Variant report

Variant rs73777865
Chromosome Location chr6:143378213-143378214
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143372000-143380400 Weak transcription K562 blood
2 chr6:143373600-143380800 Weak transcription GM12878-XiMat blood
3 chr6:143374800-143380800 Weak transcription Primary T cells from cord blood blood
4 chr6:143375200-143380000 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr6:143375200-143381200 Weak transcription Aorta Aorta
6 chr6:143375600-143379600 Weak transcription Fetal Intestine Small intestine
7 chr6:143376000-143380600 Weak transcription Adipose Nuclei Adipose
8 chr6:143376200-143380800 Weak transcription Duodenum Smooth Muscle Duodenum
9 chr6:143376400-143378600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr6:143376400-143380200 Weak transcription Fetal Intestine Large intestine
11 chr6:143376600-143380000 Weak transcription Liver Liver
12 chr6:143376800-143380200 Weak transcription Skeletal Muscle Female skeletal muscle
13 chr6:143376800-143380600 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr6:143377200-143380400 Weak transcription HUES6 Cell Line embryonic stem cell
15 chr6:143377200-143380600 Weak transcription HUES48 Cell Line embryonic stem cell
16 chr6:143377200-143380800 Weak transcription ES-WA7 Cell Line embryonic stem cell
17 chr6:143377200-143380800 Weak transcription H9 Cell Line embryonic stem cell
18 chr6:143377200-143380800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
19 chr6:143377400-143380000 Weak transcription HepG2 liver
20 chr6:143377600-143380800 Weak transcription H1 Cell Line embryonic stem cell
21 chr6:143377800-143380800 Weak transcription iPS-15b Cell Line embryonic stem cell
22 chr6:143377800-143380800 Weak transcription Fetal Lung lung
23 chr6:143378200-143378400 Enhancers HUES64 Cell Line embryonic stem cell
24 chr6:143378200-143380800 Weak transcription Stomach Mucosa stomach

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