Variant report

Variant rs9376721
Chromosome Location chr6:143400358-143400359
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143382600-143426800 Weak transcription Ovary ovary
2 chr6:143384200-143407400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr6:143384200-143407600 Weak transcription Psoas Muscle Psoas
4 chr6:143386000-143403800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr6:143386400-143431800 Weak transcription NHEK skin
6 chr6:143389600-143437000 Weak transcription HSMM muscle
7 chr6:143389800-143418800 Weak transcription Osteobl bone
8 chr6:143395800-143432200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:143396600-143402200 Enhancers Liver Liver
10 chr6:143397400-143431600 Weak transcription HMEC breast
11 chr6:143398000-143408000 Weak transcription Left Ventricle heart
12 chr6:143398800-143404000 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:143399400-143400600 Enhancers Small Intestine intestine
14 chr6:143399400-143400800 Enhancers HepG2 liver
15 chr6:143399800-143401200 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr6:143400000-143400400 Enhancers iPS-18 Cell Line embryonic stem cell
17 chr6:143400000-143400400 Enhancers Primary neutrophils fromperipheralblood blood
18 chr6:143400000-143400600 Enhancers HUES48 Cell Line embryonic stem cell
19 chr6:143400000-143400600 Enhancers iPS-20b Cell Line embryonic stem cell
20 chr6:143400000-143400800 Enhancers Fetal Intestine Large intestine
21 chr6:143400000-143401200 Enhancers HUES64 Cell Line embryonic stem cell
22 chr6:143400000-143401200 Enhancers Fetal Intestine Small intestine
23 chr6:143400200-143400400 Genic enhancers Ganglion Eminence derived primary cultured neurospheres brain

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