| Tag | Content |
|---|
EnhancerAtlas ID | HS026-06220 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr11:65555260-65556470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr11:65555898-65555909 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr11:65555899-65555909 | GGGGCGGGGC | - | 6.02 | | MEOX2 | MA0706.1 | chr11:65555958-65555968 | AGTAATTAAC | + | 6.02 | | SP2 | MA0516.2 | chr11:65555896-65555913 | TTGGGGGCGGGGCGTGG | - | 6.19 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_24650 | chr11:65554469-65556603 | Colon_Crypt_2 | | SE_24927 | chr11:65554462-65557521 | Colon_Crypt_3 | | SE_27031 | chr11:65553202-65561915 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACCGCTCAGG CGACCCTCGG CTCCGACGTC GTAAATCCAG AAAACCGGGA CTCGCATGAG 60
GCGGGAGAAG GCACTGGAGC GATGCCACTT TGGGGGGCGG GGAGCGGGCT GGAGTTTCGG 120
CCGAGATTTG TGTTAAAAGC TCAGAGCTTC AGCCGCTCGC ACAGGTCCTT CCTCCTCCCC 180
CACAACACTG GTGGCCGGGT CGGAGTGAGG GTCGGGCCGG TGGGGGGCGT GGGCCCCCAA 240
ATTTTCGTTG GGCTCCGGCT GCTAGTCCCG CGCAGTGAGC CGAGACGGTG GGACAGGCGC 300
CCGCTGCGCC CCGCTTGCCC TTAAAGCAGA GGTGGGATCG GGTCTCACCT CTGCTAGAAA 360
CGCACTTCCT TCACCTTGCG GAGGGCACAA TTGCATGGAA AGCAGCTGCA GGGAGCCCAC 420
CCCACAGCGG AGGGCCAGGC CCGGGGAAGC TGGTGTACCC AGTTATTTTT GGCAGACGCC 480
TAGACAGCGT CGACTGTGAG AGTTGCTTCT TCCTCCAGCG GCATCTTCCC CTGAACGCCC 540
CAAGAACACT CCTACCCCTT CTGTCCTCCC CCACCCCCAA CAAAGTCTTT GGTCTGGAGA 600
AAGCCTGCTT CCTTCCGAAC GCCCCCTCCC CAGGCCTTGG GGGCGGGGCG TGGACGCTCT 660
GAACGCCCAG CCCAGCCCCT CCGAGGGGGG AGGGGAGGAG TAATTAACCA ACTGACTTTG 720
ACCCTTGATC TGCAGACTCC CTGGCACCGC CCCAGGCCTT GTAGGAAAGT GGGGAAATGA 780
GGGCAGCAGT GAGGGGCCCC GTGAGGGCTC TTGCTCAGTT TCCCTCCTGA ATAAGCTGTT 840
GGAGACAGTG TCCTGGTGAG GTCTTTGTGG CCTGACCTTC CAGGACCCAG TGGCCTGTGG 900
CGCTGGCAGG ATGTTTCACA GCTTAACCTG ATCTCAAGGG GACCCCTCTT CCACCGTTCC 960
TTAAAACAAG GGAATGTGCC AGAAGACCCT GGTAACCCCA GTGGGGAAAC TGAGGCAAAA 1020
AGGGAAGTGA GTGGCCTCCC CACCTGAGGC AGATTAGGGT GTGGGCTCAG AATTCTGTGT 1080
ATAGCTTCTT GCTTGGCCAC ACTCCCTGGT GAGCTGGCTG GTTCTCTACC TGGGGGTTGG 1140
TGGGGGCACG CAGAGGGCCA GAGCCCCCTC CCCGCTCCGC CCTCCGCCCT CCACCCTCAC 1200
CTGTGTTTGA 1210
|
