| Tag | Content |
|---|
EnhancerAtlas ID | HS139-52761 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr8:22600950-22602780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr8:22601519-22601534 | AGGCCAGTGTGACCT | - | 7.12 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24334 | chr8:22600513-22601243 | Colon_Crypt_2 | | SE_24334 | chr8:22601318-22601594 | Colon_Crypt_2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I022741 | chr8 | 22599459 | 22607261 |
|
Enhancer Sequence | TTTATGGACC CGTTTCATCC TTACTTGTTC CCAAACCAGA AGGGACCATC CTGGGGGCTG 60
AGCCAGGAGC CTGATGGCAG CCCCAGACCA CAGCTGTTTG GAGTGGGGGC TAAATGGTTC 120
CTGAGCCTGA AGCCCCTCCG GAGCTGCCTT TTCCTCCTCC ATCCCTTATC TGGTTGAGAC 180
AAAGTGAGGA ATTTAGGTCA ATGGCTGACA ACAACCAGCC TTAGGAAATG GGCAGGGGAC 240
AGGGAGGGAG GAAGTGCATC CACCCTGATT CTTAAGAGTG TCAACACTTG TCACACATGG 300
AGGCCAGAAA GAGCATTCAG CACCTGCCGG CAGCACCACG CCCCTTTCCT CTGCCCAGGT 360
ACTGATAGGA GCTCCCTGAA TCATCCCAGT TGCAATTCCA ACACCTGAGC AGAACTAGAC 420
TCCGTGGAGG GTGGGGCTGG CCCGCTGAAT CACCAGTAAC ACCTGTGTTT TGCTTGTGAG 480
GTCTCCCTGC TCACTCGGGG ACCAGCCAAG CCTGACCCTG TTTGGCTTCT CGGAGCTTGG 540
TGAGATCACA GCCTGGGGGT TGTGGCTGCA GGCCAGTGTG ACCTGCTGTG CAGGGAGTAT 600
TTTTAAAGAG ATACTTGCCC TGTGTTCCCA GGATCAGCTC CCTGAGAGAC TCAAGTTGTT 660
CTTTGAATTC TGCCTCCCTC TCCCAATTTG ATTGTAGACA TTGGTCAGGG GAACATAAAA 720
TCACTTGGGA TAAAGTGTGT AGTGGAAATT AACATGCAAT CTTCTTGCCA TAGACAAGCC 780
CCTGGGGGAT GCCCAGGGAG TCTTGGTGAC TGGTAGCACC TGAGGGAGGT GGGATGAGCA 840
GAATCAGACT CCCTAATTCC CTTGAGGATG CAGAGATAGA CTCACCTGTT TTCTCCTGAG 900
TTCTAGAACT GCCTAACTGT GGTCTTCCGG TCAGAGCCTG GACAGGAGCC ACAGGCCACC 960
ATGACAGGGT CTGCCGGTGG AAAAAGACTC ATGTATGAGT CAGCCTGCTG CCTCGGTTCC 1020
CAGCCAGATG CGGGCCCAGC CCTGCCTCCA GGCCATCTGC CGAAAATTGG GGTCAGTGGA 1080
GGGCAGAGGA GCCCACGCAT GCAGGTTCCT CGTGCCCCTA ACCAAGCTCC CCTTTTCATG 1140
TCCTCTCTTC TTGCAGACAT CGCCTTCTTA CAATGCAGAA CAGACGATGC ACTGTCTCAG 1200
GTCACGCTTA GCCTCCTACG GGGGCACGAC AGAAGAAGAG GAACATTTAG AGAGGCACAG 1260
CTCCTACATC CTTGGATGGG GAGAGTGGGG AGCAAACAGG CCAGGTGAGT CACTTGGGGG 1320
TTGGGCCATG GTTGTTAGAC AGTGACAGCA GTCCTGGACC CGTATCCAGC ACTCTCCACT 1380
CTAGGGGTTT CAGGCCCTTG TGCACTGCTG TATCACTTAA TCCTCCTTCA CCAGGAGGCA 1440
GAGAGGGTAG CGTTTGCAGA TGGGGACACA AGCTCTGGAG AGGTTAATGA CTTGCCGGAG 1500
ATGGGAGTTC CAATCGGCAG CAGATCAGCA AATGGAATGC GGGTGTCCTG GCCCGTGATC 1560
TAAGTCTCCT GATTCATAGT CTAATGTTCT TTTGTCTACA CCTCAGAACA AAGAGGGGCT 1620
GTGTTCAGAA AATTGATTCT GAAGGGAAGG GAATATTTTT TTCCCTTTGC TGGAATTTCT 1680
CTGGAGACTT CGGACTTGCT CAAGTTGGAT GGAAAAGCCC GTCTAGATCT TCCCAGCTCT 1740
CTCCTGGGTT ATGCCCGGGC CTGGGGGCAG AAAGCTTTTG AGACAGGGAC AGGCCACATT 1800
CTCCAGTGCC CTCTCGACTT AGGGGACCCT 1830
|
