Variant report

Variant rs10174735
Chromosome Location chr2:188326005-188326006
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:188313000-188326200 Weak transcription Right Ventricle heart
2 chr2:188313400-188340000 Weak transcription Fetal Brain Male brain
3 chr2:188313600-188330400 Weak transcription Muscle Satellite Cultured Cells --
4 chr2:188324600-188332400 Weak transcription HUVEC blood vessel
5 chr2:188325200-188326200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr2:188325400-188330400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr2:188325400-188334200 Weak transcription Primary hematopoietic stem cells blood
8 chr2:188326000-188326200 Weak transcription Right Atrium heart
9 chr2:188326000-188326200 Active TSS HepG2 liver
10 chr2:188326000-188327000 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:188326000-188327200 Active TSS Fetal Intestine Large intestine
12 chr2:188326000-188327400 Active TSS ES-I3 Cell Line embryonic stem cell

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