| Tag | Content |
|---|
EnhancerAtlas ID | HS104-19697 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr14:91263650-91264860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYCN | MA0104.4 | chr14:91264513-91264525 | GGCCACGTGGCG | + | 6.74 | | MYCN | MA0104.4 | chr14:91264513-91264525 | GGCCACGTGGCG | - | 6.74 | | NFE2L1 | MA0089.2 | chr14:91263936-91263951 | ACTGCTGTGTCATGC | - | 6.19 | | Nfe2l2 | MA0150.2 | chr14:91263938-91263953 | TGCTGTGTCATGCTG | - | 7.07 | | Nkx3-2 | MA0122.3 | chr14:91264053-91264066 | TTTAAGTGGTTAT | - | 7.82 | | Nr2f6(var.2) | MA0728.1 | chr14:91264838-91264853 | GAGGTCAAGAGTTCG | + | 6.24 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_40377 | chr14:91263861-91264676 | K562 |
|
| | 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 |
| GH14I090794 | chr14 | 91261042 | 91266149 |
|
Enhancer Sequence | ATTATCTGGG TATGGTGGCA CACACCTGTT AATCCCAGCT ACTCGGGAGG CTAAGGCAGG 60
AGAATCACTT GAACCTGGGA GGCAGAGGTT ACAGTGAGCC GAGATGTCTC CACTGTACTC 120
CAGCCTGGGC AACAGAGTGA GACTTAGTCT AAAGAAAAAA AAAGCCTCAG AATGACCAGA 180
GTGAACTCCA GCTCCTCGTT TACTGGGCTT CCTGTAATCC CGGGTAACCC AGCATTTGCA 240
GTATTTGTGA TCCCCCTGCC TCCAGAGTGC TAACAGGAAA ACAGACACTG CTGTGTCATG 300
CTGGTGGGGG TATAAATTAG CATGAGTGTC TCCAGGGGGC AATGTAGCAA TTTCTACAAA 360
GCAACTGACA TACTCCCATA CCAGCTGACC CAGAAATTCC AGTTTTAAGT GGTTATCCCA 420
CAGATATATG CAATCTTCAG CACAAAGATG TACAGATAGG GATGTTTACT ACATACAGCC 480
CTACTGGTCA TAGCAAAAGA TACGAGACAA CCTATAAGGT CCTTGACAGG ATACCTGTTA 540
ACTGAGTTAT GGTGCACCCC ATGCAGCAGG ACCGTGCACC CATAAACACA TGGAGCAGAT 600
CTCCATACGA CTCTGTGGTG GCCTGGCTGT ACGAAAGGCC ATGTCTTCAC GTTTCCTGAA 660
TCCCATGCTC TGTGGCCTCT TGCACTGTCC CTGGGCTTGA CCCCAGGGCT TGCTCTGACT 720
GATGGAACAG TGGAAATGTT AATGCACGCA GAGGCTTAGA AAAGGGCTTA CGCACTTTTT 780
CCCTCTTGCT TCTCTGTGAC CGCCACGAGA ACGTGCCTAG GCCAGCCCAT ACCTAGCCCA 840
GGCCAACCTG CTGAACGATA AAAGGCCACG TGGCGCAGAG CTGAGCTGTC TAGGCAAGAC 900
TCCATAAGCG TAAGAGAGCC CAGCCAAGAG CAGCAAAGTC ACCGGGCTGA CCCATAGCAG 960
GCCACTGATG GATGAGCGAG CCCTGGCAAG CCCAGAATCA TGAGAAATAA TAAAAGGTGA 1020
TTGCTTTAAG GCACTAAGCT TTGGGATGGT TTGTTATGCA GTAATAGCTG ACAATCACAA 1080
AGATAGCTGA AAAAAGCAAG ACACAAAAGA GGGTATATAG TCACTATTGT GTGTAAAAAA 1140
CAATAGGCCG GACTAGGTGG CTCACACCTG TAATCCCAAC ACTCGCCTGA GGTCAAGAGT 1200
TCGAGACCAG 1210
|
