| Tag | Content |
|---|
EnhancerAtlas ID | HS093-12999 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr17:43654020-43654820 |
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 | AGACTTTCCT CTCTAATTAA GAATAAATAG TAACTTCTCT TAGAAGCAAA ATTTATTCAA 60
AGACCTGTGC TAACATTCTT AAATATCTGC TAGCCATAAT AAAGAAATCA ATGTACTTTA 120
TGTTCTTAGC TCCCACAATT TAGCCTAAAT ATTTGCCCTG GCACGCTTAG GCTGGTCCAA 180
GCAAGCATTA GGTCATAGCC TGTTCCTCTT CCTTATTTAA AAGTGTTTTT ACCTTTCTCA 240
ACATTCCACA AGTTACTTCC TCCTTCCTTT GTTCCCCTCT ACCTTTGCCT CTTTTAAAAA 300
GTTCTAAGTT ACTAACCAAT CGGGACAAAT ACAGAATGTG AGGTCCCGTT CCAGCCAAAG 360
GAAACCGGAA ACAGCAGTAA GGTAGATGCG TCAGGTTATA AATGACCCTA TCTCCTTTGT 420
TGGGTGTACT CTCATGGCAA AACTGCCCGT GAGTGTACCC TTTCTGCAGG AAGTAAAAAT 480
GGCCTTACTA AGTAAACTAA ATTTATGTTC AAGTGCTGTT TCTTCACGGC ACCGGGGAAC 540
AAGCATTTCA AACAGGAGAT TTAGAAGTCA GTTCATCCTT GACTCCTTTC CTCCCGCTCA 600
CCACATCCCA GCCTAACCAA TCTATCTCAT TCAGGATTCA TTCTAATGCC TGAATTATTT 660
TCTGCCAGGT GCTGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCC AAGGCGGGTG 720
GATCACTTGA GGTCAGAAGT TCAAGACCAG CCTGGCCACT TGAACCGAGG AAGAGGTTGC 780
AGTGAGCCAA GGTCATGCCA 800
|
