Variant report

Variant	esv1833520
Chromosome Location	chr16:70141139-70236877
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	chr16:70199076-70199303	K562	blood:	n/a	n/a
2	ARID3A	chr16:70195992-70196417	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:70191181-70192253	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:70186462-70187162	HepG2	liver:	n/a	n/a
5	ATF1	chr16:70199108-70199250	K562	blood:	n/a	n/a
6	ATF1	chr16:70143611-70143697	K562	blood:	n/a	n/a
7	ATF1	chr16:70195925-70196369	K562	blood:	n/a	n/a
8	ATF1	chr16:70147951-70148282	K562	blood:	n/a	chr16:70148098-70148112
9	ATF3	chr16:70147959-70148367	HepG2	liver:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
10	ATF3	chr16:70147962-70148260	HepG2	liver:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
11	ATF3	chr16:70147960-70148270	K562	blood:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
12	ATF3	chr16:70147950-70148330	GM12878	blood:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
13	ATF3	chr16:70147973-70148328	H1-hESC	embryonic stem cell:	n/a	chr16:70148090-70148110 chr16:70148074-70148094 chr16:70148220-70148229
14	ATF3	chr16:70143585-70143779	K562	blood:	n/a	n/a
15	ATF3	chr16:70148048-70148187	GM12878	blood:	n/a	chr16:70148090-70148110 chr16:70148074-70148094
16	BACH1	chr16:70190168-70190514	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr16:70147926-70148170	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr16:70148023-70148328	GM12878	blood:	n/a	n/a
19	BATF	chr16:70199070-70199298	GM12878	blood:	n/a	n/a
20	BHLHE40	chr16:70147910-70148574	GM12878	blood:	n/a	n/a
21	BHLHE40	chr16:70198955-70199421	K562	blood:	n/a	chr16:70199167-70199176 chr16:70199166-70199179 chr16:70199168-70199177 chr16:70199168-70199177
22	BHLHE40	chr16:70147820-70148392	HepG2	liver:	n/a	n/a
23	BHLHE40	chr16:70198964-70199392	HepG2	liver:	n/a	chr16:70199167-70199176 chr16:70199166-70199179 chr16:70199168-70199177 chr16:70199168-70199177
24	BHLHE40	chr16:70147929-70148332	HepG2	liver:	n/a	n/a
25	BHLHE40	chr16:70198996-70199289	HepG2	liver:	n/a	chr16:70199167-70199176 chr16:70199166-70199179 chr16:70199168-70199177 chr16:70199168-70199177
26	BHLHE40	chr16:70195884-70195964	K562	blood:	n/a	n/a
27	BHLHE40	chr16:70186495-70186937	HepG2	liver:	n/a	n/a
28	BHLHE40	chr16:70143609-70143654	K562	blood:	n/a	n/a
29	BHLHE40	chr16:70199031-70199331	GM12878	blood:	n/a	chr16:70199167-70199176 chr16:70199166-70199179 chr16:70199168-70199177 chr16:70199168-70199177
30	BHLHE40	chr16:70199036-70199329	A549	lung:	n/a	chr16:70199167-70199176 chr16:70199166-70199179 chr16:70199168-70199177 chr16:70199168-70199177
31	BHLHE40	chr16:70147958-70148291	A549	lung:	n/a	n/a
32	BHLHE40	chr16:70147914-70148657	K562	blood:	n/a	n/a
33	BHLHE40	chr16:70198956-70199405	HepG2	liver:	n/a	chr16:70199167-70199176 chr16:70199166-70199179 chr16:70199168-70199177 chr16:70199168-70199177
34	BRCA1	chr16:70186455-70186874	HepG2	liver:	n/a	n/a
35	BRCA1	chr16:70147907-70148167	GM12878	blood:	n/a	chr16:70148054-70148063
36	BRCA1	chr16:70147947-70148155	H1-hESC	embryonic stem cell:	n/a	chr16:70148054-70148063
37	BRCA1	chr16:70147948-70148162	HepG2	liver:	n/a	chr16:70148054-70148063
38	BRCA1	chr16:70147906-70148179	Hela-S3	cervix:	n/a	chr16:70148054-70148063
39	CBX3	chr16:70147444-70149098	K562	blood:	n/a	n/a
40	CBX3	chr16:70198885-70199357	K562	blood:	n/a	chr16:70199118-70199129
41	CCNT2	chr16:70147967-70148299	K562	blood:	n/a	chr16:70148084-70148093 chr16:70148220-70148229
42	CEBPB	chr16:70190661-70190770	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:70143583-70143813	MCF-7	breast:	n/a	chr16:70143697-70143708
44	CEBPB	chr16:70195995-70196314	IMR90	lung:	n/a	n/a
45	CEBPB	chr16:70143607-70143854	HepG2	liver:	n/a	chr16:70143697-70143708
46	CEBPB	chr16:70143605-70143762	HepG2	liver:	n/a	chr16:70143697-70143708
47	CEBPB	chr16:70181824-70181870	K562	blood:	n/a	n/a
48	CEBPB	chr16:70191818-70192121	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:70143582-70143870	Hela-S3	cervix:	n/a	chr16:70143697-70143708
50	CEBPB	chr16:70143583-70143872	K562	blood:	n/a	chr16:70143697-70143708

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70207801-70207851	IMR90	lung:	fetal
2	chr16:70207801-70207851	IMR90	lung:	fetal
3	chr16:70207801-70207851	HRE	kidney:	n/a
4	chr16:70193705-70193755	GM19239	blood:	n/a
