| Tag | Content |
|---|
EnhancerAtlas ID | HS101-29119 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr22:46329650-46331860 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr22:46329851-46329864 | TTCCGGAACATTC | + | 6.12 | | Myog | MA0500.1 | chr22:46331133-46331144 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr22:46331133-46331144 | CAGCAGCTGTC | - | 6.02 | | ZNF263 | MA0528.1 | chr22:46330173-46330194 | GGAGGAGAGGGGGGATGTGGG | + | 6.85 | | ZNF263 | MA0528.1 | chr22:46330167-46330188 | GGGGCAGGAGGAGAGGGGGGA | + | 7.6 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I045934 | chr22 | 46330041 | 46331468 |
|
Enhancer Sequence | GGCTGTGACA GGCGTGCACT CCCGGCCTGG GCACACAGAG GCAAAGATGC TGAGCTGTGG 60
AAGGGTTTGG TGAGGTCAAG AGTGGCCACA GAGGAGGGGG AGAATGTCTC GCAAGCAGGT 120
GGCACTTTCT GTCCAGGTGC CAGGGCCAGC TGCTGGGGAG GGCTGGATGT CAGGGCACTT 180
GTCTGGCCAC ACAGGCGTGG ATTCCGGAAC ATTCAGAGGC CGGTCGGCAC CAGCAACAGC 240
GTAGCCCACC CTCAGGGCTC TCCACATGCG CCGGGCGCAC ACCCAGCCCT CACATGCGCT 300
CCCATTTCAC CTGGACGTTA GGATGAGGCG CGTCCAACCA TGATTCCCGG TTTACAGAGG 360
AGGAAGCAGA GGCACAGAGA GTGGCTGGAG CAAGATTCAA ACCCAGGGAA TGAATTCAAA 420
GACCAGGAAG GCTGACGGAG GAGCAAAGTG CCTGGGGTCG GGGGCCCTGG AAGGTCCTTC 480
TGCCCCCAGC TTGGCCTCTC TGAGGCTAAG GTGACCTGGG GCAGGAGGAG AGGGGGGATG 540
TGGGCTATGC AGCCCCCAGG GAAGATGCTG CCTGTGGACA GTCTGTGGAC CTGGGGGAAA 600
GGCGCAGCTG TAGGCAGGCT CTGGGTAGGA GCTCTAGGGA GGCTGAGCTG GCTCTGGAGT 660
GGGCATGTGT CACCCGATGG AGGGGGTCTA GGAACCCCAA ATGATTGTGC GGGCCCAGCC 720
GGTGGACCTT GAGGACAGAT GTGGATGTCC CCTCAGAGGT CCTGGAACAA CAGCCTGTGA 780
CCCTCCTCTT CCTGCCCCAT AGGAAGGCTG CAGAGCGGGT CAGGGGATGC CACTGTCCTG 840
AAGTCCCTGA GCAGGCTGGC AGATCCACGG CTGGGTTTGC ACCCTTGGAG GACACTTCCC 900
ACAAGCCTCC CTTCCAGCCT CCCGCAAGCG CCTGCTCTCA CCTGGCTATG CCTGCCCCAG 960
GCTCAGACTC AGTTACTCAC CGGTTACTCA TCGCCTGCCG CTCCTGCTAA TTCCTTTTTT 1020
ATTTGCTTTT AATGAGCCAA ACCCTCTGGT CTCTCGTCAT GGAGACAAGG GGGAGGTGAG 1080
CTGCAGAGAG TCATAGTTTT GGCACAATCA GTAAGAACGA CCTTAGGTCC GGCGAGAGTC 1140
GCTGCCGTGG ACTGTGGGCT CCCGTGCGCC CGGCACGTTG CCTGTGTTGT CTGGTTTAAT 1200
TCTCACAACA GCCCACGGGG GAGGGCCCGT TACCCCATGT TACAGACCTA GACGCCCACT 1260
CCGAGGGCTT TGTCATGGTG TGCCTAGGTG TGTAGTGGGA AGGGCAGAAG GGCTGCAGGC 1320
TTCCCCCGTG TCCCTCCCCA AGTCCCTCCT GGGGCCGTGA CTGGGCACCT TGCCAGTCCG 1380
CCCACACGCC ATCCTTCCTC CAGGCTGACA GCGAGCCAGT GCTTAGACTT AGAAGCCGGT 1440
CCTCTGCAGT GGGTGCAGAC AGCCTGGACC CATGTGCCTT GCTCAGCAGC TGTCAGTGGC 1500
CCCCAAGGCC TCTGAGACGA CTTCCAGTGC CTTGGCCTGG CCCCCAAGGC CCCAGAGGCC 1560
TGACCCCACC GCTCCTCGCC CACCACTGCC TGCAGCCCAG CGTGGCCTGC CTGCAGGTTG 1620
GGCAGCCACC TCTGGTGCAC AGTAACTACT CCTGAATAAA GGACCTGCTG GCTTCCTGCC 1680
GCCTGCCCTG GGGGACAGCA GCCCCCTCCC TTCCTGGAAT ACCTGCCCAC CCTCCCACAT 1740
ATCCACACAC TCCTCAGGCT CTGGACGCAG GGAGGGAGGC TCCCTCCTCC CCGAATGCCC 1800
TCTGTAGTGG GCACACCCTC CCCTGGGCTC TCACTGGGTG CCCCTCAGGC TGCAGGCAGG 1860
ATCCACATCT GATTCTTTTC TGTACCTCCC ACCCATCGCT GTTTCCCAAA TCCCATGCAT 1920
GAGCAGGTCT GGACTGGGCA CCTCCCCCAC ACCACCTTAT CTCCAAGACA GCCCCATTCT 1980
GATCAGACCC ATTTCACAGA TGGGAAAACC GAGCCTTCAA AGCAGGAAGG GATTTGCAAT 2040
AGGCCCATGG CAGTGACGAA AGCCATCTGA GCTCAGCAGC TGCCCTAGAT GTGTGTGGTG 2100
ATGGGGAAGC TGGATGAGGG CAGCACGGAT GCTCTGTTTG GGGCCGGCAG CTGTCCTGCT 2160
GGTACACTTG GGTCTCGGGG GGCCTAGGGG CCTCTCTGAA GACCCACAGC 2210
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