Variant report

Variant rs2389264
Chromosome Location chr13:96209959-96209960
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:96205600-96210400 Weak transcription A549 lung
2 chr13:96206600-96211200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr13:96206600-96231000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr13:96206800-96230200 Weak transcription H9 Cell Line embryonic stem cell
5 chr13:96207000-96216800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr13:96207200-96211000 Enhancers Pancreas Pancrea
7 chr13:96207200-96216600 Weak transcription Primary hematopoietic stem cells blood
8 chr13:96208400-96211400 Weak transcription Primary hematopoietic stem cells short term culture blood
9 chr13:96208600-96230000 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr13:96208800-96210400 Enhancers HUES48 Cell Line embryonic stem cell
11 chr13:96208800-96210600 Enhancers Cortex derived primary cultured neurospheres brain
12 chr13:96209200-96229000 Weak transcription HUES6 Cell Line embryonic stem cell
13 chr13:96209600-96210000 Active TSS Adipose Nuclei Adipose
14 chr13:96209600-96211000 Bivalent Enhancer HepG2 liver
15 chr13:96209600-96212400 Weak transcription iPS-20b Cell Line embryonic stem cell
16 chr13:96209800-96210000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
17 chr13:96209800-96210000 Bivalent Enhancer Osteobl bone
18 chr13:96209800-96210600 Enhancers Fetal Lung lung

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