Tag | Content |
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EnhancerAtlas ID | HS104-01011 | Organism | Homo sapiens | Tissue/cell | HUVEC | Coordinate | chr1:26428360-26430030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZIC1 | MA0696.1 | chr1:26429857-26429871 | CACAGCAGGGGGGA | - | 6.42 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 26428669 | 26428883 | chr1 | 26428974 | 26429346 |
| Enhancer Sequence | GGCCTTGTGG AGTCTACAGG TTTGTCCAGG GTCCAGGAGG TCAGGACCAT CGAGAGGCTA 60 AGTGTGGTTA TCTGTGCCTC CTTCCCAGCC CCTGCTCTAA ATAACCATAG AGCAAATATT 120 TGAAGAATGT CAGCTTAAAG GAGTGTCTCA CTCTGACCCT CAAATTTCTA TTTATTTTTT 180 AAATTGACAA AAATTGTATT TATTTACTCA TATGTACAAC ATGATGCTTT GAAATATGAA 240 TACATTGTGG AATGGCTAAA TTTAAGGCCC AGTGTAAATG CTACCTCCTC TCTAAAGCTT 300 TCCTGCCCGC CATTCCCCTC CACAGAAGCA CAGTTTGGAT TTCCTCCCCT GGGCTATGTA 360 ACCTCAGCTG GCACTGGTTG AATTGTACTG TCTGCATATT TATATGTCTG TCTCCCCTCC 420 CAGAGAAAGT CCATGAGGGC AGGGACCTTA TCTTTCTGTT CACTGCTTTT TCTCAGCATC 480 AAGCACAATT TCTTGCACGT GGTGGATATT CACCAAATAG CTGTTGACTT AACGAACAAA 540 GTGCCACCAT GTGCCAGGCA CTAGTTGACT TCTGAAGAGA GGGGTATATG TCAAGACATT 600 TGTTAGCCAC CCACCAGCCT CTGAATTTAA GCCTGCCAGT AAGCCCCATC CTTCAGGACA 660 CAGAGCTTGG TCAAGGAGGG GCCCACAACC CTATCTCTTA CCCCCTACTC CCTAGCCCCT 720 AGCCAATCAG GTCCAACAAG ACTTAATTTC AGGAATGTTG TTTGAGGAAT AGAGAAGTTG 780 ACTTTCTCAT TCCTGCAGGA TATGATCTCA TAAGGCTGAA TTCCCACTGG TGACCCCGAG 840 GCCCACAAGG GAAGCCAGCC TTAAGATGAA GGCAGCATCA TGGGAGGCAG AACAGAGGAA 900 ACTAGAGTCT TTGGTGACAT GTGAGCTGCT GAATCAAACT TCCTTCCCGA AGCTAGCCCT 960 CCCACCTCCA TTTCTCTTAG GTAAATGTAC CAATCATTCC TTTCAGTCAC TTTGAGTTGA 1020 GTTTCTGCTC TTGCAACATG AAGCATCCAG AAGAGGCCAG AGAATCAGAG GAAGCCGAAG 1080 CTTTAACACT TCAGGACCTG CTGAGGAGTC GGGTGAATCC TCAGTTTGGG ACACTCCCAA 1140 CACCCCCATC CAGCATGGTT TTCAGATGGT GGCATCCCCA GCAGCTCTTG GACCCAGGGG 1200 CAGGAGATGT GAACCTGGGT CTTAACCATC AGCTGCTCCA GCTGTTCTCA GTCCTCACCA 1260 AGAAGACAAC TAGGACCCAT CCAAAGACAA AAACAGCTAA TGTTATACCT GGTGCAAGAC 1320 CTTTGTGGGC CCCCAGATCA CTTGTCTCAG GGGCTGGATC AGAAATAAAC ATTTTGATCT 1380 TCTTATTACA AGCATAGTGG AGGTGTAGGA TTCAAGAATC AGAGTGTTGG AGCTATAAGG 1440 ATCCTTAGAG ATGAGCTGGT CAGACCCCCT CATTTTGCAG ATGGGGAGAC TGAGGCCCAC 1500 AGCAGGGGGG AGTCTTTCTT GCTCAAGATG ACACAGCGTG TTAGTGCCAA AGCTAATACC 1560 CTTCCTAAAG GAGTTTCTCC CTCAGCCTCC CCCTGCAGAA ATGGGGCTGG GGTGGCTGGG 1620 CACAGTGGCT CACGCCTATA ATCCCAACAC TTTGGGAGGC CGAGGTGGGT 1670
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