| Tag | Content |
|---|
EnhancerAtlas ID | HS135-00483 |
Organism | Homo sapiens |
Tissue/cell | MM1S |
Coordinate | chr11:268770-269950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:269490-269511 | GTGTGGTTTCAGTTCCTGTTT | + | 6 | | POU2F2 | MA0507.1 | chr11:269685-269698 | TTCATTTGCATTT | + | 6.59 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_16128 | chr11:267513-270474 | CD4_Naive_Primary_7pool | | SE_21864 | chr11:267477-270412 | CD8_Naive_7pool | | SE_22226 | chr11:267090-270596 | CD8_Naive_8pool | | SE_28519 | chr11:268667-269561 | Fetal_Intestine | | SE_52556 | chr11:267492-273530 | Small_Intestine | | SE_61820 | chr11:266425-273086 | Toledo | | SE_62809 | chr11:266595-290841 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 268826 | 269269 | | chr11 | 269337 | 269903 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I000266 | chr11 | 266649 | 273455 |
|
Enhancer Sequence | GGGATCACAG ATATGAGCCA CCGCGCCCCG CCCTTGGCAC TGTTTAATCC ATGTGTTGTT 60
TATTTATGTA TCCTGTTTAT TTTCTGTCTC CCAACAAAGA CGTAGCTCCT TCTGGGTAGG 120
GCATTTTGTT CATGCTCTCA GATGCCGCCT ACCGCCCTAG AGCAGGAAAT AGCGGTCAGC 180
GCCAGCTGTG AGGAGCACAG CATTGCGGCC AACACAGGAG GCACTGACCA CGGGGCAGGC 240
GCTATTTAAA AATCGTGGCA AAGGATCAGA CGTAACAGAA CTCTTTTTGT TTTAATCATT 300
TTTAAGTGTG CAGTTCAATG ATGTTAGTTA CATGCACAAT ATTGTGTAAC CATCACCACT 360
ATTTCCAAAA TCCTTTCTAT CCGTCAGACA GAAACTCCGT CCCCATTAAA CAGCAACTCT 420
GCATTCCTCC GTCCCCCCAG CCTCTGGTCA CGTGTCTCAT CTACTTTCAG TCTCTACGGA 480
TTTGCCTGTT CTAATTATTT CATAGAAGTG GATTCATACA GTACGTGTCC TTCTGTGTCA 540
GGTTCATGTC ACTCAGCGTG ATGTGCCCAA GGTTCACCCA TGCGTCGGGC TCTCATTCCT 600
GAATCGCATT TCTCTGTACG GATAGACTGA GTTTTGTTTG TCTGTTCACC TGTTTAGGAA 660
CACTTGGTTG CTTCCACATT TTGACTGTTA TGAATAACGC TACTAGCAAA GTGAACACGA 720
GTGTGGTTTC AGTTCCTGTT TTCAATTCTT CCGCGTCTTT TAAGAAAAAA CAAACTGTTT 780
TCAACAGTTG CATCATTTTA CCGTCCCACC AGCAACATGG GAGGCTTCCC ATCACTTGTT 840
TTCTTCATGT TTGTTTTGTT TAGTTGCATA ATAATTGCCA TCCTAGTGGA GGTAAGAAGG 900
TATCTCACTG TTCTTTTCAT TTGCATTTTT GTAATGACTA ACGAGGTTGG GCAACTTTTC 960
ACGTGCTTGT CAGTCATTCG CATCTTTTTT TTTTTTTGAG AAATGTCTAT TCAAGTCCTT 1020
TGCTCATTTT GAAATTGTGC TGTTTGGGTT TTGGTTGTTG ATTTGAAGGA GTCCTTTTTA 1080
TATTACGTAT ATGAATCCTT ACCAGATATA TGATTCGCAA ACATTTTCTC CCATTCTGTG 1140
GTGATCTCTT CAGCCCCTTG ATAGTGTCCT TTGATGCACA 1180
|
