Variant report

Variant rs6957350
Chromosome Location chr7:103085410-103085411
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:103084800-103085600 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
2 chr7:103084800-103085600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
3 chr7:103085000-103085600 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
4 chr7:103085000-103085600 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
5 chr7:103085200-103085600 Bivalent Enhancer H1 Cell Line embryonic stem cell
6 chr7:103085200-103085600 Flanking Bivalent TSS/Enh iPS-20b Cell Line embryonic stem cell
7 chr7:103085200-103086000 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
8 chr7:103085400-103085600 Flanking Bivalent TSS/Enh HUES48 Cell Line embryonic stem cell
9 chr7:103085400-103085600 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
10 chr7:103085400-103085600 Bivalent/Poised TSS NH-A brain
11 chr7:103085400-103086000 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
12 chr7:103085400-103086200 Bivalent/Poised TSS Primary T cells from cord blood blood
13 chr7:103085400-103087200 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell

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