Variant report

Variant rs61985011
Chromosome Location chr14:69206887-69206888
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:69198400-69214000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr14:69200200-69207000 Enhancers Fetal Stomach stomach
3 chr14:69201200-69222600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr14:69202600-69209000 Weak transcription Primary T helper cells PMA-I stimulated --
5 chr14:69202800-69224600 Weak transcription Primary T helper naive cells from peripheral blood blood
6 chr14:69203600-69213800 Weak transcription Esophagus oesophagus
7 chr14:69203800-69207200 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr14:69203800-69207600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
9 chr14:69203800-69207600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr14:69203800-69208600 Weak transcription Fetal Thymus thymus
11 chr14:69204200-69219200 Weak transcription Adipose Nuclei Adipose
12 chr14:69204400-69213800 Weak transcription Right Atrium heart
13 chr14:69205000-69208000 Enhancers K562 blood
14 chr14:69205000-69210400 Enhancers Primary B cells from peripheral blood blood
15 chr14:69205600-69214200 Weak transcription Spleen Spleen
16 chr14:69205600-69216200 Weak transcription Lung lung
17 chr14:69206200-69207400 Weak transcription Ovary ovary
18 chr14:69206400-69207400 Weak transcription HSMMtube muscle
19 chr14:69206600-69208000 Enhancers Primary B cells from cord blood blood
20 chr14:69206800-69207600 Enhancers Fetal Heart heart

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