| Tag | Content |
|---|
EnhancerAtlas ID | HS138-11870 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr13:110746260-110747800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr13:110747606-110747627 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | | RARA | MA0729.1 | chr13:110747694-110747712 | CCTTGACCTCCTGGCCTC | - | 6.13 | | RUNX1 | MA0002.2 | chr13:110746854-110746865 | TTCTGTGGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41265 | chr13:110745758-110747965 | Left_Ventricle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I110093 | chr13 | 110745998 | 110748510 |
|
Enhancer Sequence | TCTCCACACC ACTTCCATTT CTCATCAATA GAGGGGCTAA TTGAAGTAAA GACTCTTGAA 60
GGACTCCTTC AATGGGAACA CTCTGGAGTC CTGTATTCTG GTAGCATTTG TCATAATTAG 120
GTTATTTAAT GATGAGGTAC CTGATATGAA TGGCCTGCAG AATATGCCCC AACTATGCCT 180
TCATCAAATC TCCTAGAACT GTGTACCAAA CGAGTGAGTT TCACAGCACG TGCTCACTCT 240
GTGCTCACTG TGTGTTCGTA ACAACAATGA TTTGGTAATG TGGAGGCTGT GTGCCTCCCA 300
AATTCATACA TTGAAGCCCT AACCCCCAGT ACCTCAGAAT GTGACTATAT TTAGAAATAG 360
GGTCTGTAAG CAGGTGATGA AGTTAAAACG AGGTCATTAG GATGAGCCCA CATATGACTG 420
GAGTCCTTAT AAGAAAAATA AATATGAACA CAGATGGGCA CAGAGGGACA GCCACTTGAG 480
GACATAGGGA GAAGGCGGCC ATCTGCAAGC CAAAGAGAGA GGCCTCAAGA GAAACCAGCC 540
CCACCGACAC CTTGGTCTCA GACTTCCCAG CCTCCAGAAC CGTGAGAAAT AAATTTCTGT 600
GGTTTAAGCC ACCCAGTCTG TAGTGCTTCT TAATAGAAGC CCTGGGAAGC TAATACAGGG 660
GGTTTGGCTG AAGAAAAACA GTTGGATTTA AGACTGCAGT GTGCTGACAT CGGCTCCCAT 720
AGTTAACCAG AGCAATTCCT CCTGTGCGAC TGCTGGATCC AGCCCTTCCG CCAGCTCAGC 780
ACCTCCCTCG GGATTGCACA ATGCTTTGTC AGTTGAGCCA CTAGCAAGCC CAGCCAGGTC 840
TATTTGAAAC GGTAAACAAA AACTCAGCCC CACACAATAG TGACATTTAC TGCCCTCATG 900
TTCATTCTCA GAATCTTCCA CTGCAGTTGG AACATATTAG TCAGAGTCCT TTGAAAGCTG 960
ATGCAACGTG GGCCTGGAAC TCTCAGAACA AGGCGTGATT GTGCTAGAAC TGGATCGCAG 1020
AGCCAGTGTG CCTGGTGAGC CAATACCTGC ACCGTTGTCT GCTTGACTCG AGGAGAGGCC 1080
ACAGCCCCTG CTTCCCCTTC AGCAACCTGA TGGCAGGAGC TTCATTTCTG CTGCGAGTGA 1140
GCAGGCTGCC AATCATTCTC ATGCCTGCCC TTGTCTGCTA AATGCCATAG TCGTAAATGT 1200
TCAAAGGCTG ATCTGACCAG CATTCACTTC TATTTAGCGC CATGTCTGGT CTGTGCTTCT 1260
GATCATCCTG CCTGCTCTCC CCCTAGGGTT TGTGGCTGGG GCTTACTTTC AAAGCTTTAA 1320
GATGTTTAGG ATTTTTCTTT TTTCTTTTTT TCTTTTTCTT TTTTTTTTTT TGAAACAGGG 1380
TCTCACTCTG TCACCCAGGC TGGAGTGCAG TGGGGCAATC ATGGCTCACC CCAGCCTTGA 1440
CCTCCTGGCC TCGAGCCATG CCTCCCAAAG TCCTGAGATT ACAAGTGTGA GCCACTGCGC 1500
TTGGCCAGGA AATTTCTTAG AACTGGGTTA CGCTTGCAAC 1540
|
