Variant report

Variant rs12534391
Chromosome Location chr7:66133422-66133423
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:93 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:66120600-66146000 Weak transcription Primary T cells from cord blood blood
2 chr7:66120600-66146200 Weak transcription Placenta Amnion Placenta Amnion
3 chr7:66120800-66143600 Weak transcription GM12878-XiMat blood
4 chr7:66120800-66146000 Weak transcription Rectal Mucosa Donor 29 rectum
5 chr7:66121000-66139400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr7:66121000-66143600 Weak transcription Primary B cells from peripheral blood blood
7 chr7:66121000-66144000 Weak transcription Skeletal Muscle Female skeletal muscle
8 chr7:66121000-66146200 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr7:66121000-66146200 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr7:66121200-66137800 Weak transcription HMEC breast
11 chr7:66121400-66139800 Weak transcription Rectal Smooth Muscle rectum
12 chr7:66121400-66146000 Weak transcription Adipose Nuclei Adipose
13 chr7:66121400-66146000 Weak transcription Rectal Mucosa Donor 31 rectum
14 chr7:66121600-66137800 Weak transcription NH-A brain
15 chr7:66121600-66144000 Weak transcription Primary T killer memory cells from peripheral blood blood
16 chr7:66121600-66145400 Weak transcription Primary T cells fromperipheralblood blood
17 chr7:66121600-66146200 Weak transcription Duodenum Smooth Muscle Duodenum
18 chr7:66121600-66146200 Weak transcription HSMMtube muscle
19 chr7:66121800-66134600 Weak transcription Ovary ovary
20 chr7:66121800-66144000 Weak transcription Skeletal Muscle Male skeletal muscle
21 chr7:66122200-66138200 Weak transcription NHDF-Ad bronchial
22 chr7:66122400-66134400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
23 chr7:66122600-66146000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
24 chr7:66127800-66135800 Weak transcription Monocytes-CD14+_RO01746 blood
25 chr7:66127800-66136800 Weak transcription Hela-S3 cervix
26 chr7:66127800-66146000 Weak transcription A549 lung
27 chr7:66128000-66135800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
28 chr7:66128000-66136200 Weak transcription K562 blood
29 chr7:66128000-66138400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
30 chr7:66128000-66144000 Weak transcription Pancreas Pancrea
31 chr7:66128000-66144000 Weak transcription Spleen Spleen
32 chr7:66128000-66145800 Weak transcription Primary B cells from cord blood blood
33 chr7:66128000-66146000 Weak transcription Duodenum Mucosa Duodenum
34 chr7:66128000-66146000 Weak transcription Fetal Lung lung
35 chr7:66128000-66146000 Weak transcription HSMM muscle
36 chr7:66128000-66146200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
37 chr7:66128000-66146200 Weak transcription Sigmoid Colon Sigmoid Colon
38 chr7:66128000-66146400 Weak transcription H9 Cell Line embryonic stem cell
39 chr7:66128200-66133600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
40 chr7:66128200-66133600 Weak transcription Primary hematopoietic stem cells short term culture blood
41 chr7:66128400-66133800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
42 chr7:66128400-66138200 Weak transcription Primary monocytes fromperipheralblood blood
43 chr7:66129600-66134000 Enhancers Brain Substantia Nigra brain
44 chr7:66129800-66133600 Enhancers Brain Cingulate Gyrus brain
45 chr7:66129800-66133800 Enhancers Brain Hippocampus Middle brain
46 chr7:66129800-66135200 Strong transcription Fetal Adrenal Gland Adrenal Gland
47 chr7:66129800-66136400 Strong transcription IMR90 fetal lung fibroblasts Cell Line lung
48 chr7:66130000-66133800 Weak transcription Right Atrium heart
49 chr7:66130200-66136600 Strong transcription Fetal Stomach stomach
50 chr7:66131000-66135200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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