| Tag | Content |
|---|
EnhancerAtlas ID | HS091-22214 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr18:33596820-33598220 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr18:33597819-33597838 | CTTCCACTAGATGGCACTA | + | 7.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr18 | 33597401 | 33597530 | | chr18 | 33597543 | 33598157 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH18I036017 | chr18 | 33597564 | 33597964 |
| Enhancer Sequence | AAAAAGACAC TATATAAAAT GACATGTACA GTCTGATTCT ATCCTTCTAA ATCTTGCCAA 60
AAGGTATTCA ATGGGTGATA AAAATTTTGG ATGGTATCTG CATGTGCTTA TCAATGGTTT 120
TTCAACTATG ATAAGCATGT ACTACTTTTG CAATAAAAAA AAAAACTGCC AGGTGCAGTG 180
GCTCACACCT GTAATCCCAA CACTCTGGGA GGCGAGGGCA GGTGGATCAC CTACCTGAGC 240
CCAGCAGTTC GAGACCAGCC TGGGCAACAC GGTGAAACAC TGTCTCTACA AAAAGCACAA 300
AAATTAGTCG GGAGTCGTGG CACTCGCCTG TAGTCCCAGC TACTCGGGAG GCTGATCACC 360
TGAGCCCTGG GAGGTCGAGG GTGCAGTCAG TCATGATTGT GCCACTGAGC TCCAACCTGG 420
GTAACAGAGT GAGACCTTGT CTCAAAACAC ACACACACAC ACTTCACTGC TACCACCCAC 480
TGTAGTTCAG GCTTTTACTG CTGAGCACAT TTTTCTAATT AAGTTGCATC TGGTCTCCCT 540
ACTGCTAATC TCTCTCCAAT CTAATCCACT CAACAACTAT AACCATTTTC AGACACTGCC 600
AACACCACCA CTCCTTTCTT CCCTTTGGCC TGTTATCAAC CTCTACTGGG CCTGACATTC 660
AAGTGCCCTC CACAATGTGG CTCCAAACTA CTTTTCAATC TCATCTCACT TCTAAGAACT 720
GATACAGTAA CAACAAAATG TAATCTTTGT TAGCAGTTTA TTAAGGACTT CGTCTCAAGA 780
AAGCGTAACT GCCTATATGC ATCATTGTTT TAACCATCAG AGTTCTATGA ATGCCTCTCT 840
TGACAGTAAT TAGCATTAGT ATTGATATTA CATTTCCATT CCATGAATGA GTGAACAGGC 900
ACAAAGGGCA ATAGAGTGTA AATTCCTCTC TGTTACATAC TTTAACGTAA AAGAATGAAC 960
ACTGGCTTAA GGACTCTGGT TTCATCTGTA GCTCCCGCTC TTCCACTAGA TGGCACTATT 1020
ACTCTTTACA AATTCAGTAC TTATACAATG CTAAGGATTA CTACTGTTCA TTTCTTATTC 1080
ACGTTATTCT CACATATTGT TAGTGTTATT CTCCTACAGA AGGGGAAAAA ATGCAAGCTG 1140
GTAAAATAAT TTTACAATTT CAAGACGATA ATTTACTCCT TTGTTCAAAA TGCTCAACTG 1200
CAGCTCTACA AACTGCATGC CTTGAACACA CAGCCCACTT AAGACTTTTT AAGTACTGGA 1260
CTCTGCTAAA ATGATTTAAC CAATTATGTT GGATATAATT TTATTCAAAA TCCTCAAGTG 1320
TCTTTCAATC ATTTTTATTT ATTAAAGTAT CATTCTTTTC TGATTTAGCT ACAAGTAAGT 1380
TACCAATTTT AAATATATAC 1400
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