| Tag | Content |
|---|
EnhancerAtlas ID | HS049-07411 | Organism | Homo sapiens | Tissue/cell | Fetal_spinal_cord | Coordinate | chr8:101669600-101671200 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr8:101669697-101669718 | AAAGAAAAAAAGAAAGAAAGA | - | 6.34 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACCTGGAAGG CAGAGGTTGC GGTGAGCCAA GATCGCGCCA TTGTGCTCCA GCCTGGGCAA 60
CAAGAGCAAA ACTCCAACTC AAAAAAAAAA AAAGAAAAAA GAAAAAAAGA AAGAAAGAAA 120
AGGGAGGGAA GGGAGCCCCG AGGCTGCCTC TGGGTTTGGG TGGAACAGGC TTGCTGGCCA 180
AGGAGACCTC ATTTGGGGAG GCAGCAGGTA TACCTGTGGA GTCCAGACTG TGCTTGGATG 240
TGTGGGAAGG AGGTCCAGCT GGAGGGCTTG GGAGCCAGTC TGAAGTGGAG GGACAAGATG 300
GGGATTGGGA ATACAGGTGA AGATCAGGGT CACGGGAGAT GGTGCAGTCA CCTGGTGAAG 360
GTCCAGAGGT GAAGAATGAA GTGGACTACT TGGGAGGCTG AGGCAGGAGA ATCCCTTGAA 420
CCTGGGAGGC AGAGGTTGCA GTAAGCCAAG ATCGCCCCAC TGCATTCCAG CCTGGGTGAC 480
AAAGGTAGAC TCCATCTCAA AAGAAAACAA AAAAACAAAA AATAACAACA ACAACAACAA 540
CAACAACAAA CAACTAAAAA AATTGGTCAC CACCTGTGAT TTGTTACCAC TGTGAAAAAT 600
CACAGATCCT TGGCATTTTG TTTAGACCTC GGCAGGTCAG TTCAGCCCAG CCTGGACTGA 660
CCATGGGAAT CATCTGGGAA GCTTTAAAAA AATGCTGATG TCCGGGTCCC ACCTTCAGGG 720
ATCCTGATTT AATTGTTTTT TGGAGGATAG CCTGGGCATC GGGATGCTAA TGCTCCCGAA 780
GTGTGAAAAC TACTGGCGAG TGAGTAAAAC CCACTGTGGT CAGAGCCCCT CACAGCTCTG 840
AAGATTCTAA AGGCTGCAAT TTTGGCTCAG CTTGCTGTCT AGGAGATGGA GGCTACTGTT 900
GGAAAAATGC CTCCCTGGGA AGCTACGTTA GAATCTCATC CAAGCAGCTT GCAGGGGCAA 960
AACTGCAGTG AAACATTGCC TGAGATTTTA TTCAAAGTCT TTTTCATTCA TGTGCAGAAT 1020
GAAAGTTCAT TTCTTGTGCT GCTAGAAACC TACTGAGCGA CAGTGAGTGG ATGCTCAAAT 1080
GCTGCTGCAG AGGCATTAGC CAGTATTTAA GAGCATAGTT TACATGTAGT GGGTACTTCC 1140
CATGTGTCAG ACACTACTCA GGGCACTTTA CAATATTACT TCACTTGATC CACACAACAA 1200
CCCTATGAAA TAGGTACTAC TGTTTGCACT TTACTGATAA GGAAACTGAG ATCAGAGAGG 1260
TTAAGCATCT TGCCCAAAGT TGCACAGCTG GTAAGTCCCA CAGCCAGGAT TTGAAACTCG 1320
AGTGCCCAGG CTCTGCAGTG ATCTGTGGGA CACTAGGACC ACAGTGGGGC ATGGCCAGTG 1380
TGGACTTTGT GTAAGCACAC ACGAGATGCT TCCGGGATCA CCATACTTTC AAGAGGTTCT 1440
TTGCGATGAG TCGAGGTCTT GGTTAGGGGT GAACCAATGA CTGCTGTTTG ATCACTCCTG 1500
GTGGGACCTA CTCTGTGCCC ACTGGCTGCT AGGCTTGGCG GAATTCAAAT TTGAATACAG 1560
TTGTTTCCAA CTGCATTGTA CAGGTGGAAA ATATGTTGAT 1600
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