| Tag | Content |
|---|
EnhancerAtlas ID | HS091-08647 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:107786920-107788820 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:107787476-107787495 | CAGCCGCTAGGTGGCGCAA | + | 6.25 | | ZNF263 | MA0528.1 | chr11:107787512-107787533 | CTTCCCACTCCATCCTCCTTC | - | 6.66 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I107916 | chr11 | 107787361 | 107787510 | | GH11I107917 | chr11 | 107787781 | 107787930 |
|
Enhancer Sequence | ATTATTATTA CATTTTTAAA ATGTAAATTG ACTTCTGATT CACTTTACCC CTTCTGATTC 60
ACTTCTGATA GCCTGTCCTA TTCAGAAAAT AATTGTGAAG GCATAAATGG TGATATTTTA 120
AAGTATTAAG AATGGCATGG CCAGGCATGG ATTCTTATAG GAACCACGCT ATAGGATTAT 180
AGGGTGGTTC ACACCTATAA TCCCAGCACT TTGGGAGGCC GAGGTGATAC AGGAGGGGGC 240
AGGGAAGTGC TGGGTAGAGA AAGGCGGGGT CCCTGGCAAG GGCTCCACCC TGGGGCCTGT 300
GCCTACAGAC CTAACTGAGA ACAGGTACTC CTGTTTCCAT GCCCAGATAT TGAATTTTCC 360
AAGACCACTC TGGCCCACCA TGCCCCTCAT CCTGTGCCCA TAAAAACCCA AGACCATAGC 420
AGGCACACAC ACAAGGGGCT GGATGTCGAG AGGAGCAGAA GAGCAGAAGA ACACACCAAC 480
AGACACCAGC AGACACTGAC AGGCCATCGA CAACAGGACA ACGTGGAATT CTGTCAGGGG 540
TGGTTCTTGA AGAGCCCAGC CGCTAGGTGG CGCAACTCCA GGGGAAGACC ACCTTCCCAC 600
TCCATCCTCC TTCTGGCTCC ACATCCATCT CACTGAGAGC TACTTCCCCC ACTCAATAAA 660
ACCTTGCACC CATCCTCCAA GCCCACATGT GATCCGATTT TTCCAGTACA CTAGGGCAAG 720
AAGCCGGGAT ACAGAAAGCC CTTGTGATAA GACAGAGAGT CTAATTGAGC TGCTTAACAC 780
AAGCCACCTG CAGAGAGCAA AACTGCAAGA GCACACTGTA ACACAGGCCC ACTGGGGCTT 840
CGAGAGCTGT AAACACTTAA CCCTAGATGC TGCTGTGGGG TCGGAGCCCA AAAACACTCC 900
CCAGTACCTG CATCCTCTAC ATGCTCCCCC TAGAGGTTTG AGCAGCCGAG GACTGAAGAA 960
GCGAGCCACA TCCCTGTTGC ATGCCCTGTG AGGGGGATAA GGGAACTCCT CCAGTTTCAG 1020
AGGCAGGCGG ATCGCTCGAG CCCAGGAATT TGAGACTAGC CTGGGCAACA TGGTGACATC 1080
CTGTCTGTAT CAAAAATACA AAAAAATTAG CCAGGCATGG TGGTGTGTAC TTGTGATCCC 1140
AGCTACTCAG GAGGCTGAGG TGGGAGAATC ATCAGAGCCT GGGGAGGTCG AGGCTGCAGT 1200
GAGCCATGAT CTCACCACTG CACTCTAGCC TGTGCCACAG AGTGAGACCC CGTCTCAAAA 1260
CAACAACAAC AACAACAACA AAGAATGGCA TGAACATATA TTCCAACATC ATGACATCTA 1320
ATTTTATGAA ATTACATATC AGTTCACTCT ATCCATAAAC TCTGGAAAAT TTTCCTTCTC 1380
AAGCCATCCC ATTACATAGA TGAGACTAGC TTATCAGTTC AAATCACAAC TTTGGTTCCA 1440
GTTTAGTCAG CCCCGGATTG TGAGAATAGA GGGATTAAGG ATAGTGAGGA TATTAATCAC 1500
TCCGTATGGA CCCTCAATAG TCTAGCTCAT GATTCTCAGG TAGAGCCACT AGGAAAATAT 1560
CCAGTTCTGA CATCAAATAT ATTATCAAAA GTAACCATTC ATAGAAAAAA AGTTATAAAA 1620
CATTCAGTTC ATAAACAGTG TACAAAATTG TAGCTGATAA CACCCATTCT TCACTTTCCA 1680
TAAATCAGAC GTTTTCATTT TATTTTATTT TATTTTATTT TTTGGGTGCG GGGACAGAGT 1740
CTTTCTCTGT CACCCAGGCT GGAGTGCAGT GGCACAATCT CGGCTCACTG CAAACTCTGC 1800
CTTCTGGGTT CAAGTGAGTT TTGTGCCTCA GCCTCCCAAG TAGCTGGGAC TATAGGTGCA 1860
CACAACCAGG CACAGCTAAT TTTTGTATTT TTAGCAAAGG 1900
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