| Tag | Content |
|---|
EnhancerAtlas ID | HS091-48388 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr9:117099810-117102250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:117101552-117101571 | TGCCCAGCAGGGGGCAGCA | + | 7.34 | | HNF1A | MA0046.2 | chr9:117100052-117100067 | AATTAATAATTAATA | + | 6.17 | | LBX2 | MA0699.1 | chr9:117101194-117101204 | GCTAATTGGC | - | 6.02 | | ZIC4 | MA0751.1 | chr9:117101553-117101568 | GCCCAGCAGGGGGCA | - | 6.04 | | ZNF263 | MA0528.1 | chr9:117100355-117100376 | GGAGGAGGGAGATAAAGAAGC | + | 6.59 | | ZNF263 | MA0528.1 | chr9:117100352-117100373 | GGTGGAGGAGGGAGATAAAGA | + | 6.8 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_09259 | chr9:117100351-117107360 | CD14 | | SE_10330 | chr9:117100824-117101640 | CD19_Primary | | SE_17353 | chr9:117100433-117101775 | CD4p_CD25-_CD45RAp_Naive | | SE_19978 | chr9:117100571-117101797 | CD56 | | SE_22306 | chr9:117100803-117101725 | CD8_primiary |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I114339 | chr9 | 117101461 | 117101650 |
|
Enhancer Sequence | GGTGTTCAAG GACAGGAAGT TCAATCTACC TGTTCATCTG ATTTACTGCC CATCTAGTAC 60
ATGCCAGCCA GCGTGCCAGG CTCTGGGGTT ACAGTGGGAC AAGAAAACAT GGACTCCTGC 120
AATCTTCTTG GAGCCGGATC TTGGGGAGGC CAGGATCACC CTAGGCTTGA TAGCAAAACC 180
CCCTCATGGA AGAATATCTG GGGGTTCCAT TTGCCAAGCA AGGGGTGCTG GAGAAAGGCA 240
ATAATTAATA ATTAATAATA GTAATAATAA TAATAATAGG GATTCTGCAG GAGTGGGAGG 300
GTCTGGCCCC ATGTCCTGGG AAGTGGGTAG AAGAGCATCC TTCCTAGCCC AGTCCTATAG 360
GAATGTGAGG TGTTGTTTTA AAGTGCTGTG GGAATGGGCT GACAAGCCCA TTGAGATGAA 420
GCACGGATTT CCCTAAGAGG TGACAATGGC ATCCATCAGG GCCACTAAGT TTAGGGTTCA 480
AGGAAACCAG CAGTGGGCAA GAGGGGGTGT GGCCTCAGCA CTGTTAAATA AAGGGTGTGT 540
GTGGTGGAGG AGGGAGATAA AGAAGCATGG ACCTAAATCA GGAATAAGTT TAGGAGGACG 600
CAGCAGAGTC ATTCATTGGC ATCTTGCTTG GCACACTGTA AACTCTGGCT TTATTCCTGA 660
GCCCCTGCTG TCTAACTTGC ATTGTTATAC AGTGTGTAGA AACAGATGAT CCAAACAGAC 720
ATTTCTCCAA AGGAGCTATT CAAATGGACA ATACGTACAT GAAAAGATGC ATATCCTTAG 780
CCATCAGGAA ATGCAAAGTG AAACCACTGC ACACCCTCTA ACATCAAAAA GGACAGATAG 840
CAACAAGTGT TGACAAGAAT GTGGAGAAAC TGGAATCCTC AGCACTGCTG GTGGGAATGT 900
AAATGGTGGA GCCACTGTGG AAAACAGTCT GACAGTTCCT CCAACAGTTA AACCCAGTGC 960
CTAGCCCAGG GCTGGCATCC TCATCTTTGG TACCCATGTA CCAGTTGGTG CCTTTATCTT 1020
TATTTTACAG ATGAGCAAAG CGGAGCTCAG AGAAGCTAAG TGATTCAGGA GGCAGTAGAA 1080
TGCACCAGCC TTAGCAGCTC AGGCCCTGGA GCCCTGCCCC AAATCCCAGT CATTCTGCTG 1140
GGCTACTCAT GGGACTCTGG ACAAGCTAAG TCACTTTGCA AGGCCTCTGT TTTCCCACCT 1200
AAAACGACCA CAGTTAGCAA CCTCTCAGCT TAGAGCTGAT GGAAAATTCA GGTAAAAAGC 1260
TGGCACTGCC TGGCTCCGGT AAGTGCTCCA TAAACGTGAG CTCCTAAGAC CCAGAGTCAG 1320
ACAGCTGGAA GGGGCAGCCA TGGGTTCACA CCTGGGCCCG ACTCTCCCCA CATATCTAAT 1380
GTGTGCTAAT TGGCAAGCAG CAGATGCTGA TAAAATAATC TGAACTGTAT GAACGGGCTT 1440
CTTGCATCCC CAAAACAGCA GCCTGCACTC CCTCCTCTAG GGACCGTCTG GTGTAAGTAA 1500
CTACAGAGGC TCCTCAAATT ACGATGGGGT TATGCCCCTA TAAACCCGCT GTAAAGTCGA 1560
AAAATCATAA ATCGAACCAT TGTAAAAGTA GGGACTGTCT GGGCTGGGTT TTCATACACC 1620
CCCACCTTCT GTTAATTTGA TGACCAACTT GGCCTGAAAG TTACCCAAAA CTCTCCCTAG 1680
GGCCAACACT GAAAAAGTCC CTCTGGGCTG GAAAGTCTCG GCTGCAGGGG CTATGGGACG 1740
GCTGCCCAGC AGGGGGCAGC ACAGGCCCAC TCCGCTTTCC AAACTACACT GGTCTCAACC 1800
ACTGGGCCCG TTCAGTCCTG CTGACCAGCA GCTGGAGAAA TTTCAGGGTG TCACCAGCGC 1860
AAATTCTAGC AGCATTAGAA GCACCATCAT TATTGGCAAC TTCTATGTAC TATGGGCTTT 1920
CCATGCATTA ATTCATTCAA TCCTCAGCAC AACCCATTTC GCAGAGAAGG AAACTGAGGC 1980
ATAGGTATAA CCCGCCCATC CTGAGTTGGA AACAGCAACC TGGTGAGTTC TGCCCACAGG 2040
CCTGAGCCTG GAAGAATGTG AAATGGGGCC TCAGGAGAAG TAAAGACTCC ATGGCTACCG 2100
TGGGGTCACC AAATTCTGGG CAAAACCTTT CCCGATCAAT GAGTTGGAAC ACTGGCAGGC 2160
GCTTTCCCCC GTGTCTGCTG GAGGTCTGAG CATGCAGCAT TGGTTCTCAT CTCTGCTGGA 2220
GTGGAAGATT CCTTAGCGAC TTGCTTAGAC TCAGCTGAGA GGGCAGCAAG AAAGCAAATT 2280
TACATACCGG GCGCGGTGGC TACACCTTGT AATGCCAGTG CTTTGGGAGG CCAATGCGGG 2340
CAGATCACCT GAGGCCAGGA GGTCAAGACC AGCCTGGCCA ACATGGCGAA ACCCATCTCT 2400
ACCAAAAATA CCAAAAAAAT TAGCCGGGTG TGGTGGCACA 2440
|
