| Tag | Content |
|---|
EnhancerAtlas ID | HS048-36663 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr8:145632890-145634390 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr8:145633983-145634001 | CCTTCCTTCACTCCTTTA | - | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr8:145634193-145634211 | GGTAGGAAGGGAGGCAGA | + | 6.32 | | Spz1 | MA0111.1 | chr8:145634213-145634224 | AGGGTAGCAGC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCTGTCTCT ATTAAAAATA CAAAAAAAAA ATTAGCCGGG CGTGGTGTCA CACACCTGTA 60
ATCCCAGCTA CTTGGTGGAG GGTTTAGGGA GCTGAGGCAC AAGAATTGCC TGAACCCACG 120
AGGCGGAGGT TAAAGTTAGC TGAGATCACA CCACTTCATT CCAGCCTGAG TGACACAGCA 180
AGACTCCGTC TCACCAGGAA AAACAAAAAA AAAAATTATT TGTAGAGATG GGGTCTTGCT 240
ATGTTGCTCA GGCCAGTCCT GAACTCCTGG CCTCAAGCAG TCATCCCACT TCAGCCTCCC 300
AAAGTGTGGG ACTATAGGTG TGAGCCAGTG CACCCAGCCT GAGATTCGGT TACAGGACTC 360
GCCGTGGCTT CAGTCTTGGT GGGTGTCTCA TTGTGAGGGA GGCTGCCATG TTGTGAGCTG 420
CCCCAGGGAG GGGCCCATGT GGTGAGGAAC TGCGGCCTCC TGCCAATAGT GTGTTAGGAG 480
CAGAAACTCC AGCCCTCGTC AAGCCTTCAG AGGACAGGAG CCCTGGCCAG CAAATACATA 540
TGTATGCCGG GGTAGGTGCC CAGGAGGGTT GGCCTCCTTT GGCCTGAGCT TCTGACCCAT 600
CTGCCTGCTG GGTCAGCCCC TATTCACAAC CCTCTTGTGG CTCCTCCCTG CTTTGTGGAG 660
AATAGTCCTG ACCACGGCCT ACCTCCCTCC ATCCCCACCA CCACATCCAG TCTATACCAC 720
GGCCACACTG TGCATGTCTC TCCACCCTCA ACTGCTTTGG GCCTGTGCAC AGGCTGTTTC 780
TTCTGCCTGG AACACCCTCC TCTCACCATC CCTGGGCCTG GGTAAGAGGT ACTCCTCCCT 840
TCAAGAGCAA TGGAGAAACT GCCTCTTGCA AGTTGCTTTC CTGGACCAGC TTTCAACCCT 900
CCGGCAACCA AAACACCACT GTATTTCCCA AACCCTTGAG GCGTGTGCCC CACTGTACCA 960
AGACTCCTGT CAACAGTCTG TCCCCATCCT AGACCTGGCC TTGTTCCTTG TGCTACCAAT 1020
GTCCTTCCCC CGACAAACTC CCGCTCTGCC TCAGACAGGC TCTTCTGATC ATGCGACTGG 1080
AAATACACAG TCTCCTTCCT TCACTCCTTT ATTCCCGCAG CAGCACTTGC TGCAGGGGCA 1140
GGTGTGTTTA TTTAGATGTT CCCCTTCCCC AAGTGTCTGC AGGTGTGGTT CACATGGTAT 1200
CTCTGCTACC CAGCGCACAG TGGGCGTTCG CTCCTTCCGA ACAACTTGCT GAAAAAACGG 1260
AAGAGCAAAC AAGACGGCTA GGGCAGCGCG CCCTTCCCGG TGGGGTAGGA AGGGAGGCAG 1320
AACAGGGTAG CAGCTGTGAG AAAGGATCTG AGCACAAGAG ATTCAGGGTC ATGTCCTGGC 1380
TCCTCAGGCT GAGGAACGTT AAGCAAATCA CTCAACTTGT CTGGGGCTTG GCTCTTCCAT 1440
CTGCAACCGG GGGCGGTGAG AGCACCCACG TCGCGGACAG CGGGGAGGGC TCCCAGGGCC 1500
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