Variant report

Variant	esv1793651
Chromosome Location	chr5:14575698-14584695
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:442)
CpG islands
(count:796)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:14581450-14582638	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr5:14580284-14581199	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr5:14576509-14576615	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:14576202-14576652	Hela-S3	cervix:	n/a	chr5:14576207-14576218
5	CEBPB	chr5:14580675-14581099	MCF-7	breast:	n/a	n/a
6	CEBPB	chr5:14582372-14582588	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:14582729-14582909	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr5:14580456-14581171	Hela-S3	cervix:	n/a	n/a
9	CHD1	chr5:14581346-14581369	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr5:14581645-14581935	K562	blood:	n/a	chr5:14581877-14581887
11	CHD2	chr5:14581607-14582538	H1-hESC	embryonic stem cell:	n/a	chr5:14581877-14581887 chr5:14582100-14582110
12	CHD2	chr5:14581658-14581933	GM12878	blood:	n/a	chr5:14581877-14581887
13	CHD2	chr5:14581431-14582614	Hela-S3	cervix:	n/a	chr5:14581877-14581887 chr5:14582100-14582110
14	CREB1	chr5:14581492-14582060	A549	lung:	n/a	n/a
15	CREB1	chr5:14581572-14582063	HepG2	liver:	n/a	n/a
16	CREB1	chr5:14582246-14582531	A549	lung:	n/a	n/a
17	CTCF	chr5:14582360-14582510	GM12868	blood:	n/a	n/a
18	CTCF	chr5:14582120-14582270	AG04449	skin:	n/a	n/a
19	CTCF	chr5:14583035-14583228	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr5:14583020-14583170	Caco-2	colon:	n/a	n/a
21	CTCF	chr5:14582480-14582630	NHEK	skin:	n/a	n/a
22	CTCF	chr5:14582471-14582558	GM13976	blood:	n/a	n/a
23	CTCF	chr5:14582600-14582750	A549	lung:	n/a	n/a
24	CTCF	chr5:14582660-14582810	GM12864	blood:	n/a	n/a
25	CTCF	chr5:14582400-14582550	GM12864	blood:	n/a	n/a
26	CTCF	chr5:14582475-14582592	Medullo	brain:	n/a	n/a
27	CTCF	chr5:14582420-14582570	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr5:14582420-14582570	GM12866	blood:	n/a	n/a
29	CTCF	chr5:14582480-14582630	BE2_C	brain:	n/a	n/a
30	CTCF	chr5:14582420-14582570	GM12875	blood:	n/a	n/a
31	CTCF	chr5:14582960-14583110	BJ	skin:	n/a	n/a
32	CTCF	chr5:14582420-14582570	HEK293	kidney:	n/a	n/a
33	CTCF	chr5:14582440-14582590	BE2_C	brain:	n/a	n/a
34	CTCF	chr5:14582460-14582610	HCFaa	heart:	n/a	n/a
35	CTCF	chr5:14583040-14583190	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr5:14582395-14582709	GM12878	blood:	n/a	n/a
37	CTCF	chr5:14583080-14583230	BE2_C	brain:	n/a	n/a
38	CTCF	chr5:14583080-14583230	HAc	cerebellar:	n/a	n/a
39	CTCF	chr5:14582480-14582630	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr5:14583020-14583170	A549	lung:	n/a	n/a
41	CTCF	chr5:14582460-14582610	GM12871	blood:	n/a	n/a
42	CTCF	chr5:14582440-14582613	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:14582440-14582590	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr5:14582451-14582599	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr5:14582460-14582593	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:14582000-14582150	GM12865	blood:	n/a	n/a
