Tag | Content |
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EnhancerAtlas ID | HS176-29136 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr4:74974990-74976230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr4:74974991-74975002 | TGTTGTGCAAT | - | 6.14 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_34020 | chr4:74973468-74984340 | HCC1954 | SE_34944 | chr4:74973434-74984043 | HeLa | SE_35924 | chr4:74973407-74984079 | HMEC | SE_38660 | chr4:74973379-74978167 | HUVEC | SE_46049 | chr4:74973285-74983971 | Osteoblasts | SE_55844 | chr4:74970769-74984442 | u87 | SE_64715 | chr4:74973303-74981674 | NHEK | SE_67651 | chr4:74970769-74984442 | u87 |
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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 |
GH04I074107 | chr4 | 74973459 | 74983803 |
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Enhancer Sequence | TTGTTGTGCA ATTCAGGGTG CTCACTCATA GCACATACAG TGTTGAATAT AATCATCTAT 60 AGCTTCAAAT GTGCTGGTCA TGAGTCCACT AAGAAATGCA GAAAAGAAGC AAGAGGAGAA 120 ACAGTCTGAC CTTAGCTGCA AAGGGCACCA GGATGCCAGC ATGCTAGAGT CATGCTGGTT 180 TCCCCCTTCA TGGAAGTGAC AGGCCCATGA CAAATTTACG CAAATATGAC ATGGAAAATA 240 ATTTCTTGAA GAAAACTTCT TTTGCCATAT GTTTCCTGGT TTTCTTCTGG TTTGGCCTGT 300 GAATGGTATC AGTTTATTTT CGAGTCTAGT ATCCAATATT CCTGGAAGCT AGGGCTGAGG 360 AATGTTCATT TCACAGGATG GCCAAGGTCT GATATGCAAG GCTGGGATTG AGTGAGGCCC 420 CAGGGCAGGC TGAGAACAGG AAGCGGTTTC ACTGACATTC CATTCCTTTC TCTCCCTGAC 480 CACTCCCATC TCAGAGTGGC CAAGGATCAC TGAAGAAATA GTAATTGTCA TCTAAACCTC 540 ATAACAGGGG TGTCTGGCAC TTGAGAGTTG ACCCACTTCA ATTTATTCAA GCTCCCACTC 600 AAAAAAACTC TCCTTGACTT ACAGGATATG AATACCAATT CCCTAAAGCA AAGCATAGTG 660 AGAATTTCAG TAAAAGAAAA GAAACGAAAA CCCCAGAAAA AGTATTCAGT AATTGAAGAG 720 TCACCATCCC GAGGGTCCTA TAGGAGCTCA CCCTTGGTCG GTGAGAACTA CTCAGTCAGC 780 CTCACTTACC TCATTGCTCT GGCCAGCTCA TACAGGCTTA CAAGAGCAGG TTATTAAATG 840 GTCAGGAATT TTGATAGCCA GTTATTCATT GTTGGAAGCA TAAATTTGAC CACAGTGGGA 900 GTGTTTATGG AAATCAGCAA ATGCTACAAA TCTGATTTTT TTTTAAATTT GAAAGCTGTT 960 TTACCAACAC ACCGCGGCTT ATAGCTCTGC ATAAACATAA TCTGTATCAA CTTTATCCTC 1020 TTTTTCCTCC CCTTACTATA GCCTCTGTCC TCTGCCCTCA TTATCCTCTG CTGGGATCTC 1080 TTGAATATTT TTTCCCCTTT AGCTGGTTTT CTCTTTCACT CATTGATTTG TCCTGGGTTT 1140 CATCATCTAG GCAACTCTCA CGCACAGAAA ATTCTTGGGA GTTGTTCTCA CTAGACTGAT 1200 AGCAATACCA CTTTTATTTA TTATTATTAT TATTATTATT 1240
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