Variant report

Variant	esv2761846
Chromosome Location	chr14:79522198-79629157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:240)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:240 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:79557750-79558236	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr14:79557693-79558133	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:79560132-79560350	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr14:79557757-79558076	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr14:79557773-79558093	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr14:79559878-79560134	HepG2	liver:	n/a	chr14:79560020-79560031 chr14:79560018-79560031
7	CEBPB	chr14:79557714-79558287	H1-hESC	embryonic stem cell:	n/a	chr14:79558092-79558105 chr14:79558092-79558103
8	CEBPB	chr14:79523178-79523744	IMR90	lung:	n/a	n/a
9	CEBPB	chr14:79601619-79601724	IMR90	lung:	n/a	chr14:79601695-79601708
10	CEBPB	chr14:79605965-79606029	HepG2	liver:	n/a	n/a
11	CTCF	chr14:79558020-79558170	Caco-2	colon:	n/a	n/a
12	CTCF	chr14:79558064-79558189	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr14:79558070-79558173	Lung_OC	lung:	n/a	n/a
14	CTCF	chr14:79558020-79558170	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr14:79533567-79533689	GM13977	blood:	n/a	n/a
16	CTCF	chr14:79558100-79558250	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:79558031-79558198	GM12878	blood:	n/a	n/a
18	CTCF	chr14:79558040-79558187	Pancreas_OC	pancreas:	n/a	n/a
19	CTCF	chr14:79558046-79558193	LNCaP	prostate:	n/a	n/a
20	CTCF	chr14:79558045-79558195	Medullo	brain:	n/a	n/a
21	CTCF	chr14:79558096-79558176	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr14:79546412-79546471	GM20000	blood:	n/a	n/a
23	CTCF	chr14:79558020-79558170	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr14:79557960-79558110	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr14:79558058-79558175	MCF-7	breast:	n/a	n/a
26	CTCF	chr14:79558051-79558196	MCF-7	breast:	n/a	n/a
27	CTCF	chr14:79557921-79558251	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr14:79557960-79558110	Caco-2	colon:	n/a	n/a
29	CTCF	chr14:79557980-79558130	MCF-7	breast:	n/a	n/a
30	CTCF	chr14:79546420-79546570	WERI-Rb-1	eye:	n/a	chr14:79546476-79546489
31	CTCF	chr14:79628020-79628170	GM12875	blood:	n/a	n/a
32	CTCF	chr14:79598444-79598545	GM13976	blood:	n/a	n/a
33	CTCF	chr14:79543629-79543639	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr14:79557806-79557852	Medullo	brain:	n/a	n/a
35	CTCF	chr14:79557780-79557930	HA-sp	spinal cord:	n/a	n/a
36	E2F4	chr14:79537861-79537864	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr14:79547301-79547501	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr14:79540234-79540434	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr14:79551061-79551135	MCF10A-Er-Src	breast:	n/a	n/a
40	EBF1	chr14:79567059-79567178	GM12878	blood:	n/a	n/a
41	EP300	chr14:79607504-79607901	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr14:79611286-79611501	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr14:79607564-79607965	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr14:79557712-79558212	H1-hESC	embryonic stem cell:	n/a	n/a
45	EP300	chr14:79530606-79530849	GM12878	blood:	n/a	chr14:79530730-79530744
46	EP300	chr14:79557775-79558083	H1-hESC	embryonic stem cell:	n/a	n/a
