Tag | Content |
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EnhancerAtlas ID | HS108-29392 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:178982680-178984430 |
Target genes | |
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) |
Gata1 | MA0035.3 | chr3:178983892-178983903 | ACAGATAAGGA | - | 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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| Number: 2 | ID | Chromosome | Start | End |
GH03I179268 | chr3 | 178983793 | 178983839 | GH03I179267 | chr3 | 178984389 | 178984588 |
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Enhancer Sequence | TTTTTTAATT ACAACATTAT TTAACAACTT ATTTTGAAAC AGCAAATAAG GTTAAGTCAA 60 CATAGTTCAT CAAGTTCAGC AAGAGGAAAT AGCAATAATT CAGTTGTGCA TTTCAGAAAT 120 GAAAATGGGA TACAGTAGTT TGCTTTGATG ACAACACAAC TGCCTTTATA TCTAGTTAAT 180 TGTGTGACGT ATGGGACACT AAAACTTGTT TGCTTGCATG TTTGTCATTT GATCTTTTGC 240 CATAAAGTAA TTCATTTTAA TTGTCTGTTC ACAAAAAAAT TGGTTCATGT CTAGCGAGAA 300 GAACACCTTT CTTTCCTCTG TAGTCTGTCT GGTCCTTCTT CCCTGAACCC CCATCTTATC 360 CAAACTCCTG TATCTCACTC TCCTCATGCT CCCTCTCAAA TACCCCTGAG TGCAGTTAAG 420 TGATAATGGA AGTGAGTAAC ATGATGACCA TTACCATCTT TAATGTTTTC CAATTCTCAG 480 CTCCCAACTC CACTAGAGCC AATAATAAAT CATGCATATT TCCAGATAGT GAGTGAACCT 540 GGTTCTGAAA TGTACCCCTC CCAACAGGTT TTTCTTTGTT TGAGACAGAG TTTGGCTCTT 600 GTCGCCCAGG CTGGAGTGCA ATGGCACAAT CTCTGCTCAC TGCAACCTCC TCCTCCCAGG 660 TTCAAGCAAT TCTCCAGCCT CAGCCTCCTG AGTAGCTGGG ATTACAGGCG CGCCACCACC 720 ATGCCCAGCT AATTTTTGTA TTTTTAGTAG AGACGGGGTT TCACCATGTT GGCCAGGCTG 780 CTCTCGAACT CCTGACCTCA GGTGATCCAC TCACCTCGGC CTCCCAAAGT GCTGGGATTA 840 CAGGTGTGAG CCACCGCGCC TGGCACAAAA GGTTTTAGTA TCCCATTTGT CCAACACCCT 900 CAGGCATCAC TCTTCTCTCC ATTTTGGTTC CCACATTGAC TGCCCCATGC CCCAACCCTA 960 GGGCAGGCAA AAGGGGTGCA GGTCACTAGA GGCTTTCAGC TTCTTTGCTT TTCATTTCCC 1020 TGGGGAGAAA ACGGGTCCTG AAAATAATCT CTCACTTCCC CCTTTAAGGA GAAGAGTAGG 1080 GTGGGTAATA ACAATAGCTA AAAGGCTAGA GTTTAGGGAG GTGTAGAGCG TATACCCGGT 1140 ATAACAGTAT AGTTTAGAGA GGATGTGGTA TACTGTGCTG AGACACGCAG GGGCTCTTAC 1200 TATCTGCATT TCACAGATAA GGAGATGAGG CAAACAGAGA AGTTAAGTGA CTTGCCCAGT 1260 CATATGGCTG ATTAAGTGGT GAGCTGGGTT TGAATCCAAG GGCTGTGACT CCAGGGCTTC 1320 ACCAATGGGA CCTGCCCAGT CATATGGCTG ATTAAGTGGT GAGCTGGGTT TGAATCCAAG 1380 GGCTGTGACT CCAGGGCTTC ACCAATGGGA CCAAATGCTG GTCTAATTTC TTCATTCCTC 1440 ATTCAACCAA CAGATCATTC TTGAGCACCA ACTATGGGCT GGGCTATGAT CAGTGCTGGG 1500 GAGCTACAGG TGAGTTTAAA AGGTCTCCAG TCTCCAAGAA CTGGCAACCT AGAGGATAGA 1560 GCCAACAGGA AAGGCTGCAG CCCCGTGATG TGAGTGCTAC TGGGGAAGCC TGCTGGGTAC 1620 CCTGGGAGGC ATGGCAAGTG GGCATCCTCA GAGAAAAAGG AAACACTCAC TCCCCAAGCT 1680 CGAGATGTCC CCTCTTCTTG CAACTGCTTG TTCAGCCAGA TTCCCACTAC CGGCAGAGCT 1740 TCCGGAAGTG 1750
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