Tag | Content |
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EnhancerAtlas ID | HS095-13996 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr18:55679950-55681490 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr18:55680856-55680872 | CCCAAAGTAAATAATG | + | 6.12 |
| | 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 |
GH18I058012 | chr18 | 55680017 | 55683278 |
| Enhancer Sequence | TATTTCAGAA CTCAAGAACC TTTAGCAGAT TTCATATTTA ATATAATGTC ACCACTAGTT 60 CAAAATCTAT ATATAATAAG ATAGAAAAGG GCACCACTGG TGCTGAAAAT GTCACGTTGA 120 AGAGAACAAC GAAGAACACA CAATCATCTA CAGCCTTCTC ACTCAGCGCT GTCAGGAACC 180 AACAGCACTG GCACCACCAG GAGCTTGTTG GAAATGCAAA ATCTTGGGTT CACCCCAGAC 240 CTGCTGAATC AAATCTTTAT TTTCACAAGA TCCCTGGGGA CTTGCATGCA GGTAAGATTT 300 GAGAAGCACA GGTCTAAGGT ATTTCTCTAT CAATGAACAG AGCAATGGGT AGAGCAGAGG 360 AGAGGCCCAG AAACTCAGAG TTCTGGTGTT CCTTGCATGG CCGTTGAAAA CTGTCCCTAA 420 CCTCTCTGGG TAGCAGCTTC CTCAAGTATA AACTGAGGCT CTGGTTGAAA AGGCTGTTGT 480 CATAAGCTGC TGACACAGAG CTTTTTTCAG TCCCAATTGT GTAGGACAGC TTGTGTGATG 540 AGAATTGAAT GACATGCATA TCACACATTT GGTATGCTCA ATGAATGCTA TTAATAAAAT 600 TGTGAATCAC AAATGTTACT CCCATTTCCT TCCCAGCTCA GGGAAGAAAC GGTATGCATG 660 ACATGATGCA TTGAATGGGG CAGCCTACAT CTACTTTGCC TCCTGAGAAT ATCCTGAGCA 720 TCAGGCCAGT GTTGGCTTCG CCAGGAATCC TAACTCAGGT CTTGAAAGCA AGATTGTTGC 780 TGTTAAAAAG GTGACATGGG ATTTTTCTGT TTCCTCATTA CATTGCTTTA GTTTCTCCCT 840 GCCTGAAGCT TCTTTAATCT GTAGGCTGTG GGCACCACCT TTAAAGTTTT GACTCACATT 900 ATCTATCCCA AAGTAAATAA TGACTAAAGT GGTGGCAAAG TCAACACATT CTTTGAAAGA 960 CAATGAATCT GGGTGTTGAA TGAAATCAGA TGCCAGGAAT ATATACATTG TTGTTACAAC 1020 GCTATTACAC AACAGGCCTT AGAAGAATTC CTTTTCTCCA GGTAAAAACT ACCCCCGTAC 1080 CAGTTACTCT GGGTGAAGAA AGGCGTCTAT GTTTGGCAAG GACTAAGGAA TATTTGACTT 1140 CATGAATCAA TAACTATTCT CAAAGCTGCT ATTGACCTCT GATCTGCAAA TCTGTCAGCA 1200 AAGAGAGATT ATGGTAACTA TACTGCTAGT AAAATGCAAA CCTGTTGGTT AAACATTTGC 1260 TGAAAGCCCT GCTAGTGACC CCTGTTAAAG TGAACCAAAT TTGGCCACGT GTTCTTGCAA 1320 TGTTCTGGAA CATCAGAGAA AAATAACTGC CTGACCCAAC ACAGCTTAGC TCCTAGAGAG 1380 CTAAGAGATT TCTCTGGGCC AGAAGCGTTG GCAGGGATCA TTCCTTTCTC AGTCTCTCTC 1440 TTCTACCACT GGGCCCGAGT TAGTGGGATC TGTTAGGAGG TTTTTGAATA ATAATGACTG 1500 TTCTCAATCC TTCTGAAGAT TCTCAAAATT AATTTCTTCT 1540
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