Variant report

Variant	esv2761925
Chromosome Location	chr16:81262516-81278038
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	chr16:81272071-81272314	HepG2	liver:	n/a	n/a
2	BACH1	chr16:81273333-81273632	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr16:81269179-81269377	K562	blood:	n/a	n/a
4	BHLHE40	chr16:81277384-81277610	K562	blood:	n/a	n/a
5	CBX3	chr16:81266474-81266740	K562	blood:	n/a	n/a
6	CEBPB	chr16:81276681-81276827	K562	blood:	n/a	chr16:81276770-81276781
7	CEBPB	chr16:81276587-81276957	Hela-S3	cervix:	n/a	chr16:81276770-81276781
8	CEBPB	chr16:81276588-81276951	IMR90	lung:	n/a	chr16:81276770-81276781
9	CEBPB	chr16:81276597-81276961	H1-hESC	embryonic stem cell:	n/a	chr16:81276770-81276781
10	CEBPB	chr16:81276534-81276962	MCF-7	breast:	n/a	chr16:81276770-81276781
11	CEBPB	chr16:81276593-81276926	K562	blood:	n/a	chr16:81276770-81276781
12	CEBPB	chr16:81276594-81277061	A549	lung:	n/a	chr16:81276770-81276781
13	CEBPB	chr16:81275758-81276027	K562	blood:	n/a	n/a
14	CEBPB	chr16:81276601-81277010	ECC-1	luminal epithelium:	n/a	chr16:81276770-81276781
15	CEBPB	chr16:81276586-81276961	A549	lung:	n/a	chr16:81276770-81276781
16	CEBPB	chr16:81276584-81276957	HepG2	liver:	n/a	chr16:81276770-81276781
17	CEBPB	chr16:81276594-81277004	ECC-1	luminal epithelium:	n/a	chr16:81276770-81276781
18	CEBPB	chr16:81276566-81276982	K562	blood:	n/a	chr16:81276770-81276781
19	CEBPB	chr16:81275729-81275979	A549	lung:	n/a	n/a
20	CEBPB	chr16:81276635-81276960	HepG2	liver:	n/a	chr16:81276770-81276781
21	CEBPB	chr16:81276527-81277053	MCF-7	breast:	n/a	chr16:81276770-81276781
22	CEBPB	chr16:81276678-81276818	HepG2	liver:	n/a	chr16:81276770-81276781
23	CEBPB	chr16:81276600-81277000	A549	lung:	n/a	chr16:81276770-81276781
24	CHD2	chr16:81277676-81277698	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr16:81272420-81272570	Caco-2	colon:	n/a	chr16:81272431-81272444
26	CTCF	chr16:81262560-81262710	GM12866	blood:	n/a	n/a
27	ELF1	chr16:81276943-81277301	K562	blood:	n/a	chr16:81277159-81277172
28	FOS	chr16:81272062-81272215	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr16:81270995-81271195	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr16:81270973-81271173	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr16:81270970-81271194	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr16:81272067-81272312	MCF10A-Er-Src	breast:	n/a	n/a
33	FOSL2	chr16:81271915-81272520	A549	lung:	n/a	n/a
34	FOXA2	chr16:81272306-81272590	HepG2	liver:	n/a	n/a
35	IRF1	chr16:81272004-81272363	K562	blood:	n/a	chr16:81272167-81272180 chr16:81272167-81272181 chr16:81272168-81272185 chr16:81272167-81272180 chr16:81272169-81272183 chr16:81272168-81272180 chr16:81272168-81272180 chr16:81272169-81272180 chr16:81272165-81272179 chr16:81272170-81272181 chr16:81272167-81272180 chr16:81272169-81272179 chr16:81272166-81272180
36	IRF1	chr16:81272004-81272328	K562	blood:	n/a	chr16:81272167-81272180 chr16:81272167-81272181 chr16:81272168-81272185 chr16:81272167-81272180 chr16:81272169-81272183 chr16:81272168-81272180 chr16:81272168-81272180 chr16:81272169-81272180 chr16:81272165-81272179 chr16:81272170-81272181 chr16:81272167-81272180 chr16:81272169-81272179 chr16:81272166-81272180
37	KAP1	chr16:81271832-81272421	U2OS	brain:	n/a	n/a
38	MAFF	chr16:81263526-81263784	K562	blood:	n/a	chr16:81263611-81263629
39	MAFF	chr16:81273346-81273695	HepG2	liver:	n/a	chr16:81273523-81273537 chr16:81273517-81273535
40	MAFF	chr16:81263438-81263786	HepG2	liver:	n/a	chr16:81263611-81263629
41	MAFF	chr16:81273360-81273649	K562	blood:	n/a	chr16:81273523-81273537 chr16:81273517-81273535
42	MAFK	chr16:81263474-81263736	K562	blood:	n/a	chr16:81263612-81263627
43	MAFK	chr16:81273402-81273681	H1-hESC	embryonic stem cell:	n/a	chr16:81273519-81273534 chr16:81273522-81273538 chr16:81273523-81273537 chr16:81273520-81273540 chr16:81273524-81273534
