Variant report

Variant rs12249849
Chromosome Location chr10:91413649-91413650
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:91406400-91414200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr10:91406600-91413800 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr10:91406600-91415800 Weak transcription Colonic Mucosa Colon
4 chr10:91407200-91418400 Weak transcription Psoas Muscle Psoas
5 chr10:91409000-91418800 Weak transcription Skeletal Muscle Male skeletal muscle
6 chr10:91411200-91414000 Enhancers Primary B cells from peripheral blood blood
7 chr10:91411200-91414400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr10:91411800-91414000 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr10:91412200-91414000 Flanking Active TSS GM12878-XiMat blood
10 chr10:91412400-91415800 Enhancers HepG2 liver
11 chr10:91412600-91413800 Enhancers HMEC breast
12 chr10:91412800-91414000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr10:91413400-91414600 Weak transcription Fetal Intestine Large intestine
14 chr10:91413600-91413800 Enhancers NH-A brain
15 chr10:91413600-91414000 Weak transcription Fetal Intestine Small intestine
16 chr10:91413600-91414200 Weak transcription HUES6 Cell Line embryonic stem cell
17 chr10:91413600-91416800 Weak transcription Osteobl bone

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