| Tag | Content |
|---|
EnhancerAtlas ID | HS050-71614 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chrX:39714080-39715560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFK | MA0496.2 | chrX:39715091-39715110 | GACTGATGAGTCATCAGAT | + | 6.06 | | NFE2L1 | MA0089.2 | chrX:39715092-39715107 | ACTGATGAGTCATCA | - | 6.02 | | RUNX1 | MA0002.2 | chrX:39714284-39714295 | GTCTGTGGTTT | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI039853 | chrX | 39712803 | 39715687 |
|
Enhancer Sequence | AGGTCATGAG GATGGAGCCC TCATGAAGGG GGTCAGTGCC CTTATAAAAA GCGACCCCAG 60
AGAGCTCTCT CTCCCTGTCT CTGCCATGTG AGGGCACAAG GAAAAGTTGG CAATCTACAG 120
CCCAGAAGAG GGCCCTCCCC CAAACCCGAC CGTGCTGGTA CCCTGATCTC GGCCTCTCAG 180
CCTCCAGAAC CATGAGAAGT ACGTGTCTGT GGTTTATCAG CCCCCCCGCG TGTGGTACCG 240
TGTTACAGCA GCCTGGATGG ACTAAGACCC TTCTGCAGAG GGACTTTGTC TGAAACTGGC 300
TTCCTCCCCT TCTTGGTCCT GCCCTTCCAT ACCCTTCCGT GTTTCTTGGG AGCACTTCCT 360
TAATAAATTG CTTCCACACG AATCCGCGTC TCAGAAGCTG CTTCTGAGAA AACCGAAGTG 420
ATGGGGCCCC TGGGCTGCAC AGTAATAACA GTTGTTACAG ACGGCACCTC CTCCAACCCT 480
CAGAACCAGA CGGCCACAAT GGTATTGACT GCATTGCACA GAGGAGGAAA CGGAAACCCA 540
GAGAGCAGAA GGGACTTGCC CAGGATGGTG GAGTTGGTGA GCAGAGCAGC CTACATTAAA 600
CCCAGCTCCA AAGCCAGCCC TGGGTCTTTG ATGCCCCACA GAAAATACAT GGGAGGAGCC 660
CTGCAGCTCC TGAAAGGAGC TAACATCTCC CAAGCCCCAC TTCCAGGGGC AATCTGGGGC 720
CAGCCAGGTA CTTAGATGGA CAGATGACCA AGGAGAGACC ACTCAAGCCC TCAGTTTGAG 780
AATGCATTCC TCTGCGTTCA CAGGCTTACC TGGAGCCAGT TCCCCAAAGC CCCACTGGAC 840
TTTTTAAGCC CCCAGAGGCC TTCAGACAGG AACCCACTGA GTCTTCAAAC CCCCAATCTC 900
CATGGGGTTA AAACAATCCC CAAAAGGCAG GACTTACTAG GAGTCGTTCA GAAACTGGCA 960
AAAGCACCCT CTGAATAAAT GTTCAGGGTT CCATCCGGAG ACGCCCACGG TGACTGATGA 1020
GTCATCAGAT AGCCAGCTGT CGCCACAGAG TGCTATATAT AGAAGCTGGA GGGGTGCCTG 1080
GTACCTAAAG AAAGGGGAGG AGCACACACC TAGTAGGTGG GGTCTCAGCT GGGAGGCAGG 1140
CCTAGAGCAC CTGGAAACTG CACCCTCAGC TCCCTCTGCC CCCCCAGCAA AACAGAATCT 1200
GGGTCAGCAA TTCCCCGGCA CAGAATGCCG CGTGAACTGG AAGCAAGCAG CAACAGGGCC 1260
GGACGTGGGC CATGCCAGTG CATTCATGAT GATTACTGCT AATGATGGTA ATGGGAGAAT 1320
AATGGCTCAG TGAACTTCCC GCACATCACC TCGTCGTCTT CCCATCAGAC ATACACACTG 1380
AGGACGCGCT TGTATTGCTG CCATTTAGAC AGCCGAAACA GAACTTCCAG ACCTCAGGCT 1440
TGGTAGGCTG GGCCTGTGCT GTCCAGGACA GGGGCCACTA 1480
|
