| Tag | Content |
|---|
EnhancerAtlas ID | HS098-40210 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:138999590-139001140 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr3:139000487-139000499 | CGCCCCCTGCCA | - | 6.07 | | MEF2A | MA0052.3 | chr3:139000309-139000321 | TCTAAAAATAGC | + | 6.52 | | MEF2B | MA0660.1 | chr3:139000309-139000321 | TCTAAAAATAGC | + | 6.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_44251 | chr3:138998564-139003600 | NHDF-Ad |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I139280 | chr3 | 138999221 | 139001857 |
|
Enhancer Sequence | GAAAGAGGCT GGATCTCCTG CAAAGCGGCC CAAGGGCTTC CAGCCATGAA TGGACCCAGA 60
TTCAAGTGCA AAGCTATGCT GGGAAATAAA GAAAGGCACA GCTTTGTCTA CTGAGGTCTT 120
GTGTGAAAAT CCACACCATC CCCTGCAGCG TGTTTAGTTC TGCTTCTCCA AGGTAGGTCT 180
CCTCCCGTTT TAAGCTGGAG AGCTAAAGCA CAGCAGAGTG AAGTGGCTCA CCCAAGCCCA 240
CAACAAATGG CTGGCATTTG AGCTCACATC TGTCTGACTC CAAAATCCAT ATCCCCTTGG 300
TCTCATTGTC TGAAGCTTAC TGCCTGGGGA TCCTGGGACA ACATTTCAGC TGCATTCCCA 360
GCAAACAGAT CCATGAGCCC AGAGAAGCAC CCCAGCCATG CCTGAGACTT GGTTCCCAGC 420
CACTCAGCAC CACCTCCTAT GGACAGAGCT GGAAAACTGG GCCACAGGAA GCAAGACTGC 480
ATGGCTCTCT CCTCTCCTTC CAGTATGGCA TTGAGCACTG ATTAAAAAGA TAATCTGGAG 540
GCTGCTCTAG GGCCAGGCGC CATGCACAAA ACACCAGAAT GATTTGTCAT CTGAAAAGCT 600
AAAAACATCT TGATGGGTGG AGAAATCTTG ATGAGTCGAT CATGGAAGAT TATGCAAATC 660
CCTCTGCCTT TGGTGCAGAC TTTTCCAGCC AAAAGATACC ACCTCCAGAT GTGGTACCCT 720
CTAAAAATAG CAGGTGGAGT CATCTCCCCT GGCTAATTGT TCTAAGTGGT CCCTCAGTGC 780
CATCTGGAAG TGGATCTCCT CAGTGTACCA GGACATCGCC CCAATTATCT ATGCAACGGC 840
TCCTCAATGC TGGCCTTACA ACAGAGGCGG CAGCTGTCTC CGCTTATTAC ACCTCCCCGC 900
CCCCTGCCAT GGCCGGCACT GACTCTGCCT CTGACGCTGA GGATACGCAC TGCACACGCC 960
CTGCCAGATG CCAAAGGAAG CCATTCTTCT GGAAGAAGAC TTTCTCCTGA AAGCCTCCTG 1020
GAGGCAAAGT TCTGGCAGAA CGAGGCAATT TCCCTCCCTG CAGGCGGAAG GAAGGCAATT 1080
AGAGCGGGTA AGGATGGGGG ATGCTTTCTC TTTTCTTCAC TGCTGGCGAA ATATGGGCCA 1140
GGTCACGCCA CTGGCAGATG CTGCTGGCTG TGAGTGTGCA GCATCGACTC CAGATGGGTT 1200
TCTTGCCAGC ATCTCTGGCA ACCAGGGCAG GAGAGGTGCA TGTGCCTGTT CTTCCCAGGG 1260
GCTGTGGGTG CCACAGGGCA ATGCCTATAG CAGGCAGGTC TGGGACAGCT CTCAGATGTG 1320
TGCCTGGACC CAGGTAGTCT GAGATCTTCG CCAGGGCCTC TGACCACCTT GGCCTCTGAA 1380
GCAATTAACT GGTTTCCCTG CTCTGTTCAC TGGTCAGTTC TGAGTAGCAT GAGATGGCAG 1440
AATTCTCAGA GGTCACCTGG CTCATGAGAA AGTGCCAGGA GGGCATGTGA GTGCTTGGAA 1500
AGGTCCTCCC CAGAGGGAGA AGAACCAGGT CAAAGACTTT GTGCAGCATG 1550
|
