Variant report

Variant	nsv915760
Chromosome Location	chr16:74374025-74455333
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	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
4	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
5	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
6	ATF3	chr16:74401940-74402325	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
7	ATF3	chr16:74401896-74402310	K562	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
8	ATF3	chr16:74401853-74402428	HepG2	liver:	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	BACH1	chr16:74398509-74398539	K562	blood:	n/a	n/a
11	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
12	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
13	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
14	BHLHE40	chr16:74445450-74445698	HepG2	liver:	n/a	n/a
15	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
16	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
17	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
18	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
19	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
20	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
21	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
22	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
23	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
24	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
25	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
26	CEBPB	chr16:74441969-74442184	K562	blood:	n/a	n/a
27	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
28	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
29	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
30	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
31	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
32	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
33	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
34	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
35	CHD2	chr16:74401780-74402403	GM12878	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
36	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
37	CHD2	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
38	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr16:74438089-74438284	K562	blood:	n/a	n/a
40	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
41	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
42	CREB1	chr16:74402083-74402284	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr16:74402021-74402294	K562	blood:	n/a	n/a
44	CREB1	chr16:74401943-74402336	HepG2	liver:	n/a	n/a
45	CREB1	chr16:74401934-74402414	A549	lung:	n/a	n/a
46	CREB1	chr16:74401970-74402284	GM12878	blood:	n/a	n/a
47	CREB1	chr16:74402012-74402247	A549	lung:	n/a	n/a
48	CREB1	chr16:74401959-74402277	K562	blood:	n/a	n/a
49	CTCF	chr16:74428920-74429070	GM12865	blood:	n/a	n/a
50	CTCF	chr16:74428940-74429090	GM06990	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74402336-74402386	CMK	blood:	n/a
2	chr16:74402336-74402386	CMK	blood:	n/a
3	chr16:74402329-74402379	AG09319	gingival:	n/a
4	chr16:74401986-74402036	MCF-7	breast:	n/a
5	chr16:74402329-74402379	GM12891	blood:	n/a
6	chr16:74402329-74402379	AG04450	lung:	fetal
7	chr16:74446218-74446268	GM06990	blood:	n/a
8	chr16:74441639-74441689	SK-N-SH_RA	brain:	n/a
9	chr16:74446218-74446268	BE2_C	brain:	n/a
10	chr16:74401547-74401597	Jurkat	blood:	n/a
11	chr16:74398168-74398218	ovcar-3	ovarian:	n/a
12	chr16:74398168-74398218	PrEC	prostate:	n/a
13	chr16:74455140-74455190	HRE	kidney:	n/a
14	chr16:74455140-74455190	BE2_C	brain:	n/a
15	chr16:74401794-74401844	GM19239	blood:	n/a
16	chr16:74401986-74402036	NB4	blood:	n/a
17	chr16:74406059-74406109	ovcar-3	ovarian:	n/a
18	chr16:74441639-74441689	IMR90	lung:	fetal
19	chr16:74401794-74401844	HRPEpiC	eye:	n/a
20	chr16:74403516-74403566	NT2-D1	testis:	n/a
21	chr16:74401547-74401597	HepG2	liver:	n/a
22	chr16:74402336-74402386	HCF	heart:	n/a
23	chr16:74402329-74402379	Caco-2	colon:	n/a
24	chr16:74401547-74401597	SK-N-SH	brain:	n/a
25	chr16:74402329-74402379	NH-A	brain:	n/a
26	chr16:74398168-74398218	AoSMC	blood vessel:	n/a
27	chr16:74401986-74402036	PFSK-1	brain:	n/a
28	chr16:74398168-74398218	AG10803	skin:	n/a
29	chr16:74401986-74402036	HCF	heart:	n/a
30	chr16:74441639-74441689	MCF-7	breast:	n/a
31	chr16:74403516-74403566	SK-N-SH_RA	brain:	n/a
32	chr16:74400946-74400996	Hela-S3	cervix:	n/a
33	chr16:74446218-74446268	BJ	skin:	n/a
34	chr16:74455140-74455190	SKMC	muscle:	n/a
35	chr16:74406059-74406109	HPAEpiC	pulmonary alveolar:	n/a
36	chr16:74402737-74402787	HRE	kidney:	n/a
37	chr16:74402336-74402386	HRPEpiC	eye:	n/a
38	chr16:74402329-74402379	HCT-116	colon:	n/a
39	chr16:74402737-74402787	AG04450	lung:	fetal
40	chr16:74401986-74402036	HCPEpiC	choroid plexus:	n/a
41	chr16:74402329-74402379	Jurkat	blood:	n/a
42	chr16:74455140-74455190	HPAEpiC	pulmonary alveolar:	n/a
43	chr16:74398168-74398218	NH-A	brain:	n/a
44	chr16:74401986-74402036	T-47D	breast:	n/a
45	chr16:74401547-74401597	GM12878	blood:	n/a
46	chr16:74402737-74402787	A549	lung:	n/a
47	chr16:74441639-74441689	HEEpiC	esophagus:	n/a
48	chr16:74455140-74455190	PrEC	prostate:	n/a
49	chr16:74401547-74401597	ECC-1	luminal epithelium:	n/a
50	chr16:74403516-74403566	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:74396107..74397775-chr16:74400703..74403254,2	K562	blood:
2	chr16:74329306..74331523-chr16:74400690..74402975,2	MCF-7	breast:
3	chr16:74394116..74395645-chr3:9438342..9440027,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009
2	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
3	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681
4	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
5	lnc-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain
6	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1

