Variant report

Variant	esv3425665
Chromosome Location	chr14:105056507-105061005
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:45)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:45 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr14:105058332-105059108	GM12878	blood:	n/a	n/a
2	BCL3	chr14:105058585-105059125	GM12878	blood:	n/a	n/a
3	BHLHE40	chr14:105058691-105058948	K562	blood:	n/a	n/a
4	CTCF	chr14:105059660-105059810	SK-N-SH_RA	brain:	n/a	n/a
5	CTCF	chr14:105059700-105059850	AG04449	skin:	n/a	n/a
6	CTCF	chr14:105059720-105059870	WERI-Rb-1	eye:	n/a	n/a
7	CTCF	chr14:105059800-105059950	WERI-Rb-1	eye:	n/a	n/a
8	CTCF	chr14:105058714-105058760	GM19239	blood:	n/a	n/a
9	CTCF	chr14:105059740-105059890	A549	lung:	n/a	n/a
10	CTCF	chr14:105059778-105059837	GM19239	blood:	n/a	n/a
11	CTCF	chr14:105059738-105059881	MCF-7	breast:	n/a	n/a
12	CTCF	chr14:105059779-105059863	K562	blood:	n/a	n/a
13	CTCF	chr14:105059799-105059827	MCF-7	breast:	n/a	n/a
14	CTCF	chr14:105059771-105059869	K562	blood:	n/a	n/a
15	CTCF	chr14:105059786-105059845	Gliobla	brain:	n/a	n/a
16	CTCF	chr14:105059754-105059878	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr14:105059771-105059866	MCF-7	breast:	n/a	n/a
18	CTCF	chr14:105059740-105059890	K562	blood:	n/a	n/a
19	CTCF	chr14:105059760-105059910	GM12871	blood:	n/a	n/a
20	CTCF	chr14:105059699-105059917	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr14:105059772-105059877	Fibrobl	skin:	n/a	n/a
22	CTCF	chr14:105059736-105059870	HepG2	liver:	n/a	n/a
23	CTCF	chr14:105059760-105059910	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr14:105059795-105059837	A549	lung:	n/a	n/a
25	CTCF	chr14:105060420-105060570	GM12868	blood:	n/a	n/a
26	CTCF	chr14:105059760-105059910	BE2_C	brain:	n/a	n/a
27	CTCF	chr14:105059780-105059930	HepG2	liver:	n/a	n/a
28	CTCF	chr14:105059720-105059870	SK-N-SH_RA	brain:	n/a	n/a
29	MYC	chr14:105058828-105058920	MCF-7	breast:	n/a	n/a
30	MYC	chr14:105058491-105058650	MCF-7	breast:	n/a	n/a
31	NFATC1	chr14:105058388-105059076	GM12878	blood:	n/a	n/a
32	NFATC1	chr14:105058442-105059082	GM12878	blood:	n/a	n/a
33	NFIC	chr14:105058575-105058977	GM12878	blood:	n/a	n/a
34	PBX3	chr14:105058568-105058994	GM12878	blood:	n/a	n/a
35	PBX3	chr14:105059004-105059127	GM12878	blood:	n/a	n/a
36	POLR2A	chr14:105058839-105058920	MCF-7	breast:	n/a	n/a
37	POLR2A	chr14:105058649-105058723	MCF-7	breast:	n/a	n/a
38	POLR2A	chr14:105058518-105058565	MCF-7	breast:	n/a	n/a
39	POLR2A	chr14:105058447-105058831	MCF-7	breast:	n/a	n/a
40	STAT5A	chr14:105058648-105058966	GM12878	blood:	n/a	n/a
41	STAT5A	chr14:105058528-105059029	GM12878	blood:	n/a	n/a
42	SUZ12	chr14:105058509-105058961	H1-hESC	embryonic stem cell:	n/a	n/a
43	TCF3	chr14:105058648-105059023	GM12878	blood:	n/a	n/a
44	TCF3	chr14:105058634-105058993	GM12878	blood:	n/a	n/a
45	ZNF263	chr14:105058591-105058848	HEK293-T-REx	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105058234-105058284	ECC-1	luminal epithelium:	n/a
2	chr14:105058234-105058284	PrEC	prostate:	n/a
