Variant report

Variant rs62395449
Chromosome Location chr6:11978887-11978888
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:11973200-11980200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:11975800-11979200 Enhancers K562 blood
3 chr6:11978200-11979600 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr6:11978400-11979000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr6:11978400-11979000 Enhancers GM12878-XiMat blood
6 chr6:11978400-11979000 Enhancers Hela-S3 cervix
7 chr6:11978400-11979200 Enhancers Fetal Intestine Large intestine
8 chr6:11978400-11979200 Enhancers HUVEC blood vessel
9 chr6:11978400-11979400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr6:11978600-11979000 Enhancers Primary B cells from cord blood blood
11 chr6:11978600-11979000 Enhancers Primary T helper cells PMA-I stimulated --
12 chr6:11978600-11979000 Enhancers Primary T killer naive cells fromperipheralblood blood
13 chr6:11978600-11979000 Enhancers Fetal Kidney kidney
14 chr6:11978600-11979000 Enhancers Stomach Mucosa stomach
15 chr6:11978600-11979200 Enhancers Primary T helper naive cells fromperipheralblood blood
16 chr6:11978600-11979200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr6:11978600-11979200 Enhancers Fetal Intestine Small intestine
18 chr6:11978600-11979200 Enhancers NH-A brain
19 chr6:11978600-11979400 Enhancers Primary hematopoietic stem cells blood

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