Variant report

Variant	esv3345682
Chromosome Location	chr14:70689349-70691247
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:70690400-70690968	K562	blood:	n/a	n/a
2	BHLHE40	chr14:70690031-70690525	K562	blood:	n/a	n/a
3	CBX3	chr14:70690533-70690798	K562	blood:	n/a	n/a
4	CEBPB	chr14:70690174-70690468	HepG2	liver:	n/a	n/a
5	CEBPB	chr14:70690188-70690384	A549	lung:	n/a	n/a
6	CEBPB	chr14:70690311-70690379	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr14:70690132-70690487	K562	blood:	n/a	n/a
8	CHD2	chr14:70690629-70690641	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr14:70690339-70690646	K562	blood:	n/a	n/a
10	CTCF	chr14:70690620-70690770	HRE	kidney:	n/a	n/a
11	CTCF	chr14:70690600-70690750	K562	blood:	n/a	n/a
12	CTCF	chr14:70690560-70690710	GM12874	blood:	n/a	n/a
13	CTCF	chr14:70690600-70690750	GM12869	blood:	n/a	n/a
14	CTCF	chr14:70690440-70690590	BE2_C	brain:	n/a	n/a
15	CTCF	chr14:70690600-70690750	HCM	heart:	n/a	n/a
16	CTCF	chr14:70690394-70690787	K562	blood:	n/a	n/a
17	CTCF	chr14:70690540-70690690	GM12868	blood:	n/a	n/a
18	CTCF	chr14:70690441-70690790	GM12878	blood:	n/a	n/a
19	CTCF	chr14:70690560-70690710	NB4	blood:	n/a	n/a
20	CTCF	chr14:70690580-70690730	HEK293	kidney:	n/a	n/a
21	CTCF	chr14:70690643-70690682	HepG2	liver:	n/a	n/a
22	CTCF	chr14:70690600-70690750	GM12878	blood:	n/a	n/a
23	CTCF	chr14:70690540-70690690	GM12874	blood:	n/a	n/a
24	CTCF	chr14:70690536-70690712	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr14:70690600-70690750	HEK293	kidney:	n/a	n/a
26	CTCF	chr14:70690571-70690686	GM12878	blood:	n/a	n/a
27	CTCF	chr14:70690451-70690493	K562	blood:	n/a	n/a
28	CTCF	chr14:70690520-70690670	K562	blood:	n/a	n/a
29	CTCF	chr14:70690439-70690752	K562	blood:	n/a	n/a
30	CTCF	chr14:70690580-70690730	HepG2	liver:	n/a	n/a
31	CTCF	chr14:70690580-70690730	A549	lung:	n/a	n/a
32	CTCF	chr14:70690600-70690750	HAc	cerebellar:	n/a	n/a
33	CTCF	chr14:70690600-70690750	GM12871	blood:	n/a	n/a
34	CTCF	chr14:70690546-70690652	GM12891	blood:	n/a	n/a
35	CTCF	chr14:70690552-70690696	HepG2	liver:	n/a	n/a
36	CTCF	chr14:70690498-70690737	K562	blood:	n/a	n/a
37	CTCF	chr14:70690560-70690710	HPF	lung:	n/a	n/a
38	CTCF	chr14:70690540-70690690	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr14:70690580-70690730	GM12878	blood:	n/a	n/a
40	CTCF	chr14:70690571-70690706	GM19240	blood:	n/a	n/a
41	CTCF	chr14:70690580-70690730	GM12871	blood:	n/a	n/a
42	CTCF	chr14:70690540-70690690	BE2_C	brain:	n/a	n/a
43	CTCF	chr14:70690271-70690824	K562	blood:	n/a	n/a
44	CTCF	chr14:70690600-70690750	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr14:70690476-70690754	H1-hESC	embryonic stem cell:	n/a	n/a