5	chr16:70196247-70196297	HCPEpiC	choroid plexus:	n/a
6	chr16:70207801-70207851	HMEC	breast:	n/a
7	chr16:70190513-70190563	CMK	blood:	n/a
8	chr16:70226235-70226285	SKMC	muscle:	n/a
9	chr16:70190398-70190448	LNCaP	prostate:	n/a
10	chr16:70207801-70207851	MCF-7	breast:	n/a
11	chr16:70226235-70226285	GM12891	blood:	n/a
12	chr16:70151549-70151599	GM12891	blood:	n/a
13	chr16:70193705-70193755	U87	brain:	n/a
14	chr16:70207304-70207354	LNCaP	prostate:	n/a
15	chr16:70190398-70190448	SAEC	small airway:	n/a
16	chr16:70190513-70190563	AG10803	skin:	n/a
17	chr16:70190398-70190448	T-47D	breast:	n/a
18	chr16:70226235-70226285	SK-N-MC	brain:	n/a
19	chr16:70151549-70151599	HRPEpiC	eye:	n/a
20	chr16:70146610-70146660	CMK	blood:	n/a
21	chr16:70207722-70207772	HRCEpiC	kidney:	n/a
22	chr16:70190398-70190448	NHDF-neo	bronchial:	n/a
23	chr16:70151549-70151599	HepG2	liver:	n/a
24	chr16:70220191-70220241	HUVEC	blood vessel:	n/a
25	chr16:70190398-70190448	BJ	skin:	n/a
26	chr16:70148795-70148845	HUVEC	blood vessel:	n/a
27	chr16:70147964-70148014	HCT-116	colon:	n/a
28	chr16:70193705-70193755	HPAEpiC	pulmonary alveolar:	n/a
29	chr16:70148758-70148808	LNCaP	prostate:	n/a
30	chr16:70196247-70196297	ProgFib	skin:	n/a
31	chr16:70207801-70207851	AG09319	gingival:	n/a
32	chr16:70190398-70190448	Hela-S3	cervix:	n/a
33	chr16:70190513-70190563	HMEC	breast:	n/a
34	chr16:70146610-70146660	NT2-D1	testis:	n/a
35	chr16:70145696-70145746	PANC-1	pancreas:	n/a
36	chr16:70143703-70143753	H1-hESC	embryonic stem cell:	embryo
37	chr16:70148795-70148845	PANC-1	pancreas:	n/a
38	chr16:70207297-70207347	AG10803	skin:	n/a
39	chr16:70190329-70190379	K562	blood:	n/a
40	chr16:70207297-70207347	HCT-116	colon:	n/a
41	chr16:70148795-70148845	GM12892	blood:	n/a
42	chr16:70190398-70190448	AG10803	skin:	n/a
43	chr16:70190329-70190379	T-47D	breast:	n/a
44	chr16:70196247-70196297	HUVEC	blood vessel:	n/a
45	chr16:70207722-70207772	HCM	heart:	n/a
46	chr16:70148795-70148845	GM19239	blood:	n/a
47	chr16:70147964-70148014	SK-N-SH	brain:	n/a
48	chr16:70147964-70148014	H1-hESC	embryonic stem cell:	embryo
49	chr16:70193705-70193755	ProgFib	skin:	n/a
50	chr16:70193705-70193755	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:70198641..70199632-chr16:74343397..74344233,2	K562	blood:
2	chr16:70185546..70188215-chr16:74330413..74333077,2	K562	blood:
3	chr16:70189713..70191262-chr16:70193819..70195441,2	MCF-7	breast:
4	chr16:70195628..70198229-chr16:70323197..70325854,2	MCF-7	breast:
5	chr16:70098076..70099819-chr16:70146086..70148783,2	MCF-7	breast:
6	chr16:70190180..70193178-chr16:70320490..70323768,3	K562	blood:
7	chr16:70183960..70187287-chr16:70187613..70192158,4	MCF-7	breast:
8	chr16:70194900..70197913-chr16:70284304..70286530,3	MCF-7	breast:
9	chr16:70185026..70185664-chr16:74657267..74657783,2	MCF-7	breast:
10	chr16:70190124..70192979-chr16:70192985..70196334,3	MCF-7	breast:
11	chr16:70190723..70192786-chr16:74330377..74332345,2	K562	blood:
12	chr16:70191657..70193675-chr16:70283732..70285560,2	K562	blood:
13	chr16:70194744..70197032-chr16:70317749..70321532,3	K562	blood:
14	chr16:70170309..70171136-chr16:72947288..72947878,2	MCF-7	breast:
15	chr16:70170285..70171145-chr16:72963448..72963968,2	MCF-7	breast:
16	chr16:70192894..70195380-chr16:70284264..70288568,4	MCF-7	breast:
17	chr16:70197328..70198092-chr16:70301268..70302134,2	MCF-7	breast:
18	chr16:70185001..70186006-chr16:74463672..74464734,4	MCF-7	breast:
19	chr16:70189713..70191262-chr16:70193819..70195441,2	MCF-7	breast:
20	chr16:70183960..70187287-chr16:70187613..70192158,4	MCF-7	breast:
21	chr16:70190124..70192979-chr16:70192985..70196334,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOSC6-2	chr16:70192708-70192792	ENSG00000247228.2
2	lnc-EXOSC6-2	chr16:70207031-70207322	ENSG00000247228.2
3	lnc-EXOSC6-2	chr16:70207031-70207351	ENSG00000247228
4	lnc-EXOSC6-2	chr16:70190243-70190407	ENSG00000247228.2
5	lnc-EXOSC6-2	chr16:70192860-70193983	ENSG00000247228
6	lnc-EXOSC6-2	chr16:70195347-70195796	ENSG00000247228
7	lnc-EXOSC6-2	chr16:70194075-70194214	ENSG00000247228
8	lnc-EXOSC6-2	chr16:70194638-70194844	ENSG00000247228

No.	miRNA target gene	miRNA name	Chromosome Location
1	PDPR	hsa-let-7b-5p	chr16:70191336-70191343
2	PDPR	hsa-let-7b-5p	chr16:70191322-70191343
3	PDPR	hsa-miR-155-5p	chr16:70192265-70192271
