Variant report

Variant rs6683136
Chromosome Location chr1:228670486-228670487
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:228667400-228672800 Weak transcription HUVEC blood vessel
2 chr1:228667400-228673600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr1:228667400-228674000 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr1:228667600-228673600 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr1:228667600-228673800 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
6 chr1:228667600-228674000 Weak transcription Primary T helper cells PMA-I stimulated --
7 chr1:228667800-228672000 Weak transcription Primary monocytes fromperipheralblood blood
8 chr1:228667800-228673800 Weak transcription Primary T regulatory cells fromperipheralblood blood
9 chr1:228667800-228674000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr1:228668000-228673200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr1:228668000-228673600 Weak transcription Primary T cells fromperipheralblood blood
12 chr1:228668000-228673600 Weak transcription Pancreas Pancrea
13 chr1:228668000-228674000 Weak transcription Primary T helper 17 cells PMA-I stimulated --
14 chr1:228668200-228673200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr1:228668200-228673800 Weak transcription Fetal Intestine Small intestine
16 chr1:228669000-228673000 Weak transcription Primary hematopoietic stem cells short term culture blood
17 chr1:228669800-228670800 Enhancers GM12878-XiMat blood
18 chr1:228670000-228670600 Enhancers K562 blood
19 chr1:228670000-228672800 Weak transcription HepG2 liver

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