Variant report

Variant rs190319228
Chromosome Location chr1:216998269-216998270
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:216989000-217005800 Weak transcription Left Ventricle heart
2 chr1:216989600-217000600 Weak transcription Psoas Muscle Psoas
3 chr1:216994600-217004000 Weak transcription iPS-20b Cell Line embryonic stem cell
4 chr1:216994800-216998600 Weak transcription Fetal Heart heart
5 chr1:216996400-217000400 Enhancers Fetal Intestine Small intestine
6 chr1:216996400-217004400 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr1:216997000-216999600 Enhancers Fetal Intestine Large intestine
8 chr1:216997800-216998600 Enhancers HUES48 Cell Line embryonic stem cell
9 chr1:216997800-216999400 Enhancers Duodenum Mucosa Duodenum
10 chr1:216998000-216998400 Enhancers HUES6 Cell Line embryonic stem cell
11 chr1:216998000-216998600 Enhancers HUES64 Cell Line embryonic stem cell
12 chr1:216998000-216998600 Bivalent Enhancer Fetal Lung lung
13 chr1:216998000-216999200 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr1:216998000-216999200 Enhancers H1 Cell Line embryonic stem cell
15 chr1:216998200-216998400 Enhancers Small Intestine intestine
16 chr1:216998200-216998600 Enhancers H9 Cell Line embryonic stem cell
17 chr1:216998200-216998800 Enhancers iPS-15b Cell Line embryonic stem cell

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