Variant report

Variant	rs74109990
Chromosome Location	chr12:76236023-76236024
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:76234777..76238439-chr12:76239479..76242748,4	MCF-7	breast:
2	chr12:76230979..76233331-chr12:76235384..76238133,2	MCF-7	breast:
3	chr12:76204669..76207624-chr12:76235185..76236726,2	MCF-7	breast:
4	chr12:76215518..76217462-chr12:76234728..76237383,2	K562	blood:

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs59275865	1.00[AFR][1000 genomes]
rs74110023	1.00[AFR][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	nsv1040583	chr12:75742802-76360276	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv832463	chr12:76136551-76316703	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv899315	chr12:76163309-76385096	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1041730	chr12:76198863-76331900	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:76228600-76239800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:76228600-76250000	Weak transcription	Pancreas	Pancrea
3	chr12:76231000-76237800	Weak transcription	HepG2	liver
4	chr12:76232200-76241400	Weak transcription	Fetal Stomach	stomach
5	chr12:76232800-76237400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:76234200-76236200	Enhancers	Fetal Lung	lung
7	chr12:76234600-76236400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:76234600-76236600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr12:76234600-76236800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr12:76234600-76237200	Enhancers	Brain Germinal Matrix	brain
11	chr12:76235400-76236200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr12:76235400-76236200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr12:76235400-76236200	Enhancers	Fetal Muscle Leg	muscle
14	chr12:76235400-76236400	Enhancers	Brain Substantia Nigra	brain
15	chr12:76235600-76236200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr12:76235600-76236200	Enhancers	Brain Anterior Caudate	brain
17	chr12:76235600-76236400	Enhancers	Brain Hippocampus Middle	brain
18	chr12:76235600-76236800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:76235600-76242600	Weak transcription	Left Ventricle	heart
20	chr12:76236000-76237800	Weak transcription	Fetal Brain Male	brain
21	chr12:76236000-76238400	Weak transcription	HUVEC	blood vessel
22	chr12:76236000-76239000	Weak transcription	Brain Angular Gyrus	brain
23	chr12:76236000-76239400	Weak transcription	Fetal Brain Female	brain
24	chr12:76236000-76242000	Weak transcription	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links