Variant report

Variant rs1611740
Chromosome Location chr6:29831814-29831815
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29831400-29832400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
2 chr6:29831400-29832400 Bivalent Enhancer Fetal Intestine Large intestine
3 chr6:29831600-29832000 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
4 chr6:29831600-29832000 Bivalent Enhancer Primary hematopoietic stem cells blood
5 chr6:29831600-29832000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr6:29831600-29832000 Bivalent Enhancer Ovary ovary
7 chr6:29831600-29832200 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
8 chr6:29831600-29832200 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
9 chr6:29831600-29832200 Active TSS iPS DF 6.9 Cell Line embryonic stem cell
10 chr6:29831600-29832200 Flanking Bivalent TSS/Enh ES-UCSF4 Cell Line embryonic stem cell
11 chr6:29831600-29832200 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr6:29831600-29832200 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr6:29831600-29832200 Bivalent Enhancer Fetal Stomach stomach
14 chr6:29831800-29832000 Flanking Bivalent TSS/Enh Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr6:29831800-29832000 Bivalent Enhancer Fetal Brain Male brain
16 chr6:29831800-29832000 Flanking Bivalent TSS/Enh Fetal Intestine Small intestine
17 chr6:29831800-29832000 Bivalent Enhancer Left Ventricle heart
18 chr6:29831800-29832200 Active TSS iPS DF 19.11 Cell Line embryonic stem cell
19 chr6:29831800-29832200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
20 chr6:29831800-29832400 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --

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