Variant report

Variant rs17437175
Chromosome Location chr7:27130276-27130277
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27122800-27133600 Weak transcription HMEC breast
2 chr7:27128200-27133400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr7:27128200-27133600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr7:27128400-27133000 Weak transcription NHEK skin
5 chr7:27128600-27135000 Weak transcription NHLF lung
6 chr7:27129200-27134000 Bivalent Enhancer Fetal Kidney kidney
7 chr7:27129800-27131200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
8 chr7:27129800-27134400 Bivalent Enhancer Fetal Lung lung
9 chr7:27130000-27130800 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr7:27130000-27131000 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
11 chr7:27130000-27131000 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
12 chr7:27130000-27131200 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
13 chr7:27130200-27130400 Bivalent Enhancer H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr7:27130200-27131400 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
15 chr7:27130200-27132400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
16 chr7:27130200-27132800 Bivalent Enhancer HUES64 Cell Line embryonic stem cell

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