Variant report

Variant	esv1815957
Chromosome Location	chr16:71790812-71816899
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	chr16:71792235-71792776	HepG2	liver:	n/a	n/a
2	BATF	chr16:71809888-71810218	GM12878	blood:	n/a	n/a
3	BHLHE40	chr16:71792293-71792492	HepG2	liver:	n/a	n/a
4	BHLHE40	chr16:71809826-71810229	GM12878	blood:	n/a	chr16:71810029-71810050 chr16:71810033-71810046
5	CEBPB	chr16:71792506-71792733	HepG2	liver:	n/a	n/a
6	CEBPB	chr16:71796082-71796432	IMR90	lung:	n/a	n/a
7	CTCF	chr16:71791160-71791310	HEEpiC	esophagus:	n/a	n/a
8	CTCF	chr16:71815780-71815930	HEEpiC	esophagus:	n/a	chr16:71815847-71815863 chr16:71815851-71815861
9	CTCF	chr16:71815800-71815950	AG10803	skin:	n/a	chr16:71815847-71815863 chr16:71815851-71815861
10	CTCF	chr16:71815840-71815990	RPTEC	kidney:	n/a	chr16:71815847-71815863 chr16:71815851-71815861
11	CTCF	chr16:71816700-71816850	GM12878	blood:	n/a	n/a
12	CTCF	chr16:71815720-71815870	HCPEpiC	choroid plexus:	n/a	chr16:71815847-71815863 chr16:71815851-71815861
13	CTCF	chr16:71815864-71815904	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr16:71815940-71816090	HMEC	breast:	n/a	n/a
15	CTCF	chr16:71815840-71815990	Caco-2	colon:	n/a	chr16:71815847-71815863 chr16:71815851-71815861
16	CTCF	chr16:71815820-71815970	AG10803	skin:	n/a	chr16:71815847-71815863 chr16:71815851-71815861
17	CTCF	chr16:71794547-71794577	ProgFib	skin:	n/a	n/a
18	CTCF	chr16:71811458-71811678	T-47D	breast:	n/a	n/a
19	CTCF	chr16:71794014-71794051	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr16:71815700-71815850	HAc	cerebellar:	n/a	n/a
21	CTCF	chr16:71815660-71815810	RPTEC	kidney:	n/a	n/a
22	CUX1	chr16:71810483-71810549	GM12878	blood:	n/a	n/a
23	EBF1	chr16:71809802-71810112	GM12878	blood:	n/a	chr16:71809986-71809995 chr16:71809986-71809995 chr16:71809984-71809995 chr16:71809984-71809997 chr16:71809986-71809996
24	EBF1	chr16:71809773-71810373	GM12878	blood:	n/a	chr16:71809986-71809995 chr16:71809986-71809995 chr16:71809984-71809995 chr16:71809984-71809997 chr16:71809986-71809996
25	EP300	chr16:71809834-71810166	GM12878	blood:	n/a	n/a
26	EP300	chr16:71792243-71792657	HepG2	liver:	n/a	n/a
27	EP300	chr16:71795408-71795505	K562	blood:	n/a	n/a
28	ESR1	chr16:71803114-71803447	ECC-1	luminal epithelium:	n/a	n/a
29	FOXA1	chr16:71791839-71792846	HepG2	liver:	n/a	n/a
30	FOXA1	chr16:71792197-71792825	HepG2	liver:	n/a	n/a
31	FOXA1	chr16:71792314-71792846	HepG2	liver:	n/a	n/a
32	FOXA1	chr16:71792150-71792874	HepG2	liver:	n/a	n/a
33	FOXA2	chr16:71792221-71792755	HepG2	liver:	n/a	n/a
34	GATA2	chr16:71796074-71796598	HUVEC	blood vessel:	n/a	n/a
35	GATA2	chr16:71805253-71805878	HUVEC	blood vessel:	n/a	chr16:71805636-71805657 chr16:71805640-71805654 chr16:71805638-71805654
36	GATA3	chr16:71805576-71805927	MCF-7	breast:	n/a	chr16:71805636-71805657 chr16:71805638-71805654
37	GATA3	chr16:71805338-71806026	SK-N-SH	brain:	n/a	chr16:71805636-71805657 chr16:71805638-71805654
38	GATA3	chr16:71806383-71807357	A549	lung:	n/a	n/a
39	GATA3	chr16:71805407-71805800	MCF-7	breast:	n/a	chr16:71805636-71805657 chr16:71805638-71805654
40	GATA3	chr16:71806745-71807334	SK-N-SH	brain:	n/a	n/a
41	GATA3	chr16:71805335-71805985	SK-N-SH	brain:	n/a	chr16:71805636-71805657 chr16:71805638-71805654
42	GATA3	chr16:71805275-71805996	A549	lung:	n/a	chr16:71805636-71805657 chr16:71805638-71805654
43	GATA3	chr16:71806996-71807152	SH-SY5Y	brain:	n/a	n/a
44	HDAC2	chr16:71792149-71792660	HepG2	liver:	n/a	n/a
45	HNF4A	chr16:71792295-71792691	HepG2	liver:	n/a	n/a
46	HNF4G	chr16:71792255-71792731	HepG2	liver:	n/a	n/a
47	IRF1	chr16:71804022-71804051	K562	blood:	n/a	n/a
48	MAFF	chr16:71801045-71801339	HepG2	liver:	n/a	chr16:71801205-71801223 chr16:71801183-71801201
49	MAFF	chr16:71792139-71792553	HepG2	liver:	n/a	chr16:71792307-71792325
50	MAFF	chr16:71795023-71795334	HepG2	liver:	n/a	chr16:71795191-71795209

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:71792711-71792761	NH-A	brain:	n/a
2	chr16:71800315-71800365	IMR90	lung:	fetal
3	chr16:71792711-71792761	LNCaP	prostate:	n/a
4	chr16:71800315-71800365	HEK293	kidney:	embryo