4	PDPR	hsa-miR-16-5p	chr16:70191655-70191661

Variant related genes	Relation type
PDPR	TF binding region
CLEC18C	TF binding region
ENSG00000261145	TF binding region
ENSG00000247228	TF binding region
PDPR	CpG island
CLEC18C	CpG island
ENSG00000261145	CpG island
ENSG00000247228	CpG island
ENSG00000259972	chromatin interactions
ENSG00000255185	chromatin interactions
ENSG00000090861	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000223496	chromatin interactions
ENSG00000196696	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000157349	chromatin interactions
ARHGDIA	miRNA target sites
ACOT8	miRNA target sites
FAM122B	miRNA target sites
ZNRF3	miRNA target sites
ATAD5	miRNA target sites

Extended variants
information (count: 3561 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3561 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528074521	chr16:70141156-70141157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560857291	chr16:70141158-70141159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2549619	chr16:70141219-70141220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56299818	chr16:70141234-70141235	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs552347552	chr16:70141336-70141337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7193597	chr16:70141342-70141343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189382515	chr16:70141352-70141353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567954153	chr16:70141390-70141391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564378292	chr16:70141392-70141393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs8056500	chr16:70141487-70141488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550252195	chr16:70141528-70141529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561790526	chr16:70141556-70141557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7198451	chr16:70141562-70141563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185775767	chr16:70141651-70141652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566737993	chr16:70141671-70141672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534128556	chr16:70141704-70141705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs8056999	chr16:70141715-70141716	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs8058329	chr16:70141721-70141722	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376389990	chr16:70141729-70141730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556980019	chr16:70141751-70141752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144264429	chr16:70141779-70141780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373528627	chr16:70141807-70141808	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs550161048	chr16:70141834-70141835	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs76261766	chr16:70141853-70141854	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs556247723	chr16:70141903-70141904	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs114362779	chr16:70141924-70141925	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs374335234	chr16:70141933-70141934	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs377270951	chr16:70141980-70141981	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs541786118	chr16:70141988-70141989	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs553532821	chr16:70141991-70141992	Weak transcription Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs2432369	chr16:70142002-70142003	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs572393021	chr16:70142003-70142004	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs2432370	chr16:70142018-70142019	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs148740748	chr16:70142020-70142021	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs564293265	chr16:70142043-70142044	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs531809690	chr16:70142046-70142047	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs2259706	chr16:70142048-70142049	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs562194561	chr16:70142051-70142052	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs529398022	chr16:70142081-70142082	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs545498313	chr16:70142114-70142115	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs192010170	