Variant report

Variant rs4887815
Chromosome Location chr16:75319216-75319217
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:86 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:75301000-75325000 Weak transcription Liver Liver
2 chr16:75301800-75321800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr16:75302000-75324000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr16:75306200-75325000 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr16:75306200-75325200 Weak transcription H1 Cell Line embryonic stem cell
6 chr16:75306400-75321600 Weak transcription Right Atrium heart
7 chr16:75307600-75321600 Weak transcription Lung lung
8 chr16:75307800-75320400 Weak transcription Fetal Adrenal Gland Adrenal Gland
9 chr16:75307800-75323000 Weak transcription NHLF lung
10 chr16:75307800-75325400 Weak transcription Osteobl bone
11 chr16:75311600-75321200 Weak transcription Spleen Spleen
12 chr16:75312000-75324400 Weak transcription H9 Cell Line embryonic stem cell
13 chr16:75313400-75324600 Weak transcription Stomach Smooth Muscle stomach
14 chr16:75313400-75325200 Weak transcription iPS-20b Cell Line embryonic stem cell
15 chr16:75313400-75325200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr16:75313600-75321000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
17 chr16:75313600-75321600 Weak transcription Left Ventricle heart
18 chr16:75313600-75321800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
19 chr16:75313600-75321800 Weak transcription Gastric stomach
20 chr16:75313600-75321800 Weak transcription HUVEC blood vessel
21 chr16:75313600-75322000 Weak transcription Fetal Intestine Large intestine
22 chr16:75313600-75322200 Weak transcription Adipose Nuclei Adipose
23 chr16:75313600-75323200 Weak transcription HepG2 liver
24 chr16:75313600-75323800 Weak transcription Ovary ovary
25 chr16:75313600-75325800 Weak transcription ES-I3 Cell Line embryonic stem cell
26 chr16:75313600-75330400 Weak transcription Pancreas Pancrea
27 chr16:75313800-75322200 Weak transcription Right Ventricle heart
28 chr16:75314000-75322000 Weak transcription Primary T helper naive cells fromperipheralblood blood
29 chr16:75314000-75325000 Weak transcription Brain Anterior Caudate brain
30 chr16:75314400-75321600 Weak transcription Fetal Lung lung
31 chr16:75314800-75321800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
32 chr16:75314800-75321800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
33 chr16:75314800-75325400 Weak transcription Colon Smooth Muscle Colon
34 chr16:75315000-75320800 Weak transcription Skeletal Muscle Female skeletal muscle
35 chr16:75315000-75321200 Weak transcription Placenta Placenta
36 chr16:75315000-75321800 Weak transcription HSMM muscle
37 chr16:75315000-75335600 Weak transcription Psoas Muscle Psoas
38 chr16:75315200-75321600 Weak transcription Skeletal Muscle Male skeletal muscle
39 chr16:75315200-75325200 Weak transcription Brain Hippocampus Middle brain
40 chr16:75315200-75326600 Weak transcription Brain Substantia Nigra brain
41 chr16:75315400-75325400 Weak transcription Aorta Aorta
42 chr16:75315800-75322200 Weak transcription Primary T cells from cord blood blood
43 chr16:75316000-75319400 Strong transcription Fetal Intestine Small intestine
44 chr16:75316000-75320800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
45 chr16:75316000-75320800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
46 chr16:75316600-75323000 Weak transcription Duodenum Smooth Muscle Duodenum
47 chr16:75316800-75321400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
48 chr16:75316800-75321800 Weak transcription iPS-15b Cell Line embryonic stem cell
49 chr16:75316800-75322200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
50 chr16:75316800-75325000 Weak transcription Brain Germinal Matrix brain

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