Tag | Content |
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EnhancerAtlas ID | HS196-15023 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr2:103103740-103105120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr2:103104669-103104689 | GGTCTGTGGGTGTGTTGGGC | - | 6.16 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_32242 | chr2:103103136-103105095 | Gastric |
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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 |
GH02I102487 | chr2 | 103103587 | 103105370 |
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Enhancer Sequence | GAAGAGCTTG GACTTGGCTG GGGAGGTGGG AGGACCTGGG AGAAGTGAGG AGCAGATCAG 60 TGCAGGTCCC AGTAAATGAA GGAGAGTGTT GCAGGGGGCA GAGGTTCACC AAATCTGACT 120 CCTAACCTTC CACAACAGAC AACCCCTTTA CTTCCTGCAC TTGTGGAGTC TAAGCCACAG 180 ACTTGCCCTT TAAGGAGCAG CCTGAGGGGT GTGGGCTAAT CCTTGGGAGG CATGCTAGAG 240 CAGGACAGGG CTGGAGGGGC ACTGTATTAT TTCATTGCAA TGCCTCCCAT TTGATTCATC 300 AAACACCTGT TTGGTTCATT TTCTTCTGGC TAAATAAACA GAATGGTTGA AGTTTGAATT 360 GTACAAATTG GCTTTCAACT AGACTACACT GTGAGCTACC TAGGAGTAAT TAGAACTCAC 420 TTCAGGTCAC ATGCACAAGA AAAAAGAAAA AGCCTCTCGT TATCAAGTTG TCTTTTCTTT 480 GTCAGGAGAT GGGGTTGAGC AGCTATGGAA ATGGATTTGG AAGAGAAACA GGGAGAAAAG 540 CAATGTCGCT TTAGCTTTTT AGGGAGTAAT CAGAAAGAGG GCAGAAAAGC GCATGGGAGA 600 AGTTCTCTCC CGCCAGCCTT GCTGAGTGCC TGGGATGCAG AAGCAAACAA GCTTCATCTC 660 CTGCCTTTGA GGAGCCACAG CTATGAACAC ATGACTTATT TCTTTTTGTT TGTAGATTAT 720 TCCTTTTAAC CATGGACCTG CTTGTTCTGT ATTTTATTAG AATCCTTTCT AGCCACAGAG 780 AATTCCTAGG AAGTTGCATA ATACATTAAT AGAAATTCCT GACTTGAGAG AAAAGCGTAG 840 AGCTTCAAGC ACAGCCTGGG GACTTTCCTA GTCCTGTGGT TTTCAACAGC TGTCCCACCC 900 CCAACAACAC CCGTTCATGC ATCCTTAAGG GTCTGTGGGT GTGTTGGGCT GCAGTGGGAA 960 AAAAAACATG CCCGGTGTCA CGTGAAAAAC CCCATGAGTT GGCTGTTTGG GAGGTGCTGG 1020 CTGACAAATA GTTTCCTTAT AGCTTCCTCC ATGGTTGCAT AAATGGATGA CATCCAGCAG 1080 AACCTGTTAC ACAGGCCTGG ATGGGAGCAC TAGATCCAGG CGATGGGTGA GGGAGGAAGC 1140 CATTGACCCT GACTCCAGGC TGAGGTCATC CATACTTTCC TCCTTACCCC ACAGGACCAG 1200 CTTTGATTGT TGGTGAGTAA TAGGCTAATA CCACTGAGAA AGCTGAGAGA CCATGAAATC 1260 TAATTCCTTT TTTTTTTTTT TTTTTGAGAC GGAGTCTCGC TCTGTTGCCC AGGCTGGAGT 1320 GCAGTGGCGC GATCTCAGCT CACTGTAAGC TCTGCCTCCC AGGTTCGCGA CATTCTCCTG 1380
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