| Tag | Content |
|---|
EnhancerAtlas ID | HS050-02043 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:44251820-44253070 |
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 | TAATCTACCT TTTACTCAGT TGCCAGAATA ATCAATTTAG TTCCCACATA ATGGCCCAAG 60
TTTATATTTA AAAATATAAA TCCGACTCTG TTACTCCCGG GGTTTTAAGC AGGGCTTCTC 120
ATTGCTAATG AAATAGAACA CAGACATCTT TCTGCGGCCT GTACACCCTC CTGCAGATGC 180
GGCTCCTGTC TTCCTCTCTG ACCTCGTTTT CCCACCTCCT GCTTTCTGTG CTCTGTGCGC 240
CAGCAACACT GACCTTCTGA CTTCTTCTTT AGATGTAGCA GGGCTGCTGC GCTTGCTTTT 300
CCTTCCGCCT GGAACTCTTT CTCTTGATCT TTTCTTAGCT TGCTTCTGTC TCCAGGTCTC 360
AGCCTGGGTG CCACCTCCTC AGAGAAGCCT TCCTGAAACA CCCTGTCTAA CACTGCCTGT 420
ACCTCTACCC TTGGTCTCCG TTACATGCTT TAATATTCTT CGTACTGCTT ATCACTGTTC 480
AGTATTTTGT TCATTTCATT TGTTTGGTTG TTTTGTATCT CCCTGACTAA AACAAAAATT 540
CCTTGAGAAT AAGAACATTT TTGTTCTTAC TCACCACTGT ATTTTCAAGC CTAGTGTGTC 600
GTAGTTTCTC AGTAAACATC TGTTAAACTG ATAAACAGTG AAATCTCCCT TGTTACTGTT 660
TTTCCCACGG CTGTGTCTTG TGTTTAGCTT TATATGTATT TTTATTTTAC CTGTTAGGTT 720
GTGAGCTACT TGAGGGAACA ATTTTCTTTT AGTTCATTTT TACGTCTCTC AGGCTTACAC 780
ATGGTAATTG GCTGAAGATA AGTATACCCC AAAAGGTAGC TCATTTGCTG CATAATTTGT 840
GCTCTGGAAA CTTGTCCAAT GGCAGAAAGA CTGAGCCCTA TTCTTCTTCA TACTCCCTTT 900
AGATTCCTTT TATTCCACTT CGGAAACCAG ACACAGGAAA CATCTGACTA TAATAAAAGA 960
TTGCCAGTAA ATTCTAGGTT TCCTCATTGA ACAAAGTCAT GTGCAGCAAG GCTGTGCTGT 1020
ACTTTGGTCT GGAATTCAGT TTGGTCACTT GTATGGCAGG CCACATGGCT GCCTCTGGCC 1080
TGGGAGCCAG GAACAGCTGG AGCCTGGGAT GACTGAAGTA AAAATGACAT ATTTGCTAGC 1140
CTGAGAGGGA GAAGTCTGGA TATTCTTGCT CTGTTCCTTG CAAAGCAAAC TTCTCAATTT 1200
GTTGAATACT AAGTTTTCCC GTTAGCTGTC AAAGTGGTTT ATAACTAAAA 1250
|
