Variant report

Variant	esv1819882
Chromosome Location	chr16:74366712-74440516
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	chr16:74401940-74402325	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
4	ATF3	chr16:74401896-74402310	K562	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
5	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
6	ATF3	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
7	ATF3	chr16:74401853-74402428	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
8	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
9	BACH1	chr16:74398509-74398539	K562	blood:	n/a	n/a
10	BACH1	chr16:74402015-74402440	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
12	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
13	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
14	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
15	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
16	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
17	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
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	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
21	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
22	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
23	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
24	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
25	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
26	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
27	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
28	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
29	CEBPB	chr16:74366899-74367207	HepG2	liver:	n/a	n/a
30	CEBPB	chr16:74367000-74367116	K562	blood:	n/a	n/a
31	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
32	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
33	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
34	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
35	CHD2	chr16:74438089-74438284	K562	blood:	n/a	n/a
36	CHD2	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
37	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
39	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
40	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
41	CHD2	chr16:74401780-74402403	GM12878	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
42	CREB1	chr16:74401959-74402277	K562	blood:	n/a	n/a
43	CREB1	chr16:74401970-74402284	GM12878	blood:	n/a	n/a
44	CREB1	chr16:74402021-74402294	K562	blood:	n/a	n/a
45	CREB1	chr16:74402083-74402284	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr16:74401934-74402414	A549	lung:	n/a	n/a
47	CREB1	chr16:74402012-74402247	A549	lung:	n/a	n/a
48	CREB1	chr16:74401943-74402336	HepG2	liver:	n/a	n/a
49	CTCF	chr16:74367572-74367610	GM20000	blood:	n/a	n/a
50	CTCF	chr16:74396380-74396435	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74402329-74402379	MCF10A-Er-Src	breast:	n/a
2	chr16:74400946-74400996	ProgFib	skin:	n/a
3	chr16:74402329-74402379	MCF10A-Er-Src	breast:	n/a
4	chr16:74400946-74400996	ProgFib	skin:	n/a
5	chr16:74401794-74401844	Jurkat	blood:	n/a
6	chr16:74402737-74402787	HPAEpiC	pulmonary alveolar:	n/a
7	chr16:74401547-74401597	Jurkat	blood:	n/a
8	chr16:74402336-74402386	HPAEpiC	pulmonary alveolar:	n/a
9	chr16:74402737-74402787	PrEC	prostate:	n/a
10	chr16:74403516-74403566	ovcar-3	ovarian:	n/a
11	chr16:74401794-74401844	NB4	blood:	n/a
12	chr16:74401547-74401597	AG09309	skin:	n/a
13	chr16:74406059-74406109	HIPEpiC	eye:	n/a
14	chr16:74403516-74403566	HAEpiC	amniotic membrane:	n/a
15	chr16:74401794-74401844	GM06990	blood:	n/a
16	chr16:74401986-74402036	ECC-1	luminal epithelium:	n/a
17	chr16:74402737-74402787	A549	lung:	n/a
18	chr16:74403516-74403566	SK-N-SH_RA	brain:	n/a
19	chr16:74401986-74402036	NB4	blood:	n/a
20	chr16:74402737-74402787	AG04449	skin:	fetal
21	chr16:74403516-74403566	HRE	kidney:	n/a
22	chr16:74401547-74401597	Hepatocyte	liver:	n/a
23	chr16:74403516-74403566	ECC-1	luminal epithelium:	n/a
24	chr16:74402737-74402787	NHBE	bronchial:	n/a
25	chr16:74402336-74402386	GM06990	blood:	n/a
26	chr16:74402336-74402386	GM19239	blood:	n/a
27	chr16:74402336-74402386	H1-hESC	embryonic stem cell:	embryo
28	chr16:74401986-74402036	Caco-2	colon:	n/a
29	chr16:74398168-74398218	HEK293	kidney:	embryo
30	chr16:74401547-74401597	U87	brain:	n/a
31	chr16:74398168-74398218	NHDF-neo	bronchial:	n/a
32	chr16:74401547-74401597	Caco-2	colon:	n/a
33	chr16:74398168-74398218	HCPEpiC	choroid plexus:	n/a
34	chr16:74403516-74403566	PrEC	prostate:	n/a
35	chr16:74402336-74402386	GM12878	blood:	n/a
36	chr16:74401547-74401597	HUVEC	blood vessel:	n/a
37	chr16:74403516-74403566	GM12891	blood:	n/a
38	chr16:74403516-74403566	HMEC	breast:	n/a
39	chr16:74402336-74402386	AG09319	gingival:	n/a
40	chr16:74402336-74402386	SK-N-SH_RA	brain:	n/a
41	chr16:74400946-74400996	GM12878	blood:	n/a
42	chr16:74401547-74401597	AG10803	skin:	n/a
43	chr16:74401547-74401597	MCF-7	breast:	n/a
44	chr16:74406059-74406109	HCPEpiC	choroid plexus:	n/a
45	chr16:74400946-74400996	AG04449	skin:	fetal
46	chr16:74401986-74402036	AoSMC	blood vessel:	n/a
47	chr16:74402737-74402787	HCT-116	colon:	n/a
48	chr16:74400946-74400996	HCPEpiC	choroid plexus:	n/a
49	chr16:74398168-74398218	U87	brain:	n/a
50	chr16:74402737-74402787	HNPCEpiC	eye:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain
2	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
3	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1
4	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009
5	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
6	lnc-CLEC18B-2	chr16:74368790-74369244	ENSG00000259972.1
7	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681

