Tag | Content |
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EnhancerAtlas ID | HS088-00544 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:12183880-12186000 |
Target genes | Number: 13 | Name | Ensembl ID |
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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 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_61096 | chr1:12184746-12245090 | HBL1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I012124 | chr1 | 12184887 | 12187657 |
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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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