| Tag | Content |
|---|
EnhancerAtlas ID | HS092-15886 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:52294200-52296030 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:52295183-52295201 | GGAAAAAAGGAGGGAAGG | + | 6.84 | | FOXC1 | MA0032.2 | chr14:52294368-52294379 | ATGTTTACATA | - | 6.32 | | Nfe2l2 | MA0150.2 | chr14:52294867-52294882 | AGCTGAGTCACTGTG | - | 6.04 | | ZNF263 | MA0528.1 | chr14:52295180-52295201 | GGAGGAAAAAAGGAGGGAAGG | + | 6.29 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I051827 | chr14 | 52294301 | 52295593 |
|
Enhancer Sequence | AAGAAGAAAT CCTGGTCCCG GTGATCCCTC TGAGAACAGA TGTAGTGAGA AAGCTAGGAG 60
TGGTATTTTT TGATGTCATA CAGTTCCAGA CTATAACTAG CTCAGCTTTG AGACTTGAGG 120
TCAAATAATT AAAGCTGTGA TTAGTGTGTT GGATGTTCAT CCACGTATAT GTTTACATAT 180
CCCAGAATTA CACGCAGTGG AAAAGCAGCA CCGTGGAGCT GGGTGATTCC TGAGCCCAAC 240
CTGTGCCTCT GGTCTAGGGG CATGCAGGGG AAATTGCAAC CTCCAATGGA AAGAGAAGCA 300
AGAGATGGTG TACCTTCAGG CAAAGGTAGG CTTCAACAAA TGGTGATGGA AGGATACTGC 360
AAAGAGGAAA ACGTTGAAGT GTTTATTCTC TGAGGGAATG GTGGAAAGAG TAAAGAGCTT 420
GGAGAGAGAG TCTGAGAGTG GGAGGACTCA GGAGGGAGCA TAAAGCTGCG GAAGATGAGA 480
GAATAACCCA GGATAGATGT TTGGGTTGTA GACGGTTGGG GGAAGGCAAG CACCATATGC 540
CTTGGGGGCA GTGGCCATGG ATTCTCGGGA TGAGAGGCCT CGGTAGAACT GACTAGCTTC 600
CTCAACATGA GTTATTTGGT GCCACTGTGG CTGATTGTGC AGACAGTCCT GCCATCATCC 660
CCAGGGGAGC TGAGTCACTG TGTGGTGAAA GCCACAGTCT CCGGCAAGGC TGCTTTGTGC 720
TGGGCAGGGA AGCTGCAGGG ACTGGGGAAG CCACCTCAAG GTGAACAGGA GGTGGCAGAG 780
CCTGGTCTGC GGTGAGCGCT TTCACACAGT AGGGAAGTTT TCCTACTTGC CTGAGCTCCG 840
GATTGTTTCC CCCAGCAGGG AGCTGTGCCT GCCTGAAAAT GGTTCCAGGG CACAATTGTT 900
ATCATAAAGG AAAGCAGGAC CAGAAGAACC TTGACAACTT TTTGATATTG CTTATCCTAG 960
CTCTGACTGA TAAGGGGGCA GGAGGAAAAA AGGAGGGAAG GAATAAATCA AGGAGATAAT 1020
CACAAAACAA CAAGGAGATA ATCACAAAAG CAGAAGAAAA CATGTTGTTT TCACTGGGCT 1080
GTGGTTGGCT TATGATATCT GTCTGACTCA CGGCCACACT GAGGATTCTG GAATGCATTC 1140
TACCCAGGTA TGAAGTAGGC ATCCTAACGG CCACAAGATG TAGCTTAGTT TACAGACCCA 1200
TCAAGCTGCT TGGGTTGGTC TAAGGCTGGA CTGTGAAGCT GGTGAAATTT GTTTCTGACT 1260
CTGCTATTTT CAGGCCTCTT CTCCTCCCCA GAAACCCTTC TCCTTGGTTT CTCCTGCCCC 1320
TATAGCCCTG CCCTCACCCT TCAGGAACAC CCCAGGGGCT CAGGGCTGGG GACGGCAGAG 1380
GCTTAGCCCC ACTACCTCCC CGCTGCCTGG CAGTTTGATG TGCAGACGTG ACAGGCCCTC 1440
TGTCTCAAGA TATTAGCTCT CTTCCACCAT CACACTCCCC AAACCCTCTT GTCACCATTC 1500
TTGGGAATGC CAAGGTCCAC AGTGATGATA CTTTGATTCT TTGTTGCTCA GGAATGATAG 1560
TCACAATATT TAACAAGTGA GCAAAGGCAC TGATAGGTAG AACAGACACC AGCTGTGAAC 1620
ACCTCAGTAA GGCAGCAAGG CACATGCTGG CCAAATAGCT GCATCCTCCT ATCCACCTAG 1680
CCTTTCAGTC CTCCAGTGAC CTGGTCCTCC TGTGCCTCAG CTGTCCACTC CCAGGTGTAT 1740
AGCCTAGACT TGTTACCATC CACAGCAGCA CCTTCTCAGT CATCATCTGC TGGCTTTCCA 1800
GCTTATCTCC CCAACTCCCA AAAGTTCTTT 1830
|