5	chr16:71792305-71792355	NH-A	brain:	n/a
6	chr16:71800315-71800365	PFSK-1	brain:	n/a
7	chr16:71800315-71800365	NHDF-neo	bronchial:	n/a
8	chr16:71792305-71792355	HUVEC	blood vessel:	n/a
9	chr16:71800315-71800365	AG09309	skin:	n/a
10	chr16:71792305-71792355	AG04449	skin:	fetal
11	chr16:71800315-71800365	HCPEpiC	choroid plexus:	n/a
12	chr16:71800315-71800365	Hela-S3	cervix:	n/a
13	chr16:71792711-71792761	SK-N-SH_RA	brain:	n/a
14	chr16:71800315-71800365	HMEC	breast:	n/a
15	chr16:71800315-71800365	SK-N-MC	brain:	n/a
16	chr16:71792711-71792761	HCPEpiC	choroid plexus:	n/a
17	chr16:71792305-71792355	SK-N-SH_RA	brain:	n/a
18	chr16:71792711-71792761	AG09309	skin:	n/a
19	chr16:71800315-71800365	HL-60	blood:	n/a
20	chr16:71792711-71792761	AoSMC	blood vessel:	n/a
21	chr16:71800315-71800365	AG09319	gingival:	n/a
22	chr16:71792305-71792355	A549	lung:	n/a
23	chr16:71792305-71792355	LNCaP	prostate:	n/a
24	chr16:71800315-71800365	HUVEC	blood vessel:	n/a
25	chr16:71792711-71792761	HL-60	blood:	n/a
26	chr16:71792305-71792355	IMR90	lung:	fetal
27	chr16:71800315-71800365	HIPEpiC	eye:	n/a
28	chr16:71800315-71800365	HAEpiC	amniotic membrane:	n/a
29	chr16:71792305-71792355	AoSMC	blood vessel:	n/a
30	chr16:71792305-71792355	GM12878	blood:	n/a
31	chr16:71800315-71800365	LNCaP	prostate:	n/a
32	chr16:71792711-71792761	GM19239	blood:	n/a
33	chr16:71800315-71800365	PrEC	prostate:	n/a
34	chr16:71792711-71792761	PFSK-1	brain:	n/a
35	chr16:71792711-71792761	GM06990	blood:	n/a
36	chr16:71792711-71792761	A549	lung:	n/a
37	chr16:71792711-71792761	HUVEC	blood vessel:	n/a
38	chr16:71792305-71792355	HRPEpiC	eye:	n/a
39	chr16:71800315-71800365	HNPCEpiC	eye:	n/a
40	chr16:71792305-71792355	HCPEpiC	choroid plexus:	n/a
41	chr16:71792305-71792355	MCF10A-Er-Src	breast:	n/a
42	chr16:71792711-71792761	HRPEpiC	eye:	n/a
43	chr16:71800315-71800365	AoSMC	blood vessel:	n/a
44	chr16:71800315-71800365	GM12891	blood:	n/a
45	chr16:71800315-71800365	HCT-116	colon:	n/a
46	chr16:71800315-71800365	NH-A	brain:	n/a
47	chr16:71792305-71792355	HRCEpiC	kidney:	n/a
48	chr16:71792305-71792355	HNPCEpiC	eye:	n/a
49	chr16:71800315-71800365	HPAEpiC	pulmonary alveolar:	n/a
50	chr16:71800315-71800365	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:71792577..71794560-chr16:71799391..71801593,2	MCF-7	breast:
2	chr16:71815919..71817496-chr16:71847689..71850509,2	MCF-7	breast:
3	chr16:71799645..71801237-chr16:71841138..71842836,2	MCF-7	breast:
4	chr16:71800568..71802232-chr16:71804201..71806010,2	MCF-7	breast:
5	chr16:71805065..71807022-chr16:71841800..71844542,2	MCF-7	breast:
6	chr16:71784075..71786608-chr16:71800561..71802768,2	MCF-7	breast:
7	chr16:71795022..71797414-chr16:71798658..71803314,4	MCF-7	breast:
8	chr16:71796071..71798495-chr16:71805042..71807418,2	MCF-7	breast:
9	chr16:71792577..71794560-chr16:71799391..71801593,2	MCF-7	breast:
10	chr16:71790780..71793408-chr16:71805214..71808324,3	K562	blood:
11	chr16:71802433..71805430-chr16:71808477..71810923,2	K562	blood:
12	chr16:71809920..71813337-chr16:71827529..71832113,4	K562	blood:
13	chr16:71804847..71807102-chr16:71815302..71816965,2	K562	blood:
14	chr16:71793829..71795546-chr16:71803779..71806490,2	MCF-7	breast:
15	chr16:71795022..71797414-chr16:71798658..71803314,4	MCF-7	breast:
16	chr16:71815390..71817110-chr16:71837324..71839084,3	K562	blood:
17	chr16:71809511..71811368-chr16:71813247..71816023,2	K562	blood:
18	chr16:71810112..71812013-chr16:71817233..71818739,2	MCF-7	breast:
19	chr16:71815403..71819721-chr16:71837408..71844213,7	K562	blood:
20	chr16:71809511..71811368-chr16:71813247..71816023,2	K562	blood:

Variant related genes	Relation type
SNORD71	TF binding region
AP1G1	TF binding region
SNORD71	CpG island
AP1G1	CpG island
ENSG00000223224	chromatin interactions
ENSG00000166747	chromatin interactions

Extended variants
