Variant report

Variant	rs58063463
Chromosome Location	chr14:64418348-64418349
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs35920722	1.00[AMR][1000 genomes]
rs35960129	1.00[AMR][1000 genomes]
rs41319545	1.00[AMR][1000 genomes]
rs57705252	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60136116	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1038825	chr14:64109441-64491720	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1037140	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv542119	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv1793389	chr14:64346190-64457224	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv902019	chr14:64395569-64882380	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64365000-64430200	Weak transcription	Fetal Brain Male	brain
2	chr14:64390600-64418800	Weak transcription	HepG2	liver
3	chr14:64393200-64419800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:64395000-64491000	Weak transcription	Psoas Muscle	Psoas
5	chr14:64396000-64418600	Weak transcription	Fetal Heart	heart
6	chr14:64400000-64419800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr14:64401400-64430200	Weak transcription	Stomach Mucosa	stomach
8	chr14:64401600-64427800	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr14:64403600-64432800	Weak transcription	Lung	lung
10	chr14:64405000-64423400	Weak transcription	HSMM	muscle
11	chr14:64405600-64418800	Weak transcription	HMEC	breast
12	chr14:64405800-64418800	Weak transcription	Small Intestine	intestine
13	chr14:64406200-64434400	Weak transcription	Hela-S3	cervix
14	chr14:64407200-64418800	Weak transcription	HUVEC	blood vessel
15	chr14:64408200-64432000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr14:64408400-64430200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr14:64410000-64418400	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr14:64410000-64422800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr14:64410000-64429600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr14:64411200-64424600	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr14:64411800-64425200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr14:64412200-64419000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:64414400-64439600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:64415400-64418600	Weak transcription	NHLF	lung
25	chr14:64415400-64435800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr14:64415600-64418800	Strong transcription	Primary T helper cells PMA-I stimulated	--
27	chr14:64415600-64419200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr14:64415600-64419400	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr14:64415600-64425400	Strong transcription	Dnd41	blood
30	chr14:64415600-64439000	Weak transcription	Stomach Smooth Muscle	stomach
31	chr14:64416000-64418800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr14:64416000-64419000	Strong transcription	Primary B cells from cord blood	blood
33	chr14:64416000-64419200	Strong transcription	Fetal Stomach	stomach
34	chr14:64416000-64421600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr14:64416200-64418400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr14:64416200-64418800	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr14:64416200-64418800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr14:64416200-64418800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr14:64416200-64418800	Strong transcription	Left Ventricle	heart
40	chr14:64416200-64419000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr14:64416200-64419000	Strong transcription	Fetal Intestine Small	intestine
42	chr14:64416200-64419000	Strong transcription	Fetal Kidney	kidney
43	chr14:64416200-64419000	Strong transcription	Fetal Thymus	thymus
44	chr14:64416200-64419200	Strong transcription	Fetal Intestine Large	intestine
45	chr14:64416200-64419200	Strong transcription	Thymus	Thymus
46	chr14:64416200-64419400	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr14:64416200-64419400	Strong transcription	Placenta	Placenta
48	chr14:64416200-64420200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr14:64416200-64420200	Strong transcription	GM12878-XiMat	blood
50	chr14:64416200-64420600	Strong transcription	Fetal Muscle Trunk	muscle

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