| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00342 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:7710820-7711630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr1:7711073-7711085 | AGGCACGTGGCC | - | 6.07 | | RFX1 | MA0509.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | + | 6.17 | | RFX1 | MA0509.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | - | 6.19 | | RFX2 | MA0600.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | + | 6.38 | | RFX2 | MA0600.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | - | 6.3 | | RFX5 | MA0510.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | - | 6.14 | | RFX5 | MA0510.2 | chr1:7711452-7711468 | AGTTACCATGGTGACC | + | 6.28 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAATGAGAGT TGAGTGGTGA GATCGGGAAA TTGAATAGTA TGTGGGTGTC TGGATATGAG 60
AAGTTAAATC TAATGAAAAT TTCATCCAGT TGAACCAAGA AATCAGAAAC AGGGCCTTTA 120
TTCCTGTCAA CAAGAATACA GTGAAAATTA AACCAACCCG GCTGCCATTT CCCATTGACC 180
TTGTCGCCAT GGAGACAGCC TTCTAGTGTC AACAACACCG AGGACTCCGA AGGGGCCTCA 240
TTCACTCCAG GAGAGGCACG TGGCCGCTCC CTCTCCCGTC CGCCTCCGGC ACGTGGTTCA 300
TAAGGAGAGC AGCCACACGT CCAGGGTTGC TGGAGAGCAA CCCAGCCTAT ACCAGCACCT 360
GGACAAATGA CCACAGCACC CTTTGTTGGC TCCCAAGGTG ACCTGGCTTG ACTAGTTAAA 420
TGGCCACCCT CTTTCTGGGT CTTTCTTGGG TGGCAGGGTA CCTAGGTGGG TGGACTGGAC 480
GAGCCCAGAT GGAGGAGGAG GACAGGGCCC CCCACAGCCC TCCAGAAAAG GACACTGCCC 540
CTCGTCCTTG CCACCTGCTC ATCACAGCAC CCAGAAATCT CTTCTCATGC AAAGGAAGGC 600
CAAGCGTCGA TTCCAGCAGG TGCCGCCTGT ACAGTTACCA TGGTGACCAA AGCTCCAGGT 660
GGCCTTGCCC TGTCATCCTT CCAAGAGTTA CTGCCCCACA GAGCAGAGGG GACAGGTAGC 720
TGGTTCTCAC CCGTTCCAGG AGCCACCAGG GGCTGAGGCA GACTTCTGGA GTTCTCTCTG 780
TCTCCTCGTC CAATTCCTTT CCAAAGTCTT 810
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