Tag | Content |
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EnhancerAtlas ID | HS180-03152 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:154411840-154412940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:154412339-154412357 | CCTGCCTGCCTTCCTTTG | - | 6.35 | EWSR1-FLI1 | MA0149.1 | chr1:154412335-154412353 | CCTGCCTGCCTGCCTTCC | - | 7.45 | MEF2C | MA0497.1 | chr1:154412922-154412937 | TTCTATTTTTAAATT | - | 6.5 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00437 | chr1:154410501-154413087 | Adipose_Nuclei | SE_09189 | chr1:154410306-154416288 | CD14 | SE_17632 | chr1:154411908-154416448 | CD4p_CD25-_CD45RAp_Naive | SE_18405 | chr1:154410428-154416120 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19165 | chr1:154411944-154415379 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24531 | chr1:154412197-154412478 | Colon_Crypt_2 | SE_62668 | chr1:154357227-154415486 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 154411979 | 154412800 | chr1 | 154412049 | 154412363 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154439 | chr1 | 154411601 | 154412810 |
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Enhancer Sequence | AGTGCAGTGG CGTGATCTCA GCTCAATGCA ACCTCTGCCT CCCGGGTTCA AGCAATTCTC 60 CTATCTCAGC CTCCCGAGTA GCTGGGACTA CAGGCACCTG CCACCATGAC TGGCTAATTT 120 TTATATTTTT AGTGGAGATG GGGTTTCACC ATATTGGTCA GGCTGGTCTT GAACCCCTGA 180 CCTCAGGTGA TTCACCCACC TCAGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC 240 GCGCCCTGCC CATTTATATT ATTTTTAAGT GCACAGCTCT GTGGCATTAA GTATTGTTGT 300 GCAACCATCA CCACTTTACT TCTCCAGGAC TTTTTTCATC TTGTAAAACT GAAACTCAGA 360 ATCTGTTAAA CAGTAACTTT CCTTTCACCC ACTCCTTCCC CCAGCTCGTG GCAACCACCA 420 GTCTACTTGC TTTTTCTGTG AGTTTGACTA CTCTAGTACT TCATTTGCTT GCTTGCTTGC 480 TTGCATGCCT GCCTACCTGC CTGCCTGCCT TCCTTTGTCT CTTTCTGTCT CTCTCTTTTT 540 CTCTTTTTTT TTGAGACGGA GTCTCACTCT GTCACCCACC CAGGCTGGAG TGCACTGTCG 600 TGACCTTGGC TCACTGCAAC CTCTGCCTCC CGGGTTCAAG CAATTCTCCA GCCTTAGCCT 660 CCTGAGTAGC TGAGATTACA GGCGCCTGCC ACCATGCCTG GCTAATTTTT GTATTTTTTG 720 TAGAGACAAG GTTTCACCAT GTTGCCCAGG CTGCACTCTA GGTACTTCAA ATAAGTGGAA 780 TCAGAGAGTA TTTGTCCTTT GGTGACTGAC TTATTTCACT TAGCATAATG TCCTCAAGGT 840 TTATTCATGT GGTATAACAT GTGTCAGACT TTCCTCCCTT TTTAAGGCTG AATAATATTC 900 CATTGTGTAG AGATACCACA TTGTGTTGAT TCATTCATTT GTCAGGGGAC ACTGGGTTTG 960 CTTCCCCATT TTGGTTGTGC ATAATGCTGC TATGAACACG GGTGTAAAAT ATCTGTTTAG 1020 ATTCCTGCTT TCAGTTCTTT TGTGTATATA CTCAGAATTA TAATTGTGGC ATTATATGGT 1080 AATTCTATTT TTAAATTTTC 1100
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