Variant report

Variant rs598552
Chromosome Location chr5:180208990-180208991
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:180203000-180212400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:180204400-180215400 Weak transcription Primary B cells from cord blood blood
3 chr5:180205200-180209800 Weak transcription Primary T cells fromperipheralblood blood
4 chr5:180205600-180211800 Weak transcription Liver Liver
5 chr5:180205800-180212400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
6 chr5:180206000-180212200 Weak transcription Lung lung
7 chr5:180206200-180209800 Weak transcription Primary T cells from cord blood blood
8 chr5:180206600-180212400 Weak transcription Aorta Aorta
9 chr5:180206800-180210800 Weak transcription Esophagus oesophagus
10 chr5:180207000-180214600 Weak transcription Primary monocytes fromperipheralblood blood
11 chr5:180207200-180212200 Weak transcription Right Atrium heart
12 chr5:180207200-180212400 Weak transcription Fetal Intestine Large intestine
13 chr5:180207800-180210800 Weak transcription Placenta Placenta
14 chr5:180208000-180212000 Weak transcription Stomach Smooth Muscle stomach
15 chr5:180208000-180212400 Weak transcription Psoas Muscle Psoas
16 chr5:180208400-180210000 Flanking Active TSS K562 blood

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