Variant report

Variant	nsv826972
Chromosome Location	chr14:70717268-70726035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:359)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:359 , 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	ATF1	chr14:70724287-70724576	K562	blood:	n/a	n/a
2	BACH1	chr14:70721386-70721566	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:70724301-70724501	K562	blood:	n/a	n/a
4	CCNT2	chr14:70721445-70721635	K562	blood:	n/a	n/a
5	CEBPB	chr14:70717945-70718135	A549	lung:	n/a	n/a
6	CEBPB	chr14:70724248-70724524	K562	blood:	n/a	n/a
7	CEBPB	chr14:70717958-70718139	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:70717909-70718212	K562	blood:	n/a	n/a
9	CEBPB	chr14:70718003-70718137	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr14:70724199-70724626	MCF-7	breast:	n/a	n/a
11	CHD2	chr14:70722003-70722455	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr14:70724440-70724590	HCM	heart:	n/a	n/a
13	CTCF	chr14:70724180-70724330	A549	lung:	n/a	n/a
14	CTCF	chr14:70721899-70722012	GM10266	blood:	n/a	n/a
15	CTCF	chr14:70721900-70722050	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr14:70724360-70724510	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:70724320-70724470	HepG2	liver:	n/a	n/a
18	CTCF	chr14:70724306-70724567	K562	blood:	n/a	n/a
19	CTCF	chr14:70724400-70724550	HPF	lung:	n/a	n/a
20	CTCF	chr14:70724340-70724490	GM12878	blood:	n/a	n/a
21	CTCF	chr14:70724193-70724527	A549	lung:	n/a	n/a
22	CTCF	chr14:70724340-70724490	GM12870	blood:	n/a	n/a
23	CTCF	chr14:70724400-70724550	HRE	kidney:	n/a	n/a
24	CTCF	chr14:70724316-70724552	NHEK	skin:	n/a	n/a
25	CTCF	chr14:70724100-70724250	HCM	heart:	n/a	n/a
26	CTCF	chr14:70724300-70724450	RPTEC	kidney:	n/a	n/a
27	CTCF	chr14:70724318-70724551	Gliobla	brain:	n/a	n/a
28	CTCF	chr14:70724440-70724590	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr14:70724340-70724490	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr14:70724380-70724530	HPF	lung:	n/a	n/a
31	CTCF	chr14:70724340-70724490	AG10803	skin:	n/a	n/a
32	CTCF	chr14:70724315-70724573	A549	lung:	n/a	n/a
33	CTCF	chr14:70724400-70724550	HVMF	connective:	n/a	n/a
34	CTCF	chr14:70724270-70724575	GM10266	blood:	n/a	n/a
35	CTCF	chr14:70724360-70724510	GM12868	blood:	n/a	n/a
36	CTCF	chr14:70724409-70724481	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr14:70724380-70724530	GM12864	blood:	n/a	n/a
38	CTCF	chr14:70724360-70724510	HL-60	blood:	n/a	n/a
39	CTCF	chr14:70721957-70721976	MCF-7	breast:	n/a	n/a
40	CTCF	chr14:70724335-70724516	GM20000	blood:	n/a	n/a
41	CTCF	chr14:70724362-70724522	GM10248	blood:	n/a	n/a
42	CTCF	chr14:70724074-70724719	A549	lung:	n/a	n/a
43	CTCF	chr14:70724340-70724490	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr14:70724380-70724530	GM12872	blood:	n/a	n/a
45	CTCF	chr14:70724360-70724510	HFF	foreskin:	n/a	n/a
46	CTCF	chr14:70724460-70724610	GM12870	blood:	n/a	n/a
47	CTCF	chr14:70724340-70724490	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr14:70724400-70724550	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr14:70724260-70724616	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr14:70724400-70724550	SK-N-SH_RA	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70721864-70721914	HCM	heart:	n/a
2	chr14:70721641-70721691	HNPCEpiC	eye:	n/a
3	chr14:70721531-70721581	ECC-1	luminal epithelium:	n/a
