Tag | Content |
---|
EnhancerAtlas ID | HS134-00174 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:8968200-8969570 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr1:8969097-8969112 | GACAATGACTAAGCA | + | 6.14 | SPDEF | MA0686.1 | chr1:8968655-8968666 | ACCCGGATGTG | + | 6.32 | ZNF263 | MA0528.1 | chr1:8968394-8968415 | TAAGGAGGGGATGCAGGAGGG | + | 6.08 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_56056 | chr1:8967292-8969354 | u87 | SE_67633 | chr1:8967292-8969354 | u87 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 8968400 | 8969144 | chr1 | 8968861 | 8969246 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I008908 | chr1 | 8968234 | 8969415 |
|
Enhancer Sequence | GGGGGATATA TTCTAACAGG GAACTGCCAA GCCTCTATAT CACCCTCTCT TCTAGCTTGC 60 TGAATTCCTG TCTGAATAGA ACTAAGAGCA GTCATTCGAG GCGCTGCTTG AACAGTCACT 120 GGGGCAACTA CTTTTTGCCC AGTGTCCTCT GGAAAAGAAA GATCTGGAGG TCAGGCCACT 180 TTCTGTCTTC AAAATAAGGA GGGGATGCAG GAGGGTAGGG ATGAACCTCT TCCTCCTTTG 240 CTGCTTTAGC TTTAGCTGGC AAACAAACCT GCTCTGTCAC CTCTTCTGTT ACTTCATTAT 300 ACTTTCCTTC CTCGTCATCA TCAGTGTGAA AAGCTTCCAA GGACCCTGAT GCTTCTGAGC 360 TCCTCTTCTT ACTCACCACG GGGATTGCTT AAGAGTACTC GGGTGTCCTC CAGTTTAGTT 420 TCACGTTCTC CAACTGTCGC TCCGGCGACC CTTTGACCCG GATGTGAGCC CCCATGTTGG 480 GCACCGCTTG CCGAGACCAG CTCAGTCGCG GAGACTCTAA CCCGGCGGCA CTAGAGGAAT 540 TAAAGACACA CACACAGAAA TATAGAGTGT GGAGTGGGAG ATCAGGGGAC TCACAGCCTT 600 CAGAGCTTGA CTCACATGTT TATTGACAGC AAGCCAGTGA TAAGCATTAT TTCTATAGAT 660 TATAGATTAA CTAAAAGTAT TCCCTACAGG AAACAAAGGG ATGGGCCAAG ACAAAGGGAT 720 GGGCTCTGGC TAGTTATCAC ACAAACAATA GCATGAGTGA TCTGGTCTGA AATTCCAGGG 780 CTCAAACAGT CTTCACGCTT TGGCCTCCTA AAGTGCTGGG ATTACAGATG GGAGCCACTG 840 CACCCACCAG GCCTCCAGTT TTTGAGCCAA GGCCATGCTC TGTCTGGGTA GCCCCAAGAC 900 AATGACTAAG CATGCTGGGA TACCAGGCCT GGTCATTTCT GCCCAACGGG GCTGTACTGA 960 TGGCCTGTAT TTGCTCCAGA GCTCCCCGTT GGATTAGCCA AGACGGTTCT GCATCATCGT 1020 CTGAGACTCT CCCTGATAAA TCCCGCTCTC TCCTGCTTTT TCTTTCACAG CTGCTACCCC 1080 CAATACACCC TTTTATTTTA ACAGTTTTTG GGGAATAGGT GGTTTTTGGT TACATGGATA 1140 AGTTCTTTAA TGGTGATTTC TGAGATTTTG GTACCCCCGT CACCCAGGAA GCACACACCA 1200 TACCCAACGT GTAGTCCCAA TACACTCTTT TTTGTTTTGT TTTGTTTTTT TTGTTTTTTG 1260 AGACGGAGTC TCACTCTGTC GCCAGGCTGG AGTGCAGTGG TGCGATCTCG GCTCACTGCA 1320 ACCTCTGCCT CCCGGGTTCA AGCGATTCTC CTGCCTCAGC CTCCCAAGTA 1370
|