Variant report

Variant rs6900614
Chromosome Location chr6:167701100-167701101
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167689200-167702400 Weak transcription Placenta Amnion Placenta Amnion
2 chr6:167692400-167702400 Weak transcription Thymus Thymus
3 chr6:167696800-167705800 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr6:167697000-167702400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr6:167697200-167702000 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr6:167697200-167702400 Weak transcription Fetal Thymus thymus
7 chr6:167697200-167705200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr6:167697400-167702000 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr6:167697400-167702400 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr6:167697600-167702400 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr6:167697600-167706200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr6:167699000-167702400 Weak transcription H1 Cell Line embryonic stem cell
13 chr6:167699200-167701200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr6:167699200-167701600 Weak transcription Fetal Muscle Leg muscle
15 chr6:167699200-167702400 Weak transcription Liver Liver
16 chr6:167700000-167701800 Weak transcription Fetal Intestine Small intestine
17 chr6:167700200-167704400 Enhancers HepG2 liver
18 chr6:167700800-167702800 Enhancers Fetal Brain Male brain

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