| Tag | Content |
|---|
EnhancerAtlas ID | HS045-46396 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr3:123995680-123996860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr3:123996262-123996274 | CGCCCCCTGACA | - | 7.22 | | KLF13 | MA0657.1 | chr3:123996002-123996020 | TCCAGAGGGGCGTGTCAT | - | 6.68 | | NR3C2 | MA0727.1 | chr3:123996274-123996291 | CAGAACACAGTGTCCTG | + | 6.08 | | Nkx2-5(var.2) | MA0503.1 | chr3:123995713-123995724 | CTTGAGTGGTT | - | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_01654 | chr3:123991253-123999860 | Aorta | | SE_54021 | chr3:123991236-123999461 | Spleen | | SE_54982 | chr3:123989832-123998283 | Stomach_Smooth_Muscle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I124274 | chr3 | 123993757 | 123997857 |
|
Enhancer Sequence | ATTTCACAGA TGGGAAAGCT GAGACTTGGT GTGCTTGAGT GGTTTGCTTG GGATAGAGTC 60
CTCTGCTTTG AAGCTGGTGC TCCTCCCTCT TCTCCCAACA CACGCACGCA CACATGTGCG 120
CATGCACACA CACATGTGTG CACACGTGCA CACACACACT CTCTACACCC TCTCTTTGGA 180
GGCTCCTTGC CGTGCAGGAC AGATGGTGGC ATGTGCCAGG AACCTAGGCG GTGGCTAAAG 240
GGGCTGGGGG CTAGGAGGAT AAGGGTCACT TGACATGTGT CCTCACCAGT GCTGTGGTGA 300
AGGGACAAGC ACTGGACAGG CCTCCAGAGG GGCGTGTCAT GTCTCTGTGT GGTTCAATTG 360
CCTGAGCCCT TCATGTTGGG AGGGAGGCTT CAAAGAGCTG TGACCTTCGG GTTGGCCAGA 420
AGGGCAAGGC CTTTACGGGG TGGTTGTAAT TTCCTGCTTT TTTTGGAGAA AGGCTCCGGT 480
GCCCTCTTGT TCCTGCTCTC CCCTCTCCTA CTGAGACCTT AACCACCAAA CCCCTCCACC 540
TCCTGTTGAC GGAGCTCAGG GCAAGGAAGT GTGTCTGTAT CCCGCCCCCT GACACAGAAC 600
ACAGTGTCCT GTATTATTTC CAGCCTGCTG GTCCTGGGAA TTTCGACTTA CTTTTTCTCA 660
TTTCCTCCCC TTGAACATTA GAAACATTAG ATTCCAAAAA TAATCTAAGT CACCGTGTTC 720
TACAGGCTGC ATGTGTGTGT TTTCTCCCAA AGCTGTTTTT CTCCCTCTTA AATCCTTTCT 780
CCCTCTCCTT TCTTCCCTCT CCTGCATTTT CAGCCCCATT TGTATCCTGA GATTAGCACG 840
CCTGCAGGAG GAGTGTGGGT GTGGAGAACA GAATGGAGGA AGGATGGGGA AGAATGCTCA 900
GGCATGAGGC TTGGCTCCCT TCCACGGTTC TCTCAAGAGA GTGGAAGGTG CCAAGACCTG 960
AACTGCTGTG TGTAAAAAGT CTGCCTATGC AGCCCCTGCT TATGAATGGA CCCCATAGAA 1020
CTGTGGACCC CTTAGTGACT CTTTGGAACT GAGAACTAAG ACACTGTGTT AACAGTACTT 1080
TCCAGAATCT GGGCTGTCAC ACTGACTCTG TCTGCAGCAG TTGAGGTGAG CTGTGAAAAG 1140
AAGGTCTGAT CAGAGATGAA CTATGTGTGT GTGTGTGTGT 1180
|
