Tag | Content |
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EnhancerAtlas ID | HS175-06026 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr12:50651130-50652440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr12:50651752-50651763 | TTTTATTGCTT | - | 6.32 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00355 | chr12:50650014-50654143 | Adipose_Nuclei | SE_26085 | chr12:50650803-50654789 | Duodenum_Smooth_Muscle | SE_27814 | chr12:50651160-50652435 | Fetal_Intestine | SE_28691 | chr12:50651113-50654922 | Fetal_Intestine_Large | SE_34214 | chr12:50650817-50654048 | HCC1954 | SE_35640 | chr12:50651500-50654855 | HepG2 | SE_47348 | chr12:50645040-50657360 | Panc1 |
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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 |
GH12I050257 | chr12 | 50650800 | 50654746 |
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Enhancer Sequence | CCGAAAGAGT GAGGGTCGTG ATCAACTCAG TATACCACTG GAGGCTATAT GAGTAAACAG 60 CAAACTGTTC TCATGAATGC AGAATGTTGG CAAACTGACA AATTGCATCT GCCACCCAGA 120 AGGAATGCTG AGGGCAGTCA CACCAGCAGT GTTTCTTGTG ATTAGGCATA ATTGATACCT 180 GTTAACAGTA ATATGAACCT GTGATCAATT AAGCAGCTGA CCAATCGTTA CCTCCTCCTC 240 CCTGCTCTTT CTACCCAATA AATACAAAGG GCTGTGGAAG CTCAGTGGGC TGCCTTTGCT 300 CACTAGAAGC AGGGAACTCT CTTTTTCTTC CTCTGACCCC TTCCTTTAAA ATAGTTACTT 360 TTAAGTTTTC ATTTCTGCTT TCCACACCCT TAGTTCAGTC TTATAATGAT GGTCTCAAGT 420 AGTAACAGTA GTAACTGTCA TAGTGATGGT CTCAAGTAGT AACCTTGGCA GTATGCCACA 480 AGATGATCTT CCTGCTTCGG CCCTCCAAAG TGCTAGGATT ACAGGCATGA GCCACCACGT 540 CCAGCCCAAC CATTTATTTA TATTAGGATG GTTTCATAGA TAGTTACTTT ATTCCCTGTA 600 TTATAATCCA ATACTATCCT TATTTTATTG CTTAAATTGT TCCAGCTCTT GGAGTTTTTG 660 GCTTGGCTCC AGTGTTCTCT CAACTTGCCC TGTTTTTTGT TTGTTTTGTT TTTAGCACTT 720 CCTTACTTTC TAGCACTGCA AGATGTTCCA GGCTCGTCTT GTATTTACCA TGCCTCAGCC 780 CTGGAATCAA CTATTTCCCC AAGGAGCCCT GTTTTCTTTT ATGGGAGAAG TTAGCATCTG 840 GGCACTACTA GTTATGCTCA TTGCCACTGA GATGTCACTG CTTCTAGGCG TCTTAGTGGA 900 CAAAACCAAG AATTATATGT ATGTATACTG GCCCATGTAT ACACACTGCT TTTTGTGTGT 960 GTGTGTGTGT GTGTGACAGA ATCCACTGTC ACCCAGGCTG GACTGCAGTG GTGCAATCAC 1020 AGCTCACTGC AGCCTACCTC CTGAGCACAA ATGATCCTCC CACCTCAGCC TGCCAAGTAG 1080 CTGGGACTAG ACACATGCCA CCGCGCCTGG CTAATATTTT AAATTTTTTT GTAGAGACAG 1140 AGTCTCCCCG TATTGTCCAG GCTGGTGTCA AACTCCTGGG CCTAAGTGAT CCTCACGCCT 1200 CAGCCTCCCA AAGTGCTGGG ATTATAGGTG TGAGCCACTG TGCCTGGCCT ATAGGCACAC 1260 ATTTCTTTAT TTAGCTCTAT ATCTACCTAT ACTTTTTTTT TTTTTTTTTT 1310
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