Variant report

Variant	esv3372455
Chromosome Location	chr16:81810851-81815149
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:351)
CpG islands
(count:427)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:81812290-81812455	K562	blood:	n/a	n/a
2	ATF2	chr16:81813257-81813585	GM12878	blood:	n/a	n/a
3	ATF3	chr16:81812700-81813020	K562	blood:	n/a	chr16:81812856-81812876 chr16:81812754-81812763
4	ATF3	chr16:81812752-81813041	H1-hESC	embryonic stem cell:	n/a	chr16:81812856-81812876 chr16:81812754-81812763
5	ATF3	chr16:81812646-81813043	GM12878	blood:	n/a	chr16:81812856-81812876 chr16:81812754-81812763
6	ATF3	chr16:81812752-81812969	GM12878	blood:	n/a	chr16:81812856-81812876 chr16:81812754-81812763
7	BACH1	chr16:81813254-81813652	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr16:81813517-81813630	K562	blood:	n/a	n/a
9	BCL3	chr16:81812419-81812895	A549	lung:	n/a	chr16:81812632-81812641
10	BHLHE40	chr16:81813880-81814327	GM12878	blood:	n/a	n/a
11	BHLHE40	chr16:81814127-81814151	K562	blood:	n/a	n/a
12	BHLHE40	chr16:81812217-81812265	K562	blood:	n/a	n/a
13	BHLHE40	chr16:81812545-81813116	K562	blood:	n/a	chr16:81812903-81812919
14	BHLHE40	chr16:81813359-81813510	K562	blood:	n/a	n/a
15	BHLHE40	chr16:81812593-81813593	GM12878	blood:	n/a	chr16:81812903-81812919
16	CBX3	chr16:81812727-81813034	K562	blood:	n/a	n/a
17	CBX3	chr16:81811062-81811378	K562	blood:	n/a	n/a
18	CCNT2	chr16:81812569-81813491	K562	blood:	n/a	n/a
19	CEBPB	chr16:81812097-81812436	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr16:81812568-81812617	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr16:81812922-81814034	GM12878	blood:	n/a	chr16:81813754-81813764
22	CHD2	chr16:81812586-81813014	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr16:81813467-81813504	K562	blood:	n/a	n/a
24	CHD2	chr16:81813335-81813625	GM12878	blood:	n/a	n/a
25	CHD2	chr16:81812620-81812776	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr16:81812731-81813058	GM12878	blood:	n/a	n/a
27	CHD2	chr16:81812721-81812744	K562	blood:	n/a	n/a
28	CREB1	chr16:81812583-81813058	A549	lung:	n/a	chr16:81812865-81812878
29	CTBP2	chr16:81812564-81813310	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr16:81813460-81813610	GM12869	blood:	n/a	n/a
31	CTCF	chr16:81812980-81813130	GM12866	blood:	n/a	n/a
32	CTCF	chr16:81813411-81813548	MCF-7	breast:	n/a	n/a
33	CTCF	chr16:81811529-81811807	K562	blood:	n/a	n/a
34	CTCF	chr16:81813540-81813690	GM12872	blood:	n/a	n/a
35	CTCF	chr16:81813360-81813552	GM19240	blood:	n/a	n/a
36	CTCF	chr16:81813380-81813530	MCF-7	breast:	n/a	n/a
37	CTCF	chr16:81813401-81813526	GM19238	blood:	n/a	n/a
38	CTCF	chr16:81813479-81813508	GM12891	blood:	n/a	n/a
39	CTCF	chr16:81812858-81812980	GM12892	blood:	n/a	n/a
40	CTCF	chr16:81813380-81813530	GM12865	blood:	n/a	n/a
41	CTCF	chr16:81812920-81813070	GM12873	blood:	n/a	n/a
42	CTCF	chr16:81815140-81815290	GM06990	blood:	n/a	n/a
43	CTCF	chr16:81813480-81813630	GM12864	blood:	n/a	n/a
44	CTCF	chr16:81812840-81812990	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr16:81813527-81813530	GM19238	blood:	n/a	n/a
