Variant report

Variant	esv3324236
Chromosome Location	chr14:21565662-21567360
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	chr14:21567064-21567210	HepG2	liver:	n/a	n/a
2	BACH1	chr14:21566963-21567035	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr14:21566956-21567119	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr14:21566992-21567190	H1-hESC	embryonic stem cell:	n/a	n/a
5	CCNT2	chr14:21566640-21566835	K562	blood:	n/a	chr14:21566787-21566796
6	CEBPB	chr14:21566797-21567029	Hela-S3	cervix:	n/a	n/a
7	CEBPD	chr14:21565859-21566462	HepG2	liver:	n/a	n/a
8	CEBPD	chr14:21566491-21567051	HepG2	liver:	n/a	n/a
9	CHD2	chr14:21566761-21567020	H1-hESC	embryonic stem cell:	n/a	chr14:21566788-21566798
10	CHD2	chr14:21565877-21566217	Hela-S3	cervix:	n/a	chr14:21566153-21566163
11	CHD2	chr14:21566675-21567172	HepG2	liver:	n/a	chr14:21566788-21566798
12	CHD2	chr14:21565722-21566195	HepG2	liver:	n/a	chr14:21566153-21566163
13	CHD2	chr14:21566647-21567112	Hela-S3	cervix:	n/a	chr14:21566660-21566670 chr14:21566788-21566798
14	CHD2	chr14:21566022-21566147	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr14:21566900-21567050	GM12875	blood:	n/a	n/a
16	CTCF	chr14:21566700-21566850	GM12875	blood:	n/a	chr14:21566782-21566791
17	CTCF	chr14:21566700-21566850	SK-N-SH_RA	brain:	n/a	chr14:21566782-21566791
18	CTCF	chr14:21566740-21566890	GM12866	blood:	n/a	chr14:21566782-21566791
19	CTCF	chr14:21566771-21566828	GM12878	blood:	n/a	chr14:21566782-21566791
20	CTCF	chr14:21566700-21566850	HepG2	liver:	n/a	chr14:21566782-21566791
21	CTCF	chr14:21566760-21566910	Hela-S3	cervix:	n/a	chr14:21566782-21566791
22	CTCF	chr14:21566660-21566810	HUVEC	blood vessel:	n/a	chr14:21566782-21566791
23	CTCF	chr14:21566743-21566768	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr14:21566792-21566814	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr14:21566740-21566890	AG04450	lung:	n/a	chr14:21566782-21566791
26	CTCF	chr14:21566776-21566831	IMR90	lung:	n/a	chr14:21566782-21566791
27	CTCF	chr14:21566644-21566943	K562	blood:	n/a	chr14:21566782-21566791 chr14:21566658-21566671
28	CTCF	chr14:21566680-21566830	SAEC	small airway:	n/a	chr14:21566782-21566791
29	CTCF	chr14:21566720-21566870	GM12873	blood:	n/a	chr14:21566782-21566791
30	CTCF	chr14:21566920-21567070	HRE	kidney:	n/a	n/a
31	CTCF	chr14:21566860-21567010	GM12873	blood:	n/a	n/a
32	CTCF	chr14:21566610-21566922	H1-hESC	embryonic stem cell:	n/a	chr14:21566782-21566791 chr14:21566658-21566671
33	CTCF	chr14:21566700-21566850	GM12866	blood:	n/a	chr14:21566782-21566791
34	CTCF	chr14:21566780-21566930	AG04449	skin:	n/a	chr14:21566782-21566791
35	CTCF	chr14:21566800-21566950	GM12864	blood:	n/a	n/a
36	CTCF	chr14:21566760-21566910	HMEC	breast:	n/a	chr14:21566782-21566791
37	CTCF	chr14:21566760-21566910	HRPEpiC	eye:	n/a	chr14:21566782-21566791
38	CTCF	chr14:21566740-21566890	HepG2	liver:	n/a	chr14:21566782-21566791
39	CTCF	chr14:21566700-21566850	GM12874	blood:	n/a	chr14:21566782-21566791
40	CTCF	chr14:21566740-21566890	Caco-2	colon:	n/a	chr14:21566782-21566791
41	CTCF	chr14:21566760-21566910	GM06990	blood:	n/a	chr14:21566782-21566791
42	CTCF	chr14:21566820-21566970	AG09309	skin:	n/a	n/a
43	CTCF	chr14:21566773-21566788	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr14:21566720-21566870	Caco-2	colon:	n/a	chr14:21566782-21566791
45	CTCF	chr14:21566832-21566843	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:21566645-21566908	K562	blood:	n/a	chr14:21566782-21566791 chr14:21566658-21566671
47	CTCF	chr14:21566780-21566930	AoAF	blood vessel:	n/a	chr14:21566782-21566791
48	CTCF	chr14:21566840-21566990	GM12874	blood:	n/a	n/a
49	CTCF	chr14:21566680-21566830	Hela-S3	cervix:	n/a	chr14:21566782-21566791
50	CTCF	chr14:21566920-21567070	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21566452-21566502	MCF10A-Er-Src	breast:	n/a
2	chr14:21566084-21566134	PrEC	prostate:	n/a
3	chr14:21566452-21566502	MCF10A-Er-Src	breast:	n/a
4	chr14:21566084-21566134	PrEC	prostate:	n/a
5	chr14:21566452-21566502	HRE	kidney:	n/a
6	chr14:21566698-21566748	HNPCEpiC	eye:	n/a
7	chr14:21566084-21566134	NHDF-neo	bronchial:	n/a
8	chr14:21566698-21566748	HCPEpiC	choroid plexus:	n/a
9	chr14:21566698-21566748	GM12892	blood:	n/a
10	chr14:21566698-21566748	PrEC	prostate:	n/a
11	chr14:21566452-21566502	GM06990	blood:	n/a
