Variant report

Variant	esv3423633
Chromosome Location	chr14:105053757-105056255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:245)
Chromatin interactive
region (count:9)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:105054806-105055071	LNCaP	prostate:	n/a	n/a
2	CTCF	chr14:105054815-105055063	LNCaP	prostate:	n/a	n/a
3	EGR1	chr14:105053959-105054146	K562	blood:	n/a	chr14:105054070-105054083 chr14:105054070-105054080 chr14:105054069-105054084 chr14:105054070-105054083
4	ELF1	chr14:105054021-105054232	K562	blood:	n/a	chr14:105054089-105054102
5	ELF1	chr14:105053905-105054237	K562	blood:	n/a	chr14:105054089-105054102
6	GABPA	chr14:105054698-105055000	H1-hESC	embryonic stem cell:	n/a	n/a
7	MAZ	chr14:105054004-105054217	K562	blood:	n/a	chr14:105054070-105054080
8	MXI1	chr14:105052507-105055174	SK-N-SH	brain:	n/a	n/a
9	REST	chr14:105055753-105056112	SK-N-SH	brain:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105055026-105055076	Hepatocyte	liver:	n/a
2	chr14:105055026-105055076	Hepatocyte	liver:	n/a
3	chr14:105054940-105054990	CMK	blood:	n/a
4	chr14:105054940-105054990	NHBE	bronchial:	n/a
5	chr14:105054940-105054990	BE2_C	brain:	n/a
6	chr14:105054436-105054486	MCF10A-Er-Src	breast:	n/a
7	chr14:105054436-105054486	AoSMC	blood vessel:	n/a
8	chr14:105054940-105054990	SK-N-MC	brain:	n/a
9	chr14:105054940-105054990	SKMC	muscle:	n/a
10	chr14:105055026-105055076	AG09319	gingival:	n/a
11	chr14:105054436-105054486	BJ	skin:	n/a
12	chr14:105055171-105055221	IMR90	lung:	fetal
13	chr14:105055026-105055076	RPTEC	kidney:	n/a
14	chr14:105054940-105054990	GM06990	blood:	n/a
15	chr14:105054940-105054990	K562	blood:	n/a
16	chr14:105054436-105054486	PFSK-1	brain:	n/a
17	chr14:105054436-105054486	GM12892	blood:	n/a
18	chr14:105054436-105054486	SKMC	muscle:	n/a
19	chr14:105055026-105055076	H1-hESC	embryonic stem cell:	embryo
20	chr14:105054436-105054486	RPTEC	kidney:	n/a
21	chr14:105054436-105054486	HUVEC	blood vessel:	n/a
22	chr14:105054436-105054486	GM12891	blood:	n/a
23	chr14:105054940-105054990	HRPEpiC	eye:	n/a
24	chr14:105055171-105055221	BE2_C	brain:	n/a
25	chr14:105054436-105054486	HRCEpiC	kidney:	n/a
26	chr14:105054940-105054990	GM12892	blood:	n/a
27	chr14:105054436-105054486	NHBE	bronchial:	n/a
28	chr14:105055171-105055221	Caco-2	colon:	n/a
29	chr14:105054940-105054990	HPAEpiC	pulmonary alveolar:	n/a
30	chr14:105055026-105055076	HepG2	liver:	n/a
31	chr14:105055171-105055221	CMK	blood:	n/a
32	chr14:105054436-105054486	HPAEpiC	pulmonary alveolar:	n/a
33	chr14:105054940-105054990	HepG2	liver:	n/a
34	chr14:105054436-105054486	A549	lung:	n/a
35	chr14:105055026-105055076	AG04449	skin:	fetal
36	chr14:105055171-105055221	NHBE	bronchial:	n/a
37	chr14:105055171-105055221	HCM	heart:	n/a
38	chr14:105054940-105054990	SAEC	small airway:	n/a
39	chr14:105055171-105055221	HNPCEpiC	eye:	n/a
40	chr14:105055171-105055221	SKMC	muscle:	n/a
41	chr14:105054436-105054486	AG10803	skin:	n/a
42	chr14:105055171-105055221	ProgFib	skin:	n/a
43	chr14:105054940-105054990	GM12878	blood:	n/a
44	chr14:105054940-105054990	HNPCEpiC	eye:	n/a
45	chr14:105055171-105055221	AG04450	lung:	fetal
46	chr14:105054940-105054990	H1-hESC	embryonic stem cell:	embryo
47	chr14:105054436-105054486	NHDF-neo	bronchial:	n/a
48	chr14:105055026-105055076	GM12892	blood:	n/a
49	chr14:105054940-105054990	AG09319	gingival:	n/a
50	chr14:105054436-105054486	GM19239	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105056244..105058754-chr14:105069412..105071602,2	MCF-7	breast:
2	chr14:105051680..105054326-chr14:105056453..105058154,2	K562	blood:
3	chr14:105029275..105030973-chr14:105053381..105055372,2	MCF-7	breast:
4	chr14:105053139..105055951-chr14:105056833..105058762,2	MCF-7	breast:
5	chr14:104610504..104612427-chr14:105051437..105054279,2	MCF-7	breast:
6	chr14:105052614..105054993-chr14:105059778..105063745,3	MCF-7	breast:
7	chr14:105051460..105054318-chr14:105065676..105068171,2	MCF-7	breast:
8	chr14:105048877..105053029-chr14:105053228..105056172,3	MCF-7	breast:
9	chr14:105053087..105055483-chr14:105069492..105072343,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM179-1	chr14:105055358-105055677	ENSG00000259037.1
2	lnc-TMEM179-1	chr14:105055962-105056184	ENSG00000259037.1

