Tag | Content |
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EnhancerAtlas ID | HS023-14902 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr2:136549510-136550960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr2:136550941-136550953 | GCAATCACTGCA | + | 6.14 | ZEB1 | MA0103.3 | chr2:136550022-136550033 | GGGCAGGTGGG | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 136549992 | 136550234 | chr2 | 136549800 | 136550600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I135791 | chr2 | 136548983 | 136550615 |
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Enhancer Sequence | CACATTGTTA ACTGTTGCTC CAAGAACTAC TGCTGGAACA TACCAGAAAA ACCAAAAGAA 60 TTCACAGACC TTTGAAAGAA GCAGAATGCT ACTGCAAACT CCATGAGACA GCTGCAAAAC 120 TGTGAGTTCC CAAAGTGTGA GAAGGGGAAA GTCTGCCTCT GAACACACAT CCTCTCTGGG 180 GACCTGAACA TCCAGATCAT AGGAGAAGGA TTTAACCTTA CCTAGAGCGC AAGTGGATTT 240 AGGGAGCCAA GTGAAATGTA AAAGTAGAAG AAGCAGTGGG AAGAGCCCTG TAGCCACTCC 300 CTGTCCCCAG CTTGAGCCCA GGGAAGCCAT TCCTGACTTT ATCCTACAGG GGTCCTTGTA 360 GAAGGAAGCC AGTGGAATTA GGGAGGGGCA GGATTAAGGA AGCTTCTAGC TCAACTTATT 420 AATTTCAACT AGAAGCATGA ATTTTCCTGA GCAGAATCTT GGGGGCAAAC AAGAAGTGCA 480 GATAAAAGCA CAGAAGCCAC AGCCAACAGT GTGGGCAGGT GGGGAGGGGC AAGGCCTGAA 540 AGCCCTGTTT GCTTTCTCAG AGAGAAGGCT TGTGGCCTGG GGTGAGATCT CTGCCCTGCG 600 CACTGTTGGC AGGGCACAGC AGGAGTGAGA CTGGCCTTGC TGGCTGCATG GGAGCTAGGT 660 GAGGCTTGTG ACTGCCAGCT TTCCCAACTT CCCTAGCAAC CTGTATGACA CAGCAGAGGA 720 AGCCATAATA CCCCTGGGAA CAGAACTCCA CTGGCCTGAG AACCAGCCCC CTATTCCCCC 780 ACAGTGGCCA CAGCAAGCCT CACCCGAGGA GAGTCTGAGC TCAGATATGC CTAATGCTGC 840 CCCAACCTGA TGGTCTTTCT CTACCTTTGC TGGTAGCTGA AGACAAAAGA CATAAACTCT 900 TGGGAGCTCT ATGGCCCCGC CCATAACCTG AGAAACCCAA ATACCCTGGC CAACGTAGGG 960 CAACCTTGTA ATCCCCCTTC TACTACCGCA GCTGGTGGCA GTGGAAGGGG AAAGCACCTC 1020 AAAAGTGCCA CCTCCTCTCT TGAAAGTGCC ACCTCCTGGC TGGAGACCAA CCAACTCACG 1080 CCATTATAGC AACTCATAAC AGAAGAACCC TGCTCCAAAG AAAGAGAAAA CAACAACTAA 1140 TTCCACTGCC TGCAACATCC TGGCTAACCA GAGGTCCTGA GTCTGTCCAC ATGACAACTT 1200 CACTGCTCGC ATAACCAGCG TTTGAGAAAA CCAGTGCACG AAAGAAAACT ACAACCAAGG 1260 ACCCTCACAG AATCCACTTA AGTCCCCTGC CACCTGCACT GGAGCAGGTG CTGGTATCCA 1320 TGGCTGGGAG ACCTGAAGAC AGATCACATC ACAGGACTCT TTGCAGACAT TCCTCAGCAC 1380 CAGTTCAGAT CCCAGTAATT CTGCTGGGTG GATAGACCCA GAAGGGCAAT GGCAATCACT 1440 GCAGTCTGGC 1450
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