Variant report

Variant	rs73554696
Chromosome Location	chr19:44051378-44051379
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:44050644..44056032-chr19:44057547..44060902,6	K562	blood:
2	chr19:44046417..44049052-chr19:44049423..44052069,2	MCF-7	breast:
3	chr19:44049826..44052731-chr19:44057585..44060177,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269177	Chromatin interaction
ENSG00000073050	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs168310	1.00[ASN][1000 genomes]
rs2854497	1.00[ASN][1000 genomes]
rs3213316	1.00[ASN][1000 genomes]
rs3213321	1.00[ASN][1000 genomes]
rs3213322	1.00[ASN][1000 genomes]
rs3213339	0.82[AMR][1000 genomes]
rs3213348	1.00[ASN][1000 genomes]
rs34439296	1.00[ASN][1000 genomes]
rs34471331	1.00[ASN][1000 genomes]
rs346049	1.00[ASN][1000 genomes]
rs399300	1.00[ASN][1000 genomes]
rs4251895	1.00[ASN][1000 genomes]
rs4251915	1.00[ASN][1000 genomes]
rs56015523	1.00[ASN][1000 genomes]
rs56204051	1.00[ASN][1000 genomes]
rs57817750	1.00[ASN][1000 genomes]
rs60175550	1.00[ASN][1000 genomes]
rs60273962	1.00[ASN][1000 genomes]
rs60889018	1.00[ASN][1000 genomes]
rs62113722	1.00[ASN][1000 genomes]
rs7257640	1.00[ASN][1000 genomes]
rs73554667	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73554679	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73556565	1.00[ASN][1000 genomes]
rs73556581	1.00[ASN][1000 genomes]
rs8104645	1.00[ASN][1000 genomes]
rs8110767	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055872	chr19:43173614-44075193	Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv544009	chr19:43173614-44075193	Enhancers ZNF genes & repeats Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS 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 target site	43 gene(s)	inside rSNPs	diseases
3	nsv1067126	chr19:43260649-44075194	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv544015	chr19:43260649-44075194	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv1057657	chr19:43302497-44076564	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	nsv1059631	chr19:43316978-44075054	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv544030	chr19:43316978-44075054	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	nsv532820	chr19:43807486-44080610	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv1056721	chr19:43808474-44095077	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv532821	chr19:43842383-44357315	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
11	nsv1058162	chr19:43846238-44055058	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv1056785	chr19:44010370-44081601	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv912107	chr19:44030998-44055726	Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44038600-44054000	Weak transcription	Psoas Muscle	Psoas
2	chr19:44038800-44055800	Weak transcription	Stomach Mucosa	stomach
3	chr19:44039200-44078600	Weak transcription	Hela-S3	cervix
4	chr19:44040200-44052000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr19:44040200-44052200	Strong transcription	Fetal Muscle Leg	muscle
6	chr19:44040600-44052000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr19:44040800-44051800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr19:44040800-44060800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr19:44041600-44051400	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr19:44041600-44051600	Strong transcription	Fetal Intestine Large	intestine
11	chr19:44041600-44052200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr19:44041800-44065200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr19:44042000-44051600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr19:44042000-44051600	Strong transcription	Skeletal Muscle Male	skeletal muscle
15	chr19:44042400-44052000	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr19:44042400-44058000	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr19:44042600-44052000	Strong transcription	Placenta	Placenta
18	chr19:44043200-44051800	Strong transcription	Brain Hippocampus Middle	brain
19	chr19:44043200-44064600	Weak transcription	NHDF-Ad	bronchial
20	chr19:44043400-44051400	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr19:44043400-44051400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr19:44043400-44051600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr19:44043400-44052200	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr19:44043400-44058800	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr19:44043400-44059000	Strong transcription	Fetal Muscle Trunk	muscle
26	chr19:44043400-44059200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr19:44043600-44051600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr19:44043600-44052000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr19:44043600-44054600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr19:44043600-44057800	Strong transcription	Stomach Smooth Muscle	stomach
31	chr19:44043600-44059200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr19:44043600-44065800	Strong transcription	Adipose Nuclei	Adipose
33	chr19:44043800-44051400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:44043800-44051600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr19:44043800-44051600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr19:44043800-44051600	Strong transcription	Fetal Brain Female	brain
37	chr19:44043800-44051800	Strong transcription	Lung	lung
38	chr19:44043800-44052000	Strong transcription	Fetal Intestine Small	intestine
39	chr19:44043800-44065800	Weak transcription	Fetal Heart	heart
40	chr19:44043800-44074000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr19:44044000-44051400	Strong transcription	Brain Anterior Caudate	brain
42	chr19:44044000-44051600	Strong transcription	Primary B cells from peripheral blood	blood
43	chr19:44044000-44051600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr19:44044000-44052000	Strong transcription	Fetal Stomach	stomach
45	chr19:44044200-44051400	Strong transcription	Brain Inferior Temporal Lobe	brain
46	chr19:44044600-44069000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr19:44045000-44051400	Strong transcription	Fetal Lung	lung
48	chr19:44045200-44062800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr19:44045600-44051600	Strong transcription	Brain Angular Gyrus	brain
50	chr19:44046000-44051400	Strong transcription	Gastric	stomach

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