information (count: 1091 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1091 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11075901	chr16:71790812-71790813	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78164232	chr16:71790833-71790834	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551372939	chr16:71790834-71790835	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76625340	chr16:71790836-71790837	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569764684	chr16:71790851-71790852	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531678155	chr16:71790854-71790855	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551830103	chr16:71790905-71790906	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555868559	chr16:71790978-71790979	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs28607441	chr16:71791001-71791002	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145286300	chr16:71791026-71791027	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145143250	chr16:71791038-71791039	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553363419	chr16:71791091-71791092	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373155436	chr16:71791151-71791152	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs545579006	chr16:71791169-71791170	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs377071100	chr16:71791210-71791211	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs575959139	chr16:71791218-71791219	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs534188118	chr16:71791268-71791269	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs189723197	chr16:71791273-71791274	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs554311374	chr16:71791286-71791287	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs372793292	chr16:71791287-71791288	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs528055763	chr16:71791302-71791303	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs61679457	chr16:71791304-71791305	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs72487898	chr16:71791305-71791306	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs397730917	chr16:71791309-71791310	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546588120	chr16:71791329-71791330	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564988873	chr16:71791338-71791339	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557807990	chr16:71791342-71791343	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74740498	chr16:71791352-71791353	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181398162	chr16:71791372-71791373	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548353524	chr16:71791390-71791391	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77546460	chr16:71791411-71791412	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7201228	chr16:71791429-71791430	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs186031471	chr16:71791432-71791433	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188321963	chr16:71791464-71791465	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181869518	chr16:71791520-71791521	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567769208	chr16:71791537-71791538	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534675214	chr16:71791599-71791600	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186079224	chr16:71791617-71791618	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149135249	chr16:71791630-71791631	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142250098	chr16:71791640-71791641	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557728458	chr16:71791693-71791694	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575894733	chr16:71791714-71791715	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9939455	chr16:71791798-71791799	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs554330877	chr16:71791811-71791812	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs79507857	chr16:71791824-71791825	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs398100279	chr16:71791827-71791828	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs202065063	chr16:71791854-71791855	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs572900515	chr16:71791873-71791874	