Variant report

Variant	rs12250249
Chromosome Location	chr10:118522719-118522720
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:118512400-118525400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:118516400-118523000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr10:118517200-118523000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr10:118517200-118524600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:118518800-118526200	Weak transcription	Colon Smooth Muscle	Colon
6	chr10:118521000-118524800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr10:118521200-118522800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr10:118521200-118523800	Enhancers	Brain Angular Gyrus	brain
9	chr10:118521200-118524000	Enhancers	Brain Cingulate Gyrus	brain
10	chr10:118521200-118524000	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr10:118521200-118524200	Enhancers	Brain Hippocampus Middle	brain
12	chr10:118521400-118523800	Enhancers	Brain Anterior Caudate	brain
13	chr10:118521400-118524000	Enhancers	Brain Substantia Nigra	brain
14	chr10:118521400-118524000	Enhancers	HepG2	liver
15	chr10:118521600-118522800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr10:118521800-118523000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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