Variant report

Variant rs1527363
Chromosome Location chr1:226611505-226611506
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:226596200-226622600 Weak transcription Right Atrium heart
2 chr1:226602800-226616200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr1:226606000-226616200 Weak transcription H1 Cell Line embryonic stem cell
4 chr1:226606200-226612000 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr1:226606200-226616000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr1:226607400-226612000 Weak transcription Fetal Brain Male brain
7 chr1:226607400-226614200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
8 chr1:226607600-226612000 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr1:226607600-226612000 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr1:226608200-226612200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr1:226608400-226616200 Weak transcription Fetal Brain Female brain
12 chr1:226608600-226612400 Weak transcription Brain Cingulate Gyrus brain
13 chr1:226608600-226612400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
14 chr1:226608800-226612400 Weak transcription Brain Hippocampus Middle brain
15 chr1:226608800-226613200 Weak transcription Duodenum Mucosa Duodenum
16 chr1:226609000-226612200 Weak transcription Brain Substantia Nigra brain

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