Variant report

Variant rs2693471
Chromosome Location chr15:52762506-52762507
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:52753600-52762600 Genic enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr15:52757200-52770400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr15:52757400-52771800 Weak transcription Primary T cells from cord blood blood
4 chr15:52758600-52772000 Weak transcription HUVEC blood vessel
5 chr15:52758600-52773000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr15:52758800-52773000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr15:52759000-52772000 Weak transcription Primary hematopoietic stem cells short term culture blood
8 chr15:52759200-52763800 Weak transcription Rectal Mucosa Donor 29 rectum
9 chr15:52759200-52770600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr15:52759200-52771000 Weak transcription Primary T helper cells PMA-I stimulated --
11 chr15:52759200-52778200 Weak transcription Right Atrium heart
12 chr15:52759400-52763800 Weak transcription H1 Cell Line embryonic stem cell
13 chr15:52759400-52773000 Weak transcription Brain Angular Gyrus brain
14 chr15:52759800-52773000 Weak transcription Monocytes-CD14+_RO01746 blood
15 chr15:52760400-52770600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr15:52762200-52762600 Enhancers Primary T helper cells fromperipheralblood blood
17 chr15:52762200-52763600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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