| Tag | Content |
|---|
EnhancerAtlas ID | HS050-38742 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:159058650-159059740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr2:159058748-159058761 | AAATTAATTAACG | + | 6.41 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 159058701 | 159059591 | | chr2 | 159058754 | 159059727 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I158202 | chr2 | 159059041 | 159059190 |
| Enhancer Sequence | AAAAAGGTGG GAGAGAAAGA AAAATATTGT CATTGTTCCA TATGAATTTT TTAAAGTGTT 60
CCATACACAT ACGCACAATC ACTTTCCCAC TTTGGGCAAA ATTAATTAAC GTATGTATCT 120
TGAGGAAAGA AGCTTATAAG TTTGCTCTGT TTTAGCAGAA GGGTCAGACC ATACATAAGG 180
CTCTGAGTGT TATACTGTGG AAGTGAATAG GCAGAAAGGA ATGCAATCAG ATGAGAATGG 240
TGTCTTTGGT TTAATAGAAT GTCAAGTTTT CTCAGCTTTC CTTCATTTCA GTTAAGTTTT 300
TCTAAAGGCG AGATAGAACC CAAGTATGTA AGAATATTTT GCTTTTAAGC AGCAATACTG 360
ATGTTCCCCG CTTCTTCCAC CATCCTGCTA GACCTGGGGT CAGTACACAT TTTGTGGAAA 420
CGGTGCCAAA TAATAAATAT TTCAGGCCTG CAGGCCATAC AGTCTCTGTT GGCATCTATT 480
CAACTCTGTC ACTGCAGCAC ACGAAAGCAG CCAGAGACAA ACAAAGAAGC TTGGCTCTGT 540
TCCAATAAAA CTTTACTTAT GGACACAGAA ATTTTAATTT CATATAATTT CTACACAACA 600
CAAATTCTTT TTTATCTTCT TTTTTTGACC ATTTAAACAT GCAAAAACAT ATTCTTAGCT 660
TGCAGGCAAT ACAAAAAACA GGCAGAGGGC CAGATATGGA CTAACCCAGA GAACAAAAGG 720
GAAAACTTAA AATTGAATCT TTGTGTTGGC TGCCCTTTAG CTGCCTAGCT TAACTTTGGT 780
GAAGGAAAGG GGCTCTCTTA GATGGTGTGA CAGGTCTGAG CAGCACTATA CTCTTAAGCC 840
ATTCAGCAGA GAGCAGGAGA GTCCTCTGAG ACCTCCAAGA TTAAAGAAGT CCATGAGCTG 900
CTGTAAGTAG GGAGGCTTGC TTCAAGTTTG TAATCAGTGT GATTGGAGTC ATAATGAAAG 960
TAATGGTAAC TGGAACCTTG GTCTGTTAGT CCAGCATCTA CTTAGAGTTG GAGAGCATTG 1020
TCTTATTTGC TCCCTTCTGC AAGTGAAGCC ACCTTACCCA CTGTCTGTGC CTTGAGGTCT 1080
TTACCTTGAC 1090
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