Tag | Content |
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EnhancerAtlas ID | HS158-41665 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr4:6750800-6752130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr4:6751894-6751905 | GGCCACACCCA | + | 6.62 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_23558 | chr4:6750750-6753976 | Colon_Crypt_1 | SE_24593 | chr4:6750774-6753042 | Colon_Crypt_2 | SE_27608 | chr4:6750727-6755682 | Esophagus | SE_42068 | chr4:6750932-6751798 | LNCaP | SE_42068 | chr4:6751840-6753045 | LNCaP | SE_51051 | chr4:6747543-6755479 | Sigmoid_Colon |
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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 |
GH04I006746 | chr4 | 6748122 | 6755667 |
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Enhancer Sequence | AGGATGGTCT CGGTCTCCTG ACCTCGTGAT CCTTCTGCCC TGGCCTCCCA AAGTGCTGGG 60 ATTACAGGCG TGAGCCCCCG CGCCTGGCCC CATGTGTCAG TCTTAATAAT AACATAGCAA 120 TAACAATAGT AACAGCAGCA GCAACCCTTT GCAGATGAGC CTCGGGGTTA AAATGCACTT 180 TCTCTAATTC TCTAATATTA TCTCATTGGC TGCTCTTGAG AGCTCTGAGA GGTAGGAATT 240 CTCATCTGCT TTGACAGATG GGGAAAATGA GGCACACTTC AGCCAGGCAC CTCCTCACAC 300 TACAGGGCAG ATCCAGCCCA TGCAAAGCTG GGCCTAGTTC CTGGGTGGGG CTGTGTCAGG 360 ACAGCTGGGC ACGGACGGAG CTTTCACCCA CGCTGGGGCG CCTGCTCAGC GAGGCTGCCT 420 GGTGGGGCGG TGACTGCATG ACAAACTTGC TGTGTGGCCT GGACGTCAGG GCGGGAGTAA 480 CAGCTCCAGG AAGGCCAGAG TTCAGCCCAG TCAGCCCACT CGGCCCCACT GTTCGGGCTG 540 CCCTCTGAGC ATGTGTCATC CTGCCAGGGT CCCTCCCACT GCGACCTGTC TTCCTGGCAG 600 CTGCTGTTCA GGAGTTCTGC ACCCCGCCCT GGGTGTCCTG CCAAAGCCAA GGTGGCCGTG 660 CGGTCAGAGG CAGCGTCCTC TGCCCTCCCT GTCTCCCTGC CTGTGTGTGC CCCTCCTTCC 720 ATGGCCGGGA GCCTTTCTCC TTTCCCTTCT CATTTTGCCA GACTCCCACC CTACTGTCAC 780 AACCTGCCAA AGAGGCACTG CTCCAGGCAG CTCCTGGACT CGCCCAGATG CAGCCAGACC 840 CTCTGCTGCG CTCACTGCAT CGTCGTGGAT GTAGCTGTCT CTCTGCCTTT CTGGACATCC 900 TGACTGTGGC AGAGGTCCCC AGCCCCACGG GAGGTGGGGT GGGCAGGGTC GGGGGGTCCA 960 TGTCCCCTTT TCTTAGGTGA GGGGAGTCAC TTGAAGCCAG GGCAGGTGTG GGGATGGGGG 1020 CCCCAGACTT GAGCACGTGC CAGGCAGAGG GAAAGGGAGC TCCGGAGAGG TCGAGTCAGG 1080 GTAGGGGGCT TGATGGCCAC ACCCAAGCCA GAGAGGAAGC CGGAGGCTGC GAGCCAGCCC 1140 TGAACCCGGC AGCCTCTGCC GTGATGAACC AGGGCGACCC CTCTACCCAG CGGCTCAGCC 1200 GACACCCTCA GAAACTCAAT TTTATTTAAC CAGCACATAT CATGTGCACT CTGGACCAGG 1260 AGTGGTTCAC TTACTCCTCA CAAGCAGGCT GCCAGCAGCA GGGACACGGG CACAGAGGGG 1320 CTAGGGAACT 1330
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