Tag | Content |
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EnhancerAtlas ID | HS098-33875 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:241859900-241862110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:241861269-241861290 | CCTCCCCTCCACCCCTCCACC | - | 6.67 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27042 | chr2:241860242-241861540 | Esophagus |
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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 |
GH02I240920 | chr2 | 241859889 | 241866520 |
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Enhancer Sequence | CAGTGCTCTG CCCAGCACTG GCACAAAGCT GGCACCTGCA CAGCAGAGGA AAGCAGGCCA 60 GCAGGCACCG ACCCCAACCC CAGATGGAGC TCGCAGAGAA ATGGCTCCAC CCCAGTTCCC 120 TGGCCCTTTT CTGACAACTG AGGCTGGCCG GGGCCGCTTG GACCTCAGAG GAGAGGGGAC 180 AGAGGCAGGG CTGTATCTTT GGTCCCCTGG TGGCTGTAGT GCCTTCCAGG GTGACCTGTG 240 AGGTGAGCAA GAGGCATATT TAGTCACAAA ATGTGGAGCT GGGGAAGGCC TCCCATTGTG 300 TAGACAGGGA AACCGAGGCA GAAAGGTGAA GAAACCTGCT AGGCCAGAGC CTCTCTCCTA 360 TGTCAGCCGC TCCAAGACAT GCTGGCTTCT GAGGCAGGAC TTGGCAAGGA GCCAGTGCGT 420 GGAGTGGGGT GTCCAGCCCA CCTTGTGGGG TACTCAGGGC CCCTGCCACA CCCATGCCAT 480 CTTCAGAGCC CCCCTGGTTC TGCATGGCAT GTCAGATGAC CCCACTTTCC AGATAAGGAG 540 TAGAGGCTCA GAGCCAGCCA GTGATCACCC AGGCCACACC ACCATTACTG GGGCTGAGAT 600 CTGAACCCCT GAAGCAGATC TGGCCCCTTC TTAGTCACCT GACCAGTGGC CAGTACTGAA 660 TGCCTGAGGG GTCCCCAGGG GGCCTCACCT TCTAGAAGGG TCCTTCCCAG GATCATGGCA 720 GCACCAGCCC CACAGCGGTG CCCTCAGCTC TCTGAGGGGC CCGTTCTCTG CTCCCCACCC 780 AGTTCTATCA CGCCCTGACC CCCACACGGG AAACACGTTT CCATCCATTG TTGCTGGCAC 840 CCCTGGGAGC CCCTGAGGGC AGGAGCTGGG GTCCACCCCA CCTGATGGGG GCCCCAGCAC 900 ATCCGTGAGC TGCCAGCCAG CCTACTCTTC CTGGGAGCCC CTACAGCTGT GGGGAGGCCT 960 TGGGGGAGGC ATCTTCCTAG CACAGGGTGG GGAGATGTTG GGAACAGGCC AGTGGGAATA 1020 GAAGCCACAG AAATGCTGCC GACAGATTAG TAAGCTGCGT GAGTCAGATC CAAACTCGCC 1080 AGCAGCCCAG TGCACGCCAG CTCCCGGGCG GCTCAGCAGG CAAAGTGTGG GTGCCAGGAG 1140 GCTGGGTCTA ACTCCAAGTT ACCCCCAAGA CAGGCGGAAC GGGGTCTGGG TGGCCAGAGT 1200 GCCTGACCAT GGCATCTCCA TCCTGGGGTG GCACCCCCAG ACCCCGCCCG GCTCCTCCAG 1260 GGTCTTCCAA CGCCACCTTC TCTTCCAGCT TGTGGCTGAG GAGGGGCCCC TTGGCTCTCC 1320 CATGCATTTG GCCCAGGCAT AGCCACAGCT GAGGCCCCAG GCCTGCTGCC CTCCCCTCCA 1380 CCCCTCCACC TAGGCCATCC TTGGCCCTTG ATTTCCTGGG CCCAAGTTCG GTCTTGGCCC 1440 AGTGGTGGCA GAGTGGCCCT GGGCAGTGGG CCCACATCAT GGTGGGTGTG GTCCTGCTCC 1500 CTGTAGGTGA GGTGCTGGAC TCAGGCAGGA GGCCCAGATG GAGAGGAACC ACACTCAATC 1560 TCCAGGGGGC AGCCCCAGAG GTAGCCCTGT GACCTTCCAT CCTGCCCCTG TGTGCCTGAA 1620 CCAAGCCCTG AAGCCCCTCC CCCTACACTG ACGGCTGGGC TGCCCAGGTA GCTGGGGCAG 1680 TGGGGCCTCA GTTTACCCAT CTGTAAATGA AATGTGGGCA TGCTCCAGCA GCCCCCAGAG 1740 CTATGCCCCC ACTGGGCCAC CATACTCACA CTGTCCTCAA GGCCTGATGG GATTGGCACA 1800 TCAGTGCAAC CCAGCATGCC CCTGCCCCTC CCCTCCTCTG CCAGCCGTGG GCACTTGGCA 1860 CAGGGCAGGA GGCCACCTGT CGGGTTCATT GTGTGGAAGG GCCTGGGCCT CACCAGACCC 1920 AACCCCAGCC CCTGCTGTGG GGCCCCAGGG AGCCCTCTCT TCCCCACTAA GGTCGGCTTT 1980 GTGCCCAAGA TGCCCCAGCC CCTGCCTGGC GGGTTCAGGA GCAGCCAGAC CAGGTGGGCT 2040 ATTGCTCCTC CCCAGCTGCA GGCCCGGCTG GAGACCACCG AGGCTCAGCT GCGGAGGTCA 2100 GAGCTGGAGC ACAGCGTGGA TCTGGAGGAG GCCCTTGGCC GTCTGGAGGC TGCCGAGGAG 2160 AGGTGAGGCC AGGTGCGGGG CAGTCAGGGC TGCAGGAAGC ACAGCCATCC 2210
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