| Tag | Content |
|---|
EnhancerAtlas ID | HS047-14891 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:56453850-56455000 |
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 | TATTCTCAAA TTAAAAACAA ATAATAGCCA TTTGAACTAG GACTCAGTTC AGCACCTAGC 60
AAGAAAGACA GCATTGGCAT TCCCTGGGTA TAACACAGGG GCTGTCTTTG CCCTTCCTCC 120
AAGGAATTTT CAGCCAGGAA GCGGGCTCTT GAGAAAACAG ATGCAAATAC ATCTGTCTCC 180
TTGGAATGCA AGGTCTCCTA ATCATGAAGA TGCAAACACG ATTTCTACAG TGGGCCACCT 240
GTCCCCTCAG TGACACCAGG GGAGGGTCAA GAGAAATGAG CTTGCCTGAT TTGAGAAGGG 300
TGTGGCTGTG GAGGGCTCAT GGAAACTTGG TGAATTTGAC TTCCTCAAAG GCCAGGAGTT 360
AGGACACCAC TGTCTCACAG GCTGCCATGA GGGGCAAATT AAGAGGCACT TGCTTTCAAG 420
CACGAGTTGG GTCATTCTGA CTCAGAATTC AGCTTTGCAT ACATATTTTA TACCCCCTGT 480
GTAAAGACAT GTGAACTGTC CTTCGGTGGT GTGTGTTGTA TTTCATATTC CTGAGTCTAT 540
TCTCCCTGTG TCCTCCTTAA CTTATTTGTT CTGATTTTTT CCCCTCCCTC CCAAGACAGA 600
CCTAGAGTTC AGATTCTGAC CCCATCATTT ACCTGTGTGA CCTTGGGCAT GTTAATCTTT 660
CTGAGCCTCA TATTGCTCGT CTTTGGAATG GGAACAAGAA TGCTTTGTGT AGACAGGAGA 720
TAATGGATAT CAGTGCCTAG CAAAAAGCCT GACACTTAGT AAGTGCTCAC TTAATGGCAG 780
CTGTTTTTAT TACTGCATCT ATAATAAAGT CCCTTCTTAT TCCTGGAAGG GACAAGGCCT 840
TTTCTGAACC CCTCCCCCGT TCTTTGGTAA TCAACAGTGC TTCTGAATGC CAGTGTTCTG 900
CAAGGCGCAT TCTGGGACAG CTCATTATCC ACAGTCACTT CCCTCCTGTT CTCAGCCCTC 960
CAAACCCCAC TGAACAAGCT CTTCCAGTTC TCAGCCTGCC TCCTTCCCAT GAAGGAAGCC 1020
ATGTGATCTC ATTACCTCCT CACAAAGGGC ATTTCAGGGC TCAACTGGGC CTGGAACTTA 1080
ATGCTGGTCT CCCCTTATCC ATGGCATCTC CTCCTCTTTG GGTGTGTGCT TCTGCAAGCA 1140
ATTCTTCACT 1150
|
