Variant report

Variant rs72829847
Chromosome Location chr17:46626484-46626485
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:73 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:46621200-46629600 Weak transcription Gastric stomach
2 chr17:46621600-46628000 Weak transcription Pancreas Pancrea
3 chr17:46621600-46634400 Weak transcription Hela-S3 cervix
4 chr17:46621800-46627600 Weak transcription Spleen Spleen
5 chr17:46622400-46626600 Enhancers Primary T killer naive cells fromperipheralblood blood
6 chr17:46622800-46627400 Weak transcription Placenta Placenta
7 chr17:46623200-46627400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
8 chr17:46623800-46630800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
9 chr17:46624000-46629800 Bivalent Enhancer H1 Cell Line embryonic stem cell
10 chr17:46624200-46626800 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr17:46624400-46626600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
12 chr17:46624400-46627000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr17:46624400-46627400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr17:46624600-46627000 Enhancers Primary T cells fromperipheralblood blood
15 chr17:46624600-46631600 Weak transcription Esophagus oesophagus
16 chr17:46624800-46626800 Weak transcription HSMMtube muscle
17 chr17:46624800-46627400 Weak transcription Placenta Amnion Placenta Amnion
18 chr17:46625000-46627200 Bivalent/Poised TSS Fetal Brain Male brain
19 chr17:46625200-46626600 Flanking Bivalent TSS/Enh ES-I3 Cell Line embryonic stem cell
20 chr17:46625200-46626800 Transcr. at gene 5' and 3' K562 blood
21 chr17:46625200-46627400 Weak transcription A549 lung
22 chr17:46625400-46626800 Enhancers Primary hematopoietic stem cells blood
23 chr17:46625400-46627200 Weak transcription Sigmoid Colon Sigmoid Colon
24 chr17:46625600-46626600 Enhancers Primary hematopoietic stem cells short term culture blood
25 chr17:46625600-46626600 Enhancers Primary T helper memory cells from peripheral blood 2 blood
26 chr17:46625600-46626600 Active TSS Stomach Smooth Muscle stomach
27 chr17:46625600-46626800 Weak transcription Fetal Muscle Trunk muscle
28 chr17:46625600-46627000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
29 chr17:46625600-46627400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
30 chr17:46625600-46627400 Weak transcription Colonic Mucosa Colon
31 chr17:46625600-46627400 Bivalent Enhancer NH-A brain
32 chr17:46625600-46629600 Weak transcription GM12878-XiMat blood
33 chr17:46625600-46630200 Genic enhancers Fetal Stomach stomach
34 chr17:46625600-46631600 Weak transcription Right Atrium heart
35 chr17:46625800-46627000 Enhancers HUVEC blood vessel
36 chr17:46625800-46627200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
37 chr17:46626000-46626600 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
38 chr17:46626000-46626600 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
39 chr17:46626000-46626800 Bivalent Enhancer Fetal Muscle Leg muscle
40 chr17:46626000-46627000 Enhancers Primary T helper cells fromperipheralblood blood
41 chr17:46626000-46627800 Genic enhancers HSMM muscle
42 chr17:46626200-46626600 Flanking Bivalent TSS/Enh hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
43 chr17:46626200-46626600 Enhancers Primary T helper cells PMA-I stimulated --
44 chr17:46626200-46626600 Bivalent Enhancer Fetal Lung lung
45 chr17:46626200-46626800 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
46 chr17:46626200-46626800 Enhancers Primary T cells from cord blood blood
47 chr17:46626200-46626800 Weak transcription Rectal Mucosa Donor 29 rectum
48 chr17:46626200-46626800 Genic enhancers NHLF lung
49 chr17:46626200-46627000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
50 chr17:46626200-46627000 Enhancers Fetal Thymus thymus

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