Variant report

Variant	esv3390205
Chromosome Location	chr14:105291932-105294680
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:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105289983..105292400-chr14:105295807..105297431,2	MCF-7	breast:
2	chr14:105287225..105290811-chr14:105291462..105294551,5	K562	blood:
3	chr14:105218306..105221418-chr14:105291704..105295058,3	MCF-7	breast:
4	chr14:105290213..105292759-chr8:144821047..144823089,2	MCF-7	breast:
5	chr14:105268427..105271161-chr14:105291567..105294333,2	K562	blood:
6	chr14:105234486..105235367-chr14:105292449..105293276,4	MCF-7	breast:
7	chr14:105189504..105190527-chr14:105292721..105293350,3	MCF-7	breast:
8	chr14:105234529..105236014-chr14:105292452..105293414,8	MCF-7	breast:
9	chr14:105214906..105218911-chr14:105291555..105293979,3	K562	blood:
10	chr14:105292450..105295087-chr14:105329500..105333525,7	MCF-7	breast:
11	chr14:105293628..105294624-chr14:105337330..105337838,2	MCF-7	breast:
12	chr14:105234590..105235623-chr14:105292148..105293402,8	K562	blood:
13	chr14:105214906..105217436-chr14:105291555..105293979,2	K562	blood:
14	chr14:105280966..105282808-chr14:105292129..105294295,2	K562	blood:
15	chr14:105233810..105238299-chr14:105291361..105295745,6	K562	blood:
16	chr14:105234738..105235318-chr14:105293407..105294201,2	K562	blood:
17	chr14:105190468..105192484-chr14:105291233..105293061,2	MCF-7	breast:
18	chr14:105293691..105294557-chr14:105406827..105407640,3	MCF-7	breast:
19	chr14:105294072..105294589-chr14:105362751..105363336,2	MCF-7	breast:
20	chr14:105292149..105293877-chr14:105432490..105434872,2	MCF-7	breast:
21	chr14:105235443..105237438-chr14:105291289..105294293,4	K562	blood:
22	chr14:105189826..105192403-chr14:105291424..105294271,3	MCF-7	breast:
23	chr14:105280954..105282466-chr14:105292119..105293629,2	K562	blood:
24	chr14:105291374..105295422-chr14:105328190..105336195,18	MCF-7	breast:
25	chr14:105292163..105294059-chr14:105311800..105314620,2	K562	blood:
26	chr14:105293283..105294221-chr14:105511851..105512622,2	MCF-7	breast:
27	chr14:105282552..105286026-chr14:105289483..105293569,5	K562	blood:
28	chr14:105226070..105227570-chr14:105291620..105294600,2	MCF-7	breast:
29	chr14:105197416..105200391-chr14:105289343..105292189,2	MCF-7	breast:
30	chr14:105292878..105295272-chr14:105309126..105311348,2	MCF-7	breast:
31	chr14:105292002..105293559-chr14:105403118..105405949,2	MCF-7	breast:
32	chr14:105264645..105268219-chr14:105292165..105294813,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000203499	chromatin interactions
ENSG00000185100	chromatin interactions
ENSG00000184990	chromatin interactions
ENSG00000258430	chromatin interactions
ENSG00000099814	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000258701	chromatin interactions

