Tag | Content |
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EnhancerAtlas ID | HS020-04686 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr1:246861800-246863400 |
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) |
MEF2A | MA0052.3 | chr1:246862526-246862538 | GCTATTTATAGC | - | 6.32 | MEF2B | MA0660.1 | chr1:246862526-246862538 | GCTATTTATAGC | - | 7.22 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I246698 | chr1 | 246861721 | 246863190 |
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Enhancer Sequence | CACCAAGGGT GGGCACCAGG AAACCCCATC TTCCTTTCCC ACTCATTCAG TCTCCACTCT 60 CCCAGCTTCC CTCCCACAGC CTTCTGTGTT TCATTTGCCT TGGACCCACA GATACCTCAG 120 GGAGGAGCAC CACGAAGGCA AACCAACCTC TTTCATATCA ACATCCATTG CCACCTGTTA 180 GTAAGTGTCA AATGGTGTTC TGCATGCTAG AAGATCTCCC TCCCACGGGG TGCCTGTGAG 240 CCTCCTGCTA TAGGAGACAG AATTCTGTAT GGCCCATCCA GGGAGGAGCA ACCGAAGGAA 300 AAACAGCAAC TGTGGTTCTC TGTGCCTATA TTGGATTATG TCCCATAGAT GCCCCTTACA 360 TCTTCTAATG AGGGAGTGGC TAGTGGGGCT CCTATTTGCT AGATGTTTCT GCTGCTGGGC 420 TAAAAACCGC TTAGGTGGCC GGGCGGGGTG GCTCACGCCT CTAATCCCTG CACTTTGGGA 480 GCCGAAGTGG GAGGATTACT TGAGTTTAGG AGTTTGAGAC CAGCCTGGGC AACATAGTGA 540 GACCCCCATC TCTACAAAAT GAATAAGTAG AGTTTAAATT AAAAAGAGAA AAAGAAACAT 600 GCTTAATCTA CTTCTGAGAA TGATCTCAGG AAGAGAGTGA AACAGATGGG CTCGGTCTCC 660 TGAGGGAGAC AAACAGGGCT TCAAGCAGGG CTTAGGCTGG GGACGCTGTG TGGAGCAGAG 720 TCACTGGCTA TTTATAGCCC AAACAGTAAG AAGAGTCGTT ATGAAAATGC CCAGAGGTGC 780 TTTGATCCGG GAAGTACACA AGCCAATCAA AATACGCCGC CTTCGGGCAA GAGGAGCCGG 840 AGAGCGCCAT CTAGTGACCC CACAAGTTCC CTTCCTGAAG GAAGTATTCA GTCCGGAGAA 900 ACCAAGACCC ACCTCACAGC GAGGACCAGA GAGACACCTT GGTAAGAGGC CCTGGAAACG 960 AAACACAAAG CGAGGAAGGA CAGTGCACGG GCCTCAGACG CGAAAAACAG GGGTCGGAGT 1020 GCCCATCCTA CAGGTTGTTT GATAATTAAA TGAGATATTT CCTTTTTATA TGAAATGTTT 1080 TATGTTCATA AAGATGACAA CTAAATAATC TTCATTAACT TAGGAATCCA GCCCTTACTA 1140 TGTGACACAG TGTGTGCCAA TGTATTTATC ATTTTGTTTT ATGAGTTGTA TCTTTTTTTT 1200 TTTTTTTTTT GAGACAGGGT CTCACTTTGT CACCGAGGCT GGAGTGCAGT GACACAATCT 1260 CGGCTCACTG CAACCTCTAC TTCCCAGGCT CAAGTGATTC TCCTGCCTCA GCCTCCTGAG 1320 TAGCTGGGAC TACAGGCGTG CGCCACCACG CCCAGTTGAT TTTTTGTATT TGTTTTGTTT 1380 TGTTTTGTTT TGTTTTAGTA GATATGGGGT TTTGCCGTGT TGGCCAGGCT TGTCTCGAAC 1440 TCCTGAGCTC AGGTGATCTG CCTGCCTCGG CCTCCAAAGT GCTGGGATTA CAGGCGTGAA 1500 CCACGGCGTC TGGCCAACTT GTATCATTTT TGTTATTATA GAATATTTAT TTGAAATGTT 1560 CTAGTTTGCA GTAATTTGTG GGAGTTTTGT TCTTACTAGG 1600
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