12	chr14:21567333-21567383	SAEC	small airway:	n/a
13	chr14:21567020-21567070	PANC-1	pancreas:	n/a
14	chr14:21567164-21567214	LNCaP	prostate:	n/a
15	chr14:21566863-21566913	NB4	blood:	n/a
16	chr14:21567333-21567383	HCT-116	colon:	n/a
17	chr14:21567020-21567070	AG04450	lung:	fetal
18	chr14:21566698-21566748	AG09319	gingival:	n/a
19	chr14:21566863-21566913	PANC-1	pancreas:	n/a
20	chr14:21566698-21566748	RPTEC	kidney:	n/a
21	chr14:21566084-21566134	LNCaP	prostate:	n/a
22	chr14:21566452-21566502	NB4	blood:	n/a
23	chr14:21566452-21566502	AG04449	skin:	fetal
24	chr14:21567333-21567383	Hela-S3	cervix:	n/a
25	chr14:21567333-21567383	HEEpiC	esophagus:	n/a
26	chr14:21567164-21567214	SK-N-MC	brain:	n/a
27	chr14:21566863-21566913	HUVEC	blood vessel:	n/a
28	chr14:21566863-21566913	ovcar-3	ovarian:	n/a
29	chr14:21566452-21566502	AG09309	skin:	n/a
30	chr14:21566863-21566913	LNCaP	prostate:	n/a
31	chr14:21567164-21567214	IMR90	lung:	fetal
32	chr14:21567020-21567070	HRE	kidney:	n/a
33	chr14:21566452-21566502	ECC-1	luminal epithelium:	n/a
34	chr14:21567164-21567214	HEK293	kidney:	embryo
35	chr14:21566084-21566134	PFSK-1	brain:	n/a
36	chr14:21567020-21567070	AG10803	skin:	n/a
37	chr14:21567333-21567383	ECC-1	luminal epithelium:	n/a
38	chr14:21566084-21566134	NH-A	brain:	n/a
39	chr14:21567020-21567070	IMR90	lung:	fetal
40	chr14:21566863-21566913	SK-N-SH	brain:	n/a
41	chr14:21566863-21566913	AG04449	skin:	fetal
42	chr14:21566863-21566913	BJ	skin:	n/a
43	chr14:21567333-21567383	NB4	blood:	n/a
44	chr14:21566698-21566748	PFSK-1	brain:	n/a
45	chr14:21567333-21567383	Hepatocyte	liver:	n/a
46	chr14:21567333-21567383	AG04449	skin:	fetal
47	chr14:21566452-21566502	HMEC	breast:	n/a
48	chr14:21567164-21567214	H1-hESC	embryonic stem cell:	embryo
49	chr14:21567164-21567214	ECC-1	luminal epithelium:	n/a
50	chr14:21566084-21566134	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr14:21535130..21541812-chr14:21564802..21576767,22	MCF-7	breast:
2	chr14:21566818..21567426-chr5:145582956..145583681,2	Hela-S3	cervix:
3	chr14:21560808..21562943-chr14:21563849..21565971,2	K562	blood:
4	chr14:21488163..21490230-chr14:21563775..21566660,2	K562	blood:
5	chr14:21538435..21540879-chr14:21565246..21568452,4	K562	blood:
6	chr14:21493156..21496539-chr14:21563277..21566869,4	K562	blood:
7	chr14:21559218..21562308-chr14:21563084..21566776,3	K562	blood:
8	chr14:21534879..21542621-chr14:21563384..21568050,9	MCF-7	breast:
9	chr14:21493465..21495146-chr14:21564517..21566869,2	K562	blood:
10	chr14:21529965..21532217-chr14:21564746..21566795,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDRG2-4	chr14:21566970-21567070	NONHSAT035653

Variant related genes	Relation type
TMEM253	TF binding region
ZNF219	TF binding region
TMEM253	CpG island
ZNF219	CpG island
ENSG00000165795	chromatin interactions
ENSG00000091009	chromatin interactions
ENSG00000165804	chromatin interactions
ENSG00000165801	chromatin interactions

Extended variants
information (count: 24 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551772750	chr14:21565707-21565708	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs369793244	chr14:21565732-21565733	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs537593788	chr14:21565795-21565796	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs550759574	chr14:21565834-21565835	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs567549041	chr14:21565971-21565972	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs536533535	chr14:21565989-21565990	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs2771315	chr14:21566003-21566004	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs573505502	chr14:21566030-21566031	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs10132732	chr14:21566277-21566278	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs534278641	chr14:21566642-21566643	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs557745933	chr14:21566806-21566807	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs543586855	chr14:21566926-21566927	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs563448693	chr14:21567006-21567007	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
