Variant report

Variant rs7975385
Chromosome Location chr12:49190992-49190993
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:49184200-49193800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr12:49184200-49194400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr12:49184200-49198800 Weak transcription NHLF lung
4 chr12:49184400-49194000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr12:49188400-49191200 Enhancers Fetal Intestine Large intestine
6 chr12:49188600-49191000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr12:49189600-49191000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr12:49189800-49191200 Enhancers Fetal Adrenal Gland Adrenal Gland
9 chr12:49190000-49191000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr12:49190000-49197400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr12:49190000-49197400 Weak transcription A549 lung
12 chr12:49190400-49193600 Weak transcription Fetal Intestine Small intestine
13 chr12:49190400-49204000 Weak transcription Rectal Mucosa Donor 31 rectum
14 chr12:49190800-49191000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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