| Tag | Content |
|---|
EnhancerAtlas ID | HS003-23014 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr19:33634470-33635740 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EHF | MA0598.2 | chr19:33635191-33635203 | GACTTCCGGGTT | - | 6.14 | | ELF1 | MA0473.2 | chr19:33635191-33635203 | GACTTCCGGGTT | - | 6.74 | | ELF4 | MA0641.1 | chr19:33635191-33635203 | GACTTCCGGGTT | - | 6.18 | | Nr2f6(var.2) | MA0728.1 | chr19:33635324-33635339 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH19I033143 | chr19 | 33634739 | 33635506 |
|
Enhancer Sequence | GCCCAGGAGG CCAAGGGGTG CAGTGAGCCG TGTTCTTGCC ACTGCACTCC AGCCTGGGTG 60
ATAGAGCAAG ACCCTCTCTC AAAAAAAAAA AAAAAAAGTT TGGTAGTTTT TCTCATATTA 120
TTACAAAGGT AATATGATTT TATTACAGGA AACACATGAA AACACAAGAA AGAAAAAAAC 180
TCATCTTTCC ATGACCCCAA AGTTAACGGC TGTGAAAATG TTGTCATAGG TATTTTTTTC 240
TTCTCCACGA ACATCCACAT ACATTTATGA AACTGGGACT GTACCAAAAT ACTGATATGT 300
ACTCACCATA AACGTAGACG CCAAATATTG TCACATCTCC TTTATTTTCC AACTGTTTAT 360
TAGACCCCCT TTCCCTCGTT CATTTGAAGT CTAACCAGTA TTTCCCCTTT AAATTGTCTG 420
GGTCCACAGG GATGGGGTCG TGCTTCTAAA TGCCCAGTGT GGAGGGAGTG GGCCGATCTC 480
TGCACAGCCG CTGTTCCTGC TCTTGGCCAC TTGGTGTCAC TGTCGAGTCT AAAACTGCGC 540
AGCCCCACGG ACACTGATCA TTCTGGCGCT GCCCTCAGTT GGCCCCGGCC CGCCCAGAGT 600
GCGTGCAGGG GCCTGGATCC CACAACCCAA GACGATCATT TTCTTTTCTT TTTGAGACGG 660
TGTCTCGCTC TGTCGCCCAG GCTGGAATGA AGTGGCGCAA TCTTAGCTCA CTGAAACCTC 720
CGACTTCCGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCAT GAATAGCTGG GACTACAGGC 780
GCGCGCCACC ACACCCAGCT AATTTTCATA TTTTTAGTAG AGACGAGGTT TCACCATGTT 840
GGCCAGGCTG GTCTTGAACT CCTGACCTCA GGTGATCCAC CCACCTCGGC CTCCCAAAGT 900
GCTGGGATTA CAGTCGTGAG CCACCGCGCC CGGCCTGGAA GATATTGCTA GATTCTGCAA 960
AGACTTTTTG GCCAGTAGGA AAGGAAAACA CAATCTGTTT GCAGCTCTGC CCCCAGCATG 1020
GCCAGTTTCC ACCTGGTGTC TGGAATTGCG GGGTAATTTC CCATGGATGC CAGGAATGGC 1080
AAGGGTGTCC TTCCCGCTCA GGGGACGGAC ATGTTGCAAA GTCCTTTCCT CTTTCGGAGC 1140
TGAGTGAGAG TCCCAGGACC TTGGAGTTCT CAGATTTTGC TACCAGAGAT AAGCTAAGGG 1200
CTAATGTTGA CCTCGATTTA CGACTTCAGC AAACACGGCA GTGACCACTC TCTTCTCCTC 1260
TCTCTCCCGT 1270
|
