Variant report

Variant	nsv983938
Chromosome Location	chr14:67656148-67670777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:67656240-67656390	SK-N-SH_RA	brain:	n/a	n/a
2	CTCF	chr14:67656180-67656330	HAc	cerebellar:	n/a	n/a
3	CTCF	chr14:67656080-67656230	GM12872	blood:	n/a	n/a
4	CTCF	chr14:67656240-67656390	MCF-7	breast:	n/a	n/a
5	CTCF	chr14:67656140-67656290	SK-N-SH_RA	brain:	n/a	n/a
6	CTCF	chr14:67656140-67656290	MCF-7	breast:	n/a	n/a
7	CTCF	chr14:67664800-67664950	NHEK	skin:	n/a	n/a
8	CTCF	chr14:67656285-67656296	MCF-7	breast:	n/a	n/a
9	FOSL2	chr14:67658377-67658964	SK-N-SH	brain:	n/a	n/a
10	GATA2	chr14:67664487-67664824	HUVEC	blood vessel:	n/a	n/a
11	GATA3	chr14:67664527-67664702	SH-SY5Y	brain:	n/a	n/a
12	MAFF	chr14:67656055-67656284	HepG2	liver:	n/a	n/a
13	MAFK	chr14:67656066-67656201	K562	blood:	n/a	chr14:67656074-67656085 chr14:67656070-67656086
14	MAFK	chr14:67655974-67656311	HepG2	liver:	n/a	chr14:67655999-67656014 chr14:67656074-67656085 chr14:67656070-67656086
15	MAFK	chr14:67655991-67656257	HepG2	liver:	n/a	chr14:67655999-67656014 chr14:67656074-67656085 chr14:67656070-67656086
16	MAFK	chr14:67656102-67656219	IMR90	lung:	n/a	n/a
17	MAX	chr14:67662157-67662186	NB4	blood:	n/a	n/a
18	MYC	chr14:67666479-67666481	MCF-7	breast:	n/a	n/a
19	MYC	chr14:67662050-67662229	K562	blood:	n/a	chr14:67662180-67662190
20	MYC	chr14:67666492-67666618	MCF-7	breast:	n/a	n/a
21	MYC	chr14:67666442-67666478	MCF-7	breast:	n/a	n/a
22	MYC	chr14:67666408-67666458	MCF-7	breast:	n/a	n/a
23	NFYA	chr14:67669879-67669953	GM12878	blood:	n/a	n/a
24	POLR2A	chr14:67666454-67666478	MCF-7	breast:	n/a	n/a
25	POLR2A	chr14:67666076-67666090	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr14:67666392-67666619	MCF-7	breast:	n/a	n/a
27	POLR2A	chr14:67658886-67659035	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr14:67665458-67665652	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr14:67666511-67666520	MCF-7	breast:	n/a	n/a
30	POLR2A	chr14:67666396-67666407	MCF-7	breast:	n/a	n/a
31	POLR2A	chr14:67655899-67656340	H1-neurons	neurons:	n/a	n/a
32	POLR2A	chr14:67658454-67658821	SK-N-SH	brain:	n/a	n/a
33	POLR2A	chr14:67665792-67665883	MCF-7	breast:	n/a	n/a
34	POLR2A	chr14:67666411-67666440	MCF-7	breast:	n/a	n/a
35	POLR2A	chr14:67666581-67666606	MCF-7	breast:	n/a	n/a
36	POLR2A	chr14:67666528-67666565	MCF-7	breast:	n/a	n/a
37	POLR2A	chr14:67655923-67656389	H1-neurons	neurons:	n/a	n/a
38	POLR2A	chr14:67666384-67666598	HepG2	liver:	n/a	n/a
39	POLR2A	chr14:67655906-67656407	PANC-1	pancreas:	n/a	n/a
40	REST	chr14:67655853-67656452	H1-neurons	neurons:	n/a	chr14:67656077-67656085
41	STAT3	chr14:67666243-67666295	MCF10A-Er-Src	breast:	n/a	n/a
42	TAL1	chr14:67662066-67662320	K562	blood:	n/a	n/a
43	TCF12	chr14:67659019-67659480	SK-N-SH	brain:	n/a	n/a
44	ZNF384	chr14:67661052-67661148	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67656241-67656291	SAEC	small airway:	n/a