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

Extended variants
information (count: 3264 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3264 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575357302	chr16:74366712-74366713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543866509	chr16:74366744-74366745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560996352	chr16:74366746-74366747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574471685	chr16:74366767-74366768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2911029	chr16:74366858-74366859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540401374	chr16:74366887-74366888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376261182	chr16:74366896-74366897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184577225	chr16:74366904-74366905	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs532265561	chr16:74366906-74366907	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs2911028	chr16:74366918-74366919	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552102403	chr16:74366934-74366935	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs2911027	chr16:74366936-74366937	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs187919064	chr16:74366982-74366983	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs562448127	chr16:74366992-74366993	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs370287159	chr16:74367026-74367027	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs545262046	chr16:74367065-74367066	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs375406369	chr16:74367066-74367067	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs548309315	chr16:74367086-74367087	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs568511213	chr16:74367113-74367114	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs534059749	chr16:74367116-74367117	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs547953317	chr16:74367121-74367122	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs571094339	chr16:74367123-74367124	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs540134120	chr16:74367135-74367136	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs368010426	chr16:74367189-74367190	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs191308488	chr16:74367202-74367203	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs140528269	chr16:74367213-74367214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554297862	chr16:74367248-74367249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574458654	chr16:74367264-74367265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539994181	chr16:74367279-74367280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559915087	chr16:74367370-74367371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576585688	chr16:74367383-74367384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545604858	chr16:74367424-74367425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565506968	chr16:74367652-74367653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200920029	chr16:74367687-74367688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201892208	chr16:74367771-74367772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562411031	chr16:74367784-74367785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531528212	chr16:74367786-74367787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527956128	chr16:74368019-74368020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549451057	chr16:74368134-74368135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201859289	chr16:74368274-74368275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561970876	chr16:74368359-74368360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527773623	chr16:74368363-74368364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547620972	chr16:74368366-74368367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370965798	chr16:74368393-74368394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570961068	chr16:74368402-74368403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111645977	chr16:74368415-74368416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374332136	chr16:74368429-74368430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368218294	chr16:74368443-74368444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533524095	chr16:74368484-74368485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372390407	chr16:74368522-74368523	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:1739 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

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	chr16:74341400-74371600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr16:74341400-74376200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr16:74341400-74400800	Weak transcription	NH-A	brain
8	chr16:74341600-74371200	Weak transcription	HUVEC	blood vessel
9	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
10	chr16:74355600-74382200	Weak transcription	GM12878-XiMat	blood
11	chr16:74356600-74371400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr16:74357600-74367600	Strong transcription	Fetal Stomach	stomach
13	chr16:74357800-74367600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr16:74358200-74367200	Strong transcription	Fetal Intestine Small	intestine
15	chr16:74359400-74367200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr16:74360000-74378200	Weak transcription	Primary B cells from cord blood	blood
17	chr16:74360000-74401400	Weak transcription	Small Intestine	intestine
18	chr16:74360600-74371600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr16:74360600-74382600	Weak transcription	HSMMtube	muscle
20	chr16:74360800-74383000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr16:74361000-74382000	Weak transcription	Fetal Kidney	kidney
22	chr16:74361000-74385000	Weak transcription	K562	blood
23	chr16:74361400-74384200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr16:74362000-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr16:74362200-74387400	Weak transcription	NHDF-Ad	bronchial
26	chr16:74362200-74392400	Weak transcription	HSMM	muscle
27	chr16:74362200-74394000	Weak transcription	HMEC	breast
28	chr16:74362200-74398600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr16:74362800-74398000	Weak transcription	Psoas Muscle	Psoas
30	chr16:74363400-74367200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr16:74363800-74367200	Strong transcription	Stomach Smooth Muscle	stomach
32	chr16:74364000-74367000	Strong transcription	Fetal Intestine Large	intestine
33	chr16:74364000-74367200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr16:74364000-74367200	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr16:74364000-74367400	Strong transcription	Liver	Liver
36	chr16:74364000-74367600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr16:74364000-74367600	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr16:74364200-74366800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr16:74364200-74367000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr16:74364200-74367000	Strong transcription	Esophagus	oesophagus
41	chr16:74364200-74367200	Strong transcription	H9 Cell Line	embryonic stem cell
42	chr16:74364200-74367200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr16:74364200-74367200	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr16:74364200-74367200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr16:74364200-74367200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr16:74364200-74367200	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr16:74364200-74367200	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr16:74364200-74367200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr16:74364200-74367200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr16:74364200-74367200	Strong transcription	Adipose Nuclei	Adipose

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