Variant report

Variant	nsv457532
Chromosome Location	chr16:76251275-76293394
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	chr16:76256042-76256283	HepG2	liver:	n/a	n/a
2	CEBPB	chr16:76266667-76266981	IMR90	lung:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
3	CEBPB	chr16:76276619-76276914	HepG2	liver:	n/a	chr16:76276751-76276762
4	CEBPB	chr16:76256803-76257198	H1-hESC	embryonic stem cell:	n/a	chr16:76257002-76257013
5	CEBPB	chr16:76266660-76266961	HepG2	liver:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
6	CEBPB	chr16:76266739-76266878	K562	blood:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
7	CEBPB	chr16:76266695-76266926	A549	lung:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
8	CEBPB	chr16:76266652-76266909	H1-hESC	embryonic stem cell:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
9	CEBPB	chr16:76256857-76257120	HepG2	liver:	n/a	chr16:76257002-76257013
10	CTCF	chr16:76261160-76261310	SAEC	small airway:	n/a	n/a
11	CTCF	chr16:76263161-76263202	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr16:76253820-76253970	GM12872	blood:	n/a	n/a
13	E2F4	chr16:76276713-76276959	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr16:76259558-76259746	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr16:76259967-76260192	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr16:76260449-76260740	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr16:76259965-76260724	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr16:76260397-76260652	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr16:76259949-76260248	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr16:76260430-76260726	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr16:76259967-76260199	MCF10A-Er-Src	breast:	n/a	n/a
22	FOXA1	chr16:76256745-76257085	HepG2	liver:	n/a	n/a
23	FOXA1	chr16:76255956-76256327	HepG2	liver:	n/a	n/a
24	FOXA1	chr16:76256830-76257066	HepG2	liver:	n/a	n/a
25	FOXA2	chr16:76288729-76289045	A549	lung:	n/a	n/a
26	FOXA2	chr16:76256799-76257037	HepG2	liver:	n/a	n/a
27	GATA2	chr16:76256782-76257088	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr16:76262491-76262776	MCF-7	breast:	n/a	n/a
29	GATA3	chr16:76262530-76262772	T-47D	breast:	n/a	n/a
30	GATA3	chr16:76256788-76257033	SH-SY5Y	brain:	n/a	n/a
31	HNF4A	chr16:76256016-76256306	HepG2	liver:	n/a	chr16:76256137-76256150 chr16:76256157-76256165 chr16:76256137-76256150 chr16:76256133-76256155 chr16:76256137-76256151
32	JUN	chr16:76278777-76279058	HepG2	liver:	n/a	chr16:76278894-76278907 chr16:76278895-76278904
33	JUND	chr16:76251468-76251777	HepG2	liver:	n/a	n/a
34	JUND	chr16:76278802-76279074	HepG2	liver:	n/a	chr16:76278895-76278904
35	MAFF	chr16:76266605-76266963	HepG2	liver:	n/a	chr16:76266780-76266798
36	MAFF	chr16:76277560-76277872	K562	blood:	n/a	chr16:76277705-76277723 chr16:76277711-76277725
37	MAFF	chr16:76256004-76256302	HepG2	liver:	n/a	chr16:76256116-76256134
38	MAFF	chr16:76280510-76280831	HepG2	liver:	n/a	chr16:76280670-76280688
39	MAFF	chr16:76268363-76268489	HepG2	liver:	n/a	n/a
40	MAFF	chr16:76277534-76277901	HepG2	liver:	n/a	chr16:76277705-76277723 chr16:76277711-76277725
41	MAFF	chr16:76266623-76266925	K562	blood:	n/a	chr16:76266780-76266798
42	MAFF	chr16:76280641-76280735	K562	blood:	n/a	chr16:76280670-76280688
43	MAFK	chr16:76291517-76291614	HepG2	liver:	n/a	n/a
44	MAFK	chr16:76280510-76280850	HepG2	liver:	n/a	chr16:76280671-76280686
45	MAFK	chr16:76256762-76257001	HepG2	liver:	n/a	n/a
46	MAFK	chr16:76268298-76268433	HepG2	liver:	n/a	chr16:76268373-76268387 chr16:76268375-76268386
47	MAFK	chr16:76255980-76256302	HepG2	liver:	n/a	chr16:76256118-76256128 chr16:76256117-76256132 chr16:76256119-76256128
48	MAFK	chr16:76280506-76280836	HepG2	liver:	n/a	chr16:76280671-76280686
49	MAFK	chr16:76266628-76266947	Hela-S3	cervix:	n/a	chr16:76266781-76266796 chr16:76266781-76266797 chr16:76266776-76266796
50	MAFK	chr16:76266652-76266915	K562	blood:	n/a	chr16:76266781-76266796 chr16:76266781-76266797 chr16:76266776-76266796