44	MAFK	chr16:81263446-81263793	HepG2	liver:	n/a	chr16:81263612-81263627
45	MAFK	chr16:81263451-81263784	HepG2	liver:	n/a	chr16:81263612-81263627
46	MAFK	chr16:81273365-81273679	K562	blood:	n/a	chr16:81273519-81273534 chr16:81273522-81273538 chr16:81273523-81273537 chr16:81273520-81273540 chr16:81273524-81273534
47	MAFK	chr16:81263530-81263687	Hela-S3	cervix:	n/a	chr16:81263612-81263627
48	MAFK	chr16:81277716-81277717	H1-hESC	embryonic stem cell:	n/a	n/a
49	MAFK	chr16:81273353-81273697	HepG2	liver:	n/a	chr16:81273519-81273534 chr16:81273522-81273538 chr16:81273523-81273537 chr16:81273520-81273540 chr16:81273524-81273534
50	MAFK	chr16:81273376-81273686	IMR90	lung:	n/a	chr16:81273519-81273534 chr16:81273522-81273538 chr16:81273523-81273537 chr16:81273520-81273540 chr16:81273524-81273534

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81272080-81272130	A549	lung:	n/a
2	chr16:81272281-81272331	PrEC	prostate:	n/a
3	chr16:81271937-81271987	U87	brain:	n/a
4	chr16:81272500-81272550	HRE	kidney:	n/a
5	chr16:81272080-81272130	Hepatocyte	liver:	n/a
6	chr16:81272080-81272130	AG09309	skin:	n/a
7	chr16:81272080-81272130	NHBE	bronchial:	n/a
8	chr16:81272080-81272130	NH-A	brain:	n/a
9	chr16:81271937-81271987	SK-N-SH	brain:	n/a
10	chr16:81272500-81272550	AG09319	gingival:	n/a
11	chr16:81272500-81272550	AG04450	lung:	fetal
12	chr16:81272281-81272331	NB4	blood:	n/a
13	chr16:81272500-81272550	AG09309	skin:	n/a
14	chr16:81272080-81272130	HUVEC	blood vessel:	n/a
15	chr16:81271937-81271987	PrEC	prostate:	n/a
16	chr16:81271937-81271987	HRE	kidney:	n/a
17	chr16:81272281-81272331	RPTEC	kidney:	n/a
18	chr16:81272080-81272130	SK-N-SH_RA	brain:	n/a
19	chr16:81271937-81271987	SK-N-SH_RA	brain:	n/a
20	chr16:81272429-81272479	SAEC	small airway:	n/a
21	chr16:81272500-81272550	HIPEpiC	eye:	n/a
22	chr16:81271937-81271987	HPAEpiC	pulmonary alveolar:	n/a
23	chr16:81271937-81271987	AG10803	skin:	n/a
24	chr16:81272080-81272130	AG09319	gingival:	n/a
25	chr16:81272429-81272479	LNCaP	prostate:	n/a
26	chr16:81272429-81272479	GM12891	blood:	n/a
27	chr16:81271937-81271987	PANC-1	pancreas:	n/a
28	chr16:81271937-81271987	ProgFib	skin:	n/a
29	chr16:81272429-81272479	ECC-1	luminal epithelium:	n/a
30	chr16:81272500-81272550	GM06990	blood:	n/a
31	chr16:81272281-81272331	AoSMC	blood vessel:	n/a
32	chr16:81272429-81272479	GM12892	blood:	n/a
33	chr16:81272281-81272331	MCF-7	breast:	n/a
34	chr16:81272080-81272130	MCF-7	breast:	n/a
35	chr16:81271937-81271987	T-47D	breast:	n/a
36	chr16:81272281-81272331	SK-N-MC	brain:	n/a
37	chr16:81272429-81272479	HEEpiC	esophagus:	n/a
38	chr16:81271937-81271987	GM06990	blood:	n/a
39	chr16:81272500-81272550	ProgFib	skin:	n/a
40	chr16:81272429-81272479	GM19239	blood:	n/a
41	chr16:81272080-81272130	HCT-116	colon:	n/a
42	chr16:81272281-81272331	SAEC	small airway:	n/a
43	chr16:81272281-81272331	HNPCEpiC	eye:	n/a
44	chr16:81272429-81272479	HAEpiC	amniotic membrane:	n/a
45	chr16:81272281-81272331	IMR90	lung:	fetal
46	chr16:81272429-81272479	H1-hESC	embryonic stem cell:	embryo
47	chr16:81272429-81272479	HNPCEpiC	eye:	n/a
48	chr16:81272429-81272479	AG09319	gingival:	n/a
49	chr16:81272429-81272479	Caco-2	colon:	n/a
50	chr16:81272281-81272331	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:81264245..81265836-chr16:81282203..81285157,2	K562	blood:
2	chr16:81257407..81259845-chr16:81262564..81264154,2	K562	blood:
3	chr16:81110781..81113412-chr16:81267989..81270691,2	MCF-7	breast:
4	chr16:81273374..81275112-chr16:81481220..81483509,2	MCF-7	breast:
5	chr16:81266786..81269384-chr16:81269942..81271960,2	MCF-7	breast:
6	chr16:81266786..81269384-chr16:81269942..81271960,2	MCF-7	breast:

Variant related genes	Relation type
BCMO1	TF binding region
BCMO1	CpG island
ENSG00000245059	chromatin interactions
ENSG00000166455	chromatin interactions

Extended variants