3	chr14:105058234-105058284	HNPCEpiC	eye:	n/a
4	chr14:105058234-105058284	HEEpiC	esophagus:	n/a
5	chr14:105060221-105060271	AoSMC	blood vessel:	n/a
6	chr14:105060221-105060271	ECC-1	luminal epithelium:	n/a
7	chr14:105058234-105058284	AG09309	skin:	n/a
8	chr14:105058234-105058284	PFSK-1	brain:	n/a
9	chr14:105058234-105058284	GM06990	blood:	n/a
10	chr14:105058234-105058284	NHBE	bronchial:	n/a
11	chr14:105060221-105060271	NB4	blood:	n/a
12	chr14:105058234-105058284	AG10803	skin:	n/a
13	chr14:105058234-105058284	T-47D	breast:	n/a
14	chr14:105058234-105058284	AG04449	skin:	fetal
15	chr14:105058234-105058284	ProgFib	skin:	n/a
16	chr14:105060221-105060271	NH-A	brain:	n/a
17	chr14:105060221-105060271	PrEC	prostate:	n/a
18	chr14:105060221-105060271	HPAEpiC	pulmonary alveolar:	n/a
19	chr14:105058234-105058284	GM12891	blood:	n/a
20	chr14:105060221-105060271	HIPEpiC	eye:	n/a
21	chr14:105060221-105060271	NHDF-neo	bronchial:	n/a
22	chr14:105060221-105060271	NHBE	bronchial:	n/a
23	chr14:105060221-105060271	HepG2	liver:	n/a
24	chr14:105060221-105060271	SAEC	small airway:	n/a
25	chr14:105058234-105058284	BJ	skin:	n/a
26	chr14:105060221-105060271	CMK	blood:	n/a
27	chr14:105058234-105058284	HL-60	blood:	n/a
28	chr14:105060221-105060271	HUVEC	blood vessel:	n/a
29	chr14:105060221-105060271	SK-N-SH	brain:	n/a
30	chr14:105060221-105060271	ProgFib	skin:	n/a
31	chr14:105058234-105058284	HEK293	kidney:	embryo
32	chr14:105060221-105060271	HRE	kidney:	n/a
33	chr14:105060221-105060271	HAEpiC	amniotic membrane:	n/a
34	chr14:105060221-105060271	GM12892	blood:	n/a
35	chr14:105060221-105060271	MCF10A-Er-Src	breast:	n/a
36	chr14:105058234-105058284	HepG2	liver:	n/a
37	chr14:105058234-105058284	MCF-7	breast:	n/a
38	chr14:105060221-105060271	AG09319	gingival:	n/a
39	chr14:105058234-105058284	CMK	blood:	n/a
40	chr14:105058234-105058284	IMR90	lung:	fetal
41	chr14:105058234-105058284	ovcar-3	ovarian:	n/a
42	chr14:105060221-105060271	Jurkat	blood:	n/a
43	chr14:105060221-105060271	ovcar-3	ovarian:	n/a
44	chr14:105060221-105060271	HL-60	blood:	n/a
45	chr14:105058234-105058284	HIPEpiC	eye:	n/a
46	chr14:105058234-105058284	HMEC	breast:	n/a
47	chr14:105060221-105060271	GM12878	blood:	n/a
48	chr14:105060221-105060271	BJ	skin:	n/a
49	chr14:105058234-105058284	HCPEpiC	choroid plexus:	n/a
50	chr14:105060221-105060271	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:105053625..105056399-chr14:105056665..105059451,2	MCF-7	breast:
2	chr14:105056244..105058754-chr14:105069412..105071602,2	MCF-7	breast:
3	chr14:105056847..105059828-chr14:105062201..105064275,3	MCF-7	breast:
4	chr14:105051680..105054326-chr14:105056453..105058154,2	K562	blood:
5	chr14:105046780..105049204-chr14:105060096..105062523,2	K562	blood:
6	chr14:105053139..105055951-chr14:105056833..105058762,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf180-1	chr14:105058773-105058979	NONHSAT040263
2	lnc-C14orf180-1	chr14:105058659-105058677	NONHSAT040263
3	lnc-C14orf180-1	chr14:105058611-105058858	NONHSAT040262
4	lnc-C14orf180-1	chr14:105058927-105058979	NONHSAT040262

