Variant report

Variant	rs35212883
Chromosome Location	chr14:32853312-32853313
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32847000-32854000	Weak transcription	Fetal Brain Female	brain
2	chr14:32849000-32867400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:32850800-32854200	Enhancers	NHEK	skin
4	chr14:32850800-32854400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr14:32851000-32854200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr14:32851200-32854000	Enhancers	Brain Hippocampus Middle	brain
7	chr14:32851800-32853600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:32851800-32854000	Enhancers	Brain Cingulate Gyrus	brain
9	chr14:32852000-32853400	Weak transcription	Stomach Mucosa	stomach
10	chr14:32852600-32854000	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr14:32852800-32854400	Enhancers	Brain Anterior Caudate	brain
12	chr14:32853000-32853400	Enhancers	Psoas Muscle	Psoas
13	chr14:32853000-32854600	Enhancers	Brain Substantia Nigra	brain
14	chr14:32853200-32853600	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr14:32853200-32853800	Weak transcription	Brain Angular Gyrus	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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