| Tag | Content |
|---|
EnhancerAtlas ID | HS146-13513 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr7:66017230-66018450 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF3 | MA0522.2 | chr7:66018210-66018220 | AACACCTGCT | + | 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 |
| GH07I066551 | chr7 | 66016274 | 66018466 |
|
Enhancer Sequence | TCCAAAAAAA AAAGATTAGC CGGGGTTGGT AGTGGGCGCC TGTAATCTCA GCCACTCAGG 60
AGGCTGAGGC AGGAGAATCA GTTGAACCCA GGAAGTGGAG GTTGCAATGA GCCGAGATCA 120
TGCTACTCTA CTCCAGCCTG GGGAACAAAG CCAGGCTCTG TCTCAAAAAA AAAAAAAAAA 180
AAAAAAGAGC AAACAAAAAA CAAAAAACAT GGCAGAGACA CAGAAGGCCA CATAAATGCC 240
TCAGGAAGAT TTGGGACAGA TGCCCAGAGG GTGGGCACTG TCACCCACAT CCACCACTCC 300
CTCCAATATG GCCATCTCTC ATGGTGACTC AAGGATGGCC ACAGCCCATG GACCAGTCTG 360
AGACAGAGGG TGGGGCAGCA TCTGACTTCT TTTTCATGTT GAATATCCCA CAAAAATCCC 420
TCTGACTCAT AGCCTGGGCT CCTCCTGCCT CCAGGGTCTT CTCTTTCCCA GGGTCTCTAT 480
GCCACATCAC AGACACCTAG TTTCTGACTT TTCTCCACCA ATTGAAGAGA CATTTGCCCC 540
GTGGACCGAG CCTGCCCTTA CTCTGTGTCA TTAAGACCCT TCTGGTGGGC TGAGTGCAGT 600
GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCTGAAGC AGGAGAATTC TTTGAGCCCA 660
GGAGTTCAAG ACCAGACTGG GCAACATAGA CTCCGTCTCT ACAAAAAATT AGCCAGGCAG 720
GGTGGTGTGC ACCTGTAGTC CCAGCTACTC AGGAGGCTGA GGCAGGAGGA TCGCTTGAGC 780
TTGGGAGATG GAGGCTGCAG TGAGCCAAGA CCACACCACT GCACCCCAGC ATGGGTGACA 840
GAGTGAGACC GTGTCTCAAA AAAGACAAAA AAAGCCCTTC TTTATCGGGC TGGGCGAGGT 900
TTCCATGCAG TAACCCATCC AATCAGGATG TGCTGCTCAA AGTCTTACAT CTTCACCTCA 960
AGGAAATTCA GCAACCGCAA AACACCTGCT GACTCCTGCC GAGATCCCGC CACTGCACTA 1020
CAGCCTGGGT GACAGAGCTA GACTCCGTCT CCAAAAAAAA GCATTCTTTT TTTTTTTTTT 1080
TAAAGAAATG ATCAATTAAA AAACCTTTAA TGCTCAGTTT TCACAAACAC AATCAAGTCT 1140
ATCAAATTTC CGGATTTACA GCAAAATGTG CCAGCTAAAA AGGTGTACAT TCTTCAGTTT 1200
CTCCTATACT TTTTTTTTTT 1220
|
