| Tag | Content |
|---|
EnhancerAtlas ID | HS191-16539 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr17:56453910-56455010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr17:56454146-56454157 | AGGGTGTGGCT | - | 6.02 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23473 | chr17:56453732-56455624 | Colon_Crypt_1 | | SE_27272 | chr17:56453844-56455630 | Esophagus | | SE_28098 | chr17:56451905-56456269 | Fetal_Intestine | | SE_28995 | chr17:56451897-56455936 | Fetal_Intestine_Large | | SE_34462 | chr17:56453810-56457073 | HCT-116 | | SE_50030 | chr17:56453826-56455795 | RPMI-8402 | | SE_52476 | chr17:56453755-56455731 | Small_Intestine | | SE_56729 | chr17:56453870-56454458 | VACO_400 | | SE_56729 | chr17:56454557-56455149 | VACO_400 |
|
| | 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 |
| GH17I058374 | chr17 | 56452143 | 56462492 |
|
Enhancer Sequence | AAGAAAGACA GCATTGGCAT TCCCTGGGTA TAACACAGGG GCTGTCTTTG CCCTTCCTCC 60
AAGGAATTTT CAGCCAGGAA GCGGGCTCTT GAGAAAACAG ATGCAAATAC ATCTGTCTCC 120
TTGGAATGCA AGGTCTCCTA ATCATGAAGA TGCAAACACG ATTTCTACAG TGGGCCACCT 180
GTCCCCTCAG TGACACCAGG GGAGGGTCAA GAGAAATGAG CTTGCCTGAT TTGAGAAGGG 240
TGTGGCTGTG GAGGGCTCAT GGAAACTTGG TGAATTTGAC TTCCTCAAAG GCCAGGAGTT 300
AGGACACCAC TGTCTCACAG GCTGCCATGA GGGGCAAATT AAGAGGCACT TGCTTTCAAG 360
CACGAGTTGG GTCATTCTGA CTCAGAATTC AGCTTTGCAT ACATATTTTA TACCCCCTGT 420
GTAAAGACAT GTGAACTGTC CTTCGGTGGT GTGTGTTGTA TTTCATATTC CTGAGTCTAT 480
TCTCCCTGTG TCCTCCTTAA CTTATTTGTT CTGATTTTTT CCCCTCCCTC CCAAGACAGA 540
CCTAGAGTTC AGATTCTGAC CCCATCATTT ACCTGTGTGA CCTTGGGCAT GTTAATCTTT 600
CTGAGCCTCA TATTGCTCGT CTTTGGAATG GGAACAAGAA TGCTTTGTGT AGACAGGAGA 660
TAATGGATAT CAGTGCCTAG CAAAAAGCCT GACACTTAGT AAGTGCTCAC TTAATGGCAG 720
CTGTTTTTAT TACTGCATCT ATAATAAAGT CCCTTCTTAT TCCTGGAAGG GACAAGGCCT 780
TTTCTGAACC CCTCCCCCGT TCTTTGGTAA TCAACAGTGC TTCTGAATGC CAGTGTTCTG 840
CAAGGCGCAT TCTGGGACAG CTCATTATCC ACAGTCACTT CCCTCCTGTT CTCAGCCCTC 900
CAAACCCCAC TGAACAAGCT CTTCCAGTTC TCAGCCTGCC TCCTTCCCAT GAAGGAAGCC 960
ATGTGATCTC ATTACCTCCT CACAAAGGGC ATTTCAGGGC TCAACTGGGC CTGGAACTTA 1020
ATGCTGGTCT CCCCTTATCC ATGGCATCTC CTCCTCTTTG GGTGTGTGCT TCTGCAAGCA 1080
ATTCTTCACT GTCTCCTGTT 1100
|
