Variant report

Variant	rs13132415
Chromosome Location	chr4:89827492-89827493
allele	G/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:6)

rs_ID	r²[population]
rs13109149	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13124775	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1458556	0.89[AFR][1000 genomes]
rs17815990	0.84[AFR][1000 genomes]
rs17816380	0.89[AFR][1000 genomes]
rs62310474	0.89[AFR][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	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1009354	chr4:89725914-89985155	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv998651	chr4:89800245-89933445	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv537175	chr4:89800245-89933445	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv879532	chr4:89811195-89917135	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:89809200-89828800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:89816000-89829000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:89816800-89827800	Weak transcription	Fetal Brain Male	brain
4	chr4:89818000-89829000	Weak transcription	Pancreas	Pancrea
5	chr4:89818800-89828800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr4:89820000-89859200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr4:89821600-89827800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:89821800-89829200	Weak transcription	Osteobl	bone
9	chr4:89822800-89828400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr4:89824400-89829000	Weak transcription	Fetal Intestine Large	intestine
11	chr4:89824600-89834000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr4:89824800-89829000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr4:89825000-89828600	Weak transcription	Fetal Muscle Trunk	muscle
14	chr4:89825000-89831200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr4:89825200-89829000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:89825600-89827600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr4:89825600-89878400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr4:89825800-89828800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr4:89826000-89827600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr4:89826000-89828400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr4:89826000-89829000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:89826000-89829000	Weak transcription	Colon Smooth Muscle	Colon
23	chr4:89826000-89829000	Weak transcription	Fetal Muscle Leg	muscle
24	chr4:89826000-89832600	Weak transcription	Adipose Nuclei	Adipose
25	chr4:89826000-89839600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:89826400-89828000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr4:89826400-89828200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:89826400-89838400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:89826600-89828800	Weak transcription	Fetal Intestine Small	intestine
30	chr4:89826600-89836200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:89826800-89828600	Weak transcription	Fetal Stomach	stomach
32	chr4:89827000-89828600	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr4:89827000-89828600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr4:89827200-89837400	Weak transcription	Fetal Lung	lung
35	chr4:89827200-89847000	Weak transcription	Placenta	Placenta
36	chr4:89827400-89847000	Weak transcription	Ovary	ovary

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