| Tag | Content |
|---|
EnhancerAtlas ID | HS092-15118 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:101085830-101087310 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr13:101086509-101086520 | TGTGACTCATC | + | 6.14 | | JUND | MA0491.1 | chr13:101086509-101086520 | TGTGACTCATC | + | 6.14 | | Lhx3 | MA0135.1 | chr13:101087143-101087156 | AAATTAATTTTCC | + | 6 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I100433 | chr13 | 101085268 | 101087414 |
|
Enhancer Sequence | GTAATGTTGC TACCAGGTAA TAAACAAGCC ATACTGTATT TGGGAGAGGA GGGTGTGTTT 60
CAAAGTCTAG TTCATTGTAA TATCAAAACT GGTAAAACCT CTCCTCTCTA AACTCAGTTT 120
GACCTCACAC TGAGAAACCT TTACTAGTGC AGAGGAGAAT GTTGCTTTCT TCTTGCTTGC 180
TTTATATTGT AGGGGCAAAA GGGTGTGATC CCACTCCTCC CCATCATAAG GGTGTCCATG 240
GCAGACACTC CTATAACAAA AGACAGGTTA ACAAGAGAAA AGTATAACTG ATTTATTTAA 300
TCAAAGTTTT ATGTGACATG AGAGTCTTCA GAACAGAGAT CCAAAGATAC AAGGAAAGCT 360
GTCCATTTTA ATGCTTAGGT TTAATGAAGA ATGGGCAGCC GTGTAAAACT GATGGGACAA 420
AGAATGTAAG TGAATGCTAG TAGGCTGAGA GGAACCCAGC AAGGCCTATG TTCAGATCTT 480
CCTGGCCTCT CTTGTACTAT TTCTTCCTCC CAGGTATGGG ACAAGACCCA TCTGGGATGA 540
CGGTCTTATG ACCTGCTACT GTTGTAGAGA AGGGTAGGCC AGAGAATTTC TTTATGAGCA 600
GCTCTTAGAA AGGCAGGGAG GGGTTAGAGT CCTCTTTCTG GTTTCATAGT TGTCTTTGCG 660
GGAGAGGAAT TCTGATGTCT GTGACTCATC TCAGGAGAGA ATGAGGGGTG AGAGACAGGA 720
AGGCAGAAGG TCAGAGATCT TAGTTCTGAG GTTACTTCTG AGGCCTTCTC TTTGGGGTAT 780
CATTTTCTGA GCCTCAACAA TACCCTTTTC TACTTCAGAG CTGCTATATT GGGTCTCTCA 840
GAATTTGCAG TATGGGGTAA AGATGAGAAG AGCATGGCAG GAAGAACCAG GTTTTCTGGG 900
GCAGAGGCAA CCTGGCATTC ACTCTCTTGG GGCATGGCAG ATGTCCAAAG CTGGCCGGTA 960
GCCCTGGGAT ACTTTCATGT GGATTTGGGG GAACTTCTCA CCTGCAGAAC ACTTAATGCC 1020
TCCTGTCTTT TCCAGTTGCC TTTGGTCTCC TGAGCAACTA CTGTGTTGAC TCTGAATGTT 1080
CTCACTGGGC ATGGTCCCTC ATAATGACCC CGCCTGCTTT TCTCCTGCAC AATCCACGTC 1140
TGGCCACAGG AAATAGTAAT AAGTCCTTGC CTCACCAAAC CAACAAAGTA CAAGCTTCTC 1200
TTCTTGGTCT GTCTCTAAGA ATTCGCATGA ATAAGTGATT CTCATGAAGT CGCTTTCACG 1260
TAGCTTAAGC AGAGTTCAGC CTTAAATTCT AAGCTTAAGA ATTCGACCTC CTCAAATTAA 1320
TTTTCCTCTT TTATTCTTTT AAGGTGGGAG ATGGACAGTC ACTGGTCCCA CAGCTTCCTA 1380
GCACATTCTA CCAGGTAGCC TTGGCTAGCA TCTGACTTAA AGATGTATGG GTACTTGGCG 1440
TCTACTTCTT TTTGTTGCTG AACCCCTGTG ATTCCATGAA 1480
|
