Variant report

Variant rs182005010
Chromosome Location chr6:33788864-33788865
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:33776400-33792400 Weak transcription Right Atrium heart
2 chr6:33781800-33792400 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr6:33782200-33790600 Weak transcription HUES64 Cell Line embryonic stem cell
4 chr6:33782800-33790600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr6:33785400-33790200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr6:33787600-33790000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr6:33788200-33790200 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr6:33788400-33790400 Enhancers Primary hematopoietic stem cells blood
9 chr6:33788600-33789000 Enhancers Primary T helper cells PMA-I stimulated --
10 chr6:33788800-33789000 Bivalent Enhancer Primary T cells fromperipheralblood blood
11 chr6:33788800-33789000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
12 chr6:33788800-33789200 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr6:33788800-33789200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --

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