Tag | Content |
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EnhancerAtlas ID | HS187-06417 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:122607550-122608480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:122607918-122607937 | GAGCGCCACCTGTTGGTCA | - | 7.01 | Foxd3 | MA0041.1 | chr12:122608251-122608263 | GTTTGTTTGTTT | + | 6.32 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_23525 | chr12:122607373-122609334 | Colon_Crypt_1 | SE_24216 | chr12:122607473-122607961 | Colon_Crypt_2 | SE_24216 | chr12:122608017-122608739 | Colon_Crypt_2 | SE_32300 | chr12:122607476-122608542 | Gastric | SE_41952 | chr12:122607452-122608025 | LNCaP | SE_41952 | chr12:122608310-122608759 | LNCaP | SE_48379 | chr12:122607267-122608707 | Psoas_Muscle | SE_50423 | chr12:122607276-122608773 | Sigmoid_Colon | SE_52993 | chr12:122607393-122608098 | Small_Intestine |
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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 |
GH12I122122 | chr12 | 122607349 | 122608656 |
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Enhancer Sequence | TTTAGAGCAG CTTTTCCTGA GTACCCTGTG AAGAAGGGTC CCCGTGGAGG TCTGCGTAGG 60 AAATGTCCCT GCTCCTCTCC TTGAAGATTG ACGGGGCACA GCCTAACAGC TCTGCCAGGC 120 CCATCAGGAG CCTGCCCAGG GTTTCTGGGC ATGAGTCGTC CAGGGTGTCC CTTCCTTTGT 180 GACACCTGAC GCATTCATTG CCACCTTGCC ACCTTCTGAG GCATCACAGA ACTTCACGCG 240 TTGCCTCCTC AGATCTTGAC TTGAAATTGC CTTGGGGGCG GGCTGGGGGT GCAGGCCGTC 300 GACCCTTTCC GGCCCGCCGT GGCTGGTTTG TTTGGATTTT GAGTTGGACG CCCTTCTTTG 360 TGTTTCTTGA GCGCCACCTG TTGGTCATAG AGATATTACC GAAACTCGGG GTGGAACGGT 420 GATCCCAGTT GGGAGTTCTG GTCTCTGTGT TGCTGCTGAA GTCTGACTGT GTTTGACGTA 480 AACACCCAAA GAAAAGGGAA ACATTTCAGC TCACGGAGAG GAAGAAGAGG GGACCCTCAA 540 ACTAAACTTT GAGGTTTCTA GCCTGTAAGG CTAAATTTCC CTGCGTCTTG CCGCTCCCCT 600 CATTGTGTGT GATTAAAGCT GTTGGTATGA CACCCTCTGC CCTCCAGCTT TGTCTGCTGT 660 ACCCCCTGCC TTCAGACTCC CTTTTTTGGT TGGTTATTTT TGTTTGTTTG TTTTCTGAGA 720 CGGTCTTGCT CTTTCACTTA GGCTGGAGTG CATTGGTGCC ATCATGGCTC ACTGCAACCT 780 CAAACACCTG GGCTCAAGCG ACCTTCCTGC CTCAGTCTCC CCAGTAGCTA GGACTACAGA 840 CGCATGCCAC CATGCCCTGT TCACACATTG AGGGCTTTTC ACTGCCTCGA TCAGGCTGAG 900 TTCTGCTCAC TGGGGCCACC ACAGGCCAGG 930
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