| Tag | Content |
|---|
EnhancerAtlas ID | HS091-21918 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr18:11937700-11938880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr18:11938058-11938077 | TCCCCAGCAGATGGCGCAA | + | 6.19 | | IRF1 | MA0050.2 | chr18:11937767-11937788 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
|
| | 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 |
| GH18I011938 | chr18 | 11938001 | 11938150 |
|
Enhancer Sequence | TGCAGTGAGC CAAGATGGCA CCAGTGCACT CCAGCCTGAG CAACAAGAGT GAAACTCCGT 60
CTCAAAAAAA AAAAAAAAGA AAGAAAGAAA TTAGCTATTT TTCAACTCTA TTATTTAAAC 120
CCTCCTTAGG GCATCCTTTG GAGTGACAGC AGACAGTGAC TGGGATAACT CTGCATATTT 180
TGGCTTAAAA TTATTTTTAT CTACTGAAAG GAAAACTAAA TTATACTCTG AAACATAATC 240
TAATGACGGA GGGTCTCAGA GCAAATAGCT GTTAGTCGGA GATATTGAAA GTGATCAGGT 300
TGTGAACTCA CTTGAATCGA GCCTATTACC TCATGAAATT ATAAAATGAT TAGCAATGTC 360
CCCAGCAGAT GGCGCAAGTG GCCCCTCTGC TGTGATGGGA AGCCAATCTG TTTCCTCTTC 420
ATATGACAAT TGAACAGTAG ATCCTAACCA GGTAAGGTGT TTAGTTAGGA AAGAAATCAT 480
TCATGGGATT CCAAGAGAGG CTAACTAGGA AAGACAAAAT CTGGAGGCTT TTTAATTTAC 540
TTCTCATGTT AAACAGTCTA GGAGCATGTA TTGACCTCAC CAGTAATATG GTTCCATTCA 600
CAATATTTTT AGCTCTGAAA AAGAAAATTC TCTCATGACA GAGTTTTAGA TTAAGTCCCA 660
AAGGATGACA AAGTACCAAC AATTAGAATA TCTGAAATGT TTTGATGAGC TGGTGGAATT 720
AGTGAAGGGC TCATAATGAG AAGCTCAGAG CTGTCTCCTA ACAAATTACA GGTAAACGGT 780
TTCTGAAGGA AACTGCAGGG AAGGGGATAA TGATTAAAGA TTATTGGAGT CAGCCAATGT 840
TTCTGCTGCT TTGCTAGTTA CTTGCAAACA AATATGATGT TCTTGCTCAC ATTTTGAAGC 900
TCTCGGCTAC GCATTTTTTA CGAACAAGCA AACATTTGCA TTTCTAGGCC AGAGGCAGCC 960
CACGCTGGGA AGGCAGGGGA CGGAATGTGT TATCCATCGA ATAGTCTTCG AAAGTGCAAA 1020
AGAACTTTAT TAATTAAAGC ATGTTAAATA TCTGCCTTTA TAACTTCCAA AGAAACAAGA 1080
ATTGAGAATG TTCAGGTCAA TGAATAATTT TGTGCAATAG CTGTCCTGCC AATACCTACT 1140
GCCTTCCATC CCAAACACCC ATCAATGTTT TAACCCTCTG 1180
|
