| Tag | Content |
|---|
EnhancerAtlas ID | HS047-26164 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr4:139948940-139949960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr4:139949781-139949793 | TGCCCTGAGGCA | - | 6.18 |
| | | 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 |
| GH04I139027 | chr4 | 139948913 | 139950002 |
| Enhancer Sequence | CGCGCCTGGC CTATTTATGA ACATTAAAAT TTGAATTTCA TATCATTTTC ACATGTCATG 60
AAATATTACT GTTCTTAAGG TTCCCCCCCT CCCCCTACCA TTTAAAAATA TAAAAGCCTT 120
TCTTAGCTTG CAGGCAGCAC AAAGACAGGA TGCTGCCAGA GTTAGCTCAT GGGTCACAGT 180
CGGTAGATCC CTGATCTAGA GAGGACTCTG TACAGTCAGC AGAAGGCGCC TTATAGTTTC 240
ATATTTCCAC TCACACTGTA AAAACACGTC ATTTTTCCAA GTGTCCCAGA AATGTTAGTG 300
ATGGGAGATC ACCAGATTTT TAGGTTTTGC TTTTTCACAT TTTTATTTCA GAGGATTGTG 360
CTAGAAAAGC CCAGCTTGTG GAAATGATTT GTCAGCCAAT AGACAATTGA GCACCAGTCG 420
AACATGTTAA ACTAAGCATT TATCATGGAG GGGATTCCCT TCTCTTTAGA GAGCTTTTCC 480
ATATGAGTCT GTCCTGGCTG AAGGTATGGT TCAGTCTTGT CTGGATGACG CTTCAGCTTT 540
CTTGTCTGGT CTGTGACTGC CACCTGGCAA AGAGAGGTTG TTTGGATTGT CACACTCAGT 600
CTAGGTGCTT GTATTTTTAG ACACGTTAGG TTGAGAGTTC TGACCTTCAC TTGATATCTC 660
TGGTAATGCC AAGCGGGTCG TGGCACTGCT TTGTACACTC TGTGCTGTGG CAGTGTGTGT 720
GTGCTGTGAC GACAGTGACG TCGACAGATG GAGGAGGTGC AACTCGACCT CTGTTTCTTT 780
CTGGCCTGAA GAATGGGCTG CTGTGTGCGC CTGGGGCTAG GCAGGACAGC TGCATCGCTG 840
TTGCCCTGAG GCAGTATCAG CACAGCTGGA GATGCTGACG AGCAGCAGTC CAAGGTGCAG 900
GTAACTTTCT CCAGGGCCAG CCCCCTTACT AGTTGTTCAA TCTAGAGAAA GCTGTGCAGA 960
TACCCACTTC ACCAGATTTG GGACAGAATA ATGAAAATAC ATGGAAGCAG TCTGGCACAT 1020
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