Tag | Content |
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EnhancerAtlas ID | HS153-03656 |
Organism | Homo sapiens |
Tissue/cell | Osteobl |
Coordinate | chr6:159141020-159142440 |
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 | TGAGGTGGGA GGATCGCTTG AGCCCAGGAG GTCAAGGCTG CAGTGAGCCA TGGTTGCACC 60 ACTGCACTCC AGCCTGGGTG ACAGAGTGAA ACCCTGTCTC AAATAATAAT AAATTAAAAA 120 TTTTAAAAAT TGGCCGGGCA CCATGGCTCA TGCCTGTAAT CCCAGCACTC TGGGAGGCTG 180 AAGTGGGTGG ATCACCTGAG TTCAGGCGTT CGAGAGCAGC CTAGCCAACA TGGTAAAACC 240 CCGTCTCTAC TAAAAATACA CAAATTAGCC AGGCTCATGG CGGGTGCCTG TAATCCCAAC 300 TACTCAGGAG GCCGAGGCAG GAGAATCTTT GCTTGAACCT AGGAGGCAGA GATTGCAGTA 360 AGCCGGGATC GTACTGTTAT ACGCTCCAGC CTGGGTGACA AGAGTGAAAC TTTGTCTCAA 420 AAAAAAAAAA AAAAAAAGCC TGAGTTTTAG TGAGAGGTTG ACCAACGTGC CTAATGTCAC 480 ATAGTGAATG AGAGATGGAG CCAGGAGCAG ACCTGGGATT TGACTCTGAA TTCTAAACTC 540 TATGTTCCCA TAAGAAGGAC AAATGAGGAC CGCTGAAGAA AGAGGGTTCA GGAAGGGGCG 600 TGTGGAAGCA TGAGTAATTA TCTTACTTGC TTGAGTCACA GGAAACCACT CAGAGGCTAA 660 CACTGACTTG GGGTTAACCA GATGCCTGGC ATTGTTCTCA GCGTAATGCC CTTCAGAGGT 720 ATTTAGCCTT TGTAATCCTT AAGACAGCCC TATGAAGTTG GTACTGTTCC TGTCCCTACT 780 AAAGACAGGG ACACTGGGGC AAAGAGATGA CCAAGAGCTA GGTGAAGCCT GCTCCAGAGA 840 CCAACCACAC CCTGTCCACG CCCCAGAGGT GAGACGCATT TCCCATTTGC ACCGTGATGT 900 GCTGTGTGGT GGCTCATCCC ACGCACCACA GGCTGGGCTT GTGGCGTTCT GCATGAGGAT 960 GGCCCGTGGG TCCTCGGCAC GCCCCCTCCC CTGCTGCATG TGCACATGGC CCAGAGCCTG 1020 GCCAGGGTTG TCTGAAGGGC TAAGGGAGCT CAGGGATAGA AGTGGTGGGG TGCAGGGGAG 1080 ACGGTGGGGA GACAGTGGGG AGAGAGCCAA TCCAAGTAGA CATTGTTATG CGTGTGTCCA 1140 CTTCTCAGCC ATGCTCTTGG CAGGAACGCT TCCAACTTTC TGCAGGCCTT CTCTCTCCCC 1200 ACCTTAATTG AGGTTGTGGC TGGGTTGGTT TCTTTGTTTC ATTTTGAGAC CAAGTCTCGC 1260 TGTCTTGCCC AGGCTGGAGT GCAGTGGTGA TATCGTGGGT CACTGTAGTC TCGATCTCGA 1320 AGGCTTAAGT GATCCTCCCA CCTCAGCCTC CCAAGTAGCT GGGACTACAG GGATATGGCA 1380 CCATGCCTGG CTGATTTTTT TTAATTTTTA TTTTTAGTAG 1420
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