| Tag | Content |
|---|
EnhancerAtlas ID | HS050-35138 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:9293000-9294100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr2:9293608-9293622 | CCGCTTCCTGGAAA | - | 6.63 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH02I009152 | chr2 | 9292930 | 9293129 | | GH02I009153 | chr2 | 9293215 | 9294266 |
| Enhancer Sequence | CTCCTGACGA GTACAGGGAT GTCTTTTTCA GGGCATAATC TGAGCCCCAA ACAAGTCTAT 60
ATGAACTTTG CTTCTCTACG AGGCCAGGGG AGCAACACTC ACAGAACACC TCTCTGTGGA 120
CATGGCCTGA CCCCTGCGTT TTCCTTGTCA GCTCAATCCC CACATTCAGT CGTGATGAGC 180
GGCCTTTTGC AAATCCCCTA CGCACTCTGC TCTGCAGCAG CAATATGCAT ACACTGTGTA 240
ATTTAATCCT GTCGGGTGGA ACTGCCATCT CCATTTGCAG AAGAGGGCTT CAGGGATGCT 300
AAATCCGTTA TCCAATTGGA CTAAGAGTCA GACAGGGTTT TCTCTCCTCC CCGCCCGCCC 360
CGTCCCTGTC TTTGGGAAAG CAGCCCTGCC AGGTCCTGTT TCCTGTCCCC CCCCAATTCC 420
AACCCTCCCC CGGTGCAAGA GCCACCCACT TCCTCCAGGG AGGCATCCTC CACCCTCATG 480
CTGGGCTTTG GCAGTTTTAC GACTCCATCG GTGCTAAGAG TGCGTTTTAA TGAATGGACC 540
ATCGACAGCA ATTCATCAAT TAGTTAAAAG TTGGATCAGA TCAATTCTCC CATGGGGTTT 600
GGCTCCAACC GCTTCCTGGA AAGAATGCCG GCTGTGTTCT CCACTCCACC TCAGTCTCCA 660
CCCTACGGCT TCTGATCTGT CTGGTGCCAG TGTGAAATAA ATCTATCTAA AGCCAGAGAG 720
AAGAGATCCA TTTCATTTTG TTAAGCTGTG CTCTTTTGTA GGTCACTTTT AAAATCAACA 780
AGTCAAATGC TTTAAAATCA AGAAATAAAG CAATTTCATT CGCATAGTTT CCCATTGTGC 840
AACGCCTTGT TGTCCTAGAG AGGGAGAGGT GGAGATATTC AGAGTGCCAA GCTTGATGGA 900
TCAGATATGG GGCAGAGCGA CCATGTGGAA ATCACTCAGG AGGCAGGGTG CCAGCCGAAA 960
CCAGGGGTTC ATGAGGAGCC AGTAGCTTCT CCCAGATGCT TGGCCCATAA CTCATCACCA 1020
GGGCACACTG GCACCTGCTG GGGAGTAAAC AAAGTCCTGG GTGTTGAGTC CTTTTCTCTT 1080
GCTGGCTATT AATGGCCTTT 1100
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