| Tag | Content |
|---|
EnhancerAtlas ID | HS026-08816 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr12:122598560-122599600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr12:122599512-122599527 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23525 | chr12:122598861-122599426 | Colon_Crypt_1 | | SE_24216 | chr12:122598969-122599293 | Colon_Crypt_2 | | SE_32300 | chr12:122598634-122599618 | Gastric | | SE_48379 | chr12:122598472-122599494 | Psoas_Muscle | | SE_50423 | chr12:122598519-122599479 | Sigmoid_Colon | | SE_52993 | chr12:122598571-122599430 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 122598971 | 122599178 | | chr12 | 122598572 | 122598636 | | chr12 | 122598600 | 122599533 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I122104 | chr12 | 122589301 | 122599486 |
|
Enhancer Sequence | TCACTCTTGT TGCCCAGGCT AGAGTGTAAT GGCACAATCT TGGCTCACCG CGCAACCTCT 60
GCCTCCCAGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCTA AGTAGCTGGG ATTACAGGCA 120
TGTGCTACCA CACCCGGCTA ATTTTTGTAT TTTTAGTAGA CAGGGTTTCA TCATGTTGGC 180
CAGACTGTTA TCAAACTCCT GACCTCAGGT GATCCACCCA CCTCAGCCTC CCAAAGTGCT 240
GGGATTACAG GCGTGAGCCA CTGCGCCTGG CTGACTGCCT TCATTTCTAA TACCAAATGC 300
AAGTTGGGGA GTTCCCAAAA CCACCCTCAG TTTCAATAAT TCACTAGAAA AACAGAACGC 360
ACTGAAAAGT ATTATATTCA TGGTTGCAGT ATATTATAAG GAAAGGATTC AAATTAAAAT 420
CAGCCAAGAC GCAAGTTTTT ACTGGACTTG ATCCATTCTA CCCCTGTGGT TGACCTTTAG 480
TTTCTAGCCC CGCCCAGATG TCTGGCTAAG ACCTTTAGTT AGCCTTTCCT CTGGAGGTTG 540
GAACTGATAC CCTGTGCTCC AGGCCCCCAT TGTAAGTCAG ATTGGTAACT GTTCTGTGGC 600
CAAAGCCCCC AGGCAAACAA AGACACTCCC ATCAGGCAGA ACTAATTTCT AATTCCAGGG 660
GCCTAGAATT CACCTCCCAG CAGCCCAGGG CAAAGGCTTG ACCTCTCTTT GGGAAGGTGA 720
CTTCTTTTTT TTTTTTTTTT TTGGTGGGGG GGGACAGGGT CTCACTCTGT TGCCCAGACT 780
GGAGTGCGGT GGCACGATCT CGGCTCACCT CAACCCCCAC CTCCCGGGTT CAAGCGATTC 840
TCCTGCTTCA GCCTCCTGAG TAGCTGGGAT TACAGGTATG CGCCACTACT GCCCGGTTAA 900
TTTTTTTATT TTTAGTAGAG ATGGGGTTTC ATCATGTTGG CCAGGCTGGT CTTGAACTCC 960
TGACCTCAAA TGATCCACCT GCCTCAGCCT CCCAAAGTGC TGGGATTACA ATCGTGAGCC 1020
ACCGCACCCA GCCAGGAAGA 1040
|