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76272351-76272401	HRE	kidney:	n/a
2	chr16:76269409-76269459	CMK	blood:	n/a
3	chr16:76272351-76272401	ECC-1	luminal epithelium:	n/a
4	chr16:76269297-76269347	GM19239	blood:	n/a
5	chr16:76269184-76269234	HPAEpiC	pulmonary alveolar:	n/a
6	chr16:76269409-76269459	MCF-7	breast:	n/a
7	chr16:76266534-76266584	SAEC	small airway:	n/a
8	chr16:76269409-76269459	GM12878	blood:	n/a
9	chr16:76272351-76272401	NHBE	bronchial:	n/a
10	chr16:76269297-76269347	HepG2	liver:	n/a
11	chr16:76269297-76269347	ovcar-3	ovarian:	n/a
12	chr16:76269192-76269242	BE2_C	brain:	n/a
13	chr16:76272351-76272401	U87	brain:	n/a
14	chr16:76269297-76269347	Jurkat	blood:	n/a
15	chr16:76269297-76269347	NB4	blood:	n/a
16	chr16:76256948-76256998	Caco-2	colon:	n/a
17	chr16:76266534-76266584	HCF	heart:	n/a
18	chr16:76272351-76272401	AG04449	skin:	fetal
19	chr16:76268785-76268835	HMEC	breast:	n/a
20	chr16:76269043-76269093	HUVEC	blood vessel:	n/a
21	chr16:76266534-76266584	T-47D	breast:	n/a
22	chr16:76256948-76256998	SKMC	muscle:	n/a
23	chr16:76268785-76268835	NHBE	bronchial:	n/a
24	chr16:76269297-76269347	Hela-S3	cervix:	n/a
25	chr16:76272351-76272401	SK-N-SH	brain:	n/a
26	chr16:76269184-76269234	ProgFib	skin:	n/a
27	chr16:76269043-76269093	HRCEpiC	kidney:	n/a
28	chr16:76269184-76269234	HepG2	liver:	n/a
29	chr16:76269297-76269347	PrEC	prostate:	n/a
30	chr16:76266534-76266584	HCT-116	colon:	n/a
31	chr16:76269043-76269093	HNPCEpiC	eye:	n/a
32	chr16:76272351-76272401	HPAEpiC	pulmonary alveolar:	n/a
33	chr16:76268785-76268835	AG09319	gingival:	n/a
34	chr16:76269409-76269459	GM06990	blood:	n/a
35	chr16:76269043-76269093	MCF10A-Er-Src	breast:	n/a
36	chr16:76269184-76269234	K562	blood:	n/a
37	chr16:76269043-76269093	AG09309	skin:	n/a
38	chr16:76269192-76269242	K562	blood:	n/a
39	chr16:76266534-76266584	PFSK-1	brain:	n/a
40	chr16:76269297-76269347	PANC-1	pancreas:	n/a
41	chr16:76272351-76272401	PrEC	prostate:	n/a
42	chr16:76269409-76269459	A549	lung:	n/a
43	chr16:76269043-76269093	HRE	kidney:	n/a
44	chr16:76269409-76269459	HNPCEpiC	eye:	n/a
45	chr16:76269043-76269093	SK-N-SH_RA	brain:	n/a
46	chr16:76268785-76268835	GM12878	blood:	n/a
47	chr16:76269184-76269234	HRCEpiC	kidney:	n/a
48	chr16:76269409-76269459	HCM	heart:	n/a
49	chr16:76269192-76269242	AoSMC	blood vessel:	n/a
50	chr16:76269192-76269242	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr16:76272213..76274617-chr16:76275881..76278722,3	MCF-7	breast:
2	chr16:76267035..76268706-chr16:76269783..76271539,2	K562	blood:
3	chr16:76264260..76266317-chr16:76268267..76270250,2	MCF-7	breast:
4	chr16:76272213..76274617-chr16:76275881..76278722,3	MCF-7	breast:
5	chr16:76267035..76268706-chr16:76269783..76271539,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC025287.1-3	chr16:76268585-76269326	NONHSAT143776
2	lnc-AC025287.1-3	chr16:76262283-76262757	ENSG00000260983.1
3	lnc-AC025287.1-3	chr16:76265215-76265343	ENSG00000260983.1
4	lnc-AC025287.1-3	chr16:76268953-76269521	NONHSAT143777

