| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00839 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr1:24337950-24339070 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:24338820-24338841 | TTCTTCTTTCTTTTTTTTTTT | + | 6.26 |
| | | 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 |
| GH01I024011 | chr1 | 24337999 | 24339230 |
| Enhancer Sequence | ACGGGGTTTC ACCATGTTGG CCAAGCTGGT CTTGAACCCC TGATCTCAAG TGATCTGCCT 60
GCCTTAGCCT CCCAAAATGC TGGGATTACA AGCATGAGCC ATCACGTCCA GCCGATAATA 120
ATTACATTTC AAAGGGTGGC AGCATTAAAC CCATCTATCA TCTTGAATTG TCTCAAGACA 180
AAGACTTTTA AATTATGTGA GAAGAGGACT GGTAGAATAC AGAGGTAAAA GTAAGGTCTT 240
CAGACTTAAA AGCTCTATCT AAATAAGATC TTTTGATGTG GGTCATTCAT GAAACTAAAG 300
CAAACAGATG AAGCCTACTA AGATCTTGAA GGTTTGGATT GTCAAAGAGC CTGCCCCATT 360
CAGCCGTGTC ATTCAGCACA GCCCGTGACT GTTCGGCCCC AAGGCAGTTG ATGGTGCCTG 420
ATCTACATGG GCAGGAGAGG TCTGCTAAAG CTCTTCAGCC TCTAGGAATG GCCTTCCCCA 480
CAGTGCCCTC CCCAGATGCA GCCATGGGGA ATAGCAAGCA AGGAGAATCC TTCCAGAGAA 540
CAAAACTAAG GGCTGTAGAT TGACCAGCCA AGGAACTCTA CTGCAGGGAT AGCGAGTCCC 600
CACTACTCCT GCCCTGCAGG ACTGTACAAG TGCGATGGAC CAGAGACAGC TGAGTGTTTG 660
CCATGTTCTT TTTTTCCCAA AGGGAGTTTT TATTGCACTT ATCCTGTTGG GGAGAGATAA 720
ATTGTCTTTA AGCTTACAGA TCTCTAGTCA TGAGAAGCCA CATCCTGACC CTAATCCTCT 780
AGAGATCCTG GACTTTGAGC TGGATTTAGT AACTGGATGT AACTTTATTG CTGTATCCCT 840
TGGGGAGGGC CAAATGCATT TCCTTTTTCT TTCTTCTTTC TTTTTTTTTT TTTTTTTGAG 900
ACGGAGTCTT GCTCTGTCTC CCAGGATGGA GTGCAGTGGT GCGATCTCAG GTCACTACAA 960
CCTCCACCTC CCGGTTCAAG TGATTCTCCT GCCTCAGCCT CCTGAGTAGC TGAGATTACA 1020
GGCATGCGGC ACCATGCCTG GCTAATTTTT GTATTTTTAG TAGAAACGGG GTTTCACCAC 1080
GTTGGCCAGG CTGGTCTTGA GCTCCTGACC TCCAGTGATC 1120
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