| Tag | Content |
|---|
EnhancerAtlas ID | HS148-18962 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr9:93939530-93941000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr9:93940526-93940537 | TTCTGTGGTTT | + | 6.32 | | STAT3 | MA0144.2 | chr9:93940313-93940324 | TTTCCCAGAAG | - | 6.62 | | Stat4 | MA0518.1 | chr9:93940310-93940324 | CTGTTTCCCAGAAG | - | 6.01 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_20662 | chr9:93939420-93940686 | CD56 | | SE_25080 | chr9:93939736-93941207 | Colon_Crypt_3 | | SE_27567 | chr9:93939295-93941541 | Esophagus | | SE_39461 | chr9:93939246-93940576 | Jurkat | | SE_39461 | chr9:93940602-93941251 | Jurkat | | SE_44911 | chr9:93940201-93941027 | NHLF | | SE_66540 | chr9:93939246-93940576 | Jurkat | | SE_66540 | chr9:93940602-93941251 | Jurkat |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I091177 | chr9 | 93939622 | 93943446 |
|
Enhancer Sequence | TCAGAACTCT CACGGCAATT TGACAGGACT GTGGCATCAA AGTGTGTGCC TGTGTTTCAG 60
TAATCCATGT CCTCTGTGTT TTACAAAAGC ACTGGCCCAA GACAGATTGG GGAAAAACTA 120
CAAAAAATTG CTCCTTCCCT ACAGGCTGTT CCAGGACAGC AGCTCTGGAG TGTGGCTTGG 180
CGGTCATTTC TGGGGGAAGC TGCAGACAAT TAGCCACAGA TGATACTTAG GGTCTCAGAC 240
CCCACAGTTG ATGCTTAAAA TAGATGTTAA TGACTTCAGA GATGTCCCTA AGCTTATCTG 300
ATTCATACCC TCTCATTTCC AATGTGTTTT CTGAGGGAAA AAGAAGGGTT TTCGGTCAGT 360
GTGCCAGGAG ATCCAAAATC CAGGGCATCC CTGGGTAGCC TGACCTGCTG GGACAATGAA 420
AAGGTGGAGA GAGGACTCCC AGGGACGGCA ATGAGGAAAC AGGGCTGCCA CGGCCCACAG 480
GCCTGGGTGT GATCTTGCTG CAGAGCCAGG AAGCTCCTTG CAGCGGTGAA TGTGGTGGCG 540
GTGCTGGCCG GGCACCGTGG CTGTGCCTGG CAGGCCTGCT GAGGGCACAG GGATTCATCG 600
CGCTTGGCTC AGAAGCTTCG TTTTTCTGAG ACAGCTCCCA GCTTCACTCA AACGTGGTTA 660
CCTACAGATG CAAACTGGAA ACGATGCACT GTTTGTTCCC TTGCAATCTC TACGGTGAGC 720
AGGCAGGAGC CCCAGCCAGA GTCCTGTGGT CACACACCCA CTGGTGGTCA GGTAAATTTT 780
CTGTTTCCCA GAAGGTTTTA TTTTACAGAG TTAACAGACT GTGGCCTGCT TCCATTGCTC 840
TGAAACACGC CAACTCCAGT TTCCCCACCT TTGTGAGGAC GATCAAAAAC CCAGAGAACG 900
GCAGTGTTAA GATTTGATTT CATGATAAGC CCATCTTGTG GCAAGTTGAG TCTGGCTCTG 960
GAAGGTGTGT TTGCCAGGAA ACAAGCTGTG TATTATTTCT GTGGTTTGGC AAGGGAAACT 1020
CTGAGCTGGA TGGATTTGGG AACCAGGGGA AACATAGCTC AGGCCATGAG AAGTCTGGAT 1080
GAACAGGAAA ACAGAGGAGG GGTCCCAGGT ATTGCACAGC TCAGAGAGAC AACGCCCCAG 1140
CGCCAGAACT CAGCAGCCAG CAGGGGTGTG GGCAGCACTG GGGTGTGGCT GGAAACTTCG 1200
GACACCACCC ACACGGCCCA CAGTGCCAAG CCCTGCTGCC TGGCCCTGCC CACAGAACCC 1260
CCCCATCCTT CTCAGCTGTG GGCTAAACAC CCCCAGGATG GAAATGGCTG GGCTGTCCAG 1320
GGTGTGGAGT GAGCAGAGGC GCACAGGCAG CCTGCCTATG TGGGCCTGTG TTGGTGGGGC 1380
CCCACGTGTG GACATGCCCC GCCTGACACC AGGACTTGCC CGTGAGCCTC CCTCATCCCC 1440
AGCAGGCCTT GCTGGGACTC CTGTCTGGGG 1470
|
