| Tag | Content |
|---|
EnhancerAtlas ID | HS180-12762 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr12:123734850-123736730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr12:123735629-123735644 | TCTGCTGAGTCATGC | - | 7.23 | | Nfe2l2 | MA0150.2 | chr12:123735631-123735646 | TGCTGAGTCATGCAG | - | 7.41 | | RREB1 | MA0073.1 | chr12:123736160-123736180 | TGGGGGGGTGTGTGTTCGGG | - | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_13718 | chr12:123735330-123736488 | CD34_Primary_RO01536 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 123736311 | 123736577 | | chr12 | 123734922 | 123735982 | | chr12 | 123735107 | 123736146 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I123250 | chr12 | 123734884 | 123737119 |
|
Enhancer Sequence | TACATTGGGC TTCACCTTTC TCTGGTCCTT CCCTGATTAA TAACTAACCT CCTGAATTCT 60
TTTTCAGGTA AATCAGGTAT TTCTTCTTGG TTTGGATCCA TTGCCAGTGA ACTAGTATGT 120
TTTTTGGGGG GTGTTGAAGC GTCTTGTTTT GTCATATTAC CAGGGTTTGT TCATTTGGGT 180
AGGCTCTGTC AGAGGGAAGG TCTAGGGCTG AAGGCTGTTC AGATTCTTTT GTCCCATGGG 240
GTGTTCTCTT CATGTAGTAC TCTGCCCCTT TTCCTATGGA TGTGGCTTCC TATGAGCCAA 300
ACTTGCAGTG ATTGTTGTCT CTCTTCTGGG TCTAGCCACC CAGCGAATCT TCCCAGTTCC 360
AGGCTGGTAC TGGAGGTTAT CTGCAGAGTC CTGTGATGTG AACCATCTAT GGGTCTCTCA 420
GCCATGGCTA CCAGTGCCTG TTCGGTGGAG GTGGCAGAGG GTACAATGGA GCTTTGGTGG 480
GTTAATGGTC TATTTTTTTT GCTGGTTGGC CTCCTGCCAG GAGGTGGTCC TTTCCAGAAA 540
GCATCAGCTG TGGTAATATG GGGAGGAACC AGCAGTGGGC GGGGCCCTAG AACTCCCAAG 600
ATTTATTTGC CCTTTGTCTT CCTGCCAGGG TGCATAGGGA AGGACCATCA GGTGGGGGTG 660
GAGCTAGGCG TGTCTGAGCT CAGACTCTCC TTGGGCGGGT CTTGCTGCGG CTGCTGTAGG 720
GAATGTGGGT GAGATTCCCA GGTCACTGGA GTCGTGTACC TAGGAGAGTT ATGGCTGCCT 780
CTGCTGAGTC ATGCAGGTTG TCAGGGAAGT GGGGGAAAGC TGGCAGTCAC AGGCCTCACC 840
CAGCTCCCAC ACAAACCCAA GGGCCGGTCT TACTCCCACC GTGTTCCCCC ACAACTGCCC 900
CGAGTCTGTT TCCAGGCAGA GGGTGAGACT GGCTTGAAAA TTTGCCCCAA GGCTGTGCCC 960
CTCCCAGCAG CGAAAGAAAA GGGCTGTAGT TCTTCCCCCA CCTGTGAAGT CTGCATGCTG 1020
GATTCGTGCA GTTGCCCAAG TTCTGGCCAG GAGGCTTCTC ACCCTGTTTA AATTGTTACG 1080
AAGTTCGACT AGAGAATTCT TCTCCCTGTG GAGTTTTATC CCTTGCTCCT CTGGCCACCC 1140
TCCCGATGGA TCCCTGTGGT GCCAGGCAGG AATGGGCCTT CTGGGGACCC AGCGAGCTCC 1200
CACGGCCTTT CTGCTGCTTC CTCTACCCCT GTAGTTCGCT CTGCTGAGTC TGACTTAGCT 1260
CCAGGTAAAG TTGGAAATTT CTCCTGCAAA CAGACCTTCA GCCTCTCCAG TGGGGGGGTG 1320
TGTGTTCGGG AGAGGAGGAT CTCCCTTTCC CACTTCCACA GTTGGGGCAC TCACAGTATT 1380
TGGGGGTCTC CCGGGCCCTG CAGGAGCAAT CCGCTTCCTT CAGAGGGTCT GTGGGTCCTC 1440
TCAGGATTGC TGGTTTGTTC TTGCAGTTGA TCTAGAGCTA AAATTCACAA TGCAAGCCTC 1500
TGCATGCTGC TCTGTCTGAA GCTACAATCT AGTCCTGCCT CCTGTCTGCT ATGATCCCAG 1560
GAGCTCCCAT GCAAATAAAT TATGATCACA AGGTCCCAAA ATAGGCTGTC TAGAGCTGAG 1620
GAGCAAGGAG AGCCAGTCTG AGTCCCAAAA CTGAAGAACG TGGAGTCTGA TGTTCAAGGG 1680
CAGGGAGCAT CCAGCACTGG AGAAAGATGT AGGCAGAGAG TCTAGGCCCA TCTCATCTGT 1740
CTTTTAATAT CTTCTCTAAC TAACCTGTAA GCTCCAAGAA GACAGTCCAG CTCTTTTTCA 1800
TCTCATGTCC CTTACTGTAC CTAACAAGGA CCTTATTAAA AGTTGACTGG CTGGATGCAG 1860
TGGCTCACGC CTGTAATCCC 1880
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