Variant report

Variant rs375487114
Chromosome Location chr6:210421-210422
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:196800-211800 Weak transcription Right Atrium heart
2 chr6:209600-211000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
3 chr6:209800-210800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:210000-210600 Flanking Active TSS Primary T regulatory cells fromperipheralblood blood
5 chr6:210200-210600 Enhancers Primary B cells from peripheral blood blood
6 chr6:210200-210600 Enhancers Primary T helper naive cells from peripheral blood blood
7 chr6:210200-210600 Enhancers Primary T helper cells fromperipheralblood blood
8 chr6:210400-210600 Enhancers Primary T helper memory cells from peripheral blood 1 blood
9 chr6:210400-210600 Enhancers Primary T helper 17 cells PMA-I stimulated --
10 chr6:210400-210800 Enhancers Primary T helper memory cells from peripheral blood 2 blood
11 chr6:210400-211000 Bivalent Enhancer Primary T cells fromperipheralblood blood
12 chr6:210400-211800 Weak transcription Esophagus oesophagus
13 chr6:210400-213600 Enhancers GM12878-XiMat blood
14 chr6:210400-215200 Weak transcription Primary T helper cells PMA-I stimulated --

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