Tag | Content |
---|
EnhancerAtlas ID | HS108-23056 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:111919790-111921360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr2:111920483-111920494 | AAAACAAAGCA | + | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58584 | chr2:111874506-111933083 | Ly1 |
|
| 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 |
GH02I111162 | chr2 | 111919701 | 111921293 |
|
Enhancer Sequence | ATGGCTTCCT CTGTTGAATG TCGTCCAAAA GCAATTGCTT GTCAGCTTAA AAGCGTGTGC 60 CATGTTGTCA TGCCCGCCGT CTGAGAGGGC AGGCATCCCC GCACACTTGC AGACTGGGAT 120 GCTGTAGCAT CTTCTCATGA GTCAGGGATT GGGTGTAACT TTTGCCAAAA TTTCCTGCAT 180 TTTCCCCACC CTCTCCAACA TGTCTTTGAA TACCCCATAT CCTTTACATT TGAGATGAAA 240 GTGGAACTCT AAAAACCTTG GAAAGATTCT CTTGTGAGGT GACTTCTACT TAAGCTTGGT 300 CACAGCCTCC TGCTGTCCTC AAAGAGTGGG CAGGAGATTT CTTCCCTTGG ACGCTGCCAG 360 TGCTGGAATA TGAAACTTAC CAAGTGTCAG CAGTTGGGGT CTGTCCTTCA CGTTGACCCA 420 GCCCCCTCAT TGGTGTCCTG ATGATTGTGG ACACCCAGTC AGCCCCATTT TCTGGCCACA 480 CCAAGCATGG CAATGACACC AGGTTGGCAC AAAACAACTC TGCCTGGATT GATTACTTAG 540 CCCATCATAG CGTACACTTT CTTCATTTTA GTAAGTTGTG GTTTTATTTT GAATAAGTCT 600 CTTTCAACCT ATTAATATTA GTCTACACTA AAATTAACCT TCCCCTAAAT TATTCTCACA 660 CAGAGGCAGC AAAGTAATTT TGAAAGTTAA ATCAAAACAA AGCAATCTTG TGTGTAAAAC 720 AGATAAAAAT CACAGACTGT GGTTACAGAG TGCCTCTACA GGAATCGCTT ACATAAAGCT 780 GATTTCCTCC AATCTTGTTA TGGAAGGAAA AGGGGAAATG CCCTGGCCTT ATCACAATCC 840 CATTCTGTCA AACAAGCGCG GCAGAGCTTG TGTAAACAGT GGAGCTGCAG CTGCGGCTGG 900 TGTCTGTGGG GGCCATTCGG GGTCTGAGGG GACAGTTGTC TCAGCCTGAT GCATGGCAGG 960 TGGTTCCCGC GACGGTGTGT TGGAGGTATC CCCCACCCAA TGAGAAGGGG GTTTGTGGAG 1020 AGACAGTCAT GTAGCCCGGT CTCGTGTGGA TTAGTCATTA AGAAATGTCC AGGGCAGATT 1080 TCAGACTTGA ACAGTGAACC AGGTTGTAGC TCATGGCGTC GAGGTTGAGG TGTTGTGTTG 1140 CCGCTGCCTT TGGTGACTGT GAATTTATAC CTTGCACATA CTCACAAAAT GGATTAGAAC 1200 CTGAAAGTGG GCGCTGTGGA AGACCTGAGG ACCCTGAAAG CATTGGATAA GCTGGTGATT 1260 TCCTTTTGAA CAGTTTCTCA GTTTGTAACA AACATATGCT GGTCACTGAC ACAGAGACTT 1320 TTTTATGTTC TGGATTGCTC TTTCCTTCCC ATACCGAGAA GGTGGGAGGA TGGGGGTTGA 1380 CATTGCCTGT GTCTGTGACC ATGGGCACCC CTCTGGGTCA CGGTGTTTAT CATAGCCAAG 1440 CAGCCAGAGG CACAATGGCG CATCACTGCG AGACTTTATT TAGCTTCTTA GGGCAGATTA 1500 CTCCAAATCA CTGGTTTTTC AAATAAATTA CAGCTACCAG AAATTCACCC CTGGGGGAAT 1560 CTGCAGCATA 1570
|