Tag | Content |
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EnhancerAtlas ID | HS060-27007 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr4:185703610-185705020 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr4:185704668-185704682 | GTGAGTCACCTCTT | - | 6.11 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_00065 | chr4:185702927-185706107 | Adipose_Nuclei |
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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 |
GH04I184782 | chr4 | 185703570 | 185704605 |
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Enhancer Sequence | GCCTTGAAAA CGCCTATCTG CAATGGACGT GTCTTCTCTC TTCCAGCCAC TAAACAACAG 60 AAGTAACCCA GGAGGCACAG AGGATTCCAT GATGCCTCAG GACCATCACA CACAACACAC 120 ACATGTTCAA CACACACAGG CTGTTCTTAC ACTTGTGAAA ATGAGGGATC CTGGAAACTA 180 CTATTTGTGC AAGAAACTAC TATTTGGCTC TGACAGGACA GAATAAAAAT GGGAAATCCT 240 TCCAATCATG TGAGATACTG CCCCTAGCTC CTTCTACAGG GGAGGTGTGA GAAGTTGCTT 300 CCCCTTCTCT TGAGAGACAG ATGAACACCT CTCAAGCAAA GCCTTCTGCA TCCTGTCGAC 360 CCCAGAGGAC GGACGGGGAG AAATCATGCA CTTCAGTCTG AGAAGAACCA ACAAGCACTA 420 CTGCAGGAGT GTGGCTCCGA GGCTGCAGAG AACGATCCCT TCCACAGACG CACCCCAAAT 480 ACACCAGCTC CTAAGCTGCC CTTCACACAA AACCCAGAAG GAGGAAGTGC ATTTGTATTC 540 ATGAATCCGC ATGATTACCT GCCCCGAGAG CAGGAGAAGG GGGGCCAGGG ACGGGAGCCT 600 TTCCTGGACA GCTGTGTGGA AGCAGCAGGC AGCAGAGCTG GCCTGTCTGG AGCACGTGCC 660 TGTTCCGGGG TGCCGTGTGG ACTGGGGAAG AGCTGTGGCA CCCACATTCA TTGTAATCAT 720 GATAAAAATA AAAATAAACA GCAACGTCTT CCTGCACTGC TACTGCCACT CATGAGCCGC 780 TGTTTCAACA GCTGTAGCCG TTGATGGGTG GGGACTAGAG ACCGACAAGG GCCACCATAC 840 TCAGATCCCA GCTTCCTTTG TGCTTATACA GTAACACAAG TGCCTTCCCC GAACATCTGT 900 GTTCCTCCCT ACAGCTGCCT GGGGGTAAGT GTCACACAGG TGGTGAGTTG GCCAAGGACA 960 GCTTTGAGGG TCAGCAGCAT GCACTAGGAA AGCCTACACA AGAGGCTGCA GGCCTTGCTT 1020 CTGGTCCTGG TTCTGCCACT AACCAGCTAT AACCTTGGGT GAGTCACCTC TTTTCCTGAG 1080 ACAGGTCCTC CTCATCTGTG AAATGAAGAT GTATTCCCAC GTTCCAGCTT CTGAGTTTTT 1140 CTAGTACCCC TCAAGTGGAG AGAAATAATG CTATGCCGCC AGGGGGACCG GGAGAGTTTC 1200 TAGAATTTTA TCTTAAAAAT TATACTTGAC TTCACAATGT ATCCACATCA GCTTTGAAAT 1260 ACAATGCTTT GAACCACCTG TTAAATTCCT TAACTTGTTC TCCCCAAACC TTTGTGTCAA 1320 GTTTCTCCTT GGATGCCCCA TGCTTACGGC AAGGCTCTGA GCTGGTCCAG CACATACACT 1380 CTGGAGAAAC CTTCCGGCTC CAAGAATGCA 1410
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