Variant report

Variant rs7764064
Chromosome Location chr6:167518192-167518193
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167503600-167527200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:167509000-167525200 Enhancers Primary B cells from peripheral blood blood
3 chr6:167512600-167518800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:167512800-167518400 Weak transcription Thymus Thymus
5 chr6:167515800-167518200 Enhancers Primary Natural Killer cells fromperipheralblood blood
6 chr6:167516400-167518200 Enhancers Fetal Intestine Large intestine
7 chr6:167516600-167518200 Enhancers Rectal Mucosa Donor 29 rectum
8 chr6:167517000-167519800 Enhancers Primary B cells from cord blood blood
9 chr6:167517200-167518200 Enhancers Primary T helper 17 cells PMA-I stimulated --
10 chr6:167517200-167518400 Enhancers GM12878-XiMat blood
11 chr6:167517400-167518200 Enhancers Primary hematopoietic stem cells blood
12 chr6:167517400-167523800 Weak transcription Primary T regulatory cells fromperipheralblood blood
13 chr6:167517600-167518200 Enhancers HepG2 liver
14 chr6:167517600-167523800 Weak transcription Primary T cells fromperipheralblood blood
15 chr6:167517600-167529800 Weak transcription Spleen Spleen
16 chr6:167518000-167518200 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
17 chr6:167518000-167518200 Enhancers Primary mononuclear cells fromperipheralblood Blood

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