The 2.0 version of rSNPBase

Variant report

Variant rs72693826
Chromosome Location chr1:165510929-165510930
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:165505600-165513000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:165507600-165512800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr1:165509800-165511400 Weak transcription Fetal Lung lung
4 chr1:165509800-165511800 Weak transcription Fetal Stomach stomach
5 chr1:165510200-165511000 Enhancers Fetal Muscle Trunk muscle
6 chr1:165510200-165513000 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr1:165510400-165512400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:165510400-165512800 Weak transcription Adipose Nuclei Adipose
9 chr1:165510400-165512800 Weak transcription Placenta Placenta
10 chr1:165510400-165512800 Weak transcription Right Atrium heart
11 chr1:165510400-165512800 Weak transcription Right Ventricle heart
12 chr1:165510400-165513000 Weak transcription Brain Inferior Temporal Lobe brain
13 chr1:165510600-165512000 Weak transcription Skeletal Muscle Female skeletal muscle
14 chr1:165510600-165512800 Weak transcription Left Ventricle heart
15 chr1:165510600-165512800 Weak transcription Psoas Muscle Psoas
16 chr1:165510600-165513000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
17 chr1:165510800-165511200 Weak transcription Fetal Muscle Leg muscle
18 chr1:165510800-165511200 Weak transcription Skeletal Muscle Male skeletal muscle
19 chr1:165510800-165511400 Weak transcription Fetal Heart heart

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Last update: Aug 31, 2015