14	rs191453915	chr14:21567072-21567073	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs542857911	chr14:21567075-21567076	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs559356509	chr14:21567111-21567112	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs551555110	chr14:21567132-21567133	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs528390137	chr14:21567165-21567166	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs551445571	chr14:21567195-21567196	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs565327875	chr14:21567233-21567234	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs141801608	chr14:21567236-21567237	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs564627691	chr14:21567282-21567283	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs12889457	chr14:21567333-21567334	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs143814256	chr14:21567336-21567337	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21555800-21566200	Weak transcription	HSMM	muscle
2	chr14:21558800-21566600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr14:21559800-21566600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr14:21560800-21565800	Weak transcription	Small Intestine	intestine
5	chr14:21561000-21565800	Weak transcription	Ovary	ovary
6	chr14:21561600-21566600	Weak transcription	Gastric	stomach
7	chr14:21561600-21566800	Weak transcription	Spleen	Spleen
8	chr14:21562000-21566000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr14:21562200-21566800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr14:21562600-21566800	Weak transcription	Liver	Liver
11	chr14:21563800-21565800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:21564200-21565800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr14:21564400-21565800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr14:21564400-21566000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr14:21564400-21566000	Enhancers	Left Ventricle	heart
16	chr14:21564600-21565800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
17	chr14:21564600-21565800	Flanking Active TSS	Brain Germinal Matrix	brain
18	chr14:21564600-21566000	Enhancers	Brain Cingulate Gyrus	brain
19	chr14:21564600-21566600	Weak transcription	Osteobl	bone
20	chr14:21564600-21566800	Enhancers	Placenta	Placenta
21	chr14:21564800-21565800	Flanking Active TSS	NHEK	skin
22	chr14:21564800-21566000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:21564800-21566000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:21564800-21566000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr14:21564800-21567000	Active TSS	Fetal Brain Female	brain
26	chr14:21565000-21566000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr14:21565000-21566000	Flanking Active TSS	A549	lung
28	chr14:21565000-21566000	Flanking Active TSS	HMEC	breast
29	chr14:21565000-21567400	Active TSS	Sigmoid Colon	Sigmoid Colon
30	chr14:21565200-21565800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr14:21565200-21565800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr14:21565200-21565800	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr14:21565200-21565800	Enhancers	Primary T cells fromperipheralblood	blood
34	chr14:21565200-21565800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr14:21565200-21565800	Flanking Active TSS	Colon Smooth Muscle	Colon
36	chr14:21565200-21565800	Enhancers	Lung	lung
37	chr14:21565200-21565800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr14:21565200-21565800	Flanking Active TSS	Thymus	Thymus
39	chr14:21565200-21565800	Enhancers	K562	blood
40	chr14:21565200-21565800	Flanking Active TSS	NHDF-Ad	bronchial
41	chr14:21565200-21566000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr14:21565200-21566000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr14:21565200-21566000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr14:21565200-21566000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr14:21565200-21566000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr14:21565200-21566000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr14:21565200-21566000	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr14:21565200-21566000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr14:21565200-21566000	Flanking Active TSS	Fetal Intestine Small	intestine
50	chr14:21565200-21566000	Active TSS	Fetal Kidney	kidney

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