Variant report

Variant	esv1826506
Chromosome Location	chr16:70253919-70287669
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1987)
CpG islands
(count:916)
Chromatin interactive
region (count:30)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1987 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70285693-70286285	K562	blood:	n/a	n/a
2	ARID3A	chr16:70285768-70286158	HepG2	liver:	n/a	n/a
3	ATF2	chr16:70285719-70286058	GM12878	blood:	n/a	n/a
4	ATF2	chr16:70285560-70286287	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr16:70285539-70286157	GM12878	blood:	n/a	n/a
6	ATF2	chr16:70285578-70286117	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr16:70285052-70285235	K562	blood:	n/a	n/a
8	ATF3	chr16:70285482-70286054	A549	lung:	n/a	n/a
9	ATF3	chr16:70285713-70286019	K562	blood:	n/a	n/a
10	ATF3	chr16:70285595-70286202	A549	lung:	n/a	n/a
11	BACH1	chr16:70285758-70286009	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr16:70285189-70285377	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr16:70286012-70286116	K562	blood:	n/a	n/a
14	BACH1	chr16:70285122-70285178	K562	blood:	n/a	n/a
15	BATF	chr16:70277954-70278184	GM12878	blood:	n/a	n/a
16	BATF	chr16:70270340-70270551	GM12878	blood:	n/a	n/a
17	BATF	chr16:70259711-70260057	GM12878	blood:	n/a	n/a
18	BATF	chr16:70274761-70275229	GM12878	blood:	n/a	n/a
19	BATF	chr16:70265769-70265977	GM12878	blood:	n/a	n/a
20	BATF	chr16:70274531-70275234	GM12878	blood:	n/a	n/a
21	BATF	chr16:70275352-70275629	GM12878	blood:	n/a	n/a
22	BATF	chr16:70269196-70269455	GM12878	blood:	n/a	n/a
23	BATF	chr16:70266179-70266523	GM12878	blood:	n/a	n/a
24	BATF	chr16:70269207-70269408	GM12878	blood:	n/a	n/a
25	BATF	chr16:70275330-70275612	GM12878	blood:	n/a	n/a
26	BATF	chr16:70266143-70266490	GM12878	blood:	n/a	n/a
27	BATF	chr16:70272693-70272978	GM12878	blood:	n/a	n/a
28	BATF	chr16:70272645-70272986	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:70274569-70274791	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:70272703-70272967	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:70274796-70275305	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:70266040-70266508	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:70266128-70266474	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:70272603-70273149	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:70274544-70275641	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:70273183-70273430	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:70275340-70275579	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:70260079-70260328	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:70256901-70257158	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:70267253-70267439	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:70264796-70265164	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:70265235-70265407	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:70256507-70256821	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:70256979-70257253	GM12878	blood:	n/a	n/a
45	BCL3	chr16:70285533-70286181	A549	lung:	n/a	chr16:70285921-70285929
46	BCL3	chr16:70285249-70286114	GM12878	blood:	n/a	chr16:70285921-70285929
47	BCL3	chr16:70285545-70286396	K562	blood:	n/a	chr16:70285921-70285929
48	BCL3	chr16:70285515-70286212	A549	lung:	n/a	chr16:70285921-70285929
49	BCL3	chr16:70285551-70286540	K562	blood:	n/a	chr16:70285921-70285929
50	BCLAF1	chr16:70285447-70286184	GM12878	blood:	n/a	chr16:70285921-70285929

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70283421-70283471	PANC-1	pancreas:	n/a
2	chr16:70283421-70283471	PANC-1	pancreas:	n/a
3	chr16:70285910-70285960	AG04449	skin:	fetal
4	chr16:70284928-70284978	K562	blood:	n/a
5	chr16:70285806-70285856	BJ	skin:	n/a
6	chr16:70286390-70286440	SAEC	small airway:	n/a
7	chr16:70286390-70286440	HCT-116	colon:	n/a
8	chr16:70285408-70285458	HRCEpiC	kidney:	n/a
9	chr16:70285955-70286005	GM12892	blood:	n/a
10	chr16:70285806-70285856	HCM	heart:	n/a
11	chr16:70284893-70284943	H1-hESC	embryonic stem cell:	embryo
12	chr16:70285955-70286005	HepG2	liver:	n/a
13	chr16:70285816-70285866	LNCaP	prostate:	n/a
14	chr16:70285978-70286028	HEK293	kidney:	embryo
15	chr16:70285910-70285960	A549	lung:	n/a
16	chr16:70284928-70284978	NH-A	brain:	n/a
17	chr16:70285408-70285458	HCF	heart:	n/a