46	CUX1	chr14:70690389-70690827	K562	blood:	n/a	n/a
47	E2F6	chr14:70690547-70690694	K562	blood:	n/a	n/a
48	ELF1	chr14:70690229-70690741	K562	blood:	n/a	n/a
49	ELF1	chr14:70690364-70690694	GM12878	blood:	n/a	n/a
50	EP300	chr14:70690232-70690860	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70690454-70690504	AG09319	gingival:	n/a
2	chr14:70690454-70690504	PANC-1	pancreas:	n/a
3	chr14:70690525-70690575	ovcar-3	ovarian:	n/a
4	chr14:70690454-70690504	NH-A	brain:	n/a
5	chr14:70690454-70690504	RPTEC	kidney:	n/a
6	chr14:70690538-70690588	HUVEC	blood vessel:	n/a
7	chr14:70690538-70690588	T-47D	breast:	n/a
8	chr14:70690538-70690588	GM12892	blood:	n/a
9	chr14:70690538-70690588	HCM	heart:	n/a
10	chr14:70690454-70690504	HEEpiC	esophagus:	n/a
11	chr14:70690454-70690504	HRE	kidney:	n/a
12	chr14:70690454-70690504	ovcar-3	ovarian:	n/a
13	chr14:70690538-70690588	H1-hESC	embryonic stem cell:	embryo
14	chr14:70690454-70690504	GM06990	blood:	n/a
15	chr14:70690525-70690575	AG09309	skin:	n/a
16	chr14:70690525-70690575	LNCaP	prostate:	n/a
17	chr14:70690454-70690504	SK-N-SH	brain:	n/a
18	chr14:70690454-70690504	Hela-S3	cervix:	n/a
19	chr14:70690525-70690575	HEK293	kidney:	embryo
20	chr14:70690525-70690575	NHBE	bronchial:	n/a
21	chr14:70690454-70690504	AG04450	lung:	fetal
22	chr14:70690525-70690575	SK-N-SH_RA	brain:	n/a
23	chr14:70690454-70690504	GM12891	blood:	n/a
24	chr14:70690525-70690575	NHDF-neo	bronchial:	n/a
25	chr14:70690525-70690575	SAEC	small airway:	n/a
26	chr14:70690525-70690575	HCPEpiC	choroid plexus:	n/a
27	chr14:70690525-70690575	Hela-S3	cervix:	n/a
28	chr14:70690454-70690504	HRCEpiC	kidney:	n/a
29	chr14:70690525-70690575	HepG2	liver:	n/a
30	chr14:70690454-70690504	A549	lung:	n/a
31	chr14:70690538-70690588	HEK293	kidney:	embryo
32	chr14:70690538-70690588	HepG2	liver:	n/a
33	chr14:70690454-70690504	HCF	heart:	n/a
34	chr14:70690454-70690504	PrEC	prostate:	n/a
35	chr14:70690525-70690575	RPTEC	kidney:	n/a
36	chr14:70690538-70690588	NT2-D1	testis:	n/a
37	chr14:70690538-70690588	LNCaP	prostate:	n/a
38	chr14:70690525-70690575	SK-N-MC	brain:	n/a
39	chr14:70690538-70690588	AG04450	lung:	fetal
40	chr14:70690525-70690575	BJ	skin:	n/a
41	chr14:70690454-70690504	HL-60	blood:	n/a
42	chr14:70690538-70690588	HPAEpiC	pulmonary alveolar:	n/a
43	chr14:70690454-70690504	HNPCEpiC	eye:	n/a
44	chr14:70690525-70690575	Jurkat	blood:	n/a
45	chr14:70690525-70690575	HL-60	blood:	n/a
46	chr14:70690538-70690588	MCF10A-Er-Src	breast:	n/a
47	chr14:70690454-70690504	NHBE	bronchial:	n/a
48	chr14:70690538-70690588	HEEpiC	esophagus:	n/a
49	chr14:70690454-70690504	HEK293	kidney:	embryo
50	chr14:70690525-70690575	Caco-2	colon:	n/a

