Variant report

Variant rs6682932
Chromosome Location chr1:47789314-47789315
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:47780200-47798400 Weak transcription Spleen Spleen
2 chr1:47780600-47798000 Weak transcription HSMMtube muscle
3 chr1:47780800-47791200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr1:47780800-47797800 Weak transcription Fetal Muscle Leg muscle
5 chr1:47787200-47790800 Enhancers Stomach Mucosa stomach
6 chr1:47787800-47789600 Enhancers HepG2 liver
7 chr1:47788200-47791800 Enhancers Fetal Intestine Small intestine
8 chr1:47788600-47792400 Enhancers Rectal Mucosa Donor 31 rectum
9 chr1:47788800-47789800 Enhancers K562 blood
10 chr1:47788800-47790200 Enhancers Fetal Intestine Large intestine
11 chr1:47789000-47789600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr1:47789000-47789600 Enhancers A549 lung
13 chr1:47789200-47789600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
14 chr1:47789200-47789800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr1:47789200-47790600 Enhancers Rectal Mucosa Donor 29 rectum
16 chr1:47789200-47792400 Enhancers Duodenum Mucosa Duodenum

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