Variant report

Variant rs900557
Chromosome Location chr2:111661810-111661811
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:111632000-111662000 Weak transcription H1 Cell Line embryonic stem cell
2 chr2:111652000-111662200 Weak transcription H9 Cell Line embryonic stem cell
3 chr2:111658000-111662000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr2:111658400-111662400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr2:111658800-111665000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr2:111658800-111665200 Weak transcription Fetal Intestine Small intestine
7 chr2:111660000-111662000 Enhancers Colon Smooth Muscle Colon
8 chr2:111660000-111663600 Enhancers Fetal Muscle Leg muscle
9 chr2:111660200-111663600 Enhancers Fetal Muscle Trunk muscle
10 chr2:111660600-111662000 Enhancers Placenta Placenta
11 chr2:111660600-111662200 Weak transcription Primary hematopoietic stem cells short term culture blood
12 chr2:111660800-111662800 Enhancers Brain Germinal Matrix brain
13 chr2:111661400-111662800 Weak transcription Fetal Stomach stomach
14 chr2:111661600-111663000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
15 chr2:111661600-111665000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr2:111661800-111662600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
17 chr2:111661800-111662600 Weak transcription Fetal Brain Male brain
18 chr2:111661800-111662800 Weak transcription Fetal Brain Female brain

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