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No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:70668752..70670788-chr14:70688180..70689726,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMOC1-2	chr14:70690493-70690565	ENSG00000258422
2	lnc-SMOC1-2	chr14:70690482-70690565	ENSG00000258422
3	lnc-SMOC1-2	chr14:70690724-70690914	ENSG00000258422

No data

Variant related genes	Relation type
ENSG00000258422	TF binding region
ENSG00000258422	CpG island

Extended variants
information (count: 47 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:47 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141134638	chr14:70689399-70689400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576168439	chr14:70689450-70689451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113213138	chr14:70689491-70689492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190348107	chr14:70689503-70689504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554129217	chr14:70689611-70689612	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs545059086	chr14:70689668-70689669	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs61979481	chr14:70689710-70689711	Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs117504607	chr14:70689723-70689724	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs567229272	chr14:70689744-70689745	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs535371954	chr14:70689803-70689804	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs377364016	chr14:70689852-70689853	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs553297039	chr14:70689858-70689859	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs553702972	chr14:70689993-70689994	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs114560836	chr14:70690010-70690011	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs538924028	chr14:70690049-70690050	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs67403471	chr14:70690053-70690054	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs76983211	chr14:70690073-70690074	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs527463562	chr14:70690080-70690081	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs182902031	chr14:70690169-70690170	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs202062294	chr14:70690219-70690220	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs57277684	chr14:70690240-70690241	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs140059974	chr14:70690241-70690242	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs575672056	chr14:70690251-70690252	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs556906830	chr14:70690321-70690322	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs78122957	chr14:70690387-70690388	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs561159451	chr14:70690454-70690455	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs572893666	chr14:70690471-70690472	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs10459537	chr14:70690476-70690477	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs559224510	chr14:70690492-70690493	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs533017557	chr14:70690523-70690524	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs78621863	chr14:70690557-70690558	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs551302385	chr14:70690588-70690589	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs573277687	chr14:70690589-70690590	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs8012417	chr14:70690630-70690631	Active TSS Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs530545189	chr14:70690647-70690648	Active TSS Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs549045011	chr14:70690681-70690682	Active TSS Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs74062854	chr14:70690798-70690799	Active TSS Bivalent/Poised TSS Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs9323533	chr14:70690877-70690878	Active TSS Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs546580863	chr14:70690918-70690919	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs115731577	chr14:70690924-70690925	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs6573939	chr14:70690955-70690956	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs187641510	chr14:70690985-70690986	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs532800027	chr14:70691021-70691022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575779607	chr14:70691092-70691093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75454938	chr14:70691219-70691220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555043469	chr14:70691224-70691225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544866643	chr14:70691243-70691244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70687800-70689600	Weak transcription	K562	blood
2	chr14:70689600-70690800	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr14:70689600-70690800	Active TSS	K562	blood
4	chr14:70689600-70691000	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr14:70689800-70690200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr14:70689800-70690600	Active TSS	Primary hematopoietic stem cells	blood
7	chr14:70689800-70690800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr14:70689800-70690800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr14:70690000-70690200	Active TSS	Fetal Muscle Leg	muscle
10	chr14:70690000-70690600	Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr14:70690000-70690600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr14:70690000-70690600	Active TSS	HSMM	muscle
13	chr14:70690000-70690600	Active TSS	NH-A	brain
14	chr14:70690000-70690800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr14:70690000-70691000	Active TSS	HSMMtube	muscle
16	chr14:70690200-70690400	Bivalent/Poised TSS	Fetal Intestine Large	intestine
17	chr14:70690200-70690400	Active TSS	Placenta	Placenta
18	chr14:70690200-70690400	Bivalent/Poised TSS	Left Ventricle	heart
19	chr14:70690200-70690400	Active TSS	GM12878-XiMat	blood
20	chr14:70690200-70690600	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr14:70690200-70690600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr14:70690200-70690600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:70690200-70690600	Active TSS	Brain Cingulate Gyrus	brain
24	chr14:70690200-70690600	Active TSS	Duodenum Mucosa	Duodenum
25	chr14:70690200-70690600	Bivalent/Poised TSS	Fetal Intestine Small	intestine
26	chr14:70690200-70690600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
27	chr14:70690200-70690600	Active TSS	Fetal Thymus	thymus
28	chr14:70690200-70690600	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
29	chr14:70690200-70690600	Bivalent/Poised TSS	NHEK	skin
30	chr14:70690200-70690800	Active TSS	H1 Cell Line	embryonic stem cell
31	chr14:70690200-70690800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr14:70690200-70690800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr14:70690200-70690800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr14:70690200-70690800	Active TSS	Adipose Nuclei	Adipose
35	chr14:70690200-70690800	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr14:70690200-70690800	Active TSS	Fetal Stomach	stomach
37	chr14:70690200-70690800	Active TSS	Psoas Muscle	Psoas
38	chr14:70690200-70690800	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
39	chr14:70690400-70690600	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr14:70690400-70690600	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
41	chr14:70690400-70690600	Flanking Bivalent TSS/Enh	Placenta	Placenta
42	chr14:70690400-70690600	Enhancers	Gastric	stomach
43	chr14:70690400-70690600	Flanking Bivalent TSS/Enh	Left Ventricle	heart
44	chr14:70690400-70690600	Active TSS	Pancreas	Pancrea
45	chr14:70690400-70690600	Flanking Active TSS	GM12878-XiMat	blood
46	chr14:70690600-70690800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
47	chr14:70690600-70690800	Bivalent/Poised TSS	Fetal Intestine Large	intestine
48	chr14:70690600-70690800	Flanking Active TSS	Pancreas	Pancrea
49	chr14:70690600-70690800	Flanking Active TSS	HSMM	muscle
50	chr14:70690600-70690800	Flanking Active TSS	NH-A	brain

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