Variant report

Variant rs2294765
Chromosome Location chr6:142738060-142738061
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:56 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:142718000-142763200 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr6:142721600-142749200 Weak transcription Duodenum Smooth Muscle Duodenum
3 chr6:142722000-142743400 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr6:142727000-142743400 Strong transcription HepG2 liver
5 chr6:142729200-142743200 Strong transcription Liver Liver
6 chr6:142730200-142747600 Weak transcription Fetal Intestine Small intestine
7 chr6:142730400-142738200 Weak transcription Primary hematopoietic stem cells blood
8 chr6:142733000-142738600 Enhancers NHDF-Ad bronchial
9 chr6:142733400-142739200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr6:142733400-142739200 Enhancers Osteobl bone
11 chr6:142733800-142738600 Weak transcription H1 Cell Line embryonic stem cell
12 chr6:142733800-142758000 Weak transcription Stomach Smooth Muscle stomach
13 chr6:142734200-142739200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr6:142734600-142738200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
15 chr6:142734800-142738800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr6:142734800-142743200 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr6:142735200-142738400 Genic enhancers A549 lung
18 chr6:142735200-142760200 Weak transcription Esophagus oesophagus
19 chr6:142735200-142765400 Weak transcription Hela-S3 cervix
20 chr6:142735600-142738600 Genic enhancers HUVEC blood vessel
21 chr6:142735600-142743600 Weak transcription Sigmoid Colon Sigmoid Colon
22 chr6:142735800-142740200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
23 chr6:142735800-142765400 Weak transcription Placenta Amnion Placenta Amnion
24 chr6:142736800-142738200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
25 chr6:142736800-142738200 Genic enhancers Fetal Lung lung
26 chr6:142736800-142738200 Enhancers HMEC breast
27 chr6:142736800-142738400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
28 chr6:142736800-142738600 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
29 chr6:142736800-142738600 Enhancers HSMM muscle
30 chr6:142736800-142738800 Enhancers Cortex derived primary cultured neurospheres brain
31 chr6:142736800-142739000 Enhancers HUES48 Cell Line embryonic stem cell
32 chr6:142736800-142739000 Enhancers HUES6 Cell Line embryonic stem cell
33 chr6:142736800-142739000 Enhancers iPS-20b Cell Line embryonic stem cell
34 chr6:142736800-142739200 Enhancers ES-I3 Cell Line embryonic stem cell
35 chr6:142736800-142739200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
36 chr6:142736800-142739200 Enhancers iPS-15b Cell Line embryonic stem cell
37 chr6:142736800-142743200 Strong transcription Placenta Placenta
38 chr6:142737000-142739000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
39 chr6:142737000-142739000 Enhancers HUES64 Cell Line embryonic stem cell
40 chr6:142737000-142739000 Enhancers iPS-18 Cell Line embryonic stem cell
41 chr6:142737200-142739000 Enhancers NHLF lung
42 chr6:142737400-142738200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
43 chr6:142737400-142738800 Enhancers NH-A brain
44 chr6:142737400-142742200 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
45 chr6:142737600-142738800 Enhancers ES-WA7 Cell Line embryonic stem cell
46 chr6:142737600-142741000 Weak transcription Fetal Intestine Large intestine
47 chr6:142737600-142765600 Weak transcription Duodenum Mucosa Duodenum
48 chr6:142737800-142738200 Enhancers Fetal Brain Female brain
49 chr6:142737800-142738800 Genic enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
50 chr6:142737800-142765800 Weak transcription Fetal Brain Male brain

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