| Tag | Content |
|---|
EnhancerAtlas ID | HS148-13710 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr4:141015000-141016470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:141015920-141015938 | GCTTCCTTCCTCCTTTCC | - | 7.39 | | TFAP2A | MA0003.3 | chr4:141016243-141016254 | TGCCTCAGGCA | + | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09699 | chr4:141011070-141025597 | CD14 | | SE_13803 | chr4:141014689-141023586 | CD34_Primary_RO01536 | | SE_38025 | chr4:141010149-141026808 | HUVEC | | SE_47279 | chr4:141009086-141022050 | Panc1 | | SE_50003 | chr4:141014792-141025388 | RPMI-8402 | | SE_60286 | chr4:141005600-141039792 | Ly4 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I140087 | chr4 | 141008338 | 141022818 |
|
Enhancer Sequence | GCACCTTGGC TGTATTACCC TAGCCTGAGA TTTCCTTTGG AGTGCATTCG GTCTGGCCGT 60
CAGGTTGTCC TGCTCACTGT GCAGCATGAT CCCCCTGACA TTCCATCCTT TGGAGCCCCA 120
GTAACCACAG CAGGAGGGCC AGCAGCTGAG GCTGAGCCAG AAGAGACCTG TTCTAGCTGG 180
ATCTGCACAG CCTGGTCTCT GGGTCTAAAA TAAAACTCTT AACTTCTCTG CCAATGAGCT 240
CTGCCAGGCC TGATGACGTA ACAGGTCCCT TCAGTTCTAT TTGCAGGCAA GGTCCATTTA 300
CATCAGGATT TCATCCAGGT AAGGGGGAAT TTGGGAGGGG GAGGGAGTGA GGGACTCTCA 360
GAGAATGGAC CTGTCTTCCC ATCATGCATG GAAAAGGTCT GAAAGAGCTG GTGAGGTGCC 420
AAAGTAATTG TACACGTCAT CTTGAGCTGT GCAAAGAGGA GCAGGCCTAG CTATAGCTAA 480
TTGCTATCCT CCGGCTATAT GCTCCCCACT GAATACCAGA GAGGGGAATC TGTTCGGTGC 540
ATAACAAAGA AAAATCACAA GTAAAATAAA GCTAAGCAGC AGCCGGCCAA CGCTGTGATG 600
CTGCGACCGC CAACCATGGC CAGCCACACA CAGGGAAACT CGGATTTGTC CTCACTCATC 660
TTCTCTCAGG CCTTCTAATT AAGAAAACCT TAAACTTGGA ACCAATTTAC TCCTTTCTCG 720
CTCATTTAAG TCATCACCCT GACCCATCTC TGATGAAGAC AGAGCACTTC AAACAATGGA 780
GAGTAGTTCC TAAGATAGCC GGTGGCCAAC GTGAACTTCC TAATTAAGGA CCCACACAAA 840
AGTAACTTTC TCTTCTTCTG GGCTCTTTGT GTTTGTAAAA ATGCGGCTTC AAGCTGAACA 900
AACTATTTGA TCATCTTCCC GCTTCCTTCC TCCTTTCCTG TCTGTCTGTC TGTAATGTTT 960
CTCAGCTGAT CAATAGCTGT CTCTCTGTGT CATGAAGTGT GCAATAAGCT GTTCTTTTTC 1020
TTTTGTCTCA AAGCCAGAAG ACGCTGTATG GAAAGACCAG TTCCTCTTCT CCCACCCTTC 1080
TAGCTGTGCG TGGCAGCCCA GTGGAGGTCT GGACGCTTGC CACTGAGTGC CAAGAGCAAA 1140
ACCCAGGCCA ATCAGCAGGA CGGATCCAAG CCCCTGACTG CAGCAGAGGT GCCTCTCCGC 1200
AGCCAGGCTG CAGCCACCCA CAGCCTTGGG GCTGCCCTGA CCCTGCCTCA GGCAGGAGCC 1260
CCGCCTCCTT CTCAAAGGAC GTCACAGAGT ACCTGCCCTT GGGGTGCCAC ACATCTTTCT 1320
TTGCTCTCTT TTTTCAGATT CAATTTGCCT GAATAGGAAG AACCTCTCCT TCCTGCCTAA 1380
TCTATTCCCA GAAATCCCAG CTGCTCTCCC CAACTTTCAC AGAGCAAATC AGTAGGCCCA 1440
CCACTGTCCA TGTTGGAGAT CACACTGAGC 1470
|
