Variant report

Variant	rs13090341
Chromosome Location	chr3:20108516-20108517
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:20108340..20110457-chr3:20115203..20117134,2	K562	blood:
2	chr3:20080894..20083209-chr3:20107151..20110064,3	K562	blood:

Variant related genes	Relation type
ENSG00000114166	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs6803231	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1825914	chr3:19549859-20137270	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	esv1833006	chr3:19562271-20389045	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv1833139	chr3:19579860-20121349	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv1010613	chr3:19942032-20461486	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	esv1826030	chr3:19972766-20170581	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	esv1826830	chr3:19982972-20632072	Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	nsv997486	chr3:20006702-20113989	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	esv1829542	chr3:20009231-20384627	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
9	nsv834627	chr3:20068115-20227975	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv433359	chr3:20090908-20587572	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
11	nsv470450	chr3:20096735-20389045	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20099000-20122600	Weak transcription	Aorta	Aorta
2	chr3:20099400-20108600	Weak transcription	Fetal Stomach	stomach
3	chr3:20099400-20112600	Weak transcription	HSMMtube	muscle
4	chr3:20099400-20112800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr3:20099400-20122600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr3:20099400-20122800	Weak transcription	Lung	lung
7	chr3:20100000-20109200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr3:20102800-20113400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr3:20102800-20136800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr3:20103000-20111400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr3:20103200-20108600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr3:20103200-20108600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr3:20103200-20108600	Weak transcription	NHDF-Ad	bronchial
14	chr3:20103200-20108800	Weak transcription	A549	lung
15	chr3:20103200-20110400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr3:20103200-20112600	Weak transcription	Primary T cells from cord blood	blood
17	chr3:20103200-20112800	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr3:20103200-20113000	Weak transcription	Primary B cells from cord blood	blood
19	chr3:20103200-20113000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr3:20103200-20113000	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr3:20103200-20113200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr3:20103200-20114000	Weak transcription	Liver	Liver
23	chr3:20103200-20119400	Weak transcription	Fetal Intestine Small	intestine
24	chr3:20103200-20122200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr3:20104000-20111000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr3:20104200-20111800	Enhancers	Brain Substantia Nigra	brain
27	chr3:20104400-20113400	Enhancers	Brain Hippocampus Middle	brain
28	chr3:20105000-20111000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr3:20105200-20110800	Enhancers	HMEC	breast
30	chr3:20105800-20113200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr3:20106000-20108600	Enhancers	Fetal Muscle Leg	muscle
32	chr3:20106000-20109200	Enhancers	Brain Anterior Caudate	brain
33	chr3:20106000-20111400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr3:20106400-20109200	Enhancers	Brain Cingulate Gyrus	brain
35	chr3:20106400-20109200	Enhancers	Fetal Lung	lung
36	chr3:20106400-20122600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr3:20106600-20110000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr3:20106600-20110200	Enhancers	Primary T cells fromperipheralblood	blood
39	chr3:20106800-20108600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr3:20106800-20108800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr3:20106800-20109400	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr3:20106800-20112600	Weak transcription	Fetal Heart	heart
43	chr3:20106800-20130800	Weak transcription	Fetal Intestine Large	intestine
44	chr3:20107000-20108600	Weak transcription	Brain Angular Gyrus	brain
45	chr3:20107000-20108800	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr3:20107000-20109200	Enhancers	K562	blood
47	chr3:20107000-20109400	Enhancers	NHEK	skin
48	chr3:20107000-20110000	Weak transcription	Rectal Smooth Muscle	rectum
49	chr3:20107000-20111400	Weak transcription	Right Ventricle	heart
50	chr3:20107000-20112200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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