Variant report

Variant	rs16841075
Chromosome Location	chr2:133530556-133530557
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:133529831..133532826-chr2:133534612..133536132,2	K562	blood:
2	chr2:133530106..133532173-chr2:133536887..133539675,2	K562	blood:

Variant related genes	Relation type
ENSG00000176771	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11679975	0.92[JPT][hapmap];1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs11687264	1.00[YRI][hapmap]
rs11692657	0.92[JPT][hapmap]
rs12618525	0.92[JPT][hapmap]
rs1367392	0.92[JPT][hapmap];1.00[YRI][hapmap]
rs1374739	0.92[JPT][hapmap]
rs1374740	0.92[JPT][hapmap]
rs16841087	0.83[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs16841146	0.87[ASN][1000 genomes]
rs16841210	0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs16841277	0.92[JPT][hapmap];1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs16842050	0.85[JPT][hapmap];1.00[YRI][hapmap]
rs16842369	1.00[YRI][hapmap]
rs17397380	1.00[YRI][hapmap]
rs1839003	1.00[YRI][hapmap]
rs4143562	0.92[JPT][hapmap];1.00[YRI][hapmap];0.85[ASN][1000 genomes]
rs61995744	0.82[ASN][1000 genomes]
rs72847207	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs72847208	0.87[ASN][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	nsv1011421	chr2:132895241-133682185	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv875137	chr2:133167263-133714142	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv583158	chr2:133316092-133862100	Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv875138	chr2:133410921-133761794	Enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	nsv1002955	chr2:133440142-133743211	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv834379	chr2:133471980-133665601	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs16841075	UBXN4	cis	cerebellum	SCAN

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133510400-133530600	Weak transcription	Brain Hippocampus Middle	brain
2	chr2:133512400-133539400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr2:133515800-133532200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:133517600-133539800	Weak transcription	Brain Substantia Nigra	brain
5	chr2:133519800-133539800	Weak transcription	Fetal Stomach	stomach
6	chr2:133523400-133544400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:133524200-133547800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:133525400-133531200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:133526800-133533200	Weak transcription	Fetal Brain Male	brain
10	chr2:133527400-133533000	Weak transcription	NHLF	lung
11	chr2:133527400-133538200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr2:133527600-133536800	Weak transcription	Fetal Brain Female	brain
13	chr2:133527600-133539400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr2:133527600-133544200	Weak transcription	Left Ventricle	heart
15	chr2:133527800-133531800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:133528000-133541800	Weak transcription	Fetal Muscle Trunk	muscle
17	chr2:133529000-133530800	Strong transcription	Ovary	ovary
18	chr2:133529000-133540000	Weak transcription	Brain Anterior Caudate	brain
19	chr2:133529000-133540200	Weak transcription	Lung	lung
20	chr2:133529400-133531400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr2:133529400-133540600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr2:133529400-133544400	Weak transcription	Fetal Intestine Large	intestine
23	chr2:133529600-133539400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr2:133529800-133530600	Enhancers	Brain Germinal Matrix	brain
25	chr2:133530400-133530600	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr2:133530400-133530800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:133530400-133530800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:133530400-133530800	Strong transcription	Liver	Liver
29	chr2:133530400-133530800	ZNF genes & repeats	Esophagus	oesophagus
30	chr2:133530400-133530800	Enhancers	Fetal Intestine Small	intestine

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