| Tag | Content |
|---|
EnhancerAtlas ID | HS180-12729 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr12:123306500-123307910 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:123307053-123307074 | TCCCCATCCACTCCCTCCCCA | - | 6.13 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_31427 | chr12:123307190-123308052 | Gastric |
|
| | 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 |
| GH12I122822 | chr12 | 123306650 | 123308479 |
|
Enhancer Sequence | CACAATGGCT CACACCTGTA ATCCTAGCCC TTTGGGAGGC TGAGGCAGGA GGATCACGTG 60
AAGCCAGGAA TGGGCAACAA TGGGAGACCC TGTCTCTATA AATTTAAACA CACACACACA 120
CACACACACA CACACACGAC ATTATTTATC TTTTTTTTTT TTTTTTTTGA GACAGAATGT 180
CACTCTTGTC ACCAAGCTGG AGTGCAGTGT CGTGATCTTG GCTCACTACA ACCTCCACCT 240
CCCAGGTTCA AGCGATTCTC CTGCCTTTCA GCCTCCCAAG TCGCTGGGAC TACAGGCGCG 300
TGCCACCACG CCCAGCTAAT TTTCGTCTTT TTAGTAGAGA CAGGGTTTCA CCATGTTGGC 360
CAGGATGGTC TCGAGCTCTT GACCTTGTGA TCCGCCTGCC TCGGCCTCCC AAAGTGCTGG 420
GATTACAGGC GTGAGCCACT GCACCTGGCC AATACATTAT TATTAACCAT AGTCATGGTG 480
CTGTGCAATA GATCACTAAA ACTTTTCCTC CTGTCTAATT GAAACTTTGT ACCTTTGACC 540
AATAGCTCCC CTTTCCCCAT CCACTCCCTC CCCAAGCCTC TGGTAATCAC TATTCTACTC 600
TCTGCTTCTA TGAGTTCCAC ATTTTTTTTT TTTTTTTTGA GATGGAGTCT CGGTCTGTCG 660
CCCAGGCTGG AGTGCAGTGG TGCGATCTTG GCTCACTGTA AGCTCCGCCT CCCGGGTTCA 720
CACCATTGAG TTCCACACTT TTTAGATTTC AAATATAAGT GAGATCAGGC AGTATTTGTC 780
TTTCTGTGCC TGGCTTCTTT CACGCAGTCT AATGTCCTCC AGGTTCATCC ACGCTGTTGC 840
AAATTACAGA ATTTTGTTTG TTTTTATGGC TAAATATTAC TCCATTGTGC GTATATACTA 900
CGTTTTCCTG ATCCACTCAT CTGCTGACAG GCACTTATGT TGCTTCCGCA TCTTGGCTGC 960
AGTGAACATG GAGTGGAGTG CAGATATCTC TTCATCTAAC GTCTTTTTTT CTTTTTTCTT 1020
TTTTTGAGAC AGGGTCTCAC TCTGTCGCCC AGGCTGGAGT GCAGTGGCGT GATCTTGGCT 1080
TACTGCAACC TCCACCTCCT GGGTTCAAGC AATTCTCCCA CCTCAGCTTC CCAAGTAGCT 1140
GGAATTACAG GCGGGCGCCA CGATGTCCAG CTCATTTTTG TATTTTTGGT AGAGATGGGG 1200
TTTTGCCATA CTGGCCAGGC TGCTCTTGAA TTCCTGATCT CAAGTGATCC GCCCACCCTG 1260
GCCTCCCAAA GTGCTGGGAT TATAGGCATG AGCCACCACG CCCAGCCTCA TCTAACATCT 1320
CTTAAAGGCA TTTCTGCTAT ATTTGTGTTT AGTCTTCTTA AGAATTTTTT AGTTTCTCTA 1380
TCCTGAATAC TAATCTGGGA GTTGTTTTCT 1410
|
