| Tag | Content |
|---|
EnhancerAtlas ID | HS034-14443 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:5045980-5047400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr19:5046496-5046509 | AGGAACAGCTGGT | - | 6.04 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_41729 | chr19:5045841-5049299 | LNCaP | | SE_65334 | chr19:5045698-5050618 | Pancreatic_islets |
|
| | 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 |
| GH19I005045 | chr19 | 5045762 | 5050235 |
|
Enhancer Sequence | TGTGTATTTT GGTTATCAGT TGTGACTTGC AAGTATTTTC TTTCTGACTG GGGCTTGTCT 60
TTCTCTTACG GATCCTGCCT GATTGTTTTC AAGTGAAAGT TCAGCCTCAG ACTCCAGTGC 120
ATGAGAGCCT CTGGGTTGGC TGGCCTGCAC TGCCTGCACT TGGCCTGTAG TGATGACCCG 180
GGAGGGACTC TGCAGCCGCA CGCAGGCTGT GCCAGCCCAG GCCGACCTGC CACAGGTGCC 240
AGGGGAAGCT TCAGGGCTTC CTTGCCATGT GTTTGCCATG CCTAGCCTAT GCACTAGCCT 300
ACTTTTACAG CGGGGGAAAC AGCCCACAGC AGAGAAGCGA CTTGCTGTGG TCCCAGGATG 360
AATTTGCGCC CAGCTCAGCC TGTGCCTGGG GCCTCCCTCT GCCCCATCTG GGTCTCATCA 420
CTGCCTCCCT CCTCACCTCT TCTGGGCTCC TGCCAGGGCT CACCTTGCAA AGGAACCGCT 480
GGTCTTGCCA AGTCTGAGGG CCGGTCGTGC AGGTGCAGGA ACAGCTGGTG GGGGGTGGAT 540
TCAGGCTGTG AGAGCAGCTC ACGTTCATGT GTGTCTGGGC TCCTCTCGGC CTCTCAGCAG 600
GCCATGAGCC TCTCCGGGGA CTGCAGTGAC TAATGTGTAT TTTATGAGCT CTTGGGACAG 660
GACGGGGTTT GTTTGCTTGT GGCATTAAGA ATAGATGTGC CTGGTGGGTG GGGATTCCGT 720
CCTTGTTTGC CTAGTTCTGA AAACTGTCTT CGTCTCCTCG GTCAGAAGCT GTGGAAGGGC 780
TGTCACTGGG CCTTGGCTCC GGTACCATCG CTGGGTTAGC CCCAAGTGGT GACTGTTTTT 840
CTCCTTCCGT GTCATTGACT TAGAGGCGTG TTAATTATGC ACTCCCAAAC TGCAGGCTTC 900
ACAACAAGGC CTCCACCCAG CAGGAAGCAC GCAGCTCAGT GGAATCTGAC AGGCCCTGCC 960
TGCCTGGTGC ACGCTGGCAT GTGCGATGGG GCCCTTCCTG GAAGGGCCAA GCTGGCGGTG 1020
AGCCCTTCAG AAAAGGTGTC TGGGCTGGGT ATGGCGGCTC ATGCCTGCAG CCCCAGCGCT 1080
TGGAGGGGCC AAAGTGGGAG GGACCATTGA GCCCAGGAGT TCGAGACCAG CCTGGGCAAC 1140
AGAGTGAGAC TTCATCTCTA CACAGAAAAA AGTAAAAATT AGCCAGGTGT GGTTTCTCAC 1200
GCCTATAGCC TATAGTCCCA GGTACTCAGG AGACTGAGGC TGGAGGATTA CCTGAGCCTG 1260
GGAGGTTGAG GCTGCAGTGA GCTATGATTC TGCCACTGCA CTCCAGCCTG GGCAAGAATC 1320
TCACACAGGT TAAGACCAGC CCCTGGTCTG CAGGGTATGA CCGGCCCCTG GGGGGGCCGC 1380
AGATACTGGG GTGGAGGAGG ATGGGCAGCG ACCCCTGGGA 1420
|