18	chr16:70284893-70284943	GM12892	blood:	n/a
19	chr16:70285408-70285458	Hela-S3	cervix:	n/a
20	chr16:70283421-70283471	Hepatocyte	liver:	n/a
21	chr16:70286329-70286379	CMK	blood:	n/a
22	chr16:70285955-70286005	HMEC	breast:	n/a
23	chr16:70285408-70285458	HRE	kidney:	n/a
24	chr16:70259186-70259236	ovcar-3	ovarian:	n/a
25	chr16:70259186-70259236	GM12892	blood:	n/a
26	chr16:70259186-70259236	NHDF-neo	bronchial:	n/a
27	chr16:70286779-70286829	CMK	blood:	n/a
28	chr16:70283421-70283471	HepG2	liver:	n/a
29	chr16:70286430-70286480	HMEC	breast:	n/a
30	chr16:70259186-70259236	AG10803	skin:	n/a
31	chr16:70286430-70286480	NH-A	brain:	n/a
32	chr16:70285816-70285866	A549	lung:	n/a
33	chr16:70286779-70286829	AG04450	lung:	fetal
34	chr16:70285955-70286005	SKMC	muscle:	n/a
35	chr16:70284893-70284943	ovcar-3	ovarian:	n/a
36	chr16:70286779-70286829	NH-A	brain:	n/a
37	chr16:70284893-70284943	AG09319	gingival:	n/a
38	chr16:70285978-70286028	GM19239	blood:	n/a
39	chr16:70286779-70286829	HMEC	breast:	n/a
40	chr16:70285816-70285866	HCM	heart:	n/a
41	chr16:70284893-70284943	AoSMC	blood vessel:	n/a
42	chr16:70284928-70284978	NB4	blood:	n/a
43	chr16:70283421-70283471	MCF10A-Er-Src	breast:	n/a
44	chr16:70284928-70284978	AG09309	skin:	n/a
45	chr16:70285408-70285458	AG10803	skin:	n/a
46	chr16:70286346-70286396	MCF10A-Er-Src	breast:	n/a
47	chr16:70285910-70285960	GM06990	blood:	n/a
48	chr16:70286779-70286829	ovcar-3	ovarian:	n/a
49	chr16:70286390-70286440	NH-A	brain:	n/a
50	chr16:70284928-70284978	PFSK-1	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70284271..70287113-chr16:70301564..70303205,2	MCF-7	breast:
2	chr16:70279244..70282169-chr16:70284255..70286230,4	K562	blood:
3	chr16:70279273..70282169-chr16:70284255..70286204,3	K562	blood:
4	chr16:70283799..70285737-chr6:44213868..44216847,2	K562	blood:
5	chr16:70285876..70288887-chr16:70302566..70307390,4	K562	blood:
6	chr16:70287320..70289608-chr16:70290173..70293534,4	K562	blood:
7	chr16:70279273..70282169-chr16:70284255..70286204,3	K562	blood:
8	chr16:70287173..70288856-chr16:70293033..70295926,2	MCF-7	breast:
9	chr16:70285325..70286015-chr8:117886552..117887078,2	HCT-116	colon:
10	chr16:70284505..70286615-chr16:70556732..70559559,2	MCF-7	breast:
11	chr16:70286360..70288555-chr16:70308791..70311038,2	K562	blood:
12	chr11:842040..842913-chr16:70285376..70285907,2	HCT-116	colon:
13	chr16:70278247..70283453-chr16:70284015..70287841,6	MCF-7	breast:
14	chr16:70285343..70285906-chr19:16738980..16739732,2	Hela-S3	cervix:
15	chr16:70278247..70283453-chr16:70284015..70287841,6	MCF-7	breast:
16	chr16:70279244..70282169-chr16:70284255..70286230,4	K562	blood:
17	chr16:70287090..70289744-chr16:70321659..70325168,3	MCF-7	breast:
18	chr16:70283625..70285831-chr16:70321379..70323186,2	K562	blood:
19	chr16:70285367..70286970-chr17:73718097..73720794,2	MCF-7	breast:
20	chr16:70285081..70287489-chr16:70291525..70295571,5	K562	blood:
21	chr16:70286246..70291555-chr16:70316780..70324702,12	K562	blood:
22	chr16:70284511..70286776-chr16:70330314..70334173,3	MCF-7	breast:
23	chr16:70191657..70193675-chr16:70283732..70285560,2	K562	blood:
24	chr16:70284207..70286196-chr16:70321648..70323975,3	MCF-7	breast:
25	chr16:70286317..70289211-chr16:70320911..70324702,4	K562	blood:
26	chr1:149982029..149982749-chr16:70285430..70285983,2	Hela-S3	cervix:
27	chr16:70285239..70287287-chr16:70556700..70559340,2	K562	blood:
28	chr16:70283970..70285913-chr16:70380669..70382950,2	K562	blood:
29	chr16:70284251..70286200-chr16:70298122..70301114,5	MCF-7	breast:
30	chr16:70284942..70287057-chr16:70291525..70294943,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DDX19B-2	chr16:70273803-70273904	NONHSAT143414
2	lnc-DDX19B-2	chr16:70280560-70282018	NONHSAT143414

No data

Variant related genes	Relation type
ENSG00000269866	TF binding region
EXOSC6	TF binding region
ENSG00000261556	TF binding region
ENSG00000238734	TF binding region
ENSG00000269866	CpG island
EXOSC6	CpG island
ENSG00000261556	CpG island
ENSG00000238734	CpG island
ENSG00000177700	chromatin interactions
ENSG00000261556	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000265648	chromatin interactions
ENSG00000090861	chromatin interactions
ENSG00000132470	chromatin interactions
ENSG00000105085	chromatin interactions
ENSG00000214063	chromatin interactions
ENSG00000168872	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000264875	chromatin interactions
