Variant report

Variant rs17712784
Chromosome Location chr7:22311651-22311652
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:22262200-22329000 Weak transcription Primary B cells from cord blood blood
2 chr7:22278600-22325800 Weak transcription Liver Liver
3 chr7:22282200-22364400 Weak transcription Esophagus oesophagus
4 chr7:22309200-22322400 Weak transcription Primary T cells from cord blood blood
5 chr7:22309400-22311800 Genic enhancers Dnd41 blood
6 chr7:22309600-22318400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr7:22309600-22328600 Weak transcription Sigmoid Colon Sigmoid Colon
8 chr7:22309600-22329000 Weak transcription H1 Cell Line embryonic stem cell
9 chr7:22310000-22327000 Weak transcription Rectal Mucosa Donor 29 rectum
10 chr7:22310000-22329000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr7:22310000-22335600 Weak transcription Pancreas Pancrea
12 chr7:22310000-22343400 Weak transcription Spleen Spleen
13 chr7:22310200-22311800 Enhancers HepG2 liver
14 chr7:22310200-22317200 Weak transcription Rectal Mucosa Donor 31 rectum
15 chr7:22310400-22318400 Weak transcription Duodenum Mucosa Duodenum
16 chr7:22311000-22313600 Weak transcription Thymus Thymus
17 chr7:22311000-22315000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr7:22311400-22312600 ZNF genes & repeats Fetal Intestine Small intestine
19 chr7:22311600-22311800 Enhancers Fetal Thymus thymus

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