| Tag | Content |
|---|
EnhancerAtlas ID | HS176-00404 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:24610010-24611230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:24610743-24610754 | GGGTGACTCAG | + | 6.02 | | FOXP2 | MA0593.1 | chr1:24611158-24611169 | AAGTAAACAAA | + | 6.62 | | JUNB | MA0490.1 | chr1:24610743-24610754 | GGGTGACTCAG | + | 6.02 | | LMX1B | MA0703.2 | chr1:24610367-24610378 | TTAATTAAAAT | - | 6.62 | | Nr5a2 | MA0505.1 | chr1:24611115-24611130 | GAGTTCAAGGCCAGC | + | 8.25 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_26668 | chr1:24609435-24614470 | Esophagus | | SE_35109 | chr1:24609294-24612359 | HeLa | | SE_36021 | chr1:24609234-24614068 | HMEC | | SE_64493 | chr1:24609444-24613797 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I024283 | chr1 | 24609537 | 24613932 |
|
Enhancer Sequence | TTACCCAGAG ACAGGTGGGT GCCCACGCCT CACCTACTAC TTGGAGGCCC CAGTCATAGT 60
CATCATATCA GGGAGTATGG GGGATGCCAT TTGGGGCCTC CTCAAAAAAG ATGCCACCTG 120
CTCTAGCCCA GGAAGTCAAG CTATGGTTGC TCACCTTGGG ACAGTAGGGA CAGCTTGCTG 180
GGCTTGTAAA TAAATGTGGA GCAAATCACA GTGAATGACC CGCACCTCAC TTAGGCCTTC 240
ACCAGGCATT GCCAAATGCT GCCTTCTCTT TACTCGCCCA GGAGCCCAGG CACATTGGTG 300
TCTTCATTAT TTCCGAGTGG ACCTTATTCA ATAACCCAGG GAAAATCAAC AATGTGATTA 360
ATTAAAATCT TAAGACACAC TCTGTTTTGT TATCTGTGGA CTCTACTGAG CTACTTCCTC 420
CAGGAAGAAG GAATTGGCCC ACTTGTTGGG TTTATTTATT TACTTATCTA CATGCATCTG 480
GACAGTTTTG CGTTGTGATT CATTCTGGGA AAGCTATATC AGATGGGACC ACATCCAAGG 540
AGGAACCGGG TTGGGAAAGG ATGCTGGAAT CCCGGAATTG CCTTCCCAGT CACCTCAGAA 600
TCAGGATTAT GCTCTTTTTT AATGCTTTCT CCTTCACAAT GAGTTTCCCC CCCAGAAACC 660
TCATTAACCC TGAAACTTTT TGAACATTTT CCACAGGTAA GGGAGGCTGG TCTTCTGGAC 720
TCGGCTGAGT CCTGGGTGAC TCAGGCTGAG TCCTCAGGAA AACCCCAGGG GCTCAGGATG 780
CAACCTGCTG AGTCCCAGGC CGGTGGCCGA ACCTCCTCAA GCCTCGTCTT CTCATCAGCA 840
AAATTAAAAG TTCCCTCTTA GGGTGTTGCA GGTTTCAATA GAATCACACC GCGGATCAGG 900
CTCGCTTCGG GGCCATTGCA CATGCTGTTC CCTTTTTCTG AGACACAATT CCTCTCTTCC 960
CATCACCACT CCAGCCTCTC AACTTGGTTG ACACCAACCA TCCTTCCAGC CGTAGTTTAA 1020
ATATCATTTC TGGCTGGGTG CCCTGGCTCA TGCTTGTAAT CCCGGCACTT TGGGAGGCCA 1080
AGGTGGGCAG ATTGCTTGAG TCCAGGAGTT CAAGGCCAGC CTGGGCAACA CAGACCCTGT 1140
CTCTACAGAA GTAAACAAAA TTAGCCCAGT GTGGTGGTGT GTGCCTGTGG TCCCAGCTAC 1200
TCAGGAGGCT GAGGTGGGAG 1220
|
