Variant report

Variant	esv1831365
Chromosome Location	chr16:74387587-74410258
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	chr16:74401853-74402428	HepG2	liver:	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	chr16:74401940-74402325	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
6	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
7	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
8	ATF3	chr16:74401950-74402248	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	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
12	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
13	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
14	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
15	BHLHE40	chr16:74401724-74402378	GM12878	blood:	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	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
20	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
21	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	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	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
25	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
26	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
27	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
28	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
29	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
30	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
31	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
32	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
33	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
34	CHD2	chr16:74401780-74402403	GM12878	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
35	CHD2	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
36	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
37	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
38	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
39	CREB1	chr16:74401943-74402336	HepG2	liver:	n/a	n/a
40	CREB1	chr16:74402021-74402294	K562	blood:	n/a	n/a
41	CREB1	chr16:74401970-74402284	GM12878	blood:	n/a	n/a
42	CREB1	chr16:74401959-74402277	K562	blood:	n/a	n/a
43	CREB1	chr16:74402083-74402284	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr16:74401934-74402414	A549	lung:	n/a	n/a
45	CREB1	chr16:74402012-74402247	A549	lung:	n/a	n/a
46	CTCF	chr16:74398040-74398190	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr16:74390497-74390523	GM13976	blood:	n/a	n/a
48	CTCF	chr16:74396380-74396435	HepG2	liver:	n/a	n/a
49	CTCF	chr16:74396220-74396370	GM12872	blood:	n/a	n/a
50	CTCF	chr16:74396220-74396370	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74402737-74402787	HPAEpiC	pulmonary alveolar:	n/a
2	chr16:74402737-74402787	NT2-D1	testis:	n/a
3	chr16:74402329-74402379	Jurkat	blood:	n/a
4	chr16:74402737-74402787	NB4	blood:	n/a
5	chr16:74400946-74400996	HepG2	liver:	n/a
6	chr16:74402336-74402386	IMR90	lung:	fetal
7	chr16:74406059-74406109	Hela-S3	cervix:	n/a
8	chr16:74401794-74401844	HNPCEpiC	eye:	n/a
9	chr16:74400946-74400996	NHDF-neo	bronchial:	n/a
10	chr16:74402737-74402787	BJ	skin:	n/a
11	chr16:74402329-74402379	NH-A	brain:	n/a
12	chr16:74402737-74402787	PFSK-1	brain:	n/a
13	chr16:74401547-74401597	H1-hESC	embryonic stem cell:	embryo
14	chr16:74403516-74403566	Jurkat	blood:	n/a
15	chr16:74402336-74402386	HL-60	blood:	n/a
16	chr16:74403516-74403566	MCF-7	breast:	n/a
17	chr16:74400946-74400996	SK-N-SH	brain:	n/a
18	chr16:74401794-74401844	AG09309	skin:	n/a
19	chr16:74402329-74402379	HRE	kidney:	n/a
20	chr16:74402329-74402379	PANC-1	pancreas:	n/a
21	chr16:74398168-74398218	HAEpiC	amniotic membrane:	n/a
22	chr16:74401547-74401597	HCF	heart:	n/a
23	chr16:74403516-74403566	HUVEC	blood vessel:	n/a
24	chr16:74400946-74400996	HAEpiC	amniotic membrane:	n/a
25	chr16:74398168-74398218	MCF10A-Er-Src	breast:	n/a
26	chr16:74402737-74402787	AG09319	gingival:	n/a
27	chr16:74406059-74406109	HIPEpiC	eye:	n/a
28	chr16:74402336-74402386	AG04449	skin:	fetal
29	chr16:74402336-74402386	HUVEC	blood vessel:	n/a
30	chr16:74401986-74402036	SKMC	muscle:	n/a
31	chr16:74401547-74401597	HEEpiC	esophagus:	n/a
32	chr16:74403516-74403566	HIPEpiC	eye:	n/a
33	chr16:74402336-74402386	AG04450	lung:	fetal
34	chr16:74402336-74402386	HCF	heart:	n/a
35	chr16:74402336-74402386	ovcar-3	ovarian:	n/a
36	chr16:74400946-74400996	HPAEpiC	pulmonary alveolar:	n/a
37	chr16:74401794-74401844	HepG2	liver:	n/a
38	chr16:74400946-74400996	A549	lung:	n/a
39	chr16:74402329-74402379	Caco-2	colon:	n/a
40	chr16:74401547-74401597	GM12892	blood:	n/a
41	chr16:74401547-74401597	MCF-7	breast:	n/a
42	chr16:74402336-74402386	BJ	skin:	n/a
43	chr16:74402336-74402386	HAEpiC	amniotic membrane:	n/a
44	chr16:74403516-74403566	HCF	heart:	n/a
45	chr16:74401794-74401844	GM12891	blood:	n/a
46	chr16:74400946-74400996	HEK293	kidney:	embryo
47	chr16:74401794-74401844	HRPEpiC	eye:	n/a
48	chr16:74398168-74398218	SKMC	muscle:	n/a
49	chr16:74402737-74402787	HCT-116	colon:	n/a
50	chr16:74401547-74401597	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr16:74394116..74395645-chr3:9438342..9440027,2	MCF-7	breast:
2	chr16:74396107..74397775-chr16:74400703..74403254,2	K562	blood:
3	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-2	chr16:74401963-74402046	NONHSAT143681
4	lnc-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain

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
ENSG00000214331	chromatin interactions
ENSG00000206573	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000261079	chromatin interactions
ENSG00000168137	chromatin interactions

Extended variants
information (count: 1166 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1166 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2549272	chr16:74387587-74387588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372010071	chr16:74387625-74387626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536038455	chr16:74387635-74387636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555731416	chr16:74387650-74387651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572606539	chr16:74387667-74387668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2549273	chr16:74387680-74387681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541289932	chr16:74387681-74387682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188341344	chr16:74387691-74387692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576404352	chr16:74387709-74387710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545427910	chr16:74387733-74387734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562592657	chr16:74387734-74387735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576238497	chr16:74387741-74387742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541909057	chr16:74387758-74387759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376376226	chr16:74387788-74387789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561690728	chr16:74387792-74387793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527497747	chr16:74387804-74387805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547685181	chr16:74387852-74387853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146492016	chr16:74387882-74387883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs5015743	chr16:74387896-74387897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149398838	chr16:74387908-74387909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181110471	chr16:74387939-74387940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549950202	chr16:74387940-74387941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570132282	chr16:74387950-74387951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535533136	chr16:74387955-74387956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3874592	chr16:74387958-74387959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184180136	chr16:74387972-74387973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs5015745	chr16:74387974-74387975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369100628	chr16:74388024-74388025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577955941	chr16:74388029-74388030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111691607	chr16:74388064-74388065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs5015747	chr16:74388087-74388088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190020820	chr16:74388112-74388113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs3971805	chr16:74388130-74388131	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs374407771	chr16:74388143-74388144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557836398	chr16:74388150-74388151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139050401	chr16:74388195-74388196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541525983	chr16:74388214-74388215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34562682	chr16:74388256-74388257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527458933	chr16:74388257-74388258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377446759	chr16:74388264-74388265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78200018	chr16:74388300-74388301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564364358	chr16:74388308-74388309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557712971	chr16:74388342-74388343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540692248	chr16:74388351-74388352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560573119	chr16:74388362-74388363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10451149	chr16:74388369-74388370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550052354	chr16:74388371-74388372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181686731	chr16:74388373-74388374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529306180	chr16:74388377-74388378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs118012030	chr16:74388414-74388415	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:1050 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	chr16:74340800-74400200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr16:74341400-74400800	Weak transcription	NH-A	brain
5	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
6	chr16:74360000-74401400	Weak transcription	Small Intestine	intestine
7	chr16:74362000-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr16:74362200-74392400	Weak transcription	HSMM	muscle
9	chr16:74362200-74394000	Weak transcription	HMEC	breast
10	chr16:74362200-74398600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr16:74362800-74398000	Weak transcription	Psoas Muscle	Psoas
12	chr16:74364400-74398800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr16:74365200-74394000	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr16:74367200-74398000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr16:74367200-74400800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr16:74367600-74392400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr16:74368400-74387800	Strong transcription	Placenta	Placenta
18	chr16:74368400-74389400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr16:74368600-74389200	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr16:74371200-74388400	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr16:74371800-74400800	Weak transcription	Fetal Heart	heart
22	chr16:74371800-74400800	Weak transcription	HUVEC	blood vessel
23	chr16:74371800-74401200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr16:74372200-74400800	Weak transcription	Colonic Mucosa	Colon
25	chr16:74373600-74396400	Weak transcription	NHEK	skin
26	chr16:74374000-74399800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr16:74375400-74388400	Strong transcription	Duodenum Mucosa	Duodenum
28	chr16:74375400-74388800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr16:74375600-74389200	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr16:74375600-74389200	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr16:74375600-74389600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr16:74375800-74394800	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr16:74376400-74394800	Strong transcription	Fetal Stomach	stomach
34	chr16:74376800-74388800	Strong transcription	Fetal Muscle Trunk	muscle
35	chr16:74377800-74389000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr16:74378200-74387800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr16:74379200-74388200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr16:74379200-74394000	Weak transcription	Primary B cells from cord blood	blood
39	chr16:74380200-74401400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr16:74381200-74388600	Strong transcription	Liver	Liver
41	chr16:74381400-74387600	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr16:74381400-74388200	Strong transcription	H1 Cell Line	embryonic stem cell
43	chr16:74381400-74388200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr16:74381400-74388200	Strong transcription	Spleen	Spleen
45	chr16:74381400-74388800	Strong transcription	Primary T cells fromperipheralblood	blood
46	chr16:74381600-74389400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr16:74381800-74388400	Strong transcription	Adipose Nuclei	Adipose
48	chr16:74381800-74389200	Strong transcription	Fetal Muscle Leg	muscle
49	chr16:74382000-74388200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr16:74382000-74388200	Strong transcription	Sigmoid Colon	Sigmoid Colon

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