Tag | Content |
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EnhancerAtlas ID | HS180-02333 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:92269170-92270540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr1:92269623-92269633 | ATGGGGTGAT | + | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_00014 | chr1:92266356-92273792 | Adipose_Nuclei | SE_01322 | chr1:92269351-92270603 | Adrenal_Gland | SE_16105 | chr1:92268531-92271743 | CD4_Naive_Primary_7pool | SE_22269 | chr1:92268200-92271939 | CD8_Naive_8pool | SE_29597 | chr1:92268556-92269669 | Fetal_Muscle | SE_53998 | chr1:92268130-92271658 | Spleen |
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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 |
GH01I091802 | chr1 | 92268199 | 92273987 |
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Enhancer Sequence | ATTTGTAGCT TAACCTACCC TAATTAATGT ACTTGCCTTC TTTTATTTCA TCAGAAGTGC 60 CAACCTTTGT CCCAAAGGAG CCTCTGAATA GCAAGGTTTC CTCCAGGAAC ACATTCCCCA 120 CCGTTTCTGT TCCTTCCCAC CACCATGGCC TGACAAACTC CTGCTCATTC TACTGATCTC 180 TCAAGGAAGC TCCCCAAACC TCCCTCACTG TGTTAGATCT GTATTTTTTC ATACTCTCAT 240 GGTACTCTCC GTTTCTCTCC ACAGCACTTC CTGTGATGAG ATGTACATAA TTATTTGTGC 300 AATTATTGGT TTCACATCTA CATGCTCCCA AAGACTGCAA ACACCACGAA AGAACAGAAC 360 CCAACCACTC TGTCTGCTGC TGCCTGCCTC ACCCCAGCAC AGTATCTGGC ACAAAACAGA 420 CACTCAATTA TCGCTGAGAA ATGGGGAAGA ACCATGGGGT GATGCATGCT GCATGGGCTT 480 TGTGCCAATA AGGGACTGTC TGTCTCAGAC TTCCTGCTTT CACTCTTTAC CTGAGAGCCA 540 AAGCCTCACT CTTATACTAA AAGGGGCAGA AAAAAAAAAC ACCAACCATG AAATGAAGGA 600 GGTGGCATTT TTGGTTGCTA AGAATCAAGT CCCAGTTGGG GCTTCCCCAC CTTCAACTGT 660 CACAGAAAGC AGGAAACACA AATCTGTTTT TGTCTTCTCT TCCCGGACAC TCTTCTGGCC 720 AATCCCCTCT CTCCAGGTGG CAGGACAATC CTCTATCTCT CCGTTGGCAC ACCACAGCCC 780 CAGCCTCATC CTGCCACTTC TGGGTCAGGC CCTAGCCTTC CTGTCCCTTT CCCTCTGCCA 840 CAGCCAGCTC ATGAACCTGT CTCCCATCCT TCCCCCTTGG CCTCATAGTG GTTCCTTCCG 900 CAATCTGTCT GCACAATGCC AGGGCCAGCT CCATTCAGGA AGGCTTCCAC CTGGGAACAG 960 CATGATCCAC CCCACAGGCT CTAGCACAAG TGCCTGAGTT AACACAGTGG CTCAGATTCT 1020 CACTTGACCA CCATGGGGCC CGAGTATAGC ACCTCCCAGC CACGAAGGCT TGGAAACCAG 1080 GAAAACATGC TCCGAAACCC CATCTGACTC ATCTGCTCAC TTTTGTGGTG ACCTGTGAGC 1140 TCTGGAGCTG CTACTGTAGG CCCTCACCGG CAGCCTCAAA AGGCTGGGAG TGTCTCCTGT 1200 GGCCACGGCT GAAAACCCAC ATCCCGTCTT CCCTACGCAA TCTCTTCCCT GCAGTCAAGA 1260 GCCAAGTGAG TGACATGCTC TGATGATGCT CCTTATCAGC AGCACAGCAA AAGCTGTGTT 1320 ACCACGTAAG GATCAACCAG GGCGTGGACG ATGACGAAAG AACACACCTG 1370
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