Tag | Content |
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EnhancerAtlas ID | HS102-18285 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr5:80286050-80287370 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr5:80286989-80287000 | GGTGACTCATG | + | 6.62 | HNF4G | MA0484.1 | chr5:80287339-80287354 | AGGACTTTGACCTTT | - | 6.08 | Hnf4a | MA0114.3 | chr5:80287337-80287353 | ACAGGACTTTGACCTT | - | 6.62 | JUND | MA0491.1 | chr5:80286989-80287000 | GGTGACTCATG | + | 6.02 | RREB1 | MA0073.1 | chr5:80287119-80287139 | AGTGTGTGTGTGTGTTGGGG | - | 6.63 | RREB1 | MA0073.1 | chr5:80287121-80287141 | TGTGTGTGTGTGTTGGGGGG | - | 6.69 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 80286128 | 80287179 | chr5 | 80286375 | 80287263 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I080989 | chr5 | 80285676 | 80287424 |
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Enhancer Sequence | TATTTTCTTT TTCTGCTCAC TGGAGCATCA TTGATTAAAC TGCACAAAGG CACCAATGTG 60 TTGTTTAGTG GTGGCTTGAT TTCCACGTTC TGTAGGAGGT AGGTGAGCTT CCCTCGTGCC 120 CAATTTCATG TCCAACCCAG AGCCAATACT TGGAATCCTG AGAATTTTCC AAATACTCTT 180 GTCATCCTCT TGCCAGTGAA AGGAGTCGGG AGGGGGCTCC AGGAAGAAGT CGTCTAGACC 240 CCCATTGCTA AGCCAAAAAA TTTCTGCTGT TAGGGCTTCC TATCTGCCGG GGGCATTTTC 300 CCTTCTCTAG CTGGCTTCTG TTAGGAGCTC TTTGTGGCAG GAGCCCTGTT ATGTTGAGCA 360 GGGCTGTCGG TCCACACCTT TGCTGCCTCA CCCCAGTGCC CCACTGGGCT CCTGTTTGGT 420 GTTGTCCTTT TGTACTTCCA GGCTAGGTTT TTCCTTCCCA TGGGTTGAAT TGCTGGCTGG 480 CTGGCGTCTT TCACATTCTT GTGGTTTCTA AACTCCAGTG GGAATTCCTT GGTGTAAATC 540 TGGGAATGAG CACAGGTAAG GACAGTGACT TCAAATGTCC ATTGTACACT AGAAGTGCTG 600 ACTGTTCTAG TACATGAAGG TTCACAAAAG GTGAGCTGCA TAGCTCAGGT TAGTGATAGT 660 GCTTTTGTGG GTCATAGGAG TTTGTCAGTT TGTAGGTCAT AGGAGTTTGT CAATTAGACT 720 AGAGCAGGAA AGTTATTTAC CTTGAGAAAT GGCATAATCT CATTTTTCAT ATCACTGTAG 780 ATGTCTGGGA CCCATTATTT TTGTCAGCAC TTCTTAATTT TATAAGTTCA CTGACAGAAT 840 ATCTGAACTT CAGGTACCTT AGAGCCAGGC CTCTCAAACC TTACAAAGAT CTGCAAATCC 900 CCTGGAGGCC TTGTAAAATG CAAACTTGGG GCCAGGTGTG GTGACTCATG TCTGTAATCC 960 CAGCACTTTG TAATGCCAGC AATTTGGGAG GCCAAGGCAG GCAGATTGCT TAAGCCCAGG 1020 AGGTTGAGAC CAGCCTGGGC AACATGGTGA AACTGCATCT CTACAGAAAA GTGTGTGTGT 1080 GTGTTGGGGG GCCTGAGGTG GGAGGATCAT TTGAGCCCAG GCGGTGGATG TTGCAGTGAG 1140 CTGAGATGGT GCCACTGCAC TCCAACCTAA GTGACAGATG AGACCTTGTC TTTCAATAAA 1200 TAAATAAATA GCAGAATCTC AGGCAGGACC TGAGAGTCTG CATTGCTAAC AAGGTCCAGG 1260 AAGACCTTAT CAGCCTTTTC TCACTCAACA GGACTTTGAC CTTTTTCACC TTTTTCCAGT 1320
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