Variant report

Variant rs900556
Chromosome Location chr2:111661684-111661685
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 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 chr2:111660400-111661800 Enhancers Brain Inferior Temporal Lobe brain
11 chr2:111660600-111661800 Enhancers Colonic Mucosa Colon
12 chr2:111660600-111661800 Enhancers Rectal Mucosa Donor 31 rectum
13 chr2:111660600-111661800 Enhancers Rectal Smooth Muscle rectum
14 chr2:111660600-111662000 Enhancers Placenta Placenta
15 chr2:111660600-111662200 Weak transcription Primary hematopoietic stem cells short term culture blood
16 chr2:111660800-111662800 Enhancers Brain Germinal Matrix brain
17 chr2:111661000-111661800 Enhancers Fetal Brain Female brain
18 chr2:111661200-111661800 Enhancers Skeletal Muscle Male skeletal muscle
19 chr2:111661400-111662800 Weak transcription Fetal Stomach stomach
20 chr2:111661600-111661800 Enhancers Fetal Brain Male brain
21 chr2:111661600-111663000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
22 chr2:111661600-111665000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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