| Tag | Content |
|---|
EnhancerAtlas ID | HS060-14897 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:43654150-43654840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:43654277-43654295 | TCCTCCTTCCTTTGTTCC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr17:43654748-43654763 | GAGGTCAGAAGTTCA | + | 6.38 | | RARA | MA0729.1 | chr17:43654748-43654766 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24643 | chr17:43654536-43654924 | Colon_Crypt_2 | | SE_64997 | chr17:43652951-43655118 | NHEK |
|
| | 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 |
| GH17I045576 | chr17 | 43653767 | 43655170 |
|
Enhancer Sequence | TCCCACAATT TAGCCTAAAT ATTTGCCCTG GCACGCTTAG GCTGGTCCAA GCAAGCATTA 60
GGTCATAGCC TGTTCCTCTT CCTTATTTAA AAGTGTTTTT ACCTTTCTCA ACATTCCACA 120
AGTTACTTCC TCCTTCCTTT GTTCCCCTCT ACCTTTGCCT CTTTTAAAAA GTTCTAAGTT 180
ACTAACCAAT CGGGACAAAT ACAGAATGTG AGGTCCCGTT CCAGCCAAAG GAAACCGGAA 240
ACAGCAGTAA GGTAGATGCG TCAGGTTATA AATGACCCTA TCTCCTTTGT TGGGTGTACT 300
CTCATGGCAA AACTGCCCGT GAGTGTACCC TTTCTGCAGG AAGTAAAAAT GGCCTTACTA 360
AGTAAACTAA ATTTATGTTC AAGTGCTGTT TCTTCACGGC ACCGGGGAAC AAGCATTTCA 420
AACAGGAGAT TTAGAAGTCA GTTCATCCTT GACTCCTTTC CTCCCGCTCA CCACATCCCA 480
GCCTAACCAA TCTATCTCAT TCAGGATTCA TTCTAATGCC TGAATTATTT TCTGCCAGGT 540
GCTGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCC AAGGCGGGTG GATCACTTGA 600
GGTCAGAAGT TCAAGACCAG CCTGGCCACT TGAACCGAGG AAGAGGTTGC AGTGAGCCAA 660
GGTCATGCCA CTGTACTCCA GCCTGGGCGA 690
|