Extended variants
information (count: 91 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:91 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386781077	chr14:105291932-105291933	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs183417494	chr14:105291933-105291934	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs71423203	chr14:105291935-105291936	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs565915699	chr14:105291943-105291944	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs535496679	chr14:105291949-105291950	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs534923841	chr14:105291963-105291964	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs374410558	chr14:105291976-105291977	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs578081420	chr14:105292022-105292023	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs555190528	chr14:105292027-105292028	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs189954538	chr14:105292031-105292032	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs368756613	chr14:105292073-105292074	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs534593500	chr14:105292096-105292097	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs72635200	chr14:105292123-105292124	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs542914872	chr14:105292167-105292168	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs559711251	chr14:105292192-105292193	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs142818259	chr14:105292211-105292212	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs545263557	chr14:105292242-105292243	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs66987285	chr14:105292245-105292246	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs182292188	chr14:105292255-105292256	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs550420625	chr14:105292272-105292273	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs12887198	chr14:105292281-105292282	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs187327548	chr14:105292380-105292381	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs549251112	chr14:105292392-105292393	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs369885180	chr14:105292405-105292406	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs566075902	chr14:105292409-105292410	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs534888160	chr14:105292415-105292416	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs12891602	chr14:105292434-105292435	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs551901910	chr14:105292477-105292478	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs371643282	chr14:105292546-105292547	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs76626126	chr14:105292573-105292574	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs557194369	chr14:105292608-105292609	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs67906390	chr14:105292650-105292651	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs536678129	chr14:105292652-105292653	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs553294015	chr14:105292656-105292657	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs377251134	chr14:105292657-105292658	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs573220443	chr14:105292666-105292667	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs147268612	chr14:105292713-105292714	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs545331635	chr14:105292733-105292734	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs565056704	chr14:105292737-105292738	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs56317173	chr14:105292771-105292772	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs544273881	chr14:105292775-105292776	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs560856128	chr14:105292809-105292810	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs529634633	chr14:105292871-105292872	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs56000079	chr14:105292883-105292884	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs559718257	chr14:105292955-105292956	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs528717222	chr14:105292967-105292968	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs551801669	chr14:105292976-105292977	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs73350382	chr14:105292978-105292979	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs542263285	chr14:105292994-105292995	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs544606913	chr14:105293019-105293020	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105283200-105292200	Weak transcription	Gastric	stomach
2	chr14:105283400-105292000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr14:105283400-105292000	Weak transcription	Right Atrium	heart
4	chr14:105283600-105292000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr14:105283600-105292000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr14:105283800-105292000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr14:105283800-105292200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr14:105284000-105292000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr14:105284400-105292200	Weak transcription	K562	blood
10	chr14:105285000-105292200	Weak transcription	Dnd41	blood
11	chr14:105287200-105292000	Weak transcription	NH-A	brain
12	chr14:105287200-105292600	Weak transcription	HSMMtube	muscle
13	chr14:105287400-105292000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr14:105287400-105292000	Weak transcription	Brain Hippocampus Middle	brain
15	chr14:105287400-105292000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr14:105287400-105292000	Weak transcription	Pancreas	Pancrea
17	chr14:105287400-105292000	Weak transcription	Right Ventricle	heart
18	chr14:105287600-105292000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr14:105287600-105292000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:105287600-105292000	Weak transcription	HMEC	breast
21	chr14:105287600-105292200	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr14:105287800-105292000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr14:105287800-105292000	Weak transcription	Left Ventricle	heart
24	chr14:105287800-105292000	Weak transcription	Ovary	ovary
25	chr14:105287800-105292000	Weak transcription	A549	lung
26	chr14:105287800-105292200	Weak transcription	Brain Anterior Caudate	brain
27	chr14:105288000-105292000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr14:105288000-105292000	Weak transcription	Colonic Mucosa	Colon
29	chr14:105288000-105292200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr14:105288400-105292000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr14:105291000-105292800	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr14:105291200-105292200	Enhancers	Esophagus	oesophagus
33	chr14:105291400-105292200	Weak transcription	Fetal Kidney	kidney
34	chr14:105291600-105292000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr14:105291600-105292000	Enhancers	Placenta	Placenta
36	chr14:105291800-105292000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:105291800-105292000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr14:105291800-105292000	Active TSS	Primary T helper cells fromperipheralblood	blood
39	chr14:105291800-105292000	Weak transcription	Lung	lung
40	chr14:105291800-105292200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
41	chr14:105291800-105292200	Active TSS	Primary T cells from cord blood	blood
42	chr14:105291800-105292400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr14:105291800-105294400	Enhancers	Spleen	Spleen
44	chr14:105292000-105292200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
45	chr14:105292000-105292200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr14:105292000-105292200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:105292000-105292200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr14:105292000-105292200	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr14:105292000-105292200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
50	chr14:105292000-105292200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood

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