Variant report

Variant rs143871941
Chromosome Location chr2:190450037-190450038
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:190446800-190450200 Weak transcription HUVEC blood vessel
2 chr2:190446800-190450400 Weak transcription Sigmoid Colon Sigmoid Colon
3 chr2:190447400-190452200 Weak transcription Primary T cells from cord blood blood
4 chr2:190448200-190450400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr2:190448400-190457400 Weak transcription Primary hematopoietic stem cells blood
6 chr2:190448600-190450400 Enhancers Fetal Intestine Large intestine
7 chr2:190448600-190450600 Enhancers Liver Liver
8 chr2:190448600-190450600 Enhancers Rectal Mucosa Donor 31 rectum
9 chr2:190448600-190451400 Enhancers Ovary ovary
10 chr2:190449200-190450200 Enhancers HepG2 liver
11 chr2:190449400-190450600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr2:190449600-190450600 Enhancers Stomach Mucosa stomach
13 chr2:190449800-190450600 Enhancers HMEC breast
14 chr2:190449800-190450600 Enhancers K562 blood
15 chr2:190449800-190452400 Weak transcription Primary hematopoietic stem cells short term culture blood

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