Tag | Content |
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EnhancerAtlas ID | HS048-02169 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:118188730-118189600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:118189472-118189490 | GGAAGGAATGGAGGACAG | + | 6.27 | PPARG | MA0066.1 | chr1:118189409-118189429 | AATGGGTCCACGTGCCCCAG | - | 6.24 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_31627 | chr1:118188834-118189563 | Gastric | SE_61007 | chr1:118138819-118218057 | HBL1 | SE_62427 | chr1:118147317-118217904 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I117646 | chr1 | 118188740 | 118189601 |
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Enhancer Sequence | TATATAAAGT GCTTAGCAGA ATGTCCGGAA TGTAGTAATA ACTCAGTGAA TGGTCTTAGC 60 TGTTTTTAAT AATGAAGCTC TGGAGTGAGG CCAAGAGGAA CAGTTGCCTT TGGTTACATA 120 ATCCATCTTG TCCATGACTT TGAATTTAGT CTCAGGGGCA CAATGGGCAG GTTTCTCTGG 180 AGGATGCTGG TTCCCTGAGA GGTGAGAAGC TGGGCTAGTA AGCTTGGACC CATGTTCCCA 240 CCCCACTGGG CAGCCTTACT GGGCATGGCC CTTTCCGTTC TGGCTCCCTG GGACTTGGCT 300 CACTGAGTTT GGCTCTGGGC AGAGTCGTAT GACTGGTCCT CACTGCACCC AGCTTGCTCT 360 GGCGGGTATC AGGTGGCCTG CAGCTTGAAG AACTCCTATG TCAGCAGCTC TGGAAGCCAG 420 CAGCTCTGAG GGAGAGACCA GAGGTCTTGA GCTGGAGACA CCCAGAGGCC CAGTGGCAGA 480 CTAGTCTAGA ACAGGGACAT CAGACCTGGC AGCACATGGC TCAGCCCCGT GGAGTACAGA 540 CTGCAGTGGC TTCAGCTGGC CCCCAGGCCC CTTCTCCTCT GGCCCAGATA TGAACCACGC 600 CCTGTACAGA CCGGAGGACT TTACCTCCTA GGAGCCGCAG CTTCCTACAG AAGACCAGTG 660 GGTGTGCCAG CGATGTTAGA ATGGGTCCAC GTGCCCCAGG AAGGCAGCCT TTTCCGCAGC 720 ACAGAAGTGG GAGAGCATAG CTGGAAGGAA TGGAGGACAG CGGAGCAGAA CTCAGGACCA 780 GAGGGAGGCC TGAAGGAAGT TGTCTTAGTG TAGTCTGGTA TAGAAAACTT TTTTAAAAAG 840 AAAAGTAATT TTAGTATTTT CAAATCCTGT 870
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