| Tag | Content |
|---|
EnhancerAtlas ID | HS092-16654 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:80956380-80958910 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:80958284-80958302 | CCTGCCATCCTTCATTCC | - | 6.76 | | Myog | MA0500.1 | chr14:80957665-80957676 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr14:80957665-80957676 | CTGCAGCTGTT | - | 6.62 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I080490 | chr14 | 80957084 | 80958788 |
|
Enhancer Sequence | ATTTAGTCCA TTCCTAAACA ATAAGGGGGA GGGGCATCAA CTTGATTTCA AACAAATATT 60
TCTTATTATC AATTATATTT AAGGGGGGTA CCACTGTAAG ATAAAAGGCC AAGATGAATC 120
ATATGTGGCT ATCAGTTATC AGTCTTTCAG GGACAACAAG ATGGAAAGGT AGAAAAAATC 180
CCTGATCTCG ATGTCGACAT TGAGGTAAAG CTGGAAGAGA TTGAAATGTC AAGGAATCAT 240
CAAATTAAAA TCTCCCTTCA TATGACAATG TCAAAATATG GAAATGTTAC TCTGAAACAC 300
AGTGGTTGAC TGTGAGCCAC TGGTATAGAG AAGAAAAAAT GAAATTGCAT GTGAAATGTT 360
AATGTGGAAT CAATGCCCCA AATCAGGTTG CTCTGAAGTT CCTGGGAGTG AGAGAAAACA 420
GAATTACAAC TTGACTCTAA AGACATTTGC AACTTTTATA ATCAAATACT ACTTCTGTCC 480
TTCAAGCCAA ACAGAAGAAC TATACTATAG GCCCTGATTT AATTGGATGT CTTGATGATG 540
ATCCTGATGA ATGGGCAGAG TCCTGGCATA GTCTGTTAGA AGGAGGAGGT GGGAAGTAAC 600
CTTTAGTAGT TAATCAAGCA TCTTTGGAAA TGGCTTTAAG ACCTCCACTT GGGTGAGCCT 660
CAGGACTGAA TCACAGCTCG GATACCTGGG AGAACACATG ATATTGGAAA CCAAGTTAAA 720
AAAAAATACT CTAGTACTTC ACCTGGAAAA TAGCCACTTT CATATTTTTG TTTTGGGATA 780
GGCACTAAAA CTCAGAGAAG GCTATTATAA AATGAATGTC AAGGCAGGGT TCTTGAATTT 840
GACCATTGAT CACAATCATC TGGAGGACTT GTTGTAACAC AGATCGTTGG CGCCATCACC 900
AAAGTTTCTG AATGGATAGG TCTGGGGATA GCTAGAGAAT ATGTAATTCT AACAAGCACC 960
CAGATAATAC TGCTGCTGCA GGTTTTGAGA TCACCCTTTG TGAACCATTG CTTTCAGGAA 1020
TCGTTGAACA AAAGGATACG TATCTTCCTC ACAAAACTAT GATTTACCCT CAGTGGAATC 1080
TAATCCATGA GTTTACATGC ATTTAAAATT AAGAAATGAG CAATGACCAC CACTGTTAAT 1140
TTGGAACAGT CAAACTAACC TCACAAAAGA CTTCTCCAGT GGAAAAAAAT GGGAAACTCT 1200
TTCCACGGTA CACACTGGCT TTATTGGCTG TGGTCTTGGT CAAAGCACAG AATGAACCTT 1260
GGCCAGCAGC ATGAGGTCTC TCAAGCTGCA GCTGTTGGGC GGAGGCTGCT CTGCCAGTGA 1320
CTCTGGGCAG GAAGTGCCTC GTTAGAACTG TTGCATCTAT TTTACTCAGG CCAGAGGGGG 1380
GGAAAAAGAA AGAAAGAAAA AGTCCCTAGG TTTCTCCAAA CCTCTTTTAA TGCCACCGTG 1440
TTAGATGGCT TTGCTACCCA TCACTGTTTC ACTTCTGGTA ACTAACAGCT TGGGGTTCAT 1500
TATGATGGGA AGTTTCAAAT ATGCTAAGTA TTATAAATCA AGCCTGTATC TTCACTCACA 1560
GTGGAATTAA TGACAGCATA AATAAAATGA AAATCCAAAA TGACAGACAA GCACAGGGCA 1620
CCCCGGCTGA AAAACATCAG AAAGCCGATC ACTCTGCACC CAGACCCAAA CTGCTAGCCA 1680
GCAGTCTATA AAGAACATGA AGGATTACTG CAACTTTCAT CAGAAATGTG ACTTTATAGT 1740
GAACATCAAG TTCAACAGGA CTTCTCACAA TGCTTCTTTC CAGGACCCTG CATCACATAA 1800
AGGATGAAGT GCTACCACAG TTTTTTCCTT CCAGTAAACA GTTTAAAATG TGTGTTATTA 1860
AAGGCAACCC AGCTTCCTCT GTGTTCATAT CATTTTACAG AACTCCTGCC ATCCTTCATT 1920
CCCTTATCCA GCTAAGTGCT GAGCAACAAT GGACAAACAA AATCTAAACT AGCATAACCA 1980
CTACCCTAGG GATAACACTG AATAAGAGTT ATGCAGTATG ATCTGATAAT AGCTGGCTTC 2040
AAGAGCTAAG AAGAAAAGGG GGAAAAAAGC TTGTAAAGGG GATATATTTG AAATTGAAAT 2100
TTTAAAACAG ATGTGCAACT GGACACACAT TTTGGGAACT GCTCTTTTGG CTATAAGGTG 2160
ATGAAGGTGA TATGAATAGG TTCTCTGATA TATGAAGTAC ATATAAATAC TGTATTAAAA 2220
ATAGCTGTGT ATTATCACAC AAGGATGAAG AATAATGATC TCATTTTACC AAGAGAAGCC 2280
TTTCACACCT GGTTAATAGA CCAGGTCACA CCTTAAGAAA AATAACAAAA GTGTTTCATG 2340
TATTAATCTC ACTAACTCCG CTTGCAACTA TCCTGTTATC TTAAAATACA TGCACAGGAC 2400
AAGTGAGCAC GACTCTAGCC CACAGGCTGG CCCTAATAAA GGACAGAAAG TTGCTTCTAA 2460
AGATCACTGA GGAGAGGACT GGATACCAGA GAAGGATATC AAAGAGAGAG AGACTGGGAG 2520
AGATGAAATA 2530
|