47	CTCF	chr5:14582460-14582610	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr5:14582460-14582610	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr5:14582460-14582610	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr5:14582480-14582630	GM12873	blood:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14581529-14581579	GM12891	blood:	n/a
2	chr5:14581529-14581579	GM12878	blood:	n/a
3	chr5:14582133-14582183	SK-N-SH	brain:	n/a
4	chr5:14581529-14581579	GM12891	blood:	n/a
5	chr5:14581529-14581579	GM12878	blood:	n/a
6	chr5:14582133-14582183	SK-N-SH	brain:	n/a
7	chr5:14581942-14581992	AG04450	lung:	fetal
8	chr5:14581699-14581749	NH-A	brain:	n/a
9	chr5:14581529-14581579	HAEpiC	amniotic membrane:	n/a
10	chr5:14581699-14581749	Caco-2	colon:	n/a
11	chr5:14581699-14581749	ECC-1	luminal epithelium:	n/a
12	chr5:14581529-14581579	NHDF-neo	bronchial:	n/a
13	chr5:14577586-14577636	HCF	heart:	n/a
14	chr5:14581642-14581692	HUVEC	blood vessel:	n/a
15	chr5:14577586-14577636	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:14581771-14581821	ProgFib	skin:	n/a
17	chr5:14581826-14581876	GM12892	blood:	n/a
18	chr5:14581404-14581454	MCF10A-Er-Src	breast:	n/a
19	chr5:14581642-14581692	Hela-S3	cervix:	n/a
20	chr5:14581620-14581670	AoSMC	blood vessel:	n/a
21	chr5:14581529-14581579	H1-hESC	embryonic stem cell:	embryo
22	chr5:14582133-14582183	AG10803	skin:	n/a
23	chr5:14581826-14581876	SK-N-SH_RA	brain:	n/a
24	chr5:14581651-14581701	NHBE	bronchial:	n/a
25	chr5:14581642-14581692	H1-hESC	embryonic stem cell:	embryo
26	chr5:14581404-14581454	HL-60	blood:	n/a
27	chr5:14582549-14582599	NHDF-neo	bronchial:	n/a
28	chr5:14581404-14581454	MCF-7	breast:	n/a
29	chr5:14577586-14577636	NHDF-neo	bronchial:	n/a
30	chr5:14581651-14581701	HAEpiC	amniotic membrane:	n/a
31	chr5:14581699-14581749	IMR90	lung:	fetal
32	chr5:14581529-14581579	SK-N-SH	brain:	n/a
33	chr5:14581404-14581454	NHBE	bronchial:	n/a
34	chr5:14581942-14581992	AG04449	skin:	fetal
35	chr5:14581404-14581454	NB4	blood:	n/a
36	chr5:14577586-14577636	PFSK-1	brain:	n/a
37	chr5:14582549-14582599	A549	lung:	n/a
38	chr5:14581942-14581992	HEEpiC	esophagus:	n/a
39	chr5:14581529-14581579	AG04449	skin:	fetal
40	chr5:14581529-14581579	ovcar-3	ovarian:	n/a
41	chr5:14581826-14581876	RPTEC	kidney:	n/a
42	chr5:14581826-14581876	SKMC	muscle:	n/a
43	chr5:14581942-14581992	Caco-2	colon:	n/a
44	chr5:14581529-14581579	NHBE	bronchial:	n/a
45	chr5:14581699-14581749	SAEC	small airway:	n/a
46	chr5:14577586-14577636	HIPEpiC	eye:	n/a
47	chr5:14581826-14581876	SK-N-SH	brain:	n/a
48	chr5:14581404-14581454	GM12892	blood:	n/a
49	chr5:14581620-14581670	PANC-1	pancreas:	n/a
50	chr5:14581529-14581579	NT2-D1	testis:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:14487528..14489858-chr5:14581341..14583372,2	MCF-7	breast:
2	chr5:14497681..14499439-chr5:14580941..14582507,2	MCF-7	breast:
3	chr5:14580610..14583664-chr5:14584270..14587652,5	MCF-7	breast:
4	chr5:14582284..14584528-chr5:14622359..14624603,2	MCF-7	breast:
5	chr5:14582227..14584118-chr5:14585804..14588637,2	K562	blood:
6	chr5:14582585..14585698-chr5:14586097..14589501,3	MCF-7	breast:
7	chr5:14575023..14577429-chr5:14607385..14610126,2	K562	blood:
8	chr5:14569029..14571729-chr5:14576984..14579113,2	MCF-7	breast:

