| Tag | Content |
|---|
EnhancerAtlas ID | HS095-31289 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr9:100904390-100905840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr9:100905624-100905637 | AGCAGCTGTTCCT | + | 7.22 | | TFAP2C | MA0524.2 | chr9:100905474-100905486 | TGCCCTGGGGCA | + | 6.44 | | TFAP2C | MA0524.2 | chr9:100905474-100905486 | TGCCCTGGGGCA | - | 7.22 | | ZNF263 | MA0528.1 | chr9:100905096-100905117 | CCTCCCCTCCGCCCCACCTCC | - | 6.07 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09950 | chr9:100904103-100905141 | CD14 | | SE_24386 | chr9:100904263-100906392 | Colon_Crypt_2 | | SE_26852 | chr9:100904207-100909935 | Esophagus | | SE_27659 | chr9:100903802-100910551 | Fetal_Intestine | | SE_28584 | chr9:100903818-100910565 | Fetal_Intestine_Large | | SE_42027 | chr9:100904412-100905212 | LNCaP | | SE_53152 | chr9:100904184-100910435 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I098141 | chr9 | 100904020 | 100910418 |
|
Enhancer Sequence | CAGGATTAGC CAAAAACTTC TGTTATAAAA CTGTAGCTCT TGAAGGGCTC TAGAGACCAG 60
GAATGGAGCC CACAGCTGCA CTGTCTTATC CTGCACCTGT GGCAGGCATT GCGAATGGAT 120
CCCAGCACCC TCTCTCGGAC CTCAGACTTG GGGAAATCCA GCATGGAGTA GGGACTTGCC 180
CAGGGTCACT GCAAAGGTGA GGGGCAGAGC TGGGCTTGAG CCCAGGCCTC TGGTTCCCCA 240
AGTGTGAGCC TGGTGCTGTA CTTCCTGTGC TCTGAGGGAG CACCAGTGAG TGCTCTGTGA 300
GTCCCTGCCC TGGCCTCCTT CCTGCACACA GCCTTTCCTT TCTCTGGGAT CATTTCCTGG 360
GTCAAAGGCC ATGAGCAGTA CTGTGTCTTT GGCTGTGGGG CACTGATTGC TCTCCGGGCC 420
TTTAGACTCT GGCCCAGGGC CATGCCCCAA TTTCCGCAGT GCGGTTTCCC AAGAAAAGCC 480
AGATGAGCCA ATAGTCAGGC TGCCCTCGGG CTGACGGGAG GCAAAGTGCC CAGGAGCCCC 540
ATTCAGACAC ACACCTCCCA CCTCCCACAG ACTCAGGGAA GGCGCCTTAG GGTTGGGCGT 600
GGCTCAGAAG GGCCTAGCCC TAGACAGCTT CTCTTCCTTC TCAGCCTTCT CTTCCTTCTC 660
AGCTGATGAG GGAAGGCTGC CCACTCACAC CCCAGCCCAC CCCAGCCCTC CCCTCCGCCC 720
CACCTCCCCT GCCCTGCCCT GCCCTGCGCT GCCCTGCGCT GCCCTGCGCT GCCCTGCCCT 780
GGGCTGGCAG ATTGCTCTGC TTCTAAAAGG TTTTACGCTG AGGACCACAG GCAGGAGCGG 840
ACATTAGCCA GCCTGGTGGG CTATTGACTG AGCTGCTAAA AGCCTGTCAG GGACATTTAT 900
CATCAGGAGG CCATTTCCAC CTTCTGCCCA TTAGGCCAGC ACTCAGCCAG AAACAGGCTT 960
CTGATGGATG TGGTGTACAA GCTCTAAATC AGGGGAGACA CGCCTGCTCC CCTCGCAGAC 1020
CCCACAGAAC CCTGGCTTGG GCCGCCCTGC CTGGAGAGGC ATCACCTCCA AGTCTCCAAG 1080
GGGCTGCCCT GGGGCAGAGG GGGAAGACAG GACAGAAGGA CCCAGGAGGA GTCAGGCGGG 1140
TGGGGGACCA GACTGGGGAC TCTCTACGGC TGACCTCCAT TGCCAGAAAG GGAGAGGTTG 1200
TGAGGCCACT GTCACGACCC TCAGCAGTCA AGGGAGCAGC TGTTCCTACA ACAGCATCAT 1260
AGTCATGGCC TCAAATGAGC ATCCCAACAG CTCAGGGTGG AGACTGGGAG GCAGGGGTGG 1320
CAGGACGGGC AGAGGGAGGA CACACAGTGT AGCAGAGGTG AAGTGGGCAG GCAGACTCTG 1380
GCTTCCAGGG GTGGAATCCC TGCCACATCC CTTACCATGG TGCAGCCTTG GGCAAGTGAC 1440
CTCAGTTCTC 1450
|
