| Tag | Content |
|---|
EnhancerAtlas ID | HS146-00458 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:44251810-44253020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:44252908-44252921 | AGGAACAGCTGGA | - | 6.09 | | Nr2f6(var.2) | MA0728.1 | chr1:44252069-44252084 | TGACCTTCTGACTTC | - | 6.06 | | RARA | MA0729.1 | chr1:44252066-44252084 | CACTGACCTTCTGACTTC | - | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 44252293 | 44252991 | | chr1 | 44252663 | 44252939 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043786 | chr1 | 44251760 | 44253553 |
|
Enhancer Sequence | CTCTCTCCCC TAATCTACCT TTTACTCAGT TGCCAGAATA ATCAATTTAG TTCCCACATA 60
ATGGCCCAAG TTTATATTTA AAAATATAAA TCCGACTCTG TTACTCCCGG GGTTTTAAGC 120
AGGGCTTCTC ATTGCTAATG AAATAGAACA CAGACATCTT TCTGCGGCCT GTACACCCTC 180
CTGCAGATGC GGCTCCTGTC TTCCTCTCTG ACCTCGTTTT CCCACCTCCT GCTTTCTGTG 240
CTCTGTGCGC CAGCAACACT GACCTTCTGA CTTCTTCTTT AGATGTAGCA GGGCTGCTGC 300
GCTTGCTTTT CCTTCCGCCT GGAACTCTTT CTCTTGATCT TTTCTTAGCT TGCTTCTGTC 360
TCCAGGTCTC AGCCTGGGTG CCACCTCCTC AGAGAAGCCT TCCTGAAACA CCCTGTCTAA 420
CACTGCCTGT ACCTCTACCC TTGGTCTCCG TTACATGCTT TAATATTCTT CGTACTGCTT 480
ATCACTGTTC AGTATTTTGT TCATTTCATT TGTTTGGTTG TTTTGTATCT CCCTGACTAA 540
AACAAAAATT CCTTGAGAAT AAGAACATTT TTGTTCTTAC TCACCACTGT ATTTTCAAGC 600
CTAGTGTGTC GTAGTTTCTC AGTAAACATC TGTTAAACTG ATAAACAGTG AAATCTCCCT 660
TGTTACTGTT TTTCCCACGG CTGTGTCTTG TGTTTAGCTT TATATGTATT TTTATTTTAC 720
CTGTTAGGTT GTGAGCTACT TGAGGGAACA ATTTTCTTTT AGTTCATTTT TACGTCTCTC 780
AGGCTTACAC ATGGTAATTG GCTGAAGATA AGTATACCCC AAAAGGTAGC TCATTTGCTG 840
CATAATTTGT GCTCTGGAAA CTTGTCCAAT GGCAGAAAGA CTGAGCCCTA TTCTTCTTCA 900
TACTCCCTTT AGATTCCTTT TATTCCACTT CGGAAACCAG ACACAGGAAA CATCTGACTA 960
TAATAAAAGA TTGCCAGTAA ATTCTAGGTT TCCTCATTGA ACAAAGTCAT GTGCAGCAAG 1020
GCTGTGCTGT ACTTTGGTCT GGAATTCAGT TTGGTCACTT GTATGGCAGG CCACATGGCT 1080
GCCTCTGGCC TGGGAGCCAG GAACAGCTGG AGCCTGGGAT GACTGAAGTA AAAATGACAT 1140
ATTTGCTAGC CTGAGAGGGA GAAGTCTGGA TATTCTTGCT CTGTTCCTTG CAAAGCAAAC 1200
TTCTCAATTT 1210
|
