| Tag | Content |
|---|
EnhancerAtlas ID | HS092-15327 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:111682530-111685120 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr13:111683755-111683765 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr13:111683755-111683765 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr13:111683755-111683765 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr13:111683755-111683765 | AACAGCTGTT | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I111030 | chr13 | 111683002 | 111684871 |
|
Enhancer Sequence | GGACTGCCAT CCTGGGTCGC CACTCTCTCC AGAGAGTGCC TACCATCCCC ACGCTCCAGC 60
CACGGTTACA GGGCAGAACT CCCTGTCTTC GTGGGCAAAG CATCCGTGGA CTCACCGCTT 120
TGTGCCATCG AATTGCAGCA GTGTGGCTGG AGCAGTTGGC GGCCCTGATG CCCAGCGCAC 180
AGAGAACGCA TCCGGGATGC GCTCAAGGAT GCTGCCAACA GGGTTCTCAG CCTGCCCGTG 240
GAGCCTGTCT TCCTAACTTG GCACTCGTGC CATCGTTGGA CCAAGATGTC ATTGGGCACC 300
GTCCCCTCCG GACAGATGCT TTCCAGCCCA GGCAGCCAGA AGGACACTAA GCTCGTGGCA 360
TTTGGGACGG CACTGATAGA CATGGCATTA AAGCCGACTT TAACCTCTTC TTCTTCCTCT 420
TTGTCACGGG GTAGAAAAGT GAGCCGCTCC AACACCCAGC TGCACCAATT TAAGGTCTTA 480
ACCATAGCCT CTAAAGGAGG TCTAAAGCCC TCCCAAATGT GGTTGCTGTA AAAATTGAGA 540
CCGTTTTCCA CATGCTGCTC CTAAATCCTT TACCTCTTTC CACCTTTTCT CTCCCCATAG 600
GCAAATGGCA ACTATGGCCA CAAGAGAAAG CCCAGCTCAT TTAAGTAAAG TAATTGATTT 660
TGACATCTGA AAACTAACAG CAGTTAGAAA TTTTAGAATG AATCACTGAG TAGACCAAAT 720
GAATTTAAAT CAATTATCTG AGGTTTAATG TTTAAAGGGG GTTTAATTTT ATGTATCTAG 780
TTGCACCTTG ATTATTCAGT TTTGAAGTTC CATGCATCAA AGTTTTAATC TCAGAATGAA 840
CACTAGACTC CCTGGGCTTC CCCTGCAGAC TGGTATGTGC TTAGGGAACG CAGGTGAGCC 900
ATGAGGCAGC CAGTCATGAA GTCAACCGAG GCTTCTCAGC TGCCATGCCA GCCGCTGTAG 960
TAGTTCCCGA GCAGAGTTCA CCCTCAGCGT CGTCACAGAC AACTTTTGTG GAGAGCTCAT 1020
GTGTGCTTGC CAGTTCTCTG TGCCTCTGTG GCTTTCTCAC AACGGGCAAC ATTGGGTCTA 1080
AATCTTAACT TTCTTGCAAA GAAGTCACAC TTCTCAAATA CAGGCTGTGT TAAGCGAATG 1140
ATCATTTGGG CAGCCATGTT TAATAGAAAT GCTGTTGCTA TCCCAGGCTC ATTCTTGCTA 1200
TCTTAAGATA GATTTGTTCA TCATTAACAG CTGTTTCACC AATGGGTGTC TGTTTGCTGA 1260
ATGACAAGTC CTGCAGTCTC ATGACTTCAT GCTGGATAAC GCCAGGCGCA GGTGCATTTA 1320
GAAGGGTGAA GTGGCTCTTT CTGTAGGCCC AGGCCAGCTC TGGCCTTTCT CTTGTAGCCA 1380
ATGAGCTGTG GTAGAGACAC CTGTCCCCAG GAAGCAGCTC ACTCCTGTCC TACAACCCTG 1440
AGGCGGGCAG GGCAGGCACT ACCGCCCAGC TGTCCTAGTC CTGATGTGAG TCAGTGACCT 1500
AGAATCCGGA GCCTTCCCAA CAGCCAGTGG AAACATCCTG TCACATGTGG TTTTTATTTC 1560
AGAACTCGGG CTTGTGGTGC TGCCCTGCAC CCTGAGACAC CCTTGCTGTG GTCGGATTCG 1620
TGGAAGCACA CTGGCTTACC CAAGTACCTC AGTCGATTGC TCAGCAGCTC TTACTTGTGA 1680
TCAGAGCTGA TGGGGTGAGC AACTTATTCT TGGGGAGAAT TAGCTCCTGG AAGGTCTGGC 1740
TTGGGGCTGG TGCCGCATCC CATGGCCTCA GCTTGAGGAT GGAGGAAGGG GTCAGCTGGG 1800
GAGTGTGGAG GGATGGGGAG CTGTTCCCAA GCTTCACACC ACTGCTCACC ACTGGGCAAT 1860
CCAGTGAGCT TCCATGGATC TGACCACACT TATGGGGTCT CAGGGCACAG GACTCTGCAC 1920
CGAAAGCCCA AGGTTTGAAA TGAAAATAAC ATGTCCTCCA CTCCTCCAGG GGAATGTGTG 1980
TAGAACAACC TGGGACCAGC CAGAGAAACA TGGTGGGCGG GTTCCTGGCT TGGTGCCCCT 2040
TTCCCACTCC TCTCCCAATA ATCTGGTCCT GTGAGGATGC CCCACACTCC TGACCACCTC 2100
AGGCCTGCAC CCTCGTCTGA GCTAACCCTC ATCTGAGCTG TTGGGCCTTG CTGGAGAGAT 2160
GGGGGCTGAG CAAGCACAGG CCTGCTGGGG CCTCTGGATC CTCTCACTGT GGTGATGGCC 2220
AGGCCACCTC CTGCAGGAAC TGCTGGTGTC TCCTCCATGA CCAGAGGCCA CCACTGGGGA 2280
TGCCCAGGCC TCCCTGTCAC ATCCTCCCCA CTTCTGGTGC AAACTCTCTG AGAGACACAT 2340
GCAGGACAGT GCTTGGACCC AGGCCCACAC TAGCTTCCTA CCAGTCACTG CACCCCAAAT 2400
CAACTCATCC ACTCAGCCAC AGGTGGGGCA ACTGCACCCC AGCCCAGGGG GGTTCCTGAC 2460
GGGGAGAGTG AGTGCATGTG TGTGAAGAGT GGCAGGTCCT GCAGACCGAG AGAGTCTAGA 2520
ACATCCTCTT GCGGGAGGAA TGGCCTAGAG TCAGGGGAGG TGACAGCATT CCCCTGGTAC 2580
CTCCTCAAGC 2590
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