Variant related genes	Relation type
RPL18P13	TF binding region
RPL18P13	CpG island
ENSG00000244485	chromatin interactions

Extended variants
information (count: 1004 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16943998	chr16:76251275-76251276	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556461674	chr16:76251277-76251278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576747912	chr16:76251303-76251304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542337927	chr16:76251313-76251314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112081874	chr16:76251320-76251321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527643375	chr16:76251330-76251331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143808227	chr16:76251350-76251351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560367045	chr16:76251357-76251358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546079336	chr16:76251448-76251449	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs150621881	chr16:76251552-76251553	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs139967597	chr16:76251560-76251561	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs377754554	chr16:76251576-76251577	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs76319480	chr16:76251606-76251607	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs531450526	chr16:76251632-76251633	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs144783138	chr16:76251661-76251662	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs551942070	chr16:76251700-76251701	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs558197054	chr16:76251702-76251703	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs73615426	chr16:76251706-76251707	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs553512574	chr16:76251715-76251716	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs570458419	chr16:76251815-76251816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539731691	chr16:76251865-76251866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556860590	chr16:76251882-76251883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs57474616	chr16:76251890-76251891	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs148547793	chr16:76251894-76251895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555861388	chr16:76251913-76251914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144409305	chr16:76251929-76251930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146684974	chr16:76251937-76251938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574041307	chr16:76251943-76251944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564308308	chr16:76251959-76251960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533372316	chr16:76252009-76252010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180924069	chr16:76252058-76252059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545731286	chr16:76252066-76252067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562488716	chr16:76252068-76252069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377159608	chr16:76252110-76252111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34527086	chr16:76252129-76252130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2866619	chr16:76252142-76252143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs567791152	chr16:76252167-76252168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527366124	chr16:76252174-76252175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556293290	chr16:76252261-76252262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374857098	chr16:76252274-76252275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547481444	chr16:76252305-76252306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2866620	chr16:76252360-76252361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs575866405	chr16:76252371-76252372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556571927	chr16:76252378-76252379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570398690	chr16:76252387-76252388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs8059365	chr16:76252388-76252389	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs555969541	chr16:76252444-76252445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564750244	chr16:76252447-76252448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186251458	chr16:76252448-76252449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534768551	chr16:76252470-76252471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	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
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	24585490	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76241600-76257400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr16:76249000-76254400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr16:76249800-76257400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr16:76250800-76252000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr16:76251200-76251400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr16:76251400-76251600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr16:76251400-76251800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr16:76251600-76251800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr16:76251800-76255400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr16:76252800-76253400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr16:76253400-76254600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr16:76253800-76254800	Enhancers	Small Intestine	intestine
13	chr16:76254000-76254200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
14	chr16:76254200-76254400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
15	chr16:76254400-76254600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr16:76254400-76254600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr16:76254600-76255200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr16:76254600-76255800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr16:76255200-76256800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr16:76255400-76256400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr16:76255600-76256000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr16:76255600-76257000	Enhancers	Liver	Liver
23	chr16:76255800-76256200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr16:76255800-76256600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
25	chr16:76255800-76256800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
26	chr16:76255800-76257000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr16:76255800-76258200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr16:76256000-76256200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr16:76256000-76256200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr16:76256000-76257000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
31	chr16:76256000-76257000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr16:76256000-76257000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr16:76256000-76257200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
34	chr16:76256000-76258200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
35	chr16:76256200-76256400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr16:76256200-76256800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr16:76256200-76257000	Enhancers	HepG2	liver
38	chr16:76256200-76257200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr16:76256200-76257600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr16:76256200-76258200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
41	chr16:76256400-76256600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr16:76256400-76256800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr16:76256600-76257000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
44	chr16:76256600-76257000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
45	chr16:76256600-76257600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr16:76256800-76257400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr16:76257000-76259800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr16:76257400-76258000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr16:76257400-76258200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr16:76257400-76258200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell

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