Variant report

Variant	esv3377452
Chromosome Location	chr14:105669757-105672255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105668897..105669930-chr14:105818302..105819064,4	MCF-7	breast:
2	chr14:105671811..105674041-chr14:105933944..105936633,2	MCF-7	breast:
3	chr14:105668626..105670243-chr14:105732918..105735863,2	MCF-7	breast:
4	chr14:105663679..105669180-chr14:105669363..105675708,8	K562	blood:
5	chr14:105668719..105671355-chr14:105765771..105767767,2	MCF-7	breast:
6	chr14:105669895..105672499-chr14:105780191..105782899,2	MCF-7	breast:
7	chr14:105667951..105671831-chr14:105672268..105675254,4	K562	blood:
8	chr14:105668328..105670868-chr14:105672731..105674371,2	MCF-7	breast:
9	chr14:105666418..105671078-chr14:105765699..105768969,5	MCF-7	breast:
10	chr14:105669105..105670016-chr14:105818280..105819197,4	K562	blood:
11	chr14:105668316..105670026-chr14:105722977..105725479,2	MCF-7	breast:
12	chr14:105667874..105671061-chr14:105780211..105783022,3	K562	blood:
13	chr14:105670331..105671987-chr14:105672268..105674643,2	K562	blood:
14	chr14:105668621..105671368-chr14:105688558..105691360,2	K562	blood:
15	chr14:105568093..105570383-chr14:105666909..105669878,2	K562	blood:
16	chr14:105663948..105665922-chr14:105668555..105670749,2	MCF-7	breast:
17	chr14:105668630..105671458-chr14:105740355..105743089,2	K562	blood:
18	chr14:105660777..105662281-chr14:105668696..105670709,2	K562	blood:
19	chr14:105667147..105672450-chr14:105672961..105678949,7	MCF-7	breast:
20	chr14:105671389..105673472-chr14:105681134..105682646,2	K562	blood:
21	chr14:105670960..105673149-chr14:105739734..105742723,2	MCF-7	breast:
22	chr14:105669972..105673331-chr14:105732479..105735063,3	MCF-7	breast:
23	chr14:105670645..105673390-chr14:105687925..105689985,2	MCF-7	breast:
24	chr14:105667669..105672140-chr14:105712867..105716210,4	MCF-7	breast:
25	chr14:105668503..105670075-chr14:105733985..105734945,13	MCF-7	breast:
26	chr14:105668056..105672326-chr14:105713017..105716519,4	MCF-7	breast:
27	chr14:105670122..105672901-chr14:105693966..105695750,2	K562	blood:
28	chr14:105668572..105669859-chr14:105733916..105734898,6	MCF-7	breast:
29	chr14:105671397..105673814-chr14:105677467..105679452,2	K562	blood:
30	chr14:105665384..105666955-chr14:105671405..105672932,2	K562	blood:
31	chr14:105629335..105630135-chr14:105669031..105669954,2	K562	blood:
32	chr14:105669278..105669927-chr14:105714056..105714962,2	MCF-7	breast:
33	chr14:105669002..105670184-chr14:105747515..105748746,6	MCF-7	breast:
34	chr14:105669618..105672409-chr14:105805481..105807820,2	K562	blood:
35	chr14:105671031..105673113-chr14:105678890..105680434,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000184887	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000182979	chromatin interactions
ENSG00000185024	chromatin interactions

Extended variants
information (count: 99 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587737425	chr14:105669761-105669762	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs587593736	chr14:105669770-105669771	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs587670587	chr14:105669842-105669843	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs587730478	chr14:105669930-105669931	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs587628306	chr14:105669938-105669939	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs587663070	chr14:105669947-105669948	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs75969682	chr14:105669955-105669956	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs181274112	chr14:105670026-105670027	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs587618295	chr14:105670045-105670046	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs587693202	chr14:105670067-105670068	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs587755164	chr14:105670073-105670074	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs148177735	chr14:105670088-105670089	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs587688294	chr14:105670115-105670116	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs587775666	chr14:105670168-105670169	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs587666331	chr14:105670183-105670184	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs141638611	chr14:105670244-105670245	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs28532164	chr14:105670256-105670257	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs35808550	chr14:105670262-105670263	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs376802706	chr14:105670295-105670296	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs587716355	chr14:105670352-105670353	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs368091788	chr14:105670373-105670374	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs587711791	chr14:105670404-105670405	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs142013239	chr14:105670435-105670436	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs587665887	chr14:105670436-105670437	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs371496337	chr14:105670483-105670484	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs587608288	chr14:105670513-105670514	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs587665112	chr14:105670520-105670521	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs373534442	chr14:105670525-105670526	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs587745040	chr14:105670545-105670546	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs587613202	