Tag | Content |
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EnhancerAtlas ID | HS073-00340 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr1:29535830-29537990 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr1:29537131-29537142 | CTAATCCTCTT | - | 6.62 | FOSL1 | MA0477.1 | chr1:29536802-29536813 | CATGAGTCACT | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TCACAACCTG TGGTATGAGA ACATGACCTC AGCACTGTGG TATGGAGAAC TGATCTTGTT 60 TTAGTGAATG AGTGAGTGGG AAGCCTGTAA CAAGCTTTAA GAGGAGACTG AGATGATCCG 120 ATGTATGCTT TAAGATCACT TTATTGCTGG GTGAAGACTG TGGAGTGGGG AGGGGCAGCG 180 TGGAAGCCAG AGGTCTTTGT GGGGGTCGAG GTATGAGATG ATGGCTGCCT AGTCTGGGAC 240 TTTGGCAGTG GGGATGAGGA ACAGAAGATG GATTTGAGTT CTATTTTAAA GACAGAATCA 300 ATAGGATTTG GTGAGGACTG CGTGAGGGGT CTGCACTCAC ACAGGCAGGA TCTTGTATGA 360 AGAAGGGGTG AAGAGGGTAG GCTTTGGAGT CAGAGAGACT CCAGCCTTGG TTCCACAGTG 420 TCCTCACTGT GTCACCTTAG GGAAATTGCT TGGAGCCTTG TTGGCTCAGC ATCTGGTCAC 480 AGTGGCAGCT CGGGGCCCTT GGCCTATGCT TCCAAAGCTC TTGGGCATGC CTGCTCACTA 540 TCCAGTTGCT GGGATTCTAA TGGTGTCCTG GTCCTATGTG GGTCAGCTGT GGGAAGCAGG 600 GGGCAGCCTG GGTAATCACT AACTGTGCTA TAGGAAACGG GGATGTCAAT GTGGGCTTTA 660 GGGACCAAGA ACTGGGGACA GGAGGCAGGA ACACTTTTTT TTTTTTTTTT GAGATGGAGT 720 CTTGCTTTGT CGCTCAGGCT GGAGTGCAGT GGCACGATCT CAGCTCACTG CAAGCTCTGC 780 CTCCAAGGCT CCCGCCATTC TCCTGCCTCA GCCTCCCAAG TAGCTGGGAC TACACGTGCC 840 CGCCACCACA CCCGGCTAAT TTTTTTGTAT TTTTTAGTAG AGATGGGGTT TCACTGTGTT 900 AGCCAGGATG GTCTCGATCT CCTGACCTCG TGATCCGCCC ATCTTGGCCT CCCAAAGTGC 960 TGGGATTATA GGCATGAGTC ACTGTACCCG GCCCAGGAAC ACTTTTTATA GAAGGCTGTG 1020 TCAATCCTAG AGTAGGTCTA TGGCTGAGAA AATAAGAGAC TGAAAAGGCG AGGATTCCTC 1080 TGTAATCCAG GAAGTGCCCC AGCATCCTGT GGGCTTCCCC CGGACTGGCC TTCAAATCAT 1140 CGTTCCCATT CATCTCAGCT AACACTTACT GTACTCTACC GTGCACCAAA TGCTTAGTGC 1200 AGGGCTTTCT ATGTATGAAA TCCAGGGCAT TTTCTAATTC CCCTTATGGC ACGACAATGG 1260 AAATCCAACC CTTGATATGG ATTTCTGGGG CTTAGCAGTC CCTAATCCTC TTCTCAAGAG 1320 ACTCTGGGTG GGAGGGAGGC AGCACCCGTG GTCAGAGACA AGGGCTTTCA GGGTTTCAAG 1380 TAGAACTCTT AGGCTTGAAG TTGGAGAGAC CTGCTTAAAA ACCCTGGCTC TACCACTCAC 1440 TAGTGTGTGA CTTTGAATGA TCACTTCACC TTTTTTGAGT TTCCATTTCC CTAATCTGTG 1500 AAATGCAGAG AGTAACACTT ATGTCATAGT GTGAAGATTA AACTAAAGAC ATTTGTACAG 1560 AGACTATCAC TATGCCTAGT ACACAGTGGG TGTATAACAC ACATTGTTTT CCTTTAATGA 1620 TGCTAATTCC CAGACTTTAG CTCTGAGGAT TCCCAATTCC TCAGTCATAT GCAACTGACC 1680 CTTAACCATC TCCATTGTTG AACTTGGGGG TCAGCAAACT GTGGCCTGTG GGCTAAATCT 1740 GCCTCACCAC TTGTTTTTGT AAATAAAGGG TTTTTTTTTT TTTTGTTTTG AGACAAGAGT 1800 CTTACTCTGT TGCCCAGGTT GGAGTGTGGC TTACTGCAAC TTCTGCTTCC TGGTCTCGAG 1860 CTATCCTTCC ATGTCAGCCT CCCCAGTGGC TGGGACTACA GGTGTACGCT GCCACACTTC 1920 GCTAATTTTT TGTAGAGATG GACTTTCACC AAGTTGCCCA GGCCATTCTT GAACTCTTGG 1980 ACTCAAGCGA TCTGCCCGCC TTGGCCTCCC ATGCTGGGAT TACAGGCATG AGCCACCATG 2040 CCTGGTCCTG TAAATAAAGT TTTATTGGAA CACAGCCATG TTCACTCAAT TGTTTATATA 2100 TTGCCTGTGG CTGTTTACGA TAGTAGAGTT GGGTAGTCAC AAAGATGATA TAGCCTACGA 2160
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