Variant report

Variant rs11928846
Chromosome Location chr3:140798999-140799000
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:49 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:140790600-140802800 Weak transcription Dnd41 blood
2 chr3:140792800-140808400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr3:140793400-140806600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr3:140794000-140813000 Genic enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr3:140794800-140800600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr3:140796200-140799000 Enhancers Fetal Muscle Trunk muscle
7 chr3:140796200-140799200 Enhancers Fetal Muscle Leg muscle
8 chr3:140796400-140799200 Weak transcription Primary hematopoietic stem cells short term culture blood
9 chr3:140796400-140801400 Genic enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr3:140796600-140806600 Enhancers HUES6 Cell Line embryonic stem cell
11 chr3:140796600-140807200 Enhancers Fetal Heart heart
12 chr3:140797000-140800400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr3:140797000-140804400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr3:140797000-140805000 Weak transcription Duodenum Smooth Muscle Duodenum
15 chr3:140797200-140800000 Weak transcription H9 Cell Line embryonic stem cell
16 chr3:140797200-140802200 Weak transcription Psoas Muscle Psoas
17 chr3:140797200-140802200 Weak transcription HSMM muscle
18 chr3:140797200-140802400 Weak transcription Right Ventricle heart
19 chr3:140797200-140802600 Weak transcription Fetal Intestine Large intestine
20 chr3:140797200-140802600 Weak transcription Fetal Intestine Small intestine
21 chr3:140797200-140802800 Weak transcription Fetal Kidney kidney
22 chr3:140797200-140811200 Weak transcription Fetal Brain Male brain
23 chr3:140797400-140799600 Weak transcription ES-I3 Cell Line embryonic stem cell
24 chr3:140797400-140799800 Weak transcription HUES48 Cell Line embryonic stem cell
25 chr3:140797400-140800800 Weak transcription Adipose Nuclei Adipose
26 chr3:140797400-140800800 Weak transcription HSMMtube muscle
27 chr3:140797400-140801000 Weak transcription Lung lung
28 chr3:140797400-140802000 Weak transcription Left Ventricle heart
29 chr3:140797400-140802000 Weak transcription Skeletal Muscle Female skeletal muscle
30 chr3:140797400-140802400 Weak transcription Right Atrium heart
31 chr3:140797600-140799400 Weak transcription iPS-20b Cell Line embryonic stem cell
32 chr3:140797600-140800400 Weak transcription Fetal Lung lung
33 chr3:140797800-140799200 Weak transcription iPS-18 Cell Line embryonic stem cell
34 chr3:140797800-140799200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
35 chr3:140797800-140799600 Weak transcription ES-WA7 Cell Line embryonic stem cell
36 chr3:140797800-140799800 Weak transcription Pancreas Pancrea
37 chr3:140797800-140801000 Weak transcription Placenta Placenta
38 chr3:140797800-140801600 Weak transcription Fetal Stomach stomach
39 chr3:140797800-140801600 Weak transcription Skeletal Muscle Male skeletal muscle
40 chr3:140797800-140804600 Weak transcription Fetal Brain Female brain
41 chr3:140798400-140799000 Weak transcription Cortex derived primary cultured neurospheres brain
42 chr3:140798400-140802000 Weak transcription Brain Germinal Matrix brain
43 chr3:140798400-140803000 Enhancers H1 Cell Line embryonic stem cell
44 chr3:140798400-140803800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
45 chr3:140798400-140804600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
46 chr3:140798400-140806800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
47 chr3:140798600-140799600 Genic enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
48 chr3:140798600-140801400 Enhancers HUES64 Cell Line embryonic stem cell
49 chr3:140798600-140802200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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