Variant report

Variant rs7164954
Chromosome Location chr15:59000121-59000122
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:102 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:58977200-59004400 Weak transcription Ovary ovary
2 chr15:58977200-59007800 Weak transcription HepG2 liver
3 chr15:58977200-59039200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr15:58982400-59005000 Weak transcription Rectal Mucosa Donor 29 rectum
5 chr15:58982600-59008000 Weak transcription Fetal Brain Male brain
6 chr15:58983200-59016600 Weak transcription Small Intestine intestine
7 chr15:58985200-59005000 Weak transcription HSMMtube muscle
8 chr15:58986600-59016600 Weak transcription Stomach Smooth Muscle stomach
9 chr15:58987400-59012000 Weak transcription Rectal Smooth Muscle rectum
10 chr15:58987600-59005000 Weak transcription iPS-20b Cell Line embryonic stem cell
11 chr15:58987600-59007800 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr15:58989800-59016800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr15:58990000-59004800 Weak transcription Pancreas Pancrea
14 chr15:58990000-59005000 Weak transcription Spleen Spleen
15 chr15:58990000-59005200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr15:58990000-59023400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
17 chr15:58991600-59005200 Weak transcription Brain Hippocampus Middle brain
18 chr15:58991800-59005000 Weak transcription Liver Liver
19 chr15:58991800-59005000 Weak transcription Fetal Kidney kidney
20 chr15:58991800-59005000 Weak transcription HMEC breast
21 chr15:58991800-59012200 Weak transcription Brain Inferior Temporal Lobe brain
22 chr15:58992000-59002600 Weak transcription Primary T killer naive cells fromperipheralblood blood
23 chr15:58992000-59005000 Weak transcription H1 Cell Line embryonic stem cell
24 chr15:58992000-59009000 Weak transcription Placenta Placenta
25 chr15:58992000-59010800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
26 chr15:58992000-59015800 Weak transcription Primary T helper naive cells fromperipheralblood blood
27 chr15:58992000-59023000 Weak transcription Esophagus oesophagus
28 chr15:58992000-59023800 Weak transcription Aorta Aorta
29 chr15:58992200-59004400 Weak transcription Fetal Muscle Leg muscle
30 chr15:58992200-59008600 Weak transcription Fetal Lung lung
31 chr15:58992400-59004600 Weak transcription Fetal Muscle Trunk muscle
32 chr15:58992400-59005000 Weak transcription HUES64 Cell Line embryonic stem cell
33 chr15:58992400-59005200 Weak transcription NHEK skin
34 chr15:58992400-59005600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
35 chr15:58992400-59011600 Weak transcription HUVEC blood vessel
36 chr15:58992400-59012000 Weak transcription Brain Anterior Caudate brain
37 chr15:58992600-59005000 Weak transcription Breast Myoepithelial Primary Cells Breast
38 chr15:58992600-59016600 Weak transcription Duodenum Smooth Muscle Duodenum
39 chr15:58992600-59021000 Weak transcription Primary T killer memory cells from peripheral blood blood
40 chr15:58992800-59007200 Weak transcription Primary T helper naive cells from peripheral blood blood
41 chr15:58992800-59008400 Weak transcription A549 lung
42 chr15:58993200-59005000 Weak transcription Thymus Thymus
43 chr15:58993200-59010200 Weak transcription Rectal Mucosa Donor 31 rectum
44 chr15:58993200-59010800 Weak transcription K562 blood
45 chr15:58993400-59010600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
46 chr15:58994000-59005000 Weak transcription Duodenum Mucosa Duodenum
47 chr15:58994200-59005000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
48 chr15:58994400-59003000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
49 chr15:58994400-59004800 Weak transcription Fetal Intestine Large intestine
50 chr15:58994400-59012400 Weak transcription Cortex derived primary cultured neurospheres brain

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