Variant report

Variant rs2651489
Chromosome Location chr10:1366701-1366702
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1354200-1369400 Weak transcription H9 Cell Line embryonic stem cell
2 chr10:1355000-1387800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr10:1358800-1369200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr10:1358800-1370200 Weak transcription Fetal Brain Female brain
5 chr10:1359200-1367000 Weak transcription Brain Substantia Nigra brain
6 chr10:1362600-1369200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr10:1363000-1368600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr10:1364000-1369800 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr10:1364400-1367000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr10:1366200-1366800 Enhancers Fetal Intestine Large intestine

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