47	FOS	chr14:79621609-79621812	MCF10A-Er-Src	breast:	n/a	chr14:79621722-79621729 chr14:79621721-79621729 chr14:79621720-79621729
48	FOS	chr14:79611355-79611512	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr14:79611391-79611576	MCF10A-Er-Src	breast:	n/a	n/a
50	FOXA1	chr14:79597975-79598155	T-47D	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:79529179-79529229	AG09319	gingival:	n/a
2	chr14:79558823-79558873	H1-hESC	embryonic stem cell:	embryo
3	chr14:79558823-79558873	SK-N-SH	brain:	n/a
4	chr14:79558823-79558873	MCF10A-Er-Src	breast:	n/a
5	chr14:79558823-79558873	IMR90	lung:	fetal
6	chr14:79558823-79558873	K562	blood:	n/a
7	chr14:79529179-79529229	HL-60	blood:	n/a
8	chr14:79529179-79529229	HEEpiC	esophagus:	n/a
9	chr14:79558823-79558873	CMK	blood:	n/a
10	chr14:79529179-79529229	NT2-D1	testis:	n/a
11	chr14:79529179-79529229	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:79529179-79529229	H1-hESC	embryonic stem cell:	embryo
13	chr14:79529179-79529229	HCPEpiC	choroid plexus:	n/a
14	chr14:79529179-79529229	T-47D	breast:	n/a
15	chr14:79558823-79558873	HRCEpiC	kidney:	n/a
16	chr14:79529179-79529229	SK-N-SH_RA	brain:	n/a
17	chr14:79558823-79558873	PANC-1	pancreas:	n/a
18	chr14:79558823-79558873	AG09309	skin:	n/a
19	chr14:79529179-79529229	HNPCEpiC	eye:	n/a
20	chr14:79529179-79529229	HUVEC	blood vessel:	n/a
21	chr14:79529179-79529229	MCF-7	breast:	n/a
22	chr14:79558823-79558873	HPAEpiC	pulmonary alveolar:	n/a
23	chr14:79529179-79529229	Hela-S3	cervix:	n/a
24	chr14:79558823-79558873	SAEC	small airway:	n/a
25	chr14:79558823-79558873	NHBE	bronchial:	n/a
26	chr14:79529179-79529229	GM12891	blood:	n/a
27	chr14:79529179-79529229	SAEC	small airway:	n/a
28	chr14:79558823-79558873	HEEpiC	esophagus:	n/a
29	chr14:79558823-79558873	HRE	kidney:	n/a
30	chr14:79529179-79529229	HIPEpiC	eye:	n/a
31	chr14:79558823-79558873	GM19239	blood:	n/a
32	chr14:79529179-79529229	NH-A	brain:	n/a
33	chr14:79558823-79558873	GM06990	blood:	n/a
34	chr14:79558823-79558873	SK-N-MC	brain:	n/a
35	chr14:79558823-79558873	NH-A	brain:	n/a
36	chr14:79529179-79529229	PANC-1	pancreas:	n/a
37	chr14:79529179-79529229	SK-N-MC	brain:	n/a
38	chr14:79558823-79558873	HRPEpiC	eye:	n/a
39	chr14:79558823-79558873	HNPCEpiC	eye:	n/a
40	chr14:79558823-79558873	Hepatocyte	liver:	n/a
41	chr14:79529179-79529229	IMR90	lung:	fetal
42	chr14:79558823-79558873	Hela-S3	cervix:	n/a
43	chr14:79558823-79558873	GM12892	blood:	n/a
44	chr14:79529179-79529229	BE2_C	brain:	n/a
45	chr14:79529179-79529229	ECC-1	luminal epithelium:	n/a
46	chr14:79529179-79529229	PrEC	prostate:	n/a
47	chr14:79529179-79529229	RPTEC	kidney:	n/a
48	chr14:79558823-79558873	Jurkat	blood:	n/a
49	chr14:79529179-79529229	GM12892	blood:	n/a
50	chr14:79529179-79529229	Hepatocyte	liver:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:79557622..79558152-chr15:97180235..97181024,2	MCF-7	breast:
2	chr14:79554622..79556371-chr14:79563139..79566085,2	K562	blood:
3	chr14:79554622..79556371-chr14:79563139..79566085,2	K562	blood:
4	chr14:79573779..79574636-chr15:68722745..68723313,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIO2-5	chr14:79538510-79538846	ENSG00000258829.1
2	lnc-DIO2-5	chr14:79540891-79541105	ENSG00000258829.1
3	lnc-DIO2-5	chr14:79540891-79541110	ENSG00000258829.1
4	lnc-DIO2-5	chr14:79538475-79538818	ENSG00000258829.1

