Variant report

Variant rs35296418
Chromosome Location chr6:143946592-143946593
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143917000-143973600 Weak transcription Fetal Intestine Small intestine
2 chr6:143930400-143949400 Weak transcription H9 Cell Line embryonic stem cell
3 chr6:143930800-143946600 Weak transcription Primary T cells from cord blood blood
4 chr6:143935600-143946600 Weak transcription Primary T helper cells fromperipheralblood blood
5 chr6:143937000-143946600 Weak transcription Duodenum Mucosa Duodenum
6 chr6:143937000-143947000 Weak transcription Primary T regulatory cells fromperipheralblood blood
7 chr6:143939000-143955800 Weak transcription Stomach Mucosa stomach
8 chr6:143942200-143950600 Weak transcription Esophagus oesophagus
9 chr6:143942200-143955600 Weak transcription Sigmoid Colon Sigmoid Colon
10 chr6:143942400-143947400 Weak transcription Monocytes-CD14+_RO01746 blood
11 chr6:143943600-143950400 Weak transcription Fetal Stomach stomach
12 chr6:143943800-143950600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr6:143946000-143946800 Weak transcription Primary T cells fromperipheralblood blood
14 chr6:143946200-143947400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
15 chr6:143946200-143947400 Enhancers Primary T helper cells PMA-I stimulated --
16 chr6:143946200-143947400 Enhancers Primary T helper 17 cells PMA-I stimulated --
17 chr6:143946200-143947800 Enhancers Primary T helper memory cells from peripheral blood 1 blood

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