Tag | Content |
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EnhancerAtlas ID | HS050-04156 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:153492690-153493660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:153492692-153492710 | GGAGGGAGGGAGGGAGGG | + | 6.03 | IRF1 | MA0050.2 | chr1:153492767-153492788 | AGAGAGAAAAAGAAAGAAAGA | - | 6.22 | KLF16 | MA0741.1 | chr1:153492989-153493000 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr1:153492990-153493000 | GGGGCGGGGC | - | 6.02 | PBX1 | MA0070.1 | chr1:153492921-153492933 | ACATCAATCAAT | + | 6.44 | SP1 | MA0079.4 | chr1:153492988-153493003 | AGGGGGCGGGGCTTC | - | 6.79 | SP2 | MA0516.2 | chr1:153492987-153493004 | AAGGGGGCGGGGCTTCC | - | 7.44 | SP4 | MA0685.1 | chr1:153492986-153493003 | GAAGGGGGCGGGGCTTC | - | 7.66 | ZNF263 | MA0528.1 | chr1:153492717-153492738 | GAGAGAGGGAGGGAGGGAGGG | + | 6.11 | ZNF263 | MA0528.1 | chr1:153492707-153492728 | GGGGGAGAGAGAGAGAGGGAG | + | 6.13 | ZNF263 | MA0528.1 | chr1:153492729-153492750 | GAGGGAGGGAGAGAGAGAGAG | + | 6.89 | ZNF263 | MA0528.1 | chr1:153492725-153492746 | GAGGGAGGGAGGGAGAGAGAG | + | 6.9 | ZNF263 | MA0528.1 | chr1:153492701-153492722 | GAGGGAGGGGGAGAGAGAGAG | + | 7.06 | ZNF263 | MA0528.1 | chr1:153492693-153492714 | GAGGGAGGGAGGGAGGGGGAG | + | 7.23 | ZNF263 | MA0528.1 | chr1:153492697-153492718 | GAGGGAGGGAGGGGGAGAGAG | + | 7.35 | ZNF263 | MA0528.1 | chr1:153492721-153492742 | GAGGGAGGGAGGGAGGGAGAG | + | 7.43 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23261 | chr1:153492648-153493055 | Colon_Crypt_1 | SE_23261 | chr1:153493085-153493774 | Colon_Crypt_1 | SE_23926 | chr1:153492684-153493009 | Colon_Crypt_2 | SE_23926 | chr1:153493191-153493642 | Colon_Crypt_2 | SE_25303 | chr1:153492612-153493815 | Colon_Crypt_3 | SE_28418 | chr1:153492480-153494160 | Fetal_Intestine | SE_52579 | chr1:153492604-153493885 | Small_Intestine |
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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 |
GH01I153520 | chr1 | 153492710 | 153493995 |
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Enhancer Sequence | GGGGAGGGAG GGAGGGAGGG GGAGAGAGAG AGAGGGAGGG AGGGAGGGAG AGAGAGAGAG 60 AGAGAGAAGA GAGAGAGAGA GAGAAAAAGA AAGAAAGAAA GTTTATTTTG CCAAGATTGA 120 GGACACAGCC TCAGGAGGCA CCCGTGACAC AGCCTCATGA CAGGTCCTGA TGACATGTGC 180 CCAAGGTGGT CAGGGCACAG CTTGGTTTTA AACATTTTAG GGAGACATGC GACATCAATC 240 AATATATTTA AAATGAACAT TGGTTAGGTC CGGAAAGGTG GGACAGCTTG AAGCAAGAAG 300 GGGGCGGGGC TTCCAGGTCA CAGGTAGATG AGAGACAAAG GTTGCATTCT TTTGAGTTTC 360 TGATTAGCCT CTCCAAAGGA GGCAATCAGA TATGCATTTA TCTCAGTGAG CAGAGGGGTG 420 ACTTTGAGTA GAATGGGAGG CAGGTTTGCC CTGAGCAGTT CCTAGCTTGA TTCTTCCTTT 480 TAGCTTAGTG ATCTGGGTCC AAGATATATT CCTCTCACTG AAAAAACCAC ACATATAATA 540 GTTAAAGTGA GTGTCCAAGC CAAAAGAGTC TAGGAAGAGG CCCCAGAGCC CTGGCCATAG 600 GCATGCCCCT TACTCTGTTA GCTAAATAAC ATCCCTGGGC CTGTTAAATC TACATGCTGC 660 CTTTGTACAA ATGAGAAAAA GGTGTCTCAT CCTCTAGGCA GAGGTAGCCA GGCACCGAGG 720 TGGTGGCTTA GAAAGCTCAG CACAGGCTGA ATTTCAGCCC TCACTGATTC CCCTAGCATG 780 AGCTTTTTGT GCAGGACACA GATTGGAGGG CTGTTCTCAG CAGCTCTGCC TAGGGTAACT 840 CCAGGGAGCA CAGCCTTAAC ACTATAGACT AGACCGTCTC TAACATCCCA CCCAGCTCTG 900 GTTTATCAGA CTTCTTCAAT TCCATAGCCT CACTCCTGAA CAAAGCAGTT GGGCTATGTA 960 TTTTTGTGAG 970
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