No data

Variant related genes	Relation type
ENSG00000259037	TF binding region
TMEM179	TF binding region
ENSG00000259037	CpG island
TMEM179	CpG island
ENSG00000258986	chromatin interactions
ENSG00000259037	chromatin interactions
ENSG00000184601	chromatin interactions

Extended variants
information (count: 192 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:192 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57662750	chr14:105056508-105056509	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs180963642	chr14:105056515-105056516	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs112771967	chr14:105056546-105056547	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111366167	chr14:105056595-105056596	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553031270	chr14:105056603-105056604	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370710108	chr14:105056663-105056664	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569014390	chr14:105056735-105056736	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs537839231	chr14:105056741-105056742	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs528842379	chr14:105056743-105056744	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs185880010	chr14:105056750-105056751	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548826486	chr14:105056795-105056796	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs567946997	chr14:105056796-105056797	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs12590316	chr14:105056801-105056802	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs536562199	chr14:105056817-105056818	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs553482391	chr14:105056818-105056819	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs144884164	chr14:105056819-105056820	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs112066116	chr14:105056849-105056850	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs191525448	chr14:105056880-105056881	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs558620704	chr14:105056919-105056920	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs73361836	chr14:105056945-105056946	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs371156241	chr14:105056985-105056986	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs151304510	chr14:105056986-105056987	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs528304045	chr14:105056993-105056994	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs540159771	chr14:105056998-105056999	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs182657995	chr14:105056999-105057000	Weak transcription Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187029287	chr14:105057007-105057008	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs73361837	chr14:105057049-105057050	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs529519830	chr14:105057073-105057074	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74092103	chr14:105057099-105057100	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs7155652	chr14:105057102-105057103	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs139343956	chr14:105057105-105057106	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs190656490	chr14:105057128-105057129	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs375451171	chr14:105057158-105057159	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs550808939	chr14:105057196-105057197	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536906792	chr14:105057256-105057257	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs1135471	chr14:105057295-105057296	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546967489	chr14:105057316-105057317	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs567198559	chr14:105057329-105057330	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs538834615	chr14:105057335-105057336	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs11547184	chr14:105057340-105057341	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs369511369	chr14:105057360-105057361	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs1135470	chr14:105057373-105057374	Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs537969718	chr14:105057408-105057409	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs12101279	chr14:105057469-105057470	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs574750707	chr14:105057481-105057482	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs371159046	chr14:105057497-105057498	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560185743	chr14:105057519-105057520	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs12101271	chr14:105057529-105057530	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs546007380	chr14:105057539-105057540	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs12101275	chr14:105057586-105057587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:100)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	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
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20932292	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	21980252	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105046400-105064000	Weak transcription	Brain Anterior Caudate	brain
2	chr14:105049200-105057400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr14:105049200-105057400	Bivalent Enhancer	Placenta	Placenta
4	chr14:105053800-105063800	Weak transcription	Fetal Brain Male	brain
5	chr14:105054000-105058400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr14:105054000-105059800	Weak transcription	Right Atrium	heart
7	chr14:105054000-105061800	Weak transcription	Brain Germinal Matrix	brain
8	chr14:105054200-105058400	Weak transcription	Spleen	Spleen
9	chr14:105054200-105058800	Weak transcription	Gastric	stomach
10	chr14:105055000-105058400	Weak transcription	Adipose Nuclei	Adipose
11	chr14:105055000-105058400	Weak transcription	Fetal Heart	heart
12	chr14:105055200-105056800	Strong transcription	Right Ventricle	heart
13	chr14:105055200-105066200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:105055600-105060400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr14:105056200-105057000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr14:105056200-105057400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:105056400-105059600	Weak transcription	Left Ventricle	heart
18	chr14:105056600-105057000	Enhancers	Ovary	ovary
19	chr14:105056800-105057000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:105056800-105057200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr14:105056800-105058600	Weak transcription	Right Ventricle	heart
22	chr14:105057000-105057200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
23	chr14:105057000-105057200	Bivalent Enhancer	HSMMtube	muscle
24	chr14:105057000-105057400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr14:105057000-105057400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr14:105057000-105057400	Active TSS	Ovary	ovary
27	chr14:105057000-105057400	Active TSS	Hela-S3	cervix
28	chr14:105057000-105057400	Active TSS	Osteobl	bone
29	chr14:105057400-105057600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr14:105057400-105057600	Enhancers	Fetal Muscle Leg	muscle
31	chr14:105057400-105058000	Enhancers	Ovary	ovary
32	chr14:105057400-105058600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr14:105057600-105058800	Weak transcription	Fetal Muscle Leg	muscle
34	chr14:105057600-105061600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr14:105058000-105058400	Weak transcription	Ovary	ovary
36	chr14:105058400-105058800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr14:105058400-105058800	Enhancers	Ovary	ovary
38	chr14:105058400-105059000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:105058400-105059000	Genic enhancers	Adipose Nuclei	Adipose
40	chr14:105058400-105059000	Genic enhancers	Fetal Heart	heart
41	chr14:105058400-105059400	ZNF genes & repeats	Spleen	Spleen
42	chr14:105058600-105059000	Bivalent/Poised TSS	Fetal Lung	lung
43	chr14:105058600-105060200	Enhancers	Right Ventricle	heart
44	chr14:105058800-105059000	Bivalent Enhancer	Fetal Kidney	kidney
45	chr14:105058800-105059000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
46	chr14:105058800-105059200	Enhancers	Gastric	stomach
47	chr14:105058800-105059800	Enhancers	Fetal Muscle Leg	muscle
48	chr14:105059000-105059200	Weak transcription	Pancreas	Pancrea
49	chr14:105059000-105059800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:105059000-105061000	Enhancers	Adipose Nuclei	Adipose

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