Variant report

Variant	rs8014742
Chromosome Location	chr14:25320117-25320118
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10133078	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10136693	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10138734	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12433081	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1381318	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1381319	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1887935	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2282034	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2297059	1.00[CEU][hapmap];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2877685	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3759642	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3759643	1.00[CEU][hapmap];0.92[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55951119	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6574019	0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6574033	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs749595	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs766668	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8016612	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs872978	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs872979	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9319	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041336	chr14:24726564-25527319	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542000	chr14:24726564-25527319	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv901504	chr14:25184210-25646203	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv901505	chr14:25237268-25360584	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv901506	chr14:25295551-25377188	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25288600-25322800	Weak transcription	Placenta	Placenta
2	chr14:25306600-25321200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:25309000-25328000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr14:25309800-25323000	Weak transcription	Pancreas	Pancrea
5	chr14:25309800-25324400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr14:25310000-25321000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:25310200-25320800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr14:25313800-25320800	Weak transcription	Left Ventricle	heart
9	chr14:25313800-25323400	Weak transcription	Small Intestine	intestine
10	chr14:25314600-25333600	Weak transcription	Lung	lung
11	chr14:25315400-25320800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr14:25315600-25320800	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr14:25315600-25321000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr14:25315600-25321400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr14:25315600-25330400	Weak transcription	Brain Angular Gyrus	brain
16	chr14:25315800-25320200	Weak transcription	Fetal Intestine Large	intestine
17	chr14:25315800-25320800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr14:25315800-25320800	Weak transcription	HepG2	liver
19	chr14:25315800-25324200	Weak transcription	Brain Cingulate Gyrus	brain
20	chr14:25316000-25320800	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr14:25316000-25330400	Weak transcription	Brain Hippocampus Middle	brain
22	chr14:25316600-25320800	Weak transcription	Fetal Intestine Small	intestine
23	chr14:25316800-25320200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr14:25317800-25323000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr14:25317800-25344000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr14:25318000-25321200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr14:25318000-25328400	Weak transcription	Right Ventricle	heart
28	chr14:25318200-25330200	Weak transcription	Fetal Heart	heart
29	chr14:25318400-25321200	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr14:25318400-25321400	Weak transcription	Osteobl	bone
31	chr14:25319000-25320800	Weak transcription	NH-A	brain
32	chr14:25319000-25330400	Weak transcription	Adipose Nuclei	Adipose
33	chr14:25319200-25320800	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr14:25319200-25321400	Weak transcription	HSMM	muscle
35	chr14:25319400-25321600	Strong transcription	Fetal Muscle Leg	muscle
36	chr14:25319600-25320200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr14:25319600-25320400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr14:25319600-25320800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr14:25319600-25320800	Weak transcription	Brain Anterior Caudate	brain
40	chr14:25319600-25321200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr14:25319600-25321800	Strong transcription	Fetal Lung	lung
42	chr14:25319600-25322200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr14:25319600-25344600	Weak transcription	NHDF-Ad	bronchial
44	chr14:25319800-25320600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr14:25320000-25320800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr14:25320000-25321000	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr14:25320000-25321000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:25320000-25321000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr14:25320000-25326000	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr14:25320000-25330200	Weak transcription	HSMMtube	muscle

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