| Tag | Content |
|---|
EnhancerAtlas ID | HS193-15157 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr18:9869570-9870980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr18:9870048-9870058 | TGACCTTGAT | - | 6.02 | | RUNX1 | MA0002.2 | chr18:9870654-9870665 | TTCTGTGGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09176 | chr18:9868542-9871041 | CD14 | | SE_39869 | chr18:9868511-9871949 | K562 |
|
| | 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 |
| GH18I009868 | chr18 | 9868041 | 9871892 |
|
Enhancer Sequence | GACTTTCTGA TCAAGAGAGA CAAAAGTCAA AGATCAGCTA CTACTGTTTT CTCCTTTCTT 60
TCCTCTCATT ATAAGTGCTG CACATAATAA AAGAATGAAG AAAAGGAGAT CCATGATTAA 120
TGAAAATTTC CCAGGAGCTA CTTTCAAACT GTATCTCATT TTATCCGCAA AACAAATCTG 180
AGATAGATGT GAAATTGTTC TCCTTTTACA GAAGGAGCAT GGAGAGCTTA AGGGACATAA 240
GGAGGGCAAG TGCATTCATG CGGAGGTCCG TCCTATGTCC TATTCCAAAA CCCATTGTTG 300
CATCTCAAGA GGAAGTTTTG ACAGGGGAGT TAAGGGTTAA CCAGCTCAGG CTGGAAATGC 360
TGAATCACCC AATTAAAGGA GACTTGCTGC TTTGATGGGA AGGTCTGATC CAAAACTGCT 420
GGGGTGACTC TCCTTGACCC TACCGTTTGG GCAGCTTCAT TTATCTTTTC TGTGTCCCTG 480
ACCTTGATGT TGAAACCATT ACTCAACCCT CAGTGAAGTT CTTAACCGGC TTTTTTGAAA 540
TGACTCATGC ATCAAGGTCC AGCCATCTTG ACTTTGTAGG GCCCGATGCC CTGAATTAGC 600
TTCTGAGAAC CCAGTGCCCA AACTGGTGTC CCCAGGTGGG CCTGGCAGAC CATAGGTGGC 660
AGCTTTCTCG GTTCTCCTTC ACTTCACTTC TCTCTGGATG TGTGCGTGCT TTTTCTCTCA 720
TTGCTAAGGC ACGCCCCAAG CTTTTTGCTT ATTTGTTTTT ATTTTCATCT TAAAATCACC 780
CATGCACTGT TTTACCCCTC CCATCAACCT ACCTATATGC ATAAATCTTC TCTAGTTTTG 840
ATCAGCTGTC TTTTTTTCCT CCTCCAAGCC ACCCTCTCTT CCCTTCTCAC TAAAGAAATT 900
CTTAAATGAG AATCATGATG TACTCACTTG ATCATCTAGT CACTGCTCGC CTGAATTCAG 960
TCCCTCCCCC AGCTCTGCAC TTTCAAAGCC TATCCCCTCT TTCCACTCTC CACTCTCAGA 1020
GGGCAGGTGA AGCTGTGGGC CCCTCTCTCC CTCCTGGACC CTCCTTCTCC AGCCCAGAAG 1080
CTGGTTCTGT GGTTTCTGCA CTTCTTTTAC TGCCCTTTTC ATTTTCCTTT GCTGGCTCTT 1140
CTTAGAGCTT AAATGCAGGT ACTTCCTGCA AACGTGTGTT CCTATTTCTC CTCAGTACAC 1200
CTTCCTTCTG ATTTCATCCA ACTTTATGGC TTCAACTATT GCCTCTGGGT GTCTGGCTTC 1260
TACACTGTTG TCTAGCCTGA CTGCTTTCCA GAGATCAGAG CTTGATTTCC AGCTGCGGAA 1320
TGGGTGTACT GAAGTCCCCT CTTGCATGCA AATAGTGTTG CACCTTGTTA ACAATGCCAT 1380
TCCTGCGCTG CATTCATTCT CTCAGAGGCT 1410
|
