Variant report

Variant rs2135219
Chromosome Location chr1:154857217-154857218
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:154850400-154857800 Weak transcription Lung lung
2 chr1:154851000-154857800 Weak transcription Ovary ovary
3 chr1:154854600-154859000 Weak transcription Right Atrium heart
4 chr1:154854800-154859000 Weak transcription Fetal Heart heart
5 chr1:154854800-154859200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr1:154854800-154859600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr1:154855000-154859400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr1:154855400-154858200 Enhancers Primary hematopoietic stem cells blood
9 chr1:154855800-154858000 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr1:154855800-154859800 Enhancers K562 blood
11 chr1:154856200-154859400 Enhancers Fetal Lung lung
12 chr1:154856400-154857400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr1:154856400-154858000 Enhancers Duodenum Mucosa Duodenum
14 chr1:154856400-154858200 Enhancers Fetal Stomach stomach
15 chr1:154856400-154858400 Enhancers HUVEC blood vessel
16 chr1:154856400-154861800 Enhancers Fetal Adrenal Gland Adrenal Gland
17 chr1:154856600-154859000 Weak transcription Left Ventricle heart
18 chr1:154856600-154859000 Weak transcription Spleen Spleen
19 chr1:154856800-154858000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
20 chr1:154857000-154857600 Enhancers Fetal Intestine Large intestine
21 chr1:154857000-154858000 Flanking Active TSS HepG2 liver
22 chr1:154857200-154858800 Weak transcription Skeletal Muscle Male skeletal muscle

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