Variant report

Variant rs16889066
Chromosome Location chr6:24312954-24312955
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:24308400-24313600 Weak transcription Fetal Kidney kidney
2 chr6:24308400-24313800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr6:24312000-24313800 Enhancers ES-I3 Cell Line embryonic stem cell
4 chr6:24312200-24313800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr6:24312200-24314000 Weak transcription HSMMtube muscle
6 chr6:24312400-24313800 Enhancers HUES6 Cell Line embryonic stem cell
7 chr6:24312600-24313800 Weak transcription H1 Cell Line embryonic stem cell
8 chr6:24312600-24313800 Weak transcription Fetal Intestine Small intestine
9 chr6:24312600-24314000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr6:24312800-24313000 Flanking Active TSS HUES48 Cell Line embryonic stem cell
11 chr6:24312800-24313000 Enhancers Fetal Intestine Large intestine
12 chr6:24312800-24313200 Flanking Active TSS A549 lung
13 chr6:24312800-24313600 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr6:24312800-24313800 Enhancers HepG2 liver
15 chr6:24312800-24314200 Enhancers ES-WA7 Cell Line embryonic stem cell
16 chr6:24312800-24314200 Enhancers iPS-18 Cell Line embryonic stem cell
17 chr6:24312800-24314400 Enhancers iPS-15b Cell Line embryonic stem cell
18 chr6:24312800-24314400 Enhancers NH-A brain

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