Variant report

Variant	esv1810395
Chromosome Location	chr16:72096633-72108093
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:485)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:72100631-72100890	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:72096768-72097017	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:72106673-72107165	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:72106772-72107045	K562	blood:	n/a	n/a
5	ATF1	chr16:72106727-72107177	K562	blood:	n/a	n/a
6	BHLHE40	chr16:72100638-72100838	GM12878	blood:	n/a	n/a
7	BHLHE40	chr16:72100614-72101032	K562	blood:	n/a	n/a
8	BHLHE40	chr16:72106822-72107057	K562	blood:	n/a	n/a
9	BHLHE40	chr16:72098374-72098413	HepG2	liver:	n/a	n/a
10	CBX3	chr16:72106469-72107388	K562	blood:	n/a	n/a
11	CCNT2	chr16:72106794-72107083	K562	blood:	n/a	n/a
12	CEBPB	chr16:72096826-72097080	HepG2	liver:	n/a	chr16:72097056-72097065 chr16:72097056-72097065
13	CEBPB	chr16:72100481-72100866	K562	blood:	n/a	n/a
14	CEBPB	chr16:72106854-72107148	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr16:72106867-72107147	HepG2	liver:	n/a	n/a
16	CEBPB	chr16:72096800-72097221	HepG2	liver:	n/a	chr16:72097056-72097065 chr16:72097056-72097065
17	CEBPB	chr16:72096774-72097113	HepG2	liver:	n/a	chr16:72097056-72097065 chr16:72097056-72097065
18	CEBPB	chr16:72098298-72098582	HepG2	liver:	n/a	n/a
19	CEBPB	chr16:72096795-72097213	HepG2	liver:	n/a	chr16:72097056-72097065 chr16:72097056-72097065
20	CEBPD	chr16:72096830-72097104	HepG2	liver:	n/a	chr16:72097055-72097066
21	CEBPD	chr16:72106811-72107187	K562	blood:	n/a	n/a
22	CEBPD	chr16:72096833-72097096	HepG2	liver:	n/a	chr16:72097055-72097066
23	CHD2	chr16:72106961-72107085	HepG2	liver:	n/a	n/a
24	CHD2	chr16:72106869-72107069	K562	blood:	n/a	n/a
25	CTCF	chr16:72100720-72100870	MCF-7	breast:	n/a	n/a
26	CTCF	chr16:72100680-72100830	HAc	cerebellar:	n/a	n/a
27	CTCF	chr16:72100680-72100830	GM06990	blood:	n/a	n/a
28	CTCF	chr16:72100547-72100972	GM12878	blood:	n/a	n/a
29	CTCF	chr16:72100490-72101067	HepG2	liver:	n/a	n/a
30	CTCF	chr16:72100760-72100910	GM06990	blood:	n/a	n/a
31	CTCF	chr16:72100700-72100850	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr16:72100525-72101003	MCF-7	breast:	n/a	n/a
33	CTCF	chr16:72099120-72099270	BE2_C	brain:	n/a	n/a
34	CTCF	chr16:72100660-72100810	HAc	cerebellar:	n/a	n/a
35	CTCF	chr16:72100700-72100850	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr16:72100700-72100850	AG09319	gingival:	n/a	n/a
37	CTCF	chr16:72099071-72099331	K562	blood:	n/a	n/a
38	CTCF	chr16:72100700-72100850	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr16:72100700-72100850	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr16:72100680-72100830	GM12864	blood:	n/a	n/a
41	CTCF	chr16:72100780-72100930	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr16:72101600-72101750	RPTEC	kidney:	n/a	n/a
43	CTCF	chr16:72100620-72100770	HVMF	connective:	n/a	n/a
44	CTCF	chr16:72100700-72100850	GM12873	blood:	n/a	n/a
45	CTCF	chr16:72100300-72100450	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr16:72100630-72100881	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr16:72100720-72100870	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr16:72100680-72100830	GM12867	blood:	n/a	n/a
49	CTCF	chr16:72100680-72100830	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr16:72100590-72100921	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:72096944-72096994	H1-hESC	embryonic stem cell:	embryo
2	chr16:72097718-72097768	H1-hESC	embryonic stem cell:	embryo
3	chr16:72097718-72097768	A549	lung:	n/a
4	chr16:72096944-72096994	HRE	kidney:	n/a
5	chr16:72096944-72096994	NT2-D1	testis:	n/a
6	chr16:72096944-72096994	HIPEpiC	eye:	n/a
7	chr16:72096608-72096658	Hepatocyte	liver:	n/a
8	chr16:72096944-72096994	SK-N-SH_RA	brain:	n/a
9	chr16:72096944-72096994	GM12878	blood:	n/a
10	chr16:72097718-72097768	HUVEC	blood vessel:	n/a
11	chr16:72096944-72096994	HCM	heart:	n/a
12	chr16:72096608-72096658	ovcar-3	ovarian:	n/a
13	chr16:72096608-72096658	HCF	heart:	n/a
14	chr16:72097718-72097768	PANC-1	pancreas:	n/a
15	chr16:72096944-72096994	K562	blood:	n/a
16	chr16:72096608-72096658	HMEC	breast:	n/a
17	chr16:72096944-72096994	GM06990	blood:	n/a
18	chr16:72097718-72097768	SKMC	muscle:	n/a
19	chr16:72097718-72097768	GM12892	blood:	n/a
20	chr16:72096608-72096658	HUVEC	blood vessel:	n/a
21	chr16:72096944-72096994	HPAEpiC	pulmonary alveolar:	n/a
22	chr16:72097718-72097768	GM12878	blood:	n/a
23	chr16:72097718-72097768	RPTEC	kidney:	n/a
24	chr16:72097718-72097768	AG09309	skin:	n/a
25	chr16:72096944-72096994	HepG2	liver:	n/a
26	chr16:72097718-72097768	Jurkat	blood:	n/a
27	chr16:72096608-72096658	HRE	kidney:	n/a
28	chr16:72096608-72096658	HNPCEpiC	eye:	n/a
29	chr16:72097718-72097768	HEEpiC	esophagus:	n/a
30	chr16:72096944-72096994	AG09319	gingival:	n/a
31	chr16:72096944-72096994	NHDF-neo	bronchial:	n/a
32	chr16:72096608-72096658	GM06990	blood:	n/a
33	chr16:72096608-72096658	HCPEpiC	choroid plexus:	n/a
34	chr16:72096944-72096994	RPTEC	kidney:	n/a
35	chr16:72096608-72096658	PANC-1	pancreas:	n/a
36	chr16:72096944-72096994	HMEC	breast:	n/a
37	chr16:72096608-72096658	SAEC	small airway:	n/a