4	chr14:70721531-70721581	Hepatocyte	liver:	n/a
5	chr14:70721864-70721914	Hepatocyte	liver:	n/a
6	chr14:70721531-70721581	HL-60	blood:	n/a
7	chr14:70721864-70721914	HMEC	breast:	n/a
8	chr14:70721864-70721914	MCF-7	breast:	n/a
9	chr14:70721531-70721581	HCPEpiC	choroid plexus:	n/a
10	chr14:70721641-70721691	GM12892	blood:	n/a
11	chr14:70721641-70721691	Hela-S3	cervix:	n/a
12	chr14:70721864-70721914	SKMC	muscle:	n/a
13	chr14:70721641-70721691	HCPEpiC	choroid plexus:	n/a
14	chr14:70721531-70721581	HCT-116	colon:	n/a
15	chr14:70721641-70721691	CMK	blood:	n/a
16	chr14:70721864-70721914	AG04449	skin:	fetal
17	chr14:70721864-70721914	NHDF-neo	bronchial:	n/a
18	chr14:70721641-70721691	HEEpiC	esophagus:	n/a
19	chr14:70721641-70721691	GM12891	blood:	n/a
20	chr14:70721864-70721914	HIPEpiC	eye:	n/a
21	chr14:70721531-70721581	HAEpiC	amniotic membrane:	n/a
22	chr14:70721641-70721691	SAEC	small airway:	n/a
23	chr14:70721641-70721691	HCT-116	colon:	n/a
24	chr14:70721641-70721691	Caco-2	colon:	n/a
25	chr14:70721531-70721581	AG04450	lung:	fetal
26	chr14:70721641-70721691	HIPEpiC	eye:	n/a
27	chr14:70721864-70721914	AG09309	skin:	n/a
28	chr14:70721641-70721691	MCF-7	breast:	n/a
29	chr14:70721531-70721581	HCF	heart:	n/a
30	chr14:70721864-70721914	AG04450	lung:	fetal
31	chr14:70721641-70721691	PrEC	prostate:	n/a
32	chr14:70721864-70721914	NT2-D1	testis:	n/a
33	chr14:70721531-70721581	Caco-2	colon:	n/a
34	chr14:70721864-70721914	SK-N-MC	brain:	n/a
35	chr14:70721641-70721691	AG09319	gingival:	n/a
36	chr14:70721531-70721581	MCF-7	breast:	n/a
37	chr14:70721864-70721914	U87	brain:	n/a
38	chr14:70721641-70721691	A549	lung:	n/a
39	chr14:70721531-70721581	PFSK-1	brain:	n/a
40	chr14:70721864-70721914	Caco-2	colon:	n/a
41	chr14:70721531-70721581	GM12891	blood:	n/a
42	chr14:70721641-70721691	K562	blood:	n/a
43	chr14:70721531-70721581	T-47D	breast:	n/a
44	chr14:70721641-70721691	HL-60	blood:	n/a
45	chr14:70721864-70721914	ProgFib	skin:	n/a
46	chr14:70721864-70721914	HCF	heart:	n/a
47	chr14:70721864-70721914	AoSMC	blood vessel:	n/a
48	chr14:70721531-70721581	HEEpiC	esophagus:	n/a
49	chr14:70721531-70721581	NHDF-neo	bronchial:	n/a
50	chr14:70721641-70721691	GM06990	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:70285530..70286121-chr14:70724141..70724832,2	MCF-7	breast:
2	chr14:70715795..70718866-chr14:70920555..70924612,3	MCF-7	breast:
3	chr14:70192465..70194929-chr14:70723600..70725967,2	MCF-7	breast:
4	chr14:70563059..70563930-chr14:70724005..70724836,3	MCF-7	breast:
5	chr14:70553438..70554419-chr14:70723857..70725057,7	MCF-7	breast:
6	chr14:70716825..70718477-chr14:70720427..70722449,2	MCF-7	breast:
7	chr14:70717254..70719398-chr14:70724325..70725965,2	MCF-7	breast:
8	chr14:70512590..70513297-chr14:70723854..70724631,4	MCF-7	breast:
9	chr14:70563314..70564224-chr14:70724024..70724835,3	MCF-7	breast:
10	chr14:70716825..70718477-chr14:70720427..70722449,2	MCF-7	breast:
11	chr14:70519745..70521992-chr14:70721079..70723653,2	MCF-7	breast:
12	chr14:70723245..70723897-chr14:71034403..71035282,2	MCF-7	breast:
13	chr14:70717254..70719398-chr14:70724325..70725965,2	MCF-7	breast:
14	chr14:70512608..70513510-chr14:70723957..70724907,3	MCF-7	breast:
15	chr14:70514161..70515859-chr14:70723794..70725987,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM21-3	chr14:70723079-70723550	NONHSAT037556

