74398902-74398903	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75253274	chr16:74398903-74398904	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs386792105	chr16:74398907-74398908	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146577318	chr16:74398908-74398909	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528651513	chr16:74398916-74398917	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11648390	chr16:74398917-74398918	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376572837	chr16:74398965-74398966	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552069618	chr16:74398967-74398968	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11648767	chr16:74398975-74398976	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372947011	chr16:74398976-74398977	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11648434	chr16:74398989-74398990	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551802883	chr16:74398995-74398996	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571810044	chr16:74398998-74398999	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11648435	chr16:74398999-74399000	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9929560	chr16:74399003-74399004	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549849280	chr16:74399012-74399013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11648438	chr16:74399013-74399014	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4493081	chr16:74399016-74399017	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569660438	chr16:74399024-74399025	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563659655	chr16:74399030-74399031	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548781666	chr16:74399073-74399074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs202029803	chr16:74399082-74399083	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs62055175	chr16:74399223-74399224	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534483536	chr16:74399313-74399314	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558041111	chr16:74399436-74399437	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577465773	chr16:74399514-74399515	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2549080	chr16:74399534-74399535	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113777576	chr16:74399559-74399560	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576781976	chr16:74399563-74399564	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545876640	chr16:74399574-74399575	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs369242711	chr16:74399602-74399603	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573679836	chr16:74399608-74399609	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185816966	chr16:74399617-74399618	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2549286	chr16:74399631-74399632	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2549078	chr16:74399663-74399664	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs559556499	chr16:74399665-74399666	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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	21364760	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74332800-74401200	Weak transcription	Stomach Mucosa	stomach
2	chr16:74340800-74400200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr16:74341400-74400800	Weak transcription	NH-A	brain
4	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
5	chr16:74360000-74401400	Weak transcription	Small Intestine	intestine
6	chr16:74362000-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr16:74364400-74398800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr16:74367200-74400800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr16:74371800-74400800	Weak transcription	Fetal Heart	heart
10	chr16:74371800-74400800	Weak transcription	HUVEC	blood vessel
11	chr16:74371800-74401200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr16:74372200-74400800	Weak transcription	Colonic Mucosa	Colon
13	chr16:74374000-74399800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr16:74380200-74401400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr16:74384600-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr16:74387200-74401200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr16:74388000-74400800	Weak transcription	Brain Substantia Nigra	brain
18	chr16:74388200-74400800	Weak transcription	Esophagus	oesophagus
19	chr16:74388200-74400800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr16:74390400-74399000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr16:74391000-74398800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
22	chr16:74392400-74399000	Strong transcription	Fetal Intestine Small	intestine
23	chr16:74392800-74400800	Weak transcription	Hela-S3	cervix
24	chr16:74392800-74401200	Weak transcription	HSMMtube	muscle
25	chr16:74393800-74400800	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr16:74394800-74400600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr16:74394800-74400600	Weak transcription	HMEC	breast
28	chr16:74394800-74400800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr16:74394800-74401400	Weak transcription	Gastric	stomach
30	chr16:74395000-74400800	Weak transcription	Right Ventricle	heart
31	chr16:74395200-74401000	Weak transcription	Right Atrium	heart
32	chr16:74395800-74398800	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr16:74395800-74399000	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr16:74396000-74398800	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr16:74396000-74399000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr16:74396000-74399000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr16:74396000-74399000	Strong transcription	Fetal Muscle Trunk	muscle
38	chr16:74396200-74398800	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr16:74396200-74398800	Strong transcription	Primary T cells from cord blood	blood
40	chr16:74396200-74398800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr16:74396200-74398800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr16:74396200-74398800	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr16:74396400-74398800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr16:74396400-74399000	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr16:74396400-74399000	Strong transcription	Fetal Intestine Large	intestine
46	chr16:74396600-74398800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr16:74396800-74400600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr16:74396800-74400800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr16:74397000-74398800	Strong transcription	Placenta	Placenta
50	chr16:74397000-74398800	Strong transcription	HSMM	muscle

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