ENSG00000157349	chromatin interactions
ENSG00000260537	chromatin interactions
ENSG00000163113	chromatin interactions
ENSG00000223496	chromatin interactions
ENSG00000265230	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000141979	chromatin interactions
ENSG00000164754	chromatin interactions

Extended variants
information (count: 1226 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1226 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577672038	chr16:70253926-70253927	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs368021085	chr16:70253943-70253944	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs188750559	chr16:70253957-70253958	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs28537143	chr16:70253978-70253979	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs556958912	chr16:70254090-70254091	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs565902872	chr16:70254177-70254178	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs575995653	chr16:70254205-70254206	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs3972027	chr16:70254231-70254232	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs3972028	chr16:70254251-70254252	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs543373316	chr16:70254275-70254276	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs3972029	chr16:70254280-70254281	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs181573215	chr16:70254292-70254293	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs535126843	chr16:70254300-70254301	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs75163261	chr16:70254342-70254343	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs540822806	chr16:70254343-70254344	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs3972030	chr16:70254345-70254346	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs116243250	chr16:70254376-70254377	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs3972031	chr16:70254387-70254388	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528884954	chr16:70254400-70254401	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs550683810	chr16:70254419-70254420	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs375075082	chr16:70254428-70254429	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs2379068	chr16:70254540-70254541	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs562570579	chr16:70254575-70254576	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs3972033	chr16:70254600-70254601	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs201887656	chr16:70254629-70254630	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs530059209	chr16:70254725-70254726	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs548344701	chr16:70254734-70254735	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs201149017	chr16:70254743-70254744	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs567234383	chr16:70254773-70254774	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs534465133	chr16:70254807-70254808	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs201628532	chr16:70254821-70254822	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs369539057	chr16:70254861-70254862	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs571247360	chr16:70254888-70254889	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs113167573	chr16:70254927-70254928	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs538763227	chr16:70254931-70254932	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs556663682	chr16:70255141-70255142	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs575274575	chr16:70255159-70255160	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs536260154	chr16:70255191-70255192	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs555253140	chr16:70255197-70255198	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs186373363	chr16:70255244-70255245	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs540459666	chr16:70255260-70255261	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs144761957	chr16:70255278-70255279	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs577245240	chr16:70255287-70255288	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs191274286	chr16:70255291-70255292	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs562658119	chr16:70255302-70255303	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs536026570	chr16:70255303-70255304	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs181515876	chr16:70255304-70255305	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs560847322	chr16:70255412-70255413	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs113764931	chr16:70255422-70255423	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs556072704	chr16:70255424-70255425	Weak transcription Strong transcription	TF binding 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