38	chr16:72097718-72097768	GM06990	blood:	n/a
39	chr16:72096608-72096658	PFSK-1	brain:	n/a
40	chr16:72097718-72097768	AG09319	gingival:	n/a
41	chr16:72097718-72097768	AG04449	skin:	fetal
42	chr16:72096608-72096658	LNCaP	prostate:	n/a
43	chr16:72096944-72096994	HRCEpiC	kidney:	n/a
44	chr16:72097718-72097768	BJ	skin:	n/a
45	chr16:72097718-72097768	AG04450	lung:	fetal
46	chr16:72097718-72097768	SK-N-MC	brain:	n/a
47	chr16:72097718-72097768	MCF10A-Er-Src	breast:	n/a
48	chr16:72096608-72096658	AG04449	skin:	fetal
49	chr16:72096608-72096658	HPAEpiC	pulmonary alveolar:	n/a
50	chr16:72096608-72096658	HL-60	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:72103326..72105153-chr16:72117441..72120370,2	MCF-7	breast:
2	chr16:72098170..72103448-chr16:72104419..72108463,5	K562	blood:
3	chr16:72100206..72101351-chr16:72132899..72134129,9	K562	blood:
4	chr16:72098664..72102766-chr16:72126373..72129232,5	K562	blood:
5	chr16:72100293..72101113-chr16:72132931..72133757,5	MCF-7	breast:
6	chr16:72098664..72100530-chr16:72126789..72129168,2	K562	blood:
7	chr16:72099750..72107853-chr16:72126502..72131093,10	MCF-7	breast:
8	chr16:72103116..72104667-chr16:72127883..72129694,2	K562	blood:
9	chr16:72041551..72044328-chr16:72098859..72101646,2	K562	blood:
10	chr16:72098840..72102253-chr16:72104146..72107637,4	K562	blood:
11	chr16:72107601..72110331-chr16:72118448..72121540,3	MCF-7	breast:
12	chr16:72100387..72101200-chr16:72132899..72133926,7	MCF-7	breast:
13	chr16:72097383..72100653-chr16:72133488..72135199,3	MCF-7	breast:
14	chr16:72100358..72100998-chr16:72130881..72131518,2	MCF-7	breast:
15	chr16:72100778..72101306-chr16:72127117..72128039,2	K562	blood:
16	chr16:72098840..72102253-chr16:72104146..72107637,4	K562	blood:

No data

Variant related genes	Relation type
HPR	TF binding region
HPR	CpG island
ENSG00000140829	chromatin interactions
ENSG00000261701	chromatin interactions
ENSG00000140830	chromatin interactions
ENSG00000102967	chromatin interactions
ENSG00000260252	chromatin interactions

Extended variants
information (count: 512 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2550880	chr16:72096633-72096634	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs568083997	chr16:72096638-72096639	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs551464316	chr16:72096682-72096683	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs569990051	chr16:72096708-72096709	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs530824025	chr16:72096718-72096719	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs549623658	chr16:72096762-72096763	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs567891014	chr16:72096782-72096783	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs535398626	chr16:72096805-72096806	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs553652082	chr16:72096835-72096836	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs571876041	chr16:72096871-72096872	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs538697691	chr16:72096889-72096890	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs140435387	chr16:72096905-72096906	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs575150814	chr16:72096918-72096919	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs542288289	chr16:72096924-72096925	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs199651848	chr16:72096942-72096943	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs554832433	chr16:72096944-72096945	Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs374731834	chr16:72096975-72096976	Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs182939712	chr16:72096988-72096989	Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs187995698	chr16:72096990-72096991	Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs191185168	chr16:72097024-72097025	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs144406438	chr16:72097027-72097028	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs545063207	chr16:72097028-72097029	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs369053532	chr16:72097034-72097035	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs551607270	chr16:72097042-72097043	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs563650954	chr16:72097060-72097061	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs183354204	chr16:72097061-72097062	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs530910253	chr16:72097099-72097100	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs372627491	chr16:72097118-72097119	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs571400368	chr16:72097127-72097128	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs372122150	chr16:72097173-72097174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376756183	chr16:72097192-72097193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374947215	chr16:72097209-72097210	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs375982657	chr16:72097223-72097224	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs12918905	chr16:72097225-72097226	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs12917768	chr16:72097230-72097231	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
