Variant report

Variant rs2387641
Chromosome Location chr10:1341003-1341004
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1329200-1352600 Weak transcription Right Atrium heart
2 chr10:1335800-1341400 Weak transcription Primary T cells from cord blood blood
3 chr10:1336600-1342000 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr10:1337000-1343000 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr10:1338600-1341400 Enhancers Fetal Brain Male brain
6 chr10:1339400-1342000 Enhancers Brain Cingulate Gyrus brain
7 chr10:1340200-1341400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr10:1340200-1341800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr10:1340200-1352800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr10:1340400-1344000 Weak transcription iPS-18 Cell Line embryonic stem cell
11 chr10:1340600-1342400 Enhancers Primary hematopoietic stem cells blood
12 chr10:1340800-1344000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr10:1341000-1341800 Enhancers Fetal Thymus thymus

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