| Tag | Content |
|---|
EnhancerAtlas ID | HS092-30184 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr4:57802820-57804020 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr4:57803453-57803463 | CTCAAGTGGT | - | 6.02 |
|
| | 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 |
| GH04I056936 | chr4 | 57803021 | 57804280 |
|
Enhancer Sequence | CTAGTAGAGA CGGGGTTTCA CCACGTTGGC CAGGATGGTA TCGATCTCCT GACCTCCTGA 60
TCCACCCGCC TCAGCCTCCC AAAGTGCTGG GATTACAGGC ATGAGCTACC GTGCCCGGCT 120
GTTTTTTATA AAATGAGACG GAGTTCTGTG TTGCCCAGGG TGGACTCAGA TGATCCTCCC 180
ACCTCAGTCT CCCTAAATGC TGGGATTACA GATGTGAGCC ACCATGCCTG GCCTGTGTGT 240
TTTTTTTTTT TTCTTCTCCC AGACGGAGTC TTGCTCTGTC GCCCAGACTG GAGTGCCATG 300
TCATGATCTC CTTTCACTGC AACCTCGGCC TCCAGGTTCA AGCGATTCTC CTGCCTCAGC 360
CTCCTGAGTA ACTGGGATTA CAGGTGTCCG CCACAACACC CAGCTAATTT TTGTATTTTA 420
GTAGAGATGG GGTTTCACCA TGTGGCCCAG GCTGGTCTCG AACTCCTGAG CTGAAGTATT 480
CCTCCGACTT TGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACCA CGCCCAGCCT 540
GTTGTTTTTT TGTTTTGAGA AACGGTCTTA CTCTGTCTCC CAGGCTGGAG TGTGGTGGCA 600
TGATCACAGT TCCTGCAGCC TTGAACTCCT GGGCTCAAGT GGTCTTCTTG CCTCAGCCTC 660
CTGAGTAGCT GGGACTACAG ACCTACCCCA CCACGCCTCT TGCCGCCTCC TCTCAAAAGC 720
GTTCGTATTA TAGGCATGAG CCATCATGCC TTGCCACATT TTGTTTTGAT GCAGTGTCAG 780
ATCTGGAAGA TTCTGAGTCA GGAGAATGGT ATTTCATATT TGGATTGGTG AGTTATTCAC 840
CCTCTTCCCA CTTCCTGCAA AACTCCTTAT CAGCAACAAA GCAAAATTAA CTTTTTTTTC 900
CTCTGAGACA GGGTCTTGCT CTGTTGTCCG GGCCGTAGTG CAGTGGCACC ATCATGGCTC 960
ACTTCTGCCT CAACCTTCTG GACTCAAGCA AACCTCCCAC CTCAGCCTCT TGGAGTAGCT 1020
GGAACTACAG GTGCATGCCA CACACCCAGC TAGTTTTTTT CTTTCTTCTT TTTTTTCTAT 1080
TGACAGGGTT TTGCCTTGCT CCCCAGGATG GTCTTGAACT CTTGGACTCA GGCAGTTCAC 1140
CTGCTTCGGC CTCCTAAAGT GCTGGGATTA CAGGCGTGAG CCACAATGCC CGACTACAAA 1200
|
