| Tag | Content |
|---|
EnhancerAtlas ID | HS007-00129 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:12003730-12005140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr1:12004895-12004913 | AAGCCAGGCCCCTTTGTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34570 | chr1:12003473-12004339 | HCT-116 | | SE_34570 | chr1:12004366-12005693 | HCT-116 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I011943 | chr1 | 12003568 | 12005510 |
|
Enhancer Sequence | ATAGGGAGGA AAGTGGGCAT GTGGGGAGGG CACAGCTAGA CAGCTCCCTT ACATAGATAG 60
AGAGACAGGG CCCTCTCAAC AGATGGCCTG GCCACCGTCC CTGGCTGGGC AGTGCATGCA 120
TTTAGGTTAA GAGAGGAGAC TCTGGGTTCA GGCTTGTGTC CAAGTCCTGG TGCTGCTGCT 180
TCCTAGCTCC CTTGGGCACA TTACTCGCCA GCTGTACCCT TGGTTTCCTA ACTGGAAAGT 240
CGGGGGTTAG TATGTGTGAA GTGCTTGGAA CAGCATTGGC TGGGCACGGT GGCTCATGCC 300
TGTAATCCAG CACTTTGGGA AGCTGAGGCA GGCAGATCAC CTGAGGTCAT GAGTTTGCGA 360
CCAGCCTGGC CAACATGGTG AAACCCCATC TCTACTAAAA ATACAAAAAA TTAGCTGGGC 420
GTGGTGGCCG GCACCTGTAA TCCCAACTAT TTAGGAGGCT GAGGCATGAG AATCGCTTGA 480
ACCCAGGAGA TAGAGGTTGT AGTGAGACAA GATCTAGCCA CTGCACTCCA GCCTGGGTGA 540
CAGAGCGAGA CTCTGTCTCA AAAAAAAAAA ATTGTGTCTG GCACACAGAA AATGCTCGAT 600
GAAGGTAAGC CATTATTGTT GCTGTTATTG AGAAGCAGGA ACCTGAGAAA GGGGCTTTGA 660
GCCACGCCAC CCCATCCCCT TCCCCCACCC CTGCTGCTGG AGTTCAAGAG CCTGTTCCAT 720
CAAGAATCCT GAATTGCGCA TGCACGCGTA CACACACACA CACACACACA CACACACACA 780
CTCACTCACA TGCTCTCACG CTGGCTTTTT CCATCCATGA AATGTGACAC TCTTCCTGTC 840
CCCAGCAGCC CCCTGTTGCC AAGAGGGCCT CAGAGCTGGT GGCTCTGGTT CTCTTCACCT 900
GGGGAGAGAC TTCACCGTCC TGGCAGGAGC TCGGGGGAGC CCTTCCCCAA GTGTGAGCAG 960
CATCCCTCGT TTCTGGATCC CAGGTTCAGG TAGTGAGGCC TCTCCTTCCC ACACCTGCCT 1020
GGTGTATCCA CCCCCTCCTC CCCCAGCACC GCAGCTAATC CCTGCCAATC CCTGCTGGGC 1080
CGCCTGGCGC CAGCCCTCTG CCCTGGGGCC AGCTCCCTGC CCCGGCTACC CCTGCCCCAG 1140
CTACCCCTGC CCCGCCAGCT CTGGCAAGCC AGGCCCCTTT GTTCCTACAG TCTAGGTTCC 1200
TCCTGACTTC CTGAGGTGGT GGGAGGGGAG GGCCTTACCT GCCTGCTGTC AATCTGGCCA 1260
CCAGGTGAGA AGTGTAAGCT GCAGACCCTC AGGGAGCTAA GACTCACCCA GGGAAACAAT 1320
GATGAGCACT GCAGTGTGGG TCTTGCCTCT GTGGCTTGGA GGCCAGAGAG GGCAGGAGAA 1380
ATCCGAGAAG GCTTCATAGA GGTGGAAGGG 1410
|