No data

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

Extended variants
information (count: 170 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:170 , 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	rs113618011	chr14:105053758-105053759	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs542027770	chr14:105053776-105053777	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs570473324	chr14:105053794-105053795	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs527353036	chr14:105053815-105053816	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547178280	chr14:105053866-105053867	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564069111	chr14:105053881-105053882	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532779990	chr14:105053940-105053941	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7159145	chr14:105053965-105053966	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs569429659	chr14:105053986-105053987	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73361816	chr14:105053987-105053988	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs140952034	chr14:105053999-105054000	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs564349827	chr14:105054024-105054025	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs568340704	chr14:105054027-105054028	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374207195	chr14:105054038-105054039	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs73361819	chr14:105054044-105054045	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs373047135	chr14:105054047-105054048	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553984960	chr14:105054049-105054050	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs377302831	chr14:105054050-105054051	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201727131	chr14:105054061-105054062	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs199942352	chr14:105054062-105054063	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576367205	chr14:105054078-105054079	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs144973367	chr14:105054083-105054084	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76292733	chr14:105054085-105054086	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572278637	chr14:105054118-105054119	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs202177288	chr14:105054120-105054121	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370128922	chr14:105054122-105054123	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201529094	chr14:105054123-105054124	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs112399099	chr14:105054129-105054130	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs375304625	chr14:105054139-105054140	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs139748841	chr14:105054176-105054177	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs199521419	chr14:105054177-105054178	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192674070	chr14:105054178-105054179	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs144428844	chr14:105054188-105054189	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs61743131	chr14:105054189-105054190	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs113768792	chr14:105054196-105054197	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141850398	chr14:105054201-105054202	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs144894622	chr14:105054202-105054203	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs555264092	chr14:105054208-105054209	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs146244955	chr14:105054213-105054214	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs9788527	chr14:105054260-105054261	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs138014749	chr14:105054273-105054274	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35883949	chr14:105054318-105054319	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs116669858	chr14:105054335-105054336	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs34869170	chr14:105054353-105054354	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556254029	chr14:105054359-105054360	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184171404	chr14:105054372-105054373	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149488814	chr14:105054400-105054401	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555689482	chr14:105054471-105054472	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs143966230	chr14:105054480-105054481	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112419320	chr14:105054543-105054544	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

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:63 , 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	chr14:105049200-105054800	Enhancers	Fetal Muscle Leg	muscle
3	chr14:105049200-105057400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr14:105049200-105057400	Bivalent Enhancer	Placenta	Placenta
5	chr14:105049600-105054200	Enhancers	Left Ventricle	heart
6	chr14:105050000-105053800	Weak transcription	Gastric	stomach
7	chr14:105050200-105054800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
8	chr14:105050400-105054200	Enhancers	Adipose Nuclei	Adipose
9	chr14:105050400-105055000	Enhancers	Fetal Heart	heart
10	chr14:105051000-105054000	Enhancers	Right Ventricle	heart
11	chr14:105052400-105054000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
12	chr14:105052600-105053800	Enhancers	Placenta Amnion	Placenta Amnion
13	chr14:105052800-105054200	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr14:105052800-105054400	Enhancers	Lung	lung
15	chr14:105052800-105055000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:105053000-105053800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr14:105053000-105053800	Bivalent Enhancer	Brain Hippocampus Middle	brain
18	chr14:105053200-105053800	Enhancers	Fetal Brain Male	brain
19	chr14:105053200-105054000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr14:105053200-105054000	Enhancers	Right Atrium	heart
21	chr14:105053200-105054200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:105053200-105054200	Enhancers	Fetal Intestine Small	intestine
23	chr14:105053200-105054200	Enhancers	Spleen	Spleen
24	chr14:105053200-105055000	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr14:105053200-105055000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr14:105053400-105053800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr14:105053600-105054600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr14:105053600-105054600	Weak transcription	Brain Cingulate Gyrus	brain
29	chr14:105053600-105054800	Enhancers	Brain Angular Gyrus	brain
30	chr14:105053800-105054000	Enhancers	Brain Germinal Matrix	brain
31	chr14:105053800-105054000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
32	chr14:105053800-105054200	Enhancers	Gastric	stomach
33	chr14:105053800-105056200	Enhancers	Brain Hippocampus Middle	brain
34	chr14:105053800-105063800	Weak transcription	Fetal Brain Male	brain
35	chr14:105054000-105054200	Bivalent Enhancer	Fetal Stomach	stomach
36	chr14:105054000-105055200	Genic enhancers	Right Ventricle	heart
37	chr14:105054000-105058400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr14:105054000-105059800	Weak transcription	Right Atrium	heart
39	chr14:105054000-105061800	Weak transcription	Brain Germinal Matrix	brain
40	chr14:105054200-105054400	Genic enhancers	Left Ventricle	heart
41	chr14:105054200-105054800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
42	chr14:105054200-105055000	Genic enhancers	Adipose Nuclei	Adipose
43	chr14:105054200-105055600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr14:105054200-105055600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr14:105054200-105058400	Weak transcription	Spleen	Spleen
46	chr14:105054200-105058800	Weak transcription	Gastric	stomach
47	chr14:105054400-105056400	Strong transcription	Left Ventricle	heart
48	chr14:105054600-105055000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr14:105054600-105055000	Enhancers	Brain Cingulate Gyrus	brain
50	chr14:105054800-105055000	Bivalent Enhancer	HSMMtube	muscle

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