Variant report

Variant rs4847191
Chromosome Location chr1:94329712-94329713
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94314200-94332800 Weak transcription Brain Cingulate Gyrus brain
2 chr1:94314200-94334200 Weak transcription Primary T helper cells fromperipheralblood blood
3 chr1:94314200-94334400 Weak transcription Brain Substantia Nigra brain
4 chr1:94322200-94343600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr1:94322600-94334200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:94328800-94334800 Weak transcription Hela-S3 cervix
7 chr1:94329400-94329800 Enhancers ES-WA7 Cell Line embryonic stem cell
8 chr1:94329400-94330000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr1:94329400-94330000 Enhancers K562 blood
10 chr1:94329400-94330400 Enhancers HUVEC blood vessel
11 chr1:94329400-94330600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr1:94329400-94334600 Weak transcription A549 lung
13 chr1:94329600-94329800 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr1:94329600-94330000 Active TSS ES-I3 Cell Line embryonic stem cell
15 chr1:94329600-94330200 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr1:94329600-94334000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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