information (count: 817 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4889287	chr16:81262516-81262517	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150915309	chr16:81262518-81262519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557161318	chr16:81262528-81262529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79716858	chr16:81262533-81262534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189263593	chr16:81262539-81262540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139692531	chr16:81262594-81262595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74029083	chr16:81262616-81262617	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs112585473	chr16:81262646-81262647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144430668	chr16:81262665-81262666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs60465703	chr16:81262711-81262712	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs548482253	chr16:81262724-81262725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569865186	chr16:81262732-81262733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370326638	chr16:81262749-81262750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187049867	chr16:81262776-81262777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552775697	chr16:81262784-81262785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189800134	chr16:81262799-81262800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545974915	chr16:81262808-81262809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146571535	chr16:81262819-81262820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548821905	chr16:81262857-81262858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201207404	chr16:81262866-81262867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534745627	chr16:81262880-81262881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140083776	chr16:81262884-81262885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181397015	chr16:81262962-81262963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185657974	chr16:81262963-81262964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375373902	chr16:81262973-81262974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114943688	chr16:81263002-81263003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190021227	chr16:81263005-81263006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568698783	chr16:81263029-81263030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576254971	chr16:81263045-81263046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72831390	chr16:81263054-81263055	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs112903807	chr16:81263058-81263059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557968793	chr16:81263071-81263072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182200520	chr16:81263086-81263087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377732803	chr16:81263200-81263201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs56389437	chr16:81263223-81263224	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs527426496	chr16:81263242-81263243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186551899	chr16:81263244-81263245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192367417	chr16:81263294-81263295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539511932	chr16:81263295-81263296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563628260	chr16:81263315-81263316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553072012	chr16:81263333-81263334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531268604	chr16:81263335-81263336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149763955	chr16:81263357-81263358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571048680	chr16:81263361-81263362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372433262	chr16:81263372-81263373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145709747	chr16:81263376-81263377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73599304	chr16:81263377-81263378	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs572853084	chr16:81263384-81263385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568012472	chr16:81263387-81263388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374201549	chr16:81263394-81263395	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
