Variant report

Variant	nsv974837
Chromosome Location	chr16:74642496-74646718
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	chr16:74642974-74643021	K562	blood:	n/a	n/a
2	ARID3A	chr16:74641912-74642507	HepG2	liver:	n/a	n/a
3	BHLHE40	chr16:74645453-74645724	K562	blood:	n/a	n/a
4	BHLHE40	chr16:74642934-74643081	K562	blood:	n/a	n/a
5	CCNT2	chr16:74642838-74643215	K562	blood:	n/a	n/a
6	CEBPB	chr16:74646188-74646650	IMR90	lung:	n/a	n/a
7	CEBPB	chr16:74641949-74642501	HepG2	liver:	n/a	chr16:74642122-74642133 chr16:74642121-74642134
8	CEBPB	chr16:74646343-74646450	A549	lung:	n/a	n/a
9	CEBPB	chr16:74645376-74645503	HepG2	liver:	n/a	n/a
10	CEBPB	chr16:74646345-74646487	Hela-S3	cervix:	n/a	n/a
11	CEBPD	chr16:74642782-74643228	K562	blood:	n/a	n/a
12	CEBPD	chr16:74642677-74643281	K562	blood:	n/a	n/a
13	CUX1	chr16:74642871-74643070	K562	blood:	n/a	n/a
14	EP300	chr16:74642746-74643349	SK-N-SH	brain:	n/a	n/a
15	EP300	chr16:74642833-74643207	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr16:74642742-74643233	MCF-7	breast:	n/a	n/a
17	EP300	chr16:74642871-74643123	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr16:74642852-74643177	K562	blood:	n/a	n/a
19	FOS	chr16:74646286-74646559	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr16:74645813-74645911	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr16:74646279-74646570	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr16:74646246-74646578	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr16:74646272-74646572	MCF10A-Er-Src	breast:	n/a	n/a
24	FOSL2	chr16:74646297-74646545	SK-N-SH	brain:	n/a	n/a
25	FOSL2	chr16:74646292-74646657	SK-N-SH	brain:	n/a	n/a
26	FOXA1	chr16:74642883-74643153	T-47D	breast:	n/a	n/a
27	GATA1	chr16:74642736-74643252	PBDE	blood:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
28	GATA1	chr16:74642681-74643308	K562	blood:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
29	GATA2	chr16:74642796-74643180	K562	blood:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
30	GATA2	chr16:74642750-74643236	SH-SY5Y	brain:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
31	GATA2	chr16:74642768-74643232	K562	blood:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
32	GATA2	chr16:74642875-74643178	HUVEC	blood vessel:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
33	GATA3	chr16:74642571-74643295	SK-N-SH	brain:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
34	GATA3	chr16:74642604-74643355	MCF-7	breast:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
35	GATA3	chr16:74642829-74643138	T-47D	breast:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
36	GATA3	chr16:74642784-74643229	T-47D	breast:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
37	GATA3	chr16:74642767-74643220	SH-SY5Y	brain:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
38	GATA3	chr16:74642768-74643264	MCF-7	breast:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
39	GATA3	chr16:74642604-74643443	SK-N-SH	brain:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
40	GATA3	chr16:74642816-74643201	MCF-7	breast:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
41	GATA3	chr16:74642522-74643435	MCF-7	breast:	n/a	chr16:74642953-74642962 chr16:74643003-74643011
42	HDAC2	chr16:74642829-74643130	K562	blood:	n/a	n/a
43	HDAC2	chr16:74642761-74643307	MCF-7	breast:	n/a	n/a
44	HDAC2	chr16:74642787-74643342	MCF-7	breast:	n/a	n/a
45	HMGN3	chr16:74642883-74643238	K562	blood:	n/a	n/a
46	JUN	chr16:74642763-74643223	K562	blood:	n/a	chr16:74643037-74643047
47	JUND	chr16:74646259-74646652	SK-N-SH	brain:	n/a	n/a
48	JUND	chr16:74642910-74643102	K562	blood:	n/a	chr16:74643037-74643047
49	JUND	chr16:74642805-74643236	SK-N-SH	brain:	n/a	chr16:74643037-74643047
50	JUND	chr16:74642816-74643290	SK-N-SH	brain:	n/a	chr16:74643037-74643047

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74644836-74644886	GM19239	blood:	n/a
2	chr16:74644836-74644886	U87	brain:	n/a
3	chr16:74644836-74644886	HUVEC	blood vessel:	n/a
4	chr16:74644836-74644886	HRCEpiC	kidney:	n/a
5	chr16:74644836-74644886	CMK	blood:	n/a
6	chr16:74644836-74644886	HIPEpiC	eye:	n/a
7	chr16:74644836-74644886	H1-hESC	embryonic stem cell:	embryo
8	chr16:74644836-74644886	HCT-116	colon:	n/a
9	chr16:74644836-74644886	K562	blood:	n/a
10	chr16:74644836-74644886	MCF10A-Er-Src	breast:	n/a
11	chr16:74644836-74644886	GM06990	blood:	n/a
12	chr16:74644836-74644886	Jurkat	blood:	n/a
13	chr16:74644836-74644886	PFSK-1	brain:	n/a
14	chr16:74644836-74644886	HepG2	liver:	n/a
15	chr16:74644836-74644886	ECC-1	luminal epithelium:	n/a
16	chr16:74644836-74644886	AG09319	gingival:	n/a
17	chr16:74644836-74644886	HPAEpiC	pulmonary alveolar:	n/a
18	chr16:74644836-74644886	HCPEpiC	choroid plexus:	n/a
19	chr16:74644836-74644886	GM12892	blood:	n/a
20	chr16:74644836-74644886	HMEC	breast:	n/a
21	chr16:74644836-74644886	HCF	heart:	n/a
22	chr16:74644836-74644886	HRE	kidney:	n/a
23	chr16:74644836-74644886	SAEC	small airway:	n/a
24	chr16:74644836-74644886	BE2_C	brain:	n/a
25	chr16:74644836-74644886	GM12891	blood:	n/a