2	chr14:67665364-67665414	NB4	blood:	n/a
3	chr14:67665364-67665414	SKMC	muscle:	n/a
4	chr14:67656241-67656291	NB4	blood:	n/a
5	chr14:67665364-67665414	HAEpiC	amniotic membrane:	n/a
6	chr14:67656241-67656291	GM12892	blood:	n/a
7	chr14:67665364-67665414	HCF	heart:	n/a
8	chr14:67665364-67665414	MCF-7	breast:	n/a
9	chr14:67656241-67656291	Caco-2	colon:	n/a
10	chr14:67665364-67665414	HMEC	breast:	n/a
11	chr14:67656241-67656291	MCF-7	breast:	n/a
12	chr14:67665364-67665414	GM12892	blood:	n/a
13	chr14:67665364-67665414	A549	lung:	n/a
14	chr14:67665364-67665414	Jurkat	blood:	n/a
15	chr14:67656241-67656291	PFSK-1	brain:	n/a
16	chr14:67665364-67665414	ovcar-3	ovarian:	n/a
17	chr14:67665364-67665414	SK-N-MC	brain:	n/a
18	chr14:67665364-67665414	U87	brain:	n/a
19	chr14:67656241-67656291	CMK	blood:	n/a
20	chr14:67656241-67656291	H1-hESC	embryonic stem cell:	embryo
21	chr14:67665364-67665414	HPAEpiC	pulmonary alveolar:	n/a
22	chr14:67656241-67656291	HAEpiC	amniotic membrane:	n/a
23	chr14:67656241-67656291	NHDF-neo	bronchial:	n/a
24	chr14:67656241-67656291	NHBE	bronchial:	n/a
25	chr14:67656241-67656291	HCPEpiC	choroid plexus:	n/a
26	chr14:67656241-67656291	HRCEpiC	kidney:	n/a
27	chr14:67665364-67665414	HCT-116	colon:	n/a
28	chr14:67665364-67665414	HCM	heart:	n/a
29	chr14:67656241-67656291	SK-N-MC	brain:	n/a
30	chr14:67656241-67656291	ovcar-3	ovarian:	n/a
31	chr14:67665364-67665414	MCF10A-Er-Src	breast:	n/a
32	chr14:67665364-67665414	IMR90	lung:	fetal
33	chr14:67665364-67665414	K562	blood:	n/a
34	chr14:67656241-67656291	AG09319	gingival:	n/a
35	chr14:67656241-67656291	HMEC	breast:	n/a
36	chr14:67656241-67656291	GM12891	blood:	n/a
37	chr14:67656241-67656291	BE2_C	brain:	n/a
38	chr14:67656241-67656291	Hepatocyte	liver:	n/a
39	chr14:67665364-67665414	HRE	kidney:	n/a
40	chr14:67656241-67656291	ECC-1	luminal epithelium:	n/a
41	chr14:67665364-67665414	BJ	skin:	n/a
42	chr14:67656241-67656291	PANC-1	pancreas:	n/a
43	chr14:67665364-67665414	HUVEC	blood vessel:	n/a
44	chr14:67665364-67665414	PANC-1	pancreas:	n/a
45	chr14:67656241-67656291	HCM	heart:	n/a
46	chr14:67656241-67656291	Jurkat	blood:	n/a
47	chr14:67665364-67665414	AG09309	skin:	n/a
48	chr14:67656241-67656291	RPTEC	kidney:	n/a
49	chr14:67656241-67656291	HUVEC	blood vessel:	n/a
50	chr14:67656241-67656291	AG04450	lung:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:67668079..67670109-chr14:67706345..67708659,2	MCF-7	breast:
2	chr14:67670737..67673131-chr14:67673684..67677270,3	K562	blood:
3	chr14:67663302..67666275-chr14:67670215..67672411,3	K562	blood:
4	chr14:67665237..67668000-chr14:67705488..67708368,2	MCF-7	breast:
5	chr14:67667112..67669927-chr14:67673384..67675184,2	MCF-7	breast:
6	chr14:67663302..67666275-chr14:67670215..67672411,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPHN-2	chr14:67664853-67665037	NONHSAT037431
2	lnc-GPHN-2	chr14:67669885-67670004	NONHSAT037431
3	lnc-GPHN-2	chr14:67664006-67664074	NONHSAT037431

