| Tag | Content |
|---|
EnhancerAtlas ID | HS043-12713 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr14:23466560-23467630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:23466897-23466915 | GCTTGCTTGCTTCCTTCT | - | 6.19 | | EWSR1-FLI1 | MA0149.1 | chr14:23466901-23466919 | GCTTGCTTCCTTCTTTTC | - | 6.34 | | EWSR1-FLI1 | MA0149.1 | chr14:23466905-23466923 | GCTTCCTTCTTTTCTTCC | - | 7.18 | | ZNF263 | MA0528.1 | chr14:23467182-23467203 | CCTCTCACTTTTTCCTCCTCT | - | 6.15 | | ZNF263 | MA0528.1 | chr14:23466998-23467019 | TTCCTTTCCTCTACCTCCCCC | - | 6.16 | | ZNF263 | MA0528.1 | chr14:23466632-23466653 | GGGGGAGGAGAAAAAGAGAGG | + | 6.8 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33418 | chr14:23463566-23470692 | H2171 |
|
| | 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 |
| GH14I022997 | chr14 | 23466494 | 23466910 |
|
Enhancer Sequence | AGTTTCATCC CTCCCATCTA CTCCATGTGT TCTGCTCCTT TACTCTTTAC TGGGTGTCTA 60
TGTCTTGTTG TGGGGGGAGG AGAAAAAGAG AGGACAGACG GAGAATAAGG TGGAGAGCTG 120
ACAGAACTCC AACCGTCTCT CAAGTGGCAC CACATCTGTT ATTTTCCTAT CTCTAAGATC 180
TCTATAGTTG CTCCATCTCC TTTTCATACT TCCATGTGTG ACATTCTGCA GTTCTTACTC 240
TACTCAGCCA GGATTTTCCT GCTCATATGG CCCTTAAGCA GTAAAGAAAC TGAAATAGCA 300
CAATGTACAT CTATGTCTTT TCCTGCTCAC AAAATATGCT TGCTTGCTTC CTTCTTTTCT 360
TCCCTCTTTC TCCCTATATG TTATTCTCTT ACTGTTAACA ATCAGTTGGC CATTTCTTTT 420
TCTCATTTCC CATTTTATTT CCTTTCCTCT ACCTCCCCCT CGCCTTACCT CATAGTCTCT 480
CTCCCGTGGT GTAGATTCTC TTTCCACATA GATTCACCTT TCTTCTGTGC TCCCTTTTTT 540
CACTTTTTCT CCTCCCTCAG CCCTTCATTT CTACTTGTCT CTTTCCCTCC CTATACTTGT 600
CTTCTATTAT CTTTATCTTT GTCCTCTCAC TTTTTCCTCC TCTCTCCACC TCTGCCTCTC 660
TCCCCTGTAC ATTCCCATCT CTCTTTGTAC TGAATTCCTC TTGGCAAGCA GAGGGCCTGC 720
GATAAAATAT GAATGAGCCG TCTGTGCACG GCAGGCATCC TCGCCAGGAG AGGCAGAGTC 780
CATGGAGCAG CCGAGACAGC TGTGGAAGAG AAGGTGCCAT GCGGAGCTAC TGAGAGAGAG 840
GGAAGGGCAC CCCATCACTA CACACAGCAA AAAATGACCT TCTGCCAAAG AAGCTGATGG 900
TTCAGGAAGA AAATAGAGCT GACTATCCCT GAAGGAAAAG GAAACGTGGT ACTGTTTTGC 960
TTTATCACAA ATACAAACAA AAGGTTTAAA GATGGAAAGA AAAGAACAGA AAGGAAAAAG 1020
AGTGAAAAGC CAGGAAAAGC ACCTAGGAGG AATAGCCCTC TGCTGCCATA 1070
|
