Variant report

Variant rs17052232
Chromosome Location chr6:107164225-107164226
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:107158800-107169200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr6:107161800-107164600 Weak transcription Fetal Intestine Large intestine
3 chr6:107162200-107169400 Weak transcription Small Intestine intestine
4 chr6:107162400-107164800 Weak transcription HepG2 liver
5 chr6:107162600-107169200 Weak transcription Pancreas Pancrea
6 chr6:107162800-107164800 Weak transcription Liver Liver
7 chr6:107163200-107164600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:107163200-107164800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:107163600-107164400 Flanking Active TSS Primary B cells from cord blood blood
10 chr6:107163600-107164400 Flanking Active TSS NHEK skin
11 chr6:107163600-107164600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr6:107163600-107164600 Enhancers Sigmoid Colon Sigmoid Colon
13 chr6:107163600-107165000 Enhancers HMEC breast
14 chr6:107163600-107165600 Enhancers Rectal Mucosa Donor 31 rectum
15 chr6:107163800-107165400 Enhancers Duodenum Mucosa Duodenum
16 chr6:107163800-107165800 Enhancers Stomach Mucosa stomach
17 chr6:107164000-107164400 Weak transcription iPS-20b Cell Line embryonic stem cell
18 chr6:107164000-107165400 Enhancers Rectal Mucosa Donor 29 rectum
19 chr6:107164000-107165600 Enhancers Primary B cells from peripheral blood blood
20 chr6:107164000-107165600 Enhancers Fetal Intestine Small intestine
21 chr6:107164200-107165000 Weak transcription iPS-18 Cell Line embryonic stem cell
22 chr6:107164200-107169200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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