Tag | Content |
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EnhancerAtlas ID | HS073-07808 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:46379260-46380670 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP2 | MA0516.2 | chr19:46379910-46379927 | GTCACCCCCGCCCCCTG | + | 6.05 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23551 | chr19:46379389-46382979 | Colon_Crypt_1 | SE_24599 | chr19:46379448-46380697 | Colon_Crypt_2 | SE_35762 | chr19:46376029-46383004 | HepG2 | SE_47895 | chr19:46379418-46382977 | Pancreas | SE_65443 | chr19:46378331-46381375 | Pancreatic_islets |
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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 |
GH19I045875 | chr19 | 46378522 | 46383519 |
|
Enhancer Sequence | GTGCAGTGGC GCAATCACAG CTCACTGCAG CGTCGACCTC CTGGGCTCAA GCTATCCTCC 60 CTCCTCAGCC TCTCGAGTAG CTAGGACTAC AGGTATGCAC CCCCACGCCT GGCTAATTTT 120 TTAATGTTTT ATAGAGAAGG GGTCTCCCTG TGTTGCCCAT GCTATTCTTG AACTCCTGGC 180 CTCAAGCAAT CCTCCCGCCT CAGCCTCCCA AAGTGCTGAG ATTATAGACA TGAGCCACTG 240 CGCCTGACCA GTGTCATTTC TTTCTGTATC AATCTGTCCC TCACCCTCTT TCTGTGCCTT 300 TATCTGTGTT TCTTGGTTTG AGTTGCTGGT GCTGTCTGTG TGTGTCTGTC TCTCCTATGG 360 CTCACCTCAT GCTCTCTCTC TCTCTCCCCC CTCGCTCACC CGGCCCCCGC CTTTTCTCTC 420 TACTGCTCTG ACTTCCCTCC TCCCTCCACC TGGGTCTCTG GGTTTCTCCC TCCTTCTCTC 480 AGAGTGACTC TTTCCTGGGG TCCGTCTCCC CCCACTCCTT TCCTGGATCT CTGGTCTCTC 540 TTTCTCTGGC CTCCATCCCT CTCCCAGCTC TCTGGGTTTC CGCCTCTACC TGCCACCTCG 600 CAGGCCAGGC CCTCTATTCC TGTCGCTGCG CCCCGCCTTG CCGGCTGCGT GTCACCCCCG 660 CCCCCTGCCG CGCTGGCTCC CCGTCCGTCC CACCAGCCTT GCTGTCCTGG GCAGGCCGGG 720 GAATTCCTCC CGGTTCCTGG AAAAAACAAC TGGGGCCGAG AGAAAGGCCC TCAGTCTCCC 780 CAGGCACCCG CCCCCCTCCC TCGGGCCTGG GGGTCTCTCC CGGAGTCGGC CAGCCCGAGG 840 CAGGAAGCCC TGCGGTTTCT GGCTTCTCCC AGGCGGCCTC CGGATCTGGC CCCCGCCCCC 900 CGGCCAACAG CCCAAATATT ATTCCGCGGG AGGAGTCGGT GGTGGCGGGA GGAGGCCCAG 960 GCTGAAAGAG GCTTTCAGGG CGGCCAGGCC TGGGGCTTCC TGTCCCCAGG CTCGGGCCTC 1020 AGGCCGCCCC AGTGGGGACC TCAGGTGGCC GGAGGGGCGG GGTGTTGTTG TAGGGTCCTC 1080 GGGGGAGGGT GGGGCCATCC GTCGGGGTGT CTGGTGGCCA CCAGCTCTGC TGGCGTGGGC 1140 AGGTGTGACC CCCACCCCAG GGACAGCCGG CTGATGTCCA GCGTGGAAAA GTACCACGGT 1200 CAGACATGGG ACGCATGGAC AGACACGGGA CGCCACGAAT CAGGGATGTG GGGTGGCCAT 1260 GGGGACACAG GCGGCCCTGG GCTGTGGGCC TAAGGTGACA TGGTCCAGGG GAGGGGCCTG 1320 TGGGTTGGAG CAGAGGCCGG GGCAGGGTCG CAGCTGTGGG CAGAGGGCTG TCAGCATTAG 1380 GAGGTACCAG ATGATGATGA TGATGATGGT 1410
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