| Tag | Content |
|---|
EnhancerAtlas ID | HS194-02908 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr2:28833260-28834600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr2:28833916-28833927 | CCCAATAAAAC | + | 6.62 | | HOXA13 | MA0650.2 | chr2:28833926-28833937 | CCCAATAAAAC | + | 6.62 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_01568 | chr2:28833104-28834877 | Aorta | | SE_23318 | chr2:28833216-28834463 | Colon_Crypt_1 | | SE_26630 | chr2:28833054-28834795 | Esophagus | | SE_34837 | chr2:28832222-28839258 | HeLa | | SE_36194 | chr2:28832761-28834777 | HMEC | | SE_48350 | chr2:28833124-28835658 | Psoas_Muscle | | SE_51304 | chr2:28829262-28833923 | Skeletal_Muscle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I028609 | chr2 | 28832369 | 28838981 |
|
Enhancer Sequence | TCCCACACTG GCCTCCCAAA GTGCTGGGAT TACATGTGTG AACCACCACA CTCGGCCGGA 60
ACTAGCACTT TTTGAATGGA ATGGGATAGA AAACCTCTTA GGACATCCCG TGAAATACCA 120
TTATGTCCTC CTGCCTCTGA CTGCCACCAC CCAGCTGAGA GTCTTCTCAG TTCCAGCCAC 180
TCATTGCACA CATGGCTGCC AACCCCTGCC TCATATGGGT ATTTCTCCTT GGAATGTGGC 240
CCCTTGTAAG GTGGTGACTG TACATCTGGT TTGATCCAAC CAGCACAACC AGCGAAGAAA 300
ATCACCCCTC CTTCCCCATG GAACTACACC TGGTAAAGCA GCCAGGATGT TGATGGCCTT 360
GTCCCACAGC CACTGACTCA CGTTGCTGAC TCACATCAGG AGGCTGGCTG GGCTCTGCCT 420
CCCCAGGCAG CCCACACCGT CTTTGCATGG CTGGAACTAC TAGACCGGTT CCTTGTTCTG 480
CCATTCAGTC GGCCCCCCTT TCTACTCACG GGGGCTCCAA ATCTAGCCTT CAAGAGCCAG 540
TCAGGCTCAA TCAAACCCCT CTTTCACGTC ATCTGCTTTG GCTCCAGGCC TTTAAACCAC 600
TCTGACTCAT GCATGCACCA AATGGTCAAT GGTCAATAAA CCCAGCTAAA AACAAGCCCA 660
ATAAAACCCA ATAAAACCCA TTAGACAGGA ACATAGGAGT TGGAAAAAAA AGAAAAGAAG 720
GGGAGGGGGA GGAAAGCCCT GAGGCACCCC GGCTGCCTGT CTGCCACAAC CCTGGGCTGT 780
AATTGTTCTT GCCATGGCCT CAGTCTGCAA CACATTCTAG TGTCTCCTTG ACCTCTAGCC 840
CTCTAGCTCT GCCTCCCTTT CCCCAACCTG TAGATCTTGT GATCAAATAG ATTCAATGAA 900
ACACATTGTC CAGTTGCACT CGCAGCACTT CCAAAAAGGT CAAGTTTGTC CTTCCCTCAG 960
TGCCTCCCAT TCTGGTCACG GTAGGACTGA CTCCAGCCCC TGGACCCTAA GCTGAGTCTG 1020
GGCTCCTTTG ACGTGCAGGG AGAATGCCAC TGAGTCTTGT CTCTGAGGAC CCTACCTCTC 1080
CAAATCTTGC CTCAGTTCCT CAGCAGGTAC TACACTGACT GGCCATGCCA TTCTCTGATG 1140
CTTCACTGCC TCAGCTTCTC AAGTCTGTCT CCCCACCTGA GCCAATTGTG AGTTTCTCTC 1200
TCTCCTCCTC TCATCCTGGC ACCTAGAAAT GCTCTCTAAC GCTTGAGCTG CTCAACCAGC 1260
ATGGGTCACT TGTTTATAGC ATGCTCCCAG ATCGCCCTCT TTGTTGGTGA ATGCTCAGGG 1320
AATGCTTACT GTTAACCCGA 1340
|