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81257600-81271000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:81261400-81263200	Enhancers	Duodenum Mucosa	Duodenum
3	chr16:81262000-81262600	Enhancers	Fetal Intestine Small	intestine
4	chr16:81262000-81263000	Enhancers	Fetal Intestine Large	intestine
5	chr16:81262600-81263200	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr16:81263600-81264200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr16:81264400-81264800	Bivalent Enhancer	GM12878-XiMat	blood
8	chr16:81265000-81265200	Bivalent Enhancer	GM12878-XiMat	blood
9	chr16:81266400-81267000	Active TSS	K562	blood
10	chr16:81268400-81268600	Enhancers	Left Ventricle	heart
11	chr16:81269200-81269400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr16:81269400-81269600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr16:81269400-81271000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr16:81269600-81271600	Weak transcription	Fetal Intestine Small	intestine
15	chr16:81269800-81271200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr16:81270200-81272000	Weak transcription	Left Ventricle	heart
17	chr16:81270800-81271600	Enhancers	Fetal Heart	heart
18	chr16:81270800-81271800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr16:81270800-81271800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr16:81270800-81271800	Enhancers	Duodenum Mucosa	Duodenum
21	chr16:81270800-81271800	Enhancers	Stomach Smooth Muscle	stomach
22	chr16:81270800-81272000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr16:81270800-81273200	Enhancers	Fetal Muscle Leg	muscle
24	chr16:81271000-81271200	Enhancers	Esophagus	oesophagus
25	chr16:81271000-81271200	Enhancers	Rectal Smooth Muscle	rectum
26	chr16:81271000-81271400	Enhancers	H9 Cell Line	embryonic stem cell
27	chr16:81271000-81271400	Flanking Bivalent TSS/Enh	HepG2	liver
28	chr16:81271000-81271600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr16:81271000-81271600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr16:81271000-81271600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr16:81271000-81271600	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr16:81271000-81271600	Enhancers	A549	lung
33	chr16:81271000-81271800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr16:81271000-81271800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr16:81271000-81271800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr16:81271000-81271800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr16:81271000-81271800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr16:81271000-81271800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr16:81271000-81271800	Enhancers	Brain Hippocampus Middle	brain
40	chr16:81271000-81271800	Enhancers	Fetal Kidney	kidney
41	chr16:81271000-81271800	Enhancers	Stomach Mucosa	stomach
42	chr16:81271000-81271800	Enhancers	NH-A	brain
43	chr16:81271000-81271800	Enhancers	NHEK	skin
44	chr16:81271000-81272000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr16:81271000-81272000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr16:81271000-81272000	Enhancers	Liver	Liver
47	chr16:81271000-81272000	Enhancers	Brain Cingulate Gyrus	brain
48	chr16:81271000-81272000	Enhancers	Fetal Muscle Trunk	muscle
49	chr16:81271000-81272000	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr16:81271000-81272000	Enhancers	HMEC	breast

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