26	chr16:74644836-74644886	SKMC	muscle:	n/a
27	chr16:74644836-74644886	Caco-2	colon:	n/a
28	chr16:74644836-74644886	MCF-7	breast:	n/a
29	chr16:74644836-74644886	AG04449	skin:	fetal
30	chr16:74644836-74644886	Hepatocyte	liver:	n/a
31	chr16:74644836-74644886	AG10803	skin:	n/a
32	chr16:74644836-74644886	HEEpiC	esophagus:	n/a
33	chr16:74644836-74644886	HEK293	kidney:	embryo
34	chr16:74644836-74644886	A549	lung:	n/a
35	chr16:74644836-74644886	HCM	heart:	n/a
36	chr16:74644836-74644886	LNCaP	prostate:	n/a
37	chr16:74644836-74644886	ProgFib	skin:	n/a
38	chr16:74644836-74644886	NH-A	brain:	n/a
39	chr16:74644836-74644886	ovcar-3	ovarian:	n/a
40	chr16:74644836-74644886	AG04450	lung:	fetal
41	chr16:74644836-74644886	HNPCEpiC	eye:	n/a
42	chr16:74644836-74644886	T-47D	breast:	n/a
43	chr16:74644836-74644886	HAEpiC	amniotic membrane:	n/a
44	chr16:74644836-74644886	NB4	blood:	n/a
45	chr16:74644836-74644886	RPTEC	kidney:	n/a
46	chr16:74644836-74644886	SK-N-MC	brain:	n/a
47	chr16:74644836-74644886	PANC-1	pancreas:	n/a
48	chr16:74644836-74644886	AG09309	skin:	n/a
49	chr16:74644836-74644886	GM12878	blood:	n/a
50	chr16:74644836-74644886	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr16:74641807..74643534-chr16:74646200..74648998,2	MCF-7	breast:
2	chr16:74328724..74332172-chr16:74639853..74642931,3	MCF-7	breast:
3	chr16:74638992..74641071-chr16:74646319..74648284,3	MCF-7	breast:
4	chr16:74638616..74642828-chr16:74644117..74647520,5	K562	blood:
5	chr16:74638616..74642828-chr16:74644117..74647520,5	K562	blood:
6	chr16:74640712..74642393-chr16:74644183..74645787,2	MCF-7	breast:

Variant related genes	Relation type
GLG1	TF binding region
GLG1	CpG island
ENSG00000270945	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000090863	chromatin interactions

Extended variants
information (count: 196 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:196 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185611637	chr16:74642526-74642527	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs560893997	chr16:74642532-74642533	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs7205258	chr16:74642539-74642540	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs34940915	chr16:74642548-74642549	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs11411092	chr16:74642558-74642559	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs78389495	chr16:74642566-74642567	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs79987110	chr16:74642567-74642568	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs546707706	chr16:74642572-74642573	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs550625650	chr16:74642592-74642593	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs377146342	chr16:74642610-74642611	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs113776518	chr16:74642669-74642670	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs552531110	chr16:74642691-74642692	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs569070778	chr16:74642708-74642709	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs190418021	chr16:74642736-74642737	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs150451298	chr16:74642741-74642742	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs182933444	chr16:74642752-74642753	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs574366183	chr16:74642759-74642760	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs372725262	chr16:74642789-74642790	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs534076501	chr16:74642826-74642827	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs553828977	chr16:74642842-74642843	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs577058534	chr16:74642865-74642866	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs138289094	chr16:74642920-74642921	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs148843601	chr16:74642933-74642934	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs148910115	chr16:74642980-74642981	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368911915	chr16:74642983-74642984	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs186094861	chr16:74643035-74643036	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs143507789	chr16:74643084-74643085	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs191974027	chr16:74643104-74643105	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs377187786	chr16:74643105-74643106	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560761830	chr16:74643131-74643132	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs557307629	chr16:74643155-74643156	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529688197	chr16:74643165-74643166	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184236292	chr16:74643218-74643219	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs536748585	chr16:74643222-74643223	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs560271986	chr16:74643268-74643269	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs187558461	chr16:74643275-74643276	