The 2.0 version of rSNPBase

Variant report

Variant rs34556514
Chromosome Location chr15:58333769-58333770
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:58328800-58333800 Enhancers Fetal Intestine Small intestine
2 chr15:58331000-58335000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr15:58331400-58335000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr15:58331600-58336000 Genic enhancers K562 blood
5 chr15:58331800-58335800 Weak transcription Fetal Stomach stomach
6 chr15:58332200-58338200 Weak transcription Fetal Intestine Large intestine
7 chr15:58332800-58333800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr15:58332800-58334000 Weak transcription HUVEC blood vessel
9 chr15:58332800-58334200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr15:58332800-58335000 Weak transcription Fetal Kidney kidney
11 chr15:58333200-58335600 Weak transcription HMEC breast
12 chr15:58333400-58334800 Weak transcription Fetal Lung lung
13 chr15:58333400-58336400 Weak transcription Fetal Adrenal Gland Adrenal Gland
14 chr15:58333600-58335200 Weak transcription Small Intestine intestine

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Last update: Aug 31, 2015