Variant report

Variant	esv1832916
Chromosome Location	chr16:71148958-71167731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:99)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:99 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:71155214-71155415	HepG2	liver:	n/a	n/a
2	BACH1	chr16:71165544-71165704	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr16:71149536-71149558	GM12878	blood:	n/a	n/a
4	CEBPB	chr16:71155172-71155489	HepG2	liver:	n/a	n/a
5	CEBPB	chr16:71159834-71159851	HepG2	liver:	n/a	n/a
6	CHD1	chr16:71149566-71149654	GM12878	blood:	n/a	n/a
7	CHD2	chr16:71163782-71163814	HepG2	liver:	n/a	n/a
8	CTCF	chr16:71165080-71165230	HepG2	liver:	n/a	n/a
9	CTCF	chr16:71165200-71165350	NHEK	skin:	n/a	n/a
10	CTCF	chr16:71156340-71156490	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr16:71165120-71165270	HFF-Myc	foreskin:	n/a	n/a
12	CTCF	chr16:71164980-71165130	NHEK	skin:	n/a	n/a
13	CTCF	chr16:71161540-71161690	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr16:71165124-71165244	LNCaP	prostate:	n/a	n/a
15	CTCF	chr16:71160040-71160190	GM12871	blood:	n/a	n/a
16	CTCF	chr16:71162940-71163090	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr16:71165080-71165230	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr16:71165060-71165210	NHEK	skin:	n/a	n/a
19	CUX1	chr16:71154199-71154387	GM12878	blood:	n/a	n/a
20	E2F4	chr16:71152164-71152422	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr16:71154798-71155607	MCF10A-Er-Src	breast:	n/a	n/a
22	ELK1	chr16:71166648-71166664	GM12878	blood:	n/a	n/a
23	ELK1	chr16:71150760-71150796	Hela-S3	cervix:	n/a	n/a
24	ELK1	chr16:71159054-71159162	Hela-S3	cervix:	n/a	n/a
25	ELK1	chr16:71153076-71153226	Hela-S3	cervix:	n/a	n/a
26	EP300	chr16:71164933-71164940	K562	blood:	n/a	n/a
27	EP300	chr16:71153527-71153722	GM12878	blood:	n/a	n/a
28	FAM48A	chr16:71154731-71154744	GM12878	blood:	n/a	n/a
29	FAM48A	chr16:71164069-71164116	GM12878	blood:	n/a	n/a
30	FAM48A	chr16:71160975-71161117	GM12878	blood:	n/a	n/a
31	FAM48A	chr16:71162031-71162078	GM12878	blood:	n/a	n/a
32	FOS	chr16:71155049-71155536	MCF10A-Er-Src	breast:	n/a	chr16:71155274-71155284 chr16:71155276-71155287 chr16:71155274-71155283 chr16:71155273-71155285
33	FOS	chr16:71154796-71155515	MCF10A-Er-Src	breast:	n/a	chr16:71155274-71155284 chr16:71155276-71155287 chr16:71155274-71155283 chr16:71155273-71155285
34	FOS	chr16:71155094-71155505	MCF10A-Er-Src	breast:	n/a	chr16:71155274-71155284 chr16:71155276-71155287 chr16:71155274-71155283 chr16:71155273-71155285
35	FOS	chr16:71155113-71155522	MCF10A-Er-Src	breast:	n/a	chr16:71155274-71155284 chr16:71155276-71155287 chr16:71155274-71155283 chr16:71155273-71155285
36	FOSL2	chr16:71155114-71155431	HepG2	liver:	n/a	chr16:71155274-71155284 chr16:71155276-71155287 chr16:71155274-71155283 chr16:71155273-71155285
37	GATA3	chr16:71165399-71165877	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr16:71163082-71163246	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr16:71158130-71158397	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr16:71152180-71152380	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr16:71163472-71163986	SH-SY5Y	brain:	n/a	chr16:71163505-71163515 chr16:71163731-71163742
42	GATA3	chr16:71155577-71155726	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr16:71153805-71154529	SH-SY5Y	brain:	n/a	n/a
44	GTF2F1	chr16:71164802-71164917	H1-hESC	embryonic stem cell:	n/a	n/a
45	GTF2F1	chr16:71158058-71158069	H1-hESC	embryonic stem cell:	n/a	n/a
46	GTF2F1	chr16:71150972-71151066	K562	blood:	n/a	n/a
47	GTF2F1	chr16:71165456-71165511	H1-hESC	embryonic stem cell:	n/a	n/a
48	IRF1	chr16:71161024-71161217	K562	blood:	n/a	chr16:71161075-71161089 chr16:71161063-71161070 chr16:71161078-71161091 chr16:71161073-71161087
49	IRF3	chr16:71159433-71159446	GM12878	blood:	n/a	n/a
50	JUN	chr16:71161053-71161253	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:71162835-71162885	IMR90	lung:	fetal
2	chr16:71162835-71162885	GM12878	blood:	n/a
3	chr16:71162835-71162885	SAEC	small airway:	n/a
4	chr16:71162835-71162885	Hela-S3	cervix:	n/a
