Variant report

Variant rs17465295
Chromosome Location chr7:27132577-27132578
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr7:27129800-27134400 Bivalent Enhancer Fetal Lung lung
8 chr7:27130200-27132800 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
9 chr7:27130400-27134000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr7:27131000-27134000 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr7:27131200-27134600 Weak transcription A549 lung
12 chr7:27131400-27132600 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
13 chr7:27131600-27132600 Enhancers HUVEC blood vessel
14 chr7:27131600-27133000 Bivalent Enhancer H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
15 chr7:27131800-27132600 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
16 chr7:27131800-27134200 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
17 chr7:27132200-27132600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
18 chr7:27132400-27132600 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
19 chr7:27132400-27133000 Bivalent Enhancer HUES6 Cell Line embryonic stem cell

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