Variant report

Variant	rs10865926
Chromosome Location	chr3:43145323-43145324
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:43142624..43144798-chr3:43145061..43147327,2	K562	blood:
2	chr3:43143888..43145870-chr3:43147396..43148925,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000144647	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs4683359	0.92[AFR][1000 genomes]
rs491970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs535994	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs552472	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs632013	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs664197	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs674118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs939436	0.95[AFR][1000 genomes]
rs9828191	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460522	chr3:42967597-43175207	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv590149	chr3:42967597-43175207	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv834672	chr3:43132722-43306272	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:43122400-43145800	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr3:43122800-43145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:43123000-43146400	Weak transcription	Duodenum Mucosa	Duodenum
4	chr3:43123000-43146600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr3:43123400-43146400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:43123600-43146600	Weak transcription	Fetal Intestine Small	intestine
7	chr3:43124400-43146000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr3:43124400-43146600	Weak transcription	Aorta	Aorta
9	chr3:43124600-43146800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr3:43131600-43145600	Weak transcription	Primary T cells from cord blood	blood
11	chr3:43132600-43146000	Weak transcription	Fetal Lung	lung
12	chr3:43135000-43145600	Weak transcription	HepG2	liver
13	chr3:43136200-43146000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr3:43136800-43146600	Weak transcription	Esophagus	oesophagus
15	chr3:43137000-43145600	Weak transcription	Brain Angular Gyrus	brain
16	chr3:43137000-43145800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr3:43137000-43145800	Weak transcription	Brain Hippocampus Middle	brain
18	chr3:43138800-43146200	Weak transcription	HSMMtube	muscle
19	chr3:43140000-43146200	Weak transcription	Liver	Liver
20	chr3:43140400-43145800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr3:43143200-43146200	Enhancers	Fetal Muscle Leg	muscle
22	chr3:43143200-43146600	Enhancers	Placenta	Placenta
23	chr3:43143400-43146600	Enhancers	Left Ventricle	heart
24	chr3:43143600-43146400	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr3:43143600-43146400	Enhancers	Fetal Stomach	stomach
26	chr3:43143800-43145800	Enhancers	Brain Anterior Caudate	brain
27	chr3:43143800-43146800	Enhancers	Fetal Heart	heart
28	chr3:43144000-43146400	Enhancers	Pancreas	Pancrea
29	chr3:43144200-43145400	Enhancers	K562	blood
30	chr3:43144200-43145800	Enhancers	Stomach Smooth Muscle	stomach
31	chr3:43144200-43146400	Enhancers	Lung	lung
32	chr3:43144200-43146600	Enhancers	Right Atrium	heart
33	chr3:43144400-43145800	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr3:43144400-43146000	Enhancers	Dnd41	blood
35	chr3:43144400-43146200	Enhancers	Fetal Brain Male	brain
36	chr3:43144400-43146400	Enhancers	Brain Substantia Nigra	brain
37	chr3:43144400-43146400	Enhancers	Fetal Muscle Trunk	muscle
38	chr3:43144400-43146600	Enhancers	Right Ventricle	heart
39	chr3:43144600-43145600	Weak transcription	Fetal Thymus	thymus
40	chr3:43144800-43145400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:43144800-43145400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr3:43144800-43145800	Enhancers	Brain Cingulate Gyrus	brain
43	chr3:43144800-43146200	Enhancers	Ovary	ovary
44	chr3:43145000-43145400	Weak transcription	Fetal Brain Female	brain
45	chr3:43145000-43145800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr3:43145000-43146000	Weak transcription	Spleen	Spleen
47	chr3:43145000-43146200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr3:43145000-43146200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr3:43145000-43146200	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr3:43145000-43146400	Enhancers	Colon Smooth Muscle	Colon

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