Variant report

Variant rs1765650
Chromosome Location chr1:94861387-94861388
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94859400-94861800 Enhancers Fetal Thymus thymus
2 chr1:94859800-94861600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr1:94859800-94862000 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr1:94859800-94862200 Enhancers HepG2 liver
5 chr1:94860000-94861600 Enhancers Thymus Thymus
6 chr1:94860000-94861800 Enhancers HUES6 Cell Line embryonic stem cell
7 chr1:94860000-94862000 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr1:94860200-94861400 Enhancers ES-WA7 Cell Line embryonic stem cell
9 chr1:94860200-94861600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr1:94860200-94861800 Enhancers H1 Cell Line embryonic stem cell
11 chr1:94860200-94861800 Enhancers H9 Cell Line embryonic stem cell
12 chr1:94860200-94862000 Enhancers HUES64 Cell Line embryonic stem cell
13 chr1:94860400-94861400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr1:94860400-94861400 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr1:94860400-94861800 Enhancers HUES48 Cell Line embryonic stem cell
16 chr1:94860600-94861400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
17 chr1:94861000-94861600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr1:94861000-94861600 Enhancers Fetal Intestine Small intestine
19 chr1:94861000-94861800 Enhancers Stomach Mucosa stomach
20 chr1:94861000-94862400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
21 chr1:94861200-94861400 Enhancers Gastric stomach
22 chr1:94861200-94861600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
23 chr1:94861200-94862000 Enhancers iPS-20b Cell Line embryonic stem cell

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