Tag | Content |
---|
EnhancerAtlas ID | HS116-31864 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr7:104993770-104995220 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr7:104993977-104993997 | TTGTTGTTGTTGTTTGGTGG | - | 6.42 | Tcf12 | MA0521.1 | chr7:104994500-104994511 | AACAGCTGCTG | + | 6.32 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_25374 | chr7:104991033-104995488 | DND41 | SE_66307 | chr7:104994292-104995451 | Jurkat |
|
| Number: 1 | ID | Chromosome | Start | End |
GH07I105350 | chr7 | 104990788 | 104996910 |
|
Enhancer Sequence | TCCAGGTAAT GGTTTTGTTT TTTTGTGTTT TTTTTTGAAA CAGTCTCCCT CTGTCACCCA 60 GGCTGGAATG CAGTGGTGCA ATCATGGCTC ACTGCAGCCT TGACCTCCTG GGCTCAAGCA 120 ATCCTCCCAT CTCAGCCTCC CAAGTAGCTG GGATTACAGG AGCGTGCCAT CCAGCCCAGT 180 TTGTTGTTGT TGTTGTTGTT GTTGTTGTTG TTGTTGTTGT TTGGTGGAGA CAGGGTTTTG 240 TCACGTTGCT CAGGCTGGTC TCAAACTCCT GAGCTCAAAT GATCCGCCTT CTTTGGCCTC 300 CCAAAGTGAT GGGATTACAG ACTGCCTTCA AGCAAATTCA TCAGGCCCAT GTTCCTGAAT 360 GCCCCAAGGT GAGCAGTAAG GAACAGAAAA ACACTTTCCT TCTCCAGAAA ATCCCACTCC 420 TGAGCTGATA GGAGGGGATC TCAGAAAGAA TCATCACAAA AGACAGGACA AACTAAAGAA 480 GCTGGCAGAC TTTTTTAATT CTTCCCAGTA CAAACTGGAA CTAGACATGC AGAGAGCCTT 540 CCTAAAGGCA ACGCCCAAAT CCCACGTGAG GCCAAACTTC TCCCCAGGGA GACTGAGAGC 600 CAATGTTCTT ATCATAACAC TCCTCCCCAC AGTGCACCCA CAGACAAGGA AGCCTGAGCA 660 GTTGTGGCTG TCACACAACA GATGCAGCGT TCAGGCCAGA ACCTTCCAGG ACCTTCCTCT 720 TTGCTGGCCC AACAGCTGCT GCATCTGCCT GGCCTTCGAG GAGCAGCCAG TATGTATGTG 780 GCTGTGTGGA GCAAGAATGT GCCAAAATAA GCAACCAAGT CAATCAGAGA TGGGTTTGGG 840 GCTAAGTTGA CATGGTAACA GGACCAGTCA CAGGTCTCCC CATGTATGGT GGGACCACAG 900 AGCCCTATGT CCTCCATTCA TTCTTCTCTG GGCAGTTTCT GTCCAGGACA GCTATGGGGC 960 AAATTCCACC TTATCCTTAA GACTCACCAC CTGGGTGTGC GTGGCTCTTG CCCGGCAGCT 1020 CATCCAGCTC ATCCACCCTG TACTCAGAGA TGCTTTTTTC CTCCTGCACA GGCTGTGGGT 1080 CCTTTCCCCT AACGAATCAC TCCAGGTAGT AGCCCACAGT CCTGGCCACA AAGGCCACAG 1140 GGTATGTAAC TTAAGTAGCA TAGGTAAGCA TTACGATCCA AAGCACAAGC CACACATCAT 1200 CAGGCAGCCT GGCACAATTT ACTGGGAATC CACTCATGCA TAGCAATGCA AGAGATCACA 1260 CCCTGTTTTA TGCAACAGTT GGGTACCACA AATAATCTGC AGCACAGCCC ATACTCCTCT 1320 GTCCAGCCCT GGTCTCTACC TGCTGGCTGG GAACAGACAT TGCTACTCCT AGCAGCCCAC 1380 ATGGCCTCCT GTTGTTTTTT AATAACAACT ACAGTCAGAT ATATAACTCA CATGTACAAT 1440 TCACCCAATT 1450
|