| Tag | Content |
|---|
EnhancerAtlas ID | HS091-00448 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:12183880-12186000 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:12183940-12183951 | TGTGGATTGGG | - | 6.14 | | TBX20 | MA0689.1 | chr1:12185314-12185325 | GAGGTGTGAAG | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_61096 | chr1:12184746-12245090 | HBL1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I012124 | chr1 | 12184887 | 12187657 |
|
Enhancer Sequence | GCAGGTAATG GTCCCAGCCC ACTCACCCCT ACTCCCAGCA GGGGCTTCCT CCTGGGGAAG 60
TGTGGATTGG GGGAGCCAGG AGGGAGCTTC TCCTTTGTGG GTATGGTCTG AGAAGGGGGA 120
TTAAGGTTGA CCCCAGGTTT CTGGCTTCTT GAGTTGGTGC TGTGGCTCTG GCACTTGCTA 180
GTGACTATTC TTTTCTTTTT GAAACAGTCT CACTCTGTTG CTCAGGCTGG AGGGCAGTGG 240
CACCCATCTT GGCTCACTGC AACCTCCACC TCCCAGGTTC AAGAGATTCT CCTGTCTCAG 300
CCTCCCGAGT AGCTGGGTTT ACAGGCGCTT GCCACCACGC CTGGCTAAAT TTTTTTTTAA 360
TTTTTAGTAG AGACGGGGTT TTGCCATGTT GTCCAGGTTG GTCTCAAACT CCTGACCTCA 420
GGTGATCCAC CTGCTTCAGC CTCCCAAAGT GCTAGGATTA TAGGTGTGAA CCACTGCGCC 480
TGGCTGCTAG TGACTATTCT TTAATTCTTG TAGGCAGGAA TTTTTTTCAC AGCTTCATCC 540
TCGTGGCTTA TAATTGCTAC TCAGAAAATA GGTCTTTGTT GATTGATTTC ATGACTTTGA 600
CTAGTTGTTC GAGCCTTTGA GCCTCAGTTG TCTCATCTAT ACAATGGTAA TGGCAGAGAC 660
CGTGCAGGGT TATAAGCAGT GTAGCATTGT AGACGGCCTC TGTCAGAGTT AGCTCTTAGG 720
CTGGACGCGG TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCCAAGG TGGGTGGATC 780
ACGAGGTCAG GAGTTTGAGA CCAGCCTGGC CAACACGATG AAACCACATC TCTACTAAAA 840
ATACAAAAAT TAGCCAGGCG TGGTGGCGCG CGCCTGTAAT CCCAGCTACT CAGGAGGCTG 900
AGGCAGGAGA ATCGCTTGAA CCCGGGAGGC GGAGGTTGCA AGGTTGCAGT GAGCCGAGAT 960
TGCACCGCTG CACTCCAGCC TGAGCAGCAG AATGAGAATC AGTCTCAAAC AAAACAAAAC 1020
AAAACAAAAC AAAACAAAAC AAAACAAAAC AAAACAAACA AAACCCCCAA GAGTTAGCTC 1080
TTAGGGAAAG ATGCCAGGTT ACTCATTTTA GGACTTGCAG TTCTAGTGGC TGACACGAGG 1140
TGGCAGTAGT GCTCCGGCCA GAGTTTCTGA AAGTGCGGTC CCGTCTGGCA GCATTGGCAC 1200
CGGCTGGGAA CTTGTTAGGA AAGCAAATTA TGGGCCCCAT CCCAGACCTA GAGAATCAGA 1260
AACTGCACTT TAACAAGATC TCCAGGGCAC TCATGTGCAC ATTAACGTTT GAGAAGCACT 1320
TAACTGGCAT ATACTACTTT TTAAACATCT AAACATGGAC TTCAATAAAG TGCAATCACT 1380
AGCTCTATGA TCTCTGTAAG TGACAAAAGG GAAAAACGAA GCGAGTTTAG TACCGAGGTG 1440
TGAAGAAGTA GATCTAGATA GGGGTTAAGA GCGTGGCCCT GCAGTCCCCC CGGCCTGGCC 1500
TGGCCTGGGC TGGGGCTCTG CCACTTACTC TCAGGGTGAC CTTGGGCAAC TTAACGAACT 1560
TTCGTGAGCC TCAGCTCCCC TCATTTTTAA ACTGAAGGTA GTGACGGTGC CTAGGGCATA 1620
GGGTTGGGGA TCATTCATTC AGGGAACGCT TGTGGGGTGT GTTTATGTGC AGTGGGGACT 1680
CCATGCCTGC CCTCATCAAG CAGGTCTAGA GGGTTGGCCG GGAGGGGACT GGGTTCAACC 1740
TCTTCCTTCC CCTCACTGCT TGGCCCTCCC CACCCTGACT CCGGCCACAC CAGCAGTGCT 1800
GCCAGATGCC GGTCACACCG GGCCCTCGTC CACAGTCCCC AAATTTTGGT CTATTGGACC 1860
TCAATTCCTT TGTTCTGGCT CCTAGACGCC TCAATTTCTC ACTCTCTAGA CACAGTTTGC 1920
CCTTCTCTCA GCCTTCAATA GTTGATCAGC TTCCTGGAGC CAGGCGAGGG AGGGCTGGAT 1980
GAGATAAGAG CCTTGGCTTG GAAAGGACCT GTTGTTGTTA GCCATGATGG AAGCTGTGTC 2040
CCAGGAGAAG GAGGAAGTCG TCTGGGGCTG GGGCTGTCTT GTGTGGTTGC AGCAAGGCAA 2100
AGAGTGTGGG GCGTCTCTGT 2120
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