No data

Variant related genes	Relation type
ADAM21P1	TF binding region
ADAM21P1	CpG island
ENSG00000139985	chromatin interactions
ENSG00000100650	chromatin interactions

Extended variants
information (count: 456 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532621175	chr14:70717305-70717306	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs373427716	chr14:70717343-70717344	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540271208	chr14:70717425-70717426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs17176180	chr14:70717426-70717427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184709886	chr14:70717458-70717459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532486313	chr14:70717479-70717480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs201757853	chr14:70717509-70717510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs1467688	chr14:70717510-70717511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567535255	chr14:70717517-70717518	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs1465498	chr14:70717558-70717559	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs375286547	chr14:70717598-70717599	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs75603219	chr14:70717611-70717612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs75825903	chr14:70717612-70717613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs546797245	chr14:70717676-70717677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs61979502	chr14:70717725-70717726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs189594469	chr14:70717740-70717741	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs34664547	chr14:70717783-70717784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73280734	chr14:70717795-70717796	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566994586	chr14:70717796-70717797	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs1469253	chr14:70717846-70717847	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs535836704	chr14:70717850-70717851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs554864697	chr14:70717873-70717874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573177974	chr14:70717876-70717877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147315179	chr14:70717880-70717881	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs565125854	chr14:70717891-70717892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2877625	chr14:70717923-70717924	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs577312699	chr14:70717925-70717926	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs544693338	chr14:70717958-70717959	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558937431	chr14:70718011-70718012	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs141038531	chr14:70718044-70718045	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs530124193	chr14:70718074-70718075	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs548576994	chr14:70718089-70718090	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs570494615	chr14:70718090-70718091	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs1469252	chr14:70718106-70718107	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs528380441	chr14:70718121-70718122	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs546856564	chr14:70718127-70718128	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538161906	chr14:70718145-70718146	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs150517338	chr14:70718190-70718191	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs377396743	chr14:70718226-70718227	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs149704026	chr14:70718232-70718233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs568830659	chr14:70718288-70718289	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535872658	chr14:70718299-70718300	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs370633198	chr14:70718317-70718318	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554127058	chr14:70718320-70718321	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573239251	chr14:70718355-70718356	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534214906	chr14:70718373-70718374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs181520578	chr14:70718424-70718425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs184602874	chr14:70718505-70718506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs544447445	chr14:70718514-70718515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556642053	chr14:70718515-70718516	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70697400-70719400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:70701800-70721200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:70712600-70721000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr14:70716600-70717400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:70716600-70717600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr14:70716800-70717800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr14:70716800-70718000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr14:70717200-70718000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr14:70717200-70718000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr14:70717200-70718200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr14:70717400-70717800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr14:70717400-70717800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr14:70717400-70721000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:70717600-70721200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:70717800-70721000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr14:70717800-70721200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr14:70717800-70721200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr14:70718000-70721000	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr14:70718000-70721000	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr14:70718000-70721200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr14:70718200-70721200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:70719200-70719800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr14:70719400-70719600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr14:70719400-70719600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr14:70719400-70719800	Enhancers	Stomach Mucosa	stomach
26	chr14:70719600-70721200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr14:70719600-70721200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr14:70719800-70721200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:70721000-70721200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr14:70721000-70721200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:70721000-70721600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr14:70721000-70722000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr14:70721000-70722200	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr14:70721000-70722200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr14:70721000-70722200	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr14:70721000-70722200	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
37	chr14:70721000-70722200	Active TSS	HepG2	liver
38	chr14:70721000-70722600	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr14:70721000-70722800	Active TSS	H1 Cell Line	embryonic stem cell
40	chr14:70721000-70722800	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
41	chr14:70721000-70724000	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr14:70721200-70721400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr14:70721200-70721400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr14:70721200-70721400	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr14:70721200-70721400	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr14:70721200-70721400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:70721200-70721400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
48	chr14:70721200-70721400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr14:70721200-70721400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
50	chr14:70721200-70721400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood

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