| Tag | Content |
|---|
EnhancerAtlas ID | HS104-17544 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr13:97761450-97762840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr13:97762690-97762704 | TAGTGACGTGGCAG | - | 6.43 | | CTCF | MA0139.1 | chr13:97762330-97762349 | CGTCCAGCAGAGGGCGGCA | + | 7.5 | | MEOX1 | MA0661.1 | chr13:97761920-97761930 | GCTAATTAAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_47388 | chr13:97760718-97770395 | Panc1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH13I097108 | chr13 | 97761065 | 97761530 | | GH13I097109 | chr13 | 97761796 | 97762830 |
|
Enhancer Sequence | CATCTCTCTC TCCTGGACCC TGATGAGCAT AGGATAAACA TGCTTAATTT GTAATATTCC 60
TTTCTCTGCA ACATAAATGA CGTATCTTGG GCAGGCAAGG CTGACCCTTT GATATATTTC 120
ACCCATGGTA GGATCTTTAA AACATGAAAG TTTGTTCAGA GACCACAGCT CTAAGCCTGT 180
AGATCATTTT GGAGAGGATG GAAGCCAGGT AGCCTTTGGC AGGGCCCCTG GCATGCTTGG 240
TGCTGTCTTG CTTGATGAGA AATGTGTGGT TCCACCGCCG GGGGTGGGCG GGGGGATTAT 300
CCAACAATTT ATTTCTACAC AACAACGGCA CATGAAAAAA AAAAAAAAAG GCTTGGCTCA 360
GAATGTGAGA GCTGAAATGA ACCTTCAGGG TCACCTCCAT CAACCCCTCT CTCCGCAAAC 420
AAAGAACACC AGGACCCCAC ACGGCTAAGT GGGTGGGTCC CGCTCCCATA GCTAATTAAC 480
GGCAGACTCA GGTATAGAAA CCTGGTATCT GTAATCAAAA TGGCCCTAAT TCAAAACCTG 540
GTCGGGCCAC TCAGTAAGCC ATGTTCCCCT CGGTAATTTA TCCAGTCCCC CCTGAGCCTC 600
ACTTTGCTCC GCCACAAAAC AAGAATGACC CTCCTTGCTT TTTAGGGCTC CTCTGCAGAT 660
TAAATTCATT AGCACCTCGA ACGTTGGAAA GACACAATAT TTTCTTGCCC TCCCCTCCTC 720
TTATCAGCTT GAATCGATGC GTCATGAACT CAGTGATTTC CTCTTCGCAA GCCTGCTCTG 780
GATGCAGTCT GGTGTTACAT AACCGGCTGG CTGAGGACGC AGGTCCCCTG GGCGCTGCCG 840
GCGCGCTGTG ACCAGACACG CGGGCGCGGG TGGGGGGTTC CGTCCAGCAG AGGGCGGCAA 900
AGGACGCCCG GCGCGGTCCC ACGGCCCTGC GGGCGAGCAG CAAGCTACTG CGTTCCCTTC 960
GGGAAGGCCT AATGAGCTCT TCCTGCACCG TGTTCTTTTC GGTAGAAGCA TTTTTCCTGC 1020
CTCACTTAAG TGAGTACACA GTGTTTTGGC AACTGCCATG TGTCCATATT TTTTTTTAGT 1080
TTTTGCTTTG TTTGGTTCTG GTTTACTTGA GGGGCGCTCA TGACATTTGC TAAGCATTTC 1140
CACGCTTATG GTCTTCTCGC AGTTTGATGT CTCCAGTGCC CCAAAAGGAG TCATTTTTAT 1200
TCCCAATTTA CAGATGATGA CGGCGATATT CAGATAAGTT TAGTGACGTG GCAGAAGCAG 1260
ATGCCCTTTC TAAACCAAGG AAGGGGCTGG GATGAGGAAG GGGAGGTATT TAATTTGACC 1320
GTTTCTGCCT CCTTCTGTCA GACATATTCG ACAGGATTTA TTCGGTGCTT GAGGTAAGTC 1380
AGGTACTTTT 1390
|
