Tag | Content |
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EnhancerAtlas ID | HS102-18537 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr5:130945450-130947000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr5:130945799-130945810 | AAACCACAGAC | - | 6.62 | Stat6 | MA0520.1 | chr5:130946453-130946468 | TCTTCTCAGGAAAAG | - | 6.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 130946811 | 130946985 | chr5 | 130945814 | 130946423 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I131609 | chr5 | 130944721 | 130947124 |
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Enhancer Sequence | GAACGGCCAG TAGTTCATTT CACAGTGATA GATATCTATA TTCTGGGTTT GGGTTTATCT 60 TACTTACCTC AGAGGTTCAG CCAGGATCAT AATCCAGGGG CTTCCAGAAT GCCTGAACCA 120 CAGGACTAGA ATCCCACATA CCAGAGTCCA ACCAGTGGAC CCAATTCAAA GCAAACACAG 180 GAGTATGATC ACAACCTTGG GACCACTAGT CATATCACAT ACCACACAAT CCAGAAGCAA 240 CTGGCCTCAC AGAACGCTGT AATAACCTTA TAAAGGCATA GCTGAACTTT CAGCTTAAAG 300 GCAATAATGT GAAATAATGG AATGACACCT TTTAATATGA AGATACATCA AACCACAGAC 360 CTCTATATGG AGCAGTGTAT ACAGCAGGAA GAACAGATGG GCCTAGAAAC AAATGAGTAG 420 AAGCAAGAGT CACCCATTTA TCATTATTCC CAATGAGCCA CAAAGGGATT TTGTACTTCC 480 CATTCCTACA GCTATGGACT CTGCATGTTT GCAGGTCCTG GTTCCAAAGG CCTATACTCT 540 TGCCAGGCAA CAGTACAAGA GTCTCAGTGA ACAAGTTTAC AGCTGCCACC AGGGCACTTT 600 AAACACCAGG GCCCAAGAAT CAGCAGGTAA GAAGAGTTGC CATTTTGGCA GGGATAACTG 660 ATCCTGAGCA GTAGGTGGAC GCAGGGCTGC TTTTATGTAA TGTGAACAGA GAGGAATGTG 720 TGGAATCCAC ATGACTCGCT TGGTTATTCC TTTACCTCAC TGTAACTGTA AACGGATATA 780 TATCCCAGCA TTAGCCTGAG AAGAATGATT ACCAAGGGTT CAGACATTTC AGGAAAGAAG 840 GCTTGAGTCA TACCAACATA TAAGCCACTG AGACCTGCAG AGCTGATTAT GTGAGGAGAA 900 AACAAAATGC ATAGTGGAGG AGAGAGGATA AGTACCAGTT GCAACCCCGA GATCAACCAT 960 ACAGGGGCTA TAATTCTTCC CACCACCATC TCTTGTCTAA GTTTCTTCTC AGGAAAAGAA 1020 GCTCATTGAG AGCCATGGAG GAGCTGCTCC CTGAACTTCA AACCTATGTG AAGAAGTAGA 1080 TTTGTGTGGT GCAAAGTGTA AGCTCAGGTG GCCTTGAAAA TATGCCTCTC AGATTCCAAA 1140 CTACAGGGAG TGTATTTGAA CAAAATCCCT ATTACGGGGC TCTGTAATTT ATCAACATGT 1200 TTGAACTGGG GCCCAGCTTC CCATGCGATA CTCCCAATCA ATAACTGAGC CTGGTAAAAA 1260 TACTAAGGAA TGCCTGTTCT GGGAGACTCA GGAATACTCT GATGGGTTCA AGGATTCTCC 1320 TTCCACCTTG CTAAACCACT GTTACAGTGC AGTCTAAGGC TCTTCCACTC AAACTTCCTT 1380 TCGTCTCTCC TTCACAAATG TCACATGAGC ATTCTGGTGT GAATGCTCTA CCAACTCTCT 1440 CCATTTTTGC TCAGAGGCAT TTTCCCTAAT AAATTCCTTG CATGTCTAAT ATTGTTGTGA 1500 CAACTGCTTC TAACAGAACC CAGACTAACA CGAACACTTT GTAGTATTCA 1550
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