Tag | Content |
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EnhancerAtlas ID | HS095-13917 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr18:47625720-47627290 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPIB | MA0081.2 | chr18:47627197-47627209 | GATGCGGAAGTG | + | 6.74 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 47626417 | 47626670 | chr18 | 47626028 | 47626149 |
| | Number: 1 | ID | Chromosome | Start | End |
GH18I050099 | chr18 | 47625771 | 47627215 |
| Enhancer Sequence | CAGCTGTTTG ATGTTCCAGA GTGGATAAGT GACACAGGAA GACTGTGCTT CAAGGATACT 60 TAGCAACAGT GGGACACACA GTAGAGACTT AGGGAACAGG AGGAACAGAA GTCTAACAAG 120 ATGCCATGGT TCCTTCCACT CCCAAAAGCC TGGCTTAGAT GCAAAGCCAG CCAGTCAGCC 180 AGCCTTGTAA GTAAAACGTA GTTGATTCTT GGGGTTCTAC TACCAACAGG CCACCACAGA 240 ACACAAGGAT CTTACTCTAA GTGAGACATT CTCAATTAGG GGTGATTTGG GCCCCCAGGA 300 AACATATGGC AAGGACTGGA GCTTTGAGCT GCTTTTAAGT GGTGGGGATG AAGTTCCACA 360 TAATTTCAGC AACCATCTTT ACATGAATTT GCAGAATAGT TAGCTGAGAA ATACACGGTA 420 TCTTGTACTT ATGTTCCCCC TGTAAAGCCA ACTGGCTTCG TTGATGCCAA TGGGCACCTG 480 ACATTAGATA TATAAACTTT ATCCTCCACC AAAAGGGCTA AATATAGACT ACTATTTACT 540 AGGGCCCGTG TGTGCCTGCC ATGGGTTCAC TGGGCCAGTT CAGGACACTG GACATAGGAC 600 CAGGGCTCCA CAGTCTACAC ACAGATTCTC AGTGTCCTAA AGCAACCTTC AGAGATTTAC 660 CTCCCACATC ACTATAGGTG CCTTCCAAGC TCAGATCCAA GATACACAGC CAAGATATTT 720 CAGCAACAAC CTGGCTAGAA ACCGGAAGAA CACTATAAAG TCACATGCAC ATTGGTCCAA 780 TGACAGAAGG AAGGAGCTTA TTTTCTTTTC TACATGAGCA CATCTGTTTG GATATTCACT 840 AGAGTAAATA CTTAAATGAC TAATTCACAG TTTCACTTTG TCATGGTTAA AGTATTTTAT 900 GAGACATCTG CTTCTGCTAA ATCAGGATCT TGTTTCCTCC TGAGCTGTCA CACTGAAGGC 960 AGGAACATAT GATGCTGGTT GTGTTGCACC AGCAAAAGCT TGAGAGAATA ACCTTTTCAG 1020 ACACAAGACT CCCAGCTTCC TTTGGTATCT GTGAAGCATC TATTACTGCA AGTCAACAGA 1080 CCCACTGACC ACAGGAAGAC CTCAACTAGT GCACAGAATT ATGCTTCAAC TATATTCAAG 1140 TGAGAAACGG CCTGCATGGT ATGGAGGGAA GGGAAGTTTT ACCCCTCTGC CTACCACCCT 1200 CCCCACTTTC TACTTCTCTC CTCTTTCCCC AAAGCACATC GTACTGACTG GTCAGGGTCC 1260 AAGACATTAC CTGGTACTAG CTGTTGCTCA GGCACAGTCA CTGGGGGCCA AAAGCCACAT 1320 ACTATGCATG CATCTCCCCT CTCTTTTCCA GGTCTAGGGA TCAGCAAACC AAACCAGAGC 1380 TGAAGATTCC TCCTAAAGCA CTGGGCTCTT TCTCTGCTCT CTTCTTCTTG TCTTTGCTTT 1440 GCAAGGAACA ATCAATCAGA GCATGGCAAG ACCCCTAGAT GCGGAAGTGG CTGAGGGAGA 1500 GCTGGAGCCA GCAGCATCAC CCGAAACTGC AGTTTCCCAC CCAGAACTCT GCTTTGGGAG 1560 GGACAGGGCT 1570
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