Tag | Content |
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EnhancerAtlas ID | HS048-03680 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:231622280-231623330 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NOTO | MA0710.1 | chr1:231622809-231622819 | GCTAATTAGC | + | 6.02 | NOTO | MA0710.1 | chr1:231622809-231622819 | GCTAATTAGC | - | 6.02 | OLIG2 | MA0678.1 | chr1:231623008-231623018 | ACCATATGGT | + | 6.02 | OLIG2 | MA0678.1 | chr1:231623008-231623018 | ACCATATGGT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I231486 | chr1 | 231622554 | 231623329 |
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Enhancer Sequence | AACAGAGTGA CACTCCATCT CAAAAGAAAA AAAAAAATCT CAAATTTTCA GAGTATAATG 60 TTCTTGGTTA GGTGGCTTTC CATGTGGTCA TTCAAGGACT CATACCCCTA GGACATTGTG 120 GCTCCCACCC TCCTCTAGGT CCTTGGTGTT CTCTCCATTC AGCTAGTAGA TTACAAGAGA 180 GAGAACACCT GGGAAATCGT GAAGGTATTT TTGTGGGCCA GTTCTAGCCG AGGTGTGCAT 240 CACTTCTTTG TATGCTATTA GACAGAACTT AGTCACAGGG CTTCCCTGAG ATGCAAAGGA 300 GCCTGGCTTA TGCAGTTTCT GGAGAGCGAA CCCCTTCTCA GCAATAGCTC CACACTACGG 360 AAGCAAGCAT GAGTCTACGG TGAACATTGT CATCTCTTCC ACAACCACCT TGGCTGCTTA 420 GCAACAATAT GGCTTGGGTA AAGTTTCTCA TCCCCTCTAA GCCTTAGTTT GGGATCTGCA 480 AAATGGGAAT ACAAATACAG TCTCAATGCT ACATATCTGT TTCTGCAAGG CTAATTAGCC 540 CATATGCAAT TGGTAAACAA GGATATGTTA TCCATGAACA CAGAAGTGGC ATTGGTTCAT 600 ATTTAAGTTT TCTCCTTACA GATTAACATT GTGTGTCACT GTATAATAGC AGCTGAATGC 660 AAAGTCCATG AACACAGATG AGTCAGCCAT GCATGCTTAC CCCACACGCT TCCTCTGGGC 720 TGAGTCCCAC CATATGGTCT GTCTTGCAAT TGCTTACTAC ATTGTTTCCC TGACTTTTGT 780 GCATTTTTAC CTGGTCTTCA TAACTCAGCA ACAGCAAACT TTCCTTATAT TCTCTTCTAT 840 TAAGCTGATT TAATTTTCAA CTTCTTTTAA AATAATTACA GGCTGACAGA AAAGTTTCAA 900 TAACAGTACA AAAAGTTCTA ATGTACTCTT CACCCAGGTT CCCTAAATGT TAACAGGTTA 960 CCACAATTGC TTTATCTTTA TCTGTCTATA TTGGTTTTTT TCTGAGTTAT TTGGATGATT 1020 TACATACATA ACATCCATTA ATCCCTAATC 1050
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