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs190929863	chr16:71791903-71791904	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs575492230	chr16:71791959-71791960	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Neuroblastoma	18923524	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:1174 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71761000-71805600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr16:71762200-71811400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:71763200-71799800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr16:71763200-71812600	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr16:71763400-71802200	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr16:71763600-71793000	Strong transcription	Primary B cells from peripheral blood	blood
7	chr16:71763600-71800000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr16:71763600-71801400	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr16:71763600-71812400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr16:71763800-71799600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr16:71763800-71804800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr16:71764000-71804800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr16:71764000-71813000	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr16:71764800-71802600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr16:71770600-71793000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr16:71770600-71796000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr16:71770600-71798600	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr16:71770600-71799600	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr16:71770800-71793200	Strong transcription	HSMM	muscle
20	chr16:71770800-71793600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr16:71770800-71795800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr16:71770800-71799600	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr16:71770800-71810600	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr16:71770800-71813800	Strong transcription	Liver	Liver
25	chr16:71771000-71793200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr16:71771000-71812200	Strong transcription	Placenta	Placenta
27	chr16:71774400-71792200	Weak transcription	Aorta	Aorta
28	chr16:71777200-71799800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr16:71778400-71791800	Strong transcription	HepG2	liver
30	chr16:71779000-71793000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr16:71779600-71841800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr16:71780000-71821400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr16:71782800-71792200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr16:71783400-71791400	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr16:71783800-71820600	Weak transcription	Psoas Muscle	Psoas
36	chr16:71784000-71811200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr16:71785400-71792800	Strong transcription	Primary B cells from cord blood	blood
38	chr16:71785400-71799800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr16:71785400-71808800	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr16:71785600-71793200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
41	chr16:71785800-71792800	Strong transcription	HMEC	breast
42	chr16:71786400-71792800	Strong transcription	HUVEC	blood vessel
43	chr16:71786400-71799800	Strong transcription	Adipose Nuclei	Adipose
44	chr16:71786400-71802200	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr16:71786400-71805200	Strong transcription	Duodenum Mucosa	Duodenum
46	chr16:71786600-71809800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr16:71786800-71793000	Strong transcription	Brain Germinal Matrix	brain
48	chr16:71786800-71793200	Strong transcription	Dnd41	blood
49	chr16:71786800-71793400	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr16:71786800-71793400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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