chr16:70142141-70142142	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs2549626	chr16:70142186-70142187	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs150872598	chr16:70142211-70142212	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs527543447	chr16:70142230-70142231	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs552506351	chr16:70142304-70142305	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs377466345	chr16:70142345-70142346	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs570635573	chr16:70142386-70142387	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs2549630	chr16:70142395-70142396	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs556121246	chr16:70142396-70142397	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs568142883	chr16:70142398-70142399	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:1746 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70135000-70148200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr16:70141800-70142000	Flanking Bivalent TSS/Enh	HepG2	liver
3	chr16:70141800-70142400	Enhancers	Adipose Nuclei	Adipose
4	chr16:70142000-70142400	Bivalent Enhancer	HepG2	liver
5	chr16:70142400-70147000	Weak transcription	Adipose Nuclei	Adipose
6	chr16:70143600-70144000	Enhancers	HepG2	liver
7	chr16:70144000-70145200	Weak transcription	HepG2	liver
8	chr16:70145200-70145400	Flanking Bivalent TSS/Enh	HepG2	liver
9	chr16:70145600-70146800	Weak transcription	HepG2	liver
10	chr16:70145800-70147600	Enhancers	Primary B cells from peripheral blood	blood
11	chr16:70146200-70146400	Enhancers	Primary B cells from cord blood	blood
12	chr16:70146400-70147800	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr16:70146400-70147800	Weak transcription	Primary B cells from cord blood	blood
14	chr16:70147000-70147200	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr16:70147000-70147200	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr16:70147000-70147200	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr16:70147000-70147200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr16:70147000-70147200	Enhancers	Liver	Liver
19	chr16:70147000-70147200	Enhancers	Fetal Stomach	stomach
20	chr16:70147000-70147200	Enhancers	Left Ventricle	heart
21	chr16:70147000-70147200	Enhancers	Ovary	ovary
22	chr16:70147000-70147200	Enhancers	Pancreas	Pancrea
23	chr16:70147000-70147200	Flanking Active TSS	HepG2	liver
24	chr16:70147000-70147200	Enhancers	NH-A	brain
25	chr16:70147000-70147400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr16:70147000-70147400	Enhancers	Primary T cells fromperipheralblood	blood
27	chr16:70147000-70147400	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr16:70147000-70147400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr16:70147000-70147400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr16:70147000-70147400	Enhancers	Brain Anterior Caudate	brain
31	chr16:70147000-70147400	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr16:70147000-70147400	Enhancers	Colon Smooth Muscle	Colon
33	chr16:70147000-70147400	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr16:70147000-70147400	Enhancers	Fetal Intestine Small	intestine
35	chr16:70147000-70147400	Enhancers	Fetal Muscle Trunk	muscle
36	chr16:70147000-70147400	Enhancers	Fetal Thymus	thymus
37	chr16:70147000-70147400	Enhancers	Psoas Muscle	Psoas
38	chr16:70147000-70147400	Enhancers	Right Ventricle	heart
39	chr16:70147000-70147400	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr16:70147000-70147400	Enhancers	Stomach Smooth Muscle	stomach
41	chr16:70147000-70147600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr16:70147000-70147600	Enhancers	Adipose Nuclei	Adipose
43	chr16:70147000-70147600	Enhancers	Fetal Muscle Leg	muscle
44	chr16:70147000-70147600	Enhancers	Dnd41	blood
45	chr16:70147000-70147800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr16:70147000-70147800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr16:70147000-70149600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr16:70147200-70148600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr16:70147200-70149000	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr16:70147200-70149000	Active TSS	HepG2	liver

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