46	CTCF	chr16:81812858-81812977	GM19238	blood:	n/a	n/a
47	CTCF	chr16:81813340-81813490	K562	blood:	n/a	n/a
48	CTCF	chr16:81813660-81813810	GM06990	blood:	n/a	n/a
49	CTCF	chr16:81813460-81813610	GM12873	blood:	n/a	n/a
50	CTCF	chr16:81813480-81813630	Caco-2	colon:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81812719-81812769	A549	lung:	n/a
2	chr16:81812606-81812656	K562	blood:	n/a
3	chr16:81812565-81812615	AG04450	lung:	fetal
4	chr16:81813363-81813413	HPAEpiC	pulmonary alveolar:	n/a
5	chr16:81812719-81812769	SK-N-SH	brain:	n/a
6	chr16:81812719-81812769	HCF	heart:	n/a
7	chr16:81813969-81814019	HCPEpiC	choroid plexus:	n/a
8	chr16:81812719-81812769	H1-hESC	embryonic stem cell:	embryo
9	chr16:81813363-81813413	HRCEpiC	kidney:	n/a
10	chr16:81812565-81812615	HRE	kidney:	n/a
11	chr16:81812606-81812656	IMR90	lung:	fetal
12	chr16:81812606-81812656	HCPEpiC	choroid plexus:	n/a
13	chr16:81812719-81812769	GM06990	blood:	n/a
14	chr16:81812738-81812788	SK-N-SH_RA	brain:	n/a
15	chr16:81813706-81813756	SK-N-SH_RA	brain:	n/a
16	chr16:81813969-81814019	MCF10A-Er-Src	breast:	n/a
17	chr16:81813969-81814019	NB4	blood:	n/a
18	chr16:81813363-81813413	AG04450	lung:	fetal
19	chr16:81813969-81814019	HMEC	breast:	n/a
20	chr16:81813363-81813413	GM12892	blood:	n/a
21	chr16:81812565-81812615	ProgFib	skin:	n/a
22	chr16:81812719-81812769	LNCaP	prostate:	n/a
23	chr16:81813363-81813413	AG10803	skin:	n/a
24	chr16:81813706-81813756	Caco-2	colon:	n/a
25	chr16:81812719-81812769	NH-A	brain:	n/a
26	chr16:81813706-81813756	HCPEpiC	choroid plexus:	n/a
27	chr16:81812606-81812656	HEK293	kidney:	embryo
28	chr16:81813706-81813756	MCF10A-Er-Src	breast:	n/a
29	chr16:81813706-81813756	ProgFib	skin:	n/a
30	chr16:81812606-81812656	SAEC	small airway:	n/a
31	chr16:81813363-81813413	MCF-7	breast:	n/a
32	chr16:81813969-81814019	NHBE	bronchial:	n/a
33	chr16:81812606-81812656	AG04450	lung:	fetal
34	chr16:81812738-81812788	A549	lung:	n/a
35	chr16:81813363-81813413	A549	lung:	n/a
36	chr16:81812738-81812788	GM19239	blood:	n/a
37	chr16:81812565-81812615	NT2-D1	testis:	n/a
38	chr16:81813706-81813756	GM06990	blood:	n/a
39	chr16:81813969-81814019	HPAEpiC	pulmonary alveolar:	n/a
40	chr16:81812738-81812788	U87	brain:	n/a
41	chr16:81812738-81812788	SAEC	small airway:	n/a
42	chr16:81813706-81813756	HEK293	kidney:	embryo
43	chr16:81812738-81812788	NHDF-neo	bronchial:	n/a
44	chr16:81813706-81813756	PANC-1	pancreas:	n/a
45	chr16:81812719-81812769	NT2-D1	testis:	n/a
46	chr16:81812606-81812656	HEEpiC	esophagus:	n/a
47	chr16:81813969-81814019	SKMC	muscle:	n/a
48	chr16:81812565-81812615	ovcar-3	ovarian:	n/a
49	chr16:81813706-81813756	IMR90	lung:	fetal
50	chr16:81812606-81812656	GM06990	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:81811097..81813033-chr16:81817790..81820555,3	MCF-7	breast:
2	chr16:81812978..81813631-chr16:81907214..81907808,2	K562	blood:
3	chr16:81797565..81799530-chr16:81809056..81810897,2	MCF-7	breast:
4	chr16:81801835..81805895-chr16:81806660..81810998,5	K562	blood:

