Tag | Content |
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EnhancerAtlas ID | HS187-22160 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:159141170-159142540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr6:159141864-159141875 | CCACACCCTGT | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34240 | chr6:159138493-159144118 | HCT-116 |
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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 |
GH06I158714 | chr6 | 159135608 | 159142803 |
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Enhancer Sequence | TGCCTGTAAT CCCAGCACTC TGGGAGGCTG AAGTGGGTGG ATCACCTGAG TTCAGGCGTT 60 CGAGAGCAGC CTAGCCAACA TGGTAAAACC CCGTCTCTAC TAAAAATACA CAAATTAGCC 120 AGGCTCATGG CGGGTGCCTG TAATCCCAAC TACTCAGGAG GCCGAGGCAG GAGAATCTTT 180 GCTTGAACCT AGGAGGCAGA GATTGCAGTA AGCCGGGATC GTACTGTTAT ACGCTCCAGC 240 CTGGGTGACA AGAGTGAAAC TTTGTCTCAA AAAAAAAAAA AAAAAAAGCC TGAGTTTTAG 300 TGAGAGGTTG ACCAACGTGC CTAATGTCAC ATAGTGAATG AGAGATGGAG CCAGGAGCAG 360 ACCTGGGATT TGACTCTGAA TTCTAAACTC TATGTTCCCA TAAGAAGGAC AAATGAGGAC 420 CGCTGAAGAA AGAGGGTTCA GGAAGGGGCG TGTGGAAGCA TGAGTAATTA TCTTACTTGC 480 TTGAGTCACA GGAAACCACT CAGAGGCTAA CACTGACTTG GGGTTAACCA GATGCCTGGC 540 ATTGTTCTCA GCGTAATGCC CTTCAGAGGT ATTTAGCCTT TGTAATCCTT AAGACAGCCC 600 TATGAAGTTG GTACTGTTCC TGTCCCTACT AAAGACAGGG ACACTGGGGC AAAGAGATGA 660 CCAAGAGCTA GGTGAAGCCT GCTCCAGAGA CCAACCACAC CCTGTCCACG CCCCAGAGGT 720 GAGACGCATT TCCCATTTGC ACCGTGATGT GCTGTGTGGT GGCTCATCCC ACGCACCACA 780 GGCTGGGCTT GTGGCGTTCT GCATGAGGAT GGCCCGTGGG TCCTCGGCAC GCCCCCTCCC 840 CTGCTGCATG TGCACATGGC CCAGAGCCTG GCCAGGGTTG TCTGAAGGGC TAAGGGAGCT 900 CAGGGATAGA AGTGGTGGGG TGCAGGGGAG ACGGTGGGGA GACAGTGGGG AGAGAGCCAA 960 TCCAAGTAGA CATTGTTATG CGTGTGTCCA CTTCTCAGCC ATGCTCTTGG CAGGAACGCT 1020 TCCAACTTTC TGCAGGCCTT CTCTCTCCCC ACCTTAATTG AGGTTGTGGC TGGGTTGGTT 1080 TCTTTGTTTC ATTTTGAGAC CAAGTCTCGC TGTCTTGCCC AGGCTGGAGT GCAGTGGTGA 1140 TATCGTGGGT CACTGTAGTC TCGATCTCGA AGGCTTAAGT GATCCTCCCA CCTCAGCCTC 1200 CCAAGTAGCT GGGACTACAG GGATATGGCA CCATGCCTGG CTGATTTTTT TTAATTTTTA 1260 TTTTTAGTAG AGATGTTGCC CAGGCTGGTC TCAAACTCCT GGGCTCAAGC AATCCTCCCA 1320 CCTAGGCCTC CCAAAGTGCT AGGATTACAG GTGTGAGCCA CCACGCCCAG 1370
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