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
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1121 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70231400-70258600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr16:70232400-70284800	Weak transcription	Spleen	Spleen
3	chr16:70233200-70283400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr16:70233200-70283600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr16:70234800-70260800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr16:70235600-70258600	Weak transcription	Pancreas	Pancrea
7	chr16:70235600-70284200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr16:70236200-70258600	Weak transcription	Thymus	Thymus
9	chr16:70237000-70258600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr16:70237000-70258800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr16:70237200-70267200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr16:70237200-70284800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr16:70238400-70274600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr16:70238600-70284800	Weak transcription	Esophagus	oesophagus
15	chr16:70238800-70260400	Weak transcription	Fetal Brain Female	brain
16	chr16:70238800-70283400	Weak transcription	NHEK	skin
17	chr16:70238800-70283600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr16:70239000-70260600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr16:70239000-70266800	Weak transcription	Aorta	Aorta
20	chr16:70239200-70256800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr16:70239200-70260600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr16:70239600-70283400	Weak transcription	Brain Angular Gyrus	brain
23	chr16:70239800-70259000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr16:70240200-70258600	Weak transcription	Gastric	stomach
25	chr16:70240200-70260800	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr16:70241000-70267600	Weak transcription	A549	lung
27	chr16:70241000-70283600	Weak transcription	Brain Germinal Matrix	brain
28	chr16:70241200-70255200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr16:70241200-70260600	Weak transcription	Fetal Thymus	thymus
30	chr16:70241200-70260600	Weak transcription	Osteobl	bone
31	chr16:70242200-70260000	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr16:70242200-70272600	Weak transcription	Primary B cells from cord blood	blood
33	chr16:70242200-70283400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr16:70242400-70260000	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr16:70242600-70282600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr16:70242600-70283000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr16:70242800-70283400	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr16:70243000-70261800	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr16:70243200-70283400	Weak transcription	NH-A	brain
40	chr16:70243800-70260600	Weak transcription	Left Ventricle	heart
41	chr16:70244600-70258600	Weak transcription	Ovary	ovary
42	chr16:70245000-70283400	Weak transcription	Brain Anterior Caudate	brain
43	chr16:70245600-70283000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr16:70245600-70283000	Weak transcription	Small Intestine	intestine
45	chr16:70245800-70283400	Weak transcription	Stomach Smooth Muscle	stomach
46	chr16:70246000-70267200	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr16:70246400-70283400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr16:70246400-70283400	Weak transcription	Colon Smooth Muscle	Colon
49	chr16:70247200-70260200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr16:70247800-70258600	Weak transcription	Lung	lung

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