36	rs200702148	chr16:72097255-72097256	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs112997229	chr16:72097256-72097257	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs28731397	chr16:72097279-72097280	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs567525626	chr16:72097390-72097391	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs187602002	chr16:72097410-72097411	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140307595	chr16:72097412-72097413	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs192130167	chr16:72097414-72097415	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185094388	chr16:72097475-72097476	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs568894442	chr16:72097521-72097522	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs116835266	chr16:72097560-72097561	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs536234434	chr16:72097565-72097566	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs554015154	chr16:72097571-72097572	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572507204	chr16:72097575-72097576	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs189948810	chr16:72097619-72097620	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs540095472	chr16:72097676-72097677	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	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 myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Neuroblastoma	18923524	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:72060200-72110600	Weak transcription	Esophagus	oesophagus
2	chr16:72076200-72098200	Weak transcription	Fetal Heart	heart
3	chr16:72077000-72107400	Weak transcription	Right Ventricle	heart
4	chr16:72077400-72102400	Weak transcription	Brain Substantia Nigra	brain
5	chr16:72077400-72107400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr16:72077600-72107400	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr16:72078000-72100800	Weak transcription	Brain Hippocampus Middle	brain
8	chr16:72078000-72103200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr16:72078200-72105200	Weak transcription	Brain Angular Gyrus	brain
10	chr16:72078400-72098400	Weak transcription	Primary T cells from cord blood	blood
11	chr16:72078400-72105400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr16:72078400-72108000	Weak transcription	Aorta	Aorta
13	chr16:72084600-72106800	Weak transcription	Psoas Muscle	Psoas
14	chr16:72084800-72098200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr16:72088400-72098400	Weak transcription	Adipose Nuclei	Adipose
16	chr16:72090000-72107600	Weak transcription	Primary B cells from cord blood	blood
17	chr16:72090200-72107600	Weak transcription	Gastric	stomach
18	chr16:72090200-72118400	Weak transcription	Lung	lung
19	chr16:72093200-72097200	Weak transcription	Liver	Liver
20	chr16:72093200-72118000	Weak transcription	Fetal Muscle Trunk	muscle
21	chr16:72093800-72107400	Weak transcription	Fetal Stomach	stomach
22	chr16:72093800-72118400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr16:72093800-72118400	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr16:72094800-72097400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr16:72094800-72099800	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr16:72094800-72106800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr16:72094800-72108000	Weak transcription	Fetal Muscle Leg	muscle
28	chr16:72094800-72110600	Weak transcription	Spleen	Spleen
29	chr16:72095800-72111800	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr16:72096000-72097000	Flanking Active TSS	HepG2	liver
31	chr16:72096000-72105400	Weak transcription	Brain Anterior Caudate	brain
32	chr16:72096200-72105200	Weak transcription	Ovary	ovary
33	chr16:72096400-72096800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr16:72096800-72102400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr16:72096800-72118200	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr16:72097000-72097200	Enhancers	HepG2	liver
37	chr16:72097200-72098200	Active TSS	Liver	Liver
38	chr16:72097200-72099000	Flanking Active TSS	HepG2	liver
39	chr16:72097200-72118000	Weak transcription	Primary B cells from peripheral blood	blood
40	chr16:72098200-72098600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr16:72098200-72098800	Strong transcription	Fetal Heart	heart
42	chr16:72098200-72099400	Flanking Active TSS	Liver	Liver
43	chr16:72098400-72099000	Strong transcription	Adipose Nuclei	Adipose
44	chr16:72098400-72099200	Strong transcription	Primary T cells from cord blood	blood
45	chr16:72098600-72099200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr16:72098600-72107400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr16:72098800-72099200	ZNF genes & repeats	Fetal Heart	heart
48	chr16:72099000-72101200	Enhancers	HepG2	liver
49	chr16:72099000-72107200	Weak transcription	Adipose Nuclei	Adipose
50	chr16:72099200-72100200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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