| Tag | Content |
|---|
EnhancerAtlas ID | HS050-44235 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr22:24026220-24027400 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF3 | MA0522.2 | chr22:24026776-24026786 | AACACCTGCT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 24026350 | 24026475 | | chr22 | 24026861 | 24027259 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I023684 | chr22 | 24026783 | 24029423 |
| Enhancer Sequence | GTTGATTCTA AAAGGGGCTG GGCTCGCTTT TCTCCCTGCT GCAGTCATTA CTCGTTTCCC 60
CTGGCAGAGG CAGCCGGGTG GAGGCTCATC TCTTCAAGCA GCTGGGAGAG ACACCCCACT 120
ACCCACCCTG CAGCTGCTCC AAGGATACTG GAGACAAAAA GACAGGGGCT GGGGAAGCAA 180
GATGTTCCTG CCTCGACCAA GACAGCAATT GGCCAAATGC CCTGACCCTG CTGGCATGGT 240
TACCGCAGGC CAGGCAGGCA TATTCAGGGC TCAGGATCCC TCTGCCTGAC TTTTCAAATG 300
GGCTGTTCTC AGTGACTCTG GCCCCCTCCC ACCCTGGGCT CACTCTTGAG AAACTCCTAA 360
GCCTTCTCTG GCCCTTCAGG GGCCTTAACG CTTATGTGTA GGACCAGGAT GCTCTGAGTG 420
ACCTACTTGG TCAATGGGCT GCTACAGCAG AGCTGTTGGG GAAGGCAGAG AGAAAAAGGA 480
CAATGACAGA CAAAGAACCA CTCAACACCT CAGAGACCAG CTTTGTCCCC CACCCAACCG 540
CCTTGCTCCC CACATGAACA CCTGCTTGCA GGAAGCCAAA GTGGGTCCAC AGCAGCCCAC 600
CTCTGTTCTC ACTCCCAGGG CAGACAAAGC AGCAAGAACA GGTGACACAC AGCCCCGGTG 660
ACCCTGTCCC CTCCCTACCC GTGCCTACTC TCCCATCAAA CCTGGCTTCG AGGGCTGCCC 720
GCCAGTCCTG TCCAGGCCTT ATCTGGCTCA GAGCAGATGA TCCCCTGCAC CTCCCACCCT 780
GAATCACACA GCTACACCCA GCACATGCTA CAGAGGCCCA GCACACTCTG GATCACATCC 840
AGAAACTCCA CAATAGGGGA GGAGACATGC TGTTTCCCAG GAAGGGCAGC TCCCCAGACT 900
TGGTCATTCT CAGACTCCTC CAGTCAAAGG CCGGGCACAG CCAGCTGGGA TCGCCATGCT 960
TCACTCTGAC CCACACGACT GGCCTTGCCT CCTCTATGGG AAGAGACCCC TCAGCACAAC 1020
CTCAAACCGA GACATAACAG GACAGGACAG GCTGGATGCT AGAGAGGCCA GCCAGATCTC 1080
CACACAAAGG CTCTGCTCTT AAGCAGGAGG TAGCCTGAGG GTCAAAGGTT TCCTGAAGCA 1140
ACTCAGGTGA GACCTCACAT ACAAGAGCCC CAAAGAGGCT 1180
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