Variant report

Variant	rs73428910
Chromosome Location	chr11:15848440-15848441
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:15848101..15848993-chr11:16634904..16635824,3	K562	blood:
2	chr11:15847163..15849862-chr11:15922675..15924255,2	MCF-7	breast:
3	chr11:15845677..15847198-chr11:15848084..15850314,2	K562	blood:
4	chr11:15846564..15849425-chr11:16633366..16635288,2	K562	blood:

Variant related genes	Relation type
ENSG00000110696	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11821667	1.00[EUR][1000 genomes]
rs11821691	1.00[EUR][1000 genomes]
rs6486264	1.00[EUR][1000 genomes]
rs6486265	1.00[EUR][1000 genomes]
rs67677040	1.00[EUR][1000 genomes]
rs7112764	1.00[EUR][1000 genomes]
rs7113024	1.00[EUR][1000 genomes]
rs72860688	1.00[EUR][1000 genomes]
rs72860691	1.00[EUR][1000 genomes]
rs72862108	1.00[EUR][1000 genomes]
rs72862120	1.00[EUR][1000 genomes]
rs72862126	1.00[EUR][1000 genomes]
rs72862149	1.00[EUR][1000 genomes]
rs72862152	1.00[EUR][1000 genomes]
rs72862154	1.00[EUR][1000 genomes]
rs72862159	1.00[EUR][1000 genomes]
rs7945894	1.00[EUR][1000 genomes]
rs7946754	1.00[EUR][1000 genomes]
rs7947977	0.93[EUR][1000 genomes]
rs7948085	1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832073	chr11:15822409-15984078	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15839400-15850200	Weak transcription	Aorta	Aorta
2	chr11:15841600-15848600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr11:15841800-15848600	Weak transcription	Right Atrium	heart
4	chr11:15841800-15849200	Weak transcription	Adipose Nuclei	Adipose
5	chr11:15841800-15849600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr11:15846600-15849000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:15847000-15848800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr11:15847200-15850600	Enhancers	Brain Germinal Matrix	brain
9	chr11:15847400-15848800	Enhancers	Fetal Muscle Trunk	muscle
10	chr11:15847400-15852200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr11:15847400-15853800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr11:15848000-15848600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:15848000-15848800	Enhancers	Left Ventricle	heart
14	chr11:15848000-15850600	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr11:15848000-15852800	Enhancers	Brain Hippocampus Middle	brain
16	chr11:15848000-15853400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr11:15848200-15849200	Weak transcription	Fetal Muscle Leg	muscle
18	chr11:15848200-15850000	Weak transcription	Pancreas	Pancrea
19	chr11:15848200-15850600	Enhancers	Brain Substantia Nigra	brain
20	chr11:15848400-15849200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr11:15848400-15849800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:15848400-15852400	Weak transcription	NH-A	brain
23	chr11:15848400-15853000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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