| Tag | Content |
|---|
EnhancerAtlas ID | HS050-35598 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:23658800-23660310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr2:23659414-23659425 | GATGAGTCACA | - | 6.14 | | JUND | MA0491.1 | chr2:23659414-23659425 | GATGAGTCACA | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 23659175 | 23659400 | | chr2 | 23659400 | 23659711 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I023434 | chr2 | 23657200 | 23659800 |
|
Enhancer Sequence | CTGTTGTTTC CCTCCTGGCT CTTCCCTTCT TTGCTTTCAG CTGTCATTTC TCAGTCCTAG 60
AGCTTTCGAG ACCCTCATCC TCCGGCTATT TCTAATCTTC TGCCCCGGGC TTTTCAAATC 120
TCCAACTCCT CTTAAAGTAT ACAGCCTCTG TGATGGCTGT TTCCTTAACT TGTGGGTTTC 180
TTCTTGTTGC TTCCCCTTCT ATAGCTTTAT TGCAGATGAC TGAGCTTTCA GTGCATGGGG 240
ATGTTTCTGT ATTTCTTGCG TATTCCCCGC AGTGCCTAGA TGGTGCTGAG CATGTTGCTG 300
ATACTCAGTA AACATCCATG GATTTAAGAG AAGTAAATAG CCAATCAGCT TTGTGTGTGT 360
GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTCTCAGCAC CAGAGAAGTT 420
TACCTTCAGT TTCTCAAAAG CTGGAGTTGC AAAGCCATCT TTGAGAGCCA CATTTTTTTC 480
TCCCTCAAAA TATGGTCTTA ATTGTGTGGT GATAGCCACA GACACCGCCT GGAAGCCTTC 540
CTGTGCTTCA GGAGCAGAAT GACTCTCCTC ATTGTCTGTG GGTTTAGGCA CCGAGAGCTG 600
CACAGATAAA AGCAGATGAG TCACAGGTGT GGATCTGCTG GGCGGCTCTT GTCGTTAGCA 660
GTACAAAGCC ACAGGTGCGC ATTCAGCGCT GCGAAGCGGG AAGAGGAGCC CTGACGATTC 720
TGAGGGTCTC AGGTCAAGTT AGTTACGTGG GGACTTGAAA ATGCATTGGA GATGCAGCCT 780
GGCTTCCGCA GCCGTGGAGA AAATGAGAAT GATTTTTGCT ATTTGCTTTT GGGGCACCAT 840
TTAAGCCCAT GTCTTGCTAG GTCAACGTTT TCATGCCCAT AGCTATAAAT TAAAGAGATG 900
CCTTAGACTT GGGAGCTGTT TCTCTGACTA GAAGCTGCGT CTGTTTATTC CCTTGCAGTT 960
GCTAGGAGCA TTGCAGACCA GAAGGAAGGA AATGGAGGAT GAATGATTTT AAGCATATTT 1020
TCCAAGAGTA ATGAAACCGA AAACACAAAT TCCCACACAC CAGAAAGGAA CTGGTTTCCA 1080
TCCAGTGTAG AAAAAGCTCC TGGCAAGATC CAGACTCTCT GATAATCATT CCCCTTTGCT 1140
AGGGTTTAGC TGGGCCACCG GCTTGATTGA AAGCCCGGGT TCAGCGGAAT GTGTGGGCAA 1200
AGTGTACTAA GCAGGCCAAG TCTATGCAAA CCAGGATCTG AATCAGTTAT TTAAAACAAC 1260
AGACTTGGGT AAAATCAACA GTCATTCTAA TCTAGTTTAT CTGGGAGCAG CAGTTTATCT 1320
CACAGAACCT CATTTAGTTC CATGAAATTG AGATTGGTTT CTTGATCTAT GAGATTGCAA 1380
CTTGGTGTGG TATTGTGGCC TTCCATCATT TTAATGAGGT CCTTAATGAT ATAATCCCAC 1440
TCTTGGATGA GTTGAAGGTG GCATCCCTCT TGCTGGAGAG ACTAGGATGA AAGGCATTTT 1500
CTTTTACGTA 1510
|