No data

Variant related genes	Relation type
FAM105A	TF binding region
FAM105A	CpG island
ENSG00000038382	chromatin interactions
ENSG00000145569	chromatin interactions

Extended variants
information (count: 476 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:476 , 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	rs152624	chr5:14575698-14575699	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545277649	chr5:14575721-14575722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147847649	chr5:14575723-14575724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184069484	chr5:14575785-14575786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149924898	chr5:14575832-14575833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372531779	chr5:14575873-14575874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543932760	chr5:14575876-14575877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145012100	chr5:14575898-14575899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35007304	chr5:14575906-14575907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186733069	chr5:14575908-14575909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149049575	chr5:14575950-14575951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561427114	chr5:14575954-14575955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536386980	chr5:14575972-14575973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559477844	chr5:14575986-14575987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554694674	chr5:14576043-14576044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377296926	chr5:14576130-14576131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376780561	chr5:14576134-14576135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191543732	chr5:14576138-14576139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576160546	chr5:14576259-14576260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113721860	chr5:14576312-14576313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs57185797	chr5:14576323-14576324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143083079	chr5:14576337-14576338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536626376	chr5:14576375-14576376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138503706	chr5:14576377-14576378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567270823	chr5:14576436-14576437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534675900	chr5:14576469-14576470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs59670952	chr5:14576527-14576528	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs578213706	chr5:14576572-14576573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183877778	chr5:14576595-14576596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538976270	chr5:14576630-14576631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557279757	chr5:14576660-14576661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576414004	chr5:14576683-14576684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543476228	chr5:14576698-14576699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562082465	chr5:14576729-14576730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574057659	chr5:14576774-14576775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528783430	chr5:14576902-14576903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375504086	chr5:14576920-14576921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185086	chr5:14576966-14576967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559564979	chr5:14576971-14576972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185085	chr5:14576988-14576989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533339109	chr5:14577026-14577027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545356626	chr5:14577116-14577117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536426804	chr5:14577154-14577155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369371078	chr5:14577193-14577194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551691704	chr5:14577243-14577244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140234381	chr5:14577244-14577245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531207137	chr5:14577276-14577277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548717917	chr5:14577278-14577279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560570742	chr5:14577290-14577291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567207077	chr5:14577303-14577304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14560600-14576000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr5:14570200-14576600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:14573200-14576200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr5:14574400-14576000	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr5:14574400-14576200	Enhancers	Fetal Muscle Leg	muscle
6	chr5:14574600-14581200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:14574800-14576400	Enhancers	Duodenum Mucosa	Duodenum
8	chr5:14575000-14576600	Enhancers	Hela-S3	cervix
9	chr5:14575200-14576000	Weak transcription	Adipose Nuclei	Adipose
10	chr5:14575200-14580800	Weak transcription	Fetal Brain Male	brain
11	chr5:14575200-14581200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr5:14575200-14581400	Weak transcription	Pancreas	Pancrea
13	chr5:14575400-14576800	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr5:14575400-14580200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr5:14576000-14576200	Enhancers	Adipose Nuclei	Adipose
16	chr5:14576200-14580200	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr5:14576400-14580200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr5:14576600-14579000	Weak transcription	Hela-S3	cervix
19	chr5:14576800-14579000	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr5:14576800-14580000	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr5:14577200-14577600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr5:14577400-14577800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
23	chr5:14579000-14580800	Enhancers	Hela-S3	cervix
24	chr5:14579600-14579800	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr5:14579600-14579800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr5:14579600-14581200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr5:14580000-14580400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr5:14580000-14580400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:14580000-14580800	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr5:14580200-14581200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr5:14580200-14581200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr5:14580200-14581200	Enhancers	Duodenum Mucosa	Duodenum
33	chr5:14580200-14581200	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr5:14580400-14581200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:14580600-14581200	Bivalent Enhancer	Thymus	Thymus
36	chr5:14580600-14581400	Bivalent Enhancer	Colon Smooth Muscle	Colon
37	chr5:14580800-14581000	Bivalent Enhancer	Fetal Kidney	kidney
38	chr5:14580800-14581000	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr5:14580800-14581200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
40	chr5:14580800-14581200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:14580800-14581200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr5:14580800-14581200	Bivalent Enhancer	Primary B cells from cord blood	blood
43	chr5:14580800-14581200	Enhancers	Adipose Nuclei	Adipose
44	chr5:14580800-14581200	Enhancers	Fetal Brain Female	brain
45	chr5:14580800-14581200	Enhancers	Placenta	Placenta
46	chr5:14580800-14581200	Enhancers	Fetal Stomach	stomach
47	chr5:14580800-14581200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
48	chr5:14580800-14581200	Bivalent Enhancer	NHDF-Ad	bronchial
49	chr5:14580800-14581400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr5:14580800-14581400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell

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