The 2.0 version of rSNPBase

Variant report

Variant rs28380530
Chromosome Location chr2:40490706-40490707
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:40478800-40496600 Weak transcription Right Ventricle heart
2 chr2:40478800-40499600 Weak transcription Rectal Smooth Muscle rectum
3 chr2:40485800-40492800 Weak transcription Colon Smooth Muscle Colon
4 chr2:40487600-40499600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:40487600-40503200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr2:40487600-40505600 Weak transcription HSMM muscle
7 chr2:40487800-40492200 Weak transcription Fetal Adrenal Gland Adrenal Gland
8 chr2:40487800-40499800 Weak transcription Osteobl bone
9 chr2:40487800-40502600 Weak transcription Monocytes-CD14+_RO01746 blood
10 chr2:40488200-40506200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr2:40488400-40492000 Weak transcription Fetal Intestine Large intestine
12 chr2:40488400-40492000 Weak transcription Fetal Intestine Small intestine
13 chr2:40488400-40498200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr2:40488600-40502800 Weak transcription Primary monocytes fromperipheralblood blood
15 chr2:40490200-40492000 Weak transcription Dnd41 blood
16 chr2:40490200-40493600 Weak transcription Fetal Heart heart
17 chr2:40490400-40497400 Weak transcription Aorta Aorta
18 chr2:40490400-40497800 Weak transcription Left Ventricle heart

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Last update: Aug 31, 2015