Variant report

Variant rs9261449
Chromosome Location chr6:30096005-30096006
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:30092400-30096200 Weak transcription Hela-S3 cervix
2 chr6:30092600-30097200 Weak transcription Duodenum Mucosa Duodenum
3 chr6:30094600-30096200 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
4 chr6:30094800-30096200 Bivalent/Poised TSS H9 Cell Line embryonic stem cell
5 chr6:30094800-30096200 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
6 chr6:30094800-30096200 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
7 chr6:30094800-30096200 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
8 chr6:30095000-30096200 Bivalent/Poised TSS iPS DF 6.9 Cell Line embryonic stem cell
9 chr6:30095200-30096200 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr6:30095200-30096200 Active TSS Breast Myoepithelial Primary Cells Breast
11 chr6:30095400-30096200 Bivalent Enhancer Primary B cells from peripheral blood blood
12 chr6:30095400-30096200 Bivalent Enhancer Fetal Muscle Leg muscle
13 chr6:30095800-30096200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr6:30095800-30096200 Bivalent Enhancer Fetal Muscle Trunk muscle
15 chr6:30095800-30096200 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
16 chr6:30096000-30096200 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
17 chr6:30096000-30096200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
18 chr6:30096000-30096200 Bivalent Enhancer Primary T cells effector/memory enriched fromperipheralblood blood
19 chr6:30096000-30096200 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin03 Skin
20 chr6:30096000-30096200 Bivalent Enhancer Fetal Intestine Large intestine
21 chr6:30096000-30096200 Bivalent Enhancer Fetal Intestine Small intestine

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