| Tag | Content |
|---|
EnhancerAtlas ID | HS187-25001 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr9:93939240-93941280 |
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 | CCAGGTACTT GGGAGGCTGA GGCAGGAGAA TTGCTTGAAC CTGGGAGGTG GAGGTTGCAG 60
TGAGCCAAGA TTCCATCACT GCACTCCAGC CTGGGCGACA GAGGGGAGAC TCTGTCTGTC 120
AAACAAAAAG AACAATAAGA AGGTTGTTTA TGGCTGAAAT AGGAACACAC AGAGAATCTA 180
GGGTATGGGG CTGCCAGCTC TCTCCCAGTA GAGTCCGTGG ACCAGGTCAC TTGTGAGCTG 240
CTGGTTTCTG CCCCATGATG AGATAACAGA GTGCAAGGAA GTGTACGTGT TCAGAACTCT 300
CACGGCAATT TGACAGGACT GTGGCATCAA AGTGTGTGCC TGTGTTTCAG TAATCCATGT 360
CCTCTGTGTT TTACAAAAGC ACTGGCCCAA GACAGATTGG GGAAAAACTA CAAAAAATTG 420
CTCCTTCCCT ACAGGCTGTT CCAGGACAGC AGCTCTGGAG TGTGGCTTGG CGGTCATTTC 480
TGGGGGAAGC TGCAGACAAT TAGCCACAGA TGATACTTAG GGTCTCAGAC CCCACAGTTG 540
ATGCTTAAAA TAGATGTTAA TGACTTCAGA GATGTCCCTA AGCTTATCTG ATTCATACCC 600
TCTCATTTCC AATGTGTTTT CTGAGGGAAA AAGAAGGGTT TTCGGTCAGT GTGCCAGGAG 660
ATCCAAAATC CAGGGCATCC CTGGGTAGCC TGACCTGCTG GGACAATGAA AAGGTGGAGA 720
GAGGACTCCC AGGGACGGCA ATGAGGAAAC AGGGCTGCCA CGGCCCACAG GCCTGGGTGT 780
GATCTTGCTG CAGAGCCAGG AAGCTCCTTG CAGCGGTGAA TGTGGTGGCG GTGCTGGCCG 840
GGCACCGTGG CTGTGCCTGG CAGGCCTGCT GAGGGCACAG GGATTCATCG CGCTTGGCTC 900
AGAAGCTTCG TTTTTCTGAG ACAGCTCCCA GCTTCACTCA AACGTGGTTA CCTACAGATG 960
CAAACTGGAA ACGATGCACT GTTTGTTCCC TTGCAATCTC TACGGTGAGC AGGCAGGAGC 1020
CCCAGCCAGA GTCCTGTGGT CACACACCCA CTGGTGGTCA GGTAAATTTT CTGTTTCCCA 1080
GAAGGTTTTA TTTTACAGAG TTAACAGACT GTGGCCTGCT TCCATTGCTC TGAAACACGC 1140
CAACTCCAGT TTCCCCACCT TTGTGAGGAC GATCAAAAAC CCAGAGAACG GCAGTGTTAA 1200
GATTTGATTT CATGATAAGC CCATCTTGTG GCAAGTTGAG TCTGGCTCTG GAAGGTGTGT 1260
TTGCCAGGAA ACAAGCTGTG TATTATTTCT GTGGTTTGGC AAGGGAAACT CTGAGCTGGA 1320
TGGATTTGGG AACCAGGGGA AACATAGCTC AGGCCATGAG AAGTCTGGAT GAACAGGAAA 1380
ACAGAGGAGG GGTCCCAGGT ATTGCACAGC TCAGAGAGAC AACGCCCCAG CGCCAGAACT 1440
CAGCAGCCAG CAGGGGTGTG GGCAGCACTG GGGTGTGGCT GGAAACTTCG GACACCACCC 1500
ACACGGCCCA CAGTGCCAAG CCCTGCTGCC TGGCCCTGCC CACAGAACCC CCCCATCCTT 1560
CTCAGCTGTG GGCTAAACAC CCCCAGGATG GAAATGGCTG GGCTGTCCAG GGTGTGGAGT 1620
GAGCAGAGGC GCACAGGCAG CCTGCCTATG TGGGCCTGTG TTGGTGGGGC CCCACGTGTG 1680
GACATGCCCC GCCTGACACC AGGACTTGCC CGTGAGCCTC CCTCATCCCC AGCAGGCCTT 1740
GCTGGGACTC CTGTCTGGGG CTCAGTCCCG CTCTGGGGAC ATTTTAGGAG AGGCAGGTGA 1800
GTTCCTGCTG CTCCCAGGGG CCAGTCCCAG GGGACCTCAT CTGTGACAGA GGATACCTCA 1860
TTTATGACAG AAGACGAATT GTTGGGCACA GCCCAAGGCC TACGGAGAGC AAGGTAGGGT 1920
TGTGTCAGAG TTGCCCTGAA ACCAACATCT TGTAGGTAAA GTTACTGAGG TTTGTCAAGT 1980
TGCACAGCAT GGAGTAAGCC GCAGAGTGGA GGACAGGAGG TCACTCTGTG GTTCCCGGGC 2040
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