Tag | Content |
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EnhancerAtlas ID | HS111-00352 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr1:153487880-153489130 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:153488263-153488284 | GGAGGAGGACTGGAAAGGGGT | + | 6.3 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_02992 | chr1:153487818-153488496 | Bladder | SE_23261 | chr1:153487446-153489480 | Colon_Crypt_1 | SE_23926 | chr1:153487791-153489348 | Colon_Crypt_2 | SE_25303 | chr1:153487485-153489518 | Colon_Crypt_3 | SE_28418 | chr1:153487633-153489575 | Fetal_Intestine | SE_36529 | chr1:153487745-153488859 | HMEC | SE_52579 | chr1:153487618-153489518 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 153488459 | 153488748 | chr1 | 153488088 | 153488813 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I153514 | chr1 | 153487077 | 153489449 |
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Enhancer Sequence | TGTGGAAGTC ATAAGGCCCT AGGTAACCCA TGAGGAACTC AGTCTCAGGC TTTGCATGCT 60 GCAGAGAATG ATCAGAATTG GAGGGCCCAT CCCTCCCTTC TCCTGGGTGT AGGACTGCAC 120 CGCCACCTGA AGCCTTCAGA GCCACGCAGC CTGGCTCAGG AAAGCTGCAT CTGCACTCTT 180 CAGTGCCAGG GAACTAAAGG CTGGGGCTTC CTATGCGAGG TGCAGAGCTC CCAGAGGAGC 240 AGGCACACAG ACCATGACAG GAGGCGGGGT AAGAGGCATT CATTGAAAGG TGCATCTGTG 300 TAGGATTCTT CCTAGCTGAA AACCCTAAAC TGAGCCTGGA GGCAGGAGAG GGGCTTTCTG 360 ATGCTGTGGC TCTTCCTTCC TGTGGAGGAG GACTGGAAAG GGGTCCCTTG GGGCCCTCCC 420 CAGCCTCCCT CATTCTTCTG GACAGAGGGC TGGGCTGCTG TCCCCTGGAC TTGGGGAGGA 480 CACAGGCAGG GAAGCTGGGT GCTCAGAGGA CAGAGAAAGG ATCTCCTTGG ACAGCCCACT 540 GAGCAATGGC AAGTGGCTCG CCAGGTTTCT CCTTCTCTGC TCCCTGCTCT CTTGTCACAC 600 CCTTCCTGGT ATGAAGCAAG ACAAGCTCCG GTAGTGAGCC CCTCCCTGAC TCCCTCGCCC 660 TAGGCACTGC CTATAATGGG GTGGGGCAAA ACAGCTCCCT TCTCCCAGCT TCCTCTTCAG 720 GCTCCACTGG GTCTGTCCCT GCTCACCACC TGGACTAGGT CCCTAGGTGT CAGGACAGCT 780 GGAGCTGTCT CCAGGTGTGT CATCATCACT GGCATCCTGG CCACCCAGGA GCCATACCTA 840 GGTATCCTAG ACCCCCTCTC TAGGCTCCAT CCTACCTCCT CCCACCCTGT TACCCTATAG 900 CCAACAAACC CTGCATGTTC ATCCTTGGGC ACACGTCTGC CCTCTTCCTG CTACCCTACT 960 CCACCCCAGG TCACATCCTC ATTCTCTCAC CGACCCAGGG CACCAGCCTC CTGGCGGGGG 1020 GCTCTGCCTC CACTCCAGGA CCCCTTCTCC AGGCTCCAGG TCTCCTTGAA GTCCAGGTTT 1080 TCATCACATC ACCATTCTGT TCAACCTTCA CCTACTTCAC GGCTTAGAGA TGAGGCTTTC 1140 AAACATCTGT TTATTCCTAG AACCTTTCTT TAAAATAAAA CCTTATGAGG AAGCCTGATA 1200 TATGAAAAAT ACAGGGCTCT GGCTGAAATG GGGTAAGGGA CCAGGAGTCT 1250
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