Variant report

Variant rs556165127
Chromosome Location chr6:167815308-167815309
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167813600-167815400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr6:167814200-167816000 Enhancers Fetal Intestine Large intestine
3 chr6:167814600-167815800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr6:167814600-167816000 Enhancers Fetal Intestine Small intestine
5 chr6:167814800-167815800 Enhancers Rectal Mucosa Donor 31 rectum
6 chr6:167815000-167815600 Enhancers Rectal Mucosa Donor 29 rectum
7 chr6:167815000-167816000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr6:167815000-167817400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr6:167815200-167815400 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr6:167815200-167815400 Enhancers Spleen Spleen
11 chr6:167815200-167815400 Flanking Active TSS HepG2 liver
12 chr6:167815200-167815600 Enhancers Colonic Mucosa Colon
13 chr6:167815200-167815800 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr6:167815200-167816000 Enhancers H1 Cell Line embryonic stem cell
15 chr6:167815200-167816000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland

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