chr14:105670555-105670556	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs28477712	chr14:105670559-105670560	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs587730060	chr14:105670567-105670568	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs587633952	chr14:105670582-105670583	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs587711349	chr14:105670592-105670593	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs587776004	chr14:105670613-105670614	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs587643792	chr14:105670624-105670625	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs587701222	chr14:105670664-105670665	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs35971653	chr14:105670695-105670696	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs587630836	chr14:105670735-105670736	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs189114810	chr14:105670755-105670756	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs79740181	chr14:105670759-105670760	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs144786922	chr14:105670820-105670821	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs587708453	chr14:105670836-105670837	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs78954923	chr14:105670877-105670878	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs139951625	chr14:105670878-105670879	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs373270170	chr14:105670891-105670892	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs386781128	chr14:105670892-105670893	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs587722570	chr14:105670913-105670914	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs75917492	chr14:105670988-105670989	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs12431565	chr14:105670991-105670992	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105659000-105669800	Bivalent Enhancer	Fetal Stomach	stomach
2	chr14:105659200-105670600	Bivalent Enhancer	Fetal Muscle Leg	muscle
3	chr14:105663000-105672000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr14:105663400-105674800	Enhancers	Right Ventricle	heart
5	chr14:105663800-105672400	Weak transcription	HSMMtube	muscle
6	chr14:105663800-105681600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr14:105664000-105672000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr14:105665400-105670800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr14:105665600-105670800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:105665600-105671800	Weak transcription	HSMM	muscle
11	chr14:105666000-105670600	Weak transcription	A549	lung
12	chr14:105666600-105670200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:105667200-105670000	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr14:105667400-105669800	Enhancers	Primary hematopoietic stem cells	blood
15	chr14:105667400-105669800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
16	chr14:105667400-105674000	Enhancers	Brain Hippocampus Middle	brain
17	chr14:105667400-105674400	Enhancers	Pancreas	Pancrea
18	chr14:105667600-105670000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr14:105667600-105670200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr14:105667600-105670800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr14:105667600-105672600	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr14:105667800-105669800	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr14:105667800-105669800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr14:105667800-105669800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr14:105667800-105674200	Enhancers	Spleen	Spleen
26	chr14:105668000-105669800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr14:105668000-105669800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr14:105668000-105669800	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr14:105668000-105670000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:105668000-105670200	Bivalent Enhancer	Colonic Mucosa	Colon
31	chr14:105668000-105670800	Enhancers	Adipose Nuclei	Adipose
32	chr14:105668000-105674400	Enhancers	Left Ventricle	heart
33	chr14:105668200-105670000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr14:105668200-105687200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr14:105668400-105670600	Weak transcription	Right Atrium	heart
36	chr14:105668400-105670800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr14:105668400-105670800	Weak transcription	Lung	lung
38	chr14:105668400-105672600	Enhancers	Brain Cingulate Gyrus	brain
39	chr14:105668600-105669800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
40	chr14:105668600-105669800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr14:105668600-105669800	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr14:105668600-105669800	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr14:105668600-105671800	Enhancers	Fetal Brain Male	brain
44	chr14:105668600-105672200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr14:105668600-105683000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr14:105668600-105714200	Weak transcription	HUVEC	blood vessel
47	chr14:105668800-105669800	Enhancers	Primary T cells from cord blood	blood
48	chr14:105668800-105669800	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr14:105668800-105683000	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr14:105669000-105671400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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