Variant report

Variant rs34929387
Chromosome Location chr4:121933076-121933077
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:121925600-121933800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr4:121928600-121936400 Enhancers Primary T killer naive cells fromperipheralblood blood
3 chr4:121929000-121933800 Enhancers Primary T helper cells PMA-I stimulated --
4 chr4:121930000-121933600 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr4:121930200-121934200 Enhancers HUES64 Cell Line embryonic stem cell
6 chr4:121930200-121934400 Enhancers HUES6 Cell Line embryonic stem cell
7 chr4:121930400-121934200 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr4:121930600-121933600 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr4:121931200-121933800 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr4:121931400-121933200 Weak transcription Fetal Intestine Small intestine
11 chr4:121931400-121933400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr4:121931400-121933600 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr4:121931600-121935200 Weak transcription Colon Smooth Muscle Colon
14 chr4:121931800-121933400 Enhancers Primary T helper naive cells from peripheral blood blood
15 chr4:121931800-121933600 Enhancers Primary T cells from cord blood blood
16 chr4:121932000-121933200 Weak transcription Fetal Intestine Large intestine
17 chr4:121932400-121934600 Enhancers HUES48 Cell Line embryonic stem cell
18 chr4:121932600-121933800 Weak transcription Primary T helper naive cells fromperipheralblood blood
19 chr4:121932600-121934200 Weak transcription H9 Cell Line embryonic stem cell

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