| Tag | Content |
|---|
EnhancerAtlas ID | HS092-16538 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:75163290-75165850 |
Target genes | | Number: 26 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr14:75165063-75165076 | TTCTAGAACATTC | + | 7.52 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I074697 | chr14 | 75163848 | 75166819 |
|
Enhancer Sequence | TATTCCCAAC ACTTTAGGAG GCTGAACTGG GAAGATCACT TGAGCCTAGG AGTTGAAACC 60
AGACTGGGCC CTCTCTAAAA AAATAAAAAT AAATTGGTCA GGTATGGTGG CTCACGCCTG 120
TAATCCCAGC ACTTTGGGAG GCCAAAGTGG GCAGATCACC TGAGGTCAGG GGTTTGAGAA 180
AAGCCTGGCC AACATGGCAA AACCCCATCA CTACTAAAAT ACGAAAATTA GCCACGCATG 240
GTGGCACACA CCTGTAATCC CAGCTACTCA GGAGACTGAG GCAGGAGAAT CACTTGAACT 300
TGGGAGGCTT AAGTTGTAGT GAGCCAAGAT TGCGCCACTG CACTCCATCC TGGGTGACAA 360
AGCAAGACTT CGTCTCAAAA AATAAAATAA AATAATAAAA TAAAATAAAT TAGCTGGGCG 420
TGGTAGCATG CCCCTGTTGT CCTAGCTACT CAGAAGCTAA GGCAGGAGGA TCTCCTAAGC 480
CCAGAAGTTT GAGGCTACAG TGAGCTGTGA TCACACCACA CCACTGTACT CTAGCCTGGG 540
TAACAGAGAG AGAGATCCTG TCACACATAC ACACACACAC ACACACACAG CCATGAAAAA 600
CATGATGTAA AAGTCCATTT CAAAATTTTG GTGCATACAG AGCTAGTGGC AGCAAACAGA 660
AGTTCTGATA TCACCTACTG ATGTCCACCA AATGACAAGA CAAAAGAAAG ACGTTTGTTT 720
TGTAAGATGC AATCTCCAGC ATTCTCCACA GAGAAGCACC AGCCATGAGT CCAGGGACAT 780
GAACTTAAAA AAACAAACTA TTCAATTTTC AAAAAGTGCA CAGGTTAGGG TGGTCTAACT 840
AAGGAGGTTC CAAGAATATA TCAGACACTT TGGATTATCA GTTTACATTT ACTATGGCTT 900
AATTCCACTC TTAGTTTATA CTCCCCAACC CAAAATCCCA CCATAAAAGA TTGCCCTCCT 960
CCATCAAGTT TATACTCTTG AGATATTTAT ACAGTTGTCT ATTTCTGCTA TTGTGGTTTA 1020
GCCAAGTTAC ATGGTTTTCA TTTATACTTT CTTCATCAGT CAGCCTCTCC AGTCTCTTAA 1080
TCATTCCTGT GGGTCTTCTG TGAACTCTCT CCAGCTGATC CCCAACGATC TGGTAATGAG 1140
GTGCCTCCAA ATGACTGCAG CCTTCCAGGG ACAGCCTCAT TAGTCAGCAG GATGAACTCA 1200
CTCTCCTCAG TTCCATGACA TACTACTCTT GAGCAGGCAA TCCCCCAAAT CACAGAAATC 1260
TACTGTGCTG CCGTATTAGA CTGTACCTCA TTCTATAACT CCCAGATTTG GACACTGGGG 1320
CATGCTAGAA TGTGCTAGAA GCCAGAGGAT AAATGACCCA TGTTCCTACA GCATCTGTTT 1380
CACTAGAGGA TGAGTGACTG GGGAGAAAAA AAAATTTCAT GTTAAATCAA ACTCATAGAT 1440
AATAAAACAG AATGTAATAT TTGCATGAAT TTCTAAAGAT AAAACATGGA TATGTTGAAT 1500
ATATTCATAG ATATTCTGAA CTTGAAGCAG AAAGGCTGCT TGGGCCTCTG CTCCCGGCAC 1560
CAAGGAGTTA ACATATCCTT TACCACTAGA GGTACTTGAG CCAAAACCCT CACTCAACTT 1620
CTGATCTACT GTGCATTACC TTACTCATAC CATATACTCA CATTTTAAAT GATATTATTT 1680
TTCTGCTATG TTTCCCCATC CTAGATATCT ATATTTATTT TCTCTTTGCC TAAAATCTTT 1740
TGCTGCAGGA ACACGTGTCA TTTATCTTCT GGCTTCTAGA ACATTCTTGC CTGCCCTGAT 1800
GCCCAAATCT GGGAGGCATG AAATGGGGTT ACAGTCTAAT TCACTCGATA ATTCACAGAC 1860
TACCAACATC TATAGGTTCC TCTTCATCGT TCATTCTTCA TTCATTTCAC ATTTCTTGAG 1920
CATTTGCTAT ATACTGGGCT ACGTGATAAA AGCTAAAGTC ACAAGGATAA ATAAGACAGG 1980
GTGCTTTCTT AACCTCAATG AACTTGGTCC GCCATGGGAG AAGGACAATG CAATGTTGCA 2040
AGTGCCATAA AAGAGGAATA AGCAAAGTAT GGAGGGCAGA GGAAGGAGAA GTAACTGTAT 2100
GTGCAAGTGG AAAAGCAGAG ACAACAGAGC TGATTACTTA AGAATGAGTA AGCAGGCTGA 2160
GCATGGTGGT TCATACCTGT AATCCCAGCA CTTTGGGAGG CTGAGGTGGG AGGATGGCTT 2220
GCGCCCAGGA GTTCAAGACC AATCTGGGTA ACATAGTGAG ATCCCATCTC TAAAAAAAAA 2280
AAAAAAAAAA GCTGGGTGTG GTGGTATGCA CCTATGGTCC CAGCTACTCA GGAGGCTGAG 2340
GTGGGAGGAT CATTTGAGCC CAGGAGGGTG AGGCTGCAGG GAGCCCTGAC TGCTCCACTA 2400
CACTTCAGAC CGTGTGAAGA GCAAGACTCT GTCTCCAAAA AAAACCAAGG TGTTTAGAAA 2460
GACCACCTGG GGCTAAACTA GGATGACTAC CATGTAGTGG TTAAGAGCAT GAATCTTACT 2520
ACTGAATGAT CTTAAACAAG TTACAGCAGG TCCTCAAACG 2560
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