| Tag | Content |
|---|
EnhancerAtlas ID | HS067-01122 |
Organism | Homo sapiens |
Tissue/cell | GM18522 |
Coordinate | chr11:268690-270020 |
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 | CGGGGTTTCA CCATGTTGGC CAGGCTGATC TCGAACTCCT GACCTCAAGT GATCCGCCCG 60
CCTCTGCCTC CCAAAGTGCT GGGATCACAG ATATGAGCCA CCGCGCCCCG CCCTTGGCAC 120
TGTTTAATCC ATGTGTTGTT TATTTATGTA TCCTGTTTAT TTTCTGTCTC CCAACAAAGA 180
CGTAGCTCCT TCTGGGTAGG GCATTTTGTT CATGCTCTCA GATGCCGCCT ACCGCCCTAG 240
AGCAGGAAAT AGCGGTCAGC GCCAGCTGTG AGGAGCACAG CATTGCGGCC AACACAGGAG 300
GCACTGACCA CGGGGCAGGC GCTATTTAAA AATCGTGGCA AAGGATCAGA CGTAACAGAA 360
CTCTTTTTGT TTTAATCATT TTTAAGTGTG CAGTTCAATG ATGTTAGTTA CATGCACAAT 420
ATTGTGTAAC CATCACCACT ATTTCCAAAA TCCTTTCTAT CCGTCAGACA GAAACTCCGT 480
CCCCATTAAA CAGCAACTCT GCATTCCTCC GTCCCCCCAG CCTCTGGTCA CGTGTCTCAT 540
CTACTTTCAG TCTCTACGGA TTTGCCTGTT CTAATTATTT CATAGAAGTG GATTCATACA 600
GTACGTGTCC TTCTGTGTCA GGTTCATGTC ACTCAGCGTG ATGTGCCCAA GGTTCACCCA 660
TGCGTCGGGC TCTCATTCCT GAATCGCATT TCTCTGTACG GATAGACTGA GTTTTGTTTG 720
TCTGTTCACC TGTTTAGGAA CACTTGGTTG CTTCCACATT TTGACTGTTA TGAATAACGC 780
TACTAGCAAA GTGAACACGA GTGTGGTTTC AGTTCCTGTT TTCAATTCTT CCGCGTCTTT 840
TAAGAAAAAA CAAACTGTTT TCAACAGTTG CATCATTTTA CCGTCCCACC AGCAACATGG 900
GAGGCTTCCC ATCACTTGTT TTCTTCATGT TTGTTTTGTT TAGTTGCATA ATAATTGCCA 960
TCCTAGTGGA GGTAAGAAGG TATCTCACTG TTCTTTTCAT TTGCATTTTT GTAATGACTA 1020
ACGAGGTTGG GCAACTTTTC ACGTGCTTGT CAGTCATTCG CATCTTTTTT TTTTTTTGAG 1080
AAATGTCTAT TCAAGTCCTT TGCTCATTTT GAAATTGTGC TGTTTGGGTT TTGGTTGTTG 1140
ATTTGAAGGA GTCCTTTTTA TATTACGTAT ATGAATCCTT ACCAGATATA TGATTCGCAA 1200
ACATTTTCTC CCATTCTGTG GTGATCTCTT CAGCCCCTTG ATAGTGTCCT TTGATGCACA 1260
AAAGATTTTA ATTTTGATGA AGTACAATTT ATCTTTTTGT TGTTGTTGTC ATTGCCCATG 1320
CTTTTGGTGT 1330
|