Variant related genes	Relation type
CLEC18B	TF binding region
ENSG00000261170	TF binding region
NPIPB15	TF binding region
ENSG00000259972	TF binding region
ENSG00000261079	TF binding region
ENSG00000214331	TF binding region
CLEC18B	CpG island
ENSG00000261170	CpG island
NPIPB15	CpG island
ENSG00000259972	CpG island
ENSG00000261079	CpG island
ENSG00000214331	CpG island
ENSG00000206573	chromatin interactions
ENSG00000214331	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000261079	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000168137	chromatin interactions

Extended variants
information (count: 3352 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3352 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141648250	chr16:74374039-74374040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150417848	chr16:74374060-74374061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371326766	chr16:74374074-74374075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149606595	chr16:74374108-74374109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369150772	chr16:74374149-74374150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574139196	chr16:74374152-74374153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542831529	chr16:74374200-74374201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559587697	chr16:74374202-74374203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543291663	chr16:74374203-74374204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548033713	chr16:74374215-74374216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372984667	chr16:74374226-74374227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112963042	chr16:74374234-74374235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539024129	chr16:74374271-74374272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552334690	chr16:74374281-74374282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143287110	chr16:74374305-74374306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566154082	chr16:74374309-74374310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150737856	chr16:74374311-74374312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569659337	chr16:74374312-74374313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529064390	chr16:74374336-74374337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2549263	chr16:74374347-74374348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565965936	chr16:74374366-74374367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534826984	chr16:74374369-74374370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149927776	chr16:74374376-74374377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557864960	chr16:74374386-74374387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377194194	chr16:74374425-74374426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571571930	chr16:74374438-74374439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371093253	chr16:74374476-74374477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373642188	chr16:74374485-74374486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367810217	chr16:74374493-74374494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187977571	chr16:74374528-74374529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553182517	chr16:74374554-74374555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573188400	chr16:74374557-74374558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559900979	chr16:74374575-74374576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372525377	chr16:74374576-74374577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545339185	chr16:74374604-74374605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557644116	chr16:74374617-74374618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565441100	chr16:74374622-74374623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577524910	chr16:74374638-74374639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543065826	chr16:74374643-74374644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371560680	chr16:74374648-74374649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563367917	chr16:74374732-74374733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144466002	chr16:74374748-74374749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549189054	chr16:74374760-74374761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147878507	chr16:74374867-74374868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528296796	chr16:74374895-74374896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571464550	chr16:74374899-74374900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141506145	chr16:74374914-74374915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561401236	chr16:74374951-74374952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374131349	chr16:74374976-74374977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368089053	chr16:74374986-74374987	Weak transcription Strong transcription	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:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74332800-74401200	Weak transcription	Stomach Mucosa	stomach
2	chr16:74339600-74394000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr16:74340600-74387000	Weak transcription	Hela-S3	cervix
4	chr16:74340800-74400200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr16:74341400-74376200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr16:74341400-74400800	Weak transcription	NH-A	brain
7	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
8	chr16:74355600-74382200	Weak transcription	GM12878-XiMat	blood
9	chr16:74360000-74378200	Weak transcription	Primary B cells from cord blood	blood
10	chr16:74360000-74401400	Weak transcription	Small Intestine	intestine
11	chr16:74360600-74382600	Weak transcription	HSMMtube	muscle
12	chr16:74360800-74383000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr16:74361000-74382000	Weak transcription	Fetal Kidney	kidney
14	chr16:74361000-74385000	Weak transcription	K562	blood
15	chr16:74361400-74384200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr16:74362000-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr16:74362200-74387400	Weak transcription	NHDF-Ad	bronchial
18	chr16:74362200-74392400	Weak transcription	HSMM	muscle
19	chr16:74362200-74394000	Weak transcription	HMEC	breast
20	chr16:74362200-74398600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr16:74362800-74398000	Weak transcription	Psoas Muscle	Psoas
22	chr16:74364200-74374200	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr16:74364200-74380200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr16:74364400-74398800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr16:74365200-74377000	Weak transcription	Brain Germinal Matrix	brain
26	chr16:74365200-74384000	Weak transcription	Right Ventricle	heart
27	chr16:74365200-74394000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr16:74366800-74387000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr16:74367000-74377000	Weak transcription	Esophagus	oesophagus
30	chr16:74367200-74376200	Weak transcription	Brain Angular Gyrus	brain
31	chr16:74367200-74381400	Weak transcription	Fetal Brain Female	brain
32	chr16:74367200-74382000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr16:74367200-74382000	Weak transcription	Aorta	Aorta
34	chr16:74367200-74382000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr16:74367200-74384200	Weak transcription	Colon Smooth Muscle	Colon
36	chr16:74367200-74386600	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr16:74367200-74387000	Weak transcription	A549	lung
38	chr16:74367200-74398000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr16:74367200-74400800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr16:74367600-74392400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr16:74368400-74374200	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr16:74368400-74374200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
43	chr16:74368400-74374400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr16:74368400-74374800	Strong transcription	Primary neutrophils fromperipheralblood	blood
45	chr16:74368400-74374800	Strong transcription	Fetal Stomach	stomach
46	chr16:74368400-74375000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr16:74368400-74380200	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr16:74368400-74384400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr16:74368400-74387800	Strong transcription	Placenta	Placenta
50	chr16:74368400-74389400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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