Variant report

Variant rs10799567
Chromosome Location chr1:224542122-224542123
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:224529200-224544000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr1:224536800-224544200 Weak transcription Primary T helper cells PMA-I stimulated --
3 chr1:224536800-224544400 Weak transcription Primary T killer naive cells fromperipheralblood blood
4 chr1:224536800-224544600 Weak transcription Primary T killer memory cells from peripheral blood blood
5 chr1:224538400-224544400 Weak transcription Right Atrium heart
6 chr1:224540600-224544400 Enhancers Fetal Intestine Small intestine
7 chr1:224540800-224544400 Weak transcription H1 Cell Line embryonic stem cell
8 chr1:224540800-224544400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr1:224540800-224544400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr1:224541200-224544200 Enhancers Rectal Mucosa Donor 31 rectum
11 chr1:224541200-224544400 Enhancers Fetal Intestine Large intestine
12 chr1:224541400-224542400 Enhancers Primary T cells from cord blood blood
13 chr1:224541600-224543200 Enhancers HepG2 liver
14 chr1:224541800-224542600 Enhancers K562 blood
15 chr1:224541800-224543200 Weak transcription Rectal Mucosa Donor 29 rectum
16 chr1:224542000-224542400 Flanking Active TSS Duodenum Mucosa Duodenum
17 chr1:224542000-224543000 Weak transcription Small Intestine intestine

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