Variant report

Variant rs576741619
Chromosome Location chr17:46640904-46640905
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:62 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:46633400-46641000 Enhancers Rectal Mucosa Donor 31 rectum
2 chr17:46635000-46654600 Weak transcription Hela-S3 cervix
3 chr17:46636400-46641000 Bivalent Enhancer Fetal Intestine Small intestine
4 chr17:46636600-46641000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
5 chr17:46636800-46641200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr17:46637400-46641400 Enhancers Sigmoid Colon Sigmoid Colon
7 chr17:46637800-46641400 Weak transcription Aorta Aorta
8 chr17:46638000-46643800 Enhancers Primary hematopoietic stem cells blood
9 chr17:46638600-46641000 Bivalent Enhancer Fetal Intestine Large intestine
10 chr17:46638600-46641000 Bivalent Enhancer Fetal Muscle Leg muscle
11 chr17:46638600-46641600 Flanking Active TSS Stomach Smooth Muscle stomach
12 chr17:46638800-46641200 Flanking Bivalent TSS/Enh Fetal Lung lung
13 chr17:46638800-46641400 Transcr. at gene 5' and 3' NHLF lung
14 chr17:46639000-46641200 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
15 chr17:46639000-46641400 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr17:46639200-46641800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr17:46639200-46642000 Weak transcription HSMMtube muscle
18 chr17:46639400-46641400 Enhancers Placenta Amnion Placenta Amnion
19 chr17:46639400-46641800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
20 chr17:46639600-46641400 Flanking Active TSS Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
21 chr17:46639800-46641000 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
22 chr17:46639800-46642000 Bivalent/Poised TSS NH-A brain
23 chr17:46639800-46642600 Transcr. at gene 5' and 3' Fetal Stomach stomach
24 chr17:46639800-46648600 Weak transcription Gastric stomach
25 chr17:46640000-46645600 Genic enhancers Primary hematopoietic stem cells short term culture blood
26 chr17:46640200-46641000 Transcr. at gene 5' and 3' Fetal Kidney kidney
27 chr17:46640200-46641200 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
28 chr17:46640200-46641400 Enhancers Spleen Spleen
29 chr17:46640200-46641400 Flanking Active TSS NHDF-Ad bronchial
30 chr17:46640200-46642800 Transcr. at gene 5' and 3' IMR90 fetal lung fibroblasts Cell Line lung
31 chr17:46640400-46641000 Bivalent Enhancer Lung lung
32 chr17:46640400-46641200 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
33 chr17:46640400-46641400 Flanking Active TSS Colon Smooth Muscle Colon
34 chr17:46640400-46643800 Weak transcription A549 lung
35 chr17:46640600-46641000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
36 chr17:46640600-46641000 Flanking Bivalent TSS/Enh Duodenum Mucosa Duodenum
37 chr17:46640600-46641000 Transcr. at gene 5' and 3' Rectal Smooth Muscle rectum
38 chr17:46640600-46641000 Strong transcription K562 blood
39 chr17:46640600-46641400 Flanking Active TSS Adipose Nuclei Adipose
40 chr17:46640600-46641400 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
41 chr17:46640600-46641400 Flanking Active TSS HUVEC blood vessel
42 chr17:46640600-46641600 Bivalent Enhancer H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
43 chr17:46640600-46641800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
44 chr17:46640600-46641800 Weak transcription Pancreas Pancrea
45 chr17:46640800-46641000 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
46 chr17:46640800-46641000 Flanking Bivalent TSS/Enh Breast Myoepithelial Primary Cells Breast
47 chr17:46640800-46641000 Bivalent Enhancer Liver Liver
48 chr17:46640800-46641000 Flanking Active TSS Colonic Mucosa Colon
49 chr17:46640800-46641000 Bivalent/Poised TSS Duodenum Smooth Muscle Duodenum
50 chr17:46640800-46641000 Transcr. at gene 5' and 3' Rectal Mucosa Donor 29 rectum

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