5	chr16:71162835-71162885	SKMC	muscle:	n/a
6	chr16:71162835-71162885	HRE	kidney:	n/a
7	chr16:71162835-71162885	NT2-D1	testis:	n/a
8	chr16:71162835-71162885	GM12891	blood:	n/a
9	chr16:71162835-71162885	ovcar-3	ovarian:	n/a
10	chr16:71162835-71162885	GM12892	blood:	n/a
11	chr16:71162835-71162885	Hepatocyte	liver:	n/a
12	chr16:71162835-71162885	Caco-2	colon:	n/a
13	chr16:71162835-71162885	GM06990	blood:	n/a
14	chr16:71162835-71162885	Jurkat	blood:	n/a
15	chr16:71162835-71162885	AG04449	skin:	fetal
16	chr16:71162835-71162885	HepG2	liver:	n/a
17	chr16:71162835-71162885	HPAEpiC	pulmonary alveolar:	n/a
18	chr16:71162835-71162885	HEEpiC	esophagus:	n/a
19	chr16:71162835-71162885	LNCaP	prostate:	n/a
20	chr16:71162835-71162885	AG09309	skin:	n/a
21	chr16:71162835-71162885	HNPCEpiC	eye:	n/a
22	chr16:71162835-71162885	PANC-1	pancreas:	n/a
23	chr16:71162835-71162885	AG10803	skin:	n/a
24	chr16:71162835-71162885	HMEC	breast:	n/a
25	chr16:71162835-71162885	MCF10A-Er-Src	breast:	n/a
26	chr16:71162835-71162885	GM19239	blood:	n/a
27	chr16:71162835-71162885	CMK	blood:	n/a
28	chr16:71162835-71162885	NH-A	brain:	n/a
29	chr16:71162835-71162885	H1-hESC	embryonic stem cell:	embryo
30	chr16:71162835-71162885	HEK293	kidney:	embryo
31	chr16:71162835-71162885	K562	blood:	n/a
32	chr16:71162835-71162885	NHBE	bronchial:	n/a
33	chr16:71162835-71162885	MCF-7	breast:	n/a
34	chr16:71162835-71162885	HCT-116	colon:	n/a
35	chr16:71162835-71162885	AG04450	lung:	fetal
36	chr16:71162835-71162885	BE2_C	brain:	n/a
37	chr16:71162835-71162885	ECC-1	luminal epithelium:	n/a
38	chr16:71162835-71162885	HIPEpiC	eye:	n/a
39	chr16:71162835-71162885	SK-N-SH_RA	brain:	n/a
40	chr16:71162835-71162885	HL-60	blood:	n/a
41	chr16:71162835-71162885	SK-N-SH	brain:	n/a
42	chr16:71162835-71162885	HUVEC	blood vessel:	n/a
43	chr16:71162835-71162885	SK-N-MC	brain:	n/a
44	chr16:71162835-71162885	PrEC	prostate:	n/a
45	chr16:71162835-71162885	HAEpiC	amniotic membrane:	n/a
46	chr16:71162835-71162885	U87	brain:	n/a
47	chr16:71162835-71162885	NHDF-neo	bronchial:	n/a
48	chr16:71162835-71162885	T-47D	breast:	n/a
49	chr16:71162835-71162885	PFSK-1	brain:	n/a
50	chr16:71162835-71162885	NB4	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:71156761..71157534-chr4:86089661..86090552,2	MCF-7	breast:
2	chr16:71150001..71154234-chr16:71156760..71158464,4	K562	blood:
3	chr16:71161173..71163942-chr16:71164810..71166980,2	MCF-7	breast:
4	chr16:71157663..71161844-chr16:71162616..71166129,4	K562	blood:
5	chr16:71158993..71163306-chr16:71165421..71171777,6	MCF-7	breast:
6	chr1:146554737..146556264-chr16:71167039..71168689,2	K562	blood:
7	chr16:71148009..71150710-chr16:71161315..71165106,3	K562	blood:
8	chr16:71153294..71157404-chr16:71158865..71161936,4	K562	blood:
9	chr1:146554686..146556365-chr16:71154584..71156445,2	K562	blood:
10	chr16:71158993..71163306-chr16:71165421..71171777,6	MCF-7	breast:
11	chr16:71164439..71166621-chr16:71171910..71174347,2	MCF-7	breast:
12	chr16:71164216..71166696-chr16:71169224..71171116,2	K562	blood:
13	chr16:71153052..71156401-chr16:71159001..71163450,6	K562	blood:
14	chr16:71137230..71139618-chr16:71153836..71156298,2	MCF-7	breast:
15	chr16:71145435..71147324-chr16:71148805..71150825,2	K562	blood:
16	chr16:71153052..71156401-chr16:71159001..71163450,6	K562	blood:
17	chr16:71151955..71154632-chr16:71157353..71159392,2	MCF-7	breast:
18	chr16:71150001..71154234-chr16:71156760..71158464,4	K562	blood:
19	chr1:146713329..146715162-chr16:71157129..71158866,2	K562	blood:
20	chr16:71151955..71154632-chr16:71157353..71159392,2	MCF-7	breast:
21	chr16:71153149..71155855-chr16:71181405..71183905,2	K562	blood:
22	chr16:71145606..71148394-chr16:71150978..71154581,3	K562	blood:
23	chr16:71153294..71157404-chr16:71158865..71161936,4	K562	blood:
24	chr16:71141833..71144484-chr16:71148437..71150878,2	K562	blood:

No data

Variant related genes	Relation type
HYDIN	TF binding region
HYDIN	CpG island
ENSG00000131781	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000259798	chromatin interactions
ENSG00000157423	chromatin interactions
ENSG00000230832	chromatin interactions