No data

Variant related genes	Relation type
ENSG00000258829	TF binding region
ENSG00000258829	CpG island

Extended variants
information (count: 2304 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2304 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149379199	chr14:79522271-79522272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528180146	chr14:79522310-79522311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374702647	chr14:79522314-79522315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545486319	chr14:79522344-79522345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13379131	chr14:79522345-79522346	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs529695259	chr14:79522384-79522385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546557421	chr14:79522388-79522389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs368019703	chr14:79522392-79522393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12147740	chr14:79522393-79522394	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs143985920	chr14:79522428-79522429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs8011782	chr14:79522436-79522437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs571831037	chr14:79522441-79522442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532412191	chr14:79522446-79522447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190855633	chr14:79522532-79522533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569692867	chr14:79522596-79522597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550939522	chr14:79522606-79522607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557734432	chr14:79522610-79522611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574378946	chr14:79522642-79522643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536284323	chr14:79522664-79522665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183072208	chr14:79522680-79522681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187413524	chr14:79522688-79522689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12432817	chr14:79522732-79522733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs138016075	chr14:79522737-79522738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564739237	chr14:79522742-79522743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575141326	chr14:79522768-79522769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10134650	chr14:79522772-79522773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs560880224	chr14:79522773-79522774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529976599	chr14:79522840-79522841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77153591	chr14:79522854-79522855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560063435	chr14:79522859-79522860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549400253	chr14:79522862-79522863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559478521	chr14:79522880-79522881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552258385	chr14:79522881-79522882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568971389	chr14:79522910-79522911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368534863	chr14:79522921-79522922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371799041	chr14:79522989-79522990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537684273	chr14:79523094-79523095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567720064	chr14:79523140-79523141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368484840	chr14:79523167-79523168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534823279	chr14:79523207-79523208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553517097	chr14:79523235-79523236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551851451	chr14:79523264-79523265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551181242	chr14:79523312-79523313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113386251	chr14:79523385-79523386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370197787	chr14:79523387-79523388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567893177	chr14:79523394-79523395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536916672	chr14:79523456-79523457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148676016	chr14:79523477-79523478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7155818	chr14:79523647-79523648	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs373988047	chr14:79523651-79523652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79517200-79528200	Weak transcription	Brain Germinal Matrix	brain
2	chr14:79518200-79522200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr14:79519200-79523000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr14:79519200-79524000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr14:79519800-79523600	Weak transcription	Colon Smooth Muscle	Colon
6	chr14:79522200-79522400	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr14:79522400-79522800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr14:79522800-79523800	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr14:79523000-79524000	Enhancers	NH-A	brain
10	chr14:79523000-79524200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr14:79523000-79524200	Enhancers	Psoas Muscle	Psoas
12	chr14:79523000-79524200	Enhancers	Stomach Smooth Muscle	stomach
13	chr14:79523600-79524400	Enhancers	Colon Smooth Muscle	Colon
14	chr14:79523800-79524000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr14:79524000-79524200	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr14:79524000-79524600	Enhancers	Rectal Smooth Muscle	rectum
17	chr14:79524200-79527600	Weak transcription	Stomach Smooth Muscle	stomach
18	chr14:79524400-79525000	Weak transcription	Colon Smooth Muscle	Colon
19	chr14:79524600-79527800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr14:79525000-79525200	Enhancers	Colon Smooth Muscle	Colon
21	chr14:79526400-79526600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:79527600-79527800	Active TSS	Stomach Smooth Muscle	stomach
23	chr14:79527600-79529000	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr14:79527600-79529400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:79527800-79528000	Flanking Active TSS	Stomach Smooth Muscle	stomach
26	chr14:79527800-79529000	Enhancers	Rectal Smooth Muscle	rectum
27	chr14:79527800-79529400	Enhancers	Colon Smooth Muscle	Colon
28	chr14:79528000-79529000	Enhancers	Stomach Smooth Muscle	stomach
29	chr14:79528000-79529600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr14:79528200-79529600	Enhancers	Brain Germinal Matrix	brain
31	chr14:79528600-79529400	Bivalent Enhancer	Fetal Brain Male	brain
32	chr14:79528800-79529600	Bivalent Enhancer	Fetal Brain Female	brain
33	chr14:79529800-79530800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr14:79530000-79530600	Enhancers	GM12878-XiMat	blood
35	chr14:79530200-79530800	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr14:79540800-79541200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:79540800-79541200	Enhancers	Gastric	stomach
38	chr14:79540800-79541400	Enhancers	Pancreas	Pancrea
39	chr14:79540800-79543800	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr14:79541000-79541200	Enhancers	Colon Smooth Muscle	Colon
41	chr14:79541000-79541400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr14:79541200-79541800	Weak transcription	Colon Smooth Muscle	Colon
43	chr14:79541200-79543200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr14:79541400-79541800	Weak transcription	Pancreas	Pancrea
45	chr14:79541800-79542800	Enhancers	Pancreas	Pancrea
46	chr14:79541800-79543200	Enhancers	Colon Smooth Muscle	Colon
47	chr14:79542600-79545000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:79543000-79543600	Enhancers	NHEK	skin
49	chr14:79543000-79543800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:79543000-79543800	Enhancers	HMEC	breast

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