Tag | Content |
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EnhancerAtlas ID | HS108-00067 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:1814270-1815460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata1 | MA0035.3 | chr1:1815074-1815085 | ACAGATAAGGA | - | 6.14 | IRF1 | MA0050.2 | chr1:1814724-1814745 | AAAAAAAAAGAAAAAGAAAAA | - | 6.09 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_09353 | chr1:1814365-1815631 | CD14 | SE_23324 | chr1:1814292-1814742 | Colon_Crypt_1 | SE_23324 | chr1:1814937-1815320 | Colon_Crypt_1 | SE_41740 | chr1:1814988-1815306 | LNCaP | SE_58439 | chr1:1751668-1840814 | Ly1 | SE_61572 | chr1:1814774-1842316 | Toledo |
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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 |
GH01I001883 | chr1 | 1814451 | 1815268 |
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Enhancer Sequence | AATTGTTTGA ACCCAGGAGG TGGAGGTTGC AGTGAGCCGA GATCATGTCA CTGCACTCCA 60 GCCTGGGTGA CAGGGCAAGA CTCCGTCTCA AAAAAAAAAA AAGGACATAA ACTTACCAGT 120 TTTCAAAATG AGGCATAGTT CAAGATTATT CTACAAAGGT AAAGGAAAGC CTTTAAGAGC 180 AGGTTACTGT GGCTCACATC TATAATCCCA ACATTTTGGG AGGCTAAGGC AGGAGGATCA 240 CTTGAACCCA GGAGTTGGAG ACCAGCCTGT CTCTACAAAC AATAAAAAAA ATTAGCTGGG 300 CACGGTGGCA TGTGCCCGTG GTCCTAGCTA CTTGTGAGAC TGAGAGAAGA AGATCGTATG 360 AGCCCAGGAG GTCCAGGCTG CAGTGAACCA TGATCATACC ATCACATTCC ACACTCCAGC 420 CTGGGTGACA CAGCAAAACC CTGTCCCAAA AAAAAAAAAA AAAGAAAAAG AAAAAAAAAC 480 CTTTCAAGAA AAGATAAGGA TGTGAGAGAT TTAGTAGAAA GTAAGGCAGT AAATAAGTGA 540 TAGGGATTTG CAAAGATAGC TAATATGCAT GTTCCACACC CTGAATTAAT ATTCTTCTGG 600 AACCATGGAG AAAAAAAGAA AAATCTCAGT AAACTGTCAT CTTATAACAT TTGTTAACCT 660 TGCCATAAAA GAAATTTTTA CAAAGCAAGG CCATCAGCAA CAGAAATAGC TAATCCTTGC 720 ACTGAGCTCT GTTATCAGTG CCCACATCAG GACTCATTTA ATCCTCACAA TGACCCCATG 780 AAGGAGGCTC TAGGAGCCTG TTTCACAGAT AAGGACAGAC ACAGAAGTCC TAACACTGCA 840 GGTGGCCTAA ATTAAGGCAG GCTCAGGGAG GACAGAAAGC TCCTGTGGAG TGGAAGGGTA 900 GAAGTTGAAC TGATCTTGAT TTTCAGTGCG AATAAAAGTC CTAACACTGC AAATCAGCCA 960 GTGAGGCAAC AGAGCTGAGC TGGGCTCTAA CTCAGACAGT GCCAATCCTT TTGAAAACTA 1020 CTGAATTTCT CTCACTCCCT AGATTTTAGG AATTATTTTA AAATTCCTAT GAGAAATTTT 1080 CTGAAACCTA TTGTAGACTC TTTTGACATG CTCATCTAAT TATAAAGTGT CCGGACTTTT 1140 TTTTTTTTTT TTTGACCGAG TTTCACTCTT GTTGCCCAGG CTGCAGTACA 1190
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