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs552420164	chr16:74643279-74643280	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs562653483	chr16:74643316-74643317	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs531550015	chr16:74643337-74643338	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs192779369	chr16:74643343-74643344	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs568392360	chr16:74643345-74643346	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs35537685	chr16:74643362-74643363	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556595256	chr16:74643370-74643371	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs137867788	chr16:74643372-74643373	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs547354290	chr16:74643385-74643386	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs143422068	chr16:74643409-74643410	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs539501440	chr16:74643441-74643442	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs34872893	chr16:74643451-74643452	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs79582635	chr16:74643466-74643467	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs11860292	chr16:74643493-74643494	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
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	21364760	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Epilepsy	20502679	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74641200-74643000	Weak transcription	Small Intestine	intestine
2	chr16:74641200-74653800	Weak transcription	Spleen	Spleen
3	chr16:74641400-74642800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr16:74641400-74655800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr16:74641400-74656000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr16:74641600-74642600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr16:74641600-74643000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr16:74641600-74643000	Enhancers	Placenta	Placenta
9	chr16:74641600-74643200	Enhancers	Pancreas	Pancrea
10	chr16:74641600-74643400	Enhancers	Fetal Thymus	thymus
11	chr16:74641600-74643800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr16:74641600-74644200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr16:74641600-74644200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr16:74641600-74644600	Enhancers	Primary T cells fromperipheralblood	blood
15	chr16:74641600-74644600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr16:74641600-74644800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr16:74641600-74651000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr16:74641600-74656000	Weak transcription	Aorta	Aorta
19	chr16:74641600-74657000	Weak transcription	Gastric	stomach
20	chr16:74641600-74657800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr16:74641800-74642600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr16:74641800-74642600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr16:74641800-74642800	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr16:74641800-74643600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr16:74641800-74643800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr16:74641800-74644000	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr16:74641800-74644600	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr16:74641800-74644800	Enhancers	Primary T cells from cord blood	blood
29	chr16:74641800-74653600	Weak transcription	GM12878-XiMat	blood
30	chr16:74641800-74654600	Weak transcription	Primary B cells from peripheral blood	blood
31	chr16:74641800-74655200	Weak transcription	Primary B cells from cord blood	blood
32	chr16:74641800-74655400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr16:74641800-74655400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr16:74641800-74655800	Weak transcription	NHEK	skin
35	chr16:74641800-74656200	Weak transcription	HUVEC	blood vessel
36	chr16:74641800-74656600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr16:74642000-74642600	Enhancers	HepG2	liver
38	chr16:74642000-74642800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr16:74642000-74642800	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr16:74642000-74642800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr16:74642000-74643000	Enhancers	Hela-S3	cervix
42	chr16:74642000-74643000	Enhancers	K562	blood
43	chr16:74642000-74643200	Enhancers	Primary hematopoietic stem cells	blood
44	chr16:74642000-74643600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr16:74642000-74643800	Enhancers	Dnd41	blood
46	chr16:74642000-74645600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr16:74642000-74647800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr16:74642000-74651000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr16:74642000-74652200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr16:74642000-74653200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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