Variant report

Variant	rs11195365
Chromosome Location	chr10:112643037-112643038
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUN	chr10:112643002-112644280	K562	blood:	n/a	n/a
2	POLR2A	chr10:112642992-112643191	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:112639114..112641206-chr10:112642389..112644492,2	MCF-7	breast:
2	chr10:112642885..112644521-chr10:112667962..112669630,2	K562	blood:

Variant related genes	Relation type
PDCD4	TF binding region
ENSG00000150593	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11195364	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11195377	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12358859	1.00[CEU][hapmap]
rs35369916	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045608	chr10:112524813-112677557	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1041758	chr10:112552897-112677557	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1051566	chr10:112580049-112730573	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv1035602	chr10:112636053-112781413	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:112632800-112643800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:112632800-112643800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:112632800-112678000	Weak transcription	Lung	lung
4	chr10:112632800-112678200	Weak transcription	Spleen	Spleen
5	chr10:112633200-112643800	Weak transcription	Esophagus	oesophagus
6	chr10:112633200-112643800	Weak transcription	Left Ventricle	heart
7	chr10:112633200-112656000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:112633200-112656800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:112633400-112662000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr10:112633600-112653800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr10:112633600-112655200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr10:112633800-112643800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr10:112633800-112659800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr10:112634000-112643400	Weak transcription	Fetal Muscle Leg	muscle
15	chr10:112634000-112643800	Weak transcription	Thymus	Thymus
16	chr10:112634000-112647000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr10:112634000-112649400	Weak transcription	Brain Hippocampus Middle	brain
18	chr10:112634000-112655000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr10:112634000-112655800	Weak transcription	Psoas Muscle	Psoas
20	chr10:112634000-112656000	Weak transcription	Right Ventricle	heart
21	chr10:112634000-112662400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr10:112634200-112643600	Weak transcription	Brain Germinal Matrix	brain
23	chr10:112634200-112643600	Weak transcription	Right Atrium	heart
24	chr10:112634200-112646600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr10:112634200-112655800	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr10:112634400-112643200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr10:112634400-112643400	Weak transcription	NHLF	lung
28	chr10:112634600-112643400	Weak transcription	A549	lung
29	chr10:112634600-112656600	Weak transcription	NHEK	skin
30	chr10:112634800-112643400	Weak transcription	K562	blood
31	chr10:112634800-112643800	Weak transcription	Fetal Stomach	stomach
32	chr10:112634800-112646000	Weak transcription	Fetal Brain Male	brain
33	chr10:112634800-112661800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr10:112634800-112677400	Weak transcription	HUVEC	blood vessel
35	chr10:112635400-112657000	Strong transcription	HSMM	muscle
36	chr10:112635400-112661800	Strong transcription	Placenta	Placenta
37	chr10:112635600-112660600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr10:112635600-112662200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr10:112635600-112663400	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr10:112635800-112647800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
41	chr10:112635800-112662200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr10:112636000-112643400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr10:112636000-112652000	Strong transcription	Fetal Intestine Large	intestine
44	chr10:112636000-112664400	Strong transcription	Fetal Thymus	thymus
45	chr10:112636200-112643400	Strong transcription	Primary B cells from peripheral blood	blood
46	chr10:112636200-112643400	Weak transcription	Small Intestine	intestine
47	chr10:112636200-112643800	Weak transcription	Fetal Intestine Small	intestine
48	chr10:112636200-112656200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr10:112636400-112664800	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr10:112637200-112646400	Strong transcription	Rectal Mucosa Donor 29	rectum

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