Variant report

Variant rs1611738
Chromosome Location chr6:29831706-29831707
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29831400-29831800 Bivalent Enhancer Fetal Intestine Small intestine
2 chr6:29831400-29832400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
3 chr6:29831400-29832400 Bivalent Enhancer Fetal Intestine Large intestine
4 chr6:29831600-29831800 Flanking Active TSS iPS DF 19.11 Cell Line embryonic stem cell
5 chr6:29831600-29831800 Bivalent Enhancer Fetal Brain Female brain
6 chr6:29831600-29832000 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
7 chr6:29831600-29832000 Bivalent Enhancer Primary hematopoietic stem cells blood
8 chr6:29831600-29832000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr6:29831600-29832000 Bivalent Enhancer Ovary ovary
10 chr6:29831600-29832200 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
11 chr6:29831600-29832200 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
12 chr6:29831600-29832200 Active TSS iPS DF 6.9 Cell Line embryonic stem cell
13 chr6:29831600-29832200 Flanking Bivalent TSS/Enh ES-UCSF4 Cell Line embryonic stem cell
14 chr6:29831600-29832200 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr6:29831600-29832200 Bivalent Enhancer Fetal Muscle Trunk muscle
16 chr6:29831600-29832200 Bivalent Enhancer Fetal Stomach stomach

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