Variant report

Variant	rs73043022
Chromosome Location	chr19:38839104-38839105
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:38834987..38838242-chr19:38838656..38842905,5	MCF-7	breast:
2	chr19:38838273..38840146-chr19:38846615..38848893,2	MCF-7	breast:
3	chr19:38836592..38840441-chr19:38840696..38845039,4	K562	blood:

Variant related genes	Relation type
ENSG00000099338	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs3885340	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61734615	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73037321	0.87[EUR][1000 genomes]
rs73037333	0.84[EUR][1000 genomes]
rs73037343	0.87[EUR][1000 genomes]
rs73037346	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs73041292	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73043012	1.00[EUR][1000 genomes]
rs73043013	1.00[EUR][1000 genomes]
rs73043014	1.00[EUR][1000 genomes]
rs73043015	1.00[EUR][1000 genomes]
rs73043019	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73043021	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73043027	1.00[EUR][1000 genomes]
rs73043028	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73043029	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73043030	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73043033	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73043098	0.81[EUR][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	nsv1063471	chr19:38734744-39148392	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
2	nsv833822	chr19:38760748-38945105	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
3	nsv911658	chr19:38785318-39002140	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38828200-38840400	Weak transcription	Left Ventricle	heart
2	chr19:38828200-38841400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr19:38828200-38842000	Weak transcription	Brain Angular Gyrus	brain
4	chr19:38828200-38842600	Weak transcription	Esophagus	oesophagus
5	chr19:38828200-38844800	Weak transcription	Brain Substantia Nigra	brain
6	chr19:38828200-38852000	Weak transcription	Right Atrium	heart
7	chr19:38828400-38839200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr19:38828400-38839600	Weak transcription	Primary T cells from cord blood	blood
9	chr19:38828400-38839800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr19:38828400-38839800	Weak transcription	Right Ventricle	heart
11	chr19:38828400-38840000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr19:38828600-38839600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr19:38829400-38839800	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr19:38829600-38839400	Weak transcription	Thymus	Thymus
15	chr19:38830200-38844800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr19:38832200-38840400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr19:38833800-38840400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr19:38834200-38845000	Weak transcription	Spleen	Spleen
19	chr19:38835000-38842600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:38835200-38839400	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr19:38835200-38840200	Weak transcription	Brain Hippocampus Middle	brain
22	chr19:38835200-38840200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr19:38835200-38842600	Weak transcription	Fetal Muscle Leg	muscle
24	chr19:38835200-38847000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr19:38835200-38852000	Weak transcription	Pancreas	Pancrea
26	chr19:38836800-38845000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr19:38837200-38840200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr19:38837400-38842600	Weak transcription	Brain Germinal Matrix	brain
29	chr19:38837400-38842600	Weak transcription	Fetal Muscle Trunk	muscle
30	chr19:38837800-38843000	Weak transcription	Fetal Intestine Small	intestine
31	chr19:38837800-38843800	Weak transcription	Fetal Brain Female	brain
32	chr19:38838200-38841800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr19:38838200-38843200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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