Extended variants
information (count: 623 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142617674	chr16:71149004-71149005	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs11639641	chr16:71149044-71149045	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs565483334	chr16:71149045-71149046	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532144956	chr16:71149087-71149088	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs111708649	chr16:71149130-71149131	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs568959062	chr16:71149135-71149136	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs7189874	chr16:71149137-71149138	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs529780750	chr16:71149140-71149141	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs372621847	chr16:71149155-71149156	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs548002427	chr16:71149160-71149161	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs566620610	chr16:71149206-71149207	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11645024	chr16:71149285-71149286	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373717942	chr16:71149287-71149288	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533786941	chr16:71149306-71149307	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs552442274	chr16:71149307-71149308	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs111844844	chr16:71149319-71149320	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs1859372	chr16:71149322-71149323	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs1859373	chr16:71149384-71149385	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs193091755	chr16:71149392-71149393	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs556900900	chr16:71149396-71149397	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs575255536	chr16:71149433-71149434	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs536297404	chr16:71149444-71149445	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs554777836	chr16:71149472-71149473	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs369467847	chr16:71149487-71149488	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs540519031	chr16:71149518-71149519	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs1859374	chr16:71149536-71149537	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs113476215	chr16:71149538-71149539	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565553189	chr16:71149553-71149554	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185787147	chr16:71149559-71149560	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375174106	chr16:71149564-71149565	ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs544937612	chr16:71149609-71149610	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs562441084	chr16:71149617-71149618	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs371718151	chr16:71149637-71149638	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552008331	chr16:71149659-71149660	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs11075865	chr16:71149660-71149661	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs529717289	chr16:71149668-71149669	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs8053920	chr16:71149720-71149721	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs548258784	chr16:71149759-71149760	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs916997	chr16:71149782-71149783	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs28477272	chr16:71149785-71149786	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs200667608	chr16:71149786-71149787	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs370336227	chr16:71149828-71149829	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs916998	chr16:71149887-71149888	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs571420858	chr16:71149888-71149889	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs916999	chr16:71149926-71149927	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs375404209	chr16:71149971-71149972	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs377571511	chr16:71149977-71149978	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs193041137	chr16:71150063-71150064	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs917000	chr16:71150072-71150073	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs549665307	chr16:71150077-71150078	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	18923524	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71135000-71149200	Weak transcription	Brain Anterior Caudate	brain
