| Tag | Content |
|---|
EnhancerAtlas ID | HS048-38471 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chrX:9834510-9835650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chrX:9835496-9835510 | AACTTCCTCATTTG | - | 6.2 |
| | | 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 |
| GH0XI009865 | chrX | 9833709 | 9836165 |
| Enhancer Sequence | GTGATTTTCC AAATCCCTCA AGCTGAAAAC CCTGCGGCAG GTGACATGTC CAGATCTTCC 60
TTCCCAGCCT CTGGAGTTGG TGCATTACTC CCGTGATTTT TCTCTGCCTC TTACCCCAGG 120
AGTTCTGCAG AGATGTAGGG GTAGTGCCCA TCAGGGTCGT TGTCCTTGTC GTTTTATTCT 180
TATTGCCAAA TAAATTCATT TGTGTGTGAC TATAAGACGA GTCTTCCAGA AGCAGCTGCT 240
GTAGTGATGA GTTCACTCCT CCACTGCCAT GGCTGCCTTC GCTGGGCCCC CACTGCCTGC 300
AGGACAGCGT CCAGATTCCC ATTCCAGGGC GGGGTCCTCG TCTTCCCCCA CTTCGGCCCT 360
ATCTTCAGAC ACTCCCCTGC ACACACACTC ATGCCTCAGG CCTCCTGCCT CCACGCCCTT 420
CTTCACGGGG AAGCCTCTGC GGAAGGCCTT CCCAGCTTTT TCTAGTTGCC GTTTCTATTT 480
GGAGGCCTTC TTATCTCCAC CCGAGACAGA GGGTCACATC CCCCTCATGC TGCCACTGCA 540
GGGACCCCAT TCTTTTCAGC GTGAGCCTGC TCCCCCGCTG CACTCAGGAT GCCCTTGCCC 600
TTATGGGACT TCATTTGGAT TGTCTCTTCA ACGAAGTATC AACAACTTTG TTCCATAAAA 660
GACTTTGATT AACTGTTTTT TTCCTGCTGT TCCTAGAGAA AACATTTCCA TGAGAACAAT 720
GAGGCATTCT GCACGTTAGG AGACGTTGAA CTCTAATCGG GGCCATAAGA GTGAGTTTCC 780
ACACAGAATA TCAGTTAATA ACTAAAACAA CAGTATTTGC CCGGGTGTGT GGACTTGGTG 840
CTTTGGGTCT GTGAGTGCCC ATAGCATGGC ACCTGGGCCG GCATCGTCAT GGGTCGGGGA 900
TGATTGACTT CCTAGCTTTT TGTAGAGGGG CTTTTTGAGG TTAGAGCAAG TGAGAGCAAA 960
GATTTTTCCT AAGTACTACA GGACAGAACT TCCTCATTTG TGGCTCTGGC ACTCCACAGA 1020
CATTAAGCGG CTGTCACTAA TCGGTGCAGT GCCAAGTGCT TCCTTACCTT GTAGACCTGG 1080
GACTGTGACA AAATGAGCAT CATTGTGATG CTATCACGCA TGCGGCACCT TCCCTAAGGT 1140
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