| Tag | Content |
|---|
EnhancerAtlas ID | HS050-60652 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr6:157632850-157634260 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr6:157633874-157633887 | CCGCCCCCCCCAA | + | 6.54 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CGTGTCCAAC AAACAGCATT GTTCCATGTG AGCAGCCATC AATGCACTTG GCAAGAATAA 60
GGACTTGGAA CACGCTGGTG ATTATTTTTA ATTGGATGGG CCTCGTGGCT GTAACAAAAA 120
TCGATGTATT TCTGACGCGG CTGCGGATAC ACTGATCCAT CTTGGCCCTG CGGCGCTCCG 180
GCGGCCAAAG GAGGCCAGCA CTCCAGAGAG CAGCCCCCTT TTGGCTTTGG GGCCCTGAGG 240
ACCAGAGGCT CAGGGCTTCC CCGCAACAAG GCCACAGGAC CCCGCTGGTG GGAGGGCCGG 300
GGCCCCGCGC TGACCAGACC CAATAGAGGC CCCCATTGGG GGACAGGCCC CGCGGTGCGG 360
GAGAAAGTGG GTCTGGGGAA GGAGGGGGCT GTGCAGGGGG CCGCCTGCAC CCTCCGCTCC 420
GGCTGTGGGC TTGGAGGGTT TGCGTTTCAT GGAAAGTGCA GGCCTGCTAA GCATTTGCCA 480
CTTGCATCAG GAGTGACGAC CTGCCCACGC AGGACAGGGC CAGGCAGGGG GCTTATGAGC 540
CAGAGAGCCT TTTAATGCTT TCATTTCTGG CTGGAATCAC CATTGTGAAA TATTAAAACC 600
AAACAACAGA ACATGGCCTC CCTGGTGTAA TGAAAAGCAC GTGGCTCTTA TCCCTGCCGG 660
CAGCTGCCCA AGGTCTTTGA GGAGATGGGG TTGCTGTCTG GGGGAGACTG GGGTTTGTCT 720
TTCTTGCGGG GAGAGTGGGG GTTGTCTGTG AGCTAAACAG ATGAGACAAG TGTTCTATGG 780
AGCCAATTTT TTTAATGACG CATTGGGGGA AAAGAAAAGT AATCGGATAC CCACCCAAGG 840
CTTAAGGAAC CCTTGAACCT GGTTTAAAGG TTTTTCTCAA GAAAGACAAT AGCATGGCCA 900
CTCTTGTCTC CAGCAGTTCA TGGACAGGGT GAGGCCTCCA TGCCGCTCAC ATGGAACAAT 960
GCTGTTTGTT TAACACGGAC TCATTTTCAC AGCTGATCAG AGAGGACATT GTGAAGCACC 1020
GCCCCCGCCC CCCCCAACCG TCCCCAATCA GGAGAGGACC CCGAGTCTGG AAAGCGTTCC 1080
TCTCAGGAGT GGCCTGGGAG CAGGTAAGTG CCGCAGGCAG ATCCCGGGGT GCAGACAGCA 1140
AACCGCAGCA CCGTTGCTTC CACAGCTGCA GCGGGGAAGT GTTTTTATGC ACGCAGGAGC 1200
TCAGAGAGTG AGCAGCCACC ATCTCAGTGA TGTGTCTTTT GAAGATTTTT GGAAGCTGCT 1260
TCTAGACCAC AGTGCAGCCT CACTAGCAAT AAAAGGAGAA ATTCCCTGGA GCACCAGGAA 1320
TGCTACTGCC ATTCCCGTGA ACTGTGCCAC CTGCCACCCC CATGCCCTAA CTGAAAAGCT 1380
CCCCATTCAC ACTCAACAGA ATCAATAACA 1410
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