| Tag | Content |
|---|
EnhancerAtlas ID | HS051-13279 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:742940-743720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr19:743330-743344 | GGTCCCTGGGGATT | - | 6.24 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23277 | chr19:742554-744111 | Colon_Crypt_1 | | SE_23981 | chr19:742605-743916 | Colon_Crypt_2 | | SE_24804 | chr19:742608-744206 | Colon_Crypt_3 | | SE_27769 | chr19:736895-745751 | Fetal_Intestine | | SE_28712 | chr19:742261-744533 | Fetal_Intestine_Large | | SE_50925 | chr19:742545-744097 | Sigmoid_Colon | | SE_52481 | chr19:741469-744219 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I000737 | chr19 | 737127 | 744196 |
|
Enhancer Sequence | GGCGACTGTG TGGAGCTCCG TGAGGACCTG CTGTTTTCCA CGGAGGCTGC ACCGTCCCGT 60
TCCCACAGGT CGTGGATGAG GGCCCAGTTT CTCCACGTCC TCACCAGCGC TCGTAGCCCA 120
TTCTCGTGGC TGTCCTGGTG GCGTGACGTG GGGTCTCCCT GTGGTTTGGA TTCCCAAAGC 180
CTTCTGTTCT CAGAGGCAGC TTGGCCTCTG CGGTGCCCCA GATGCTGTCA GAGGGGTCCC 240
CGCAGCCCAG CTCTGGAGTG GCTTTGGGGT GTGGCGTTGG TGGCATCTCA GCTCTAGCTC 300
TCCCCAGCTG TGTGGCCCTG GGAAGTCCCC ATGCCTCGTC TTCCGGATGA GGTCCTCACC 360
CCCATCACTC CACCCTCCTC AGCCTCACCT GGTCCCTGGG GATTCCAGAC CTGCCAGGCT 420
GGACACTGGT TGCTTAGCAA CGGGCAGGTG ATCCGTTTCC ATGGCAGCCG AGGGCTCCAA 480
TTCCTGTCTT GGGGCAGCGG CCAGTGGGAC ACACTGAGTT CAGTTCCGCC TGATCCAGAC 540
ACACCCCACC CTCTGGGCCT CCAGCCCAAA GTCATTGAGA TGCCTTGAAG CATGGACTCC 600
CCTCCCTGGG GGCTTAGAAA CTGAAAGTGG AGAACACTTT CCTTCTGGTC TGTAGCCAGG 660
AACAGGAGCC CTGACCCTTG GCCGAGAGGA GGCGAGTCCC TGGGACCCCC CTTGCGTCCC 720
TCCCAACTCC CAGCGTGGCC CAGGCAGCCG TGTTTCTAGA AGGAATTTGC AGGGCTGTGA 780
|
