| Tag | Content |
|---|
EnhancerAtlas ID | HS092-10959 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:130967750-130970040 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:130969829-130969847 | CATTCCTCTCTCCCTTCC | - | 6.23 | | REST | MA0138.2 | chr11:130969895-130969916 | TTCAGCACCCAGCACAGTGCC | + | 7.06 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I131098 | chr11 | 130968625 | 130969581 |
|
Enhancer Sequence | TCAAGCTCAT ACTTTCAGAC TCCAGAGCCA TGGTCTGTCC CCCACTGGTT GTGACCAGGC 60
CTAAACAATA GGTAGGATGA GTTTCTACCT ATTGGTTATT ATATAAGAAA AGTCAAGCAG 120
GGAAGGTGAA GTCACAGCCC AACTGCCCAC TGGAACAGTG ACATCTTGAT CACTGTTTCA 180
GATCACTACC CAGGAAAAGC TGTAACTCAT GGGATAAATC AGGCTCCAAT CTTCCCCTGA 240
GGCTCTGGGA AGCCTTAAGC CAAGGACTTG CACTTACCGT CTAGGGGATC AAGGGTGCAA 300
GATAGTGTAG AAAACAGCCT TGCAGGCTGT CTCCTCAGAC TGGACTGAAA CTGGCATTCA 360
AATACTTCCC AAAGATTGCA GAACTGCTCC CCAAGAGCAA TGACTTTCAG CTGCAGCCAT 420
CCCTTGGGCT GGAAGTGAGG CAGTGACTTC AAGGTGAAAG TCTCCATATC CCATTACCAA 480
TCCAATTACC TGGCACTTGC AGGTTAGATG GGAACTGCCA GACCGGAACC CAGCCATGGA 540
TCATTTAGAC CTGTGTCTTG TCTCTGACAG TACTCAGGGC CGAGCGTCTC ACTCAGGTGC 600
TTCTTATTGT CAACCTGCCG ACACACCAGC ACACTTTCCC TTAAATGAGG GAATAGAGCT 660
GGTAATGGGG ATGATGAGCA GCAAGAAACC CACTCTATTA CCAATGCTCC CACCCAGCCC 720
CAGCCCCAGC CTGTATCCCT GGATTCATTA GTTCATTGAA CAAATATTTA CTGAGCAGCT 780
ACTATACACT AGGCAGTACT AGGCAGAGGA TATGGTGATG AGCAAAGTCT CTGATCTCCT 840
GGACTTCCAT TGTAGTGGGA GAGTGCAGGC AATTGCACAG ATGGTCATGC ATCATGACAT 900
TCGTTATCAA CACAGTGTGA TAAAGGGGGC AGACAGTGAT GAAGAGTTGG TGATTTGTAT 960
ACTGGGTGGT CAGGGAAGTC TCTCGGACAA GGTGACATTT CAGCAGAGGC TTGAAGGCAT 1020
TGTAGGAGAA AGACATGACT ATCTGAAGAT ATGTGGGGGA CACCTGTCTT TGTCTTTTAT 1080
ATTGGGGGTT GATGCTGGAA GCAGAAATGT AAGCAGGCAC AAAATAGAAA TACATTTGCA 1140
GTGAACGAGG AATAGTGGAA GAGCAACGTG GCTGGTGTGG CTGGATAGGA ATGAGTGAAG 1200
GGAGAGGTGG AGGTGACTTC AGAGAGGTTT GGGCCCTGGA GGACTTACGG ACCATTGTTT 1260
GGCCATGGCT TTTACTCTGA GGGATGCAGG AAGTCACTTG AAGTGTTTTG AGCAGTGTAG 1320
AACACCGTAA CTAAGCATTC ATTAAACATG CCTTCAGATA AATATTTGTT GAATGAATAC 1380
ATGAAATACT TGTTGGATGA CTGAAAGAAC AAATAGCACT GAGTCACATG AGTAAGTACA 1440
CAGAGATTTC GAGAATAACA CATCTGTCCA TATTTGCTCA GAAGAGAGCA AAGTCTTCTC 1500
ACTGAAAGAG GGATTAACTA TCGGCCGCAA CCCAAATGGA GGGTAGATGG TGGTAGAGGA 1560
AGAAAGGTGA GGGTAGACAG AGCACACAAC AGATAGCCTG CAGCCCAGTA TCCTTTGAGG 1620
ACTGGGGTCT GGAGAGAAGG TGAGCACCAC AGGGATTCTT AAGTTTTGAC ATGAAATCAC 1680
AGACCCTCTA GACGAGGCCA CTTCTTTTGG AGACGCAGGA TAGGTGCCCT GTGCTGGGTG 1740
TGGTTTGAGA TGCTCTTTTT GTTTTCACCC CAAATATCTA CCTGCCCCCT GTCTCAGTGC 1800
TTGGAATGCC ACATCATAGT GCCATGCTTT TCTTGAGCCT CAGAGTCATT TTTTTTCTTC 1860
GAGAGTATCT TCTCAAACAG AATGGGAGGA TAAATCCATT CTGTGTTCTT CCCCTCTTTT 1920
CAGCAAAGGT TCTCTTCAAA TGTTACTTTT AAAAGATGCC TTTCTTTAGT CTTCTCCTTG 1980
ACTCCCTTTC TTACAAAATG AACAGCTGCC TTCTTCCCTC TATCTGCATC CATAGTTCTA 2040
CAAAGGACCC TGGGCCACTG TCCTGAGATC AACAGTTTGC ATTCCTCTCT CCCTTCCAGA 2100
CCAGAAGTTT TTTGATGCCA AGAAGCATAC AATATCCTCT TTGTCTTCAG CACCCAGCAC 2160
AGTGCCTGCA AAGTGTTTGT TTTTCTTTTC CTTCTCTCTT TTTTAATCTT TTCTTCCGTT 2220
TTTTATTGTT TTCTTGCTTT TGTTTTTTAA TCAACCAGAA TGAAAGTTTT TAAGAGCATG 2280
TTTTTCAATC 2290
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