2	chr16:71135000-71160200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr16:71142200-71153000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr16:71143000-71154400	Weak transcription	Fetal Kidney	kidney
5	chr16:71143800-71149400	Weak transcription	Pancreas	Pancrea
6	chr16:71143800-71152800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr16:71144000-71149000	Weak transcription	Brain Hippocampus Middle	brain
8	chr16:71144000-71149400	Weak transcription	Brain Substantia Nigra	brain
9	chr16:71144000-71152400	Weak transcription	Fetal Muscle Trunk	muscle
10	chr16:71144000-71162200	Weak transcription	Brain Angular Gyrus	brain
11	chr16:71145400-71162800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr16:71146600-71149400	Weak transcription	Dnd41	blood
13	chr16:71148200-71149800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr16:71148200-71149800	Strong transcription	Fetal Brain Female	brain
15	chr16:71148200-71160400	Weak transcription	Fetal Stomach	stomach
16	chr16:71148400-71149000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr16:71148400-71149200	Weak transcription	Ovary	ovary
18	chr16:71148400-71149600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
19	chr16:71148400-71149800	Strong transcription	Brain Germinal Matrix	brain
20	chr16:71148600-71149200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr16:71148600-71149600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr16:71148600-71155600	Weak transcription	Fetal Intestine Large	intestine
23	chr16:71148800-71149600	ZNF genes & repeats	Fetal Intestine Small	intestine
24	chr16:71148800-71162600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr16:71148800-71172200	Weak transcription	Fetal Brain Male	brain
26	chr16:71149000-71150000	Strong transcription	Brain Hippocampus Middle	brain
27	chr16:71149000-71162600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr16:71149200-71149800	Strong transcription	Brain Anterior Caudate	brain
29	chr16:71149200-71150000	Strong transcription	Stomach Smooth Muscle	stomach
30	chr16:71149400-71149600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr16:71149400-71149600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr16:71149400-71149600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
33	chr16:71149400-71149600	ZNF genes & repeats	Fetal Heart	heart
34	chr16:71149400-71149600	ZNF genes & repeats	Pancreas	Pancrea
35	chr16:71149400-71149600	ZNF genes & repeats	Dnd41	blood
36	chr16:71149400-71149800	ZNF genes & repeats	Brain Substantia Nigra	brain
37	chr16:71149600-71152800	Weak transcription	Fetal Heart	heart
38	chr16:71149600-71158000	Weak transcription	Pancreas	Pancrea
39	chr16:71149600-71158000	Weak transcription	Dnd41	blood
40	chr16:71149600-71159800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr16:71149800-71152800	Weak transcription	Fetal Brain Female	brain
42	chr16:71149800-71158400	Weak transcription	Brain Germinal Matrix	brain
43	chr16:71149800-71160000	Weak transcription	Brain Anterior Caudate	brain
44	chr16:71149800-71162800	Weak transcription	Brain Substantia Nigra	brain
45	chr16:71150000-71152000	Weak transcription	Stomach Smooth Muscle	stomach
46	chr16:71150000-71161600	Weak transcription	Brain Hippocampus Middle	brain
47	chr16:71151400-71168600	Weak transcription	Fetal Lung	lung
48	chr16:71152800-71153400	Strong transcription	Brain Cingulate Gyrus	brain
49	chr16:71152800-71153400	Strong transcription	Fetal Brain Female	brain
50	chr16:71152800-71153400	Enhancers	Fetal Heart	heart

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