Tag | Content |
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EnhancerAtlas ID | HS092-18698 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr15:89610220-89612040 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr15:89611904-89611914 | ACCATATGGC | - | 6.02 | SPI1 | MA0080.4 | chr15:89611976-89611990 | AGCTTCCTCTTTTT | - | 6.24 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_13697 | chr15:89611215-89612033 | CD34_Primary_RO01536 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I089066 | chr15 | 89609940 | 89612430 |
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Enhancer Sequence | GAGATTCACA GCTCTTTCTG CTCCAGATTC TATACAGTTG AGGAAGGAGA TGTGAATTGA 60 TGGTGGGGCC CCATGTTGGG GTGATCAGAC CCAACACCAG GCCATGGGGG CTACGAAGTC 120 CAGTGGAGTT AAAGGAATGA GACAAGACAA GAGTGCATAA AGTGGGATCA GGGGGCCAAT 180 GCTAGTATGG AGGCTGCTAA GGCCCGGAGC TCTGGAAGCC CACACTATTT ATTGGTGATC 240 AAACAAAGAA GCAGGTGGTG AGGATGTGGG GGTTGAAAGA AAGCAGTGTA TCAAGCACAT 300 GATCTACAAC TGTGACAGTT TAGCATTTTC TTTGAAGCAT ATGGAACATG TTCTGCTACT 360 TGAGATAATG GGAAACATGT TCTTCTAGTT TAAGTTACAA TCGATCTAAT AGCCTGGGAG 420 TGCTAGAAGC AAGAAGCCAG CAAGTCTAGA CACATTCCAG AGGCCACAAG GAGTTTTAAG 480 CCCTGAGCCC TGGATTCTGT CCAAGCCACA AGGGGTTTTA TGCCCTGGGC TTAGATTGTG 540 GTGTGGCAGG GCAGGTTTCC ACCCTTTGGC ACAGAGCTTG GTGTTCCAAA GGCCATGAGG 600 GGTTTTAGAC CCTGGACCCC AGGCATGTTC CAAGACTGTT TTACATTATG TCAGCCATGC 660 AAGCCCTGCC TCAGCCTTTT TCCCAATACT CAGCTTTTCT CGAACACCCC AGATGTCTTC 720 TGTGAGACCT GGCTGGAGTT CTACAGCACC TCCTGCCTGC TACTATCCTA ACACTCTGTG 780 GAGCAAACTC TATTCACTTG TTCTCCATCT TTTCCTTCTG GGCTCTGAGA GTCCAAACCT 840 TGAGGTAGGT ACCATGACAC ATTGGGGTCT CCACTCACAG CCTGATGCCT GTAGATGATC 900 AGCCACTGTG TAATGAATGA ACTCATTCTT CAATAAACCA GTGAATGATC ACATGAAAGA 960 AACGGTCTAG TGGGACTCTC TGGCCACAAA TACTGAATCA CCTTCCTCTT CTTTACCATA 1020 GAAGAAGGGA GAATTTCTTT CTCAAAGACC AAACCCTAGA CTTCATAGTC TTTTTCTGTT 1080 TTTCTCCCCT ACAGGACTTC TACCCCTCAG GGTCTCCCAC AGAGCATTCT GTGGGCAACT 1140 AACCATCTAA TGTTATTTTT ATAGGGCCCA AGGGAGAAAT TCTTATACAT ACACACATGT 1200 GCGCGTGCAC ACACACACAC ACACACACAC ACAAACTCTG TGTGTGTGCA TGTATAAATG 1260 ATTTCAGTTA TGTACTGCTA CATAACAAAC CACCCCTAAT GTAAGTAGCA CAAAACAACC 1320 ATTTTATTTT GCATACAGAG TCTTTGAGTC AGGAAATTAG ACAGCAACTA GCAGGGGTGG 1380 CTAGCCTCTG CTCCCTGGTG TCTGAGACCT CAGCTGGAAA GACTTGAAAG CTGAGAATGA 1440 CTCAACAATT GGGGGCTAGA GTCATCCGGA GGCGTCTTCA CCCACATGTC TGGTGGTTTG 1500 GCTGGAACCT CAGCTGGGCT TTCAGCCCAA ACACCTACAC GTGGTCCCTC CATGTGTTCT 1560 CTCCACACGG GCTAGCTGGG CTTCATCAGA CTAGCTGGTA ACTGGGGTCC AAGGGAAGGT 1620 GTCCCGAGAA AGCAAAGCAC AAGTGCATGG CATTTTTATG ACCTGGCCTC AGAAGTCACA 1680 GAGCACCATA TGGCATCATA TGATATTGGT CAAGGTTACA GAGTTTTCCC AGGTTCAAGG 1740 CATGAGGAAG TGGGCAAGCT TCCTCTTTTT TTTTTTTTTT TTTTTTTTTT TTTTGTCAAG 1800 AGGGAGTCTC TCTCTGTTGC 1820
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