No data

Variant related genes	Relation type
PLCG2	TF binding region
PLCG2	CpG island
ENSG00000197943	chromatin interactions

Extended variants
information (count: 271 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191680422	chr16:81810851-81810852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563367277	chr16:81810900-81810901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530718519	chr16:81810923-81810924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575725566	chr16:81810933-81810934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550050360	chr16:81810948-81810949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7194672	chr16:81810950-81810951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144240099	chr16:81810959-81810960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs36033508	chr16:81810992-81810993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543563928	chr16:81810996-81810997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547401475	chr16:81811003-81811004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115021547	chr16:81811085-81811086	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs7195041	chr16:81811118-81811119	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548455920	chr16:81811138-81811139	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs7198995	chr16:81811208-81811209	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs183892919	chr16:81811215-81811216	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs558839100	chr16:81811224-81811225	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs186723409	chr16:81811230-81811231	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534672770	chr16:81811253-81811254	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs72528154	chr16:81811263-81811264	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs11415278	chr16:81811264-81811265	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs75693931	chr16:81811265-81811266	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs553027971	chr16:81811268-81811269	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs111504749	chr16:81811269-81811270	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs60780862	chr16:81811342-81811343	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs563592327	chr16:81811350-81811351	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs7198003	chr16:81811397-81811398	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs545985490	chr16:81811407-81811408	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs564089959	chr16:81811436-81811437	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs532489953	chr16:81811440-81811441	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs373110092	chr16:81811447-81811448	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs541103928	chr16:81811448-81811449	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs559354443	chr16:81811449-81811450	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs7198169	chr16:81811457-81811458	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs548647478	chr16:81811466-81811467	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs7199605	chr16:81811478-81811479	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs7198191	chr16:81811485-81811486	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552755115	chr16:81811511-81811512	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs537962004	chr16:81811512-81811513	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs376315313	chr16:81811520-81811521	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs193291199	chr16:81811527-81811528	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs568105404	chr16:81811562-81811563	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545194240	chr16:81811571-81811572	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs139935992	chr16:81811576-81811577	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs58271299	chr16:81811582-81811583	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs575507722	chr16:81811596-81811597	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs75452105	chr16:81811608-81811609	Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs371834132	chr16:81811622-81811623	Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs111288642	chr16:81811626-81811627	Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs56027201	chr16:81811635-81811636	Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs566484508	chr16:81811637-81811638	Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	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
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
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16461572	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81792000-81812200	Weak transcription	Right Atrium	heart
2	chr16:81807200-81812200	Weak transcription	Adipose Nuclei	Adipose
3	chr16:81807600-81812400	Weak transcription	Left Ventricle	heart
4	chr16:81808400-81812000	Weak transcription	Fetal Thymus	thymus
5	chr16:81808600-81811800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr16:81808800-81812400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr16:81809600-81811600	Weak transcription	Primary B cells from cord blood	blood
8	chr16:81809600-81811800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr16:81809600-81811800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr16:81809600-81812000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr16:81809600-81812000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr16:81809600-81812200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr16:81809800-81812000	Weak transcription	Primary hematopoietic stem cells	blood
14	chr16:81810200-81812200	Weak transcription	GM12878-XiMat	blood
15	chr16:81810400-81812200	Weak transcription	Placenta	Placenta
16	chr16:81811600-81811800	Bivalent/Poised TSS	K562	blood
17	chr16:81811600-81812200	Enhancers	Primary B cells from cord blood	blood
18	chr16:81811800-81812000	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr16:81811800-81812000	Enhancers	A549	lung
20	chr16:81811800-81812000	Enhancers	Hela-S3	cervix
21	chr16:81811800-81812400	Enhancers	Primary B cells from peripheral blood	blood
22	chr16:81811800-81812400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr16:81811800-81812400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr16:81811800-81813400	Active TSS	K562	blood
25	chr16:81812000-81812200	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr16:81812000-81812200	Enhancers	Primary hematopoietic stem cells	blood
27	chr16:81812000-81812200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr16:81812000-81812200	Enhancers	Fetal Thymus	thymus
29	chr16:81812000-81812400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
30	chr16:81812000-81812400	Bivalent Enhancer	Fetal Intestine Large	intestine
31	chr16:81812000-81812400	Flanking Active TSS	A549	lung
32	chr16:81812000-81812400	Flanking Active TSS	Hela-S3	cervix
33	chr16:81812000-81812600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr16:81812000-81812600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr16:81812000-81812600	Bivalent Enhancer	Stomach Mucosa	stomach
36	chr16:81812000-81813200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr16:81812000-81814000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
38	chr16:81812200-81812400	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr16:81812200-81812400	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr16:81812200-81812400	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr16:81812200-81812400	Enhancers	Primary T cells from cord blood	blood
42	chr16:81812200-81812400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
43	chr16:81812200-81812400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr16:81812200-81812400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
45	chr16:81812200-81812400	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr16:81812200-81812400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr16:81812200-81812400	Bivalent Enhancer	Fetal Intestine Small	intestine
48	chr16:81812200-81812400	Enhancers	Placenta	Placenta
49	chr16:81812200-81812400	Bivalent Enhancer	Fetal Thymus	thymus
50	chr16:81812200-81812400	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum

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