| Tag | Content |
|---|
EnhancerAtlas ID | HS112-03899 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr12:108989240-108991740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LBX2 | MA0699.1 | chr12:108990855-108990865 | GCCAATTAGC | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_50734 | chr12:108988785-108994320 | Sigmoid_Colon |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I108596 | chr12 | 108989377 | 108989576 |
|
Enhancer Sequence | CACATGCACA CACACCCCAC ACACAAACAT GCACACACGC CACACATACC CATATACACC 60
CCACACACAA CCACGTACAC ACATGCCCCA CACACACCCC TATACACACA TTCACATACT 120
ACACACAATC ATACACACAT GCACACACCA CACATATATG CATACACTCC ACATACACAC 180
AACCATACAC ATACACCACA CACACTCACC TACACAACCA CACACACATG CACACACCAC 240
ACACTCTGAG CCAGGAATGG CTTGTTCCCG CTGGTGGACA TCACCTGTCA GATGCTAAAT 300
GAGGAAAGGA CCCCCTCACC TCTCTGGCAC CTGTTAGCAA AGGTTCCTAC AGACAACCTT 360
GAGCTTTGGG GTCTGTGACC TGCCAGTCAC CTCCCTGCCT CCCACCCCCA GTCAAGCCTA 420
GGAGAGAGCT TTTGTGGCAA CAACTACCAC TTCTCACTGC AGAGGGCAGC TGGGACCATG 480
GGTGGCTGGA GACCCACTCA AGTTCTGGCT GGGTCAAGAA TCCCGGCTCC ATCGCATCCA 540
GCTCTGTGGT CTGGCTCCTG TGGGCCTCAC TTTCCCCATC CGTAAGTTGG GACAGGGTGA 600
CCACAGGTAG CACCTCTCAG AGCTGTTAGG GCCAAATGAG ACAACTTTCA GAGAGTGCCT 660
GGTGCGAAGT AGCTGAGCCC CGAGGAAAGA TAGGGTCTGG GGTAGCTGAA TTCCTTCCCT 720
AGCCGAACTC CAGGTTCAGC CAGCAATTTC CCACCCTGAG TCGACAAATG AGCACCATCG 780
CCGGATGGGA ACATGCGCTC ACTGTCTGGT CCGGCCGCCA CCCAGTGAAA GACCAACCTT 840
TTCACCCCGT TCAGTGAAAC CTCTTTAGCT CTGGCCGCCA AGGAATGCAG AACCAAACAC 900
ACACATGCAC ACACATACAC ATACACACAC ATGCACACAT ACACCTACAC ACACATATAC 960
ATACAACACA CACACACACA CACACACGAA GTCAGAGGCA GAGGGCAAGA AAGGAGAACA 1020
CACAAACTGC CACTGGCTCT TTAAGGCTGA GACCCTGACT CTCAGAGTCC CCTGCACCCC 1080
ACAACCCCTC CTGGCTTCCA GGGAAAGGTG GGGGCAACGT ATGGAGGACC CAGCCCCACC 1140
TGCAGTCAGC AGAGCCTCAA AAAAGATGGT TGTGTGGCCC TGGACGGCCC CTGCCCTCTC 1200
TGGGCCTCAG TTTCCCATCT GTGGAATGAA GCACTGTTCT GGGCAGCTCT GAAGTCATTA 1260
TTCTGCCTAC CTCCCCCCGG ACCCTAATTT TTTCAAGGAC TCAGAATCTA ACAGGCCATT 1320
AGGAGCTGGG GTCAGGCCCA ACGCCTCTTG CTTCACCTTA GAGGTAACTC AGGTCCAGAG 1380
ACTGGAAACA GCCTGCCCAG GTCACACAGA AAGTCAGGGG TGAGCCCAGC AGAGCCCTGG 1440
ACAGAGAAGC CTGTCTTGGT ATATCCCAGA GGAGGTCACT TCCCGGCTAT GTGTCCTTGG 1500
GCTGGGCATG TCACCTCTCT GAGCCTCGGT TTCCATATCT GTACAATGGG GATAAGAGCC 1560
ACCTCCCTGG ACTGCTGTTA GGACAAGATG CGGCCATGCC TGGTGCACAG TGGGTGCCAA 1620
TTAGCAGGTA CCACGTGATT GCCCAGGACT CCCTGCCTGG GGACATGTCA GGCAGGGCTG 1680
GCCGTGTGTA AGTGTGGCAA ATGCCCTAAG ATGGTCCTGA GTCTGTGGAG GAGTGCAGAT 1740
GCACCCCTGA GGCCTGGGGG CCCCAAGACT TGAAGCTAGG GGACCGGGGG CTGCCCCACC 1800
CCCACCCAGA GACTGGTGGC CTTTGGGGGA GGGGCGGCCC ACGGAAACCT GGCTTCAATC 1860
AGTGGCCTTG TGGGGGAGGG GTGTTCTGGT TGGAGCACTG CACATGCCCC CGACCCCAGG 1920
GCCAGCCAAG GACAGGGACC TGGGCCCTGG AGGTCTGGAT GGGGAGGGGG GTCCTGGGGG 1980
CACAATCCCC CTCCACACAC ACACACACAC ACAGAGCAGC ATGGACACAC AATATAAAGA 2040
CACACAACAC AGGCACACCG ACTCACACAG CACTGAGACA CCCAACAGCA CTCTCATGGC 2100
CCATGCACAC AATACACAGA GAACACACAC GGACACACAA CACATATACA TACACAACCC 2160
CCTGACACAC AGCCGATCCC TGCACACAGG ACAATACCGT CCACATCACC CTCACACAGA 2220
TCCTGGAAGC AACAGCCTGG CATCCACTTG CAGAAAAGTG GAAGCAACAC ACCCCCTACA 2280
CCAAGGCCCC AGCCGCACAC ACACAACACT CCGGCCCACC CTGGCCCACC CCAGCACCGC 2340
ACACGGGACT CAGATTCCAC CACACTCATG CACACAACAC CAAACACACA CTCAAAGCCC 2400
ACACACACTT AGAGAGGCCC CCCAGAGTGC TCCAACAGTC CCCAGTCCCT AAGCTCCAAG 2460
ATAGCTCCAG GCTCTCAGGA CAGAGGAGGG GACCCCAGGA 2500
|