No data

Variant related genes	Relation type
FAM71D	TF binding region
ENSG00000258988	TF binding region
FAM71D	CpG island
ENSG00000258988	CpG island
ENSG00000258988	chromatin interactions
ENSG00000172717	chromatin interactions
ENSG00000072415	chromatin interactions

Extended variants
information (count: 556 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530948716	chr14:67656204-67656205	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs549550488	chr14:67656210-67656211	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs567820873	chr14:67656283-67656284	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs535247089	chr14:67656310-67656311	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs549727080	chr14:67656342-67656343	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs547287672	chr14:67656347-67656348	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs557498628	chr14:67656361-67656362	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs571999899	chr14:67656368-67656369	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs567946790	chr14:67656393-67656394	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs372960086	chr14:67656408-67656409	Weak transcription Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs539406315	chr14:67656432-67656433	Weak transcription Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs557511063	chr14:67656454-67656455	Weak transcription Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs373247796	chr14:67656546-67656547	Weak transcription Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs528914458	chr14:67656594-67656595	Weak transcription Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs186078043	chr14:67656639-67656640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536703311	chr14:67656661-67656662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555051007	chr14:67656682-67656683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573464192	chr14:67656683-67656684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376544347	chr14:67656691-67656692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7150934	chr14:67656715-67656716	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs565785536	chr14:67656731-67656732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111315013	chr14:67656732-67656733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559197684	chr14:67656761-67656762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143684729	chr14:67656767-67656768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35176263	chr14:67656785-67656786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs28552859	chr14:67656786-67656787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs71129813	chr14:67656805-67656806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs8014435	chr14:67656807-67656808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs199680550	chr14:67656808-67656809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373691563	chr14:67656832-67656833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545375002	chr14:67656901-67656902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543133394	chr14:67656911-67656912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112895464	chr14:67656917-67656918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368581468	chr14:67656944-67656945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142361812	chr14:67656945-67656946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs57073031	chr14:67656951-67656952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs397978046	chr14:67656958-67656959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371703406	chr14:67657004-67657005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530945113	chr14:67657043-67657044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549175497	chr14:67657044-67657045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561391143	chr14:67657050-67657051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528677270	chr14:67657051-67657052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373353330	chr14:67657096-67657097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547251008	chr14:67657117-67657118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190402475	chr14:67657121-67657122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113066287	chr14:67657142-67657143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375309721	chr14:67657143-67657144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571963225	chr14:67657160-67657161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147672991	chr14:67657220-67657221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111659767	chr14:67657227-67657228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67618400-67658200	Weak transcription	Brain Angular Gyrus	brain
2	chr14:67639600-67658600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr14:67645800-67656400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr14:67645800-67658200	Weak transcription	Brain Anterior Caudate	brain
5	chr14:67646200-67656200	Weak transcription	Psoas Muscle	Psoas
6	chr14:67647800-67658400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr14:67648200-67656200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:67648200-67658200	Weak transcription	Brain Hippocampus Middle	brain
9	chr14:67648200-67658200	Weak transcription	Brain Substantia Nigra	brain
10	chr14:67648200-67660400	Weak transcription	Ovary	ovary
11	chr14:67648400-67658000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr14:67648400-67658000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr14:67648400-67658400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr14:67648400-67658800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr14:67652400-67656200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr14:67652600-67656200	Enhancers	HMEC	breast
17	chr14:67653200-67656200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr14:67653200-67656400	Enhancers	Osteobl	bone
19	chr14:67653400-67656200	Enhancers	NH-A	brain
20	chr14:67653600-67656200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr14:67653600-67656400	Enhancers	Placenta	Placenta
22	chr14:67654200-67656200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr14:67654600-67657800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr14:67654800-67658200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr14:67654800-67658600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr14:67654800-67658600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr14:67655000-67658400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr14:67655000-67661800	Weak transcription	A549	lung
29	chr14:67655200-67658200	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr14:67655400-67656800	Enhancers	Fetal Thymus	thymus
31	chr14:67655400-67658200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr14:67655400-67658200	Weak transcription	HSMMtube	muscle
33	chr14:67655400-67658800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr14:67655800-67656200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr14:67655800-67656200	Active TSS	HepG2	liver
36	chr14:67655800-67656400	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr14:67656000-67656200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr14:67656000-67656200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr14:67656000-67656200	Enhancers	Aorta	Aorta
40	chr14:67656000-67656200	Enhancers	Liver	Liver
41	chr14:67656000-67656200	Enhancers	Fetal Stomach	stomach
42	chr14:67656000-67656200	Enhancers	Spleen	Spleen
43	chr14:67656000-67656200	Enhancers	HSMM	muscle
44	chr14:67656000-67656400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr14:67656000-67656400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr14:67656000-67656400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr14:67656000-67656400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr14:67656000-67656400	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr14:67656000-67656400	Active TSS	Rectal Mucosa Donor 29	rectum
50	chr14:67656000-67656400	Flanking Active TSS	GM12878-XiMat	blood

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